1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function
artículo científico publicado en 2017
25-Hydroxyvitamin D and osteoarthritis: A meta-analysis including new data
artículo científico publicado en 2015
52 Genetic Loci Influencing Myocardial Mass
artículo científico publicado en 2016
A Combined Linkage and Exome Sequencing Analysis for Electrocardiogram Parameters in the Erasmus Rucphen Family Study
artículo científico publicado en 2016
A Comprehensive Evaluation of the Genetic Architecture of Sudden Cardiac Arrest
A Genome-Wide Association Study Identifies the Skin Color Genes IRF4, MC1R, ASIP, and BNC2 Influencing Facial Pigmented Spots
artículo científico publicado en 2015
A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure
artículo científico publicado en 2018
A Large-Scale Population-Based Analysis of Common Genetic Variation in the Thyroid Hormone Receptor Alpha Locus and Bone
scholarly article by Marco Medici et al published February 2012 in Thyroid
A Randomized Controlled Trial to Examine the Effect of 2-Year Vitamin B12 and Folic Acid Supplementation on Physical Performance, Strength, and Falling: Additional Findings from the B-PROOF Study
artículo científico publicado en 2015
A bone overgrowth disorder due to a gain-of-function mutation in the kinase homology domain of guanylyl cyclase B, the receptor for CNP.
artículo científico publicado en 2013
A catalog of genetic loci associated with kidney function from analyses of a million individuals
scientific article published on 31 May 2019
A child with a deletion in the monocarboxylate transporter 8 gene: 7-year follow-up and effects of thyroid hormone treatment
artículo científico publicado en 2011
A combined linkage, microarray and exome analysis suggests MAP3K11 as a candidate gene for left ventricular hypertrophy
artículo científico publicado en 2018
A common NOS1AP genetic polymorphism is associated with increased cardiovascular mortality in users of dihydropyridine calcium channel blockers
artículo científico publicado en 2008
A common polymorphism in the complement factor H gene is associated with increased risk of myocardial infarction: the Rotterdam Study
artículo científico publicado en 2006
A common polymorphism renders the luteinizing hormone receptor protein more active by improving signal peptide function and predicts adverse outcome in breast cancer patients.
artículo científico publicado en 2006
A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease
artículo científico publicado en 2015
A first update on mapping the human genetic architecture of COVID-19
artículo científico publicado en 2022
A functional anti-mullerian hormone gene polymorphism is associated with follicle number and androgen levels in polycystic ovary syndrome patients
artículo científico publicado en 2008
A functional polymorphism in the catechol-O-methyltransferase gene is associated with osteoarthritis-related pain
artículo científico publicado en 2009
A functional variant in the CFI gene confers a high risk of age-related macular degeneration
artículo científico publicado en 2013
A genetic deconstruction of neurocognitive traits in schizophrenia and bipolar disorder
artículo científico publicado en 2013
A genetic epidemiologic study of candidate genes involved in the optic nerve head morphology
artículo científico publicado en 2012
A genetic risk score based on direct associations with coronary heart disease improves coronary heart disease risk prediction in the Atherosclerosis Risk in Communities (ARIC), but not in the Rotterdam and Framingham Offspring, Studies
artículo científico publicado en 2012
A genetic risk score for thyroid peroxidase antibodies associates with clinical thyroid disease in community-based populations
artículo científico publicado en 2015
A genetic variant in the seed region of miR-4513 shows pleiotropic effects on lipid and glucose homeostasis, blood pressure, and coronary artery disease
artículo científico publicado en 2014
A genome wide association study links glutamate receptor pathway to sporadic Creutzfeldt-Jakob disease risk
artículo científico publicado en 2014
A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance
artículo científico publicado en 2012
A genome-wide association meta-analysis identifies new childhood obesity loci
artículo científico publicado en 2012
A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation
artículo científico publicado en 2012
A genome-wide association meta-analysis of plasma Aβ peptides concentrations in the elderly
artículo científico publicado en 2014
A genome-wide association search for type 2 diabetes genes in African Americans
artículo científico publicado en 2012
A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium
scientific article published on 05 May 2013
A genome-wide association study identifies LIPA as a susceptibility gene for coronary artery disease
artículo científico publicado en 2011
A genome-wide association study identifies a susceptibility locus for refractive errors and myopia at 15q14.
artículo científico publicado en 2010
A genome-wide association study identifies an osteoarthritis susceptibility locus on chromosome 7q22
scientific journal article
A genome-wide association study identifies five loci influencing facial morphology in Europeans
artículo científico publicado en 2012
A genome-wide association study identifies new loci for factor VII and implicates factor VII in ischemic stroke etiology
scientific article published on 14 January 2019
A genome-wide association study identifies nucleotide variants at SIGLEC5 and DEFA1A3 as risk loci for periodontitis
artículo científico publicado en 2017
A genome-wide association study identifies nucleotide variants at SIGLEC5 and DEFA1A3 as risk loci for periodontitis
artículo científico publicado en 2018
A genome-wide association study of acenocoumarol maintenance dosage.
artículo científico publicado en 2009
A genome-wide association study of corneal astigmatism: The CREAM Consortium
artículo científico publicado en 2018
A genome-wide association study of depressive symptoms
scientific journal article
A genome-wide association study of early menopause and the combined impact of identified variants
artículo científico publicado en 2013
A genome-wide association study of early-onset breast cancer identifies PFKM as a novel breast cancer gene and supports a common genetic spectrum for breast cancer at any age.
artículo científico publicado en 2014
A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation
artículo científico publicado en 2009
A genome-wide association study of optic disc parameters
artículo científico publicado en 2010
A genome-wide copy number association study of osteoporotic fractures points to the 6p25.1 locus.
artículo científico publicado en 2013
A genome-wide screen for depression in two independent Dutch populations
artículo científico publicado en 2010
A genome-wide screen for interactions reveals a new locus on 4p15 modifying the effect of waist-to-hip ratio on total cholesterol
artículo científico publicado en 2011
A haplotype block downstream of plasminogen is associated with chronic and aggressive periodontitis
artículo científico publicado en 2017
A high-quality human reference panel reveals the complexity and distribution of genomic structural variants
scientific article published on 06 October 2016
A large genome scan for rare CNVs in amyotrophic lateral sclerosis
artículo científico publicado en 2010
A large-scale association analysis of 68 thyroid hormone pathway genes with serum TSH and FT4 levels
article
A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration
artículo científico publicado en 2015
A meta-analysis of four genome-wide association studies of survival to age 90 years or older: the Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium
artículo científico publicado en 2010
A meta-analysis of gene expression signatures of blood pressure and hypertension
artículo científico publicado en 2015
A meta-analysis of genome-wide association studies identifies multiple longevity genes
scientific article published on 14 August 2019
A meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hip
artículo científico publicado en 2014
A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11.
artículo científico publicado en 2012
A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function
artículo científico publicado en 2013
A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure
scientific article published on 10 April 2019
A network of investigator networks in human genome epidemiology
artículo científico publicado en 2005
A new polymorphism in the type II deiodinase gene is associated with circulating thyroid hormone parameters.
artículo científico publicado en 2005
A novel common variant in DCST2 is associated with length in early life and height in adulthood
artículo científico publicado en 2014
A novel variant of FGFR3 causes proportionate short stature
artículo científico publicado en 2015
A pharmacogenetic analysis of determinants of hypertension and blood pressure response to angiotensin-converting enzyme inhibitor therapy in patients with vascular disease and healthy individuals
article
A polymorphism in the glucocorticoid receptor gene, which decreases sensitivity to glucocorticoids in vivo, is associated with low insulin and cholesterol levels
artículo científico publicado en 2002
A polymorphism in type I deiodinase is associated with circulating free insulin-like growth factor I levels and body composition in humans.
artículo científico publicado en 2004
A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape
artículo científico publicado en 2016
A road map for efficient and reliable human genome epidemiology
artículo científico publicado en 2006
A study of the SORL1 gene in Alzheimer's disease and cognitive function
artículo científico publicado en 2009
A systematic analysis highlights multiple long non-coding RNAs associated with cardiometabolic disorders.
artículo científico publicado en 2018
A trans-ancestral meta-analysis of genome-wide association studies reveals loci associated with childhood obesity
scientific article published on 01 October 2019
A variant in MCF2L is associated with osteoarthritis
artículo científico publicado en 2011
ABCB1 gene variants, digoxin and risk of sudden cardiac death in a general population
artículo científico publicado en 2015
ARHGEF12 influences the risk of glaucoma by increasing intraocular pressure
artículo científico publicado en 2015
Adiposity as a cause of cardiovascular disease: a Mendelian randomization study
artículo científico publicado en 2015
Adverse outcomes of frailty in the elderly: the Rotterdam Study
artículo científico publicado en 2014
Age- and sex-specific causal effects of adiposity on cardiovascular risk factors
artículo científico publicado en 2015
Age-related accrual of methylomic variability is linked to fundamental ageing mechanisms
artículo científico publicado en 2016
Alzheimer's disease genes and cognition in the nondemented general population
artículo científico publicado en 2012
An Epigenome-Wide Association Study (EWAS) of Obesity-Related Traits
An activating mutation in the kinase homology domain of the natriuretic peptide receptor-2 causes extremely tall stature without skeletal deformities
artículo científico publicado en 2013
An epigenome-wide association study meta-analysis of educational attainment.
artículo científico publicado en 2017
An integrative cross-omics analysis of DNA methylation sites of glucose and insulin homeostasis.
artículo científico publicado en 2019
Analysis of rare variants in the C3 gene in patients with age-related macular degeneration
artículo científico publicado en 2014
Androgen receptor gene CAG repeat polymorphism in longitudinal height and body composition in children and adolescents
artículo científico publicado en 2011
Annotation of loci from genome-wide association studies using tissue-specific quantitative interaction proteomics
artículo científico publicado en 2014
Anti-Müllerian hormone and anti-Müllerian hormone type II receptor polymorphisms are associated with follicular phase estradiol levels in normo-ovulatory women
article by Marlies E. Kevenaar et al published 2 March 2007 in Human Reproduction
ApoE gene polymorphisms, BMD, and fracture risk in elderly men and women: the Rotterdam study
artículo científico publicado en 2004
Are Bone Mineral Density and Fractures Related to the Incidence and Progression of Radiographic Osteoarthritis of the Knee, Hip, and Hand in Elderly Men and Women? The Rotterdam Study
artículo científico publicado en 2019
Arterial Stiffness and Decline in Kidney Function
artículo científico publicado en 2015
Assessment of Advanced Glycation End Products and Receptors and the Risk of Dementia
artículo científico publicado en 2021
Assessment of cumulative evidence on genetic associations: interim guidelines
artículo científico publicado en 2007
Assessment of gene-by-sex interaction effect on bone mineral density
artículo científico publicado en 2012
Assessment of osteoarthritis candidate genes in a meta-analysis of nine genome-wide association studies
artículo científico publicado en 2014
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
artículo científico publicado en 2010
Association analyses of 47,500 individuals identifies six fracture loci and 82 BMD loci clustering in biological pathways that regulate osteoblast and osteoclast activity
Association between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant data
artículo científico publicado en 2014
Association between an insulin-like growth factor I gene promoter polymorphism and bone mineral density in the elderly: the Rotterdam Study
artículo científico publicado en 2003
Association between biomarkers of tissue inflammation and progression of osteoarthritis: evidence from the Rotterdam study cohort
artículo científico publicado en 2016
Association between chromosome 9p21 variants and the ankle-brachial index identified by a meta-analysis of 21 genome-wide association studies
artículo científico publicado en 2011
Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe
artículo científico publicado en 2011
Association between mutations in a thyroid hormone transporter and severe X-linked psychomotor retardation
artículo científico publicado en 2004
Association between schizophrenia and common variation in neurocan (NCAN), a genetic risk factor for bipolar disorder
artículo científico publicado en 2012
Association of 5' estrogen receptor alpha gene polymorphisms with bone mineral density, vertebral bone area and fracture risk
artículo científico publicado en 2003
Association of BRCA2 K3326* With Small Cell Lung Cancer and Squamous Cell Cancer of the Skin
scientific article published on 01 September 2018
Association of Birth Weight With Type 2 Diabetes and Glycemic Traits: A Mendelian Randomization Study
scientific article published on 04 September 2019
Association of HSP70 and its co-chaperones with Alzheimer's disease
artículo científico publicado en 2011
Association of Lipid-Related Genetic Variants with the Incidence of Atrial Fibrillation: The AFGen Consortium
artículo científico publicado en 2016
Association of Methylation Signals With Incident Coronary Heart Disease in an Epigenome-Wide Assessment of Circulating Tumor Necrosis Factor α.
artículo científico publicado en 2018
Association of Rare Loss-Of-Function Alleles in HAL, Serum Histidine: Levels and Incident Coronary Heart Disease
artículo científico publicado en 2015
Association of Uric Acid Genetic Risk Score With Blood Pressure
Association of Whole-Genome and NETRIN1 Signaling Pathway–Derived Polygenic Risk Scores for Major Depressive Disorder and White Matter Microstructure in the UK Biobank
scholarly article by Miruna C. Barbu et al published July 2018 in Biological Psychiatry: Cognitive Neuroscience and Neuroimaging
Association of adiposity genetic variants with menarche timing in 92,105 women of European descent
artículo científico publicado en 2013
Association of candidate pharmacogenetic markers with platinum-induced ototoxicity: PanCareLIFE dataset
scientific article published on 24 August 2020
Association of dietary folate and vitamin B-12 intake with genome-wide DNA methylation in blood: a large-scale epigenome-wide association analysis in 5841 individuals
scientific article published on 01 August 2019
Association of eGFR-Related Loci Identified by GWAS with Incident CKD and ESRD.
artículo científico publicado en 2011
Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium
scientific journal article
Association of heat shock proteins with Parkinson's disease
artículo científico publicado en 2011
Association of heat shock proteins with all-cause mortality
artículo científico publicado en 2012
Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks
artículo científico publicado en 2014
Association of maternal prenatal smoking GFI1-locus and cardio-metabolic phenotypes in 18,212 adults
Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts
scientific article published on April 2009
Association of the ER22/23EK polymorphism in the glucocorticoid receptor gene with survival and C-reactive protein levels in elderly men.
artículo científico publicado en 2004
Association of the exon 3 deleted/full-length GHR polymorphism with recombinant growth hormone dose in growth hormone-deficient adults
artículo científico publicado en 2009
Associations between joint effusion in the knee and gene expression levels in the circulation: a meta-analysis.
artículo científico publicado en 2016
Associations between medication use and homocysteine levels in an older population, and potential mediation by vitamin B12 and folate: data from the B-PROOF Study
artículo científico publicado en 2014
Associations of Mitochondrial and Nuclear Mitochondrial Variants and Genes with Seven Metabolic Traits
article
Associations of autozygosity with a broad range of human phenotypes
scientific article published on 31 October 2019
Associations of polymorphisms of eight muscle- or metabolism-related genes with performance in Mount Olympus marathon runners
artículo científico publicado en 2009
Asymptomatic radiographic hip osteoarthritis is associated with gait differences, especially in women: A population-based study
artículo científico publicado en 2017
Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
artículo científico publicado en 2022
Author Correction: Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases
artículo científico
Author Correction: Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps
artículo científico publicado en 2018
Author Correction: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing
scientific article published on 01 September 2019
Author Correction: Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function
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scientific article published on 01 May 2019
B-vitamins and body composition: integrating observational and experimental evidence from the B-PROOF study
artículo científico publicado en 2019
BMD Loci Contribute to Ethnic and Developmental Differences in Skeletal Fragility across Populations: Assessment of Evolutionary Selection Pressures
artículo científico publicado en 2015
BMI-associated alleles do not constitute risk alleles for polycystic ovary syndrome independently of BMI: a case-control study.
artículo científico publicado en 2014
BMP-2 gene polymorphisms and osteoporosis: the Rotterdam Study
artículo científico publicado en 2006
BclI glucocorticoid receptor polymorphism and smoking in the general population
Best practices and joint calling of the HumanExome BeadChip: the CHARGE Consortium
artículo científico publicado en 2013
Beta-blocker use and fall risk in older individuals: Original results from two studies with meta-analysis
artículo científico publicado en 2017
Bidirectional associations between circulating vitamin D and cholesterol levels: The Rotterdam Study
artículo científico publicado en 2015
Biological, clinical and population relevance of 95 loci for blood lipids
artículo científico publicado en 2010
Birth size, postnatal growth and growth during growth hormone treatment in small-for-gestational-age children: associations with IGF1 gene polymorphisms and haplotypes?
artículo científico publicado en 2009
Bivariate genome-wide association meta-analysis of pediatric musculoskeletal traits reveals pleiotropic effects at the SREBF1/TOM1L2 locus
artículo científico publicado en 2017
Bivariate genome-wide association study identifies novel pleiotropic loci for lipids and inflammation
artículo científico publicado en 2016
Blood RNA expression profiles undergo major changes during the seventh decade
artículo científico publicado en 2016
Blood lipids influence DNA methylation in circulating cells
artículo científico publicado en 2016
Bone Mass and Strength in School-Age Children Exhibit Sexual Dimorphism Related to Differences in Lean Mass: The Generation R Study
artículo científico publicado en 2015
Bone health and coronary artery calcification: The Rotterdam Study
artículo científico publicado en 2015
Bone mineral density and chronic lung disease mortality: the rotterdam study
artículo científico publicado en 2014
Bone mineral density, osteoporosis, and osteoporotic fractures: a genome-wide association study.
artículo científico publicado en 2008
Bone parameters across different types of hip osteoarthritis and their relationship to osteoporotic fracture risk
artículo científico publicado en 2013
Breast-feeding modifies the association of PPARgamma2 polymorphism Pro12Ala with growth in early life: the Generation R Study
artículo científico publicado en 2009
Burden of genetic risk variants in multiple sclerosis families in the Netherlands
artículo científico publicado en 2016
C-reactive protein gene haplotypes and risk of coronary heart disease: the Rotterdam Study
artículo científico publicado en 2006
C-reactive protein levels, variation in the C-reactive protein gene, and cancer risk: the Rotterdam Study
artículo científico publicado en 2006
C9orf72 and UNC13A are shared risk loci for amyotrophic lateral sclerosis and frontotemporal dementia: a genome-wide meta-analysis
artículo científico publicado en 2014
COPD GWAS variant at 19q13.2 in relation with DNA methylation and gene expression
artículo científico publicado en 2018
CYP1A2 and coffee intake and the modifying effect of sex, age, and smoking
artículo científico publicado en 2012
CYP2C9 Genotypes Modify Benzodiazepine-Related Fall Risk: Original Results From Three Studies With Meta-Analysis.
artículo científico publicado en 2016
Cam Deformity and Acetabular Dysplasia as Risk Factors for Hip Osteoarthritis
artículo científico publicado en 2016
Candidate CSPG4 mutations and induced pluripotent stem cell modeling implicate oligodendrocyte progenitor cell dysfunction in familial schizophrenia.
artículo científico publicado en 2018
Candidate gene studies and the quest for the entrepreneurial gene
article
Cataract surgery and the risk of aging macula disorder: the rotterdam study
artículo científico publicado en 2008
Causal mechanisms and balancing selection inferred from genetic associations with polycystic ovary syndrome
artículo científico publicado en 2015
Cdx-2 polymorphism in the promoter region of the human vitamin D receptor gene determines susceptibility to fracture in the elderly
artículo científico publicado en 2003
Cell Specific eQTL Analysis without Sorting Cells
artículo científico publicado en 2015
Cell specific eQTL analysis without sorting cells
Characteristics of de novo structural changes in the human genome
artículo científico publicado en 2015
Characterization of pathogenic SORL1 genetic variants for association with Alzheimer's disease: a clinical interpretation strategy
artículo científico publicado en 2017
Chronic joint pain in the lower body is associated with gait differences independent from radiographic osteoarthritis
artículo científico publicado en 2015
Clinical Implications of Old and New Genes for Open-Angle Glaucoma
article
Clinical impact of cytokine gene polymorphisms in heart and lung transplantation
artículo científico publicado en 2004
Cognitive Performance: A Cross-Sectional Study on Serum Vitamin D and Its Interplay With Glucose Homeostasis in Dutch Older Adults
artículo científico publicado en 2015
Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium: Design of prospective meta-analyses of genome-wide association studies from 5 cohorts
artículo científico publicado en 2009
Collaborative meta-analysis: associations of 150 candidate genes with osteoporosis and osteoporotic fracture
artículo científico publicado en 2009
Common ATP-binding cassette B1 variants are associated with increased digoxin serum concentration
artículo científico publicado en 2008
Common DNA variants predict tall stature in Europeans
artículo científico publicado en 2013
Common Genetic Determinants of Vitamin D Insufficiency: A Genome-Wide Association Study
Common Genetic Variation of the Low-Density Lipoprotein Receptor-Related Protein 5 and 6 Genes Determines Fracture Risk in Elderly White Men
article
Common NOS1AP variants are associated with a prolonged QTc interval in the Rotterdam Study
artículo científico publicado en 2007
Common Variants Affecting Susceptibility to Develop Multiple Basal Cell Carcinomas
artículo científico publicado en 2015
Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR Interval
Common and rare variant association analyses in Amyotrophic Lateral Sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
artículo científico
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
artículo científico
Common genes underlying asthma and COPD? Genome-wide analysis on the Dutch hypothesis
artículo científico publicado en 2014
Common genetic determinants of intraocular pressure and primary open-angle glaucoma
artículo científico publicado en 2012
Common genetic determinants of vitamin D insufficiency: a genome-wide association study
artículo científico publicado en 2010
Common genetic loci influencing plasma homocysteine concentrations and their effect on risk of coronary artery disease
artículo científico publicado en 2013
Common genetic variants associate with serum phosphorus concentration
artículo científico publicado en 2010
Common genetic variants associated with cognitive performance identified using the proxy-phenotype method
artículo científico publicado en 2014
Common genetic variants associated with open-angle glaucoma
artículo científico publicado en 2011
Common genetic variation in the 3'-BCL11B gene desert is associated with carotid-femoral pulse wave velocity and excess cardiovascular disease risk: the AortaGen Consortium
artículo científico publicado en 2011
Common genetic variation in the ABCB1 gene is associated with the cholesterol-lowering effect of simvastatin in males
artículo científico publicado en 2009
Common genetic variation in the Estrogen Receptor Beta (ESR2) gene and osteoarthritis: results of a meta-analysis
artículo científico publicado en 2010
Common variants associated with plasma triglycerides and risk for coronary artery disease
artículo científico publicado en 2013
Common variants at 12q14 and 12q24 are associated with hippocampal volume
artículo científico publicado en 2012
Common variants at 12q15 and 12q24 are associated with infant head circumference
artículo científico publicado en 2012
Common variants at 6q22 and 17q21 are associated with intracranial volume
artículo científico publicado en 2012
Common variants at ten loci influence QT interval duration in the QTGEN Study
artículo científico publicado en 2009
Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction
artículo científico publicado en 2010
Common variants in KCNN3 are associated with lone atrial fibrillation
artículo científico publicado en 2010
Common variants in Mendelian kidney disease genes and their association with renal function
artículo científico publicado en 2013
Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysis
scientific article published on 24 October 2008
Common variants in the calcium-sensing receptor gene are associated with total serum calcium levels
artículo científico publicado en 2010
Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration
artículo científico publicado en 2011
Common variation in the NOS1AP gene is associated with reduced glucose-lowering effect and with increased mortality in users of sulfonylurea
artículo científico publicado en 2008
Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study
artículo científico publicado en 2017
Complement component C3 and risk of age-related macular degeneration
artículo científico publicado en 2009
Complement factor H polymorphism, complement activators, and risk of age-related macular degeneration
artículo científico publicado en 2006
Complement factor h polymorphism, inflammatory mediators, and retinal vessel diameters: the rotterdam study
artículo científico publicado en 2007
Comprehensive and accurate mutation scanning of theCFTR gene by two-dimensional DNA electrophoresis
article
Comprehensive candidate gene study highlights UGT1A and BNC2 as new genes determining continuous skin color variation in Europeans
artículo científico publicado en 2012
Comprehensive evaluation of smoking exposures and their interactions on DNA methylation
artículo científico publicado en 2024
Correction: Epigenetic Profiles in Children with a Neural Tube Defect; A Case-Control Study in Two Populations.
artículo científico publicado en 2014
Correction: Four Novel Loci (19q13, 6q24, 12q24, and 5q14) Influence the Microcirculation In Vivo.
artículo científico publicado en 2010
Correction: Genome-Wide Association Scan Meta-Analysis Identifies Three Loci Influencing Adiposity and Fat Distribution.
artículo científico publicado en 2009
Correction: Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults
artículo científico publicado en 2017
Correction: Large-Scale Evidence for the Effect of the COLIA1 Sp1 Polymorphism on Osteoporosis Outcomes: The GENOMOS Study
artículo científico publicado en 2006
Correction: Susceptibility to chronic mucus hypersecretion, a genome wide association study
artículo científico publicado en 2015
Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study
artículo científico publicado en 2016
Correction: The complex genetics of gait speed: genome-wide meta-analysis approach
artículo científico publicado en 2017
Correction: Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria
scientific article published on 05 December 2019
Correlation between genetic and geographic structure in Europe
artículo científico publicado en 2008
Correlation of breast cancer susceptibility loci with patient characteristics, metastasis-free survival, and mRNA expression of the nearest genes
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artículo científico publicado el 12 de julio de 2011
Corrigendum to “A genome-wide association study identifies a common variant near the GPR22 gene as a new locus involved in prevalence and progression of osteoarthritis” [Bone. 44S2 (2009) S224]
article
Corrigendum: 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function
artículo científico publicado en 2017
Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses
artículo científico publicado en 2016
Corrigendum: Rare coding variants and X-linked loci associated with age at menarche
artículo científico publicado en 2015
Corrigendum: Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis
scholarly article published in Nature Genetics
Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations
artículo científico publicado en 2016
Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases.
artículo científico publicado en 2018
Cross-ethnic meta-analysis of genetic variants for polycystic ovary syndrome.
artículo científico publicado en 2013
Cytochrome P450 3A gene variation, steroid hormone serum levels and prostate cancer--The Rotterdam Study
artículo científico publicado en 2010
DNA Methylation Signatures of Depressive Symptoms in Middle-aged and Elderly Persons: Meta-analysis of Multiethnic Epigenome-wide Studies
article published in 2018
DNA methylation age is associated with an altered hemostatic profile in a multi-ethnic meta-analysis
article
DNA methylation profiles at birth and child ADHD symptoms
artículo científico publicado en 2013
DNA methylation signatures of chronic low-grade inflammation are associated with complex diseases
artículo científico publicado en 2016
DNA methylation-based measures of biological age: meta-analysis predicting time to death
artículo científico publicado en 2016
Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations
artículo científico publicado en 2021
Defining the role of common variation in the genomic and biological architecture of adult human height
artículo científico publicado en 2014
Dependency of phenprocoumon dosage on polymorphisms in the VKORC1, CYP2C9, and CYP4F2 genes
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artículo científico publicado el 1 de enero de 2011
Detecting low frequent loss-of-function alleles in genome wide association studies with red hair color as example
artículo científico publicado en 2011
Determinants for Quantitative Sensory Testing and the Association with Chronic Musculoskeletal Pain in the General Elderly Population
artículo científico publicado en 2015
Determinants of maternal pregnancy one-carbon metabolism and newborn human DNA methylation profiles
scholarly article by Nina H van Mil et al published December 2014 in Reproduction
Development of a Food Group-Based Diet Score and Its Association with Bone Mineral Density in the Elderly: The Rotterdam Study
artículo científico publicado en 2015
Dietary Advanced Glycation End-Products (dAGEs) Intake and Bone Health: A Cross-Sectional Analysis in the Rotterdam Study
artículo científico publicado en 2020
Dietary patterns explaining differences in bone mineral density and hip structure in the elderly: the Rotterdam Study
artículo científico publicado en 2016
Dietary patterns in an elderly population and their relation with bone mineral density: the Rotterdam Study
artículo científico publicado en 2016
Differential Genetic Effects of ESR1 Gene Polymorphisms on Osteoporosis Outcomes
scientific article published in The Journal of the American Medical Association
Digital quantification of human eye color highlights genetic association of three new loci
artículo científico publicado en 2010
Directional dominance on stature and cognition in diverse human populations
artículo científico publicado en 2015
Discovery and fine mapping of serum protein loci through transethnic meta-analysis
artículo científico publicado en 2012
Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps
artículo científico publicado en 2016
Discovery and refinement of loci associated with lipid levels
artículo científico publicado en 2013
Discovery of Genetic Variation on Chromosome 5q22 Associated with Mortality in Heart Failure
artículo científico publicado en 2016
Discovery of novel heart rate-associated loci using the Exome Chip
artículo científico publicado en 2017
Disease variants alter transcription factor levels and methylation of their binding sites
artículo científico publicado en 2016
Disentangling the genetics of lean mass
article
Diversity, compositional and functional differences between gut microbiota of children and adults
scientific article published on 23 January 2020
Do Vitamin D Level and Dietary Calcium Intake Modify the Association Between Loop Diuretics and Bone Health?
scientific article published on 14 October 2019
Dopaminergic, serotonergic, and oxytonergic candidate genes associated with infant attachment security and disorganization? In search of main and interaction effects
artículo científico publicado en 2011
Drug-Gene Interactions of Antihypertensive Medications and Risk of Incident Cardiovascular Disease: A Pharmacogenomics Study from the CHARGE Consortium
artículo científico publicado en 2015
Drug-gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval
artículo científico publicado en 2013
EIF2AK3 variants in Dutch patients with Alzheimer's disease
artículo científico publicado en 2018
Education influences the role of genetics in myopia
artículo científico publicado en 2013
Effect of HLA-DR matching on acute rejection after clinical heart transplantation might be influenced by an IL-2 gene polymorphism
artículo científico publicado en 2002
Effect of Vitamin B12 and Folic Acid Supplementation on Bone Mineral Density and Quantitative Ultrasound Parameters in Older People with an Elevated Plasma Homocysteine Level: B-PROOF, a Randomized Controlled Trial
artículo científico publicado en 2015
Effect of daily vitamin B-12 and folic acid supplementation on fracture incidence in elderly individuals with an elevated plasma homocysteine concentration: B-PROOF, a randomized controlled trial
artículo científico publicado en 2014
Effect of dietary B vitamins on BMD and risk of fracture in elderly men and women: the Rotterdam study
artículo científico publicado en 2007
Effect of genetic variants associated with plasma homocysteine levels on stroke risk
artículo científico publicado en 2014
Effect of vitamin B12 and folic acid supplementation on biomarkers of endothelial function and inflammation among elderly individuals with hyperhomocysteinemia
artículo científico
Effects of 2-year vitamin B12 and folic acid supplementation in hyperhomocysteinemic elderly on arterial stiffness and cardiovascular outcomes within the B-PROOF trial
artículo científico publicado en 2015
Effects of Calcium, Magnesium, and Potassium Concentrations on Ventricular Repolarization in Unselected Individuals
artículo científico publicado en 2019
Effects of Two-Year Vitamin B12 and Folic Acid Supplementation on Depressive Symptoms and Quality of Life in Older Adults with Elevated Homocysteine Concentrations: Additional Results from the B-PROOF Study, an RCT.
artículo científico publicado en 2016
Effects of long-term averaging of quantitative blood pressure traits on the detection of genetic associations
artículo científico publicado en 2014
Effects of serum TSH and FT4 levels and the TSHR-Asp727Glu polymorphism on bone: the Rotterdam Study
Efficient strategy for detecting gene × gene joint action and its application in schizophrenia
artículo científico publicado en 2013
Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms
artículo científico publicado en 2011
Eight genetic loci associated with variation in lipoprotein-associated phospholipase A2 mass and activity and coronary heart disease: meta-analysis of genome-wide association studies from five community-based studies
artículo científico publicado en 2011
Eight-fold increased risk for congenital heart defects in children carrying the nicotinamide N-methyltransferase polymorphism and exposed to medicines and low nicotinamide
artículo científico publicado en 2008
Enterococccus faecium abundance in gut microbiome is associated with higher bone mineral density in school age children
scholarly article
Epigenetic profiles in children with a neural tube defect; a case-control study in two populations
artículo científico publicado en 2013
Epigenome-wide Association Study Identifies Methylation Sites Associated With Liver Enzymes and Hepatic Steatosis
artículo científico
Epigenome-wide association study (EWAS) on lipids: the Rotterdam Study
artículo científico publicado en 2017
Epigenome-wide association study of body mass index, and the adverse outcomes of adiposity
artículo científico publicado en 2016
Erratum: Common variants at 12q15 and 12q24 are associated with infant head circumference
scholarly article published in Nature Genetics
Erratum: Common variants at 6q22 and 17q21 are associated with intracranial volume
article
Erratum: Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms and neuroticism identified through genome-wide analyses
article
Erratum: Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine
artículo científico publicado en 2016
Erratum: Genetic loci associated with heart rate variability and their effects on cardiac disease risk
artículo científico publicado en 2017
Erratum: Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia
article
Erratum: Large meta-analysis of genome-wide association studies identifies five loci for lean body mass
artículo científico publicado en 2017
Erratum: Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation
artículo científico publicado en 2017
Erratum: Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution
artículo científico publicado en 2011
Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
artículo científico publicado en 2010
Establishing the role of rare coding variants in known Parkinson's disease risk loci
artículo científico publicado en 2017
Estrogen Receptor α Gene Variation Is Associated With Risk of Myocardial Infarction in More Than Seven Thousand Men From Five Cohorts
article
Estrogen Receptor-Alpha Gene Polymorphisms and Body Composition in Children and Adolescents
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artículo científico publicado el 17 de junio de 2011
Estrogen receptor alpha gene haplotype is associated with radiographic osteoarthritis of the knee in elderly men and women
artículo científico publicado en 2003
Estrogen receptor alpha gene polymorphisms and risk of myocardial infarction
artículo científico publicado en 2004
Estrogen receptor alpha gene polymorphisms are associated with estradiol levels in postmenopausal women
artículo científico publicado en 2005
Estrogen receptor alpha gene polymorphisms associated with incident aging macula disorder
artículo científico publicado en 2007
Estrogen receptor beta (ESR2) polymorphisms in interaction with estrogen receptor alpha (ESR1) and insulin-like growth factor I (IGF1) variants influence the risk of fracture in postmenopausal women
artículo científico publicado en 2006
Estrogen receptors alpha and beta and the risk of open-angle glaucoma: the Rotterdam Study
artículo científico publicado en 2008
Evaluation of Presumably Disease Causing SCN1A Variants in a Cohort of Common Epilepsy Syndromes
artículo científico publicado en 2016
Evaluation of a Genetic Risk Score to Improve Risk Prediction for Alzheimer's Disease
artículo científico publicado en 2016
Evaluation of the Myocilin Mutation Gln368Stop Demonstrates Reduced Penetrance for Glaucoma in European Populations
artículo científico publicado en 2016
Evidence of inbreeding depression on human height
artículo científico publicado en 2012
Evidence that the mitochondrial leucyl tRNA synthetase (LARS2) gene represents a novel type 2 diabetes susceptibility gene
artículo científico publicado en 2005
Excessive burden of lysosomal storage disorder gene variants in Parkinson's disease
artículo científico publicado en 2017
Exercise with food withdrawal at thermoneutrality impacts fuel use, the microbiome, AMPK phosphorylation, muscle fibers, and thyroid hormone levels in rats
artículo científico publicado en 2020
Exercise, fasting, and mimetics: toward beneficial combinations?
artículo científico publicado en 2016
Exome Chip Analysis Identifies Low-Frequency a on Brain Magnetic Imaging
Exome Sequencing Analysis Identifies Rare Variants in ATM and RPL8 That Are Associated With Shorter Telomere Length
scientific article published on 30 April 2020
Exome sequencing and functional analyses suggest that SIX6 is a gene involved in an altered proliferation-differentiation balance early in life and optic nerve degeneration at old age.
artículo científico publicado en 2013
Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology
artículo científico publicado en 2019
Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology
scientific article published on 01 September 2019
Exome-Wide Meta-Analysis Identifies Rare 3'-UTR Variant in ERCC1/CD3EAP Associated with Symptoms of Sleep Apnea
artículo científico publicado en 2017
Exome-chip meta-analysis identifies novel associations of coding variants in BSN and GLRA4 with lumbar spine BMD in 27 339 adults of European descent
scholarly article
Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6
Exome-sequencing in a large population-based study reveals a rare Asn396Ser variant in the LIPG gene associated with depressive symptoms.
artículo científico publicado en 2016
ExomeChip-Wide Analysis of 95 626 Individuals Identifies 10 Novel Loci Associated With QT and JT Intervals
Expression and Gene Variation Studies Deny Association of Human HSD3B1 Gene With Aldosterone Production or Blood Pressure
article
Eye color and the prediction of complex phenotypes from genotypes.
artículo científico publicado en 2009
FTO genotype is associated with phenotypic variability of body mass index
artículo científico publicado en 2012
Facial Wrinkles in Europeans: a Genome-Wide Association Study.
artículo científico publicado en 2018
Fast linear mixed model computations for genome-wide association studies with longitudinal data
artículo científico publicado en 2012
Femoral neck BMD is a strong predictor of hip fracture susceptibility in elderly men and women because it detects cortical bone instability: the Rotterdam Study
artículo científico publicado en 2007
Femoral stress is prominently associated with fracture risk in children: The Generation R Study
artículo científico publicado en 2019
Fibrinogen gene haplotypes in relation to risk of coronary events and coronary and extracoronary atherosclerosis: the Rotterdam Study
scientific article published on 01 February 2007
Fifteen Genetic Loci Associated With the Electrocardiographic P Wave
artículo científico publicado en 2017
Fine mapping the CETP region reveals a common intronic insertion associated to HDL-C
artículo científico publicado en 2015
Fine-mapping the effects of Alzheimer's disease risk loci on brain morphology
artículo científico publicado en 2016
Finger length pattern as a biomarker for osteoarthritis and chronic joint pain: a population-based study and meta-analysis after systematic review
artículo científico
Folic Acid and Vitamin B12 Supplementation and the Risk of Cancer: Long-term Follow-up of the B Vitamins for the Prevention of Osteoporotic Fractures (B-PROOF) Trial
Folic acid and vitamin-B12 supplementation and the risk of cancer: long-term follow-up of the B-vitamins for the Prevention Of Osteoporotic Fractures (B-PROOF) trial
article published in 2018
Follicle-stimulating hormone receptor polymorphism affects the outcome of ovulation induction in normogonadotropic (World Health Organization class 2) anovulatory subfertility
artículo científico publicado en 2015
Four Susceptibility Loci for Gallstone Disease Identified in a Meta-analysis of Genome-Wide Association Studies
artículo científico publicado en 2016
Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo
artículo científico publicado en 2010
Fraction of exhaled nitric oxide values in childhood are associated with 17q11.2-q12 and 17q12-q21 variants
artículo científico publicado en 2013
Fracture incidence and secular trends between 1989 and 2013 in a population based cohort: The Rotterdam Study
scientific article published on 07 June 2018
Fractures in school age children in relation to sex and ethnic background: The Generation R Study
artículo científico publicado en 2019
Fractures in school age children in relation to sex, ethnic background and bone mineral density: the generation R Study
scholarly article
Functional heme oxygenase-1 promoter polymorphism in relation to heart failure and cardiac transplantation.
artículo científico publicado en 2005
Fundamental role for HO-1 in the self-protection of renal allografts
artículo científico publicado en 2004
GRIMP: a web- and grid-based tool for high-speed analysis of large-scale genome-wide association using imputed data
artículo científico publicado en 2009
GWAS analysis of handgrip and lower body strength in older adults in the CHARGE consortium
artículo científico publicado en 2016
GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes
artículo científico publicado en 2018
GWAS for executive function and processing speed suggests involvement of the CADM2 gene.
artículo científico publicado en 2015
GWAS of 126,559 individuals identifies genetic variants associated with educational attainment
artículo científico publicado en 2013
GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures
artículo científico publicado en 2019
GWAS of longevity in CHARGE consortium confirms APOE and FOXO3 candidacy
artículo científico publicado en 2014
GWAS on longitudinal growth traits reveals different genetic factors influencing infant, child, and adult BMI
artículo científico publicado en 2019
GWAS with longitudinal phenotypes: performance of approximate procedures
artículo científico publicado en 2015
Gene set analysis of GWAS data for human longevity highlights the relevance of the insulin/IGF-1 signaling and telomere maintenance pathways
artículo científico publicado en 2011
Gene transcripts associated with muscle strength: a CHARGE meta-analysis of 7,781 persons
artículo científico publicado en 2015
Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia
artículo científico publicado en 2014
Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci
artículo científico publicado en 2014
Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci
scientific article published on 05 May 2020
Gene-gene Interaction Analyses for Atrial Fibrillation
artículo científico publicado en 2016
Genetic Architecture of Subcortical Brain Structures in Over 40,000 Individuals Worldwide
scholarly article published 28 August 2017
Genetic Biomarkers to Identify the Risk of Osteonecrosis in Children with Acute Lymphoblastic Leukemia
artículo científico publicado en 2016
Genetic Determinants of Circulating Estrogen Levels, and Evidence of a Causal Effect of Estradiol on Bone Density in Men.
artículo científico publicado en 2018
Genetic Determinants of Cortical Structure (Thickness, Surface Area and Volumes) among Disease Free Adults in the CHARGE Consortium
article published in 2018
Genetic Determinants of Osteoporosis
Genetic Determinants of Ototoxicity During and After Childhood Cancer Treatment: Protocol for the PanCareLIFE Study
scientific article published on 19 March 2019
Genetic Determinants of Unruptured Intracranial Aneurysms in the General Population
artículo científico publicado en 2015
Genetic Interactions with Age, Sex, Body Mass Index, and Hypertension in Relation to Atrial Fibrillation: The AFGen Consortium
artículo científico publicado en 2017
Genetic Polymorphism of miR-196a-2 is Associated with Bone Mineral Density (BMD).
artículo científico publicado en 2017
Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity
scientific article published on 11 September 2020
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits
scientific article published on 17 September 2018
Genetic analysis of over one million people identifies 535 novel loci for blood pressure
Genetic and lifestyle factors related to the periconception vitamin B12 status and congenital heart defects: a Dutch case-control study
artículo científico publicado en 2008
Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting
Genetic architecture of circulating lipid levels
artículo científico publicado en 2011
Genetic architecture of early childhood growth phenotypes gives insights into their link with later obesity
Genetic architecture of open angle glaucoma and related determinants
artículo científico publicado en 2010
Genetic architecture of subcortical brain structures in 38,851 individuals
scientific article published on 21 October 2019
Genetic association analysis of 13 nuclear-encoded mitochondrial candidate genes with type II diabetes mellitus: the DAMAGE study
artículo científico publicado en 2009
Genetic association analysis of LARS2 with type 2 diabetes
artículo científico publicado en 2010
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization
artículo científico publicado en 2014
Genetic association study of childhood aggression across raters, instruments, and age
artículo científico publicado en 2021
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function
artículo científico publicado en 2016
Genetic basis of falling risk susceptibility in the UK Biobank Study
artículo científico publicado en 2020
Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53949).
artículo científico publicado en 2015
Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults
scientific article published on 22 September 2020
Genetic determinants of heel bone properties: genome-wide association meta-analysis and replication in the GEFOS/GENOMOS consortium
artículo científico publicado en 2014
Genetic determinants of mortality. Can findings from genome-wide association studies explain variation in human mortality?
artículo científico publicado en 2013
Genetic determinants of ototoxicity during and after childhood cancer treatment: design of PanCareLIFE studies (Preprint)
Genetic determinants of serum testosterone concentrations in men.
artículo científico publicado en 2011
Genetic determinants of treatment benefit of the angiotensin-converting enzyme-inhibitor perindopril in patients with stable coronary artery disease
artículo científico publicado en 2010
Genetic determination of human facial morphology: links between cleft-lips and normal variation
artículo científico publicado en 2011
Genetic diversity is a predictor of mortality in humans
artículo científico publicado en 2014
Genetic evidence of assortative mating in humans
article
Genetic insights into biological mechanisms governing human ovarian ageing
artículo científico publicado en 2021
Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosis
artículo científico publicado en 2017
Genetic loci associated with prevalent and incident myocardial infarction and coronary heart disease in the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium
artículo científico publicado en 2020
Genetic loci for retinal arteriolar microcirculation
artículo científico publicado en 2013
Genetic loci for serum lipid fractions and intracerebral hemorrhage
artículo científico publicado en 2016
Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing
artículo científico publicado en 2019
Genetic polymorphisms in the locus control region and promoter of GH1 are related to serum IGF-I levels and height in patients with isolated growth hormone deficiency and healthy controls
artículo científico publicado en 2010
Genetic predictors of fibrin D-dimer levels in healthy adults
artículo científico publicado en 2011
Genetic risk of Parkinson's disease in the general population
artículo científico publicado en 2016
Genetic risk of neurodegenerative diseases is associated with mild cognitive impairment and conversion to dementia
artículo científico publicado en 2015
Genetic risk profiles for depression and anxiety in adult and elderly cohorts
artículo científico publicado en 2010
Genetic screening of a Dutch population with isolated GH deficiency (IGHD).
artículo científico publicado en 2008
Genetic studies of body mass index yield new insights for obesity biology
artículo científico publicado en 2015
Genetic susceptibility to multiple sclerosis: Brain structure and cognitive function in the general population
artículo científico publicado en 2016
Genetic testing in clinical practice
artículo científico publicado en 2009
Genetic variance in CYP2C8 and increased risk of myocardial infarction
artículo científico publicado en 2010
Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data
artículo científico publicado en 2009
Genetic variants associated with earlier age at menopause increase the risk of cardiovascular events in women
artículo científico publicado en 2017
Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses
artículo científico publicado en 2016
Genetic variants in RBFOX3 are associated with sleep latency
artículo científico publicado en 2016
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
artículo científico publicado en 2011
Genetic variants in the ADAMTS13 and SUPT3H genes are associated with ADAMTS13 activity
article
Genetic variation and bone mineral density in long-term adult survivors of childhood cancer
artículo científico publicado en 2016
Genetic variation at the phospholipid transfer protein locus affects its activity and high-density lipoprotein size and is a novel marker of cardiovascular disease susceptibility
artículo científico publicado en 2010
Genetic variation in NOS1AP is associated with sudden cardiac death: evidence from the Rotterdam Study
artículo científico publicado en 2009
Genetic variation in gonadal impairment in female survivors of childhood cancer: a PanCareLIFE study protocol
Genetic variation in homocysteine metabolism, cognition, and white matter lesions
artículo científico publicado en 2008
Genetic variation in the ABCC2 gene is associated with dose decreases or switches to other cholesterol-lowering drugs during simvastatin and atorvastatin therapy
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artículo científico publicado el 20 de diciembre de 2011
Genetic variation in the PPARA gene is associated with simvastatin-mediated cholesterol reduction in the Rotterdam Study.
artículo científico publicado en 2013
Genetic variation in the fibrinogen-alpha and fibrinogen-gamma genes in relation to arterial stiffness: the Rotterdam Study
artículo científico publicado en 2009
Genetic variation in the multidrug and toxin extrusion 1 transporter protein influences the glucose-lowering effect of metformin in patients with diabetes: a preliminary study
artículo científico publicado en 2009
Genetic variation in the renin-angiotensin system and arterial stiffness. The Rotterdam Study
artículo científico publicado en 2009
Genetic variation may modify ovarian reserve in female childhood cancer survivors
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artículo científico publicado el 29 de enero de 2013
Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profile
artículo científico publicado en 2011
Genetic variation of cisplatin-induced ototoxicity in non-cranial-irradiated pediatric patients using a candidate gene approach: The International PanCareLIFE Study
scientific article published on 31 October 2019
Genetic variation underlying cognition and its relation with neurological outcomes and brain imaging
Genetic variation, C-reactive protein levels, and incidence of diabetes.
artículo científico publicado en 2007
Genetic, physiological, and lifestyle predictors of mortality in the general population
Genetically defined elevated homocysteine levels do not result in widespread changes of DNA methylation in leukocytes
artículo científico publicado en 2017
Genetics and biology of vitamin D receptor polymorphisms
artículo científico publicado en 2004
Genetics of cortisol secretion and depressive symptoms: a candidate gene and genome wide association approach
scientific article published on 12 February 2011
Genetics of osteoporosis
artículo científico publicado en 2010
Genetics of skin color variation in Europeans: genome-wide association studies with functional follow-up
artículo científico publicado en 2015
Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders
artículo científico publicado en 2018
Genome Scanning of Human Breast Carcinomas Using Micro- and Minisatellite Core Probes
Genome of The Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levels
artículo científico publicado en 2015
Genome wide association identifies common variants at the SERPINA6/SERPINA1 locus influencing plasma cortisol and corticosteroid binding globulin
artículo científico publicado en 2014
Genome-Wide Association Studies Identify Multiple Genetic Loci Influencing Eyebrow Color Variation in Europeans
artículo científico publicado en 2019
Genome-Wide Association Studies of Multiple Keratinocyte Cancers
artículo científico publicado en 2017
Genome-Wide Association Study for Incident Myocardial Infarction and Coronary Heart Disease in Prospective Cohort Studies: The CHARGE Consortium
artículo científico publicado en 2016
Genome-Wide Association Study of Vascular Dementia
scholarly article by Elisabeth M.C. Schrijvers et al published February 2012 in Stroke Journal
Genome-Wide Association Transethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels
Genome-wide Association Analysis in Humans Links Nucleotide Metabolism to Leukocyte Telomere Length
scientific article published on 27 February 2020
Genome-wide Association Study Links APOEϵ4 and BACE1 Variants with Plasma Amyloid β Levels
Genome-wide Association Study for Radiographic Vertebral Fractures: A Potential Role for the 16q24 BMD Locus versus Lessons Learned from Challenging Phenotype Definition
Genome-wide Meta-analysis of 158,000 Individuals of European Ancestry Identifies Three Loci Associated with Chronic Back Pain
Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis
artículo científico publicado en 2016
Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation
artículo científico publicado en 2018
Genome-wide analyses using UK Biobank data provide insights into the genetic architecture of osteoarthritis.
artículo científico publicado en 2018
Genome-wide analysis identifies 12 loci influencing human reproductive behavior
artículo científico publicado en 2016
Genome-wide analysis of genetic loci associated with Alzheimer disease
artículo científico publicado en 2010
Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma
artículo científico publicado en 2014
Genome-wide association analyses identify 18 new loci associated with serum urate concentrations
artículo científico publicado en 2013
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression
artículo científico publicado en 2018
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis
artículo científico publicado en 2016
Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention
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artículo científico publicado en 2022
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences
artículo científico publicado en 2019
Genome-wide association analysis identifies multiple loci related to resting heart rate
artículo científico publicado en 2010
Genome-wide association analysis identifies six new loci associated with forced vital capacity
artículo científico publicado en 2014
Genome-wide association analysis identifies susceptibility loci for migraine without aura
artículo científico publicado en 2012
Genome-wide association analysis identifies three new breast cancer susceptibility loci
artículo científico publicado en 2012
Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index
artículo científico publicado en 2015
Genome-wide association analysis of coffee drinking suggests association with CYP1A1/CYP1A2 and NRCAM
artículo científico publicado en 2011
Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure
scientific article published on 09 January 2020
Genome-wide association and functional follow-up reveals new loci for kidney function
artículo científico publicado en 2012
Genome-wide association and functional studies identify a role for IGFBP3 in hip osteoarthritis
artículo científico publicado en 2014
Genome-wide association and functional studies identify the DOT1L gene to be involved in cartilage thickness and hip osteoarthritis
scientific journal article
Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption
scientific journal article
Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.
artículo científico publicado en 2011
Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria
artículo científico publicado en 2019
Genome-wide association meta-analysis for total serum bilirubin levels
artículo científico publicado en 2009
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
artículo científico publicado en 2018
Genome-wide association meta-analysis identifies five novel loci for age-related hearing impairment
artículo científico publicado en 2019
Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits
artículo científico publicado en 2019
Genome-wide association meta-analysis of PR interval identifies 47 novel loci associated with atrial and atrioventricular electrical activity
Genome-wide association meta-analysis of coronary artery disease and periodontitis reveals a novel shared risk locus
scientific article published in Scientific Reports
Genome-wide association meta-analysis of fish and EPA+DHA consumption in 17 US and European cohorts.
artículo científico publicado en 2017
Genome-wide association meta-analysis of human longevity identifies a novel locus conferring survival beyond 90 years of age.
artículo científico publicado en 2014
Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability
artículo científico publicado en 2018
Genome-wide association of phenotypes based on clustering patterns of hand osteoarthritis identify WNT9A as novel osteoarthritis gene
scientific article published on 14 October 2020
Genome-wide association scan identifies a prostaglandin-endoperoxide synthase 2 variant involved in risk of knee osteoarthritis
scientific journal article
Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution
artículo científico publicado en 2009
Genome-wide association scan of neuropathic pain symptoms post total joint replacement highlights a variant in the protein-kinase C gene
artículo científico publicado en 2017
Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging
artículo científico publicado en 2021
Genome-wide association studies identify four ER negative-specific breast cancer risk loci
artículo científico publicado en 2013
Genome-wide association studies in Asians confirm the involvement of ATOH7 and TGFBR3, and further identify CARD10 as a novel locus influencing optic disc area
article
Genome-wide association studies in economics and entrepreneurship research: promises and limitations
scholarly article by Philipp D. Koellinger et al published 13 May 2010 in Small Business Economics
Genome-wide association studies of MRI-defined brain infarcts: meta-analysis from the CHARGE Consortium
artículo científico publicado en 2009
Genome-wide association studies of cerebral white matter lesion burden: the CHARGE consortium
artículo científico publicado en 2011
Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels
artículo científico publicado en 2010
Genome-wide association study confirms extant PD risk loci among the Dutch
artículo científico publicado en 2011
Genome-wide association study for acute otitis media in children identifies FNDC1 as disease contributing gene
artículo científico publicado en 2016
Genome-wide association study for circulating tissue plasminogen activator levels and functional follow-up implicates endothelial STXBP5 and STX2.
artículo científico publicado en 2014
Genome-wide association study for coronary artery calcification with follow-up in myocardial infarction
artículo científico publicado en 2011
Genome-wide association study for radiographic vertebral fractures: a potential role for the 16q24 BMD locus
artículo científico publicado en 2014
Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium
artículo científico publicado en 2014
Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis
artículo científico publicado en 2009
Genome-wide association study identifies 48 common genetic variants associated with handedness
artículo científico publicado en 2020
Genome-wide association study identifies 74 loci associated with educational attainment
artículo científico publicado en 2016
Genome-wide association study identifies a single major locus contributing to survival into old age; the APOE locus revisited
artículo científico publicado en 2011
Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma
artículo científico publicado en 2011
Genome-wide association study identifies novel breast cancer susceptibility loci
artículo científico publicado en 2007
Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations
artículo científico publicado en 2012
Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure
artículo científico publicado en 2011
Genome-wide association study in 176,678 Europeans reveals genetic loci for tanning response to sun exposure.
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artículo científico publicado en 2018
Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levels
artículo científico publicado en 2018
Genome-wide association study in an admixed case series reveals IL12A as a new candidate in Behçet disease
artículo científico publicado en 2015
Genome-wide association study meta-analysis of chronic widespread pain: evidence for involvement of the 5p15.2 region
artículo científico publicado en 2013
Genome-wide association study of 23,500 individuals identifies 7 loci associated with brain ventricular volume
artículo científico publicado en 2018
Genome-wide association study of PR interval
artículo científico publicado en 2010
Genome-wide association study of blood pressure and hypertension
scientific journal article
Genome-wide association study of height-adjusted BMI in childhood identifies functional variant in ADCY3
artículo científico publicado en 2014
Genome-wide association study of kidney function decline in individuals of European descent
artículo científico publicado en 2014
Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1.
artículo científico publicado en 2010
Genome-wide association study of retinopathy in individuals without diabetes
artículo científico publicado en 2013
Genome-wide association study of smoking initiation and current smoking
artículo científico publicado en 2009
Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk
artículo científico publicado en 2011
Genome-wide associations for birth weight and correlations with adult disease
artículo científico publicado en 2016
Genome-wide compound heterozygote analysis highlights alleles associated with adult height in Europeans
artículo científico publicado en 2017
Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function
artículo científico publicado en 2012
Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia
artículo científico publicado en 2013
Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity
artículo científico publicado en 2017
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture
scientific journal article
Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture
artículo científico publicado en 2012
Genome-wide meta-analysis identifies eight new susceptibility loci for cutaneous squamous cell carcinoma
scientific article published on 10 February 2020
Genome-wide meta-analysis identifies new susceptibility loci for migraine
artículo científico publicado en 2013
Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption
artículo científico publicado en 2014
Genome-wide meta-analysis of 158,000 individuals of European ancestry identifies three loci associated with chronic back pain
artículo científico publicado en 2018
Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits.
artículo científico publicado en 2017
Genome-wide meta-analysis of SNP-by9-ACEI/ARB and SNP-by-thiazide diuretic and effect on serum potassium in cohorts of European and African ancestry
artículo científico publicado en 2018
Genome-wide meta-analysis of common variant differences between men and women
artículo científico publicado en 2012
Genome-wide meta-analysis of macronutrient intake of 91,114 European ancestry participants from the cohorts for heart and aging research in genomic epidemiology consortium
artículo científico publicado en 2018
Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 loci
artículo científico publicado en 2014
Genome-wide meta-analysis of variant-by-diuretic interactions as modulators of lipid traits in persons of European and African ancestry
scientific article published on 06 December 2019
Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels
artículo científico publicado en 2016
Genome-wide methylation analysis identifies novel CpG loci for perimembranous ventricular septal defects in human
artículo científico publicado en 2017
Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults
artículo científico publicado en 2017
Genome-wide profiling of blood pressure in adults and children
artículo científico publicado en 2011
Genome-wide study links MTMR7 gene to variant Creutzfeldt-Jakob risk
scientific journal article
Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci
artículo científico publicado en 2013
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
artículo científico publicado en 2014
Genomewide association studies of stroke
artículo científico publicado en 2009
Genomic analyses for age at menarche identify 389 independent signals and indicate BMI-independent effects of puberty timing on cancer susceptibility
artículo científico publicado en 2016
Genomic analysis of diet composition finds novel loci and associations with health and lifestyle
article
Genomic analysis of diet composition finds novel loci and associations with health and lifestyle
scientific article published on 11 May 2020
Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation
artículo científico publicado en 2021
Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium
artículo científico publicado en 2010
Glucocorticoid receptor gene and risk of cardiovascular disease
artículo científico publicado en 2008
Glucocorticoid receptor gene polymorphisms and childhood adversity are associated with depression: New evidence for a gene-environment interaction
artículo científico publicado en 2009
Glucocorticoid receptor variant and risk of dementia and white matter lesions
artículo científico publicado en 2006
GnRH and LHR gene variants predict adverse outcome in premenopausal breast cancer patients
artículo científico publicado en 2007
Growth hormone dose in growth hormone-deficient adults is not associated with IGF-1 gene polymorphisms
artículo científico publicado en 2009
Gut microbiome-wide association study of depressive symptoms
Haplotype reference consortium panel: Practical implications of imputations with large reference panels
artículo científico publicado en 2017
Haplotypes of the NR4A2/NURR1 gene and cardiovascular disease: the Rotterdam Study
artículo científico publicado en 2009
Height in pre- and postmenopausal women is influenced by estrogen receptor alpha gene polymorphisms
artículo científico publicado en 2004
Helicobacter pylori colonization and obesity - a Mendelian randomization study
artículo científico publicado en 2017
Heritability and Genome-Wide Association Analyses of Human Gait Suggest Contribution of Common Variants
artículo científico publicado en 2015
Heritability and Genome-Wide Association Analyses of Intracranial Carotid Artery Calcification: The Rotterdam Study
artículo científico publicado en 2016
Heritability and Genome-Wide Association Analyses of Sleep Duration in Children: The EAGLE Consortium
artículo científico publicado en 2016
Heritability and genome-wide association study to assess genetic differences between advanced age-related macular degeneration subtypes
scientific journal article
Heritability and genome-wide associations studies of cerebral blood flow in the general population
artículo científico publicado en 2017
Heritability of the shape of subcortical brain structures in the general population
artículo científico publicado en 2016
Heterogeneity of breast cancer associations with five susceptibility loci by clinical and pathological characteristics
artículo científico publicado en 2008
High bone mineral density and fracture risk in type 2 diabetes as skeletal complications of inadequate glucose control: the Rotterdam Study
artículo científico publicado en 2013
Hippocampal transcriptome profiling combined with protein-protein interaction analysis elucidates Alzheimer's disease pathways and genes
scientific article published on 29 October 2018
History of tuberculosis as an independent prognostic factor for lung cancer survival
artículo científico publicado en 2012
Homocysteine and fracture prevention
artículo científico publicado en 2005
Homocysteine level is associated with aortic stiffness in elderly
artículo científico publicado en 2013
Homocysteine levels and the risk of osteoporotic fracture
artículo científico publicado en 2004
Homocysteine levels associate with subtle changes in leukocyte DNA methylation: an epigenome-wide analysis
artículo científico publicado en 2017
Host polymorphisms in interleukin 4, complement factor H, and C-reactive protein associated with nasal carriage of Staphylococcus aureus and occurrence of boils
artículo científico publicado en 2008
How to deal with the early GWAS data when imputing and combining different arrays is necessary
artículo científico publicado en 2011
Human age estimation from blood using mRNA, DNA methylation, DNA rearrangement, and telomere length
artículo científico publicado en 2016
Hundreds of variants clustered in genomic loci and biological pathways affect human height
artículo científico publicado en 2010
IRF4, MC1R and TYR genes are risk factors for actinic keratosis independent of skin color
artículo científico publicado en 2015
Identification of DIO2 as a new susceptibility locus for symptomatic osteoarthritis
artículo científico publicado en 2008
Identification of IDUA and WNT16 Phosphorylation-Related Non-Synonymous Polymorphisms for Bone Mineral Density in Meta-Analyses of Genome-Wide Association Studies
scientific article published on 08 August 2015
Identification of a candidate gene for astigmatism
scientific journal article
Identification of a common variant at the NOS1AP locus strongly associated to QT-interval duration
artículo científico publicado en 2008
Identification of a novel FGFRL1 MicroRNA target site polymorphism for bone mineral density in meta-analyses of genome-wide association studies
artículo científico publicado en 2015
Identification of a novel locus on chromosome 2q13, which predisposes to clinical vertebral fractures independently of bone density
artículo científico publicado en 2017
Identification of a sudden cardiac death susceptibility locus at 2q24.2 through genome-wide association in European ancestry individuals
artículo científico publicado en 2011
Identification of context-dependent expression quantitative trait loci in whole blood
artículo científico publicado en 2016
Identification of genetic loci associated with Helicobacter pylori serologic status
artículo científico publicado en 2013
Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders
artículo científico publicado en 2013
Identification of new susceptibility loci for osteoarthritis (arcOGEN): a genome-wide association study
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artículo científico publicado el 3 de julio de 2012
Identification of novel genetic Loci associated with thyroid peroxidase antibodies and clinical thyroid disease
artículo científico publicado en 2014
Identification of the BCAR1-CFDP1-TMEM170A locus as a determinant of carotid intima-media thickness and coronary artery disease risk
artículo científico publicado en 2012
Identification of the BclI polymorphism in the glucocorticoid receptor gene: association with sensitivity to glucocorticoids in vivo and body mass index
artículo científico publicado en 2003
Identifying genetic loci associated with antidepressant drug response with drug-gene interaction models in a population-based study
artículo científico publicado en 2015
Identifying genetic risk variants for coronary heart disease in familial hypercholesterolemia: an extreme genetics approach
artículo científico publicado en 2014
Impact of inherited genetic variants associated with lipid profile, hypertension, and coronary artery disease on the risk of intracranial and abdominal aortic aneurysms
artículo científico publicado en 2013
Impact of thyroid function and polymorphisms in the type 2 deiodinase on blood pressure: the Rotterdam Study and the Rotterdam Scan Study
Improvement of Risk Prediction by Genomic Profiling: Reclassification Measures Versus the Area Under the Receiver Operating Characteristic Curve
article by Raluca Mihaescu et al published 18 June 2010 in American Journal of Epidemiology
Improving accuracy of rare variant imputation with a two-step imputation approach
artículo científico publicado en 2014
Increased paternal age and the influence on burden of genomic copy number variation in the general population
artículo científico publicado en 2013
Incremental predictive value of 152 single nucleotide polymorphisms in the 10-year risk prediction of incident coronary heart disease: the Rotterdam Study
artículo científico publicado en 2015
Influence of Dietary Approaches to Stop Hypertension-Type Diet, Known Genetic Variants and Their Interplay on Blood Pressure in Early Childhood: ABCD Study
scientific article published on 02 December 2019
Influence of LRP5 Polymorphisms on Normal Variation in BMD
article
Influence of estrogen receptor alpha and progesterone receptor polymorphisms on the effects of hormone therapy on mammographic density
artículo científico publicado en 2006
Influence of genetic variation in CYP3A4 and ABCB1 on dose decrease or switching during simvastatin and atorvastatin therapy
artículo científico publicado en 2010
Inhibin alpha-subunit (INHA) expression in adrenocortical cancer is linked to genetic and epigenetic INHA promoter variation
artículo científico publicado en 2014
Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis
artículo científico publicado en 2013
Integrating genetic, transcriptional, and functional analyses to identify 5 novel genes for atrial fibrillation
artículo científico publicado en 2014
Integration of epidemiologic, pharmacologic, genetic and gut microbiome data in a drug-metabolite atlas
scientific article published on 13 January 2020
Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function
artículo científico publicado en 2012
Interaction between plasma homocysteine and the MTHFR c.677C > T polymorphism is associated with site-specific changes in DNA methylation in humans
artículo científico publicado en 2018
Interaction between polymorphisms in the OCT1 and MATE1 transporter and metformin response
artículo científico publicado en 2010
Interactions between dietary vitamin E intake and SIRT1 genetic variation influence body mass index.
artículo científico publicado en 2010
Interactions of dietary whole-grain intake with fasting glucose- and insulin-related genetic loci in individuals of European descent: a meta-analysis of 14 cohort studies
artículo científico publicado en 2010
Interferon gamma receptor 2 gene variants are associated with liver fibrosis in the general population: the Rotterdam Study
artículo científico publicado en 2014
Interleukin 6 -174 g/c promoter polymorphism and risk of coronary heart disease: results from the rotterdam study and a meta-analysis
scientific article published on 03 November 2005
Interleukin-6 receptor pathways in abdominal aortic aneurysm
scientific article published on 30 October 2012
International Genome-Wide Association Study Consortium Identifies Novel Loci Associated With Blood Pressure in Children and Adolescents
artículo científico publicado en 2016
Intestinal microbiome composition and its relation to joint pain and inflammation
scientific article published on 25 October 2019
Intrinsic and extrinsic risk factors for sagging eyelids
artículo científico publicado en 2014
KCND3 potassium channel gene variant confers susceptibility to electrocardiographic early repolarization pattern
artículo científico publicado en 2019
LPIN2 Is Associated With Type 2 Diabetes, Glucose Metabolism, and Body Composition
article
Large common deletions associate with mortality at old age.
artículo científico publicado en 2011
Large meta-analysis of genome-wide association studies identifies five loci for lean body mass
artículo científico publicado en 2017
Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium
artículo científico publicado en 2012
Large scale replication and meta-analysis of variants on chromosome 4q25 associated with atrial fibrillation
artículo científico publicado en 2009
Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated Diseases
artículo científico publicado en 2016
Large-Scale Genomic Analyses Link Reproductive Aging to Hypothalamic Signaling, Breast Cancer Susceptibility, and BRCA1-Mediated DNA Repair
artículo científico publicado en 2015
Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.
artículo científico publicado en 2017
Large-scale analysis of association between GDF5 and FRZB variants and osteoarthritis of the hip, knee, and hand
artículo científico publicado en 2009
Large-scale analysis of association between LRP5 and LRP6 variants and osteoporosis
artículo científico publicado en 2008
Large-scale analysis of association between polymorphisms in the transforming growth factor beta 1 gene (TGFB1) and osteoporosis: the GENOMOS study
artículo científico publicado en 2007
Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways
artículo científico publicado en 2012
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
artículo científico publicado en 2011
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes
artículo científico publicado en 2012
Large-scale evidence for the effect of the COLIA1 Sp1 polymorphism on osteoporosis outcomes: the GENOMOS study
artículo científico publicado en 2006
Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function
artículo científico publicado en 2017
Large-scale genome-wide association studies and meta-analyses of longitudinal change in adult lung function
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artículo científico publicado en 2014
Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria
artículo científico publicado en 2018
Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair
artículo científico publicado en 2015
Large-scale genomic studies reveal central role of ABO in sP-selectin and sICAM-1 levels
artículo científico publicado en 2010
Large-scale genotyping identifies 41 new loci associated with breast cancer risk
artículo científico publicado en 2013
Large-scale meta-analysis of interleukin-1 beta and interleukin-1 receptor antagonist polymorphisms on risk of radiographic hip and knee osteoarthritis and severity of knee osteoarthritis
artículo científico publicado en 2010
Large-scale whole-exome sequencing association studies identify rare functional variants influencing serum urate levels
artículo científico publicado en 2018
Leukocyte telomere length associates with prospective mortality independent of immune-related parameters and known genetic markers
artículo científico publicado en 2014
Levels of antibodies against tissue transglutaminase during pregnancy are associated with reduced fetal weight and birth weight
artículo científico publicado en 2013
Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects
artículo científico publicado en 2018
Linkage analysis and whole exome sequencing identify a novel candidate gene in a Dutch multiple sclerosis family
artículo científico publicado en 2018
Lipoprotein receptor-related protein 1 variants and dietary fatty acids: meta-analysis of European origin and African American studies
artículo científico publicado en 2013
List of Contributors
Loci at chromosomes 13, 19 and 20 influence age at natural menopause
artículo científico publicado en 2009
Loci for regulation of bone mineral density in men and women identified by genome wide linkage scan: the FAMOS study.
artículo científico publicado en 2005
Loci influencing blood pressure identified using a cardiovascular gene-centric array
artículo científico publicado en 2013
Loci influencing blood pressure identified using a cardiovascular gene-centric array.
artículo científico publicado en 2013
Long-term Effect of Folic Acid and Vitamin B12 Supplementation on Fracture Risk and Cardiovascular Disease: Follow-up Study of B-PROOF Trial (P24-031-19)
Long-term effects of folic acid and vitamin-B12 supplementation on fracture risk and cardiovascular disease: Extended follow-up of the B-PROOF trial
scientific article published on 05 August 2020
Low dietary riboflavin but not folate predicts increased fracture risk in postmenopausal women homozygous for the MTHFR 677 T allele
artículo científico publicado en 2008
Low prevalence of NOD2 SNPs in Behçet's disease suggests protective association in Caucasians
artículo científico publicado en 2009
Low serum vitamin D is associated with axial length and risk of myopia in young children
artículo científico publicado en 2016
Low-density lipoprotein receptor mutations generate synthetic genome-wide associations
artículo científico publicado en 2012
Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility
artículo científico publicado en 2015
Lower sex hormone levels are associated with more chronic musculoskeletal pain in community-dwelling elderly women
artículo científico publicado en 2016
MON-208 Association Study of AMH Promoter Polymorphisms and Serum AMH Levels in PCOS Patients
Mapping of 34 minisatellite loci resolved by two-dimensional DNA typing
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artículo científico publicado el 1 de enero de 1997
Mapping of gene expression reveals CYP27A1 as a susceptibility gene for sporadic ALS.
artículo científico publicado en 2012
Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors
Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors
artículo científico publicado en 2019
Maternal environmental risk factors and the development of internalizing and externalizing problems in childhood: The complex role of genetic factors
scientific article published on 24 August 2019
Maternal plasma folate impacts differential DNA methylation in an epigenome-wide meta-analysis of newborns
artículo científico publicado en 2016
Medication-related fall incidents in an older, ambulant population: the B-PROOF study
artículo científico
Mendelian randomization evaluation of causal effects of fibrinogen on incident coronary heart disease
artículo científico publicado en 2019
Mendelian randomization study of interleukin-6 in chronic obstructive pulmonary disease
artículo científico publicado en 2011
Menopause: Genome stability as new paradigm
artículo científico publicado en 2016
Meta-GWAS Accuracy and Power (MetaGAP) Calculator Shows that Hiding Heritability Is Partially Due to Imperfect Genetic Correlations across Studies
artículo científico publicado en 2017
Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways
artículo científico publicado en 2012
Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function
artículo científico publicado en 2010
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution
artículo científico publicado en 2010
Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci
artículo científico publicado en 2016
Meta-analysis identifies loci affecting levels of the potential osteoarthritis biomarkers sCOMP and uCTX-II with genome wide significance
artículo científico publicado en 2014
Meta-analysis identifies six new susceptibility loci for atrial fibrillation
artículo científico publicado en 2012
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine
artículo científico publicado en 2016
Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels
artículo científico publicado en 2016
Meta-analysis of Genome-Wide Association Studies Identifies Novel Loci Associated With Optic Disc Morphology
artículo científico publicado en 2015
Meta-analysis of epigenome-wide association studies of cognitive abilities
artículo científico publicado en 2018
Meta-analysis of exome array data identifies six novel genetic loci for lung function
scientific article published on 12 January 2018
Meta-analysis of exome array data identifies six novel genetic loci for lung function
Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error
artículo científico publicado en 2016
Meta-analysis of genome-wide association data identifies two loci influencing age at menarche
artículo científico publicado en 2009
Meta-analysis of genome-wide association for migraine in six population-based European cohorts
artículo científico publicado en 2011
Meta-analysis of genome-wide association studies confirms a susceptibility locus for knee osteoarthritis on chromosome 7q22
artículo científico publicado en 2010
Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque
artículo científico publicado en 2011
Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process
artículo científico publicado en 2014
Meta-analysis of genome-wide association studies identifies six new Loci for serum calcium concentrations
artículo científico publicado en 2013
Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis
artículo científico publicado en 2012
Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels
artículo científico publicado en 2011
Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error
artículo científico publicado en 2013
Meta-analysis of genome-wide association studies of aggressive and chronic periodontitis identifies two novel risk loci
artículo científico publicado en 2018
Meta-analysis of genome-wide association studies of anxiety disorders.
artículo científico publicado en 2016
Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size
artículo científico publicado en 2009
Meta-analysis of genome-wide scans for total body BMD in children and adults reveals allelic heterogeneity and age-specific effects at the WNT16 locus
artículo científico publicado en 2012
Meta-analysis of genome-wide scans for total body BMD in children and adults reveals allelic heterogeneity, pleiotropy and age-specific effects at the WNT16 locus
article published in 2012
Meta-analysis of genome-wide scans provides evidence for sex- and site-specific regulation of bone mass
artículo científico publicado en 2007
Meta‐Analysis of Genomewide Association Studies Reveals Genetic Variants for Hip Bone Geometry
artículo científico publicado en 2019
Methylation of BoneSOST, Its mRNA, and Serum Sclerostin Levels Correlate Strongly With Fracture Risk in Postmenopausal Women
article
Methylation of migraine-related genes in different tissues of the rat
artículo científico publicado en 2014
Methylenetetrahydrofolate reductase C677T genotype and PD.
artículo científico publicado en 2005
Microbiome measurement: Possibilities and pitfalls
artículo científico publicado en 2017
Microbiomics, metabolomics, predicted metagenomics and hepatic steatosis in a population-based study of 1355 adults
artículo científico publicado en 2020
Migraine without aura: genome-wide association analysis identifies several novel susceptibility.
artículo científico publicado en 2013
Mild hyponatremia as a risk factor for fractures: The rotterdam study
article
Modulation of genetic associations with serum urate levels by body-mass-index in humans
artículo científico publicado en 2015
Molecular Alterations in Dog Pheochromocytomas and Paragangliomas.
artículo científico publicado en 2019
Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions
Multi-Omics Analysis Reveals MicroRNAs Associated With Cardiometabolic Traits
scientific article published on 27 February 2020
Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction
scientific article published on 21 May 2020
Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk
Multi-ancestry genome-wide association study accounting for gene-psychosocial factor interactions identifies novel loci for blood pressure traits
artículo científico publicado en 2021
Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis
artículo científico publicado en 2015
Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids
article
Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration
artículo científico publicado en 2019
Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity
artículo científico publicado en 2019
Multi-ethnic genome-wide association study for atrial fibrillation
article
Multi-functionality of computer-aided quantitative vertebral fracture morphometry analyses
artículo científico publicado en 2013
Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks.
artículo científico publicado en 2017
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes
artículo científico publicado en 2018
Multicenter cohort association study of SLC2A1 single nucleotide polymorphisms and age-related macular degeneration
artículo científico publicado en 2012
Multiethnic Exome-Wide Association Study of Subclinical Atherosclerosis.
artículo científico publicado en 2016
Multiethnic Meta-analysis Identifies New Loci for Pulmonary Function
Multiethnic genome-wide association study of cerebral white matter hyperintensities on MRI
artículo científico publicado en 2015
Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function
scientific article published in Nature Communications
Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease
artículo científico publicado en 2013
Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors
artículo científico publicado en 2010
Multiple loci are associated with white blood cell phenotypes
artículo científico publicado en 2011
Multiple loci associated with indices of renal function and chronic kidney disease
scientific journal article
Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium
artículo científico publicado en 2009
Multistage genome-wide association meta-analyses identified two new loci for bone mineral density
artículo científico publicado en 2013
Multi‐phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations
artículo científico publicado en 2022
Mutations in nucleophosmin (NPM1) in acute myeloid leukemia (AML): association with other gene abnormalities and previously established gene expression signatures and their favorable prognostic significance
artículo científico publicado en 2005
NFAT5 and SLC4A10 Loci Associate with Plasma Osmolality
artículo científico
NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium
artículo científico publicado en 2009
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
artículo científico publicado en 2010
New genetic loci link adipose and insulin biology to body fat distribution
artículo científico publicado en 2015
New insights into the genetic etiology of Alzheimer's disease and related dementias
artículo científico publicado en 2022
New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism
artículo científico publicado en 2012
New loci associated with kidney function and chronic kidney disease
artículo científico publicado en 2010
New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk
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artículo científico publicado en 2016
Newborn DNA-methylation, childhood lung function, and the risks of asthma and COPD across the life course
artículo científico publicado en 2019
Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error
artículo científico publicado en 2013
Ninety-nine independent genetic loci influencing general cognitive function include genes associated with brain health and structure (N = 280,360)
No causal association between 25-hydroxyvitamin D and features of skin aging: evidence from a bidirectional Mendelian Randomization Study
artículo científico publicado en 2017
No evidence for genome-wide interactions on plasma fibrinogen by smoking, alcohol consumption and body mass index: results from meta-analyses of 80,607 subjects
artículo científico publicado en 2014
Non-linear associations between serum 25-OH vitamin D and indices of arterial stiffness and arteriosclerosis in an older population.
artículo científico publicado en 2014
Nonsynonymous Variation in NKPD1 Increases Depressive Symptoms in European Populations
artículo científico publicado en 2016
Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney
artículo científico publicado en 2017
Novel CYP3A4 intron 6 single nucleotide polymorphism is associated with simvastatin-mediated cholesterol reduction in the Rotterdam Study
artículo científico publicado en 2011
Novel Genetic Loci Associated With Retinal Microvascular Diameter
artículo científico publicado en 2015
Novel Genetic Variants for Cartilage Thickness and Hip Osteoarthritis
artículo científico publicado en 2016
Novel Leptin Receptor Mutations Identified in Two Girls with Severe Obesity Are Associated with Increased Bone Mineral Density
artículo científico publicado en 2016
Novel associations of multiple genetic loci with plasma levels of factor VII, factor VIII, and von Willebrand factor: The CHARGE (Cohorts for Heart and Aging Research in Genome Epidemiology) Consortium
artículo científico publicado en 2010
Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries.
artículo científico publicado en 2018
Novel genetic loci affecting facial shape variation in humans
artículo científico publicado en 2019
Novel genetic loci associated with hippocampal volume
scientific article published on 18 January 2017
Novel genetic loci underlying human intracranial volume identified through genome-wide association
artículo científico publicado en 2016
Novel genetic markers associate with atrial fibrillation risk in Europeans and Japanese
artículo científico publicado en 2014
Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects
artículo científico publicado en 2012
Novel loci associated with usual sleep duration: the CHARGE Consortium Genome-Wide Association Study
artículo científico publicado en 2014
Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals
artículo científico publicado en 2012
Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traits
artículo científico publicado en 2020
Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways
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artículo científico publicado en 2018
Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways
Novel taxonomy-independent deep learning microbiome approach allows for accurate classification of different forensically relevant human epithelial materials
scientific article published on 04 April 2019
Nucleotide excision DNA repair is associated with age-related vascular dysfunction
artículo científico publicado en 2012
OCT1 polymorphism is associated with response and survival time in anti-Parkinsonian drug users
artículo científico publicado en 2010
Objectives, design and main findings until 2020 from the Rotterdam Study
scientific article published on 04 May 2020
Omega-3 Fatty Acids and Genome-Wide Interaction Analyses Reveal DPP10-Pulmonary Function Association
artículo científico publicado en 2019
Organic anion transporter 1B1: an important factor in hepatic thyroid hormone and estrogen transport and metabolism
artículo científico publicado en 2008
Orthostatic hypotension and novel blood pressure-associated gene variants: Genetics of Postural Hemodynamics (GPH) Consortium
artículo científico publicado en 2012
Oscillometry and applanation tonometry measurements in older individuals with elevated levels of arterial stiffness
artículo científico publicado en 2013
Osteoarthritis of the knee is associated with vertebral and nonvertebral fractures in the elderly: the Rotterdam Study
artículo científico publicado en 2003
Osteoporosis
Osteoporosis Genes Identified by Genome-wide Association Studies
article
PAPSS2 deficiency causes androgen excess via impaired DHEA sulfation--in vitro and in vivo studies in a family harboring two novel PAPSS2 mutations
artículo científico publicado en 2015
PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study
artículo científico publicado en 2016
PLD3 variants in population studies
artículo científico publicado en 2015
PLS3 mutations in X-linked osteoporosis with fractures
artículo científico publicado en 2013
PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity
artículo científico publicado en 2018
PROP1, HESX1, POU1F1, LHX3 and LHX4 mutation and deletion screening and GH1 P89L and IVS3+1/+2 mutation screening in a Dutch nationwide cohort of patients with combined pituitary hormone deficiency
artículo científico publicado en 2010
PROTEIN-CODING VARIANTS IMPLICATE NOVEL GENES RELATED TO LIPID HOMEOSTASIS CONTRIBUTING TO BODY FAT DISTRIBUTION
article
PTHR1 Polymorphisms Influence BMD Variation through Effects on the Growing Skeleton
article
PanCareLIFE: The scientific basis for a European project to improve long-term care regarding fertility, ototoxicity and health-related quality of life after cancer occurring among children and adolescents
article
Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche
artículo científico publicado en 2014
Peripheral Blood Transcriptomic Signatures of Fasting Glucose and Insulin Concentrations
artículo científico publicado en 2016
Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins
artículo científico publicado en 2014
Pharmacogenetic risk factors for altered bone mineral density and body composition in pediatric acute lymphoblastic leukemia
artículo científico publicado en 2009
Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9
scientific article published on 29 October 2019
Phenotypic dissection of bone mineral density reveals skeletal site specificity and facilitates the identification of novel loci in the genetic regulation of bone mass attainment
artículo científico publicado en 2014
Physical activity attenuates the influence of FTO variants on obesity risk: a meta-analysis of 218,166 adults and 19,268 children
artículo científico publicado en 2011
Pigmentation-Independent Susceptibility Loci for Actinic Keratosis Highlighted by Compound Heterozygosity Analysis
artículo científico publicado en 2016
Pleiotropic genes for metabolic syndrome and inflammation
artículo científico publicado en 2014
Pleiotropy among common genetic loci identified for cardiometabolic disorders and C-reactive protein
artículo científico publicado en 2015
Polymorphic variations in exon 10 of the luteinizing hormone receptor: functional consequences and associations with breast cancer
artículo científico publicado en 2007
Polymorphisms Near IL28B and Serologic Response to Peginterferon in HBeAg-Positive Patients With Chronic Hepatitis B
article
Polymorphisms in the GATA-Binding Sites of the Vitamin D Receptor Gene Affect Its Transcription in the Esophagus, and Are Associated With a Reduced Risk for Esophageal Disease
artículo científico publicado en 2011
Polymorphisms in the estrogen receptor alpha gene and mammographic density.
artículo científico publicado en 2005
Polymorphisms in the interleukin 6 and transforming growth factor beta1 gene and risk of dementia. The Rotterdam Study
artículo científico publicado en 2006
Polymorphisms in the sclerosteosis/van Buchem disease gene (SOST) region are associated with bone-mineral density in elderly whites
artículo científico publicado en 2004
Polymorphisms in the vascular endothelial growth factor gene and risk of age-related macular degeneration: the Rotterdam Study
artículo científico publicado en 2008
Polymorphisms in thyroid hormone pathway genes are associated with plasma TSH and iodothyronine levels in healthy subjects
artículo científico publicado en 2003
Population analysis of the collagen type IIα1 3′ variable number of tandem repeat polymorphism by heteroduplex genotyping
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artículo científico publicado el 1 de mayo de 1998
Population genomics in a disease targeted primary cell model
artículo científico publicado en 2009
Population-based meta-analysis in Caucasians confirms association with COL5A1 and ZNF469 but not COL8A2 with central corneal thickness.
artículo científico publicado en 2012
Population-specific genetic variation in large sequencing data sets: why more data is still better
artículo científico publicado en 2017
Potential Interplay between Dietary Saturated Fats and Genetic Variants of the NLRP3 Inflammasome to Modulate Insulin Resistance and Diabetes Risk: Insights from a Meta-Analysis of 19 005 Individuals
scientific article published on 12 September 2019
Predicting human height by Victorian and genomic methods
artículo científico publicado en 2009
Predicting stroke through genetic risk functions: the CHARGE Risk Score Project
artículo científico publicado en 2014
Predicting type 2 diabetes based on polymorphisms from genome-wide association studies: a population-based study
artículo científico publicado en 2008
Prediction of age-related macular degeneration in the general population: the Three Continent AMD Consortium
artículo científico publicado en 2013
Prediction of male-pattern baldness from genotypes
artículo científico publicado en 2015
Prenatal parental tobacco smoking, gene specific DNA methylation, and newborns size: the Generation R study
artículo científico publicado en 2015
Profiling of complex microbial populations by denaturing gradient gel electrophoresis analysis of polymerase chain reaction-amplified genes coding for 16S rRNA
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artículo científico publicado el 1 de marzo de 1993
Promoter and 3'-untranslated-region haplotypes in the vitamin d receptor gene predispose to osteoporotic fracture: the rotterdam study
artículo científico publicado en 2005
Protective effect of a GRK5 polymorphism on heart failure and its interaction with beta-adrenergic receptor antagonists
artículo científico publicado en 2008
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution
article
Prothrombotic genetic risk factors are associated with an increased risk of liver fibrosis in the general population: The Rotterdam Study
artículo científico publicado en 2015
Proton pump inhibitors and the risk of overanticoagulation during acenocoumarol maintenance treatment
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artículo científico publicado el 21 de marzo de 2011
Publisher Correction: GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures
scientific article published on 24 May 2019
Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits
scholarly article published in Nature Genetics
Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits
erratum
Publisher Correction: Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability
artículo científico publicado en 2019
Publisher Correction: Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways
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artículo científico publicado en 2019
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
artículo científico publicado en 2018
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
artículo científico publicado en 2018
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
artículo científico publicado en 2019
Quantifying prion disease penetrance using large population control cohorts
artículo científico publicado en 2016
Rapid Low-Cost Microarray-Based Genotyping for Genetic Screening in Primary Immunodeficiency
scientific article published on 15 April 2020
Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer's Disease
artículo científico publicado en 2016
Rare and low-frequency coding variants alter human adult height
artículo científico publicado en 2017
Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWF
artículo científico publicado en 2015
Rare coding variants and X-linked loci associated with age at menarche
artículo científico publicado en 2015
Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study
article
Rare gene deletions in genetic generalized and Rolandic epilepsies
artículo científico publicado en 2018
Rare variants in γ-aminobutyric acid type A receptor genes in rolandic epilepsy and related syndromes
artículo científico publicado en 2015
Rationale and design of the B-PROOF study, a randomized controlled trial on the effect of supplemental intake of vitamin B12 and folic acid on fracture incidence
artículo científico publicado en 2011
Recognition of scared faces and the serotonin transporter gene in young children: the Generation R Study
artículo científico publicado en 2011
Reduced penetrance of pathogenic ACMG variants in a deeply phenotyped cohort study and evaluation of ClinVar classification over time
artículo científico publicado en 2020
Reducing the Genetic Risk of Age-Related Macular Degeneration With Dietary Antioxidants, Zinc, and ω-3 Fatty Acids
scientific article published on 01 June 2011
Refined mapping of autoimmune disease associated genetic variants with gene expression suggests an important role for non-coding RNAs
artículo científico publicado en 2016
Refining The Accuracy Of Validated Target Identification Through Coding Variant Fine-Mapping In Type 2 Diabetes
article
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes
artículo científico publicado en 2018
Relationship between gut microbiota and circulating metabolites in population-based cohorts
scientific article published on 20 December 2019
Relationship between the functional exon 3 deleted growth hormone receptor polymorphism and symptomatic osteoarthritis in women
artículo científico publicado en 2013
Relative importance of summer sun exposure, vitamin D intake, and genes to vitamin D status in Dutch older adults: The B-PROOF study
artículo científico publicado en 2015
Replication of association of a novel insulin receptor gene polymorphism with polycystic ovary syndrome
artículo científico publicado en 2011
Replication study of chr17q25 with cerebral white matter lesion volume
artículo científico publicado en 2011
Reproductive aging-associated common genetic variants and the risk of breast cancer
artículo científico publicado en 2012
Response to Letter by Markoula et al
Results of 2-year vitamin B treatment on cognitive performance: secondary data from an RCT.
artículo científico publicado en 2014
Review of radiological scoring methods of osteoporotic vertebral fractures for clinical and research settings
artículo científico
Risk of Frailty in Elderly With COPD: A Population-Based Study
artículo científico publicado en 2015
Risk scores of common genetic variants for lipid levels influence atherosclerosis and incident coronary heart disease
artículo científico publicado en 2013
Runs of homozygosity do not influence survival to old age.
artículo científico publicado en 2011
SIRT1 genetic variation and mortality in type 2 diabetes: interaction with smoking and dietary niacin
artículo científico publicado en 2009
SIRT1 genetic variation is related to BMI and risk of obesity
artículo científico publicado en 2009
Sarcopenia and Its Clinical Correlates in the General Population: The Rotterdam Study
artículo científico publicado en 2018
Scheuermann disease: evaluation of radiological criteria and population prevalence
artículo científico publicado en 2013
Scheuermann's Disease: Evaluation of Radiological Criteria and Population Prevalence
artículo científico publicado en 2013
Scrutinizing the Genetic Underpinnings of Bone Strength
artículo científico publicado en 2017
Secretory phospholipase A(2)-IIA and cardiovascular disease: a mendelian randomization study
scientific article published on 31 July 2013
Selective serotonin re‐uptake inhibiting antidepressants and the risk of overanticoagulation during acenocoumarol maintenance treatment
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artículo científico publicado el 1 de noviembre de 2011
Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior
artículo científico publicado en 2010
Serum 25-hydroxyvitamin D is associated with advanced glycation end products (AGEs) measured as skin autofluorescence: The Rotterdam Study
artículo científico publicado en 2018
Serum C reactive protein levels and genetic variation in the CRP gene are not associated with the prevalence, incidence or progression of osteoarthritis independent of body mass index
artículo científico publicado en 2010
Serum Phosphate Is Associated With Fracture Risk: The Rotterdam Study and MrOS.
artículo científico publicado en 2017
Serum fasting cortisol in relation to bone, and the role of genetic variations in the glucocorticoid receptor
artículo científico publicado en 2007
Serum phosphate levels are related to all-cause, cardiovascular and COPD mortality in men
scholarly article by Natalia Campos-Obando et al published 15 May 2018 in European Journal of Epidemiology
Serum testosterone levels in males are not associated with entrepreneurial behavior in two independent observational studies
artículo científico publicado en 2013
Seven new loci associated with age-related macular degeneration
artículo científico publicado en 2013
Severe osteoarthritis of the hand associates with common variants within the ALDH1A2 gene and with rare variants at 1p31.
artículo científico publicado en 2014
Sex Hormone-Binding Globulin Is Associated With Markers Of Vertebral Fracture And Vertebral Fracture Risk
artículo científico publicado en 2018
Sex differences in bone acquisition of pre-pubertal children are consequence of differential responsiveness to mechanical loading
scholarly article
Sex-specific differences in the effects of local androgen metabolism in the heart as an indicator for the risk of myocardial infarction
Sex-specific effects of naturally occurring variants in the dopamine receptor D2 locus on insulin secretion and type 2 diabetes susceptibility.
artículo científico publicado en 2014
Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits
artículo científico publicado en 2013
Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms
artículo científico publicado en 2016
Short-Term, Combined Fasting and Exercise Improves Body Composition in Healthy Males
artículo científico publicado en 2020
Single nucleotide polymorphisms in CRTC1 and BARX1 are associated with esophageal adenocarcinoma
artículo científico publicado en 2015
Six new loci associated with body mass index highlight a neuronal influence on body weight regulation
artículo científico publicado en 2009
Skeletal maturation in relation to ethnic background in children of school age: The Generation R Study
scientific article published on 28 November 2019
Skin autofluorescence, a non-invasive biomarker for advanced glycation end-products, is associated with prevalent vertebral and major osteoporotic fractures: The Rotterdam Study
artículo científico publicado en 2020
Smoking-by-genotype interaction in type 2 diabetes risk and fasting glucose
artículo científico publicado en 2020
Smoking-related changes in DNA methylation and gene expression are associated with cardio-metabolic traits
artículo científico publicado en 2020
Somatic TARDBP variants as cause of semantic dementia
artículo científico publicado en 2020
Somatic, positive and negative domains of the Center for Epidemiological Studies Depression (CES-D) scale: a meta-analysis of genome-wide association studies
artículo científico publicado en 2016
Staphylococcus aureus nasal carriage is associated with glucocorticoid receptor gene polymorphisms
artículo científico publicado en 2006
Staphylococcus aureus nasal carriage is not associated with known polymorphism in the Vitamin D receptor gene
artículo científico publicado en 2005
Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases
artículo científico publicado en 2012
Structural geometry of bones is prominently associated with risk of fracture in children
scholarly article
Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function
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artículo científico publicado en 2018
Subclinical thyroid dysfunction and fracture risk: a meta-analysis
artículo científico publicado en 2015
Sugar-sweetened beverage intake associations with fasting glucose and insulin concentrations are not modified by selected genetic variants in a ChREBP-FGF21 pathway: a meta-analysis
artículo científico publicado en 2017
Susceptibility to chronic mucus hypersecretion, a genome wide association study
artículo científico publicado en 2014
Systematic identification of trans eQTLs as putative drivers of known disease associations
artículo científico publicado en 2013
TGF-β1 Polymorphisms and Risk of Myocardial Infarction and Stroke
TMEM106B influences volume of left-sided temporal lobe and interhemispheric structures in the general population
article by Hieab H.H. Adams et al published 15 September 2014 in Biological Psychiatry
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels
artículo científico publicado en 2019
Targeted sequencing of genome wide significant loci associated with bone mineral density (BMD) reveals significant novel and rare variants: the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) targeted sequencing study
artículo científico publicado en 2016
The -1997 G/T and Sp1 polymorphisms in the collagen type I alpha1 (COLIA1) gene in relation to changes in femoral neck bone mineral density and the risk of fracture in the elderly: the Rotterdam study
artículo científico publicado en 2007
The -G1245A IGF1 polymorphism is related with small head size and less brain sparing in small for gestational age born children
artículo científico publicado en 2009
The Asp727Glu polymorphism in the TSH receptor is associated with insulin resistance in healthy elderly men.
artículo científico publicado en 2007
The Association between Metabolic Syndrome, Bone Mineral Density, Hip Bone Geometry and Fracture Risk: The Rotterdam Study
artículo científico publicado en 2015
The DOT1L rs12982744 polymorphism is associated with osteoarthritis of the hip with genome-wide statistical significance in males
artículo científico publicado en 2013
The ERCC6 gene and age-related macular degeneration
artículo científico publicado en 2010
The GDF5 rs143383 polymorphism is associated with osteoarthritis of the knee with genome-wide statistical significance
artículo científico publicado en 2010
The Generation R Study Biobank: a resource for epidemiological studies in children and their parents
artículo científico publicado en 2007
The Generation R Study: Biobank update 2015.
artículo científico publicado en 2014
The Generation R Study: a review of design, findings to date, and a study of the 5-HTTLPR by environmental interaction from fetal life onward
artículo científico
The Generation R Study: design and cohort update 2010.
artículo científico publicado en 2010
The Generation R Study: design and cohort update 2012.
artículo científico publicado en 2012
The Generation R Study: design and cohort update 2017
artículo científico publicado en 2017
The Generation R Study: design and cohort update until the age of 4 years
article
The Genome of the Netherlands: design, and project goals
artículo científico publicado en 2014
The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study
artículo científico publicado en 2015
The Influence of Serum Uric Acid on Bone Mineral Density, Hip Geometry, and Fracture Risk: The Rotterdam Study
artículo científico publicado en 2015
The M235T polymorphism in the angiotensinogen gene is associated with the risk of malignant hypertension in white patients
artículo científico publicado en 2007
The MC1R Gene and Youthful Looks
artículo científico publicado en 2016
The PCLO gene and depressive disorders: replication in a population-based study
article
The RIZ Pro704 insertion-deletion polymorphism, bone mineral density and fracture risk: the Rotterdam study
artículo científico publicado en 2007
The Rotterdam Study: 2010 objectives and design update
artículo científico publicado en 2009
The Rotterdam Study: 2012 objectives and design update
artículo científico publicado en 2011
The Rotterdam Study: 2014 objectives and design update
artículo científico publicado en 2013
The Rotterdam Study: 2016 objectives and design update
artículo científico publicado en 2015
The Rotterdam Study: 2018 update on objectives, design and main results
artículo científico publicado en 2017
The Rotterdam Study: objectives and design update
artículo científico publicado en 2007
The SLCO1B1 c.521T>C polymorphism is associated with dose decrease or switching during statin therapy in the Rotterdam Study
artículo científico publicado en 2014
The T-13910C polymorphism in the lactase phlorizin hydrolase gene is associated with differences in serum calcium levels and calcium intake
artículo científico publicado en 2010
The activin A-follistatin system: potent regulator of human extracellular matrix mineralization
artículo científico publicado en 2007
The association between common vitamin D receptor gene variations and osteoporosis: a participant-level meta-analysis
artículo científico publicado en 2006
The association between dietary and skin advanced glycation end products: the Rotterdam Study
scientific article published on 26 May 2020
The association of mitochondrial content with prevalent and incident type 2 diabetes.
artículo científico publicado en 2010
The association of polymorphisms in the type 1 and 2 deiodinase genes with circulating thyroid hormone parameters and atrophy of the medial temporal lobe
artículo científico publicado en 2006
The association of serum testosterone levels and ventricular repolarization
artículo científico publicado en 2009
The beneficial effects of recipient-derived vascular endothelial growth factor on graft survival after kidney transplantation
scientific article published on 01 May 2005
The catechol-O-methyltransferase Met158 low-activity allele and association with nonvertebral fracture risk in elderly men
artículo científico publicado en 2007
The challenges of genome-wide interaction studies: lessons to learn from the analysis of HDL blood levels
artículo científico publicado en 2014
The complement component 5 gene and age-related macular degeneration
artículo científico publicado en 2009
The complex genetics of gait speed: genome-wide meta-analysis approach
scientific article published on 10 January 2017
The dystrophin gene and cognitive function in the general population
artículo científico publicado en 2014
The effect of catechol-O-methyltransferase Met/Val functional polymorphism on smoking cessation: retrospective and prospective analyses in a cohort study
artículo científico publicado en 2009
The effect of genetic variation in the type 1 deiodinase gene on the interindividual variation in serum thyroid hormone levels: an investigation in healthy Danish twins
artículo científico publicado en 2008
The effects of long-term daily folic acid and vitamin B12 supplementation on genome-wide DNA methylation in elderly subjects
artículo científico publicado en 2015
The emergence of networks in human genome epidemiology: challenges and opportunities
scholarly article published 18 December 2009
The epithelial Ca2+ channel TRPV5 is essential for proper osteoclastic bone resorption
artículo científico publicado en 2005
The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals
artículo científico publicado en 2016
The genetics of seborrheic dermatitis: a candidate gene approach and pilot genome-wide association study
artículo científico publicado en 2017
The impact of thiazide diuretics on bone mineral density and the trabecular bone score: The Rotterdam study
artículo científico publicado en 2020
The increase in cholesterol with menopause is associated with the apolipoprotein E genotype. A population-based longitudinal study
artículo científico publicado en 2004
The interleukin-6-174 G/C promoter polymorphism and arterial stiffness; the Rotterdam Study
artículo científico publicado en 2008
The latest news from the GENOMOS study.
artículo científico publicado en 2009
The maternal homocysteine pathway is influenced by riboflavin intake and MTHFR polymorphisms without affecting the risk of orofacial clefts in the offspring.
artículo científico publicado en 2009
The molecular genetic architecture of self-employment
artículo científico publicado en 2013
The relationship between fertility and lifespan in humans
artículo científico publicado en 2011
The risk of myocardial infarction in patients with reduced activity of cytochrome P450 2C9.
artículo científico publicado en 2007
The role of adiposity in cardiometabolic traits: a Mendelian randomization analysis
artículo científico publicado en 2013
The role of body mass index, insulin, and adiponectin in the relation between fat distribution and bone mineral density
artículo científico publicado en 2009
The role of vitamin D receptor gene polymorphisms in bone biology
artículo científico publicado en 2002
The rs13064411 polymorphism in the WDR52 gene, associated with PCSK9 levels, modifies statin-induced changes in serum total and LDL cholesterol levels
artículo científico publicado en 2015
The trans-ancestral genomic architecture of glycemic traits
The transcriptional landscape of age in human peripheral blood
artículo científico publicado en 2015
Thiazide-associated hyponatremia: a population-based study
artículo científico publicado en 2013
Thiazides and the risk of hypokalemia in the general population
artículo científico publicado en 2014
Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies
artículo científico publicado en 2010
Three Genome-wide Association Studies and a Linkage Analysis Identify HERC2 as a Human Iris Color Gene
artículo científico publicado en 2008
Three genome-wide association studies and a linkage analysis identify HERC2 as a human iris color gene
artículo científico publicado en 2008
Thyroid Function Characteristics and Determinants: The Rotterdam Study
artículo científico publicado en 2016
Thyroid Function Tests in the Reference Range and Fracture: Individual Participant Analysis of Prospective Cohorts.
artículo científico publicado en 2017
Tissue effect on genetic control of transcript isoform variation
artículo científico publicado en 2009
Tobacco smoking is associated with DNA methylation of diabetes susceptibility genes
artículo científico publicado en 2016
Tobacco smoking is associated with methylation of genes related to coronary artery disease
artículo científico publicado en 2015
Total zinc intake may modify the glucose-raising effect of a zinc transporter (SLC30A8) variant: a 14-cohort meta-analysis
artículo científico publicado en 2011
Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation
artículo científico publicado en 2015
Trans-ethnic meta-analysis of white blood cell phenotypes
artículo científico publicado en 2014
Translation of mouse model to human gives insights into periodontitis etiology
artículo científico publicado en 2020
Treatment factors rather than genetic variation determine metabolic syndrome in childhood cancer survivors
artículo científico publicado en 2012
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis
artículo científico publicado en 2010
Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies
artículo científico publicado en 2009
Two MTHFR polymorphisms, maternal B-vitamin intake, and CHDs
artículo científico publicado en 2008
Type 2 diabetes gene TCF7L2 polymorphism is not associated with fetal and postnatal growth in two birth cohort studies
artículo científico publicado en 2009
Uncompromised 10-year survival of oldest old carrying somatic mutations in DNMT3A and TET2.
artículo científico publicado en 2016
Understanding the role of the chromosome 15q25.1 in COPD through epigenetics and transcriptomics
artículo científico publicado en 2018
Update on the predictability of tall stature from DNA markers in Europeans
artículo científico publicado en 2019
Use of Selective Serotonin Reuptake Inhibitors and Bone Mineral Density Change: A Population-Based Longitudinal Study in Middle-Aged and Elderly Individuals
artículo científico publicado en 2017
Use of statins is associated with lower serum total and non-sex hormone-binding globulin-bound testosterone levels in male participants of the Rotterdam Study
artículo científico publicado en 2015
Usefulness of Combining Complement Factor H and C-Reactive Protein Genetic Profiles for Predicting Myocardial Infarction (from the Rotterdam Study)
scientific article published on 26 June 2007
Usefulness of current candidate genetic markers to identify childhood cancer patients at risk for platinum-induced ototoxicity: Results of the European PanCareLIFE cohort study
scientific article published on 06 September 2020
VEGF polymorphisms are associated with endocardial cushion defects: a family-based case-control study
artículo científico publicado en 2010
Validated inference of smoking habits from blood with a finite DNA methylation marker set
scientific article published on 07 September 2019
Validation of the BOADICEA model and a 313-variant polygenic risk score for breast cancer risk prediction in a Dutch prospective cohort
artículo científico publicado en 2020
Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight
artículo científico publicado en 2010
Variants in MTNR1B influence fasting glucose levels
artículo científico publicado en 2008
Variants in SULT2A1 affect the DHEA sulphate to DHEA ratio in patients with polycystic ovary syndrome but not the hyperandrogenic phenotype.
artículo científico publicado en 2013
Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry
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scientific article published on 13 July 2009
Variants in the ACVR1 gene are associated with AMH levels in women with polycystic ovary syndrome
artículo científico publicado en 2008
Variation at the ANP32A gene is associated with risk of hip osteoarthritis in women.
artículo científico publicado en 2009
Variation in the Estrogen Receptor α Gene and Risk of Stroke
article
Vertebral Fractures in Individuals With Type 2 Diabetes: More Than Skeletal Complications Alone
artículo científico publicado en 2019
Vitamin D Receptor Polymorphisms Are Associated with Reduced Esophageal Vitamin D Receptor Expression and Reduced Esophageal Adenocarcinoma Risk.
artículo científico publicado en 2015
Vitamin D and C-Reactive Protein: A Mendelian Randomization Study
artículo científico publicado en 2015
Vitamin D and body composition in the elderly
artículo científico publicado en 2016
Vitamin D and retinal microvascular damage: The Rotterdam Study
scientific article published on December 2016
Vitamin D binding protein genotype and osteoporosis
artículo científico publicado en 2009
Vitamin D receptor gene BsmI and TaqI polymorphisms and fracture risk: A meta-analysis
article
Vitamin D receptor gene haplotype is associated with body height and bone size
artículo científico publicado en 2007
Vitamin D receptor gene polymorphisms in relation to Vitamin D related disease states
artículo científico publicado en 2004
Vitamin D receptor: a new risk marker for clinical restenosis after percutaneous coronary intervention
artículo científico publicado en 2010
Vitamin D status, bone mineral density, and the development of radiographic osteoarthritis of the knee: The Rotterdam Study
artículo científico publicado en 2009
Vitamin D-binding protein polymorphisms are not associated with development of (multiple) basal cell carcinomas
artículo científico publicado en 2010
WNT10A exonic variant increases the risk of keratoconus by decreasing corneal thickness
artículo científico publicado en 2015
Whole Blood DNA Methylation Signatures of Diet Are Associated with Cardiovascular Disease Risk Factors and All-cause Mortality
scientific article published on 11 June 2020
Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis
article
Whole-Genome Linkage Scan Combined With Exome Sequencing Identifies Novel Candidate Genes for Carotid Intima-Media Thickness
article
Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol
artículo científico publicado en 2014
Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture
artículo científico publicado en 2015
[Cost] effectiveness of withdrawal of fall-risk increasing drugs versus conservative treatment in older fallers: design of a multicenter randomized controlled trial (IMPROveFALL-study).
artículo científico publicado en 2011
β2-Adrenergic Receptor (ADRB2) Gene Polymorphisms and Risk of COPD Exacerbations: The Rotterdam Study
artículo científico publicado en 2019