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A PheWAS study of a large observational epidemiological cohort of African Americans from the REGARDS study

scholarly article by Xueyan Zhao et al published 31 January 2019 in BMC Medical Genomics

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

scientific article published on 31 May 2019

A comprehensive evaluation of IL4 variants in ethnically diverse populations: association of total serum IgE levels and asthma in white subjects

artículo científico publicado en 2004

A continuum of admixture in the Western Hemisphere revealed by the African Diaspora genome

scientific article published on 11 October 2016

A fully adjusted two-stage procedure for rank-normalization in genetic association studies

scientific article published on 17 January 2019

A gene-centric association scan for Coagulation Factor VII levels in European and African Americans: the Candidate Gene Association Resource (CARe) Consortium

artículo científico publicado en 2011

A genetic risk score is associated with statin-induced low-density lipoprotein cholesterol lowering

artículo científico publicado en 2016

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 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 and genome-wide association study of platelet count and mean platelet volume in african americans

artículo científico publicado en 2012

A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry

artículo científico publicado en 2013

A variational Bayes discrete mixture test for rare variant association

artículo científico publicado en 2014

APOL1 Nephropathy Risk Alleles and Risk of Sepsis in Blacks

scientific article published on 08 November 2019

Abstract 25: Epigenome-Wide DNA Methylation Analysis Reveals Novel Hematologic Trait Associations for African Americans in The Jackson Heart Study

artículo científico publicado en 2020

Adult height, coronary heart disease and stroke: a multi-locus Mendelian randomization meta-analysis

artículo científico publicado en 2016

Allelic Heterogeneity at the CRP Locus Identified by Whole-Genome Sequencing in Multi-ancestry Cohorts

artículo científico publicado en 2019

Assembly of a pan-genome from deep sequencing of 910 humans of African descent

Association between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant data

artículo científico publicado en 2014

Association of Exome Sequences With Cardiovascular Traits Among Blacks in the Jackson Heart Study

artículo científico publicado en 2016

Association of FTO with obesity-related traits in the Cebu Longitudinal Health and Nutrition Survey (CLHNS) Cohort

artículo científico publicado en 2008

Association of HLA-DRB1∗09:01 with tIgE levels among African-ancestry individuals with asthma

artículo científico publicado en 2020

Association of West African ancestry and blood pressure control among African Americans taking antihypertensive medication in the Jackson Heart Study

artículo científico publicado en 2020

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

artículo científico publicado en 2014

Association of genomic loci from a cardiovascular gene SNP array with fibrinogen levels in European Americans and African-Americans from six cohort studies: the Candidate Gene Association Resource (CARe).

artículo científico publicado en 2010

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 CASP10 and CASP8 with FEV(1)/FVC and bronchial hyperresponsiveness in ethnically diverse asthmatics

artículo científico publicado en 2008

Association of polymorphisms in the CRP gene with circulating C-reactive protein levels and cardiovascular events

artículo científico publicado en 2006

Association of protein tyrosine phosphatase 1B gene polymorphisms with type 2 diabetes

artículo científico publicado en 2004

Association of sickle cell trait with atrial fibrillation: The REGARDS cohort

scientific article published on 16 April 2019

Association studies with imputed variants using expectation-maximization likelihood-ratio tests

artículo científico publicado en 2014

Association study in African-admixed populations across the Americas recapitulates asthma risk loci in non-African populations

artículo científico publicado en 2019

Associations between common fibrinogen gene polymorphisms and cardiovascular disease in older adults. The Cardiovascular Health Study

scientific article published on 01 February 2008

Author Correction: Assembly of a pan-genome from deep sequencing of 910 humans of African descent

scientific article published on 01 February 2019

Author Correction: Association study in African-admixed populations across the Americas recapitulates asthma risk loci in non-African populations

scientific article published on 04 September 2019

Autosomal genome-wide scan for coronary artery calcification loci in sibships at high risk for hypertension

artículo científico publicado en 2002

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

artículo científico publicado en 2010

Causal effects of body mass index on cardiometabolic traits and events: a Mendelian randomization analysis

artículo científico publicado en 2014

Chromosome 8q24 risk variants in hereditary and non-hereditary prostate cancer patients

artículo científico publicado en 2008

Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices

artículo científico publicado en 2021

Coagulation factor VIII: Relationship to cardiovascular disease risk and whole genome sequence and epigenome-wide analysis in African Americans

scientific article published on 27 January 2020

Common coding variants of the HNF1A gene are associated with multiple cardiovascular risk phenotypes in community-based samples of younger and older European-American adults: the Coronary Artery Risk Development in Young Adults Study and The Cardiov

artículo científico publicado en 2009

Common variants in the CRP gene in relation to longevity and cause-specific mortality in older adults: the Cardiovascular Health Study

artículo científico publicado en 2007

Common α-globin variants modify hematologic and other clinical phenotypes in sickle cell trait and disease.

artículo científico publicado en 2018

Comparison of ENCODE region SNPs between Cebu Filipino and Asian HapMap samples

artículo científico publicado en 2007

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

artículo científico publicado en 2015

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

Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes

artículo científico publicado en 2020

Device-measured physical activity data for classification of patients with ventricular arrhythmia events: A pilot investigation

artículo científico publicado en 2018

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 replication of SNP-SNP interactions for quantitative lipid traits in over 60,000 individuals

artículo científico publicado en 2017

Dopamine transporter, gender, and number of sexual partners among young adults

artículo científico publicado en 2007

Drug-Gene Interactions of Antihypertensive Medications and Risk of Incident Cardiovascular Disease: A Pharmacogenomics Study from the CHARGE Consortium

artículo científico publicado en 2015

ERRATUM: Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

article by Matthew B. Lanktree et al published June 2012 in American Journal of Human Genetics

Enhanced statistical tests for GWAS in admixed populations: assessment using African Americans from CARe and a Breast Cancer Consortium

artículo científico publicado en 2011

Epistatic effects between two genes in the renin-angiotensin system and systolic blood pressure and coronary artery calcification.

artículo científico publicado en 2006

Estrogen receptor 1 polymorphisms are associated with airway hyperresponsiveness and lung function decline, particularly in female subjects with asthma

artículo científico publicado en 2006

Evidence for Association between SH2B1 Gene Variants and Glycated Hemoglobin in Nondiabetic European American Young Adults: The Add Health Study

artículo científico publicado en 2016

Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits

artículo científico publicado en 2016

Exome sequencing and directed clinical phenotyping diagnose cholesterol ester storage disease presenting as autosomal recessive hypercholesterolemia

artículo científico publicado en 2013

Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction

artículo científico publicado en 2014

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

Exploring pleiotropy using principal components

artículo científico publicado en 2003

Family-based samples can play an important role in genetic association studies

artículo científico publicado en 2008

Fine mapping the CETP region reveals a common intronic insertion associated to HDL-C

artículo científico publicado en 2015

Gene-centric approach identifies new and known loci for FVIII activity and VWF antigen levels in European Americans and African Americans

artículo científico publicado en 2015

Gene-centric meta-analyses for central adiposity traits in up to 57 412 individuals of European descent confirm known loci and reveal several novel associations

artículo científico publicado en 2013

Gene-centric meta-analyses of 108 912 individuals confirm known body mass index loci and reveal three novel signals

artículo científico publicado en 2012

Genetic Risk Score for Type 2 Diabetes and Traits Related to Glucose-Insulin Homeostasis in Youth: The Exploring Perinatal Outcomes Among Children (EPOCH) Study

artículo científico publicado en 2021

Genetic Risk for Hepatic Fat among an Ethnically Diverse Cohort of Youth: The Exploring Perinatal Outcomes among Children Study

scientific article published on 03 March 2020

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

scientific article published on 11 September 2020

Genetic association analysis highlights new loci that modulate hematological trait variation in Caucasians and African Americans.

artículo científico publicado en 2010

Genetic epidemiology of BMI and body mass change from adolescence to young adulthood

artículo científico publicado en 2009

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 meta-analysis of 15,901 African Americans identifies variation in EXOC3L1 is associated with HDL concentration.

artículo científico publicado en 2015

Genetic polymorphisms in CYP17, CYP3A4, CYP19A1, SRD5A2, IGF-1, and IGFBP-3 and prostate cancer risk in African-American men: the Flint Men's Health Study.

artículo científico publicado en 2008

Genetic underpinnings of regional adiposity distribution in African Americans: Assessments from the Jackson Heart Study

artículo científico publicado en 2021

Genetics of asthma and COPD. Similar results for different phenotypes

artículo científico publicado en 2004

Genetics of coronary artery calcification among African Americans, a meta-analysis

artículo científico publicado en 2013

Genome of The Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levels

artículo científico publicado en 2015

Genome- and exome-wide association study of serum lipoprotein (a) in the Jackson Heart Study.

artículo científico publicado en 2015

Genome-Wide Association Study Meta-Analysis of Stroke in 22 000 Individuals of African Descent Identifies Novel Associations With Stroke

artículo científico publicado en 2020

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 Blood Pressure Traits by Hispanic/Latino Background: the Hispanic Community Health Study/Study of Latinos.

artículo científico publicado en 2017

Genome-wide Association Study of Lipid Traits in Youth With Type 2 Diabetes

artículo científico publicado en 2021

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 admixture and association study of serum iron, ferritin, transferrin saturation and total iron binding capacity in African Americans

artículo científico publicado en 2014

Genome-wide and gene-centric analyses of circulating myeloperoxidase levels in the charge and care consortia

artículo científico publicado en 2013

Genome-wide association analysis identifies six new loci associated with forced vital capacity

artículo científico publicado en 2014

Genome-wide association analysis of red blood cell traits in African Americans: the COGENT Network

artículo científico publicado en 2013

Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria

artículo científico publicado en 2019

Genome-wide association of body fat distribution in African ancestry populations suggests new loci

artículo científico publicado en 2013

Genome-wide association study for adiponectin levels in Filipino women identifies CDH13 and a novel uncommon haplotype at KNG1–ADIPOQ ⬇️

artículo científico publicado el 27 de septiembre de 2010

Genome-wide association study of heart rate and its variability in Hispanic/Latino cohorts.

artículo científico publicado en 2017

Genome-wide association study of homocysteine in African Americans from the Jackson Heart Study, the Multi-Ethnic Study of Atherosclerosis, and the Coronary Artery Risk in Young Adults study

artículo científico publicado en 2018

Genome-wide association study of homocysteine levels in Filipinos provides evidence for CPS1 in women and a stronger MTHFR effect in young adults

artículo científico publicado en 2010

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 white blood cell count in 16,388 African Americans: the continental origins and genetic epidemiology network (COGENT).

artículo científico publicado en 2011

Genome-wide association with C-reactive protein levels in CLHNS: evidence for the CRP and HNF1A loci and their interaction with exposure to a pathogenic environment

artículo científico publicado en 2012

Genome-wide comparison of African-ancestry populations from CARe and other cohorts reveals signals of natural selection

artículo científico publicado en 2011

Genome-wide linkage scan for prostate cancer susceptibility genes in men with aggressive disease: significant evidence for linkage at chromosome 15q12.

artículo científico publicado en 2006

Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity

artículo científico publicado en 2017

Genome-wide meta-analysis of SNP and antihypertensive medication interactions on left ventricular traits in African Americans

artículo científico publicado en 2019

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 Association Study of Anthropometric Traits and Evidence of Interactions With Age and Study Year in Filipino Women ⬇️

artículo científico publicado el 21 de octubre de 2010

Gut microbiota phenotypes of obesity

scientific article published on 01 July 2019

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

artículo científico publicado en 2014

Harmonization of Respiratory Data From 9 US Population-Based Cohorts: The NHLBI Pooled Cohorts Study

artículo científico publicado en 2018

Heritability and expression of C-reactive protein in type 2 diabetes in the Diabetes Heart Study

artículo científico publicado en 2006

Heritability of carotid artery intima-medial thickness in type 2 diabetes

artículo científico publicado en 2002

IL-6 gene variation is associated with IL-6 and C-reactive protein levels but not cardiovascular outcomes in the Cardiovascular Health Study

scientific article published on 13 September 2007

Identification and functional analysis of glycemic trait loci in the China Health and Nutrition Survey.

artículo científico publicado en 2018

Identifying gene-gene interactions that are highly associated with four quantitative lipid traits across multiple cohorts

artículo científico publicado en 2016

Imputation of coding variants in African Americans: better performance using data from the exome sequencing project

artículo científico publicado en 2013

Imputation of exome sequence variants into population- based samples and blood-cell-trait-associated loci in African Americans: NHLBI GO Exome Sequencing Project.

artículo científico publicado en 2012

Inactivating mutations in NPC1L1 and protection from coronary heart disease

artículo científico publicado en 2014

Inflammation and stress-related candidate genes, plasma interleukin-6 levels, and longevity in older adults

artículo científico publicado en 2009

Inherited causes of clonal haematopoiesis in 97,691 whole genomes

artículo científico publicado en 2020

Interaction between fibrinogen and IL-6 genetic variants and associations with cardiovascular disease risk in the Cardiovascular Health Study

artículo científico publicado en 2010

Interaction of smoking and obesity susceptibility loci on adolescent BMI: The National Longitudinal Study of Adolescent to Adult Health

artículo científico publicado en 2015

Interferon gamma-induced protein 10 (IP-10) and cardiovascular disease in African Americans

scientific article published on 02 April 2020

KCNJ11 variants and their effect on the association between serum potassium and diabetes risk in the Atherosclerosis Risk in Communities (ARIC) Study and Jackson Heart Study (JHS) cohorts

artículo científico publicado en 2018

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 32 studies identifies multiple lipid loci

artículo científico publicado en 2012

Leveraging population admixture to characterize the heritability of complex traits

artículo científico publicado en 2014

Lipids, obesity and gallbladder disease in women: insights from genetic studies using the cardiovascular gene-centric 50K SNP array

artículo científico publicado en 2015

Long-term Absolute Risk for Cardiovascular Disease Stratified by Fasting Glucose Level

scientific article published on 07 January 2019

Loss-of-function mutations in APOC3, triglycerides, and coronary disease

artículo científico publicado en 2014

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

artículo científico publicado en 2015

Mapping adipose and muscle tissue expression quantitative trait loci in African Americans to identify genes for type 2 diabetes and obesity

artículo científico publicado en 2016

Mendelian randomization of blood lipids for coronary heart disease

artículo científico publicado en 2014

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 Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

artículo científico publicado en 2010

Meta-analysis of exome array data identifies six novel genetic loci for lung function

scientific article published on 12 January 2018

Meta-analysis of exome array data identifies six novel genetic loci for lung function

Meta-analysis of the INSIG2 association with obesity including 74,345 individuals: does heterogeneity of estimates relate to study design?

artículo científico publicado en 2009

Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline

artículo científico publicado en 2020

Multi-omics subtyping pipeline for chronic obstructive pulmonary disease

artículo científico publicado en 2021

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

artículo científico publicado en 2018

Multiethnic Meta-analysis Identifies New Loci for Pulmonary Function

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

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

artículo científico publicado en 2022

Novel genetic risk factors influence progression of islet autoimmunity to type 1 diabetes

artículo científico publicado en 2020

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

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

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

artículo científico publicado en 2016

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

article

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

scientific article published on 29 October 2019

Physical Function and Its Response to Exercise: Associations With Cytokine Gene Variation in Older Adults With Knee Osteoarthritis

article

Plasma Levels of Soluble Interleukin-2 Receptor α: Associations With Clinical Cardiovascular Events and Genome-Wide Association Scan

artículo científico publicado en 2015

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

Polymorphisms in the ICAM1 gene predict circulating soluble intercellular adhesion molecule-1(sICAM-1).

artículo científico publicado en 2011

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

artículo científico publicado en 2008

Polymorphisms of the IL1-receptor antagonist gene (IL1RN) are associated with multiple markers of systemic inflammation

artículo científico publicado en 2008

Population-specific coding variant underlies genome-wide association with adiponectin level

artículo científico publicado en 2011

Promoter polymorphisms in the nitric oxide synthase 3 gene are associated with ischemic stroke susceptibility in young black women

artículo científico publicado en 2005

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

artículo científico publicado en 2019

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

artículo científico publicado en 2019

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

artículo científico publicado en 2018

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

artículo científico publicado en 2018

Rare and Coding Region Genetic Variants Associated With Risk of Ischemic Stroke: The NHLBI Exome Sequence Project

artículo científico publicado en 2015

Rare and low-frequency coding variants alter human adult height

artículo científico publicado en 2017

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

artículo científico publicado en 2015

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

Recent developments in genome and exome-wide analyses of plasma lipids

artículo científico publicado en 2015

Refining The Accuracy Of Validated Target Identification Through Coding Variant Fine-Mapping In Type 2 Diabetes

article

Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes.

artículo científico publicado en 2018

Regulatory polymorphisms in human DBH affect peripheral gene expression and sympathetic activity

artículo científico publicado en 2014

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 Androgens and Risk of Atrial Fibrillation in Older Men: The Cardiovascular Health Study.

artículo científico publicado en 2018

Single-nucleotide polymorphisms at five loci are associated with C-reactive protein levels in a cohort of Filipino young adults

artículo científico publicado en 2011

Skin-blanching is associated with FEV(1), allergy, age and gender in asthma families

artículo científico publicado en 2012

Soluble CD14: genomewide association analysis and relationship to cardiovascular risk and mortality in older adults

artículo científico publicado en 2012

Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels

artículo científico publicado en 2019

Testing genetic association with rare variants in admixed populations

artículo científico publicado en 2012

The Polygenic and Monogenic Basis of Blood Traits and Diseases

artículo científico publicado en 2020

The impact of pedigree structure on heritability estimates for pulse pressure in three studies

scientific article published on 08 September 2005

The interleukin-6 receptor as a target for prevention of coronary heart disease: a mendelian randomisation analysis

artículo científico publicado en 2012

The paternal gene of the DDK syndrome maps to the Schlafen gene cluster on mouse chromosome 11.

artículo científico publicado en 2005

The relationship between C-reactive protein and subclinical cardiovascular disease in the Diabetes Heart Study (DHS).

artículo científico publicado en 2005

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

Two-locus genome-wide linkage scan for prostate cancer susceptibility genes with an interaction effect

article

Type 2 Diabetes Genetic Risk Scores Are Associated With Increased Type 2 Diabetes Risk Among African Americans by Cardiometabolic Status

artículo científico publicado en 2018

Ultraconserved elements in the human genome: association and transmission analyses of highly constrained single-nucleotide polymorphisms

artículo científico publicado en 2012

Variant Near FGF5 Has Stronger Effects on Blood Pressure in Chinese With a Higher Body Mass Index

artículo científico publicado en 2015

Variants Associated with the Ankle Brachial Index Differ by Hispanic/Latino Ethnic Group: a genome-wide association study in the Hispanic Community Health Study/Study of Latinos

artículo científico publicado en 2019

Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight

artículo científico publicado en 2010

West African ancestry and nocturnal blood pressure in African Americans: the Jackson Heart Study.

artículo científico publicado en 2018

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 sequence association with E-selectin levels reveals Loss-of-function variant in African Americans

artículo científico publicado en 2019

Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis

artículo científico publicado en 2016

Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis

article

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

beta1- and beta2-adrenergic receptor gene variation, beta-blocker use and risk of myocardial infarction and stroke

scientific article published on 24 January 2008

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