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Lista de obras de Myriam Fornage

17q25 Locus is associated with white matter hyperintensity volume in ischemic stroke, but not with lacunar stroke status

artículo científico publicado en 2013

19th Workshop of the International Stroke Genetics Consortium, April 28-29, 2016, Boston, Massachusetts, USA: 2016.001 MRI-defined cerebrovascular genomics-The CHARGE consortium

artículo científico publicado en 2017

27-year time trends in dementia incidence in Europe and the US: the Alzheimer Cohorts Consortium

artículo científico publicado en 2020

A DNA methylation biomarker of alcohol consumption.

artículo científico publicado en 2016

A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure

artículo científico publicado en 2018

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

artículo científico publicado en 2020

A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation

artículo científico publicado en 2012

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 depressive symptoms

scientific journal article

A genotype risk score predicts type 2 diabetes from young adulthood: the CARDIA study

artículo científico publicado en 2012

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 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 phenomics-based strategy identifies loci on APOC1, BRAP, and PLCG1 associated with metabolic syndrome phenotype domains

artículo científico publicado en 2011

A prospective study of serum metabolites and risk of ischemic stroke

artículo científico publicado en 2019

A research framework for cognitive aging and Alzheimer's disease among diverse US Latinos: Design and implementation of the Hispanic Community Health Study/Study of Latinos-Investigation of Neurocognitive Aging (SOL-INCA)

artículo científico publicado en 2019

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

artículo científico publicado en 2008

APOE alleles' association with cognitive function differs across Hispanic/Latino groups and genetic ancestry in the study of Latinos-investigation of neurocognitive aging (HCHS/SOL)

scientific article published on 06 November 2020

APOL1 Genotype and Race Differences in Incident Albuminuria and Renal Function Decline

artículo científico publicado en 2015

APOL1 variants associate with increased risk of CKD among African Americans

artículo científico publicado en 2013

Ala54Thr polymorphism of the fatty acid binding protein 2 gene and saturated fat intake in relation to lipid levels and insulin resistance: the Coronary Artery Risk Development in Young Adults (CARDIA) study

artículo científico publicado en 2009

Allele frequency distribution of the (TG)n(AG)m microsatellite in the apolipoprotein C-II gene

article

Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility.

scientific article published on 09 April 2013

Altered soluble epoxide hydrolase gene expression and function and vascular disease risk in the stroke-prone spontaneously hypertensive rat.

artículo científico publicado en 2007

An Analysis of Two Genome-wide Association Meta-analyses Identifies a New Locus for Broad Depression Phenotype

artículo científico publicado en 2016

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

artículo científico publicado en 2016

An Epigenome-Wide Association Study (EWAS) of Obesity-Related Traits

Analysis of Whole-Exome Sequencing Data for Alzheimer Disease Stratified by APOE Genotype

scientific article published on 10 June 2019

Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics

scientific article published on 14 March 2020

Ankle brachial index and cognitive function among Hispanics/Latinos: Results from the Hispanic Community Health Study/Study of Latinos

artículo científico publicado en 2018

Apolipoprotein E genotypes among diverse middle-aged and older Latinos: Study of Latinos-Investigation of Neurocognitive Aging results (HCHS/SOL)

artículo científico publicado en 2018

Association among sickle cell trait, fitness, and cardiovascular risk factors in CARDIA.

artículo científico publicado en 2016

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

artículo científico publicado en 2014

Association between patterns of nucleotide variation across the three fibrinogen genes and plasma fibrinogen levels: the Coronary Artery Risk Development in Young Adults (CARDIA) study

artículo científico publicado en 2006

Association of 25-Hydroxyvitamin D status and genetic variation in the vitamin D metabolic pathway with FEV1 in the Framingham Heart Study

artículo científico publicado en 2015

Association of Alzheimer's disease GWAS loci with MRI markers of brain aging

artículo científico publicado en 2015

Association of Body Mass Index with DNA Methylation and Gene Expression in Blood Cells and Relations to Cardiometabolic Disease: A Mendelian Randomization Approach

artículo científico publicado en 2017

Association of CD14 with incident dementia and markers of brain aging and injury

scientific article published on 09 December 2019

Association of blood pressure with cognitive function at midlife: a Mendelian randomization study

scientific article published on 26 August 2020

Association of coagulation-related and inflammation-related genes and factor VIIc levels with stroke: the Cardiovascular Health Study

artículo científico publicado en 2011

Association of common genetic variants with brain microbleeds: A Genome-wide Association Study

scientific article published on 10 September 2020

Association of dietary folate and vitamin B-12 intake with genome-wide DNA methylation in blood: a large-scale epigenome-wide association analysis in 5841 individuals

scientific article published on 01 August 2019

Association of functional polymorphism rs2231142 (Q141K) in the ABCG2 gene with serum uric acid and gout in 4 US populations: the PAGE Study

artículo científico publicado en 2013

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 single-nucleotide polymorphisms from 17 candidate genes with baseline symptom-limited exercise test duration and decrease in duration over 20 years: the Coronary Artery Risk Development in Young Adults (CARDIA) fitness study

artículo científico publicado en 2010

Association of the V122I Transthyretin Amyloidosis Genetic Variant With Cardiac Structure and Function in Middle-aged Black Adults: Coronary Artery Risk Development in Young Adults (CARDIA) Study

artículo científico publicado en 2020

Association of variants in HTRA1 and NOTCH3 with MRI-defined extremes of cerebral small vessel disease in older subjects

Associations between incident ischemic stroke events and stroke and cardiovascular disease-related genome-wide association studies single nucleotide polymorphisms in the Population Architecture Using Genomics and Epidemiology study

artículo científico publicado en 2012

Associations of Brain Structure With Adiposity and Changes in Adiposity in a Middle-Aged and Older Biracial Population.

artículo científico publicado en 2016

Associations of NINJ2 sequence variants with incident ischemic stroke in the Cohorts for Heart and Aging in Genomic Epidemiology (CHARGE) consortium

artículo científico publicado en 2014

Associations of lipoprotein lipase gene polymorphisms with longitudinal plasma lipid trends in young adults: The Coronary Artery Risk Development in Young Adults (CARDIA) study

artículo científico publicado en 2010

Associations of plasma clusterin and Alzheimer's disease-related MRI markers in adults at mid-life: The CARDIA Brain MRI sub-study

artículo científico publicado en 2018

Author Correction: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

scientific article published on 01 September 2019

Basic concepts and potential applications of genetics and genomics for cardiovascular and stroke clinicians: a scientific statement from the American Heart Association

artículo científico publicado en 2015

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

artículo científico publicado en 2013

Biomarkers of Inflammation and MRI-Defined Small Vessel Disease of the Brain: The Cardiovascular Health Study

artículo científico publicado en 2008

Blood Leukocyte DNA Methylation Predicts Risk of Future Myocardial Infarction and Coronary Heart Disease

scientific article published on 19 August 2019

Blood Pressure and Hispanic/Latino Cognitive Function: Hispanic Community Health Study/Study of Latinos Results

artículo científico publicado en 2017

Blood methylomics in response to arsenic exposure in a low-exposed US population

artículo científico publicado en 2013

Brain Aging in African-Americans: The Atherosclerosis Risk in Communities (ARIC) Experience

artículo científico publicado en 2015

Candidate molecular pathway genes related to appetite regulatory neural network, adipocyte homeostasis and obesity: results from the CARDIA Study

artículo científico publicado en 2010

Cardiovascular biomarkers and subclinical brain disease in the atherosclerosis risk in communities study.

artículo científico publicado en 2013

Causal Effects of Body Mass Index on Cardiometabolic Traits and Events: A Mendelian Randomization Analysis

Cerebral small vessel disease genomics and its implications across the lifespan

artículo científico publicado en 2020

Cerebral white matter hyperintensities on MRI and acceleration of epigenetic aging: the atherosclerosis risk in communities study

artículo científico publicado en 2017

Changes over 14 years in androgenicity and body mass index in a biracial cohort of reproductive-age women

artículo científico publicado en 2008

Characterization of a human 12/15-lipoxygenase promoter variant associated with atherosclerosis identifies vimentin as a promoter binding protein

artículo científico publicado en 2012

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

artículo científico publicado en 2021

Circulating Monocyte Chemoattractant Protein-1 and Risk of Stroke: Meta-Analysis of Population-Based Studies Involving 17 180 Individuals

scientific article published on 03 September 2019

Combined genealogical, mapping, and expression approaches to identify spontaneously hypertensive rat hypertension candidate genes

scientific article published on 14 February 2005

Combined linkage and association analysis identifies rare and low frequency variants for blood pressure at 1q31

artículo científico publicado en 2018

Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities

artículo científico publicado en 2020

Common INSIG2 polymorphisms are associated with age-related changes in body size and high-density lipoprotein cholesterol from young adulthood to middle age.

artículo científico publicado en 2009

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 at 12q14 and 12q24 are associated with hippocampal volume

artículo científico publicado en 2012

Common variants at 12q15 and 12q24 are associated with infant head circumference

artículo científico publicado en 2012

Common variants at 6q22 and 17q21 are associated with intracranial volume

artículo científico publicado en 2012

Common variants in Alzheimer's disease and risk stratification by polygenic risk scores

artículo científico publicado en 2021

Common variation in COL4A1/COL4A2 is associated with sporadic cerebral small vessel disease

artículo científico publicado en 2015

Comparison of smoking-related DNA methylation between newborns from prenatal exposure and adults from personal smoking

scientific article published on 19 September 2019

Complexity in the genetic architecture of leukoaraiosis in hypertensive sibships from the GENOA Study

artículo científico publicado en 2009

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

artículo científico publicado en 2008

Consistent effects of genes involved in reverse cholesterol transport on plasma lipid and apolipoprotein levels in CARDIA participants

artículo científico publicado en 2006

Contribution of common non-synonymous variants in PCSK1 to body mass index variation and risk of obesity: a systematic review and meta-analysis with evidence from up to 331 175 individuals

artículo científico publicado en 2015

Correction to: Transethnic insight into the genetics of glycaemic traits: fine-mapping results from the Population Architecture using Genomics and Epidemiology (PAGE) consortium

artículo científico publicado en 2017

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

artículo científico publicado en 2017

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

artículo científico publicado en 2018

Correction: The complex genetics of gait speed: genome-wide meta-analysis approach

artículo científico publicado en 2017

Correction: Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation

artículo científico publicado en 2019

D-dimer, inflammatory markers, and lower extremity functioning in patients with and without peripheral arterial disease

artículo científico publicado en 2003

DNA Methylation Analysis Identifies Loci for Blood Pressure Regulation

artículo científico publicado en 2017

DNA Methylation Signatures of Depressive Symptoms in Middle-aged and Elderly Persons: Meta-analysis of Multiethnic Epigenome-wide Studies

article published in 2018

DNA methylation signatures of chronic low-grade inflammation are associated with complex diseases

artículo científico publicado en 2016

DNA methylation-based measures of biological age: meta-analysis predicting time to death

artículo científico publicado en 2016

Diabetes, Cognitive Decline, and Mild Cognitive Impairment Among Diverse Hispanics/Latinos: Study of Latinos-Investigation of Neurocognitive Aging Results (HCHS/SOL)

scientific article published on 05 March 2020

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

artículo científico publicado en 2015

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

artículo científico publicado en 2020

Discovery, fine-mapping, and conditional analyses of genetic variants associated with C-reactive protein in multiethnic populations using the Metabochip in the Population Architecture using Genomics and Epidemiology (PAGE) study

scientific article published on 01 August 2018

Effect of genetic variants associated with plasma homocysteine levels on stroke risk

artículo científico publicado en 2014

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

artículo científico publicado en 2014

Epigenetic Age Acceleration and Cognitive Function in African American Adults in Midlife: The Atherosclerosis Risk in Communities Study

scientific article published on 01 February 2020

Epigenetic Loci of Blood Pressure

artículo científico publicado en 2019

Epigenome-wide association studies identify DNA methylation associated with kidney function

artículo científico publicado en 2017

Epigenome-wide association study (EWAS) of BMI, BMI change and waist circumference in African American adults identifies multiple replicated loci

artículo científico publicado en 2015

Epigenome-wide study identifies novel methylation loci associated with body mass index and waist circumference

artículo científico publicado en 2015

Erratum to "Ankle brachial index and cognitive function among Hispanics/Latinos: Results from the Hispanic Community Health Study/Study of Latinos." [Atherosclerosis 271 (April 2018) 61-69]

scientific article published on 23 September 2018

Erratum. Polygenic Type 2 Diabetes Prediction at the Limit of Common Variant Detection. Diabetes 2014;63:2172-2182.

artículo científico publicado en 2018

Erratum: Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function and bipolar disorder susceptibility

scholarly article published in Molecular Psychiatry

Erratum: Common variants at 12q15 and 12q24 are associated with infant head circumference

scholarly article published in Nature Genetics

Erratum: Common variants at 6q22 and 17q21 are associated with intracranial volume

article

Evaluation of microarray-based DNA methylation measurement using technical replicates: the Atherosclerosis Risk In Communities (ARIC) Study

artículo científico publicado en 2014

Evidence for large-scale gene-by-smoking interaction effects on pulmonary function.

artículo científico publicado en 2017

Exome Chip Analysis Identifies Low-Frequency a on Brain Magnetic Imaging

Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits

artículo científico publicado en 2016

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

artículo científico publicado en 2017

Exosome miR-371b-5p promotes proliferation of lung alveolar progenitor type II cells by using PTEN to orchestrate the PI3K/Akt signaling

artículo científico publicado en 2017

Factors influencing the decline in stroke mortality: a statement from the American Heart Association/American Stroke Association

artículo científico publicado en 2013

Family history of stroke among Mexican-American and non-Hispanic white patients with stroke and TIA: implications for the feasibility and design of stroke genetics research

artículo científico publicado en 2004

Family-based association study of matrix metalloproteinase-3 and -9 haplotypes with susceptibility to ischemic white matter injury

artículo científico publicado en 2006

Fat mass and obesity gene and cognitive decline: the Atherosclerosis Risk in Communities Study

artículo científico publicado en 2012

Field of needs: the genetics of stroke.

artículo científico publicado en 1999

Fine Mapping and Identification of BMI Loci in African Americans

artículo científico publicado en 2013

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 for executive function and processing speed suggests involvement of the CADM2 gene.

artículo científico publicado en 2015

Gene expression profiling and functional proteomic analysis reveal perturbed kinase-mediated signaling in genetic stroke susceptibility

artículo científico publicado en 2003

Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia

artículo científico publicado en 2014

Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci

artículo científico publicado en 2014

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

scientific article published on 05 May 2020

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

artículo científico publicado en 2016

Generalization and fine mapping of red blood cell trait genetic associations to multi-ethnic populations: The PAGE study

artículo científico publicado en 2018

Genes from a translational analysis support a multifactorial nature of white matter hyperintensities

artículo científico publicado en 2015

Genetic Architecture of Subcortical Brain Structures in Over 40,000 Individuals Worldwide

scholarly article published 28 August 2017

Genetic Determinants of Cortical Structure (Thickness, Surface Area and Volumes) among Disease Free Adults in the CHARGE Consortium

article published in 2018

Genetic Diversity Turns a New PAGE in Our Understanding of Complex Traits

Genetic analyses of diverse populations improves discovery for complex traits

scientific article published on 19 June 2019

Genetic ancestry in lung-function predictions

artículo científico publicado en 2010

Genetic ancestry-smoking interactions and lung function in African Americans: a cohort study

artículo científico publicado en 2012

Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting

Genetic architecture of subcortical brain structures in 38,851 individuals

scientific article published on 21 October 2019

Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults

scientific article published on 22 September 2020

Genetic determinants of lipid traits in diverse populations from the population architecture using genomics and epidemiology (PAGE) study

artículo científico publicado en 2011

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

artículo científico publicado en 2014

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

artículo científico publicado en 2016

Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

artículo científico publicado en 2019

Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies

artículo científico publicado en 2012

Genetic variation at 16q24.2 is associated with small vessel stroke

artículo científico publicado en 2016

Genetic variation in soluble epoxide hydrolase (EPHX2) and risk of coronary heart disease: the Atherosclerosis Risk in Communities (ARIC) study

artículo científico publicado en 2006

Genetics of Chronic Kidney Disease Stages Across Ancestries: The PAGE Study

artículo científico publicado en 2019

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

artículo científico publicado en 2013

Genetics of leukoaraiosis

artículo científico publicado en 2002

Genetics of stroke

artículo científico publicado en 2009

Genetics of the thrombomodulin-endothelial cell protein C receptor system and the risk of early-onset ischemic stroke

artículo científico publicado en 2018

Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders

artículo científico publicado en 2018

Genome-Wide Association Analysis of Young-Onset Stroke Identifies a Locus on Chromosome 10q25 Near HABP2

artículo científico publicado en 2016

Genome-Wide Association Analysis of the Sense of Smell in U.S. Older Adults: Identification of Novel Risk Loci in African-Americans and European-Americans.

artículo científico publicado en 2016

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

Genome-Wide Interaction with Insulin Secretion Loci Reveals Novel Loci for Type 2 Diabetes in African Americans

artículo científico publicado en 2016

Genome-wide Association Study Links APOEϵ4 and BACE1 Variants with Plasma Amyloid β Levels

Genome-wide Meta-analysis on the Sense of Smell Among US Older Adults

artículo científico publicado en 2015

Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis

artículo científico publicado en 2016

Genome-wide analysis of mitochondrial DNA copy number reveals loci implicated in nucleotide metabolism, platelet activation, and megakaryocyte proliferation

scientific article published on 02 December 2021

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

artículo científico publicado en 2013

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

artículo científico publicado en 2013

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

artículo científico publicado en 2022

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

artículo científico publicado en 2014

Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.

artículo científico publicado en 2011

Genome-wide association meta-analysis of circulating odd-numbered chain saturated fatty acids: Results from the CHARGE Consortium.

artículo científico publicado en 2018

Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging

artículo científico publicado en 2021

Genome-wide association studies of MRI-defined brain infarcts: meta-analysis from the CHARGE Consortium

artículo científico publicado en 2009

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

artículo científico publicado en 2011

Genome-wide association studies suggest sex-specific loci associated with abdominal and visceral fat.

artículo científico publicado en 2015

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 novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology [...]

artículo científico publicado en 2013

Genome-wide association study identifies novel loci for type 2 diabetes-attributed end-stage kidney disease in African Americans

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 23,500 individuals identifies 7 loci associated with brain ventricular volume

artículo científico publicado en 2018

Genome-wide association study of L-arginine and dimethylarginines reveals novel metabolic pathway for symmetric dimethylarginine

artículo científico publicado en 2014

Genome-wide association study of cognitive function in diverse Hispanics/Latinos: results from the Hispanic Community Health Study/Study of Latinos

artículo científico publicado en 2020

Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project

artículo científico publicado en 2011

Genome-wide association study of intracranial aneurysms confirms role of Anril and SOX17 in disease risk

artículo científico publicado en 2012

Genome-wide association study of selenium concentrations

artículo científico publicado en 2015

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 identification of DNA methylation QTLs in whole blood highlights pathways for cardiovascular disease

scientific article published on 19 September 2019

Genome-wide identification of allelic expression in hypertensive rats

artículo científico publicado en 2009

Genome-wide interaction with the insulin secretion locus MTNR1B reveals CMIP as a novel type 2 diabetes susceptibility gene in African Americans.

artículo científico publicado en 2018

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

artículo científico publicado en 2012

Genome-wide linkage analysis for loci affecting pulse pressure: the Family Blood Pressure Program

artículo científico publicado en 2005

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

artículo científico publicado en 2012

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

artículo científico publicado en 2017

Genomewide association studies of stroke

artículo científico publicado en 2009

Genomic susceptibility Loci for brain atrophy, ventricular volume, and leukoaraiosis in hypertensive sibships

artículo científico publicado en 2009

Genomic susceptibility loci for brain atrophy in hypertensive sibships from the GENOA study

artículo científico publicado en 2005

Genomics and epigenomics of hypertension.

artículo científico publicado en 2006

Global and Regional Development of the Human Cerebral Cortex: Molecular Architecture and Occupational Aptitudes

artículo científico publicado en 2020

Guidelines for the primary prevention of stroke: a statement for healthcare professionals from the American Heart Association/American Stroke Association

artículo científico publicado en 2014

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

artículo científico publicado en 2014

Heart Disease and Stroke Statistics-2017 Update: A Report From the American Heart Association

artículo científico publicado en 2017

Heart Disease and Stroke Statistics-2018 Update: A Report From the American Heart Association

artículo científico publicado en 2018

Heart Disease and Stroke Statistics-2020 Update: A Report From the American Heart Association

artículo científico publicado en 2020

Heart Disease and Stroke Statistics—2019 Update: A Report From the American Heart Association

artículo científico publicado en 2019

Hemostatic Factors, APOL1 Risk Variants, and the Risk of ESRD in the Atherosclerosis Risk in Communities Study.

artículo científico publicado en 2015

Hepatic gene expression profiling reveals perturbed calcium signaling in a mouse model lacking both LDL receptor and Apobec1 genes

artículo científico publicado en 2003

Hepatocyte nuclear factor 1 and hypertensive nephropathy

artículo científico publicado en 2008

Heritability of leukoaraiosis in hypertensive sibships

artículo científico publicado en 2004

Identification, Heritability, and Relation With Gene Expression of Novel DNA Methylation Loci for Blood Pressure

artículo científico publicado en 2020

Imaging Endophenotypes of Stroke as a Target for Genetic Studies

scientific article published on 14 May 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

Imputation of missing covariate values in epigenome-wide analysis of DNA methylation data

artículo científico publicado en 2016

Inherited causes of clonal haematopoiesis in 97,691 whole genomes

artículo científico publicado en 2020

Insulin Resistance Exacerbates Genetic Predisposition to Nonalcoholic Fatty Liver Disease in Individuals Without Diabetes

artículo científico publicado en 2019

Inverse effects of the PPAR(gamma)2 Pro12Ala polymorphism on measures of adiposity over 15 years in African Americans and whites. The CARDIA study

artículo científico publicado en 2005

Investigation of gene-by-sex interactions for lipid traits in diverse populations from the population architecture using genomics and epidemiology study

artículo científico publicado en 2013

Ischemic stroke is associated with the ABO locus: the EuroCLOT study

artículo científico publicado en 2013

L5, the most electronegative subfraction of plasma LDL, induces endothelial vascular cell adhesion molecule 1 and CXC chemokines, which mediate mononuclear leukocyte adhesion

artículo científico publicado en 2006

Lack of association of the angiotensinogen-6 polymorphism with blood pressure levels in the comprehensive NHLBI Family Blood Pressure Program. National Heart, Lung and Blood Institute

artículo científico publicado en 2000

Large Meta-Analysis in the CHARGE Consortium Provides Evidence For an Association of Serum Vitamin D With Pulmonary Function

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

Leukocyte Traits and Exposure to Ambient Particulate Matter Air Pollution in the Women's Health Initiative and Atherosclerosis Risk in Communities Study

artículo científico publicado en 2020

Loci influencing blood pressure identified using a cardiovascular gene-centric array

artículo científico publicado en 2013

Loci influencing blood pressure identified using a cardiovascular gene-centric array.

artículo científico publicado en 2013

Longitudinal association of PCSK9 sequence variations with low-density lipoprotein cholesterol levels: the Coronary Artery Risk Development in Young Adults Study

artículo científico publicado en 2009

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

artículo científico publicado en 2015

Mapping functions

artículo científico publicado en 2007

Matrix Gla protein and osteopontin genetic associations with coronary artery calcification and bone density: the CARDIA study

scientific article published on 03 March 2005

Meta-Analysis of Genome-Wide Association Studies Identifies Genetic Risk Factors for Stroke in African Americans

artículo científico publicado en 2015

Meta-analysis across Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium provides evidence for an association of serum vitamin D with pulmonary function

artículo científico publicado en 2018

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

artículo científico publicado en 2016

Meta-analysis of epigenome-wide association studies of cognitive abilities

artículo científico publicado en 2018

Metabolic Traits and Stroke Risk in Individuals of African Ancestry: Mendelian Randomization Analysis

artículo científico publicado en 2021

Methylome-wide association study of central adiposity implicates genes involved in immune and endocrine systems

artículo científico publicado en 2020

Methylome-wide association study provides evidence of particulate matter air pollution-associated DNA methylation

scientific article published on 14 June 2019

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 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

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 association study of cerebral white matter hyperintensities on MRI

artículo científico publicado en 2015

Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function

scientific article published in Nature Communications

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

artículo científico publicado en 2013

Multilocus genetic risk score associates with ischemic stroke in case-control and prospective cohort studies

artículo científico publicado en 2014

Multiomics integrative analysis identifies allele-specific blood biomarkers associated to Alzheimer's disease etiopathogenesis

artículo científico publicado en 2021

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

artículo científico publicado en 2022

Mutation of FOXC1 and PITX2 induces cerebral small-vessel disease

artículo científico publicado en 2014

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

artículo científico publicado en 2017

New insights into the genetic etiology of Alzheimer's disease and related dementias

artículo científico publicado en 2022

No association of ALOX5AP polymorphisms with risk of MRI-defined brain infarcts.

artículo científico publicado en 2011

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

No evidence of interaction between known lipid-associated genetic variants and smoking in the multi-ethnic PAGE population

artículo científico publicado en 2013

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

artículo científico publicado en 2018

Novel genetic loci associated with hippocampal volume

scientific article published on 18 January 2017

Novel genetic loci underlying human intracranial volume identified through genome-wide association

artículo científico publicado en 2016

Omega-3 Fatty Acids and Genome-Wide Interaction Analyses Reveal DPP10-Pulmonary Function Association

artículo científico publicado en 2019

Overlap between common genetic polymorphisms underpinning kidney traits and cardiovascular disease phenotypes: the CKDGen consortium

artículo científico publicado en 2013

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

article

Parent-child pair design for detecting gene-environment interactions in complex diseases

scientific article published on 10 May 2007

Parental history of stroke and myocardial infarction predicts coronary artery calcification: The Coronary Artery Risk Development in Young Adults (CARDIA) study

artículo científico publicado en 2004

Partial derivatives meta-analysis: pooled analyses when individual participant data cannot be shared

Patterns of association between PPARgamma genetic variation and indices of adiposity and insulin action in African-Americans and whites: the CARDIA Study

artículo científico publicado en 2006

Plasma metabolites associated with cognitive function across race/ethnicities affirming the importance of healthy nutrition

artículo científico publicado en 2022

Polygenic Prediction of Weight and Obesity Trajectories from Birth to Adulthood

artículo científico publicado en 2019

Polygenic Risk, Fitness, and Obesity in the Coronary Artery Risk Development in Young Adults (CARDIA) Study

scientific article published on 08 January 2020

Polygenic type 2 diabetes prediction at the limit of common variant detection

artículo científico publicado en 2014

Polymorphism in soluble epoxide hydrolase and blood pressure in spontaneously hypertensive rats

artículo científico publicado en 2002

Polymorphism of the soluble epoxide hydrolase is associated with coronary artery calcification in African-American subjects: The Coronary Artery Risk Development in Young Adults (CARDIA) study

artículo científico publicado en 2004

Polymorphisms within the C-Reactive Protein (CRP) Promoter Region Are Associated with Plasma CRP Levels

Polymorphisms within the C-reactive protein (CRP) promoter region are associated with plasma CRP levels

artículo científico publicado en 2005

Population genetics of hypervariable loci: analysis of PCR based VNTR polymorphism within a population

scientific article published on 01 January 1991

Post-genome-wide association study challenges for lipid traits: describing age as a modifier of gene-lipid associations in the Population Architecture using Genomics and Epidemiology (PAGE) study

artículo científico publicado en 2013

Predicted gene expression in ancestrally diverse populations leads to discovery of susceptibility loci for lifestyle and cardiometabolic traits

artículo científico publicado en 2022

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

artículo científico publicado en 2014

Prevalence and correlates of mild cognitive impairment among diverse Hispanics/Latinos: Study of Latinos-Investigation of Neurocognitive Aging results

scientific article published on 18 November 2019

Prevention of Stroke in Patients With Silent Cerebrovascular Disease: A Scientific Statement for Healthcare Professionals From the American Heart Association/American Stroke Association

artículo científico publicado en 2016

Proceedings from the Albert Charitable Trust Inaugural Workshop on white matter and cognition in aging

scientific article published on 06 December 2019

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 2018

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

artículo científico publicado en 2018

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

artículo científico publicado en 2019

Ranking analysis of F-statistics for microarray data

artículo científico publicado en 2008

Ranking analysis of microarray data: a powerful method for identifying differentially expressed genes

artículo científico publicado en 2006

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

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 coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease

artículo científico publicado en 2017

Relationships of Clinical and Computed Tomography-Imaged Adiposity with Cognition in Middle-Aged and Older African Americans

artículo científico publicado en 2017

Replication of genetic loci for ages at menarche and menopause in the multi-ethnic Population Architecture using Genomics and Epidemiology (PAGE) study

artículo científico publicado en 2013

Report of the National Heart, Lung, and Blood Institute Working Group on epigenetics and hypertension

scientific article published on 19 March 2012

Reversal of endothelial dysfunction reduces white matter vulnerability in cerebral small vessel disease in rats

scientific article published on 01 July 2018

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

artículo científico publicado en 2020

SNP-by-fitness and SNP-by-BMI interactions from seven candidate genes and incident hypertension after 20 years of follow-up: the CARDIA Fitness Study.

artículo científico publicado en 2010

Segregation at three loci explains familial and population risk in Hirschsprung disease

artículo científico publicado en 2002

Sequence variation in the soluble epoxide hydrolase gene and subclinical coronary atherosclerosis: interaction with cigarette smoking

artículo científico publicado en 2006

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

artículo científico publicado en 2019

Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms

artículo científico publicado en 2016

Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants

artículo científico publicado en 2014

Single-nucleotide polymorphism genotyping for disease association studies

artículo científico publicado en 2005

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

artículo científico publicado en 2017

Somatic, positive and negative domains of the Center for Epidemiological Studies Depression (CES-D) scale: a meta-analysis of genome-wide association studies

artículo científico publicado en 2016

Stroke Genetics Network (SiGN) study: design and rationale for a genome-wide association study of ischemic stroke subtypes

artículo científico publicado en 2013

Structural Brain MRI Trait Polygenic Score Prediction of Cognitive Abilities

artículo científico publicado en 2015

The Alzheimer's Disease Sequencing Project: Study design and sample selection

artículo científico publicado en 2017

The Expressed Genome in Cardiovascular Diseases and Stroke: Refinement, Diagnosis, and Prediction: A Scientific Statement From the American Heart Association

artículo científico publicado en 2017

The Gene, Environment Association Studies consortium (GENEVA): maximizing the knowledge obtained from GWAS by collaboration across studies of multiple conditions

artículo científico publicado en 2010

The INSIG2 rs7566605 genetic variant does not play a major role in obesity in a sample of 24,722 individuals from four cohorts

artículo científico publicado en 2009

The cis and trans effects of the risk variants of coronary artery disease in the Chr9p21 region

artículo científico publicado en 2015

The complex genetics of gait speed: genome-wide meta-analysis approach

scientific article published on 10 January 2017

The copy number variation and stroke (CaNVAS) risk and outcome study

artículo científico publicado en 2021

The emerging genetic landscape of cerebral white matter hyperintensities

artículo científico publicado en 2019

The genetic architecture of the human cerebral cortex

The genetic architecture of the human cerebral cortex

artículo científico publicado en 2020

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

artículo científico publicado en 2016

The soluble epoxide hydrolase gene harbors sequence variation associated with susceptibility to and protection from incident ischemic stroke

artículo científico publicado en 2005

The transcribed genome and the heritable basis of essential hypertension

artículo científico publicado en 2005

The transcriptional landscape of age in human peripheral blood

artículo científico publicado en 2015

The uncoupling protein 2 Ala55Val polymorphism is associated with diabetes mellitus: the CARDIA study

artículo científico publicado en 2005

Top research priorities for stroke genetics

artículo científico publicado en 2018

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

artículo científico publicado en 2016

Trans-ethnic analysis of metabochip data identifies two new loci associated with BMI.

artículo científico publicado en 2017

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

Transcriptome-Wide Association Study of Blood Cell Traits in African Ancestry and Hispanic/Latino Populations

artículo científico publicado en 2021

Transethnic insight into the genetics of glycaemic traits: fine-mapping results from the Population Architecture using Genomics and Epidemiology (PAGE) consortium

artículo científico publicado en 2017

Transferability and fine-mapping of glucose and insulin quantitative trait loci across populations: CARe, the Candidate Gene Association Resource

artículo científico publicado en 2012

Treatment of leukoaraiosis

artículo científico publicado en 2005

Trends in the incidence of dementia: design and methods in the Alzheimer Cohorts Consortium

artículo científico publicado en 2017

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

artículo científico publicado en 2023

Unraveling hypertension: epigenomics comes of age

scientific article published on 01 February 2007

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

Using previously genotyped controls in genome-wide association studies (GWAS): application to the Stroke Genetics Network (SiGN)

artículo científico publicado en 2014

Variant Discovery and Fine Mapping of Genetic Loci Associated with Blood Pressure Traits in Hispanics and African Americans

artículo científico publicado en 2016

Variation at the M235T locus of the angiotensinogen gene and essential hypertension: a population-based case-control study from Rochester, Minnesota

artículo científico publicado en 1995

Variation in the Region of the Angiotensin-Converting Enzyme Gene Influences Interindividual Differences in Blood Pressure Levels in Young White Males ⬇️

artículo científico publicado el 12 de mayo de 1998

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

artículo científico publicado en 2015

White blood cell count in young adulthood and coronary artery calcification in early middle age: coronary artery risk development in young adults (CARDIA) study.

artículo científico publicado en 2013

Whole Blood DNA Methylation Signatures of Diet Are Associated with Cardiovascular Disease Risk Factors and All-cause Mortality

scientific article published on 11 June 2020

Whole exome sequence-based association analyses of plasma amyloid-β in African and European Americans; the Atherosclerosis Risk in Communities-Neurocognitive Study

artículo científico

Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation

article

Whole genome sequence analyses of brain imaging measures in the Framingham Study

artículo científico publicado en 2017

Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol

artículo científico publicado en 2014

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

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