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Peter Lichtner

Helmholtz Zentrum MünchenORCID https://orcid.org/0000-0001-5981-7996

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Impact (2-yr)

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Top Publications

Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology

Neuron20043,023 citations

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

Nature Genetics20142,087 citations

Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores

The American Journal of Human Genetics20151,472 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

Peter Lichtner · Scinovex