Daan C. Velseboer

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

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

Evolution of mild cognitive impairment in Parkinson disease

Mark Broeders, Rob M.A. de Bie, Daan C. Velseboer et al. · Neurology · 2013 · 199 citations

Genome-wide association study confirms extant PD risk loci among the Dutch

Javier Simón‐Sánchez, Jacobus J. van Hilten, Bart van de Warrenburg et al. · European Journal of Human Genetics · 2011 · 181 citations · Full text

Genome-wide Association Study, Genotype-phenotype Association, Genetics +6