Justus C. Dächsel

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

DCTN1 mutations in Perry syndrome

Matthew J. Farrer, Mary Hulihan, Jennifer M. Kachergus et al. · Nature Genetics · 2009 · 319 citations · Full text

Perry Syndrome, Mendelian Disorder, Genetic Disorder +4

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

Impaired dopaminergic neurotransmission and microtubule-associated protein tau alterations in human LRRK2 transgenic mice

Heather L. Melrose, Justus C. Dächsel, Bahareh Behrouz et al. · Neurobiology of Disease · 2010 · 276 citations · Full text

Knockout Mouse, Neurodegenerative Diseases, Signal Transduction +10

Parkinsonism, Lrrk2 G2019S, and tau neuropathology

Ali H. Rajput, Dennis W. Dickson, Christopher A. Robinson et al. · Neurology · 2006 · 212 citations