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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 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 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 IVGTT-Based Measures of First-Phase Insulin Secretion Refines the Underlying Physiology of Type 2 Diabetes Variants

artículo científico publicado en 2017

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 Multinomial Ordinal Probit Model with Singular Value Decomposition Method for a Multinomial Trait

artículo científico publicado en 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 catalog of genetic loci associated with kidney function from analyses of a million individuals

scientific article published on 31 May 2019

A favorable cardiometabolic profile is associated with the G allele of the genetic variant rs5068 in African Americans: The Multi-Ethnic Study of Atherosclerosis (MESA).

artículo científico publicado en 2017

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 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 genetic loci associated with specific lobar brain volumes

scientific article published on 02 August 2019

A genome-wide association study identifies new loci for factor VII and implicates factor VII in ischemic stroke etiology

scientific article published on 14 January 2019

A genome-wide association study of carotid atherosclerosis in HIV-infected men

artículo científico publicado en 2010

A genome-wide association study of central corneal thickness in Latinos

artículo científico publicado en 2013

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

artículo científico publicado en 2021

A large-scale exome array analysis of venous thromboembolism

artículo científico publicado en 2019

A locus for spondylocarpotarsal synostosis syndrome at chromosome 3p14.

artículo científico publicado en 2004

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

artículo científico publicado en 2015

A meta-analysis of four genome-wide association studies of survival to age 90 years or older: the Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium

artículo científico publicado en 2010

A meta-analysis of genome-wide association studies identifies multiple longevity genes

scientific article published on 14 August 2019

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 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 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

Actionable exomic incidental findings in 6503 participants: challenges of variant classification

artículo científico publicado en 2015

Admixture mapping identifies novel loci for obstructive sleep apnea in hispanic/latino americans

scientific article published on 01 February 2019

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

Allele-specific expression changes dynamically during T cell activation in HLA and other autoimmune loci

artículo científico publicado en 2020

Amino acid position 37 of HLA-DRβ1 affects susceptibility to Crohn's disease in Asians

article

An Islet-Targeted Genome-Wide Association Scan Identifies Novel Genes Implicated in Cytokine-Mediated Islet Stress in Type 2 Diabetes

artículo científico publicado en 2015

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

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

artículo científico publicado en 2018

Anti-flagellin (CBir1) phenotypic and genetic Crohn's disease associations.

artículo científico publicado en 2007

Appendectomy does not decrease the risk of future colectomy in UC: results from a large cohort and meta-analysis

artículo científico publicado en 2016

Assessment of reliability and validity of IBD phenotyping within the National Institutes of Diabetes and Digestive and Kidney Diseases (NIDDK) IBD Genetics Consortium (IBDGC)

article

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

article published in 2019

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 angiotensinogen, angiotensin II receptor genes, and blood pressure response to an angiotensin-converting enzyme inhibitor

artículo científico publicado en 2007

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 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 androgen receptor CAG repeat polymorphism and polycystic ovary syndrome

artículo científico publicado en 2008

Association of antibody responses to microbial antigens and complications of small bowel Crohn's disease

artículo científico publicado en 2004

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 novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts

scientific article published on April 2009

Association of 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 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 of Mitochondrial and Nuclear Mitochondrial Variants and Genes with Seven Metabolic Traits

article

Associations of SNPs in ADIPOQ and subclinical cardiovascular disease in the multi-ethnic study of atherosclerosis (MESA).

artículo científico publicado en 2010

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 ⬇️

artículo científico publicado en 2013

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: Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function ⬇️

scientific article published on 01 May 2019

Best practices and joint calling of the HumanExome BeadChip: the CHARGE Consortium

artículo científico publicado en 2013

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

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

Carotid intima-media thickness (cIMT) cosegregates with blood pressure and renal function in hypertensive Hispanic families

artículo científico publicado en 2007

Cerivastatin, genetic variants, and the risk of rhabdomyolysis

artículo científico publicado en 2011

Characterization of genetic loci that affect susceptibility to inflammatory bowel diseases in African Americans

artículo científico publicado en 2015

Classification of Type 2 Diabetes Genetic Variants and a Novel Genetic Risk Score Association With Insulin Clearance

artículo científico publicado en 2020

Combination of innate and adaptive immune alterations increased the likelihood of fibrostenosis in Crohn's disease

artículo científico publicado en 2010

Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR Interval

Common variants at five new loci associated with early-onset inflammatory bowel disease

artículo científico publicado en 2009

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

Concept, design and implementation of a cardiovascular gene-centric 50 k SNP array for large-scale genomic association studies

artículo científico publicado en 2008

Contribution of higher risk genes and European admixture to Crohn's disease in African Americans

scientific article published on 12 March 2012

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

Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses

artículo científico publicado en 2016

Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases.

artículo científico publicado en 2018

Deleterious Effect of Butyrylcholinesterase K-Variant in Donepezil Treatment of Mild Cognitive Impairment

artículo científico publicado en 2016

Deletion polymorphism upstream of IRGM associated with altered IRGM expression and Crohn's disease

artículo científico publicado en 2008

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

Differences in First-Trimester Maternal Metabolomic Profiles in Pregnancies Conceived From Fertility Treatments

scientific article published on 01 April 2019

Directional dominance on stature and cognition in diverse human populations

artículo científico publicado en 2015

Discovery of Genetic Variation on Chromosome 5q22 Associated with Mortality in Heart Failure

artículo científico publicado en 2016

Discovery of novel heart rate-associated loci using the Exome Chip

artículo científico publicado en 2017

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

artículo científico publicado en 2020

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

artículo científico publicado en 2015

Effects of Calcium, Magnesium, and Potassium Concentrations on Ventricular Repolarization in Unselected Individuals

artículo científico publicado en 2019

Empirical characteristics of family-based linkage to a complex trait: the ADIPOQ region and adiponectin levels

artículo científico publicado en 2014

Epigenetic Signatures of Cigarette Smoking

artículo científico publicado en 2016

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: Genetic variants associated with subjective well-being, depressive symptoms and neuroticism identified through genome-wide analyses

article

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-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.

artículo científico publicado en 2017

Ethnic, Geographic, and Genetic Differences in Arsenic Metabolism at Low Arsenic Exposure: A Preliminary Analysis in the Multi-Ethnic Study of Atherosclerosis (MESA)

artículo científico publicado en 2018

Evaluation of mitochondrial DNA copy number estimation techniques

scientific article published on 31 January 2020

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-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology

artículo científico publicado en 2019

Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology

scientific article published on 01 September 2019

Exome-wide association study of plasma lipids in >300,000 individuals

artículo científico publicado en 2017

ExomeChip-Wide Analysis of 95 626 Individuals Identifies 10 Novel Loci Associated With QT and JT Intervals

FEM1A and FEM1B: novel candidate genes for polycystic ovary syndrome

artículo científico publicado en 2008

Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms

artículo científico publicado en 2017

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 type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

artículo científico publicado en 2018

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

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 and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes

artículo científico publicado en 2018

GWAS of QRS duration identifies new loci specific to Hispanic/Latino populations

artículo científico publicado en 2019

GWAS of the electrocardiographic QT interval in Hispanics/Latinos generalizes previously identified loci and identifies population-specific signals

artículo científico publicado en 2017

Gene responsible for mitochondrial myopathy and sideroblastic anemia (MSA) maps to chromosome 12q24.33

scientific article published on 01 May 2004

Gene-centric association mapping of chromosome 3p implicates MST1 in IBD pathogenesis

artículo científico publicado en 2008

Generalization and fine mapping of European ancestry-based central adiposity variants in African ancestry populations

artículo científico publicado en 2016

Genes linked to energy metabolism and immunoregulatory mechanisms are associated with subcutaneous adipose tissue distribution in HIV-infected men.

artículo científico publicado en 2011

Genetic Architecture of Primary Open Angle Glaucoma in Individuals of African Descent: The African Descent & Glaucoma Evaluation Study (ADAGES) III

article

Genetic Associations with Obstructive Sleep Apnea Traits in Hispanic/Latino Americans

artículo científico publicado en 2016

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

artículo científico publicado en 2017

Genetic Risk Prediction of Atrial Fibrillation

artículo científico publicado en 2016

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

scientific article published on 11 September 2020

Genetic 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 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 architecture of lipid traits in the Hispanic community health study/study of Latinos

artículo científico publicado en 2017

Genetic association of COL5A1 variants in keratoconus patients suggests a complex connection between corneal thinning and keratoconus

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 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 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 nonobstructive coronary artery disease in Caucasian women

artículo científico publicado en 2015

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 predictors of medically refractory ulcerative colitis

scientific journal article

Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses

artículo científico publicado en 2016

Genetic variants in the region harbouring IL2/IL21 associated with ulcerative colitis

artículo científico publicado en 2009

Genetic variants synthesize to produce paneth cell phenotypes that define subtypes of Crohn's disease.

artículo científico publicado en 2013

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 inflammatory bowel disease

article

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

artículo científico publicado en 2017

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 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 association analyses identify multiple loci associated with central corneal thickness and keratoconus

artículo científico publicado en 2013

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 defines more than 30 distinct susceptibility loci for Crohn's disease

artículo científico publicado en 2008

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 of pericardial fat identifies a unique locus for ectopic fat

artículo científico publicado en 2012

Genome-wide association of white blood cell counts in Hispanic/Latino Americans: the Hispanic Community Health Study/Study of Latinos

artículo científico publicado en 2017

Genome-wide association studies of cerebral white matter lesion burden: the CHARGE consortium

artículo científico publicado en 2011

Genome-wide association study and follow-up analysis of adiposity traits in Hispanic Americans: the IRAS Family Study

artículo científico publicado en 2009

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 circulating levels of PAI-1 provides novel insights into its regulation

artículo científico publicado en 2012

Genome-wide association study for circulating tissue plasminogen activator levels and functional follow-up implicates endothelial STXBP5 and STX2.

artículo científico publicado en 2014

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

artículo científico publicado en 2011

Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease

artículo científico publicado en 2010

Genome-wide association study identifying novel variant for fasting insulin and allelic heterogeneity in known glycemic loci in Chilean adolescents: The Santiago Longitudinal Study

scientific article published on 30 December 2020

Genome-wide association study in a Chinese population with diabetic retinopathy

artículo científico publicado en 2013

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 dental caries in the Hispanic Communities Health Study/Study of Latinos (HCHS/SOL)

artículo científico publicado en 2015

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

artículo científico publicado en 2017

Genome-wide association study of heavy smoking and daily/nondaily smoking in the Hispanic Community Health Study / Study of Latinos (HCHS/SOL).

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 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: which do you want first: the good news, the bad news, or the good news?

artículo científico publicado en 2007

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 linkage and association analysis of cardiometabolic phenotypes in Hispanic Americans

artículo científico publicado en 2016

Genome-wide linkage scans for type 2 diabetes mellitus in four ethnically diverse populations-significant evidence for linkage on chromosome 4q in African Americans: the Family Investigation of Nephropathy and Diabetes Research Group

artículo científico publicado en 2009

Genome-wide meta-analyses of smoking behaviors in African Americans

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 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits.

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 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 scan for estimated glomerular filtration rate in multi-ethnic diabetic populations: the Family Investigation of Nephropathy and Diabetes (FIND).

artículo científico publicado en 2007

Genome-wide scans for diabetic nephropathy and albuminuria in multiethnic populations: the family investigation of nephropathy and diabetes (FIND).

artículo científico publicado en 2007

Genomewide association studies of stroke

artículo científico publicado en 2009

Genomewide linkage scan in a multigeneration Caucasian pedigree identifies a novel locus for keratoconus on chromosome 5q14.3-q21.1.

artículo científico publicado en 2005

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

artículo científico publicado en 2019

Genotype Imputation for Latinos Using the HapMap and 1000 Genomes Project Reference Panels

artículo científico publicado en 2012

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

High-frequency haplotypes in the X chromosome locus TLR8 are associated with both CD and UC in females

scientific article published on March 2009

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

Hypertension genes are genetic markers for insulin sensitivity and resistance

artículo científico publicado en 2005

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 of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease

artículo científico publicado en 2017

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 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

Increased immune reactivity predicts aggressive complicating Crohn's disease in children

artículo científico publicado en 2008

Individual and Combined Associations of Genetic Variants in CYP3A4, CYP3A5, and SLCO1B1 With Simvastatin and Simvastatin Acid Plasma Concentrations

artículo científico publicado en 2015

Inflammatory bowel disease. I. Genetic epidemiology

artículo científico publicado en 2001

Inflammatory bowel disease. II. Gene mapping

artículo científico publicado en 2001

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: confirmation as a highly heritable trait, and genome-wide linkage analysis

artículo científico publicado en 2012

Interactions between commensal fungi and the C-type lectin receptor Dectin-1 influence colitis

artículo científico publicado en 2012

Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated Diseases

artículo científico publicado en 2016

Large-Scale Genomic Analyses Link Reproductive Aging to Hypothalamic Signaling, Breast Cancer Susceptibility, and BRCA1-Mediated DNA Repair

artículo científico publicado en 2015

Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.

artículo científico publicado en 2017

Large-scale gene-centric analysis identifies polymorphisms for resistant hypertension.

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

Linkage Analysis of High-density SNPs Confirms Keratoconus Locus at 5q Chromosomal Region

artículo científico publicado en 2014

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

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

Long-range LD can confound genome scans in admixed populations

artículo científico publicado en 2008

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

artículo científico publicado en 2015

Lymphocyte activation gene 3 and coronary artery disease

artículo científico publicado en 2016

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

MAST3: a novel IBD risk factor that modulates TLR4 signaling

artículo científico publicado en 2008

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

artículo científico publicado en 2019

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

artículo científico publicado en 2015

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 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 East Asian-ancestry populations identifies four new loci for body mass index

artículo científico publicado en 2014

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 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

Mitochondrial DNA copy number can influence mortality and cardiovascular disease via methylation of nuclear DNA CpGs

artículo científico publicado en 2020

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

article

Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration

artículo científico publicado en 2019

Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity

artículo científico publicado en 2019

Multi-ethnic Genome-wide Association Study 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 genome-wide association study for atrial fibrillation

article

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

artículo científico publicado en 2018

Multidimensional prognostic risk assessment identifies association between IL12B variation and surgery in Crohn's disease

artículo científico publicado en 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 meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function

scientific article published in Nature Communications

Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease

artículo científico publicado en 2013

Multiple loci are associated with white blood cell phenotypes

artículo científico publicado en 2011

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

Native American ancestry is associated with severe diabetic retinopathy in Latinos.

artículo científico publicado en 2014

New gene functions in megakaryopoiesis and platelet formation

artículo científico publicado en 2011

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 evidence for genome-wide interactions on plasma fibrinogen by smoking, alcohol consumption and body mass index: results from meta-analyses of 80,607 subjects

artículo científico publicado en 2014

Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney

artículo científico publicado en 2017

Novel Genetic Loci Associated With Retinal Microvascular Diameter

artículo científico publicado en 2015

Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries.

artículo científico publicado en 2018

Novel genetic markers associate with atrial fibrillation risk in Europeans and Japanese

artículo científico publicado en 2014

Novel loci associated with increased risk of sudden cardiac death in the context of coronary artery disease

artículo científico publicado en 2013

OR15-6 Epigenetic Differences in First Trimester Pregnancies Conceived with Infertility.

artículo científico publicado en 2019

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

article

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

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

Predicting stroke through genetic risk functions: the CHARGE Risk Score Project

artículo científico publicado en 2014

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

artículo científico publicado en 2017

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

article

Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

scholarly article published in Nature Genetics

Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

erratum

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

artículo científico publicado en 2019

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

artículo científico publicado en 2019

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

artículo científico publicado en 2018

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

artículo científico publicado en 2018

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

RGS6 Variants Are Associated With Dietary Fat Intake in Hispanics: The IRAS Family Study ⬇️

artículo científico publicado el 13 de enero de 2011

Rare Genetic Variants Associated With Sudden Cardiac Death in Adults

scientific article published on 11 November 2019

Rare Non-coding Variation Identified by Large Scale Whole Genome Sequencing Reveals Unexplained Heritability of Type 2 Diabetes

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

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

Relationship between proximal Crohn's disease location and disease behavior and surgery: a cross-sectional study of the IBD Genetics Consortium

artículo científico publicado en 2012

Replication of association of a novel insulin receptor gene polymorphism with polycystic ovary syndrome

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

SORCS1: a novel human type 2 diabetes susceptibility gene suggested by the mouse

artículo científico publicado en 2007

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

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

artículo científico publicado en 2019

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

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 ⬇️

artículo científico publicado en 2018

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

artículo científico publicado en 2013

Systems Genetics Reveals the Functional Context of PCOS Loci and Identifies Genetic and Molecular Mechanisms of Disease Heterogeneity

artículo científico publicado en 2015

TNFRSF1B Is Associated with ANCA in IBD.

artículo científico publicado en 2016

TNFSF15 is an ethnic-specific IBD gene

artículo científico publicado en 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 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 HMG-CoA reductase gene and lipid and lipoprotein levels: the multi-ethnic study of atherosclerosis

artículo científico publicado en 2009

The IBD International Genetics Consortium Provides Further Evidence for Linkage to IBD4 and Shows Gene-Environment Interaction

article

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 retinopathy of prematurity: a model for neovascular retinal disease

article

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

The uncoupling protein 1 gene, UCP1, is expressed in mammalian islet cells and associated with acute insulin response to glucose in African American families from the IRAS Family Study

artículo científico publicado en 2007

Trans-ethnic Meta-analysis and Functional Annotation Illuminates the Genetic Architecture of Fasting Glucose and Insulin

artículo científico publicado en 2016

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 kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies

artículo científico publicado en 2019

Trans-ethnic meta-analysis identifies common and rare variants associated with hepatocyte growth factor levels in the Multi-Ethnic Study of Atherosclerosis (MESA).

artículo científico publicado en 2015

Two-stage genome-wide linkage scan in keratoconus sib pair families

artículo científico publicado en 2006

Type 2 Diabetes Modifies the Association of CAD Genomic Risk Variants With Subclinical Atherosclerosis

artículo científico publicado en 2023

Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study

artículo científico publicado en 2009

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 ZNF365 isoform D are associated with Crohn's disease ⬇️

artículo científico publicado el 21 de enero de 2011

Variants in the HMG-CoA reductase (HMGCR) gene influence component phenotypes in polycystic ovary syndrome

artículo científico publicado en 2009

Variants of the caveolin-1 gene: a translational investigation linking insulin resistance and hypertension

artículo científico publicado en 2011

Variation in PPARG is associated with longitudinal change in insulin resistance in Mexican Americans at risk for type 2 diabetes

artículo científico publicado en 2015

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

White Matter Lesion Progression: Genome-Wide Search for Genetic Influences

artículo científico publicado en 2015

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

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 ⬇️

artículo

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