Ryan J. Uitti

Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology

Alexander Zimprich, Saskia Biskup, Petra Leitner et al. · Neuron · 2004 · 3.1K citations · Full text

Life Sciences, Genetics, Neuroscience +14

VPS35 Mutations in Parkinson Disease

Carles Vilariño‐Güell, Christian Wider, Owen A. Ross et al. · The American Journal of Human Genetics · 2011 · 893 citations · Full text

Life Sciences, Genetics, Neuroscience +13

Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy

Günter U. Höglinger, Dennis W. Dickson, Patrick Sleiman et al. · Nature Genetics · 2011 · 632 citations · Full text

Life Sciences, Genetics, Neurology +10

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 · 579 citations · Full text

Life Sciences, Molecular Genetics, Neuroscience +5

Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration

Jennifer Gass, Ashley Cannon, Ian R. Mackenzie et al. · Human Molecular Genetics · 2006 · 578 citations

Life Sciences, Genetics, Molecular Genetics +17