52 Genetic Loci Influencing Myocardial Mass
artículo científico publicado en 2016
73-OR: Clonal Hematopoiesis of Indeterminate Potential (CHIP), Glycemic Traits, and Type 2 Diabetes (T2D) Risk
artículo científico publicado en 2021
A Comprehensive Analysis of Common and Rare Variants to Identify Adiposity Loci in Hispanic Americans: The IRAS Family Study (IRASFS).
artículo científico publicado en 2015
A Comprehensive Evaluation of the Genetic Architecture of Sudden Cardiac Arrest
A Frameshift in CSF2RB Predominant Among Ashkenazi Jews Increases Risk for Crohn's Disease and Reduces Monocyte Signaling via GM-CSF.
artículo científico publicado en 2016
A Gene for Arthrogryposis Multiplex Congenita Neuropathic Type Is Linked to D5S394 on Chromosome 5qter
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artículo científico publicado el 1 de noviembre de 1997
A Genetic Risk Score Associated with Chronic Obstructive Pulmonary Disease Susceptibility and Lung Structure on Computed Tomography
scientific article published on 01 September 2019
A Genome-Wide Association Study Identifies Blood Disorder-Related Variants Influencing Hemoglobin A1c With Implications for Glycemic Status in U.S. Hispanics/Latinos
artículo científico publicado en 2019
A Genome-Wide Association Study of Vertical Cup-Disc Ratio in a Latino Population
artículo científico publicado en 2017
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 Long Non-coding RNA, LOC157273, Is an Effector Transcript at the Chromosome 8p23.1-PPP1R3B Metabolic Traits and Type 2 Diabetes Risk Locus
scientific article published on 10 July 2020
A Multinomial Ordinal Probit Model with Singular Value Decomposition Method for a Multinomial Trait
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artículo científico publicado el 31 de marzo de 2012
A Pilot Genome-Wide Analysis Study Identifies Loci Associated With Response to Obeticholic Acid in Patients With NASH
artículo científico publicado en 2019
A bioinformatics pipeline for estimating mitochondrial DNA copy number and heteroplasmy levels from whole genome sequencing data
artículo científico publicado en 2022
A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium
scientific journal article
A catalog of genetic loci associated with kidney function from analyses of a million individuals
scientific article published on 31 May 2019
A form of sensorineural deafness is determined by a mitochondrial and an autosomal locus: evidence from pedigree segregation analysis
artículo científico publicado en 1993
A functional variant of SUMO4, a new I kappa B alpha modifier, is associated with type 1 diabetes
artículo científico publicado en 2004
A generalized least-squares framework for rare-variant analysis in family data
artículo científico publicado en 2014
A genome scan for familial combined hyperlipidemia reveals evidence of linkage with a locus on chromosome 11.
artículo científico publicado en 1999
A genome scan for fasting insulin and fasting glucose identifies a quantitative trait locus on chromosome 17p: the insulin resistance atherosclerosis study (IRAS) family study.
artículo científico publicado en 2005
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 scan for acute insulin response to glucose in Hispanic-Americans: the Insulin Resistance Atherosclerosis Family Study (IRAS FS).
artículo científico publicado en 2009
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 IL23R as an inflammatory bowel disease gene
artículo científico publicado en 2006
A genome-wide association study identifies a potential novel gene locus for keratoconus, one of the commonest causes for corneal transplantation in developed countries
artículo científico publicado en 2011
A genome-wide association study identifies novel loci associated with circulating IGF-I and IGFBP-3
artículo científico publicado en 2011
A genome-wide association study meta-analysis of clinical fracture in 10,012 African American women
artículo científico publicado en 2016
A genome-wide association study of aging
artículo científico publicado en 2011
A genome-wide association study of central corneal thickness in Latinos
artículo científico publicado en 2013
A genome-wide association study of chronic obstructive pulmonary disease in Hispanics
artículo científico publicado en 2015
A genome-wide association study of depressive symptoms
scientific journal article
A genome-wide association study suggests new evidence for an association of the NADPH Oxidase 4 (NOX4) gene with severe diabetic retinopathy in type 2 diabetes
article
A genome-wide interaction analysis of tricyclic/tetracyclic antidepressants and RR and QT intervals: a pharmacogenomics study from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium
artículo científico publicado en 2016
A genome-wide linkage and association analysis of imputed insertions and deletions with cardiometabolic phenotypes in Mexican Americans: The Insulin Resistance Atherosclerosis Family Study
artículo científico publicado en 2017
A genome-wide scan for carotid artery intima-media thickness: the Mexican-American Coronary Artery Disease family study
artículo científico publicado en 2005
A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci
scientific journal article
A genome-wide study of lipid response to fenofibrate in Caucasians: a combined analysis of the GOLDN and ACCORD studies
artículo científico publicado en 2016
A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart disease
artículo científico publicado en 2016
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 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 genome-wide association studies identifies multiple longevity genes
scientific article published on 14 August 2019
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 new syndrome of Crohn's disease and pachydermoperiostosis in a family
scientific article published on 01 January 1997
A noncoding variant near PPP1R3B promotes liver glycogen storage and MetS, but protects against myocardial infarction
artículo científico publicado en 2020
A novel Alzheimer disease locus located near the gene encoding tau protein.
artículo científico publicado en 2015
A novel NOD2/CARD15 haplotype conferring risk for Crohn disease in Ashkenazi Jews
artículo científico publicado en 2003
A novel method for testing association of multiple genetic markers with a multinomial trait.
artículo científico publicado en 2010
A phenomics-based strategy identifies loci on APOC1, BRAP, and PLCG1 associated with metabolic syndrome phenotype domains
artículo científico publicado en 2011
A prevalent caveolin-1 gene variant is associated with the metabolic syndrome in Caucasians and Hispanics
artículo científico publicado en 2015
A search for heterogeneity in insulin dependent diabetes mellitus (IDDM): HLA and autoimmune studies in simplex, multiplex and multigenerational families
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artículo científico publicado el 1 de mayo de 1983
A statin-dependent QTL for GATM expression is associated with statin-induced myopathy
artículo científico publicado en 2013
A structural variation reference for medical and population genetics
artículo científico publicado en 2020
ANCA pattern and LTA haplotype relationship to clinical responses to anti-TNF antibody treatment in Crohn's disease
artículo científico publicado en 2001
APOM and high-density lipoprotein cholesterol are associated with lung function and per cent emphysema
artículo científico publicado en 2013
Abstract 14629: Rare Variants for Electrocardiographic Traits Identify Arrhythmia Susceptibility Genes
artículo científico publicado en 2020
Actionable exomic incidental findings in 6503 participants: challenges of variant classification
artículo científico publicado en 2015
Additional comments on the ulcer-multiple lentigines syndrome
artículo científico publicado en 1982
Adiponectin Isoform Patterns in Ethnic-Specific ADIPOQ Mutation Carriers: The IRAS Family Study
artículo científico publicado en 2017
Adiponectin, Insulin Sensitivity and Diabetic Retinopathy in Latinos With Type 2 Diabetes
artículo científico publicado en 2015
Adiposity-Independent Effects of Aging on Insulin Sensitivity and Clearance in Mice and Humans
scientific article published on 01 March 2019
Admixture Mapping of Subclinical Atherosclerosis and Subsequent Clinical Events Among African Americans in 2 Large Cohort Studies
artículo científico publicado en 2017
Admixture mapping identifies novel loci for obstructive sleep apnea in hispanic/latino americans
scientific article published on 01 February 2019
Admixture mapping of coronary artery calcified plaque in African Americans with type 2 diabetes mellitus
artículo científico publicado en 2012
African Ancestry Analysis and Admixture Genetic Mapping for Proliferative Diabetic Retinopathy in African Americans
artículo científico publicado en 2015
African Ancestry Is Associated with Higher Intraocular Pressure in Latinos
artículo científico publicado en 2015
African Ancestry-Specific Alleles and Kidney Disease Risk in Hispanics/Latinos
artículo científico publicado en 2016
Air pollution and percent emphysema identified by computed tomography in the Multi-Ethnic study of Atherosclerosis
artículo científico publicado en 2014
Allele-specific expression changes dynamically during T cell activation in HLA and other autoimmune loci
artículo científico publicado en 2020
Allelic Heterogeneity at the CRP Locus Identified by Whole-Genome Sequencing in Multi-ancestry Cohorts
artículo científico publicado en 2019
Alterations of a Cellular Cholesterol Metabolism Network Are a Molecular Feature of Obesity-Related Type 2 Diabetes and Cardiovascular Disease
artículo científico publicado en 2015
Alternative splicing of 3-hydroxy-3-methylglutaryl coenzyme A reductase is associated with plasma low-density lipoprotein cholesterol response to simvastatin
artículo científico publicado en 2008
Amino acid position 37 of HLA-DRβ1 affects susceptibility to Crohn's disease in Asians
article
Amyloidosis in familial mediterranean fever is associated with a specific ancestral haplotype in the MEFV locus
artículo científico publicado en 1998
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 Outbreak of Polygenic Scores for Coronary Artery Disease
scientific article published on 01 June 2020
An SNP linkage scan identifies significant Crohn's disease loci on chromosomes 13q13.3 and, in Jewish families, on 1p35.2 and 3q29.
artículo científico publicado en 2008
An association between the calpastatin (CAST) gene and keratoconus
artículo científico publicado en 2013
An integrative cross-omics analysis of DNA methylation sites of glucose and insulin homeostasis.
artículo científico publicado en 2019
An open resource of structural variation for medical and population genetics
artículo científico publicado en 2019
Analysis commons, a team approach to discovery in a big-data environment for genetic epidemiology
artículo científico publicado en 2017
Analysis of HLA-DQA1 and -DQB1 genes in Mexican Americans with insulin-dependent diabetes mellitus
artículo científico publicado en 1993
Analysis of HLA-DQA1 and -DQB1 genes in Mexican Americans with insulin-dependent diabetes mellitus
article
Analysis of Whole Exome Sequencing with Cardiometabolic Traits Using Family-Based Linkage and Association in the IRAS Family Study
artículo científico publicado en 2017
Analysis of cardiac magnetic resonance imaging in 36,000 individuals yields genetic insights into dilated cardiomyopathy
scientific article published on 07 May 2020
Analysis of family- and population-based samples in cohort genome-wide association studies
artículo científico publicado en 2011
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
Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits—The Hispanic/Latino Anthropometry Consortium
artículo científico publicado en 2022
Ancestry and other genetic associations with plasma PCSK9 response to simvastatin
artículo científico publicado en 2014
Anti-flagellin (CBir1) phenotypic and genetic Crohn's disease associations.
artículo científico publicado en 2007
Application of Bayesian classification with singular value decomposition method in genome-wide association studies
artículo científico publicado en 2009
Application of Bayesian regression with singular value decomposition method in association studies for sequence data
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artículo científico publicado el 29 de noviembre de 2011
Application of synthetic oligonucleotides to detect DQ beta genes transmission within insulin-dependent diabetes families
artículo científico publicado en 1989
Arthrogryposis multiplex congenita in an Arab kindred: update
scientific article published on 01 January 1995
Assessment of gene-by-sex interaction effect on bone mineral density
artículo científico publicado en 2012
Assessment of the Relationship Between Genetic Determinants of Thyroid Function and Atrial Fibrillation: A Mendelian Randomization Study
article published in 2019
Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study
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artículo científico publicado en 2017
Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels
artículo científico publicado en 2017
Association between ADIPOQ SNPs with plasma adiponectin and glucose homeostasis and adiposity phenotypes in the IRAS Family Study
artículo científico publicado en 2012
Association between Site-specific Bone Mineral Density and Glucose Homeostasis and Anthropometric Traits in Healthy Men and Women
artículo científico publicado en 2018
Association between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant data
artículo científico publicado en 2014
Association between angiotensinogen, angiotensin II receptor genes, and blood pressure response to an angiotensin-converting enzyme inhibitor
artículo científico publicado en 2007
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 serum amyloid A proteins and coronary artery disease: evidence from two distinct arteriosclerotic processes
artículo científico publicado en 1997
Association between sleep disordered breathing and epigenetic age acceleration: Evidence from the Multi-Ethnic Study of Atherosclerosis
scientific article published on 21 November 2019
Association of APOL1 Genotypes With Measures of Microvascular and Endothelial Function, and Blood Pressure in MESA
artículo científico publicado en 2020
Association of Directly Measured Plasma Free 25(OH)D With Insulin Sensitivity and Secretion: The IRAS Family Study
artículo científico publicado en 2017
Association of FADS1/2 Locus Variants and Polyunsaturated Fatty Acids With Aortic Stenosis
artículo científico publicado en 2020
Association of Genetic Variants with Primary Open-Angle Glaucoma among Individuals with African Ancestry
artículo científico publicado en 2019
Association of Genetic Variation With Keratoconus
artículo científico publicado en 2019
Association of HLA-DPB1*0301 with IDDM in Mexican-Americans
artículo científico publicado en 1996
Association of Mitochondrial DNA Copy Number With Cardiovascular Disease
artículo científico publicado en 2017
Association of NOD2 and IL23R with inflammatory bowel disease in Puerto Rico
artículo científico publicado en 2014
Association of PNPLA3 with non-alcoholic fatty liver disease in a minority cohort: the Insulin Resistance Atherosclerosis Family Study
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artículo científico publicado el 13 de enero de 2011
Association of TCF7L2 gene polymorphisms with reduced acute insulin response in Hispanic Americans
artículo científico publicado en 2007
Association of Triglyceride-Related Genetic Variants With Mitral Annular Calcification
artículo científico publicado en 2017
Association of a 62 Variants Type 2 Diabetes Genetic Risk Score With Markers of Subclinical Atherosclerosis: A Transethnic, Multicenter Study.
artículo científico publicado en 2015
Association of antibody responses to microbial antigens and complications of small bowel Crohn's disease
artículo científico publicado en 2004
Association of fasting insulin and C peptide with diabetic retinopathy in Latinos with type 2 diabetes
artículo científico publicado en 2014
Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study
artículo científico publicado en 2011
Association of genome-wide variation with highly sensitive cardiac troponin-T levels in European Americans and Blacks: a meta-analysis from atherosclerosis risk in communities and cardiovascular health studies
artículo científico publicado en 2012
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 all-cause mortality
artículo científico publicado en 2012
Association of insulin sensitivity and glucose tolerance with the c.825C>T variant of the G protein beta-3 subunit gene
artículo científico publicado en 2008
Association of levels of fasting glucose and insulin with rare variants at the chromosome 11p11.2-MADD locus: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study
artículo científico publicado en 2014
Association of low-density lipoprotein cholesterol-related genetic variants with aortic valve calcium and incident aortic stenosis
artículo científico publicado en 2014
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 polymorphisms in the hepatocyte growth factor gene promoter with keratoconus
artículo científico publicado en 2011
Association of severity of primary open-angle glaucoma with serum vitamin D levels in patients of African descent
scientific article published on 09 August 2019
Association of the IGF1 gene with fasting insulin levels
artículo científico publicado en 2016
Association of the Kir6.2 E23K variant with reduced acute insulin response in African-Americans
artículo científico publicado en 2008
Association of the diabetes gene calpain-10 with subclinical atherosclerosis: the Mexican-American Coronary Artery Disease Study
artículo científico publicado en 2005
Associations between SLC16A11 variants and diabetes in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL)
scientific article published in Scientific Reports
Associations between adherence to the dietary approaches to stop hypertension (DASH) diet and six glucose homeostasis traits in the Microbiome and Insulin Longitudinal Evaluation Study (MILES)
artículo científico publicado en 2022
Associations between genetic variants in the ACE, AGT, AGTR1 and AGTR2 genes and renal function in the Multi-ethnic Study of Atherosclerosis
artículo científico publicado en 2010
Associations between two common polymorphisms in the ABCA1 gene and subclinical atherosclerosis: Multi-Ethnic Study of Atherosclerosis (MESA)
article
Associations of Mitochondrial and Nuclear Mitochondrial Variants and Genes with Seven Metabolic Traits
article
Associations of adiponectin with body fat distribution and insulin sensitivity in nondiabetic Hispanics and African-Americans
artículo científico publicado en 2007
Associations of autozygosity with a broad range of human phenotypes
scientific article published on 31 October 2019
Associations of candidate genes to age-related macular degeneration among racial/ethnic groups in the multi-ethnic study of atherosclerosis
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artículo científico publicado en 2013
Associations of pentraxin 3 with cardiovascular disease: the Multi-Ethnic Study of Atherosclerosis
artículo científico publicado en 2014
Associations of variants In the hexokinase 1 and interleukin 18 receptor regions with oxyhemoglobin saturation during sleep
artículo científico publicado en 2019
Author Correction: Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases
artículo científico
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
Autoantibodies and human leucocyte antigen class II in first-degree family members of Mexican-American type 1 diabetic patients
artículo científico publicado en 2001
Benchmarking association analyses of continuous exposures with RNA-seq in observational studies
artículo científico publicado en 2021
Best practices and joint calling of the HumanExome BeadChip: the CHARGE Consortium
artículo científico publicado en 2013
Bidirectional Mendelian randomization to explore the causal relationships between body mass index and polycystic ovary syndrome
scientific article published on 01 January 2019
Biological, clinical and population relevance of 95 loci for blood lipids
artículo científico publicado en 2010
Blood Leukocyte DNA Methylation Predicts Risk of Future Myocardial Infarction and Coronary Heart Disease
scientific article published on 19 August 2019
Blood monocyte transcriptome and epigenome analyses reveal loci associated with human atherosclerosis
artículo científico
Body Adiposity Index versus Body Mass Index and Other Anthropometric Traits as Correlates of Cardiometabolic Risk Factors
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artículo científico publicado el 11 de junio de 2013
Both preoperative perinuclear antineutrophil cytoplasmic antibody and anti-CBir1 expression in ulcerative colitis patients influence pouchitis development after ileal pouch-anal anastomosis
artículo científico publicado en 2008
C-reactive protein gene polymorphism 1009A>G is associated with serum CRP levels in Chinese men: a TCVGHAGE study
artículo científico publicado en 2007
CELF4 Variant and Anthracycline-Related Cardiomyopathy: A Children's Oncology Group Genome-Wide Association Study
artículo científico publicado en 2016
CRTC3 links catecholamine signalling to energy balance
scientific journal article
CUBN is a gene locus for albuminuria
artículo científico publicado en 2011
Candidate gene association resource (CARe): design, methods, and proof of concept
artículo científico publicado en 2010
Candidate gene association study for diabetic retinopathy in persons with type 2 diabetes: the Candidate gene Association Resource (CARe).
artículo científico publicado en 2011
Candidate loci for insulin sensitivity and disposition index from a genome-wide association analysis of Hispanic participants in the Insulin Resistance Atherosclerosis (IRAS) Family Study
artículo científico publicado en 2009
Candidate locus for a nuclear modifier gene for maternally inherited deafness
artículo científico publicado en 2000
Carotid intima-media thickness (cIMT) cosegregates with blood pressure and renal function in hypertensive Hispanic families
artículo científico publicado en 2007
Catechol-O-Methyltransferase and Cardiovascular Disease: MESA
scientific article published on 16 December 2019
Cerebral small vessel disease genomics and its implications across the lifespan
artículo científico publicado en 2020
Cerivastatin, genetic variants, and the risk of rhabdomyolysis
artículo científico publicado en 2011
Challenges in elucidating the genetics of diabetic retinopathy
artículo científico publicado en 2014
Characterization of genetic loci that affect susceptibility to inflammatory bowel diseases in African Americans
artículo científico publicado en 2015
Characterization of statin dose response in electronic medical records
scientific article published on 04 October 2013
Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices
artículo científico publicado en 2021
Classification of Type 2 Diabetes Genetic Variants and a Novel Genetic Risk Score Association With Insulin Clearance
artículo científico publicado en 2020
Clinical utility of pharmacogenetic biomarkers in cardiovascular therapeutics: a challenge for clinical implementation
artículo científico publicado en 2012
Clinical, serologic, and genetic factors associated with pyoderma gangrenosum and erythema nodosum in inflammatory bowel disease patients
artículo científico publicado en 2014
Clonal hematopoiesis associated with epigenetic aging and clinical outcomes
artículo científico publicado en 2021
Close genetic linkage between diabetes mellitus and kidd blood group
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artículo científico publicado el 24 de octubre de 1981
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
Coincident linkage of fasting plasma insulin and blood pressure to chromosome 7q in hypertensive hispanic families
artículo científico publicado en 2001
Combination of genetic and quantitative serological immune markers are associated with complicated Crohnʼs disease behavior
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artículo científico publicado el 9 de marzo de 2011
Combination of innate and adaptive immune alterations increased the likelihood of fibrostenosis in Crohn's disease
artículo científico publicado en 2010
Combined admixture mapping and association analysis identifies a novel blood pressure genetic locus on 5p13: contributions from the CARe consortium
artículo científico publicado en 2011
Combined analysis of genome scans of dutch and finnish families reveals a susceptibility locus for high-density lipoprotein cholesterol on chromosome 16q
artículo científico publicado en 2003
Combined influence of LDLR and HMGCR sequence variation on lipid-lowering response to simvastatin
artículo científico publicado en 2010
Common Coding Variants in Are Associated With the Nav1.8 Late Current and Cardiac Conduction
artículo científico publicado en 2018
Common Variants in the Periostin Gene Influence Development of Atherosclerosis in Young Persons
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artículo científico publicado el 7 de abril de 2011
Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR Interval
Common genetic variants and subclinical atherosclerosis: The Multi-Ethnic Study of Atherosclerosis (MESA).
artículo científico publicado en 2015
Common genetic variants differentially influence the transition from clinically defined states of fasting glucose metabolism
artículo científico publicado en 2011
Common genetic variation near the connexin-43 gene is associated with resting heart rate in African Americans: a genome-wide association study of 13,372 participants.
artículo científico publicado en 2012
Common genetic variation, residential proximity to traffic exposure, and left ventricular mass: the Multi-Ethnic Study of Atherosclerosis
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 five new loci associated with early-onset inflammatory bowel disease
artículo científico publicado en 2009
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 variation in fatty acid metabolic genes and risk of incident sudden cardiac arrest
artículo científico publicado en 2014
Community Partnership in Precision Medicine: Themes from a Community Engagement Conference.
artículo científico publicado en 2018
Comparative genetic analysis of inflammatory bowel disease and type 1 diabetes implicates multiple loci with opposite effects
artículo científico publicado en 2010
Comparison of Genome-Wide and Gene-Specific DNA Methylation Profiling in First-Trimester Chorionic Villi From Pregnancies Conceived With Infertility Treatments
artículo científico publicado en 2016
Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study
artículo científico publicado en 2017
Comparison of Proteomic Assessment Methods in Multiple Cohort Studies
artículo científico publicado en 2020
Complex genetic contribution of the Apo AI-CIII-AIV gene cluster to familial combined hyperlipidemia. Identification of different susceptibility haplotypes
artículo científico publicado en 1997
Confirmation of three susceptibility genes to insulin-dependent diabetes mellitus: IDDM4, IDDM5 and IDDM8
artículo científico publicado en 1996
Consanguinity and common adult diseases in Israeli Arab communities
artículo científico publicado en 1997
Construction of a 1-Mb restriction-mapped cosmid contig containing the candidate region for the familial Mediterranean fever locus (MEFV) on chromosome 16p 13.3.
artículo científico publicado en 1997
Consumption of meat is associated with higher fasting glucose and insulin concentrations regardless of glucose and insulin genetic risk scores: a meta-analysis of 50,345 Caucasians
artículo científico publicado en 2015
Coronary Heart Disease Genetic Risk Score Predicts Cardiovascular Disease Risk in Men, Not Women
artículo científico publicado en 2018
Correction: Four Novel Loci (19q13, 6q24, 12q24, and 5q14) Influence the Microcirculation In Vivo.
artículo científico publicado en 2010
Correction: Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations.
artículo científico publicado en 2018
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
Correlates and heritability of nonalcoholic fatty liver disease in a minority cohort
artículo científico publicado en 2009
Cosegregation of albuminuria and blood pressure: the Insulin Resistance Atherosclerosis (IRAS) family study
artículo científico publicado en 2005
Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases.
artículo científico publicado en 2018
D-Dimer in African Americans: Whole Genome Sequence Analysis and Relationship to Cardiovascular Disease Risk in the Jackson Heart Study
artículo científico publicado en 2017
DNA Methylation Analysis Identifies Loci for Blood Pressure Regulation
artículo científico publicado en 2017
DPB1 alleles are associated with type 1 diabetes susceptibility in multiple ethnic groups
artículo científico publicado en 2004
Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries.
artículo científico publicado en 2018
Deep-coverage whole genome sequences and blood lipids among 16,324 individuals
artículo científico publicado en 2018
Deep-coverage whole genome sequences and blood lipids among 16,324 individuals
Defining the role of common variation in the genomic and biological architecture of adult human height
artículo científico publicado en 2014
Deleterious Effect of Butyrylcholinesterase K-Variant in Donepezil Treatment of Mild Cognitive Impairment
artículo científico publicado en 2016
Detailed analysis of association between common single nucleotide polymorphisms and subclinical atherosclerosis: The Multi-ethnic Study of Atherosclerosis
artículo científico publicado en 2016
Detection of genetic loci associated with plasma fetuin-A: a meta-analysis of genome-wide association studies from the CHARGE Consortium
artículo científico publicado en 2017
Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes
artículo científico publicado en 2020
Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes
Determination and use of haplotypes: ethnic comparison and association of the lipoprotein lipase gene and coronary artery disease in Mexican-Americans
artículo científico publicado en 2003
Diabetes Mellitus: The Search for Genetic Markers
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artículo científico publicado el 1 de marzo de 1979
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
Differences in First-Trimester Maternal Metabolomic Profiles in Pregnancies Conceived From Fertility Treatments
scientific article published on 01 April 2019
Different HLA haplotypes in Mexican Americans with IDDM.
artículo científico publicado en 1989
Differential effects of ramipril on ambulatory blood pressure in African Americans and Caucasians
artículo científico publicado en 2007
Differential gene expression during placentation in pregnancies conceived with different fertility treatments compared with spontaneous pregnancies
scientific article published on 02 January 2019
Differential gene expression of blood-derived cell lines in familial combined hyperlipidemia
artículo científico publicado en 2004
Differentially expressed genes in adipocytokine signaling pathway of adipose tissue in pregnancy
artículo científico publicado en 2013
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 fine-mapping of adiposity loci using high density imputation of genome-wide association studies in individuals of African ancestry: African Ancestry Anthropometry Genetics Consortium.
artículo científico publicado en 2017
Discovery and refinement of loci associated with lipid levels
artículo científico publicado en 2013
Discovery of novel heart rate-associated loci using the Exome Chip
artículo científico publicado en 2017
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals
artículo científico publicado en 2020
Disentangling the genetics of lean mass
article
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
Duodenal-ulcer disease associated with elevated serum pepsinogen I: an inherited autosomal dominant disorder
artículo científico publicado el 11 de enero de 1979
Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale
artículo científico publicado en 2020
Effects of Calcium, Magnesium, and Potassium Concentrations on Ventricular Repolarization in Unselected Individuals
artículo científico publicado en 2019
Effects of long-term averaging of quantitative blood pressure traits on the detection of genetic associations
artículo científico publicado en 2014
Efficient Variant Set Mixed Model Association Tests for Continuous and Binary Traits in Large-Scale Whole-Genome Sequencing Studies
scientific article published on 10 January 2019
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
Electrocardiographic abnormalities associated with the metabolic syndrome and its components: the multi-ethnic study of atherosclerosis
artículo científico publicado en 2011
Elevated plasma free fatty acids are associated with sudden death: a prospective community-based evaluation at the time of cardiac arrest
artículo científico publicado en 2014
Empirical characteristics of family-based linkage to a complex trait: the ADIPOQ region and adiponectin levels
artículo científico publicado en 2014
Epigenome-wide association analysis of daytime sleepiness in the Multi-Ethnic Study of Atherosclerosis reveals African-American-specific associations
scientific article published on 01 August 2019
Erratum. Multiethnic Genome-Wide Association Study of Diabetic Retinopathy Using Liability Threshold Modeling of Duration of Diabetes and Glycemic Control. Diabetes 2019;68:441-456
scientific article published on 27 April 2020
Erratum: Corrigendum: Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47
scholarly article published in Nature Genetics
Erratum: Corrigendum: Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study
scholarly article published in Nature Genetics
Erratum: Genetic loci associated with heart rate variability and their effects on cardiac disease risk
artículo científico publicado en 2017
Erratum: Genome-wide association identifies multiple ulcerative colitis susceptibility loci
scholarly article published in Nature Genetics
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: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
artículo científico publicado en 2010
Estimating the Contributions of Rare and Common Genetic Variations and Clinical Measures to a Model Trait: Adiponectin
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artículo científico publicado el 2 de octubre de 2012
Estimating the recombination frequency for the MN and the Ss loci
scientific article published on 01 January 1984
Evaluating gene x gene and gene x smoking interaction in rheumatoid arthritis using candidate genes in GAW15.
artículo científico publicado en 2007
Evaluation of mitochondrial DNA copy number estimation techniques
scientific article published on 31 January 2020
Evidence for a major dominance component in the variation of serum pepsinogen I levels
artículo científico publicado en 1982
Evidence for complex nuclear inheritance in a pedigree with nonsyndromic deafness due to a homoplasmic mitochondrial mutation
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artículo científico publicado el 5 de junio de 1998
Evidence for joint genetic control of insulin sensitivity and systolic blood pressure in hispanic families with a hypertensive proband
artículo científico publicado en 2001
Evidence for linkage of a candidate chromosome 1 region to human systemic lupus erythematosus
scientific article published on February 1997
Evidence of a non-MHC susceptibility locus in type I diabetes linked to HLA on chromosome 6.
artículo científico publicado en 1997
Evidence of insulin resistant lipid metabolism in adipose tissue in familial combined hyperlipidemia, but not type 2 diabetes mellitus
artículo científico publicado en 2002
Exome Chip Analysis Identifies Low-Frequency a on Brain Magnetic Imaging
Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits
artículo científico publicado en 2016
Exome Sequencing Identifies Genetic Variants Associated with Circulating Lipid Levels in Mexican Americans: The Insulin Resistance Atherosclerosis Family Study (IRASFS).
artículo científico publicado en 2018
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls
article by Jason Flannick et al published 22 May 2019 in Nature
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-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6
Exome-wide association study of plasma lipids in >300,000 individuals
artículo científico publicado en 2017
ExomeChip-Wide Analysis of 95 626 Individuals Identifies 10 Novel Loci Associated With QT and JT Intervals
Familial Mediterranean fever in Armenians: autosomal recessive inheritance with high gene frequency
artículo científico publicado en 1989
Familial Mediterranean fever--linkage studies with genetic markers on chromosome 6.
artículo científico publicado en 1990
Familial Mediterranean fever: analysis of inheritance and current linkage data
artículo científico publicado el 15 de septiembre de 1992
Familial Mediterranean fever: effects of genotype and ethnicity on inflammatory attacks and amyloidosis
artículo científico publicado en 2000
Familial empiric risk estimates of inflammatory bowel disease in Ashkenazi Jews
artículo científico publicado en 1989
Familial empirical risks for inflammatory bowel disease: differences between Jews and non-Jews
artículo científico publicado en 1993
Familial expression of anti-Escherichia coli outer membrane porin C in relatives of patients with Crohn's disease
artículo científico publicado en 2006
Familial expression of anti-Saccharomyces cerevisiae mannan antibodies in affected and unaffected relatives of patients with Crohn's disease
artículo científico publicado en 2000
Families with Familial Combined Hyperlipidemia and Families Enriched for Coronary Artery Disease Share Genetic Determinants for the Atherogenic Lipoprotein Phenotype
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artículo científico publicado el 1 de agosto de 1998
Family history and serology predict Crohn's disease after ileal pouch-anal anastomosis for ulcerative colitis
artículo científico publicado en 2007
Family history: A comprehensive genetic risk assessment method for the chronic conditions of adulthood
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artículo científico publicado el 22 de agosto de 1997
Fasting insulin reflects heterogeneous physiological processes: role of insulin clearance
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artículo científico publicado el 31 de mayo de 2011
Fifteen Genetic Loci Associated With the Electrocardiographic P Wave
artículo científico publicado en 2017
Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms
artículo científico publicado en 2017
Fine mapping of QT interval regions in global populations refines previously identified QT interval loci and identifies signals unique to African and Hispanic descent populations
artículo científico publicado en 2016
Fine mapping the CETP region reveals a common intronic insertion associated to HDL-C
artículo científico publicado en 2015
Fine-mapping of an expanded set of type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps
Fine-mapping of lipid regions in global populations discovers ethnic-specific signals and refines previously identified lipid loci
artículo científico publicado en 2016
Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps
artículo científico publicado en 2018
Fine-mapping, novel loci identification, and SNP association transferability in a genome-wide association study of QRS duration in African Americans
artículo científico publicado en 2016
Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo
artículo científico publicado en 2010
Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease
artículo científico publicado en 2010
Further investigation in europeans of susceptibility variants for polycystic ovary syndrome discovered in genome-wide association studies of Chinese individuals
artículo científico publicado en 2015
GENOME-WIDE INTERACTION WITH SELECTED TYPE 2 DIABETES LOCI REVEALS NOVEL LOCI FOR TYPE 2 DIABETES IN AFRICAN AMERICANS.
artículo científico publicado en 2016
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 QRS duration identifies new loci specific to Hispanic/Latino populations
artículo científico publicado en 2019
GWAS of longevity in CHARGE consortium confirms APOE and FOXO3 candidacy
artículo científico publicado en 2014
GWAS of the electrocardiographic QT interval in Hispanics/Latinos generalizes previously identified loci and identifies population-specific signals
artículo científico publicado en 2017
Gain-of-function lipoprotein lipase variant rs13702 modulates lipid traits through disruption of a microRNA-410 seed site
artículo científico publicado en 2012
Gene expression in thiazide diuretic or statin users in relation to incident type 2 diabetes
artículo científico publicado en 2014
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 of lipid traits in African, East Asian and Hispanic populations
artículo científico publicado en 2012
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
Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease
artículo científico publicado en 2014
General Framework for Meta-Analysis of Haplotype Association Tests
artículo científico publicado en 2016
Generalization and fine mapping of European ancestry-based central adiposity variants in African ancestry populations
artículo científico publicado en 2016
Generalized correlation measure using count statistics for gene expression data with ordered samples.
artículo científico publicado en 2017
Genes associated with risk of type 2 diabetes identified by a candidate-wide association scan: as a trickle becomes a flood
artículo científico publicado en 2008
Genes linked to energy metabolism and immunoregulatory mechanisms are associated with subcutaneous adipose tissue distribution in HIV-infected men
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artículo científico publicado el 1 de diciembre de 2011
Genetic Architecture of Primary Open Angle Glaucoma in Individuals of African Descent: The African Descent & Glaucoma Evaluation Study (ADAGES) III
article
Genetic Architecture of Subcortical Brain Structures in Over 40,000 Individuals Worldwide
scholarly article published 28 August 2017
Genetic Associations with Obstructive Sleep Apnea Traits in Hispanic/Latino Americans
artículo científico publicado en 2016
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 Electrocardiographic P-wave Duration and Relation to Atrial Fibrillation
artículo científico publicado en 2020
Genetic Diversity and Association Studies in US Hispanic/Latino Populations: Applications in the Hispanic Community Health Study/Study of Latinos
artículo científico publicado en 2016
Genetic Heterogeneity of Hyperpepsinogenemic I and Normopepsinogenemic I Duodenal Ulcer Disease
artículo científico publicado el 1 de septiembre de 1979
Genetic Interactions with Age, Sex, Body Mass Index, and Hypertension in Relation to Atrial Fibrillation: The AFGen Consortium
artículo científico publicado en 2017
Genetic Marker Associations With Proliferative Retinopathy in Persons Diagnosed With Diabetes Before 30 yr of age
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artículo científico publicado el 1 de julio de 1992
Genetic Risk Prediction of Atrial Fibrillation
artículo científico publicado en 2016
Genetic Risk Score in Diabetes Associated With Chronic Pancreatitis Versus Type 2 Diabetes Mellitus
artículo científico publicado en 2019
Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity
scientific article published on 11 September 2020
Genetic Variants Associated With Obesity and Insulin Resistance in Hispanic Boys With Nonalcoholic Fatty Liver Disease
artículo científico publicado en 2018
Genetic Variants Associated With Quantitative Glucose Homeostasis Traits Translate to Type 2 Diabetes in Mexican Americans: The GUARDIAN (Genetics Underlying Diabetes in Hispanics) Consortium
artículo científico publicado en 2014
Genetic Variants Associated with Circulating Fibroblast Growth Factor 23
Genetic Variants Associated with Circulating Parathyroid Hormone
artículo científico publicado en 2016
Genetic Variation in the Human SORBS1 Gene is Associated With Blood Pressure Regulation and Age at Onset of Hypertension: A SAPPHIRe Cohort Study
artículo científico publicado en 2016
Genetic analysis of adiponectin variation and its association with type 2 diabetes in African Americans
artículo científico publicado en 2013
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 ancestry and the relationship of cigarette smoking to lung function and per cent emphysema in four race/ethnic groups: a cross-sectional study
artículo científico publicado en 2013
Genetic and Pharmacologic Inactivation of ANGPTL3 and Cardiovascular Disease
artículo científico publicado en 2017
Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting
Genetic and physical mapping of a type 1 diabetes susceptibility gene (IDDM12) to a 100-kb phagemid artificial chromosome clone containing D2S72-CTLA4-D2S105 on chromosome 2q33
article
Genetic architecture of gene expression traits across diverse populations
scholarly article published 10 January 2018
Genetic architecture of gene expression traits across diverse populations
article
Genetic architecture of subcortical brain structures in 38,851 individuals
scientific article published on 21 October 2019
Genetic association of COL5A1 variants in keratoconus patients suggests a complex connection between corneal thinning and keratoconus
artículo científico publicado en 2013
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization
artículo científico publicado en 2014
Genetic associations with lipoprotein subfraction measures differ by ethnicity in the multi-ethnic study of atherosclerosis (MESA).
artículo científico publicado en 2017
Genetic associations with valvular calcification and aortic stenosis
artículo científico publicado en 2013
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 osteoporosis susceptibility in a female Ashkenazi Jewish population
artículo científico publicado en 2004
Genetic determinants of the ankle-brachial index: a meta-analysis of a cardiovascular candidate gene 50K SNP panel in the candidate gene association resource (CARe) consortium
artículo científico publicado en 2012
Genetic effects on obesity assessed by bivariate genome scan: the Mexican-American coronary artery disease study
artículo científico publicado en 2006
Genetic epistasis of IL23/IL17 pathway genes in Crohn's disease
artículo científico publicado en 2009
Genetic heterogeneity in common disease
scientific article published on 01 January 1982
Genetic heterogeneity in diabetes mellitus and diabetic microangiopathy
scientific article published on 01 January 1981
Genetic heterogeneity in peptic ulcer
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artículo científico publicado el 19 de mayo de 1979
Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes.
artículo científico publicado en 2018
Genetic interactions drive heterogeneity in causal variant effect sizes for gene expression and complex traits
artículo científico publicado en 2022
Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies
artículo científico publicado en 2022
Genetic loci associated with heart rate variability and their effects on cardiac disease risk
artículo científico publicado en 2017
Genetic loci associated with ideal cardiovascular health: A meta-analysis of genome-wide association studies
artículo científico publicado en 2016
Genetic loci associated with nonobstructive coronary artery disease in Caucasian women
artículo científico publicado en 2015
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 loci for retinal arteriolar microcirculation
artículo científico publicado en 2013
Genetic mapping of a susceptibility locus for insulin-dependent diabetes mellitus on chromosome llq
artículo científico publicado en 1994
Genetic mapping of disposition index and acute insulin response loci on chromosome 11q. The Insulin Resistance Atherosclerosis Study (IRAS) Family Study
artículo científico publicado en 2006
Genetic marker family studies in familial Mediterranean fever (FMF) in Armenians
artículo científico publicado en 1990
Genetic markers: progress and potential for cardiovascular disease
artículo científico publicado en 2004
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 predictors of medically refractory ulcerative colitis
scientific journal article
Genetic variants associated with VLDL, LDL and HDL particle size differ with race/ethnicity
artículo científico publicado en 2012
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 in novel pathways influence blood pressure and cardiovascular disease risk
artículo científico publicado en 2011
Genetic variants modulate gene expression statin response in human lymphoblastoid cell lines
artículo científico publicado en 2020
Genetic variants of the NOTCH3 gene in the elderly and magnetic resonance imaging correlates of age-related cerebral small vessel disease
artículo científico publicado en 2011
Genetic variation associated with plasma von Willebrand factor levels and the risk of incident venous thrombosis
artículo científico publicado en 2010
Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge
scientific journal article
Genetic variation in lipoprotein (a) levels in families enriched for coronary artery disease is determined almost entirely by the apolipoprotein (a) gene locus.
artículo científico publicado en 1995
Genetic variation of SORBS1 gene is associated with glucose homeostasis and age at onset of diabetes: A SAPPHIRe Cohort Study.
artículo científico publicado en 2018
Genetically Determined Plasma Lipid Levels and Risk of Diabetic Retinopathy: A Mendelian Randomization Study
artículo científico publicado en 2017
Genetics of Coronary Artery Disease in Taiwan: A Cardiometabochip Study by the Taichi Consortium
artículo científico publicado en 2016
Genetics of Type 2 Diabetes in U.S. Hispanic/Latino Individuals: Results From the Hispanic Community Health Study/Study of Latinos (HCHS/SOL).
artículo científico
Genetics of coronary artery calcification among African Americans, a meta-analysis
artículo científico publicado en 2013
Genetics of diabetes
artículo científico publicado en 1983
Genetics of inflammatory bowel disease
article
Genetics, diabetes mellitus heterogeneity, and coronary heart disease.
artículo científico publicado en 1984
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 Scan for Blood Pressure in Dutch Dyslipidemic Families Reveals Linkage to a Locus on Chromosome 4p
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artículo científico publicado el 1 de octubre de 2001
Genome of The Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levels
artículo científico publicado en 2015
Genome scan for adiposity in Dutch dyslipidemic families reveals novel quantitative trait loci for leptin, body mass index and soluble tumor necrosis factor receptor superfamily 1A
artículo científico publicado en 2000
Genome wide association (GWA) predictors of anti-TNFalpha therapeutic responsiveness in pediatric inflammatory bowel disease
artículo científico publicado en 2010
Genome-Wide Analysis of Left Ventricular Image-Derived Phenotypes Identifies Fourteen Loci Associated With Cardiac Morphogenesis and Heart Failure Development
artículo científico publicado en 2019
Genome-Wide Association Studies
artículo científico publicado en 2019
Genome-Wide Association Study Highlights APOH as a Novel Locus for Lipoprotein(a) Levels
artículo científico publicado en 2020
Genome-Wide Association Study Identifies Loci for Liver Enzyme Concentrations in Mexican Americans: The GUARDIAN Consortium
scientific article published on 20 June 2019
Genome-Wide Association Study Meta-Analysis of Long-Term Average Blood Pressure in East Asians.
artículo científico
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 Apparent Treatment-Resistant Hypertension in the CHARGE Consortium: The CHARGE Pharmacogenetics Working Group
artículo científico publicado en 2019
Genome-Wide Association Study of the Modified Stumvoll Insulin Sensitivity Index Identifies BCL2 and FAM19A2 as Novel Insulin Sensitivity Loci
artículo científico publicado en 2016
Genome-Wide Association Transethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels
Genome-Wide Association and Trans-ethnic Meta-Analysis for Advanced Diabetic Kidney Disease: Family Investigation of Nephropathy and Diabetes (FIND)
artículo científico publicado en 2015
Genome-Wide Associations Related to Hepatic Histology in Nonalcoholic Fatty Liver Disease in Hispanic Boys
artículo científico publicado en 2017
Genome-Wide Interaction with Insulin Secretion Loci Reveals Novel Loci for Type 2 Diabetes in African Americans
artículo científico publicado en 2016
Genome-Wide Interactions with Dairy Intake for Body Mass Index in Adults of European Descent
artículo científico publicado en 2017
Genome-Wide Linkage of Plasma Adiponectin Reveals a Major Locus on Chromosome 3q Distinct From the Adiponectin Structural Gene: The IRAS Family Study
article
Genome-Wide Study of Subcutaneous and Visceral Adipose Tissue Reveals Novel Sex-Specific Adiposity Loci in Mexican Americans
artículo científico publicado en 2017
Genome-wide Association Study of Platelet Count Identifies Ancestry-Specific Loci in Hispanic/Latino Americans
artículo científico publicado en 2016
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 analysis of genetic loci associated with Alzheimer disease
artículo científico publicado en 2010
Genome-wide and gene-centric analyses of circulating myeloperoxidase levels in the charge and care consortia
artículo científico publicado en 2013
Genome-wide association analyses identify 18 new loci associated with serum urate concentrations
artículo científico publicado en 2013
Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus
artículo científico publicado en 2013
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 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 and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure
scientific article published on 09 January 2020
Genome-wide association and functional studies identify 46 novel loci for alcohol consumption and suggest common genetic mechanisms with neuropsychiatric disorders
Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.
artículo científico publicado en 2011
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease
artículo científico publicado en 2008
Genome-wide association identifies OBFC1 as a locus involved in human leukocyte telomere biology
artículo científico publicado en 2010
Genome-wide association identifies multiple ulcerative colitis susceptibility loci
artículo científico publicado en 2010
Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria
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 fish and EPA+DHA consumption in 17 US and European cohorts.
artículo científico publicado en 2017
Genome-wide association of body fat distribution in African ancestry populations suggests new loci
artículo científico publicado en 2013
Genome-wide association of copy-number variation reveals an association between short stature and the presence of low-frequency genomic deletions.
artículo científico publicado en 2011
Genome-wide association of lipid-lowering response to statins in combined study populations
artículo científico publicado en 2010
Genome-wide association of pericardial fat identifies a unique locus for ectopic fat
artículo científico publicado en 2012
Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging
artículo científico publicado en 2021
Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction
artículo científico publicado en 2012
Genome-wide association studies in East Asians identify new loci for waist-hip ratio and waist circumference
artículo científico publicado en 2016
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 study and meta-analysis identify loci associated with ventricular and supraventricular ectopy.
artículo científico publicado en 2018
Genome-wide association study for coronary artery calcification with follow-up in myocardial infarction
artículo científico publicado en 2011
Genome-wide association study identifies WNT7B as a novel locus for central corneal thickness in Latinos
artículo científico publicado en 2016
Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis
artículo científico publicado en 2007
Genome-wide association study identifies novel loci for type 2 diabetes-attributed end-stage kidney disease in African Americans
Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease
artículo científico publicado en 2010
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 a Chinese population with diabetic retinopathy
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artículo científico publicado el 4 de abril de 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 PR interval in Hispanics/Latinos identifies novel locus at ID2.
artículo científico publicado en 2017
Genome-wide association study of blood pressure and hypertension
scientific journal article
Genome-wide association study of body fat distribution traits in Hispanics/Latinos from the HCHS/SOL
artículo científico publicado en 2021
Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project
artículo científico publicado en 2011
Genome-wide association study of depressive symptoms in the Hispanic Community Health Study/Study of Latinos
artículo científico publicado en 2017
Genome-wide association study of generalized anxiety symptoms in the Hispanic Community Health Study/Study of Latinos
artículo científico publicado en 2016
Genome-wide association study of heart rate and its variability in Hispanic/Latino cohorts.
artículo científico publicado en 2017
Genome-wide association study of iron traits and relation to diabetes in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL): potential genomic intersection of iron and glucose regulation?
artículo científico publicado en 2017
Genome-wide association study of primary open-angle glaucoma in continental and admixed African populations
scientific article published on 13 October 2018
Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos.
artículo científico publicado en 2017
Genome-wide association study of retinopathy in individuals without diabetes
artículo científico publicado en 2013
Genome-wide association study of vitamin D concentrations in Hispanic Americans: the IRAS family study
artículo científico publicado en 2010
Genome-wide association: which do you want first: the good news, the bad news, or the good news?
artículo científico publicado en 2007
Genome-wide comparison of African-ancestry populations from CARe and other cohorts reveals signals of natural selection
artículo científico publicado en 2011
Genome-wide family-based linkage analysis of exome chip variants and cardiometabolic risk
artículo científico publicado en 2014
Genome-wide interaction with the insulin secretion locus MTNR1B reveals CMIP as a novel type 2 diabetes susceptibility gene in African Americans.
artículo científico publicado en 2018
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 linkage and association analysis of cardiometabolic phenotypes in Hispanic Americans
artículo científico publicado en 2016
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 increases to 71 the number of confirmed Crohn's disease susceptibility loci
artículo científico publicado en 2010
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 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 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 observational studies shows common genetic variants associated with macronutrient intake
artículo científico publicado en 2013
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 points to CTC1 and ZNF676 as genes regulating telomere homeostasis in humans
artículo científico publicado en 2012
Genome-wide scans for diabetic nephropathy and albuminuria in multiethnic populations: the family investigation of nephropathy and diabetes (FIND).
artículo científico publicado en 2007
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
Genomewide association studies of stroke
artículo científico publicado en 2009
Genomewide meta-analysis identifies loci associated with IGF-I and IGFBP-3 levels with impact on age-related traits
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artículo científico publicado en 2016
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
Genotype Imputation for Latinos Using the HapMap and 1000 Genomes Project Reference Panels
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artículo científico publicado el 27 de junio de 2012
Geographic origins of Jewish patients with inflammatory bowel disease
artículo científico publicado en 1989
Glucose, insulin, and incident hypertension in the multi-ethnic study of atherosclerosis
artículo científico publicado en 2010
Growth curves in achondroplasia
artículo científico publicado en 1977
HDAC9 is implicated in atherosclerotic aortic calcification and affects vascular smooth muscle cell phenotype
scientific article published on 28 October 2019
HLA class II haplotype associations with inflammatory bowel disease in Jewish (Ashkenazi) and non-Jewish caucasian populations
artículo científico publicado en 2000
HLA genotypic study of insulin-dependent diabetes the excess of DR3/DR4 heterozygotes allows rejection of the recessive hypothesis
artículo científico publicado en 1983
HLA haplotype sharing and proband genotype in IDDM
scientific article published on 01 January 1986
HLA on chromosome 6: the story gets longer and longer
artículo científico publicado en 2008
HLA-B5 associated with duodenal ulcer
artículo científico publicado en 1977
HLA-DR and the 5' insulin gene polymorphism in insulin-dependent diabetes
artículo científico publicado en 1991
HLA-DR3 and DR4 and their relation to the incidence and progression of diabetic retinopathy1 1The authors have no proprietary interest in any of the products mentioned in this study
article
Habitual sleep duration is associated with BMI and macronutrient intake and may be modified by CLOCK genetic variants
artículo científico publicado en 2014
Haplotypes in the lipoprotein lipase gene influence fasting insulin and discovery of a new risk haplotype
artículo científico publicado en 2006
Haplotypes in the lipoprotein lipase gene influence high-density lipoprotein cholesterol response to statin therapy and progression of atherosclerosis in coronary artery bypass grafts
scientific article published on 06 June 2006
Harnessing expression data to identify novel candidate genes in polycystic ovary syndrome
artículo científico publicado en 2011
Hemodynamic fluid shear stress response genes and carotid intima-media thickness: a candidate gene association analysis in the cardiovascular health study
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artículo científico publicado el 21 de mayo de 2012
Heritability of dehydroepiandrosterone sulfate in women with polycystic ovary syndrome and their sisters
scientific article published on 30 October 2006
Heritability of subclinical atherosclerosis in Latino families ascertained through a hypertensive parent
artículo científico publicado en 2002
Heritability of the severity of diabetic retinopathy: the FIND-Eye study
artículo científico publicado en 2008
Heritability patterns in hand osteoarthritis: the role of osteophytes
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artículo científico publicado el 28 de septiembre de 2010
Hermansky-Pudlak syndrome: an immunologic assessment of 15 cases
artículo científico publicado en 1988
Heterogeneity in Diabetes Mellitus—Update, 1978: Evidence for Further Genetic Heterogeneity within Juvenile-onset Insulin-dependent Diabetes Mellitus
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artículo científico publicado el 1 de mayo de 1978
High-frequency haplotypes in the X chromosome locus TLR8 are associated with both CD and UC in females
scientific article published on March 2009
High-resolution linkage mapping for susceptibility genes in human polygenic disease: insulin-dependent diabetes mellitus and chromosome 11q.
artículo científico publicado en 1991
Higher magnesium intake is associated with lower fasting glucose and insulin, with no evidence of interaction with select genetic loci, in a meta-analysis of 15 CHARGE Consortium Studies
artículo científico publicado en 2013
Home use of a compact, 12‑lead ECG recording system for newborns
artículo científico publicado en 2019
Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease
artículo científico publicado en 2012
Human genetic variation in VAC14 regulates Salmonella invasion and typhoid fever through modulation of cholesterol.
artículo científico publicado en 2017
Hundreds of variants clustered in genomic loci and biological pathways affect human height
artículo científico publicado en 2010
Hypertension genes are genetic markers for insulin sensitivity and resistance
artículo científico publicado en 2005
Hypothesis: familial Mediterranean fever--a genetic disorder of the lipocortin family?
artículo científico publicado en 1989
IBD-associated TL1A gene (TNFSF15) haplotypes determine increased expression of TL1A protein
artículo científico publicado en 2009
IL-23 receptor (IL-23R) gene protects against pediatric Crohn's disease
artículo científico publicado en 2007
IL23R haplotypes provide a large population attributable risk for Crohn's disease
artículo científico publicado en 2008
Identification and validation of N-acetyltransferase 2 as an insulin sensitivity gene
artículo científico publicado en 2015
Identification and validation of N-acetyltransferase 2 as an insulin sensitivity gene
artículo científico publicado en 2016
Identification of TNFRSF1B as a novel modifier gene in familial combined hyperlipidemia
scientific article published on 01 September 2000
Identification of candidate genes and pathways in retinopathy of prematurity by whole exome sequencing of preterm infants enriched in phenotypic extremes
artículo científico publicado en 2021
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 type 2 diabetes and shared etiological pathways with coronary heart disease
artículo científico publicado en 2017
Identification of novel genetic Loci associated with thyroid peroxidase antibodies and clinical thyroid disease
artículo científico publicado en 2014
Identification of quantitative trait loci for glucose homeostasis: the Insulin Resistance Atherosclerosis Study (IRAS) Family Study
artículo científico publicado en 2004
Identification of type 2 diabetes loci in 433,540 East Asian individuals
artículo científico publicado en 2020
Identifying association under a previous linkage peak on chromosome 16 for body mass index using cross-sectional and longitudinal data of the Framingham Heart Study
artículo científico publicado en 2009
Immunochip analysis identification of 6 additional susceptibility loci for Crohn's disease in Koreans
artículo científico publicado en 2015
Immunochip meta-analysis of inflammatory bowel disease identifies three novel loci and four novel associations in previously reported loci.
artículo científico publicado en 2018
Impact of Rare and Common Genetic Variants on Diabetes Diagnosis by Hemoglobin A1c in Multi-Ancestry Cohorts: The Trans-Omics for Precision Medicine Program
artículo científico publicado en 2019
Impact of ancestry and common genetic variants on QT interval in African Americans
artículo científico publicado en 2012
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
Improved Performance of Dynamic Measures of Insulin Response Over Surrogate Indices to Identify Genetic Contributors of Type 2 Diabetes: The GUARDIAN Consortium
artículo científico publicado en 2016
Improved imputation accuracy in Hispanic/Latino populations with larger and more diverse reference panels: applications in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL).
artículo científico publicado en 2016
Inactivating mutations in NPC1L1 and protection from coronary heart disease
artículo científico publicado en 2014
Incidence of Age-Related Macular Degeneration in a Multi-Ethnic United States Population: The Multi-Ethnic Study of Atherosclerosis
artículo científico publicado en 2016
Increased immune reactivity predicts aggressive complicating Crohn's disease in children
artículo científico publicado en 2008
Increased intestinal permeability in patients with Crohn's disease and their relatives. A possible etiologic factor
artículo científico publicado en 1986
Increased risk for type I (insulin-dependent) diabetes in relatives of patients with alopecia areata (AA).
artículo científico publicado en 1994
Individualizing therapies in type 2 diabetes mellitus based on patient characteristics: what we know and what we need to know
artículo científico publicado en 2010
Inflammation and the incidence of type 2 diabetes: the Multi-Ethnic Study of Atherosclerosis (MESA).
artículo científico publicado en 2010
Inherited causes of clonal haematopoiesis in 97,691 whole genomes
artículo científico publicado en 2020
Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis
artículo científico publicado en 2013
Insulin Clearance Is Associated with Hepatic Lipase Activity and Lipid and Adiposity Traits in Mexican Americans
artículo científico publicado en 2016
Insulin Resistance Exacerbates Genetic Predisposition to Nonalcoholic Fatty Liver Disease in Individuals Without Diabetes
artículo científico publicado en 2019
Insulin and islet cell autoantibodies as time-dependent covariates in the development of insulin-dependent diabetes: a prospective study in relatives
artículo científico publicado en 1993
Insulin clearance and the incidence of type 2 diabetes in Hispanics and African Americans: the IRAS Family Study
artículo científico publicado en 2012
Insulin clearance: confirmation as a highly heritable trait, and genome-wide linkage analysis
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artículo científico publicado el 16 de mayo de 2012
Insulin sensitivity and insulin clearance are heritable and have strong genetic correlation in Mexican Americans
artículo científico publicado en 2014
Insulin sensitivity, body fat distribution, and family diabetes history: the IRAS Family Study.
artículo científico publicado en 2004
Insulin-IGF2 region on chromosome 11p encodes a gene implicated in HLA-DR4-dependent diabetes susceptibility
artículo científico publicado en 1991
Insulin-dependent diabetes mellitus (IDDM) is associated with CTLA4 polymorphisms in multiple ethnic groups
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artículo científico publicado el 1 de agosto de 1997
Integrative predictive model of coronary artery calcification in atherosclerosis
artículo científico publicado en 2009
Interaction of HLA and immunoglobulin antigens in Type 1 (insulin-dependent) diabetes
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artículo científico publicado el 1 de noviembre de 1984
Interactions between candidate cardiovascular disease genes, traffic proximity, and left ventricular mass: the Multi-Ethnic Study of Atherosclerosis (MESA)
abstract published in 2010
Interactions between commensal fungi and the C-type lectin receptor Dectin-1 influence colitis
artículo científico publicado en 2012
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
Intercellular adhesion molecule 1 gene associations with immunologic subsets of inflammatory bowel disease
artículo científico publicado en 1995
Intestinal permeability in patients with Crohn's disease and their healthy relatives
artículo científico publicado en 1989
Investigation of the Interplay between Circulating Lipids and IGF-I and Relevance to Breast Cancer Risk: An Observational and Mendelian Randomization Study
artículo científico publicado en 2021
Israel-Gaza conflict
artículo científico publicado en 2009
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
LDL Cholesterol and Dysglycemia: an Intriguing Physiological Relationship
scientific article published on 01 October 2020
LPA Variants Are Associated With Residual Cardiovascular Risk in Patients Receiving Statins
Lack of an association between polymorphisms of the T-cell receptor alpha-chain and ulcerative colitis
artículo científico publicado en 1989
Large Meta-Analysis in the CHARGE Consortium Provides Evidence For an Association of Serum Vitamin D With Pulmonary Function
Large meta-analysis of genome-wide association studies identifies five loci for lean body mass
artículo científico publicado en 2017
Large multiethnic Candidate Gene Study for C-reactive protein levels: identification of a novel association at CD36 in African Americans
artículo científico publicado en 2014
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 Gene-Centric Meta-Analysis across 39 Studies Identifies Type 2 Diabetes Loci.
artículo científico publicado en 2012
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 in whites and African Americans identifies IL6R polymorphism in relation to atrial fibrillation: the National Heart, Lung, and Blood Institute's Candidate Gene Association Resource (CARe) project
artículo científico publicado en 2011
Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci
artículo científico publicado en 2012
Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci
artículo científico publicado en 2012
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 genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair
artículo científico publicado en 2015
Large-scale pharmacogenomic study of sulfonylureas and the QT, JT and QRS intervals: CHARGE Pharmacogenomics Working Group.
artículo científico publicado en 2016
Leptin-mediated increases in catecholamine signaling reduce adipose tissue inflammation via activation of macrophage HDAC4
scientific journal article
Levels of Free Fatty Acids (FFA) Are Associated with Insulin Resistance But Do Not Explain the Relationship between Adiposity and Insulin Resistance in Hispanic Americans: The IRAS Family Study
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artículo científico publicado el 3 de julio de 2012
Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing data
artículo científico publicado en 2019
Linkage Analysis of High-density SNPs Confirms Keratoconus Locus at 5q Chromosomal Region
artículo científico publicado en 2014
Linkage disequilibrium mapping places the gene causing familial Mediterranean fever close to D16S246.
artículo científico publicado en 1996
Linkage of Crohn's disease to the major histocompatibility complex region is detected by multiple non-parametric analyses
artículo científico publicado en 1999
Linkage of Crohn's disease-related serological phenotypes: NFKB1 haplotypes are associated with anti-CBir1 and ASCA, and show reduced NF-kappaB activation
artículo científico publicado en 2008
Linkage of the metabolic syndrome to 1q23-q31 in Hispanic families: the Insulin Resistance Atherosclerosis Study Family Study
artículo científico publicado en 2004
Lipoprotein lipase is a gene for insulin resistance in Mexican Americans
artículo científico publicado en 2004
Lipoprotein lipase locus and progression of atherosclerosis in coronary-artery bypass grafts
artículo científico publicado en 2004
Lipoprotein receptor-related protein 1 variants and dietary fatty acids: meta-analysis of European origin and African American studies
artículo científico publicado en 2013
Locus for elevated apolipoprotein B levels on chromosome 1p31 in families with familial combined hyperlipidemia
artículo científico publicado en 2002
Long-range LD can confound genome scans in admixed populations
artículo científico publicado en 2008
Low oxygen saturation during sleep reduces CD1D and RAB20 expressions that are reversed by CPAP therapy
artículo científico publicado en 2020
Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis
artículo científico publicado en 2017
Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis
scientific article published on 01 December 2018
Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility
artículo científico publicado en 2015
Lysine-specific demethylase 1: an epigenetic regulator of salt-sensitive hypertension
artículo científico publicado en 2012
MAGI2 genetic variation and inflammatory bowel disease
artículo científico publicado en 2009
Marked parental consanguinity as a cause for increased major malformations in an Israeli Arab community
artículo científico publicado el 1 de septiembre de 1992
Mendelian Randomization Analysis of Hemoglobin A1c as a Risk Factor for Coronary Artery Disease
artículo científico publicado en 2019
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-analyses of genome-wide association studies identify multiple loci associated with pulmonary function
artículo científico publicado en 2010
Meta-analysis across Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium provides evidence for an association of serum vitamin D with pulmonary function
artículo científico publicado en 2018
Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47
scientific journal article
Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci
artículo científico publicado en 2016
Meta-analysis identifies six new susceptibility loci for atrial fibrillation
artículo científico publicado en 2012
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 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
artículo científico publicado en 2013
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 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 African Americans provides insights into the genetic architecture of type 2 diabetes
artículo científico publicado en 2014
Meta-analysis of genome-wide association studies in East Asian-ancestry populations identifies four new loci for body mass index
artículo científico publicado en 2014
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 HDL cholesterol response to statins
artículo científico publicado en 2016
Meta-analysis of lipid-traits in Hispanics identifies novel loci, population-specific effects, and tissue-specific enrichment of eQTLs
artículo científico publicado en 2016
Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline
artículo científico publicado en 2020
Metabolic Syndrome Derived from Principal Component Analysis and Incident Cardiovascular Events: The Multi Ethnic Study of Atherosclerosis (MESA) and Health, Aging, and Body Composition (Health ABC).
artículo científico publicado en 2012
Metabolic and cardiovascular genes in polycystic ovary syndrome: a candidate-wide association study (CWAS).
artículo científico publicado en 2011
Metabolomics Identifies Distinctive Metabolite Signatures for Measures of Glucose Homeostasis: The Insulin Resistance Atherosclerosis Family Study (IRAS-FS).
artículo científico publicado en 2018
Minimal model-based insulin sensitivity has greater heritability and a different genetic basis than homeostasis model assessment or fasting insulin
artículo científico publicado en 2003
Mitochondrial DNA copy number and incident atrial fibrillation
artículo científico publicado en 2020
Molecular basis of a linkage peak: exome sequencing and family-based analysis identify a rare genetic variant in the ADIPOQ gene in the IRAS Family Study
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artículo científico publicado el 5 de agosto de 2010
Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions
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 study accounting for gene-psychosocial factor interactions identifies novel loci for blood pressure traits
artículo científico publicado en 2021
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 GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE Study
artículo científico publicado en 2021
Multi-ethnic Genome-wide Association Study of Decomposed Cardioelectric Phenotypes Illustrates Strategies to Identify and Characterize Evidence of Shared Genetic Effects for Complex Traits
artículo científico publicado en 2020
Multi-ethnic Meta-analysis Identifies RAI1 as a Possible Obstructive Sleep Apnea Related Quantitative Trait Locus in Men.
artículo científico publicado en 2017
Multi-ethnic analysis of lipid-associated loci: the NHLBI CARe project
artículo científico publicado en 2012
Multi-ethnic genome-wide association study for atrial fibrillation
article
Multi-ethnic genome-wide association study of decomposed cardioelectric phenotypes illustrates strategies to identify and characterize evidence of shared genetic effects for complex traits
artículo científico publicado en 2019
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes
artículo científico publicado en 2018
Multidimensional Prognostic Risk Assessment Identifies Association Between IL12B Variation and Surgery in Crohn’s Disease
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artículo científico publicado el 1 de julio de 2013
Multiethnic Exome-Wide Association Study of Subclinical Atherosclerosis.
artículo científico publicado en 2016
Multiethnic Genome-Wide Association Study of Diabetic Retinopathy Using Liability Threshold Modeling of Duration of Diabetes and Glycemic Control
scientific article published on 28 November 2018
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 genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation
artículo científico publicado en 2016
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
Multilocus genetic determinants of LDL particle size in coronary artery disease families
artículo científico publicado en 1996
Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium
artículo científico publicado en 2009
Multiple nonglycemic genomic loci are newly associated with blood level of glycated hemoglobin in East Asians
artículo científico publicado en 2014
Multi‐phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations
artículo científico publicado en 2022
Mutations in NOD2 are associated with fibrostenosing disease in patients with Crohn's disease
artículo científico publicado en 2002
NOD2 variants and antibody response to microbial antigens in Crohn's disease patients and their unaffected relatives.
artículo científico publicado en 2006
NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium
artículo científico publicado en 2009
Native American ancestry is associated with severe diabetic retinopathy in Latinos.
artículo científico publicado en 2014
Natural Selection on Genes Related to Cardiovascular Health in High-Altitude Adapted Andeans
artículo científico publicado en 2017
Neutrophil autoantibodies in ulcerative colitis: Familial aggregation and genetic heterogeneity
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artículo científico publicado el 1 de agosto de 1992
New Blood Pressure-Associated Loci Identified in Meta-Analyses of 475 000 Individuals
artículo científico publicado en 2017
New alcohol-related genes suggest shared genetic mechanisms with neuropsychiatric disorders
scientific article published on 29 July 2019
New gene functions in megakaryopoiesis and platelet formation
artículo científico publicado en 2011
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
artículo científico publicado en 2010
Ninety-nine independent genetic loci influencing general cognitive function include genes associated with brain health and structure (N = 280,360)
No association of 9p21 with arterial elasticity and retinal microvascular findings
artículo científico publicado en 2013
No interactions between previously associated 2-hour glucose gene variants and physical activity or BMI on 2-hour glucose levels
artículo científico publicado en 2012
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 Genetic Loci Associated With Retinal Microvascular Diameter
artículo científico publicado en 2015
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 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 human alpha1a-adrenoceptor single nucleotide polymorphisms alter receptor pharmacology and biological function
artículo científico publicado en 2005
Novel loci associated with PR interval in a genome-wide association study of 10 African American cohorts
artículo científico publicado en 2012
Novel loci associated with increased risk of sudden cardiac death in the context of coronary artery disease
artículo científico publicado en 2013
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
OR15-6 Epigenetic Differences in First Trimester Pregnancies Conceived with Infertility.
artículo científico publicado en 2019
Ocular Manifestations in Inflammatory Bowel Disease Are Associated with Other Extra-intestinal Manifestations, Gender, and Genes Implicated in Other Immune-related Traits.
artículo científico publicado en 2015
Omega-3 Fatty Acids and Genome-Wide Interaction Analyses Reveal DPP10-Pulmonary Function Association
artículo científico publicado en 2019
Optimization of techniques for multiple platform testing in small, precious samples such as human chorionic villus sampling
artículo científico publicado en 2016
Orthostatic hypotension and novel blood pressure-associated gene variants: Genetics of Postural Hemodynamics (GPH) Consortium
artículo científico publicado en 2012
Outdoor air pollution and mosaic loss of chromosome Y in older men from the Cardiovascular Health Study
artículo científico publicado en 2018
Overlap of Genetic Risk between Interstitial Lung Abnormalities and Idiopathic Pulmonary Fibrosis
scientific article published on 01 December 2019
PCSK9 Loss-of-Function Variants, Low-Density Lipoprotein Cholesterol, and Risk of Coronary Heart Disease and Stroke: Data From 9 Studies of Blacks and Whites
artículo científico publicado en 2017
PLD3 variants in population studies
artículo científico publicado en 2015
PPIP5K2 and PCSK1 are Candidate Genetic Contributors to Familial Keratoconus
artículo científico publicado en 2019
PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity
artículo científico publicado en 2018
PROTEIN-CODING VARIANTS IMPLICATE NOVEL GENES RELATED TO LIPID HOMEOSTASIS CONTRIBUTING TO BODY FAT DISTRIBUTION
article
Parent-of-Origin Effects of the APOB Gene on Adiposity in Young Adults
artículo científico publicado en 2015
Pathological acid secretion not due to gastrinoma
scientific article published on 01 January 1983
Pattern recognition receptor and autophagy gene variants are associated with development of antimicrobial antibodies in Crohn's disease
artículo científico publicado en 2012
Peptic Ulcer Disease-A Heterogeneous Group of Disorders?
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artículo científico publicado el 1 de septiembre de 1977
Perinuclear antineutrophil cytoplasmic antibodies in patients with Crohn's disease define a clinical subgroup
artículo científico publicado en 1996
Personalized Medicine in Ophthalmology: From Pharmacogenetic Biomarkers to Therapeutic and Dosage Optimization
artículo científico publicado en 2013
Personalized medicine and pharmacogenetic biomarkers: progress in molecular oncology testing
artículo científico publicado en 2012
Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins
artículo científico publicado en 2014
Pharmacogenomics study of thiazide diuretics and QT interval in multi-ethnic populations: the cohorts for heart and aging research in genomic epidemiology
artículo científico publicado en 2017
Pharmacometabolomic signature links simvastatin therapy and insulin resistance
artículo científico publicado en 2016
Phenotype-genotype correlation in familial Mediterranean fever: evidence for an association between Met694Val and amyloidosis
artículo científico publicado en 1999
Phenotypic predictors of response to simvastatin therapy among African-Americans and Caucasians: the Cholesterol and Pharmacogenetics (CAP) Study
artículo científico publicado en 2006
Physical Activity Associations with Bone Mineral Density and Modification by Metabolic Traits
scientific article published on 07 July 2020
Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals
artículo científico publicado en 2016
Pleiotropic genes for metabolic syndrome and inflammation
artículo científico publicado en 2014
Pleiotropy and heterogeneity in the expression of atherogenic lipoproteins: the IRAS Family Study
artículo científico publicado en 2003
Polycystic ovary syndrome in Mexican-Americans: prevalence and association with the severity of insulin resistance
artículo científico publicado en 2005
Polymorphic gene markers in Mexican-Americans residing in southern California
artículo científico publicado en 1995
Polymorphisms of the HNF1A gene encoding hepatocyte nuclear factor-1 alpha are associated with C-reactive protein
artículo científico publicado en 2008
Pooled analysis of iron-related genes in Parkinson's disease: association with transferrin
artículo científico publicado en 2013
Population structure of Hispanics in the United States: the multi-ethnic study of atherosclerosis
artículo científico publicado en 2012
Precise gene dosage determination by polymerase chain reaction: theory, methodology, and statistical approach
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artículo científico publicado el 1 de agosto de 1991
Predicting stroke through genetic risk functions: the CHARGE Risk Score Project
artículo científico publicado en 2014
Predictive Accuracy of a Polygenic Risk Score Compared With a Clinical Risk Score for Incident Coronary Heart Disease
artículo científico publicado en 2020
Predictors of mortality in hospitalized COVID-19 patients: A systematic review and meta-analysis
scientific article published on 22 May 2020
Preferential transmission of diabetic alleles within the HLA gene complex
artículo científico publicado en 1986
Prognostic Significance of Large Airway Dimensions on Computed Tomography in the General Population: The Multi-Ethnic Study of Atherosclerosis (MESA) Lung Study
artículo científico publicado en 2018
Progress in understanding the genetics of diabetes mellitus.
artículo científico publicado en 1985
Prospective study of particulate air pollution exposures, subclinical atherosclerosis, and clinical cardiovascular disease: the Multi-Ethnic Study of Atherosclerosis and Air Pollution (MESA Air)
artículo científico publicado en 2012
Protein-Truncating Variants at the Cholesteryl Ester Transfer Protein Gene and Risk for Coronary Heart Disease
artículo científico publicado en 2017
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: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries
artículo científico publicado en 2018
Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries
artículo científico publicado en 2020
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 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
Quality of dietary fat and genetic risk of type 2 diabetes: individual participant data meta-analysis
artículo científico publicado en 2019
Quantifying rare, deleterious variation in 12 human cytochrome P450 drug-metabolism genes in a large-scale exome dataset
artículo científico publicado en 2013
Quantifying the health benefits of genetic tests: a clinical perspective
artículo científico publicado en 2006
Quantitative Trait Locus Analysis of SIX1-SIX6 With Retinal Nerve Fiber Layer Thickness in Individuals of European Descent
artículo científico publicado en 2015
Quantitative serum pepsinogen: genetics and relationship to urinary and gastric phenotypes
artículo científico publicado en 1985
Quantitative trait analysis of type 2 diabetes susceptibility loci identified from whole genome association studies in the Insulin Resistance Atherosclerosis Family Study
artículo científico publicado en 2008
Quantitative trait locus mapping of human blood pressure to a genetic region at or near the lipoprotein lipase gene locus on chromosome 8p22.
artículo científico publicado en 1996
Rare Exome Sequence Variants in CLCN6 Reduce Blood Pressure Levels and Hypertension Risk
artículo científico publicado en 2015
Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer's Disease
artículo científico publicado en 2016
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 in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease
artículo científico publicado en 2017
Rare variant associations with waist-to-hip ratio in European-American and African-American women from the NHLBI-Exome Sequencing Project
artículo científico publicado en 2016
Rationale, Design, and Baseline Characteristics of the Microbiome and Insulin Longitudinal Evaluation Study (MILES)
artículo científico publicado en 2020
Refined genomic localization and ethnic differences observed for the IBD5 association with Crohn's disease
article
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
Regional mapping of the gene for familial Mediterranean fever on human chromosome 16p13.
artículo científico publicado en 1993
Relationship of sex to diabetes risk in statin trials
artículo científico publicado en 2013
Relationships among serum pepsinogen I, serum pepsinogen II, and gastric mucosal histology. A study in relatives of patients with pernicious anemia
artículo científico publicado en 1982
Relationships between the human pepsinogen DNA and protein polymorphisms
artículo científico publicado en 1986
Relative predispositional effects of HLA class II DRB1-DQB1 haplotypes and genotypes on type 1 diabetes: a meta-analysis
artículo científico publicado en 2007
Replication of association of DENND1A and THADA variants with polycystic ovary syndrome in European cohorts
artículo científico publicado en 2011
Replication of calpain-10 genetic association with carotid intima-media thickness
artículo científico publicado en 2009
Reply
artículo científico publicado en 2016
Restriction fragment length polymorphism (RFLP) heterogeneity of HLA-DQ beta genes associated with DNA fragment identical to the DR1-beta DNA structure
scientific article published on 01 September 1991
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
SORCS1: a novel human type 2 diabetes susceptibility gene suggested by the mouse
artículo científico publicado en 2007
Sample-size calculations in segregation analysis.
artículo científico publicado en 1984
Sample-size considerations and strategies for linkage analysis in autosomal recessive disorders.
artículo científico publicado en 1986
Saturated fat intake modulates the association between an obesity genetic risk score and body mass index in two US populations
artículo científico publicado en 2014
Selecting SNPs informative for African, American Indian and European Ancestry: application to the Family Investigation of Nephropathy and Diabetes (FIND).
artículo científico publicado en 2016
Sensorineural deafness inherited as a tissue specific mitochondrial disorder
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artículo científico publicado el 1 de febrero de 1992
Sequencing Analysis at 8p23 Identifies Multiple Rare Variants in DLC1 Associated with Sleep-Related Oxyhemoglobin Saturation Level
scientific article published on 24 October 2019
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program
artículo científico publicado en 2019
Sequencing of SCN5A identifies rare and common variants associated with cardiac conduction: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium
artículo científico publicado en 2014
Serum amyloid A and P protein genes in familial Mediterranean fever
artículo científico publicado en 1990
Serum immune responses predict rapid disease progression among children with Crohn's disease: immune responses predict disease progression
artículo científico publicado en 2006
Serum metabolic signatures of coronary and carotid atherosclerosis and subsequent cardiovascular disease
artículo científico publicado en 2019
Sex differences in the late first trimester human placenta transcriptome
artículo científico publicado en 2018
Single nucleotide polymorphisms in the apolipoprotein M gene are associated with percent emphysema, HDL and HDL subfractions among European- And African-Americans: the MESA Lung and SNP Health Association Resource (SHARe) studies
abstract published in 2012
Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations.
artículo científico publicado en 2017
Smoking-by-genotype interaction in type 2 diabetes risk and fasting glucose
artículo científico publicado en 2020
Standard growth curves for achondroplasia
artículo científico publicado en 1978
Statin-induced LDL cholesterol response and type 2 diabetes: a bidirectional two-sample Mendelian randomization study
scientific article published on 05 December 2019
Statin-induced changes in gene expression in EBV-transformed and native B-cells
artículo científico publicado en 2013
Statin-induced expression change of INSIG1 in lymphoblastoid cell lines correlates with plasma triglyceride statin response in a sex-specific manner
artículo científico publicado en 2016
Statin-induced expression change of INSIG1 in lymphoblastoid cell lines correlates with plasma triglyceride statin response in a sex-specific manner.
artículo científico publicado en 2016
Steroidogenic regulatory factor FOS is underexpressed in polycystic ovary syndrome (PCOS) adipose tissue and genetically associated with PCOS susceptibility
artículo científico publicado en 2012
Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function
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artículo científico publicado en 2018
Susceptibility locus for inflammatory bowel disease on chromosome 16 has a role in Crohn's disease, but not in ulcerative colitis
artículo científico publicado en 1996
Susceptibility to Crohn's disease is mediated by KIR2DL2/KIR2DL3 heterozygosity and the HLA-C ligand
artículo científico publicado en 2009
Systematic evaluation of validated type 2 diabetes and glycaemic trait loci for association with insulin clearance
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artículo científico publicado el 14 de marzo de 2013
Systemic Soluble Tumor Necrosis Factor Receptors 1 and 2 Are Associated with Severity of Diabetic Retinopathy in Hispanics
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artículo científico publicado el 11 de febrero de 2012
TNFRSF1B Is Associated with ANCA in IBD.
artículo científico publicado en 2016
TNFSF15 is an ethnic-specific IBD gene
artículo científico publicado en 2007
Targeted sequencing in candidate genes for atrial fibrillation: the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Targeted Sequencing Study
artículo científico publicado en 2014
Testing the gene or testing a variant? The case of TCF7L2
scientific article published on 01 October 2007
The 3' untranslated region of the lipoprotein lipase gene: haplotype structure and association with post-heparin plasma lipase activity
artículo científico publicado en 2005
The 5' insulin gene polymorphism and the genetics of vascular complications in type 1 (insulin-dependent) diabetes mellitus
artículo científico publicado en 1991
The African Descent and Glaucoma Evaluation Study (ADAGES) III: Contribution of Genotype to Glaucoma Phenotype in African Americans: Study Design and Baseline Data
artículo científico publicado en 2018
The Association of Estrogen Receptor-β Gene Variation With Salt-Sensitive Blood Pressure
artículo científico publicado en 2017
The GENNID Study. A resource for mapping the genes that cause NIDDM.
artículo científico publicado en 1996
The GLP-1 response to glucose does not mediate beta and alpha cell dysfunction in Hispanics with abnormal glucose metabolism
artículo científico publicado en 2017
The HMG-CoA reductase gene and lipid and lipoprotein levels: the multi-ethnic study of atherosclerosis
artículo científico publicado en 2009
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 M694V mutation in Armenian-Americans: a 10-year retrospective study of MEFV mutation testing for familial Mediterranean fever at UCLA.
artículo científico publicado en 2012
The Polygenic and Monogenic Basis of Blood Traits and Diseases
artículo científico publicado en 2020
The aggregation of the 5' insulin gene polymorphism in insulin dependent (type I) diabetes mellitus families
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artículo científico publicado el 1 de julio de 1992
The chromosome 9p21 variant not predicting long-term cardiovascular mortality in Chinese with established coronary artery disease: an eleven-year follow-up study
artículo científico publicado en 2014
The gene for familial Mediterranean fever in both Armenians and non-Ashkenazi Jews is linked to the alpha-globin complex on 16p: evidence for locus homogeneity
artículo científico publicado en 1992
The gene for familial Mediterranean fever is mapped to 16p 13.3- p13.1 with evidence for homogeneity.
artículo científico publicado en 1995
The genetic syndromology of peptic ulcer
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artículo científico publicado el 1 de enero de 1981
The genetic underpinnings of variation in ages at menarche and natural menopause among women from the multi-ethnic Population Architecture using Genomics and Epidemiology (PAGE) Study: A trans-ethnic meta-analysis
artículo científico publicado en 2018
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 diabetes
scientific article published on 01 May 1987
The genetics of retinopathy of prematurity: a model for neovascular retinal disease
article
The genetics of the glucose intolerance disorders
scientific article published on 01 January 1981
The landscape of recombination in African Americans
artículo científico publicado en 2011
The lipoprotein lipase (LPL) S447X gain of function variant involves increased mRNA translation
artículo científico publicado en 2011
The role of the Toll receptor pathway in susceptibility to inflammatory bowel diseases
article
The transcriptional landscape of age in human peripheral blood
artículo científico publicado en 2015
The triglyceride to high-density lipoprotein cholesterol (TG/HDL-C) ratio as a predictor of insulin resistance, β-cell function, and diabetes in Hispanics and African Americans
artículo científico publicado en 2018
Trans-ethnic Evaluation Identifies Novel Low Frequency Loci Associated with 25-Hydroxyvitamin D Concentrations.
artículo científico publicado en 2018
Trans-ethnic Meta-analysis and Functional Annotation Illuminates the Genetic Architecture of Fasting Glucose and Insulin
artículo científico publicado en 2016
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations
artículo científico publicado en 2020
Trans-ethnic fine mapping identifies a novel independent locus at the 3' end of CDKAL1 and novel variants of several susceptibility loci for type 2 diabetes in a Han Chinese population
artículo científico publicado en 2013
Trans-ethnic fine-mapping of genetic loci for body mass index in the diverse ancestral populations of the Population Architecture using Genomics and Epidemiology (PAGE) Study reveals evidence for multiple signals at established loci
artículo científico publicado en 2017
Trans-ethnic fine-mapping of lipid loci identifies population-specific signals and allelic heterogeneity that increases the trait variance explained
artículo científico publicado en 2013
Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies
artículo científico publicado en 2019
Trans-ethnic meta-analysis of white blood cell phenotypes
artículo científico publicado en 2014
Transcriptome-Wide Analysis Identifies Novel Associations With Blood Pressure
artículo científico
Transcriptome-Wide Association Study of Blood Cell Traits in African Ancestry and Hispanic/Latino Populations
artículo científico publicado en 2021
Transethnic Transferability of a Genome-wide Polygenic Score for Coronary Artery Disease
artículo científico publicado en 2020
Transferability and fine mapping of type 2 diabetes loci in African Americans: the Candidate Gene Association Resource Plus Study
artículo científico publicado en 2012
Transferability and fine-mapping of glucose and insulin quantitative trait loci across populations: CARe, the Candidate Gene Association Resource
artículo científico publicado en 2012
Tumor necrosis factor microsatellites define a Crohn's disease-associated haplotype on chromosome 6.
artículo científico publicado en 1996
Two-locus mitochondrial and nuclear gene models for mitochondrial disorders
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artículo científico publicado el 1 de enero de 1992
Type 2 Diabetes Modifies the Association of CAD Genomic Risk Variants With Subclinical Atherosclerosis
artículo científico publicado en 2023
Ulcerative colitis and total alopecia in a mother and her son
artículo científico publicado en 1993
Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study
artículo científico publicado en 2009
Ulcerative colitis: a genetically heterogeneous disorder defined by genetic (HLA class II) and subclinical (antineutrophil cytoplasmic antibodies) markers
artículo científico publicado en 1993
Ultraconserved elements in the human genome: association and transmission analyses of highly constrained single-nucleotide polymorphisms
artículo científico publicado en 2012
Unusual congenital anomalies
artículo científico publicado el 1 de enero de 1975
Upregulated heme biosynthesis increases obstructive sleep apnea severity: a pathway-based Mendelian randomization study
artículo científico publicado en 2022
Uridine monophosphate kinase and susceptibility to invasive Haemophilus influenzae type B disease
artículo científico publicado en 1986
Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations
artículo científico publicado en 2019
Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations
artículo científico publicado en 2019
Variants identified in a GWAS meta-analysis for blood lipids are associated with the lipid response to fenofibrate
artículo científico publicado en 2012
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 ZNF365 isoform D are associated with Crohn's disease
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artículo científico publicado el 21 de enero de 2011
Variants in angiopoietin-2 (ANGPT2) contribute to variation in nocturnal oxyhaemoglobin saturation level
artículo científico publicado en 2016
Variants of the caveolin-1 gene: a translational investigation linking insulin resistance and hypertension
artículo científico publicado en 2011
Variation in the 3-hydroxyl-3-methylglutaryl coenzyme a reductase gene is associated with racial differences in low-density lipoprotein cholesterol response to simvastatin treatment
artículo científico publicado en 2008
Variation in the gene for muscle-specific AMP deaminase is associated with insulin clearance, a highly heritable trait
artículo científico publicado en 2005
Variation in the lysyl oxidase (LOX) gene is associated with keratoconus in family-based and case-control studies
artículo científico publicado en 2012
Visceral fat and prevalence of hypertension among African Americans and Hispanic Americans: findings from the IRAS family study
artículo científico publicado en 2008
Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium
artículo científico publicado en 2021
Whole genome sequence analysis of pulmonary function and COPD in 19,996 multi-ethnic participants
scientific article published on 14 October 2020
Whole-Genome Sequencing to Characterize Monogenic and Polygenic Contributions in Patients Hospitalized With Early-Onset Myocardial Infarction
scientific article published on 01 March 2019
Whole-exome imputation of sequence variants identified two novel alleles associated with adult body height in African Americans.
artículo científico publicado en 2014
Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol
artículo científico publicado en 2014
Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program
artículo científico publicado en 2021
Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program
artículo científico publicado en 2021
Workshop on genetics of diabetes
artículo científico publicado en 1982
X chromosome dosage of histone demethylase KDM5C determines sex differences in adiposity
scientific article published on 23 July 2020
rs641738C>T near MBOAT7 is associated with liver fat, ALT, and fibrosis in NAFLD: a meta-analysis
scientific article published on 31 August 2020
40 EASD Annual Meeting of the European Association for the Study of Diabetes : Munich, Germany, 5-9 September 2004
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