Dong-Hui Chen - Concepedia

Author

Dong-Hui Chen

University of Washington

Also Known As

Dong-Hui Chen

Publications

809

Citations

H-Index

Concepts

All Affiliations

University of Washington Geriatric Research Education and Clinical Center VA Puget Sound Health Care System

About

Dong-Hui Chen is an author at University of Washington specializing in medicine, genetics, and neurogenetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	556
2	Natural Sciences	1	1	50
3	Genetic Medicine	1	1	50
4	Molecular Biology	1	1	50
5	Molecular Genetics	1	1	50

Dong-Hui Chen

Publications

771

Citations

H-Index

Page 1

	Year	Citations
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, The American Journal of Human Genetics Neurodegenerative DiseasesRegulatory DomainMolecular NeuroscienceMissense MutationsGenetic Disorder	2003	238
Ataxia-Pancytopenia Syndrome Is Caused by Missense Mutations in SAMD9L Dong-Hui Chen, Jennifer E. Below, Akiko Shimamura, The American Journal of Human Genetics Genetic DisorderGeneticsAtaxia-pancytopenia Syndrome IsPathologyDisease Gene Identification	2016	174
Spinocerebellar Ataxia Type 14 Caused by a Mutation in Protein Kinase C γ Ichiro Yabe, Hidenao Sasaki, Dong-Hui Chen, Archives of Neurology	2003	123
Presence of Alanine-to-Valine Substitutions in Myofibrillogenesis Regulator 1 in Paroxysmal Nonkinesigenic Dyskinesia Dong-Hui Chen, Mark Matsushita, Shirley Rainier, Archives of Neurology	2005	53
Cerebral cavernous malformation: novel mutation in a Chinese family and evidence for heterogeneity Dong-Hui Chen, Hillary Lipe, Zhen Qin, Journal of the Neurological Sciences Developmental AnomalyNovel MutationChinese FamilyGenetic DisorderCerebral Cavernous Malformation	2002	52
Two Novel Mutations in<i>ABHD12</i>: Expansion of the Mutation Spectrum in PHARC and Assessment of Their Functional Effects Dong-Hui Chen, Alipi V. Naydenov, Jacqueline L. Blankman, Human Mutation Short StatureGeneticsMolecular BiologyMolecular GeneticsDisease Gene Identification	2013	50
A novel mutation in FHL1 in a family with X-linked scapuloperoneal myopathy: Phenotypic spectrum and structural study of FHL1 mutations Dong-Hui Chen, Wendy H. Raskind, William W. Parson, Journal of the Neurological Sciences X-linked Scapuloperoneal MyopathyMendelian DisorderGenetic DisorderMedicineGenetics	2010	42
Novel mutations highlight the key role of the ankyrin repeat domain in <i>TRPV4</i> -mediated neuropathy Jeremy M. Sullivan, Christina M. Zimanyi, William H. Aisenberg, Neurology Genetics	2015	25
Assessment of mutations in KCNN2 and ZNF135 to patient neurological symptoms Vijeta Raghuram, Sydney Weber, Jacob Raber, Neuroreport	2017	14

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