Alexander Zimprich

Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology

Alexander Zimprich, Saskia Biskup, Petra Leitner et al. · Neuron · 2004 · 3K citations · Full text

Mendelian Disorder, Genetic Disorder, Parkinson Disease +5

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

Alexander Zimprich, Anna Benet‐Pagès, Walter Struhal et al. · The American Journal of Human Genetics · 2011 · 876 citations · Full text

Late-onset Parkinson Disease, Retromer Complex, Neurodegenerative Diseases +8

Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions

Juliane Winkelmann, Barbara Schormair, Peter Lichtner et al. · Nature Genetics · 2007 · 690 citations

Genome-wide Association Study, Genetic Disorder, Genetics +5

Mutations in the gene encoding ɛ-sarcoglycan cause myoclonus–dystonia syndrome

Alexander Zimprich, Monika Grabowski, Friedrich Asmus et al. · Nature Genetics · 2001 · 474 citations

Mendelian Disorder, Genetic Disorder, Medicine +5

Genetic Structure of Europeans: A View from the North–East

Mari Nelis, Tōnu Esko, Reedik Mägi et al. · PLoS ONE · 2009 · 432 citations · Full text

Genotype-phenotype Association, Molecular Ecology, Human Variation +15