Alexander Zimprich

Overview

Best Publications

• Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology

  Alexander Zimprich;Alexander Zimprich;Saskia Biskup;Petra Leitner;Peter Lichtner

  3515
  Citations

• Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies

  Mike A Nalls;Cornelis Blauwendraat;Costanza L Vallerga;Karl Heilbron

  2354
  Citations

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

  Alexander Zimprich;Anna Benet-Pagès;Walter Struhal;Elisabeth Graf

  1067
  Citations

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

  Juliane Winkelmann;Barbara Schormair;Peter Lichtner;Stephan Ripke

  780
  Citations

• Mutations in the gene encoding epsilon-sarcoglycan cause myoclonus-dystonia syndrome.

  Alexander Zimprich;Monika Grabowski;Friedrich Asmus;Markus Naumann

  563
  Citations

• Genetic structure of Europeans: a view from the North-East

  Mari Nelis;Mari Nelis;Tõnu Esko;Tõnu Esko;Reedik Mägi;Fritz Zimprich

  412
  Citations

• Type and frequency of mutations in the LRRK2 gene in familial and sporadic Parkinson's disease*

  Daniela Berg;Katherine J. Schweitzer;Petra Leitner;Alexander Zimprich

  352
  Citations

• Autosomal dominant parkinsonism associated with variable synuclein and tau pathology

  Zbigniew K. Wszolek;R. F. Pfeiffer;Y. Tsuboi;R. J. Uitti

  339
  Citations

• PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome.

  Barbara Schormair;David Kemlink;Darina Roeske;Gertrud Eckstein

  336
  Citations

• Multiple regions of alpha-synuclein are associated with Parkinson's disease.

  Jakob C. Mueller;Julia Fuchs;Anne Hofer;Alexander Zimprich

  280
  Citations

• Variant in the sequence of the LINGO1 gene confers risk of essential tremor.

  Hreinn Stefansson;Stacy Steinberg;Hjorvar Petursson;Omar Gustafsson

  271
  Citations

• Cloning and expression of an isoform of the rat μ opioid receptor (rMOR1B) which differs in agonist induced desensitization from rMOR1

  Alexander Zimprich;Tatiana Simon;Volker Höllt

  269
  Citations

• The PARK8 Locus in Autosomal Dominant Parkinsonism: Confirmation of Linkage and Further Delineation of the Disease-Containing Interval

  Alexander Zimprich;Bertram Müller-Myhsok;Matthew Farrer;Petra Leitner

  251
  Citations

• Association of an ABCB1 gene haplotype with pharmacoresistance in temporal lobe epilepsy.

  F. Zimprich;R. Sunder-Plassmann;E. Stogmann;A. Gleiss

  245
  Citations

• Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1.

  Juliane Winkelmann;Darina Czamara;Barbara Schormair;Franziska Knauf

  215
  Citations

• The epsilon-sarcoglycan gene (SGCE), mutated in myoclonus-dystonia syndrome, is maternally imprinted

  Monika Grabowski;Alexander Zimprich;Bettina Lorenz-Depiereux;Vera Kalscheuer

  205
  Citations

• Myoclonus-dystonia syndrome: epsilon-sarcoglycan mutations and phenotype.

  Friedrich Asmus;Alexander Zimprich;Sophie Tezenas Du Montcel;Christian Kabus

  198
  Citations

• The Parkinson's disease VPS35[D620N] mutation enhances LRRK2-mediated Rab protein phosphorylation in mouse and human.

  Rafeeq Mir;Francesca Tonelli;Pawel Lis;Thomas Macartney

  187
  Citations

• Mitochondrial damage-associated inflammation highlights biomarkers in PRKN/PINK1 parkinsonism.

  Max Borsche;Inke R König;Sylvie Delcambre;Simona Petrucci;Simona Petrucci

  172
  Citations

• An allelic variation in the human prodynorphin gene promoter alters stimulus-induced expression.

  Alexander Zimprich;Jürgen Kraus;Michael Wöltje;Peter Mayer

  141
  Citations