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Author Details

Dan E Arking
2002
226
70
PMIDPaper TitleJournal TitlePublished Year
37916415Polygenic Risk Score Associates With Atherosclerotic Plaque Characteristics at Autopsy.Arterioscler Thromb Vasc Biol2024
37292692Clonal Hematopoiesis of Indeterminate Potential is Associated with Acute Kidney Injury.medRxiv2023
38028628Gene-educational attainment interactions in a multi-population genome-wide meta-analysis identify novel lipid loci.Front Genet2023
37804200Association Between Whole Blood-Derived Mitochondrial DNA Copy Number, Low-Density Lipoprotein Cholesterol, and Cardiovascular Disease Risk.J Am Heart Assoc2023
37571804Genetic variant annotation scores in congenital long QT syndrome.Ann Noninvasive Electrocardiol2023
37891237Mitochondrial DNA copy number is associated with incident chronic kidney disease and proteinuria in the AIDS linked to the intravenous experience cohort.Sci Rep2023
37777527Deleterious heteroplasmic mitochondrial mutations are associated with an increased risk of overall and cancer-specific mortality.Nat Commun2023
37868038The functional impact of rare variation across the regulatory cascade.Cell Genom2023
37461703Polygenic Risk Score Associates with Atherosclerotic Plaque Characteristics at Autopsy.bioRxiv2023
37192320Long-Term Air Pollution Exposure and Mitochondrial DNA Copy Number: An Analysis of UK Biobank Data.Environ Health Perspect2023
37365616Transcriptome- and proteome-wide association studies nominate determinants of kidney function and damage.Genome Biol2023
36927883Association of Mitochondrial DNA Copy Number With Brain MRI Markers and Cognitive Function: A Meta-analysis of Community-Based Cohorts.Neurology2023
37101120Priors, population sizes, and power in genome-wide hypothesis tests.BMC Bioinformatics2023
36918541Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease.Nat Commun2023
35120996Trans-ethnic genome-wide association study of blood metabolites in the Chronic Renal Insufficiency Cohort (CRIC) study.Kidney Int2022
36311265Whole-exome sequencing in 415,422 individuals identifies rare variants associated with mitochondrial DNA copy number.HGG Adv2022
35594314Resting heart rate and incident atrial fibrillation: A stratified Mendelian randomization in the AFGen consortium.PLoS One2022
35525425Sex hormones and repolarization dynamics during the menstrual cycle in women with congenital long QT syndrome.Heart Rhythm2022
35591888A bioinformatics pipeline for estimating mitochondrial DNA copy number and heteroplasmy levels from whole genome sequencing data.NAR Genom Bioinform2022
35389749Monogenic and Polygenic Contributions to QTc Prolongation in the Population.Circulation2022
35870639Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension.Kidney Int2022
35365950Frequency of the PNPLA3 rs738409 polymorphism and other genetic loci for liver disease in a Guatemalan adult population.Liver International2022
35474272<i>APOL1</i> Kidney Risk Variants and Proteomics.Clin J Am Soc Nephrol2022
36448986Biological Life-Stage and the Burden of Cardiac Events in Women With Congenital Long QT Syndrome.Circ Arrhythm Electrophysiol2022
36050321Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways.Nat Commun2022
35849594Mitochondrial DNA copy number, metabolic syndrome, and insulin sensitivity: Insights from the Sugar, Hypertension, and Physical Exercise studies.PLoS One2022
35777833Association of Mitochondrial DNA Copy Number with Risk of Progression of Kidney Disease.Clin J Am Soc Nephrol2022
34339849Use of oral contraceptives in women with congenital long QT syndrome.Heart Rhythm2022
35265679Rare Genetic Variants Associated With Myocardial Fibrosis: Multi-Ethnic Study of Atherosclerosis.Front Cardiovasc Med2022
34415308Epigenome-wide association study of mitochondrial genome copy number.Hum Mol Genet2021
34238014Risk Prediction in Women With Congenital Long QT Syndrome.J Am Heart Assoc2021
33859359Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure.Mol Psychiatry2021
33893282Publisher Correction: A meta-analysis of genome-wide association studies identifies multiple longevity genes.Nat Commun2021
33838163Genome-wide association study of serum metabolites in the African American Study of Kidney Disease and Hypertension.Kidney Int2021
33441415Blood-derived mitochondrial DNA copy number is associated with gene expression across multiple tissues and is predictive for incident neurodegenerative disease.Genome Research2021
34319147Rare Coding Variants Associated With Electrocardiographic Intervals Identify Monogenic Arrhythmia Susceptibility Genes: A Multi-Ancestry Analysis.Circ Genom Precis Med2021
34465608Proteins Associated with Risk of Kidney Function Decline in the General Population.J Am Soc Nephrol2021
35036986Association of mitochondrial DNA copy number with cardiometabolic diseases.Cell Genom2021
34548389Polygenic Risk Scores for Kidney Function and Their Associations with Circulating Proteome, and Incident Kidney Diseases.J Am Soc Nephrol2021
34378773Development and optimization of an in vivo electrocardiogram recording method and analysis program for adult zebrafish.Dis Model Mech2021
34587750Epigenetic Age and the Risk of Incident Atrial Fibrillation.Circulation2021
33021160Outcome by Sex in Patients With Long QT Syndrome With an Implantable Cardioverter Defibrillator.J Am Heart Assoc2020
32027831High-Risk, High-Reward Genetics in ASD.Neuron2020
32321923Consistent RNA sequencing contamination in GTEx and other data sets.Nature Communications2020
32004343Evaluation of mitochondrial DNA copy number estimation techniques.PLoS One2020
32479199Mitochondrial DNA Copy Number and Incident Heart Failure: The Atherosclerosis Risk in Communities (ARIC) Study.Circulation2020
32439900Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction.Nat Commun2020
32436959Analysis of putative cis-regulatory elements regulating blood pressure variation.Hum Mol Genet2020
33380473<i>NAT8</i> Variants, N-Acetylated Amino Acids, and Progression of CKD.Clin J Am Soc Nephrol2020
32602732Multi-Ethnic Genome-Wide Association Study of Decomposed Cardioelectric Phenotypes Illustrates Strategies to Identify and Characterize Evidence of Shared Genetic Effects for Complex Traits.Circ Genom Precis Med2020
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