Hereditary Early-Onset Parkinson's Disease Caused by Mutations in <i>PINK1</i>Enza Maria Valente, Nicholas Wood, Patrick M. Abou‐Sleiman et al.|Science|2004Cited by 3.5k
PINK1 cleavage at position A103 by the mitochondrial protease PARLEmma Deas, Nicholas Wood|Human Molecular Genetics|2010Cited by 485
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
PINK1 Is Necessary for Long Term Survival and Mitochondrial Function in Human Dopaminergic NeuronsAlison Wood‐Kaczmar, Nicholas Wood|PLoS ONE|2008Cited by 313
Glucocerebrosidase inhibition causes mitochondrial dysfunction and free radical damageMichael W. J. Cleeter, Anthony H.V. Schapira, Kai‐Yin Chau et al.|Neurochemistry International|2012Cited by 204