Jan Aasly

Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease

E. Sidransky, Mike A. Nalls, Jan Aasly et al. · New England Journal of Medicine · 2009 · 2.1K citations · Full text

Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study

Daniel G. Healy, Mario Falchi, Sean S. O’Sullivan et al. · The Lancet Neurology · 2008 · 1.5K citations · Full text

VPS35 Mutations in Parkinson Disease

Carles Vilariño‐Güell, Christian Wider, Owen A. Ross et al. · The American Journal of Human Genetics · 2011 · 867 citations · Full text

Mendelian Disorder, Parkinson Disease, Genetics +3

Alpha‐synuclein p.H50Q, a novel pathogenic mutation for Parkinson's disease

Silke Appel‐Cresswell, Carles Vilariño‐Güell, Mary Joy Encarnacion et al. · Movement Disorders · 2013 · 650 citations

Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids

Rosa Rademakers, Matt Baker, Alexandra M. Nicholson et al. · Nature Genetics · 2011 · 566 citations · Full text

Inflammation, Disease Mechanism, Pathogenesis +8