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Lista de obras de Alanna Morrison

73-OR: Clonal Hematopoiesis of Indeterminate Potential (CHIP), Glycemic Traits, and Type 2 Diabetes (T2D) Risk

artículo científico publicado en 2021

A Genome-wide Association Study Discovers 46 Loci of the Human Metabolome in the Hispanic Community Health Study/Study of Latinos

artículo científico publicado en 2020

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 Mendelian randomization of γ' and total fibrinogen levels on venous thromboembolism and ischemic stroke

artículo científico publicado en 2020

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

artículo científico publicado en 2015

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 large-scale transcriptome-wide association study (TWAS) of ten blood cell phenotypes reveals complexities of TWAS fine-mapping

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

artículo científico publicado en 2015

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 whole-genome scan for stroke or myocardial infarction in family blood pressure program families

artículo científico publicado en 2008

ACAT: A Fast and Powerful p Value Combination Method for Rare-Variant Analysis in Sequencing Studies

artículo científico publicado en 2019

ADAM19 and HTR4 variants and pulmonary function: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study

artículo científico publicado en 2014

ADD1 460W Allele Associated With Cardiovascular Disease in Hypertensive Individuals

artículo científico publicado en 2002

Allelic variations in angiogenic pathway genes are associated with preeclampsia.

artículo científico publicado en 2010

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

Analysis commons, a team approach to discovery in a big-data environment for genetic epidemiology

artículo científico publicado en 2017

Analysis of loss-of-function variants and 20 risk factor phenotypes in 8,554 individuals identifies loci influencing chronic disease

artículo científico publicado en 2015

Aptamer-Based Proteomic Platform Identifies Novel Protein Predictors of Incident Heart Failure and Echocardiographic Traits

artículo científico publicado en 2020

Association Between SLC20A1 and Sodium-Lithium Countertransport

artículo científico publicado en 2011

Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study ⬇️

artículo científico publicado en 2017

Association between NEDD4L gene and sodium lithium countertransport

artículo científico publicado en 2010

Association of NOS3 Glu298Asp SNP with hypertension and possible effect modification of dietary fat intake in the ARIC study

artículo científico publicado en 2009

Association of Rare Loss-Of-Function Alleles in HAL, Serum Histidine: Levels and Incident Coronary Heart Disease

artículo científico publicado en 2015

Association of SERPINA9 gene variants with carotid artery atherosclerosis: the Atherosclerosis Risk in Communities (ARIC) Carotid MRI Study

artículo científico publicado en 2013

Association of SLC34A2 variation and sodium-lithium countertransport activity in humans and baboons

artículo científico publicado en 2009

Association of Variants with Blood Pressure in the Atherosclerosis Risk in Communities Study

Association of copper-zinc superoxide dismutase (SOD1) and manganese superoxide dismutase (SOD2) genes with nonsyndromic myelomeningocele

artículo científico publicado en 2012

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

artículo científico publicado en 2014

Association of folate receptor (FOLR1, FOLR2, FOLR3) and reduced folate carrier (SLC19A1) genes with meningomyelocele

artículo científico publicado en 2010

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 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 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-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 retinoic acid receptor genes with meningomyelocele

artículo científico publicado en 2010

Association of the IGF1 gene with fasting insulin levels

artículo científico publicado en 2016

Associations of autozygosity with a broad range of human phenotypes

scientific article published on 31 October 2019

Author Correction: GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk.

artículo científico publicado en 2018

Burden of rare deleterious variants in WNT signaling genes among 511 myelomeningocele patients

scientific article published on 24 September 2020

CD163+ macrophages promote angiogenesis and vascular permeability accompanied by inflammation in atherosclerosis

artículo científico publicado en 2018

Causal Role of Alcohol Consumption in an Improved Lipid Profile: The Atherosclerosis Risk in Communities (ARIC) Study

artículo científico publicado en 2016

Characteristics of a spina bifida population including North American Caucasian and Hispanic individuals

artículo científico publicado en 2008

Chromosome 9p21 single nucleotide polymorphisms are not associated with recurrent myocardial infarction in patients with established coronary artery disease

scientific article published on 09 February 2012

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

artículo científico publicado en 2021

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

Common Coding Variants in Are Associated With the Nav1.8 Late Current and Cardiac Conduction

artículo científico publicado en 2018

Common and rare von Willebrand factor (VWF) coding variants, VWF levels, and factor VIII levels in African Americans: the NHLBI Exome Sequencing Project

artículo científico publicado en 2013

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

artículo científico publicado en 2017

Comprehensive linkage and linkage heterogeneity analysis of 4344 sibling pairs affected with hypertension from the Family Blood Pressure Program.

artículo científico publicado en 2007

Contributions of rare coding variants in hypotension syndrome genes to population blood pressure variation

article

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

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

artículo científico publicado en 2015

Cystatin C and Cardiovascular Disease: A Mendelian Randomization Study

artículo científico publicado en 2016

DNA Methylation Analysis Identifies Loci for Blood Pressure Regulation

artículo científico publicado en 2017

DNA methylation age is associated with an altered hemostatic profile in a multi-ethnic meta-analysis

article

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

artículo científico publicado en 2020

Diabetes genes and prostate cancer in the Atherosclerosis Risk in Communities study

artículo científico publicado en 2010

Diagnostic Yield and Clinical Utility of Sequencing Familial Hypercholesterolemia Genes in Patients With Severe Hypercholesterolemia

artículo científico publicado en 2016

Direct Estimates of the Genomic Contributions to Blood Pressure Heritability within a Population-Based Cohort (ARIC).

artículo científico publicado en 2015

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

artículo científico publicado en 2020

Duffy antigen receptor for chemokines (Darc) polymorphism regulates circulating concentrations of monocyte chemoattractant protein-1 and other inflammatory mediators

artículo científico publicado en 2009

Dynamic Scan Procedure for Detecting Rare-Variant Association Regions in Whole-Genome Sequencing Studies

artículo científico publicado en 2019

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

ESR1 polymorphism is associated with plasma lipid and apolipoprotein levels in Caucasians of the Rochester Family Heart Study

artículo científico publicado en 2008

Effects of Gender-Specific Differences, Inflammatory Response, and Genetic Variation on the Associations Among Depressive Symptoms and the Risk of Major Adverse Coronary Events in Patients With Acute Coronary Syndrome

artículo científico publicado en 2018

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

artículo científico publicado en 2014

Effects of rare and common blood pressure gene variants on essential hypertension: results from the Family Blood Pressure Program, CLUE, and Atherosclerosis Risk in Communities studies

artículo científico publicado en 2012

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

Efficient gene-environment interaction tests for large biobank-scale sequencing studies

scientific article published on 30 August 2020

Evaluating the Context-Dependent Effect of Family History of Stroke in a Genome Scan for Hypertension

scientific article published on 24 April 2003

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

artículo científico publicado en 2017

FastSKAT: Sequence kernel association tests for very large sets of markers

artículo científico publicado en 2018

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

artículo científico publicado en 2015

Five common gene variants identify elevated genetic risk for coronary heart disease

artículo científico publicado en 2007

Folate metabolism gene 5,10-methylenetetrahydrofolate reductase (MTHFR) is associated with ADHD in myelomeningocele patients

artículo científico publicado en 2012

Functionally oriented analysis of cardiometabolic traits in a trans-ethnic sample

artículo científico publicado en 2019

GOSR2 Lys67Arg is associated with hypertension in whites

artículo científico publicado en 2008

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

artículo científico publicado en 2018

GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk.

artículo científico publicado en 2017

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-by-Psychosocial Factor Interactions Influence Diastolic Blood Pressure in European and African Ancestry Populations: Meta-Analysis of Four Cohort Studies

artículo científico publicado en 2017

Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci

scientific article published on 05 May 2020

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

scientific article published on 17 September 2018

Genetic analysis of over one million people identifies 535 novel loci for blood pressure

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

artículo científico publicado en 2017

Genetic association of the glycine cleavage system genes and myelomeningocele.

artículo científico publicado en 2016

Genetic association study of putative functional single nucleotide polymorphisms of genes in folate metabolism and spina bifida

scientific article published on 15 August 2009

Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function

artículo científico publicado en 2016

Genetic determinants influencing human serum metabolome among African Americans

artículo científico publicado en 2014

Genetic loci associated with ideal cardiovascular health: A meta-analysis of genome-wide association studies

artículo científico publicado en 2016

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 variants in microRNA genes and targets associated with cardiovascular disease risk factors in the African-American population

artículo científico publicado en 2017

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

artículo científico publicado en 2011

Genetic variation in solute carrier genes is associated with preeclampsia.

artículo científico publicado en 2010

Gene–environment interaction and the GNB3 gene in the Atherosclerosis Risk in Communities Study

article

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 hypertension in nonobese African Americans: the National Heart, Lung, and Blood Institute Family Blood Pressure Program

artículo científico publicado en 2004

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 Serum Fructosamine and Glycated Albumin in Adults Without Diagnosed Diabetes: Results From the Atherosclerosis Risk in Communities Study

article published in 2018

Genome-Wide Association Transethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels

Genome-Wide Linkage Study of Erythrocyte Sodium-Lithium Countertransport

artículo científico publicado en 2005

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 studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction

artículo científico publicado en 2012

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

artículo científico publicado en 2011

Genome-wide association study of 1,5-anhydroglucitol identifies novel genetic loci linked to glucose metabolism

artículo científico publicado en 2017

Genome-wide association study of blood pressure and hypertension

scientific journal article

Genome-wide association study of cardiac structure and systolic function in African Americans: the Candidate Gene Association Resource (CARe) study

artículo científico publicado en 2013

Genome-wide association study of gene by smoking interactions in coronary artery calcification

artículo científico publicado en 2013

Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function

artículo científico publicado en 2012

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

Hypertension Susceptibility Loci are Associated with Anthracycline-related Cardiotoxicity in Long-term Childhood Cancer Survivors

artículo científico publicado en 2017

Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders

artículo científico publicado en 2013

Identification of novel candidate risk genes for myelomeningocele within the glucose homeostasis/oxidative stress and folate/one-carbon metabolism networks

scientific article published on 22 September 2020

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

artículo científico publicado en 2020

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

Inactivating mutations in NPC1L1 and protection from coronary heart disease

artículo científico publicado en 2014

Inherited coding variants at the CDKN2A locus influence susceptibility to acute lymphoblastic leukaemia in children

artículo científico publicado en 2015

Integrative pathway genomics of lung function and airflow obstruction

artículo científico publicado en 2015

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

LPL polymorphism predicts stroke risk in men

artículo científico publicado en 2002

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 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 ⬇️

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 whole-exome sequencing association studies identify rare functional variants influencing serum urate levels

artículo científico publicado en 2018

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

Loss-of-function variants influence the human serum metabolome

scientific article published on 31 August 2016

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

artículo científico publicado en 2015

Maternal gene-micronutrient interactions related to one-carbon metabolism and the risk of myelomeningocele among offspring.

artículo científico publicado en 2017

Maternal hypertension and risk for hypospadias in offspring

artículo científico publicado en 2016

Maternal hypertension-related genotypes and congenital heart defects

artículo científico publicado en 2020

Matrix metalloproteinase-1 and tissue inhibitors do not predict incident coronary artery disease in the atherosclerosis risk in communities (ARIC) study

artículo científico publicado en 2008

Mendelian Randomization Analysis of Hemostatic Factors and Their Contribution to Peripheral Artery Disease

scientific article published on 27 August 2020

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

artículo científico publicado en 2019

Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function

artículo científico publicado en 2010

Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci

artículo científico publicado en 2016

Meta-analysis 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 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

Metabolomic Pattern Predicts Incident Coronary Heart Disease

scientific article published on 16 May 2019

Metabolomics Identifies Novel Blood Biomarkers of Pulmonary Function and COPD in the General Population.

artículo científico publicado en 2019

Mining gold dust under the genome wide significance level: a two-stage approach to analysis of GWAS.

artículo científico publicado en 2010

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

Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk

Multi-ancestry genome-wide association study accounting for gene-psychosocial factor interactions identifies novel loci for blood pressure traits

artículo científico publicado en 2021

Multi-ancestry genome-wide 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

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

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

artículo científico publicado en 2022

Mutations in folate transporter genes and risk for human myelomeningocele

article

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

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

artículo científico publicado en 2018

Parental History of Stroke Predicts Subclinical But Not Clinical Stroke

scientific article published on 01 September 2000

Pharmacogenomics of statin-related myopathy: Meta-analysis of rare variants from whole-exome sequencing

artículo científico publicado en 2019

Plasma MCP-1 level and risk for peripheral arterial disease and incident coronary heart disease: Atherosclerosis Risk in Communities study

scientific article published on 14 April 2005

Pleiotropic genes for metabolic syndrome and inflammation

artículo científico publicado en 2014

Population genomic analysis of 962 whole genome sequences of humans reveals natural selection in non-coding regions.

artículo científico publicado en 2015

Practical Approaches for Whole-Genome Sequence Analysis of Heart- and Blood-Related Traits

artículo científico publicado en 2017

Prediction of Coronary Heart Disease Risk using a Genetic Risk Score: The Atherosclerosis Risk in Communities Study

article

Prospective Study of Epigenetic Age Acceleration and Incidence of Cardiovascular Disease Outcomes in the ARIC Study (Atherosclerosis Risk in Communities)

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

RNA sequence analysis of inducible pluripotent stem cell-derived cardiomyocytes reveals altered expression of DNA damage and cell cycle genes in response to doxorubicin

scientific article published on 19 July 2018

Rare Exome Sequence Variants in CLCN6 Reduce Blood Pressure Levels and Hypertension Risk

artículo científico publicado en 2015

Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWF

artículo científico publicado en 2015

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

artículo científico publicado en 2015

Rare coding variants associated with blood pressure variation in 15 914 individuals of African ancestry

artículo científico publicado en 2017

Rare, low frequency and common coding variants in CHRNA5 and their contribution to nicotine dependence in European and African Americans

artículo científico publicado en 2016

Regional association-based fine-mapping for sodium-lithium countertransport on chromosome 10.

artículo científico publicado en 2008

Replication of the Wellcome Trust genome-wide association study of essential hypertension: the Family Blood Pressure Program

artículo científico publicado en 2008

Reply to 'Misestimation of heritability and prediction accuracy of male-pattern baldness'.

artículo científico publicado en 2018

Resequencing and clinical associations of the 9p21.3 region: a comprehensive investigation in the Framingham heart study

artículo científico publicado en 2013

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

artículo científico publicado en 2020

Secondary findings and carrier test frequencies in a large multiethnic sample

artículo científico publicado en 2015

Sequence analysis of six blood pressure candidate regions in 4,178 individuals: the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) targeted sequencing study

artículo científico publicado en 2014

Sequence variation in TMEM18 in association with body mass index: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study

artículo científico publicado en 2014

Sequence-Based Analysis of Lipid-Related Metabolites in a Multiethnic Study.

artículo científico publicado en 2018

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

Single nucleotide polymorphisms associated with coronary heart disease predict incident ischemic stroke in the atherosclerosis risk in communities study

artículo científico publicado en 2008

Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations.

artículo científico publicado en 2017

Sodium intake and cardiovascular disease

artículo científico publicado en 2011

Strategies to design and analyze targeted sequencing data: cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study

artículo científico publicado en 2014

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

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

artículo científico publicado en 2016

The impact of data quality on the identification of complex disease genes: experience from the Family Blood Pressure Program

artículo científico publicado en 2006

The impact of multiple single day blood pressure readings on cardiovascular risk estimation: The Atherosclerosis Risk in Communities study

artículo científico publicado en 2016

The power of genetic diversity in genome-wide association studies of lipids

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

artículo científico publicado en 2023

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

Use of wrapper algorithms coupled with a random forests classifier for variable selection in large-scale genomic association studies

artículo científico publicado en 2009

Variants for HDL-C, LDL-C, and triglycerides identified from admixture mapping and fine-mapping analysis in African American families

artículo científico publicado en 2014

Variants in ANGPTL4 and the Risk of Coronary Artery Disease

artículo científico publicado en 2016

Variants in CXADR and F2RL1 are associated with blood pressure and obesity in African-Americans in regions identified through admixture mapping

artículo científico publicado en 2012

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 analysis of serum amino acid levels

artículo científico publicado en 2016

Whole-genome sequence-based analysis of high-density lipoprotein cholesterol

artículo científico publicado en 2013

Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program

Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program

artículo científico publicado en 2021

Whole-genome sequencing study of serum peptide levels: the Atherosclerosis Risk in Communities study

artículo científico publicado en 2017

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