John Wolff

Missense Mutations in the Regulatory Domain of PKCγ: A New Mechanism for Dominant Nonepisodic Cerebellar Ataxia

Dong-Hui Chen, Zoran Brkanac, Christophe L. M. J. Verlinde et al. · The American Journal of Human Genetics · 2003 · 238 citations · Full text

Neurodegenerative Diseases, Regulatory Domain, Molecular Neuroscience +10

Ataxia-Pancytopenia Syndrome Is Caused by Missense Mutations in SAMD9L

Dong-Hui Chen, Jennifer E. Below, Akiko Shimamura et al. · The American Journal of Human Genetics · 2016 · 174 citations · Full text

Genetic Disorder, Genetics, Ataxia-pancytopenia Syndrome Is +3

CMT2C with vocal cord paresis associated with short stature and mutations in the <i>TRPV4</i> gene

D.-H. Chen, Youngmee Sul, MaryAnn Weiss et al. · Neurology · 2010 · 85 citations · Full text

The clinical and genetic spectrum of spinocerebellar ataxia 14

D. -H. Chen, Patrick J. Cimino, Laura P.W. Ranum et al. · Neurology · 2005 · 81 citations

Autosomal dominant sensory/motor neuropathy with Ataxia (SMNA): Linkage to chromosome 7q22‐q32

Zoran Brkanac, Magali Fernandez, Mark Matsushita et al. · American Journal of Medical Genetics · 2002 · 81 citations