Lista de obras - Nona Sotoodehnia - Dominio Público Uruguay

52 Genetic Loci Influencing Myocardial Mass

artículo científico publicado en 2016

A Comprehensive Evaluation of the Genetic Architecture of Sudden Cardiac Arrest

A common SCN5A variant is associated with PR interval and atrial fibrillation among African Americans

artículo científico publicado en 2014

A genome-wide association study of depressive symptoms

scientific journal article

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

artículo científico publicado en 2021

An integrative cross-omics analysis of DNA methylation sites of glucose and insulin homeostasis.

artículo científico publicado en 2019

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

article published in 2019

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

artículo científico publicado en 2017

Association Between Titin Loss-of-Function Variants and Early-Onset Atrial Fibrillation

Associations of autozygosity with a broad range of human phenotypes

scientific article published on 31 October 2019

Atrial fibrillation in an African-American cohort: The Jackson Heart Study

artículo científico publicado en 2018

B-type natriuretic peptide and C-reactive protein in the prediction of atrial fibrillation risk: the CHARGE-AF Consortium of community-based cohort studies

artículo científico publicado en 2014

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

artículo científico publicado en 2018

Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR Interval

Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction

artículo científico publicado en 2010

DNA Methylation Analysis Identifies Loci for Blood Pressure Regulation

artículo científico publicado en 2017

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

artículo científico publicado en 2016

Directional dominance on stature and cognition in diverse human populations

artículo científico publicado en 2015

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

artículo científico publicado en 2017

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

Epigenetic Signatures of Cigarette Smoking

artículo científico publicado en 2016

Erratum: Genetic loci associated with heart rate variability and their effects on cardiac disease risk

artículo científico publicado en 2017

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

artículo científico publicado en 2017

European ancestry as a risk factor for atrial fibrillation in African Americans

artículo científico publicado en 2010

Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6

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

Fatty acid biomarkers of dairy fat consumption and incidence of type 2 diabetes: A pooled analysis of prospective cohort studies

artículo científico publicado en 2018

Fatty acids in the de novo lipogenesis pathway and incidence of type 2 diabetes: A pooled analysis of prospective cohort studies

artículo científico publicado en 2020

Fibroblast growth factor 23 and sudden versus non-sudden cardiac death: the Cardiovascular Health Study

artículo científico publicado en 2015

Fifteen Genetic Loci Associated With the Electrocardiographic P Wave

artículo científico publicado en 2017

Fine-mapping, novel loci identification, and SNP association transferability in a genome-wide association study of QRS duration in African Americans

artículo científico publicado en 2016

Genetic Determinants of Electrocardiographic P-wave Duration and Relation to Atrial Fibrillation

artículo científico publicado en 2020

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 association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization

artículo científico publicado en 2014

Genetic loci associated with heart rate variability and their effects on cardiac disease risk

artículo científico publicado en 2017

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

Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk

scientific article published on 05 March 2013

Genome-wide association analysis identifies multiple loci related to resting heart rate

artículo científico publicado en 2010

Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits

artículo científico publicado en 2019

Genome-wide association meta-analysis of PR interval identifies 47 novel loci associated with atrial and atrioventricular electrical activity

Genome-wide association studies of the PR interval in African Americans

artículo científico publicado en 2011

Genome-wide association study of PR interval

artículo científico publicado en 2010

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

artículo científico publicado en 2017

Identification of a sudden cardiac death susceptibility locus at 2q24.2 through genome-wide association in European ancestry individuals

artículo científico publicado en 2011

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

artículo científico publicado en 2013

Impact of ancestry and common genetic variants on QT interval in African Americans

artículo científico publicado en 2012

Interaction of methylation-related genetic variants with circulating fatty acids on plasma lipids: a meta-analysis of 7 studies and methylation analysis of 3 studies in the Cohorts for Heart and Aging Research in Genomic Epidemiology consortium

artículo científico publicado en 2016

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

artículo científico publicado en 2017

Large-scale candidate gene analysis in whites and African Americans identifies IL6R polymorphism in relation to atrial fibrillation: the National Heart, Lung, and Blood Institute's Candidate Gene Association Resource (CARe) project

artículo científico publicado en 2011

Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function

artículo científico publicado en 2017

Meta-analysis identifies six new susceptibility loci for atrial fibrillation

artículo científico publicado en 2012

Meta-analysis of genome-wide association studies of HDL cholesterol response to statins

artículo científico publicado en 2016

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-ethnic genome-wide association study for atrial fibrillation

article

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 PR interval in a genome-wide association study of 10 African American cohorts

artículo científico publicado en 2012

PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity

artículo científico publicado en 2018

Pericardial fat volume and incident atrial fibrillation in the Multi-Ethnic Study of Atherosclerosis and Jackson Heart Study

artículo científico publicado en 2017

Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins

artículo científico publicado en 2014

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

artículo científico publicado en 2019

Sequencing of SCN5A identifies rare and common variants associated with cardiac conduction: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium

artículo científico publicado en 2014

Simple risk model predicts incidence of atrial fibrillation in a racially and geographically diverse population: the CHARGE-AF consortium

artículo científico publicado en 2013

Targeted sequencing in candidate genes for atrial fibrillation: the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Targeted Sequencing Study

artículo científico publicado en 2014

Testing the role of predicted gene knockouts in human anthropometric trait variation

artículo científico publicado en 2016

The Relation of Serum Potassium Concentration with Cardiovascular Events and Mortality in Community-Living Individuals

artículo científico publicado en 2017

Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry ⬇️

scientific article published on 13 July 2009

Ventricular Ectopy as a Predictor of Heart Failure and Death

artículo científico publicado en 2015

Whole Exome Sequencing in Atrial Fibrillation

artículo científico publicado en 2016

Lista de obras de Nona Sotoodehnia

52 Genetic Loci Influencing Myocardial Mass

A Comprehensive Evaluation of the Genetic Architecture of Sudden Cardiac Arrest

A common SCN5A variant is associated with PR interval and atrial fibrillation among African Americans

A genome-wide association study of depressive symptoms

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

An integrative cross-omics analysis of DNA methylation sites of glucose and insulin homeostasis.

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

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

Association Between Titin Loss-of-Function Variants and Early-Onset Atrial Fibrillation

Associations of autozygosity with a broad range of human phenotypes

Atrial fibrillation in an African-American cohort: The Jackson Heart Study

B-type natriuretic peptide and C-reactive protein in the prediction of atrial fibrillation risk: the CHARGE-AF Consortium of community-based cohort studies

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

Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR Interval

Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction

DNA Methylation Analysis Identifies Loci for Blood Pressure Regulation

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

Directional dominance on stature and cognition in diverse human populations

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

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

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

Epigenetic Signatures of Cigarette Smoking

Erratum: Genetic loci associated with heart rate variability and their effects on cardiac disease risk

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

European ancestry as a risk factor for atrial fibrillation in African Americans

Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6

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

Fatty acid biomarkers of dairy fat consumption and incidence of type 2 diabetes: A pooled analysis of prospective cohort studies

Fatty acids in the de novo lipogenesis pathway and incidence of type 2 diabetes: A pooled analysis of prospective cohort studies

Fibroblast growth factor 23 and sudden versus non-sudden cardiac death: the Cardiovascular Health Study

Fifteen Genetic Loci Associated With the Electrocardiographic P Wave

Fine-mapping, novel loci identification, and SNP association transferability in a genome-wide association study of QRS duration in African Americans

Genetic Determinants of Electrocardiographic P-wave Duration and Relation to Atrial Fibrillation

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

Genetic Risk Prediction of Atrial Fibrillation

Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization

Genetic loci associated with heart rate variability and their effects on cardiac disease risk

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

Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk

Genome-wide association analysis identifies multiple loci related to resting heart rate

Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits

Genome-wide association meta-analysis of PR interval identifies 47 novel loci associated with atrial and atrioventricular electrical activity

Genome-wide association studies of the PR interval in African Americans

Genome-wide association study of PR interval

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

Identification of a sudden cardiac death susceptibility locus at 2q24.2 through genome-wide association in European ancestry individuals

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

Impact of ancestry and common genetic variants on QT interval in African Americans

Interaction of methylation-related genetic variants with circulating fatty acids on plasma lipids: a meta-analysis of 7 studies and methylation analysis of 3 studies in the Cohorts for Heart and Aging Research in Genomic Epidemiology consortium

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

Large-scale candidate gene analysis in whites and African Americans identifies IL6R polymorphism in relation to atrial fibrillation: the National Heart, Lung, and Blood Institute's Candidate Gene Association Resource (CARe) project

Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function

Meta-analysis identifies six new susceptibility loci for atrial fibrillation

Meta-analysis of genome-wide association studies of HDL cholesterol response to statins

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

Multi-ethnic genome-wide association study for atrial fibrillation

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

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

Novel loci associated with PR interval in a genome-wide association study of 10 African American cohorts

PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity

Pericardial fat volume and incident atrial fibrillation in the Multi-Ethnic Study of Atherosclerosis and Jackson Heart Study

Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins

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

Sequencing of SCN5A identifies rare and common variants associated with cardiac conduction: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium

Simple risk model predicts incidence of atrial fibrillation in a racially and geographically diverse population: the CHARGE-AF consortium

Targeted sequencing in candidate genes for atrial fibrillation: the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Targeted Sequencing Study

Testing the role of predicted gene knockouts in human anthropometric trait variation

The Relation of Serum Potassium Concentration with Cardiovascular Events and Mortality in Community-Living Individuals

Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry ⬇️

Ventricular Ectopy as a Predictor of Heart Failure and Death

Whole Exome Sequencing in Atrial Fibrillation