Stephanie A. Cobb

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

Translation Initiator EIF4G1 Mutations in Familial Parkinson Disease

Marie‐Christine Chartier‐Harlin, Justus C. Dächsel, Carles Vilariño‐Güell et al. · The American Journal of Human Genetics · 2011 · 299 citations · Full text

Familial Parkinson Disease, Mendelian Disorder, Genetic Disorder +5

Lrrk2 pathogenic substitutions in Parkinson's disease

Ignácio F. Mata, Jennifer M. Kachergus, Julie P. Taylor et al. · Neurogenetics · 2005 · 231 citations

Mitophagy, Lrrk2 Pathogenic Substitutions, Receptor Tyrosine Kinase +5

Parkinsonism, Lrrk2 G2019S, and tau neuropathology

Ali H. Rajput, Dennis W. Dickson, Christopher A. Robinson et al. · Neurology · 2006 · 212 citations

LINGO1 and LINGO2 variants are associated with essential tremor and Parkinson disease

Carles Vilariño‐Güell, Christian Wider, Owen A. Ross et al. · Neurogenetics · 2010 · 127 citations · Full text

Essential Tremor, Parkinson Disease, Neurolinguistics +5