Alexandra I. Soto‐Ortolaza

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

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

Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case–control study

Owen A. Ross, Alexandra I. Soto‐Ortolaza, Michael G. Heckman et al. · The Lancet Neurology · 2011 · 339 citations · Full text

Case–control Study, Parkinson Disease, Lrrk2 Exonic Variants +5

Chronic traumatic encephalopathy pathology in a neurodegenerative disorders brain bank

Kevin F. Bieniek, Owen A. Ross, Kerry A. Cormier et al. · Acta Neuropathologica · 2015 · 322 citations · Full text

Neurodegenerative Diseases, Neuropsychology, Neurological Disorder +11

Translation Initiator EIF4G1 Mutations in Familial Parkinson Disease

Marie‐Christine Chartier‐Harlin, Justus C. Dächsel, Carles Vilariño‐Güell et al. · The American Journal of Human Genetics · 2011 · 299 citations · Full text

Familial Parkinson Disease, Mendelian Disorder, Genetic Disorder +5