William P. Gilks

Hereditary Early-Onset Parkinson's Disease Caused by Mutations in <i>PINK1</i>

Enza Maria Valente, Patrick M. Abou‐Sleiman, Viviana Caputo et al. · Science · 2004 · 3.4K citations · Full text

Neurodegenerative Diseases, Mitophagy, Mitochondrial Function +14

Cloning of the Gene Containing Mutations that Cause PARK8-Linked Parkinson's Disease

Coro Paisán‐Ruíz, Shushant Jain, E. Whitney Evans et al. · Neuron · 2004 · 2.4K citations · Full text

Neurodegenerative Diseases, Genetic Disorder, Parkinson Disease +9

A common LRRK2 mutation in idiopathic Parkinson's disease

William P. Gilks, Patrick M. Abou‐Sleiman, Sonia Gandhi et al. · The Lancet · 2005 · 777 citations

Mendelian Disorder, Parkinson Disease, Pathology +3

Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data

Naheed L. Khan, Shushant Jain, John Lynch et al. · Brain · 2005 · 319 citations

Motor Dysfunction, Neurological Disorder, Corticobasal Degeneration +22

Altered cleavage and localization of PINK1 to aggresomes in the presence of proteasomal stress

Miratul M. K. Muqit, Patrick M. Abou‐Sleiman, Adrian T. Saurin et al. · Journal of Neurochemistry · 2006 · 166 citations · Full text

Mitophagy, Proteasome, Molecular Biology +17