Sarah Lincoln

Overview

Best Publications

• α-Synuclein Locus Triplication Causes Parkinson's Disease

  A. B. Singleton;M. Farrer;J. Johnson;A. Singleton

  5039
  Citations

• Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17

  M. Hutton;C. L. Lendon;P. Rizzu;M. Baker

  4256
  Citations

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

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

  3515
  Citations

• α-synuclein locus duplication as a cause of familial Parkinson's disease

  Marie-Christine Chartier-Harlin;Jennifer M. Kachergus;Christophe Roumier;Vincent Mouroux

  2401
  Citations

• VPS35 Mutations in Parkinson Disease

  Carles Vilariño-Güell;Christian Wider;Owen A. Ross;Justus C. Dachsel

  1056
  Citations

• Comparison of kindreds with parkinsonism and α‐synuclein genomic multiplications

  Matt Farrer;Jennifer Kachergus;Lysia Forno;Sarah Lincoln

  834
  Citations

• Lewy bodies and parkinsonism in families with parkin mutations.

  M Farrer;P Chan;R Chen;L Tan

  632
  Citations

• Identification of a Novel LRRK2 Mutation Linked to Autosomal Dominant Parkinsonism: Evidence of a Common Founder across European Populations

  Jennifer Kachergus;Ignacio F. Mata;Mary Hulihan;Julie P. Taylor

  621
  Citations

• Collaborative analysis of alpha-synuclein gene promoter variability and Parkinson disease.

  Demetrius M. Maraganore;Mariza De Andrade;Alexis Elbaz;Matthew J. Farrer

  620
  Citations

• Human whole genome genotype and transcriptome data for Alzheimer’s and other neurodegenerative diseases

  Mariet Allen;Minerva M. Carrasquillo;Cory Funk;Benjamin D. Heavner

  486
  Citations

• A variant of Alzheimer's disease with spastic paraparesis and unusual plaques due to deletion of exon 9 of presenilin 1

  Richard Crook;Auli Verkkoniemi;Jordi Perez-Tur;Nitin Mehta

  452
  Citations

• A loss of function mutation of presenilin-2 interferes with amyloid beta-peptide production and notch signaling.

  Harald Steiner;Karen Duff;Anja Capell;Helmut Romig

  402
  Citations

• Translation initiator EIF4G1 mutations in familial Parkinson disease

  Marie Christine Chartier-Harlin;Marie Christine Chartier-Harlin;Justus C. Dachsel;Carles Vilariño-Güell;Sarah J. Lincoln

  389
  Citations

• A Chromosome 4P Haplotype Segregating with Parkinson's Disease and Postural Tremor

  Matt Farrer;Katrina Gwinn-Hardy;Manfred Muenter;Fabienne Wavrant DeVrieze

  354
  Citations

• Lack of nigral pathology in transgenic mice expressing human alpha-synuclein driven by the tyrosine hydroxylase promoter.

  Yasuji Matsuoka;Miquel Vila;Sarah Lincoln;Alison McCormack

  339
  Citations

• Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementia

  Rosa Rademakers;Jason L. Eriksen;Matt Baker;Todd Robinson

  333
  Citations

• Impaired dopaminergic neurotransmission and microtubule-associated protein tau alterations in human LRRK2 transgenic mice.

  H. L. Melrose;J. C. Dächsel;B. Behrouz;S. J. Lincoln

  309
  Citations

• Case-control study of the ubiquitin carboxy-terminal hydrolase L1 gene in Parkinson's disease.

  D. M. Maraganore;M. J. Farrer;J. A. Hardy;S. J. Lincoln

  303
  Citations

• Parkinsonism, Lrrk2 G2019S, and tau neuropathology.

  A. Rajput;D. W. Dickson;C. A. Robinson;C. A. Robinson;O. A. Ross

  280
  Citations

• Lrrk2 pathogenic substitutions in Parkinson's disease

  Ignacio F. Mata;Jennifer M. Kachergus;Julie P. Taylor;Sarah Lincoln

  273
  Citations