Timothy Lynch

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

Mike Hutton, Corinne Lendon, Patrizia Rizzu et al. · Nature · 1998 · 3.5K citations

Neurodegenerative Diseases, Mendelian Disorder, Genetic Disorder +8

Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study

Daniel G. Healy, Mario Falchi, Sean S. O’Sullivan et al. · The Lancet Neurology · 2008 · 1.5K citations · Full text

VPS35 Mutations in Parkinson Disease

Carles Vilariño‐Güell, Christian Wider, Owen A. Ross et al. · The American Journal of Human Genetics · 2011 · 867 citations · Full text

Mendelian Disorder, Parkinson Disease, Genetics +3

Association of an Extended Haplotype in the Tau Gene with Progressive Supranuclear Palsy

Mary V. Baker, Irene Litvan, Henry Houlden et al. · Human Molecular Genetics · 1999 · 793 citations · Full text

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

Jennifer M. Kachergus, Ignácio F. Mata, Mary Hulihan et al. · The American Journal of Human Genetics · 2005 · 534 citations · Full text

Molecular Neuroscience, Mendelian Disorder, Genetic Disorder +7