Identification of a Japanese family with LRRK2 p.R1441G-related Parkinson's disease

Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology

Alexander Zimprich, Saskia Biskup, Petra Leitner et al. · Neuron · 2004 · 3K citations · Full text

Mendelian Disorder, Genetic Disorder, Parkinson Disease +5

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

The spectrum of nonmotor symptoms in early Parkinson disease

Tien K. Khoo, Alison J. Yarnall, Gordon W. Duncan et al. · Neurology · 2013 · 420 citations · Full text

Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case–control study

Owen A. Ross, Alexandra I. Soto‐Ortolaza, Michael G. Heckman et al. · The Lancet Neurology · 2011 · 339 citations · Full text

Case–control Study, Parkinson Disease, Lrrk2 Exonic Variants +5

Lrrk2 and Lewy body disease

Owen A. Ross, Mathias Toft, Andrew J. Whittle et al. · Annals of Neurology · 2006 · 266 citations