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Author Details

Arne Pfeufer
German Research Center for Environmental Health
1996
94
52
PMIDPaper TitleJournal TitlePublished Year
32121570Metabolite Shifts Induced by Marathon Race Competition Differ between Athletes Based on Level of Fitness and Performance: A Substudy of the Enzy-MagIC Study.Metabolites2020
32121570Metabolite Shifts Induced by Marathon Race Competition Differ between Athletes Based on Level of Fitness and Performance: A Substudy of the Enzy-MagIC Study.Metabolites2020
31022234VarWatch-A stand-alone software tool for variant matching.PLoS One2019
31022234VarWatch-A stand-alone software tool for variant matching.PLoS One2019
29315961REduction of THRomboembolic EVents during Ablation using the laserballoon: The RETHREVA registry.J Cardiovasc Electrophysiol2018
30046033PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity.Nat Commun2018
29315961REduction of THRomboembolic EVents during Ablation using the laserballoon: The RETHREVA registry.J Cardiovasc Electrophysiol2018
30046033PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity.Nat Commun2018
28394258Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function.J Clin Invest2017
28360221<i>NFAT5</i> and <i>SLC4A10</i> Loci Associate with Plasma Osmolality.J Am Soc Nephrol2017
28394258Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function.J Clin Invest2017
28360221<i>NFAT5</i> and <i>SLC4A10</i> Loci Associate with Plasma Osmolality.J Am Soc Nephrol2017
26098842The cost-effectiveness of UGT1A1 genotyping before colorectal cancer treatment with irinotecan from the perspective of the German statutory health insurance.Acta Oncol2016
26975745Candidate gene variants of the immune system and sudden infant death syndrome.Int J Legal Med2016
27287068Electrophysiological characterization of a large set of novel variants in the SCN5A-gene: identification of novel LQTS3 and BrS mutations.Pflugers Arch2016
26098842The cost-effectiveness of UGT1A1 genotyping before colorectal cancer treatment with irinotecan from the perspective of the German statutory health insurance.Acta Oncol2016
2765946652 Genetic Loci Influencing Myocardial Mass.J Am Coll Cardiol2016
2765946652 Genetic Loci Influencing Myocardial Mass.J Am Coll Cardiol2016
27287068Electrophysiological characterization of a large set of novel variants in the SCN5A-gene: identification of novel LQTS3 and BrS mutations.Pflugers Arch2016
26975745Candidate gene variants of the immune system and sudden infant death syndrome.Int J Legal Med2016
25248395Points to consider for prioritizing clinical genetic testing services: a European consensus process oriented at accountability for reasonableness.Eur J Hum Genet2015
25737393Analysis for Genetic Modifiers of Disease Severity in Patients With Long-QT Syndrome Type 2.Circ Cardiovasc Genet2015
25431330SNiPA: an interactive, genetic variant-centered annotation browser.Bioinformatics2015
25248395Points to consider for prioritizing clinical genetic testing services: a European consensus process oriented at accountability for reasonableness.Eur J Hum Genet2015
25737393Analysis for Genetic Modifiers of Disease Severity in Patients With Long-QT Syndrome Type 2.Circ Cardiovasc Genet2015
25431330SNiPA: an interactive, genetic variant-centered annotation browser.Bioinformatics2015
23853074A genome-wide association study identifies 6p21 as novel risk locus for dilated cardiomyopathy.Eur Heart J2014
27202308Cost-Effectiveness Analysis of Ugt1a1 Genotyping Before Colorectal Cancer Treatment with Irinotecan.Value Health2014
23853074A genome-wide association study identifies 6p21 as novel risk locus for dilated cardiomyopathy.Eur Heart J2014
24952909Annotation of loci from genome-wide association studies using tissue-specific quantitative interaction proteomics.Nat Methods2014
24952745Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization.Nat Genet2014
24857694An enhancer polymorphism at the cardiomyocyte intercalated disc protein NOS1AP locus is a major regulator of the QT interval.Am J Hum Genet2014
27202308Cost-Effectiveness Analysis of Ugt1a1 Genotyping Before Colorectal Cancer Treatment with Irinotecan.Value Health2014
24952909Annotation of loci from genome-wide association studies using tissue-specific quantitative interaction proteomics.Nat Methods2014
24952745Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization.Nat Genet2014
24857694An enhancer polymorphism at the cardiomyocyte intercalated disc protein NOS1AP locus is a major regulator of the QT interval.Am J Hum Genet2014
23280596SNP prioritization using a Bayesian probability of association.Genet Epidemiol2013
23280596SNP prioritization using a Bayesian probability of association.Genet Epidemiol2013
23307621Importance of different types of prior knowledge in selecting genome-wide findings for follow-up.Genet Epidemiol2013
23583979Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.Nat Genet2013
23583979Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.Nat Genet2013
23307621Importance of different types of prior knowledge in selecting genome-wide findings for follow-up.Genet Epidemiol2013
22100668A large candidate gene survey identifies the KCNE1 D85N polymorphism as a possible modulator of drug-induced torsades de pointes.Circ Cardiovasc Genet2012
22544366Meta-analysis identifies six new susceptibility loci for atrial fibrillation.Nat Genet2012
22876189The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits.PLoS Genet2012
22988944Network-based SNP meta-analysis identifies joint and disjoint genetic features across common human diseases.BMC Genomics2012
22606281Cis-acting polymorphisms affect complex traits through modifications of microRNA regulation pathways.PLoS One2012
22359512Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.PLoS Genet2012
22100668A large candidate gene survey identifies the KCNE1 D85N polymorphism as a possible modulator of drug-induced torsades de pointes.Circ Cardiovasc Genet2012
22988944Network-based SNP meta-analysis identifies joint and disjoint genetic features across common human diseases.BMC Genomics2012
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Collaborators

Thomas Meitinger
Technical University of Munich, Institute of Human Genetics
Co-authored papers 38
H-Erich Wichmann
Co-authored papers 32
Christopher Newton-Cheh
Co-authored papers 18
Andr?? G Uitterlinden
Erasmus University Medical Center
Co-authored papers 17
Christian Gieger
German Research Center for Cardiovascular Disease (DZHK)
Co-authored papers 16
Dan E Arking
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Martina M??ller-Nurasyid
Institute for Medical Information Processing
Co-authored papers 16
Albert Hofman
Harvard T.H. Chan School of Public Health
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Jacqueline C M Witteman
Co-authored papers 14
Andrew A Hicks
Institute for Biomedicine, Affiliated institute of the University of Lubeck
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Peter P Pramstaller
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Joshua C Bis
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Rollins School of Public Health, Emory University
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Cornelia M van Duijn
University of Oxford
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Patrick T Ellinor
Cardiovascular Research Center, Massachusetts General Hospital
Co-authored papers 12
Susan R Heckbert
Co-authored papers 12
Lenore J Launer
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Jerome I Rotter
Co-authored papers 11
Annette Peters
Ludwig-Maximilians-Universitat Munchen
Co-authored papers 11
Nona Sotoodehnia
Johns Hopkins University School of Medicine
Co-authored papers 11
Serena Sanna
Co-authored papers 10
Kenneth Rice
Co-authored papers 10
Harold Snieder
University of Groningen, University Medical Center Groningen
Co-authored papers 10
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