Shu Wu

A Homozygous Mutation in Human PRICKLE1 Causes an Autosomal-Recessive Progressive Myoclonus Epilepsy-Ataxia Syndrome

Alexander G. Bassuk, Robyn H. Wallace, Aimee C. Buhr et al. · The American Journal of Human Genetics · 2008 · 241 citations · Full text

Life Sciences, Genetics, Neurology +16

Mutations in Prickle Orthologs Cause Seizures in Flies, Mice, and Humans

Hirotaka Tao, J. Robert Manak, Levi P. Sowers et al. · The American Journal of Human Genetics · 2011 · 149 citations · Full text

Life Sciences, Genetics, Neuroscience +11

The PDZ Binding Motif of Human Papillomavirus Type 16 E6 Induces PTPN13 Loss, Which Allows Anchorage-Independent Growth and Synergizes with Ras for Invasive Growth

William C. Spanos, A. Hoover, George F. Harris et al. · Journal of Virology · 2007 · 141 citations · Full text

Medicine, Molecular Biology, Oncology +17

Disruption of the non-canonical Wnt gene PRICKLE2 leads to autism-like behaviors with evidence for hippocampal synaptic dysfunction

Levi P. Sowers, Lipin Loo, Ying Cheng Wu et al. · Molecular Psychiatry · 2013 · 91 citations · Full text

Life Sciences, Neurobiology, Neuroscience +16

Seizures Are Regulated by Ubiquitin-specific Peptidase 9 X-linked (USP9X), a De-Ubiquitinase

Lily Paemka, Vinit B. Mahajan, Salleh N. Ehaideb et al. · PLoS Genetics · 2015 · 76 citations · Full text

Life Sciences, Genetics, Neuroscience +17