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52 Genetic Loci Influencing Myocardial Mass

artículo científico publicado en 2016

A Comprehensive Evaluation of the Genetic Architecture of Sudden Cardiac Arrest

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 common connexin-40 gene promoter variant affects connexin-40 expression in human atria and is associated with atrial fibrillation

artículo científico publicado en 2010

A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization

artículo científico publicado en 2006

A genome-wide association analysis of serum iron concentrations

artículo científico publicado en 2009

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

artículo científico publicado en 2021

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

scientific article published on 14 August 2019

A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure

scientific article published on 10 April 2019

Analysis of shared heritability in common disorders of the brain

artículo científico publicado en 2018

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

Association between microdeletion and microduplication at 16p11.2 and autism

artículo científico publicado en 2008

Association of Lipid-Related Genetic Variants with the Incidence of Atrial Fibrillation: The AFGen Consortium

artículo científico publicado en 2016

Associations between genetic variants in the NOS1AP (CAPON) gene and cardiac repolarization in the old order Amish

artículo científico publicado en 2007

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

article

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

scientific article published on 01 May 2019

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

artículo científico publicado en 2018

CUBN is a gene locus for albuminuria

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 Coding Genetic Variation Underlying the Electrocardiographic PR Interval

Common genetic variants associate with serum phosphorus concentration

artículo científico publicado en 2010

Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways

artículo científico publicado en 2010

Common variants at ten loci modulate the QT interval duration in the QTSCD Study

artículo científico publicado en 2009

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

artículo científico publicado en 2010

Common variants in KCNN3 are associated with lone atrial fibrillation

artículo científico publicado en 2010

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

artículo científico publicado en 2017

Disruption of p16 and activation of Kras in pancreas increase ductal adenocarcinoma formation and metastasis in vivo

artículo científico publicado en 2011

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

artículo científico publicado en 2017

Evaluation of mitochondrial DNA copy number estimation techniques

scientific article published on 31 January 2020

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

Fifteen Genetic Loci Associated With the Electrocardiographic P Wave

artículo científico publicado en 2017

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

artículo científico publicado en 2015

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

GWAS analysis of handgrip and lower body strength in older adults in the CHARGE consortium

artículo científico publicado en 2016

GWAS meta-analysis (N=279,930) identifies new genes and functional links to intelligence

article

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

scientific article published on 05 May 2020

Gene-gene Interaction Analyses for Atrial Fibrillation

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 Investigation Into the Differential Risk of Atrial Fibrillation Among Black and White Individuals

artículo científico publicado en 2016

Genetic Obesity and the Risk of Atrial Fibrillation: Causal Estimates from Mendelian Randomization

artículo científico publicado en 2016

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

artículo científico publicado en 2014

Genetic diversity is a predictor of mortality in humans

artículo científico publicado en 2014

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

artículo científico publicado en 2013

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

artículo científico publicado en 2011

Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation

artículo científico publicado en 2018

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

artículo científico publicado en 2010

Genome-wide association and functional studies identify 46 novel loci for alcohol consumption and suggest common genetic mechanisms with neuropsychiatric disorders

Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence

article

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 study of PR interval

artículo científico publicado en 2010

Genome-wide association study of blood pressure and hypertension

scientific journal article

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

Identifying allelic loss and homozygous deletions in pancreatic cancer without matched normals using high-density single-nucleotide polymorphism arrays

artículo científico publicado en 2006

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

artículo científico publicado en 2012

Impact of genetic variants on the upstream efficacy of renin-angiotensin system inhibitors for the prevention of atrial fibrillation

artículo científico publicado en 2016

Independent susceptibility markers for atrial fibrillation on chromosome 4q25.

artículo científico publicado en 2010

Large-Scale Cognitive GWAS Meta-Analysis Reveals Tissue-Specific Neural Expression and Potential Nootropic Drug Targets

artículo científico publicado en 2017

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

Meta-analysis identifies six new susceptibility loci for atrial fibrillation

artículo científico publicado en 2012

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 genome-wide association studies identifies six new Loci for serum calcium concentrations

artículo científico publicado en 2013

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-Trait Analysis of GWAS and Biological Insights Into Cognition: A Response to Hill (2018)

artículo científico publicado en 2018

Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction

scientific article published on 21 May 2020

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

article

Multi-ethnic genome-wide association study for atrial fibrillation

article

Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors

artículo científico publicado en 2010

Multiple loci associated with indices of renal function and chronic kidney disease

scientific journal article

New loci associated with kidney function and chronic kidney disease

artículo científico publicado en 2010

Ninety-nine independent genetic loci influencing general cognitive function include genes associated with brain health and structure (N = 280,360)

No interactions between previously associated 2-hour glucose gene variants and physical activity or BMI on 2-hour glucose levels

artículo científico publicado en 2012

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

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

Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways

artículo científico publicado en 2019

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

SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function

artículo científico publicado en 2016

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

Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases

artículo científico publicado en 2012

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

artículo científico publicado en 2018

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 QT interval and risk of incident atrial fibrillation

artículo científico publicado en 2013

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

artículo científico publicado en 2016

Toward the human cellular microRNAome.

artículo científico publicado en 2017

Trans-ethnic Evaluation Identifies Novel Low Frequency Loci Associated with 25-Hydroxyvitamin D Concentrations.

artículo científico publicado en 2018

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

scientific article published on 13 July 2009

Whole Exome Sequencing in Atrial Fibrillation

artículo científico publicado en 2016