Author: Marcus Dörr

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Preprints

Genetic analysis of over one million people identifies 535 novel loci for blood pressure.

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Genome-wide association study provides new insights into the genetic architecture and pathogenesis of heart failure

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  • Site-wide: 11,676
  • In genetics: 569
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Atrial Fibrillation Genetic Risk Differentiates Cardioembolic Stroke from other Stroke Subtypes

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  • In genetics: 1,331
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Novel blood pressure locus and gene discovery using GWAS and expression datasets from blood and the kidney

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  • Site-wide: 31,271
  • In genomics: 2,798
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Multi-ancestry GWAS of the electrocardiographic PR interval identifies 210 loci underlying cardiac conduction

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  • In genetics: 1,949
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Discovering patterns of pleiotropy in genome-wide association studies

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  • In genetics: 2,068
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  • Site-wide: 113,088
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Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9

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  • In genetics: 2,089
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Genome-wide association meta-analysis of PR interval identifies 47 novel loci associated with atrial and atrioventricular electrical activity

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Genome wide association analysis in dilated cardiomyopathy reveals two new key players in systolic heart failure on chromosome 3p25.1 and 22q11.23

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  • In genomics: 3,893
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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

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  • In genetics: 4,081
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Evaluation of the causal effect of fibrinogen on incident coronary heart disease via Mendelian randomization

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KCND3 is a novel susceptibility locus for early repolarization

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  • Site-wide: 95,638
  • In genetics: 4,296
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Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure

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  • Site-wide: 104,515
  • In genomics: 6,111
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  • Site-wide: 96,101
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Expression of a transcript encoding for cytosolic renin in the diseased human heart

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  • In physiology: 1,598
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