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Thomas Meitinger

Klinikum rechts der IsarORCID https://orcid.org/0000-0002-8838-8403

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Impact (2-yr)

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Top Publications

A reference panel of 64,976 haplotypes for genotype imputation

Nature Genetics20163,228 citations

Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology

Neuron20043,023 citationsCorresponding

Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index

Nature Genetics20102,969 citations

Defining the role of common variation in the genomic and biological architecture of adult human height

Nature Genetics20142,087 citations

A Mutation in VPS35, Encoding a Subunit of the Retromer Complex, Causes Late-Onset Parkinson Disease

The American Journal of Human Genetics2011898 citations

Hypothetical LOC387715 is a second major susceptibility gene for age-related macular degeneration, contributing independently of complement factor H to disease risk

Human Molecular Genetics2005789 citations

Genetics Meets Metabolomics: A Genome-Wide Association Study of Metabolite Profiles in Human Serum

PLoS Genetics2008765 citations

Meta-Analysis of 28,141 Individuals Identifies Common Variants within Five New Loci That Influence Uric Acid Concentrations

PLoS Genetics2009655 citations

Thomas Meitinger · Scinovex