Bahareh Behrouz

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

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

Progressive dopaminergic alterations and mitochondrial abnormalities in LRRK2 G2019S knock-in mice

Mei Yue, Kelly M. Hinkle, Paul Davies et al. · Neurobiology of Disease · 2015 · 270 citations · Full text

Progressive Dopaminergic Alterations, Mitophagy, Mitochondrial Abnormalities +8

LRRK2 knockout mice have an intact dopaminergic system but display alterations in exploratory and motor co-ordination behaviors

Kelly M. Hinkle, Mei Yue, Bahareh Behrouz et al. · Molecular Neurodegeneration · 2012 · 188 citations · Full text