Ming-Hui Wei - Concepedia

Author

Ming-Hui Wei

National Cancer Institute ORCID

Also Known As

Ming-Hui Wei

Publications

1.8K

Citations

H-Index

Concepts

All Affiliations

National Cancer Institute National Institutes of Health Science Applications International Corporation (United States)Center for Cancer Research Frederick National Laboratory for Cancer Research

About

Ming-Hui Wei is an author at National Cancer Institute specializing in medicine, cell biology, and cancer genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	816
2	Cell Biology	3	3	188
3	Cellular Physiology	1	1	64
4	Neurology	1	1	106
5	Neuroscience	1	1	106

Ming-Hui Wei

Publications

1.7K

Citations

H-Index

Page 1

	Year	Citations
Mutations in the Fumarate Hydratase Gene Cause Hereditary Leiomyomatosis and Renal Cell Cancer in Families in North America Jorge R. Toro, Michael L. Nickerson, Ming-Hui Wei, The American Journal of Human Genetics UrologyNorth AmericaMedicineGeneticsPathology	2003	628
Down-regulation of transmembrane carbonic anhydrases in renal cell carcinoma cell lines by wild-type von Hippel-Lindau transgenes Sergey V. Ivanov, Igor Kuzmin, Ming-Hui Wei, Proceedings of the National Academy of Sciences	1998	393
Lung Cysts, Spontaneous Pneumothorax, and Genetic Associations in 89 Families with Birt-Hogg-Dubé Syndrome Jorge R. Toro, Stephen E. Pautler, Laveta Stewart, American Journal of Respiratory and Critical Care Medicine	2007	349
Cerebellar Ataxia, Seizures, Premature Death, and Cardiac Abnormalities in Mice with Targeted Disruption of the Cacna2d2 Gene Sergey V. Ivanov, Jerrold M. Ward, Lino Tessarollo, American Journal Of Pathology Knockout MouseSynaptic SignalingDegenerative DiseaseNeuroscienceCerebellar Ataxia	2004	106
In silico-initiated cloning and molecular characterization of a novel human member of the L1 gene family of neural cell adhesion molecules Ming-Hui Wei, Irina Karavanova, Sergey V. Ivanov, Human Genetics Novel Human MemberDevelopmental BiologyL1 Gene FamilyCell InteractionCell Adhesion	1998	64
Computerized polymorphic marker identification: Experimental validation and a predicted human polymorphism catalog John W. Fondon, Gina M. Mele, Ruth I. Brezinschek, Proceedings of the National Academy of Sciences	1998	55
The chromosome 2p21 region harbors a complex genetic architecture for association with risk for renal cell carcinoma Summer S. Han, Meredith Yeager, Lee E. Moore, Human Molecular Genetics	2011	41
H255Y and K508R missense mutations in tumour suppressor<i>folliculin (FLCN)</i>promote kidney cell proliferation Hisashi Hasumi, Yukiko Hasumi, Masaya Baba, Human Molecular Genetics Germline H255yPathologyDisease Gene IdentificationFlcn FunctionCancer Biology	2016	18

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