Fei-Feng Li - Concepedia

Author

Fei-Feng Li

Harbin Medical University ORCID

Also Known As

FEI-FENG LI, Fei-Feng Li, Fei-Feng 飞凤 Li 黎, Fei-feng Li

Publications

521

Citations

H-Index

Concepts

All Affiliations

Harbin Medical University University of Calgary Second Affiliated Hospital of Harbin Medical University Chinese Academy of Medical Sciences & Peking Union Medical College Heilongjiang Academy of Sciences

About

Fei-Feng Li is an author at Harbin Medical University specializing in medicine, genetics, and genetic epidemiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	153
2	Public Health	2	2	30
3	Natural Sciences	1	1	33
4	Biochemistry	1	1	33
5	Cell Biology	1	1	33

Fei-Feng Li

Publications

471

Citations

H-Index

Page 1

	Year	Citations
MiR-101 Is Involved in Human Breast Carcinogenesis by Targeting Stathmin1 Rui Wang, Hongbin Wang, Chan Juan Hao, PLoS ONE	2012	74
Characterization of Transcriptional Repressor Gene MSX1 Variations for Possible Associations with Congenital Heart Diseases Fei-Feng Li, Ying Han, Shuai Shi, PLoS ONE	2015	34
The Congenital Cataract-Linked G61C Mutation Destabilizes γD-Crystallin and Promotes Non-Native Aggregation Wang Zhang, Hongchen Cai, Fei-Feng Li, PLoS ONE Ocular DiseaseBiochemistryOphthalmologyProtein FoldingPromotes Non-native Aggregation	2011	33
Characterization of Nodal/TGF-Lefty Signaling Pathway Gene Variants for Possible Roles in Congenital Heart Diseases Xia Deng, Jing Zhou, Fei-Feng Li, PLoS ONE	2014	33
Nonsense mutation in the CRYBB2 gene causing autosomal dominant progressive polymorphic congenital coronary cataracts. Fei-Feng Li, Siquan Zhu, Shuzhen Wang, PubMed	2008	32
A Novel Mutation in CACNA1S Gene Associated with Hypokalemic Periodic Paralysis Which has a Gender Difference in the Penetrance Fei-Feng Li, Qianqian Li, Zhen-Xuan Tan, Journal of Molecular Neuroscience Novel MutationGender DifferenceGenetic DisorderGeneticsPhysiology	2011	28
Characterization of SMAD3 Gene Variants for Possible Roles in Ventricular Septal Defects and Other Congenital Heart Diseases Fei-Feng Li, Jing Zhou, Dandan Zhao, PLoS ONE	2015	28
Identification of a Known Mutation in Notch 3 in Familiar CADASIL in China Zhen-Xuan Tan, Fei-Feng Li, Youyang Qu, PLoS ONE	2012	27
A new mutation in BFSP2 (G1091A) causes autosomal dominant congenital lamellar cataracts. Xu Ma, Fei-Feng Li, Shuzhen Wang, PubMed	2008	23
Polymorphisms in the CHIT1 gene: Associations with colorectal cancer Fei-Feng Li, Peng Yan, Zhixun Zhao, Oncotarget Tumor BiologyChinese Han PopulationsMedicineGeneticsGenetic Epidemiology	2016	23

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