List of works - Dan E Arking

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

scientific article published on 6 October 2011

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

scientific article

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

scientific article

Genome-wide association study of blood pressure and hypertension

scientific journal article

New loci associated with kidney function and chronic kidney disease

scientific article

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

scientific journal article

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

scientific article

Meta-analysis identifies six new susceptibility loci for atrial fibrillation

scientific article published on 29 April 2012

Common variants in KCNN3 are associated with lone atrial fibrillation

scientific article

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

scientific article

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

scientific article

Analysis of shared heritability in common disorders of the brain

scientific article published on 21 June 2018

Genome-wide association study of PR interval

scientific article

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

scientific article published on 13 July 2009

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

scientific article

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

scientific article

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

scientific article published on 12 September 2016

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

scientific article published on 14 April 2013

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

scientific article

CUBN is a gene locus for albuminuria

scientific article

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

scientific article published on 23 February 2017

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

scientific article

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

article

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

scientific article published on August 2006

52 Genetic Loci Influencing Myocardial Mass

scientific article

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

scientific article published on 17 September 2018

Independent susceptibility markers for atrial fibrillation on chromosome 4q25.

scientific article

A genome-wide association analysis of serum iron concentrations

scientific article

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

scientific article

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

scientific article

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

scientific article published on 30 January 2014

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

scientific article

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

scientific article published on 29 May 2018

Common genetic variants associate with serum phosphorus concentration

scientific article

Multi-ethnic genome-wide association study for atrial fibrillation

article

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

scientific article

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

scientific article

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

scientific article

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

scientific article

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

scientific article published on 16 August 2011

Toward the human cellular microRNAome.

scientific article published on 6 September 2017

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

scientific article published on 19 February 2018

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

scientific article

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

scientific article

The QT interval and risk of incident atrial fibrillation

scientific article published on 18 July 2013

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

scientific article

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

scientific article

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

scientific article

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

scientific article published on 14 December 2016

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

scientific article published on 5 December 2016

List of works by Dan E Arking

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

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

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

Genome-wide association study of blood pressure and hypertension

New loci associated with kidney function and chronic kidney disease

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

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

Meta-analysis identifies six new susceptibility loci for atrial fibrillation

Common variants in KCNN3 are associated with lone atrial fibrillation

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

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

Analysis of shared heritability in common disorders of the brain

Genome-wide association study of PR interval

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

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

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

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

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

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

CUBN is a gene locus for albuminuria

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

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

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

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

52 Genetic Loci Influencing Myocardial Mass

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

Independent susceptibility markers for atrial fibrillation on chromosome 4q25.

A genome-wide association analysis of serum iron concentrations

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

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

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

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

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

Common genetic variants associate with serum phosphorus concentration

Multi-ethnic genome-wide association study for atrial fibrillation

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

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

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

A common connexin-40 gene promoter variant affects connexin-40 expression in human atria and is 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

Toward the human cellular microRNAome.

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

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

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

The QT interval and risk of incident atrial fibrillation

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

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

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

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

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