Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent MitophagySuzanne Lesage, Michel Borg, Valérie Drouet et al.|The American Journal of Human Genetics|2016Cited by 449
A Multicenter Study of Glucocerebrosidase Mutations in Dementia With Lewy BodiesMichael A. Nalls, John Q. Trojanowski, Raquel Durán et al.|JAMA Neurology|2013Cited by 444
Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson diseaseAlexandria Beilina, Sean Chong, Iakov N. Rudenko et al.|Proceedings of the National Academy of Sciences|2014Cited by 367
Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case–control studyOwen A. Ross, Hiroyuki Tomiyama, Alexandra I. Soto‐Ortolaza et al.|The Lancet Neurology|2011Cited by 344
Penetrance estimate of <i>LRRK2</i> p.G2019S mutation in individuals of non‐Ashkenazi Jewish ancestryAnnie Lee, Karen Marder, Yuanjia Wang et al.|Movement Disorders|2017Cited by 170