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1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function

artículo científico publicado en 2017

A Common Variant in MIR182 Is Associated With Primary Open-Angle Glaucoma in the NEIGHBORHOOD Consortium

artículo científico publicado en 2016

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 catalog of genetic loci associated with kidney function from analyses of a million individuals

scientific article published on 31 May 2019

A common missense variant of LILRB5 is associated with statin intolerance and myalgia.

artículo científico publicado en 2017

A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer

artículo científico publicado en 2011

A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease

artículo científico publicado en 2015

A genome-wide analysis of 'Bounty' descendants implicates several novel variants in migraine susceptibility

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 of bitter and sweet beverage consumption

artículo científico publicado en 2019

A genome-wide association study of early menopause and the combined impact of identified variants

artículo científico publicado en 2013

A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine

artículo científico publicado en 2020

A hierarchical Bayesian model for predicting the functional consequences of amino-acid polymorphisms

article

A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response

artículo científico publicado en 2021

A kinesin family member 6 variant is associated with coronary heart disease in the Women's Health Study

artículo científico publicado en 2008

A large-scale candidate gene association study of age at menarche and age at natural menopause

artículo científico publicado en 2010

A large-scale exome array analysis of venous thromboembolism

artículo científico publicado en 2019

A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration

artículo científico publicado en 2015

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 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 multivariate genome-wide association analysis of 10 LDL subfractions, and their response to statin treatment, in 1868 Caucasians

artículo científico publicado en 2015

A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape

artículo científico publicado en 2016

A statin-dependent QTL for GATM expression is associated with statin-induced myopathy

artículo científico publicado en 2013

Adiposity and Genetic Factors in Relation to Triglycerides and Triglyceride-Rich Lipoproteins in the Women's Genome Health Study

article

Age at natural menopause genetic risk score in relation to age at natural menopause and primary open-angle glaucoma in a US-based sample

artículo científico publicado en 2017

An Empirical Comparison of Joint and Stratified Frameworks for Studying G × E Interactions: Systolic Blood Pressure and Smoking in the CHARGE Gene-Lifestyle Interactions Working Group

artículo científico publicado en 2016

An X chromosome association scan of the Norfolk Island genetic isolate provides evidence for a novel migraine susceptibility locus at Xq12.

artículo científico publicado en 2012

Analysis of potential protein-modifying variants in 9000 endometriosis patients and 150000 controls of European ancestry

artículo científico publicado en 2017

Analysis of predicted loss-of-function variants in UK Biobank identifies variants protective for disease.

artículo científico publicado en 2018

Analysis of shared heritability in common disorders of the brain

artículo científico publicado en 2018

Are Genetic Tests for Atherosclerosis Ready for Routine Clinical Use?

artículo científico publicado en 2016

Assessing the causal relationship between obesity and venous thromboembolism through a Mendelian Randomization study.

artículo científico publicado en 2017

Assessment of Risk Factors and Biomarkers Associated With Risk of Cardiovascular Disease Among Women Consuming a Mediterranean Diet

scholarly article published 7 December 2018

Assessment of the Relationship Between Genetic Determinants of Thyroid Function and Atrial Fibrillation: A Mendelian Randomization Study

article published in 2019

Association Between Titin Loss-of-Function Variants and Early-Onset Atrial Fibrillation

Association between Vitamin D Genetic Risk Score and Cancer Risk in a Large Cohort of U.S. Women

artículo científico publicado en 2018

Association between a literature-based genetic risk score and cardiovascular events in women

artículo científico publicado en 2010

Association of Birth Weight With Type 2 Diabetes and Glycemic Traits: A Mendelian Randomization Study

scientific article published on 04 September 2019

Association of Lipid-Related Genetic Variants with the Incidence of Atrial Fibrillation: The AFGen Consortium

artículo científico publicado en 2016

Association of adiposity genetic variants with menarche timing in 92,105 women of European descent

artículo científico publicado en 2013

Association of cyclooxygenase-2 genetic variant with cardiovascular disease

artículo científico publicado en 2014

Association of exome sequences with plasma C-reactive protein levels in >9000 participants

artículo científico publicado en 2014

Association of hypertension drug target genes with blood pressure and hypertension in 86,588 individuals

artículo científico publicado en 2011

Association of the Mediterranean Diet With Onset of Diabetes in the Women's Health Study

scientific article published on 02 November 2020

Association of variation at the ABO locus with circulating levels of soluble intercellular adhesion molecule-1, soluble P-selectin, and soluble E-selectin: a meta-analysis

artículo científico publicado en 2011

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 dairy intake with risk of mortality in women and men: three prospective cohort studies

scientific article published on 27 November 2019

Atherogenic Lipoprotein Determinants of Cardiovascular Disease and Residual Risk Among Individuals With Low Low-Density Lipoprotein Cholesterol

artículo científico publicado en 2017

Biological, clinical and population relevance of 95 loci for blood lipids

artículo científico publicado en 2010

Blood Eosinophil Count and Metabolic, Cardiac and Pulmonary Outcomes: A Mendelian Randomization Study.

artículo científico publicado en 2018

CKM Glu83Gly Is Associated With Blunted Creatine Kinase Variation, but Not With Myalgia

artículo científico

COMT Effects on Vitamin E and Colorectal Cancer, in-vitro and in Two Randomized Trials (P15-005-19)

COMT and Alpha-Tocopherol Effects in Cancer Prevention: Gene-Supplement Interactions in Two Randomized Clinical Trials

scientific article published on 08 January 2019

Cardiovascular disease risk prediction with and without knowledge of genetic variation at chromosome 9p21.3.

artículo científico publicado en 2009

Cardiovascular risks associated with incident and prevalent periodontal disease

artículo científico publicado en 2015

Catechol-O-Methyltransferase and Cardiovascular Disease: MESA

scientific article published on 16 December 2019

Catechol-O-methyltransferase association with hemoglobin A1c

artículo científico publicado en 2016

Circulating branched-chain amino acids and long-term risk of obesity-related cancers in women

scientific article published on 06 October 2020

Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease

artículo científico publicado en 2016

Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families

article by Padhraig Gormley et al published September 2018 in Neuron

Common genetic loci influencing plasma homocysteine concentrations and their effect on risk of coronary artery disease

artículo científico publicado en 2013

Common genetic variations in the vitamin D pathway in relation to blood pressure

artículo científico publicado en 2014

Common variants associated with plasma triglycerides and risk for coronary artery disease

artículo científico publicado en 2013

Common variants in Mendelian kidney disease genes and their association with renal function

artículo científico publicado en 2013

Common variants in cardiac ion channel genes are associated with sudden cardiac death

artículo científico publicado en 2010

Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study

artículo científico publicado en 2017

Concordance of genetic risk across migraine subgroups: Impact on current and future genetic association studies

artículo científico publicado en 2014

Coronary heart disease risk, aspirin use, and apolipoprotein(a) 4399Met allele in the Atherosclerosis Risk in Communities (ARIC) study

artículo científico publicado en 2009

Correction to: Assessing the causal relationship between obesity and venous thromboembolism through a Mendelian Randomization study

artículo científico publicado en 2018

Correction: Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults

artículo científico publicado en 2017

Correction: Selectivity in Genetic Association with Sub-classified Migraine in Women

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

Corrigendum: 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function

artículo científico publicado en 2017

Corrigendum: Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk

artículo científico publicado en 2017

Corrigendum: Rare coding variants and X-linked loci associated with age at menarche

artículo científico publicado en 2015

Could vitamin D reduce obesity-associated inflammation? Observational and Mendelian randomization study

scientific article published on 31 March 2020

Cumulative psychological stress and cardiovascular disease risk in middle aged and older women: Rationale, design, and baseline characteristics

artículo científico publicado en 2017

Currently available versions of genome-wide association studies cannot be used to query the common haptoglobin copy number variant

artículo científico publicado en 2013

DNA mismatch repair gene MSH6 implicated in determining age at natural menopause

scientific article published on 19 December 2013

Defining the role of common variation in the genomic and biological architecture of adult human height

artículo científico publicado en 2014

Detection of protein folding defects caused by BRCA1-BRCT truncation and missense mutations

artículo científico publicado en 2003

Diet quality and genetic association with body mass index: results from 3 observational studies

scientific article published on 01 December 2018

Dietary fatty acids modulate associations between genetic variants and circulating fatty acids in plasma and erythrocyte membranes: Meta-analysis of nine studies in the CHARGE consortium

artículo científico publicado en 2015

Differential Genetic Effects on Statin-Induced Changes Across Low-Density Lipoprotein-Related Measures

artículo científico publicado en 2015

Directional dominance on stature and cognition in diverse human populations

artículo científico publicado en 2015

Discordance between Circulating Atherogenic Cholesterol Mass and Lipoprotein Particle Concentration in Relation to Future Coronary Events in Women

artículo científico publicado en 2017

Discovery and refinement of loci associated with lipid levels

artículo científico publicado en 2013

Discovery and replication of novel blood pressure genetic loci in the Women's Genome Health Study

artículo científico publicado en 2011

Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals

artículo científico publicado en 2020

Effect of Vitamin D and ω-3 Fatty Acid Supplementation on Risk of Age-Related Macular Degeneration: An Ancillary Study of the VITAL Randomized Clinical Trial

artículo científico publicado en 2020

Effect of genetic liability to migraine on cognition and brain volume: A Mendelian randomization study

scientific article published on 04 April 2020

Effects of long-term averaging of quantitative blood pressure traits on the detection of genetic associations

artículo científico publicado en 2014

Efficient Bayesian mixed-model analysis increases association power in large cohorts.

artículo científico publicado en 2015

Endophenotype Network Models: Common Core of Complex Diseases

artículo científico publicado en 2016

Erratum: A genome-wide association study of bitter and sweet beverage consumption

artículo científico publicado en 2019

Erratum: Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

artículo científico publicado en 2016

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

Evidence in the UK Biobank for the underdiagnosis of erythropoietic protoporphyria

scientific article published on 02 September 2020

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 association study of plasma lipids in >300,000 individuals

artículo científico publicado en 2017

FTO genetic variants, dietary intake and body mass index: insights from 177,330 individuals.

artículo científico publicado en 2014

FTO genotype is associated with phenotypic variability of body mass index

artículo científico publicado en 2012

Fish intake, genetic predisposition to alzheimer's disease and decline in global cognition and memory in five cohorts of older persons.

artículo científico publicado en 2017

Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis

artículo científico publicado en 2009

Four Susceptibility Loci for Gallstone Disease Identified in a Meta-analysis of Genome-Wide Association Studies

artículo científico publicado en 2016

Fried food consumption, genetic risk, and body mass index: gene-diet interaction analysis in three US cohort studies

artículo científico publicado en 2014

Functional classification of proteins and protein variants.

artículo científico publicado en 2004

GOSR2 Lys67Arg is associated with hypertension in whites

artículo científico publicado en 2008

Gene Variation of Endoplasmic Reticulum Aminopeptidases 1 and 2, and Risk of Blood Pressure Progression and Incident Hypertension among 17,255 Initially Healthy Women.

artículo científico publicado en 2018

Gene co-expression analysis identifies brain regions and cell types involved in migraine pathophysiology: a GWAS-based study using the Allen Human Brain Atlas

artículo científico publicado en 2016

Gene variations of ROCKs and risk of ischaemic stroke: the Women's Genome Health Study

artículo científico publicado en 2014

Gene × physical activity interactions in obesity: combined analysis of 111,421 individuals of European ancestry

artículo científico publicado en 2013

Gene-Based Elevated Triglycerides and Type 2 Diabetes Mellitus Risk in the Women's Genome Health Study

artículo científico publicado en 2019

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-based pleiotropy across migraine with aura and migraine without aura patient groups

artículo científico publicado en 2015

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 Correlations Between Diabetes and Glaucoma: An Analysis of Continuous and Dichotomous Phenotypes

artículo científico publicado en 2019

Genetic Interactions with Age, Sex, Body Mass Index, and Hypertension in Relation to Atrial Fibrillation: The AFGen Consortium

artículo científico publicado en 2017

Genetic Obesity and the Risk of Atrial Fibrillation: Causal Estimates from Mendelian Randomization

artículo científico publicado en 2016

Genetic Risk, Adherence to a Healthy Lifestyle, and Coronary Disease

artículo científico publicado en 2016

Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity

scientific article published on 11 September 2020

Genetic analyses of gynecological disease identify genetic relationships between uterine fibroids and endometrial cancer, and a novel endometrial cancer genetic risk region at the WNT4 1p36.12 locus

artículo científico publicado en 2021

Genetic analysis for a shared biological basis between migraine and coronary artery disease

artículo científico publicado en 2015

Genetic analysis of dietary intake identifies new loci and functional links with metabolic traits

artículo científico publicado en 2021

Genetic analysis of endometriosis and depression identifies shared loci and implicates causal links with gastric mucosa abnormality

scientific article published on 21 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 associations at 53 loci highlight cell types and biological pathways relevant for kidney function

artículo científico publicado en 2016

Genetic correlations between intraocular pressure, blood pressure and primary open-angle glaucoma: a multi-cohort analysis

artículo científico

Genetic determinants of cardiovascular events among women with migraine: a genome-wide association study

scientific journal article

Genetic determinants of statin-induced low-density lipoprotein cholesterol reduction: the Justification for the Use of Statins in Prevention: an Intervention Trial Evaluating Rosuvastatin (JUPITER) trial.

artículo científico

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 circulating levels of very long-chain saturated fatty acids

artículo científico publicado en 2014

Genetic loci associated with circulating phospholipid trans fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium

artículo científico publicado en 2014

Genetic loci associated with plasma concentration of low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, triglycerides, apolipoprotein A1, and Apolipoprotein B among 6382 white women in genome-wide analysis with replication

artículo científico publicado en 2008

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 risk, coronary heart disease events, and the clinical benefit of statin therapy: an analysis of primary and secondary prevention trials

artículo científico publicado en 2015

Genetic studies of body mass index yield new insights for obesity biology

artículo científico publicado en 2015

Genetic variants at 2q24 are associated with susceptibility to type 2 diabetes

artículo científico publicado en 2010

Genetic variants in eleven telomere-associated genes and the risk of incident cardio/cerebrovascular disease: The Women's Genome Health Study ⬇️

artículo científico publicado el 16 de octubre de 2010

Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

artículo científico publicado en 2011

Genetic variants of 11 telomere-pathway gene loci and the risk of incident type 2 diabetes mellitus: the Women's Genome Health Study

artículo científico publicado en 2011

Genetic variation at the coronary artery disease risk locus GUCY1A3 modifies cardiovascular disease prevention effects of aspirin

scientific article published on 01 November 2019

Genetic variation of fifteen folate metabolic pathway associated gene loci and the risk of incident head and neck carcinoma: the Women's Genome Health Study

artículo científico publicado en 2012

Genetics for Monitoring Prescription Practices of Commonly Used Drugs in Populations ⬇️

artículo científico publicado el 12 de enero de 2011

Genetics, ancestry, and hypertension: implications for targeted antihypertensive therapies

artículo científico publicado en 2014

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-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 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 analysis identifies 12 loci influencing human reproductive behavior

artículo científico publicado en 2016

Genome-wide analysis of dental caries and periodontitis combining clinical and self-reported data.

artículo científico publicado en 2019

Genome-wide association analyses identify 18 new loci associated with serum urate concentrations

artículo científico publicado en 2013

Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention ⬇️

artículo científico publicado en 2022

Genome-wide association analysis identifies 27 novel loci associated with uterine leiomyomata revealing common genetic origins with endometriosis

Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma

artículo científico publicado en 2016

Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk.

artículo científico publicado en 2017

Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations

artículo científico publicado en 2013

Genome-wide association analysis of soluble ICAM-1 concentration reveals novel associations at the NFKBIK, PNPLA3, RELA, and SH2B3 loci

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 meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing loss

artículo científico publicado en 2022

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 of lipid-lowering response to statins in combined study populations

artículo científico publicado en 2010

Genome-wide association studies identify four ER negative-specific breast cancer risk loci

artículo científico publicado en 2013

Genome-wide association studies identify loci associated with age at menarche and age at natural menopause

artículo científico publicado en 2009

Genome-wide association study evaluating lipoprotein-associated phospholipase A2 mass and activity at baseline and after rosuvastatin therapy

artículo científico publicado en 2012

Genome-wide association study identifies 48 common genetic variants associated with handedness

artículo científico publicado en 2020

Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure

artículo científico publicado en 2011

Genome-wide association study identifies variants at the IL18-BCO2 locus associated with interleukin-18 levels

artículo científico publicado en 2010

Genome-wide association study of kidney function decline in individuals of European descent

artículo científico publicado en 2014

Genome-wide association study of relative telomere length

artículo científico publicado en 2011

Genome-wide association study of selenium concentrations

artículo científico publicado en 2015

Genome-wide association study reveals three susceptibility loci for common migraine in the general population

artículo científico publicado en 2011

Genome-wide linkage and association analyses implicate FASN in predisposition to Uterine Leiomyomata

artículo científico publicado en 2012

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 new susceptibility loci for migraine

artículo científico publicado en 2013

Genome-wide meta-analysis identifies regions on 7p21 (AHR) and 15q24 (CYP1A2) as determinants of habitual caffeine consumption

artículo científico publicado en 2011

Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption

artículo científico publicado en 2014

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 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 observational studies shows common genetic variants associated with macronutrient intake

artículo científico publicado en 2013

Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels

artículo científico publicado en 2016

Genome-wide pharmacogenetics of anti-drug antibody response to bococizumab highlights key residues in HLA DRB1 and DQB1

artículo científico publicado en 2022

Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults

artículo científico publicado en 2017

Genome-wide studies of verbal declarative memory in nondemented older people: the Cohorts for Heart and Aging Research in Genomic Epidemiology consortium

artículo científico publicado en 2014

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 analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk

artículo científico publicado en 2017

Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism

artículo científico publicado en 2019

Getting closer to p-selectin.

artículo científico publicado en 2009

Group IIA Secretory Phospholipase A2, Vascular Inflammation, and Incident Cardiovascular Disease

scientific article published on 01 June 2019

HMG-coenzyme A reductase inhibition, type 2 diabetes, and bodyweight: evidence from genetic analysis and randomised trials

artículo científico publicado en 2014

Habitual sleep disturbances and migraine: a Mendelian randomization study

artículo científico publicado en 2020

Homocysteine, B Vitamins, MTHFR Genotype, and Incident Age-related Macular Degeneration

artículo científico publicado en 2018

Hundreds of variants clustered in genomic loci and biological pathways affect human height

artículo científico publicado en 2010

Hypothyroidism and Kidney Function: A Mendelian Randomization Study

artículo científico publicado en 2020

Identifying Novel Gene Variants in Coronary Artery Disease and Shared Genes With Several Cardiovascular Risk Factors

artículo científico publicado en 2015

Identifying blood pressure loci whose effects are modulated by multiple lifestyle exposures

artículo científico publicado en 2020

Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis.

artículo científico publicado en 2017

Inactivating mutations in NPC1L1 and protection from coronary heart disease

artículo científico publicado en 2014

Informed conditioning on clinical covariates increases power in case-control association studies

artículo científico publicado en 2012

Integrating genetic, transcriptional, and functional analyses to identify 5 novel genes for atrial fibrillation

artículo científico publicado en 2014

Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function

artículo científico publicado en 2012

Interaction of methylation-related genetic variants with circulating fatty acids on plasma lipids: a meta-analysis of 7 studies and methylation analysis of 3 studies in the Cohorts for Heart and Aging Research in Genomic Epidemiology consortium

artículo científico publicado en 2016

Interleukin-6 receptor pathways in coronary heart disease: a collaborative meta-analysis of 82 studies

artículo científico publicado en 2012

Interpreting metabolomic profiles using unbiased pathway models

artículo científico publicado en 2010

Investigating methotrexate toxicity within a randomized double-blinded, placebo-controlled trial: Rationale and design of the Cardiovascular Inflammation Reduction Trial-Adverse Events (CIRT-AE) Study

artículo científico publicado en 2017

Islet amyloid polypeptide gene variation (IAPP) and the risk of incident type 2 diabetes mellitus: the Women's Genome Health Study.

artículo científico publicado en 2011

KLB is associated with alcohol drinking, and its gene product β-Klotho is necessary for FGF21 regulation of alcohol preference

artículo científico publicado en 2016

Kinesin-like protein 6 (KIF6) polymorphism and the efficacy of rosuvastatin in primary prevention

artículo científico

Lack of Association Between Genetic Variation in 9 Innate Immunity Genes and Baseline CRP Levels

article

Lack of association between SLCO1B1 polymorphisms and clinical myalgia following rosuvastatin therapy.

artículo científico

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 candidate gene analysis of HDL particle features

artículo científico publicado en 2011

Large-scale genome-wide association meta-analysis of endometriosis reveals 13 novel loci and genetically-associated comorbidity with other pain conditions

Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair

artículo científico publicado en 2015

Lifestyle interaction with fat mass and obesity-associated (FTO) genotype and risk of obesity in apparently healthy U.S. women ⬇️

artículo científico publicado en 2011

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

Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study

artículo científico publicado en 2008

Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility

artículo científico publicado en 2015

Mendelian randomization analysis does not support causal associations of birth weight with hypertension risk and blood pressure in adulthood

artículo científico publicado en 2020

Mendelian randomization evaluation of causal effects of fibrinogen on incident coronary heart disease

artículo científico publicado en 2019

Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways

artículo científico publicado en 2012

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 five novel loci associated with endometriosis highlighting key genes involved in hormone metabolism

artículo científico publicado en 2017

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 65,734 individuals identifies TSPAN15 and SLC44A2 as two susceptibility loci for venous thromboembolism

artículo científico publicado en 2015

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 of HDL cholesterol response to statins

artículo científico publicado en 2016

Migraine genetics: from genome-wide association studies to translational insights

artículo científico publicado en 2016

Mitochondrial genome-wide association study of migraine - the HUNT Study

artículo científico publicado en 2020

Mitochondrial uncoupling protein gene cluster variation (UCP2–UCP3) and the risk of incident type 2 diabetes mellitus: The Women's Genome Health Study ⬇️

artículo científico publicado el 20 de octubre de 2010

Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores

artículo científico publicado en 2015

Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores

Morphogenesis signaling components influence cell cycle regulation by cyclin dependent kinase

artículo científico publicado en 2009

Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions

Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids

article

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

Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

artículo científico publicado en 2018

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 associated with indices of renal function and chronic kidney disease

scientific journal article

Multi‐phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations

artículo científico publicado en 2022

New Blood Pressure-Associated Loci Identified in Meta-Analyses of 475 000 Individuals

artículo científico publicado en 2017

New genetic loci link adipose and insulin biology to body fat distribution

artículo científico publicado en 2015

New loci associated with kidney function and chronic kidney disease

artículo científico publicado en 2010

New pathway for tissue-type plasminogen activator regulation.

artículo científico publicado en 2014

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

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 association of ABO histo-blood group antigen with soluble ICAM-1: results of a genome-wide association study of 6,578 women

artículo científico publicado en 2008

Novel association of HK1 with glycated hemoglobin in a non-diabetic population: a genome-wide evaluation of 14,618 participants in the Women's Genome Health Study

artículo científico publicado en 2008

Novel associations of CPS1, MUT, NOX4, and DPEP1 with plasma homocysteine in a healthy population: a genome-wide evaluation of 13 974 participants in the Women's Genome Health Study

artículo científico publicado en 2009

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 markers associate with atrial fibrillation risk in Europeans and Japanese

artículo científico publicado en 2014

Novel genetic markers improve measures of atrial fibrillation risk prediction

artículo científico publicado en 2013

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, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study

artículo científico publicado en 2009

Novel locus including FGF21 is associated with dietary macronutrient intake

artículo científico publicado en 2013

On the use of variance per genotype as a tool to identify quantitative trait interaction effects: a report from the Women's Genome Health Study

artículo científico publicado en 2010

On the utility of gene set methods in genomewide association studies of quantitative traits

artículo científico publicado en 2008

PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study

artículo científico publicado en 2016

PROTEIN-CODING VARIANTS IMPLICATE NOVEL GENES RELATED TO LIPID HOMEOSTASIS CONTRIBUTING TO BODY FAT DISTRIBUTION

article

Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche

artículo científico publicado en 2014

Peering Into the Future of CAD Genomics

artículo científico publicado en 2018

Pharmacogenetic determinants of statin-induced reductions in C-reactive protein.

artículo científico

Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins

artículo científico publicado en 2014

Pharmacogenetic study of statin therapy and cholesterol reduction

artículo científico publicado en 2004

Pharmacogenetics: the outlook for genetic testing in statin therapy

artículo científico publicado en 2005

Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9

scientific article published on 29 October 2019

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

Physical activity modifies the effect of LPL, LIPC, and CETP polymorphisms on HDL-C levels and the risk of myocardial infarction in women of European ancestry

artículo científico publicado en 2011

Physical activity, genes for physical fitness, and risk of coronary heart disease

artículo científico publicado en 2013

Physical and neurobehavioral determinants of reproductive onset and success

artículo científico publicado en 2016

Plasma levels of the proinflammatory chitin-binding glycoprotein YKL-40, variation in the chitinase 3-like 1 gene (CHI3L1), and incident cardiovascular events

artículo científico publicado en 2014

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

Pleiotropy-Based Decomposition of Genetic Risk Scores: Association and Interaction Analysis for Type 2 Diabetes and CAD

scientific article published on 14 April 2020

Polygenic Overlap Between C-Reactive Protein, Plasma Lipids, and Alzheimer Disease

artículo científico publicado en 2015

Polygenic Risk Score Predicts Sudden Death in Patients With Coronary Disease and Preserved Systolic Function

scientific article published in 2022

Polymorphism in the CETP gene region, HDL cholesterol, and risk of future myocardial infarction: Genomewide analysis among 18 245 initially healthy women from the Women's Genome Health Study

artículo científico publicado en 2009

Polymorphism in the apolipoprotein(a) gene, plasma lipoprotein(a), cardiovascular disease, and low-dose aspirin therapy

artículo científico publicado en 2009

Polymorphisms in catechol-O-methyltransferase modify treatment effects of aspirin on risk of cardiovascular disease

artículo científico publicado en 2014

Polymorphisms of the HNF1A gene encoding hepatocyte nuclear factor-1 alpha are associated with C-reactive protein

artículo científico publicado en 2008

Population analysis of large copy number variants and hotspots of human genetic disease

artículo científico publicado en 2009

Population genetic differentiation of height and body mass index across Europe

artículo científico publicado en 2015

Population-based approaches to genetics of migraine

artículo científico publicado en 2016

Population-based genomewide genetic analysis of common clinical chemistry analytes

artículo científico publicado en 2008

Prospective evaluation of B-type natriuretic peptide concentrations and the risk of type 2 diabetes in women

artículo científico publicado en 2013

Prospective study of common variants in CX3CR1 and risk of macular degeneration: pooled analysis from 5 long-term studies

artículo científico publicado en 2014

Prospective study of common variants in the retinoic acid receptor-related orphan receptor α gene and risk of neovascular age-related macular degeneration ⬇️

artículo científico publicado el 1 de noviembre de 2010

Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

artículo científico publicado en 2017

Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution

article

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: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

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 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

Purinergic receptor P2Y, G-protein coupled, 12 gene variants and risk of incident ischemic stroke, myocardial infarction, and venous thromboembolism

artículo científico publicado en 2007

Quality of dietary fat and genetic risk of type 2 diabetes: individual participant data meta-analysis

artículo científico publicado en 2019

Ranking and characterization of established BMI and lipid associated loci as candidates for gene-environment interactions

artículo científico publicado en 2017

Rare Genetic Variants Associated With Sudden Cardiac Death in Adults

scientific article published on 11 November 2019

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

Rationale, design, and methodology of the Women's Genome Health Study: a genome-wide association study of more than 25,000 initially healthy american women

artículo científico publicado en 2007

Recent Positive Selection Drives the Expansion of a Schizophrenia Risk Nonsynonymous Variant at SLC39A8 in Europeans

artículo científico publicado en 2015

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

Reproductive aging-associated common genetic variants and the risk of breast cancer

artículo científico publicado en 2012

Residual Risk of Atherosclerotic Cardiovascular Events in Relation to Reductions in Very-Low-Density Lipoproteins

artículo científico publicado en 2017

Response by Chatterjee et al to Letter Regarding Article, "Genetic Obesity and the Risk of Atrial Fibrillation: Causal Estimates From Mendelian Randomization"

artículo científico publicado en 2017

Role of Rare and Low-Frequency Variants in Gene-Alcohol Interactions on Plasma Lipid Levels

artículo científico publicado en 2020

Rooted in risk: genetic predisposition for low-density lipoprotein cholesterol level associates with diminished low-density lipoprotein cholesterol response to statin treatment

artículo científico publicado en 2016

Rosuvastatin, proprotein convertase subtilisin/kexin type 9 concentrations, and LDL cholesterol response: the JUPITER trial

artículo científico publicado en 2011

SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function

artículo científico publicado en 2016

Selectivity in genetic association with sub-classified migraine in women

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 Molecular Genetic Mechanisms Underlie Endometriosis and Migraine Comorbidity

artículo científico publicado en 2020

Shared genetic basis for migraine and ischemic stroke: A genome-wide analysis of common variants.

artículo científico publicado en 2015

Shared genetic risk between migraine and coronary artery disease: A genome-wide analysis of common variants

artículo científico publicado en 2017

Smoking-by-genotype interaction in type 2 diabetes risk and fasting glucose

artículo científico publicado en 2020

Statin-induced LDL cholesterol response and type 2 diabetes: a bidirectional two-sample Mendelian randomization study

scientific article published on 05 December 2019

Sugar-sweetened beverages and genetic risk of obesity

artículo científico publicado en 2012

Testosterone Pathway Genetic Polymorphisms in Relation to Primary Open-Angle Glaucoma: An Analysis in Two Large Datasets

artículo científico publicado en 2018

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 fat-mass and obesity-associated (FTO) gene, physical activity, and risk of incident cardiovascular events in white women

artículo científico publicado en 2010

The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals

artículo científico publicado en 2016

Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies

artículo científico publicado en 2010

Tracing sub-structure in the European American population with PCA-informative markers

artículo científico publicado en 2008

Trans-ethnic association study of blood pressure determinants in over 750,000 individuals

scientific article published on 21 December 2018

Tryptophanyl-tRNA synthetase gene polymorphisms and risk of incident myocardial infarction

scientific article published on 17 February 2005

Tumour necrosis factor gene polymorphisms and migraine: a systematic review and meta-analysis

artículo científico publicado en 2011

Understanding AAA Pathobiology: A GWAS Leads the Way.

artículo científico publicado en 2017

Understanding multicellular function and disease with human tissue-specific networks

artículo científico publicado en 2015

Using genetics to test the causal relationship of total adiposity and periodontitis: Mendelian randomization analyses in the Gene-Lifestyle Interactions and Dental Endpoints (GLIDE) Consortium

artículo científico publicado en 2015

Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers

artículo científico publicado en 2022

Vitamin D-associated genetic variation and risk of breast cancer in the breast and prostate cancer cohort consortium (BPC3).

artículo científico publicado en 2014

Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture

artículo científico publicado en 2015

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