Sophie Winder‐Rhodes

Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease

Laurie Robak, Iris E. Jansen, Jeroen van Rooij et al. · Brain · 2017 · 440 citations · Full text

Genetics, Genetic Epidemiology, Variant Burden +16

Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy

Suzanne Lesage, Valérie Drouet, Elisa Majounie et al. · The American Journal of Human Genetics · 2016 · 427 citations · Full text

Cell Autophagy, Mitophagy, Mitochondrial Function +7

Characterizing mild cognitive impairment in incident Parkinson disease

Alison J. Yarnall, David P. Breen, Gordon W. Duncan et al. · Neurology · 2013 · 409 citations · Full text

Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease

Alexandria Beilina, Iakov N. Rudenko, Alice Kaganovich et al. · Proceedings of the National Academy of Sciences · 2014 · 362 citations · Full text

Glucocerebrosidase mutations influence the natural history of Parkinson’s disease in a community-based incident cohort

Sophie Winder‐Rhodes, Jonathan Evans, Maria Ban et al. · Brain · 2013 · 287 citations · Full text