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Author: Thomas Meitinger

  • ORCiD: http://orcid.org/0000-0002-8838-8403
  • Most recently observed institution: Institute of Human Genetics, Technische Universitaet Muenchen, Munich, Germany, German Center for Cardiovascular Research (DZHK), Partner Site Munich Heart Alliance, Munich, Germany, Institute of Human Genetics, Helmholtz Zentrum Muenchen, German Researc

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    • genomics: 5,354 (rank: 3,455 out of 42,763)
    • systems biology: 4,166 (rank: 630 (tie) out of 11,761)

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Preprints

A reference panel of 64,976 haplotypes for genotype imputation

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DeepWAS: Multivariate genotype-phenotype associations by directly integrating regulatory information using deep learning

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Fine-mapping of an expanded set of type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

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Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

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Genetic diagnosis of Mendelian disorders via RNA sequencing

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Cell specific eQTL analysis without sorting cells

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Refining The Accuracy Of Validated Target Identification Through Coding Variant Fine-Mapping In Type 2 Diabetes

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Genetic discovery and translational decision support from exome sequencing of 20,791 type 2 diabetes cases and 24,440 controls from five ancestries

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Genomic analyses for age at menarche identify 389 independent signals and indicate BMI-independent effects of puberty timing on cancer susceptibility

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Narrow-sense heritability estimation of complex traits using identity-by-descent information.

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Genome-wide methylation data mirror ancestry information

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Multi-ancestry GWAS of the electrocardiographic PR interval identifies 210 loci underlying cardiac conduction

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Discovering patterns of pleiotropy in genome-wide association studies

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Genome-wide association meta-analysis of PR interval identifies 47 novel loci associated with atrial and atrioventricular electrical activity

genetics more details view paper
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A Comprehensive Evaluation of the Genetic Architecture of Sudden Cardiac Arrest

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Multi-ancestry analysis of gene-sleep interactions in 126,926 individuals identifies multiple novel blood lipid loci that contribute to our understanding of sleep-associated adverse blood lipid profile

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Cis-epistasis at the LPA locus and risk of coronary artery disease

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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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Evaluation of the causal effect of fibrinogen on incident coronary heart disease via Mendelian randomization

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A genome-wide analysis of DNA methylation identifies a novel association signal for Lp(a) concentrations in the LPA promoter

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Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure

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Genome-wide association study in European patients with congenital heart disease identifies risk loci for transposition of the great arteries and anomalies of the thoracic arteries and veins and expression of discovered candidate genes in the developing heart

genomics more details view paper
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