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Human Mutation|September 13, 2013
Two novel mutations in ABHD12: expansion of the mutation spectrum in PHARC and assessment of their functional effectsDong-Hui Chen, Alipi Naydenov, Jacqueline L Blankman, et al.
Frontiers in Immunology|August 1, 2022
NOTCH1 mutation associates with impaired immune response and decreased relapse-free survival in patients with resected T1-2N0 laryngeal cancerXiao-Yang Gong, Hai-Bin Chen, Li-Qing Zhang, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 15, 2026
Heterogenous Neuropathology in a Pedigree with RAB39B-Related Parkinson's DiseaseCaitlin Latimer, Oswaldo Lorenzo-Betancor, Dong-Hui Chen, et al.
European Journal of Medicinal Chemistry|May 18, 2026
Discovery of NTQ2494, a potent and orally bioavailable inhibitor of AXL kinase for the treatment of human tumorsLin-Lin Zhang, Ben Niu, Dong-Hui Chen, et al.
Science Signaling|September 27, 2022
Mutations in protein kinase Cγ promote spinocerebellar ataxia type 14 by impairing kinase autoinhibitionCaila A Pilo, Timothy R Baffi, Alexandr P Kornev, et al.
Human Molecular Genetics|April 19, 2013
Altered splicing of ATP6AP2 causes X-linked parkinsonism with spasticity (XPDS)Olena Korvatska, Nicholas S Strand, Jason D Berndt, et al.
Annals of Neurology|April 5, 2014
Gain-of-function ADCY5 mutations in familial dyskinesia with facial myokymiaYing-Zhang Chen, Jennifer R Friedman, Dong-Hui Chen, et al.
Neurology|November 6, 2015
ADCY5-related dyskinesia: Broader spectrum and genotype-phenotype correlationsDong-Hui Chen, Aurélie Méneret, Jennifer R Friedman, et al.
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