Fei-Feng Li

528 citations

29 papers · 377 · h-index 14

Impact in

Cancer Research
- MicroRNA in disease regulation
- Cancer-related molecular mechanisms research
Molecular Biology
- Connexins and lens biology
- Circular RNAs in diseases
- Congenital heart defects research

Papers in

Molecular Biology 16
- Congenital heart defects research 6
- Connexins and lens biology 4
Oncology 6

Co-authors: Shu‐Lin Liu (17 shared papers)Xu Ma (5 shared papers)Meng Zhang (4 shared papers)Shuzhen Wang (3 shared papers)Peng Yan (6 shared papers)Yi Cui (1 shared paper)Yi Hu (1 shared paper)Xiaochen Han (1 shared paper)
Journals: PLoS ONE (6 papers)Oncotarget (3 papers)Bioscience Reports (1 paper)Gene (1 paper)The European Physical Journal D (1 paper)
Partner nations: China Canada

In The Last Decade

Fei-Feng Li

27 papers receiving 374 citations

Peers

Countries citing papers authored by Fei-Feng Li

Since Specialization

Citations

This map shows the geographic impact of Fei-Feng Li's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Fei-Feng Li with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Fei-Feng Li more than expected).

Fields of papers citing papers by Fei-Feng Li

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Fei-Feng Li. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Fei-Feng Li. The network helps show where Fei-Feng Li may publish in the future.

Co-authors

The 25 scholars most cited alongside Fei-Feng Li, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Fei-Feng Li Line = papers co-authored together Fei-Feng Li links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 29 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	MiR-101 Is Involved in Human Breast Carcinogenesis by Targeting Stathmin1 PLoS ONE ·Rui Wang, Hongbin Wang, Chan Juan Hao, Yi Cui, Xiaochen Han, Yi Hu, Fei-Feng Li, Hong-Fei Xia, Xu Ma	2012	63
2	Nonsense mutation in the CRYBB2 gene causing autosomal dominant progressive polymorphic congenital coronary cataracts. PubMed ·Fei-Feng Li, Siquan Zhu, Shuzhen Wang, Chang Gao, Shangzhi Huang, Meng Zhang, Xu Ma	2008	30
3	The Congenital Cataract-Linked G61C Mutation Destabilizes γD-Crystallin and Promotes Non-Native Aggregation PLoS ONE ·Wang Zhang, Hongchen Cai, Fei-Feng Li, Yibo Xi, Xu Ma, Yong‐Bin Yan	2011	29
4	A Novel Mutation in CACNA1S Gene Associated with Hypokalemic Periodic Paralysis Which has a Gender Difference in the Penetrance Journal of Molecular Neuroscience ·Fei-Feng Li, Qianqian Li, Zhen-Xuan Tan, Siyao Zhang, Ji Liu, Erying Zhao, Guichun Yu, Jin Zhou, Liming Zhang, Shu‐Lin Liu	2011	24
5	Characterization of Nodal/TGF-Lefty Signaling Pathway Gene Variants for Possible Roles in Congenital Heart Diseases PLoS ONE ·Xia Deng, Jing Zhou, Fei-Feng Li, Peng Yan, Erying Zhao, Hao Ling, Kaijiang Yu, Shu‐Lin Liu	2014	21
6	Identification of a Known Mutation in Notch 3 in Familiar CADASIL in China PLoS ONE ·Zhen-Xuan Tan, Fei-Feng Li, Youyang Qu, Ji Liu, Guirong Liu, Jin Zhou, Yulan Zhu, Shu‐Lin Liu	2012	20
7	A new mutation in BFSP2 (G1091A) causes autosomal dominant congenital lamellar cataracts. PubMed ·Xu Ma, Fei-Feng Li, Shuzhen Wang, Chang Gao, Meng Zhang, Siquan Zhu	2008	19
8	Identification of two novel critical mutations in PCNT gene resulting in microcephalic osteodysplastic primordial dwarfism type II associated with multiple intracranial aneurysms Metabolic Brain Disease ·Fei-Feng Li, Xudong Wang, Minwei Zhu, Zhi-Hong Lou, Qiong Zhang, Chunyu Zhu, Honglin Feng, Zhiguo Lin, Shu‐Lin Liu	2015	17
9	Characterization of SMAD3 Gene Variants for Possible Roles in Ventricular Septal Defects and Other Congenital Heart Diseases PLoS ONE ·Fei-Feng Li, Jing Zhou, Dandan Zhao, Peng Yan, Xia Li, Ying Han, Xian-Shu Li, Guiyu Wang, Kaijiang Yu, Shu‐Lin Liu	2015	16
10	Characterization of variations in IL23A and IL23R genes: possible roles in multiple sclerosis and other neuroinflammatory demyelinating diseases Aging ·Fei-Feng Li, Xidong Zhu, Peng Yan, Meihua Jin, Hui Yue, Qiong Zhang, Jin Fu, Shu‐Lin Liu	2016	16
11	Autosomal Dominant Congenital Nuclear Cataracts Caused by a CRYAA Gene Mutation Current Eye Research ·Fei-Feng Li, Min Yang, Xu Ma, Qiong Zhang, Meng Zhang, Shuzhen Wang, Siquan Zhu	2010	14
12	Exciting rogue waves, breathers, and solitons in coherent atomic media Communications in Theoretical Physics ·Z. Y. Li, Fei-Feng Li, Hui‐jun Li	2020	13
13	Polymorphisms in the CHIT1 gene: Associations with colorectal cancer Oncotarget ·Fei-Feng Li, Peng Yan, Zhixun Zhao, Zheng Liu, Dawei Song, Xingwang Zhao, Xishan Wang, Guiyu Wang, Shu‐Lin Liu	2016	13
14	Identification of epigenetic factor KAT2B gene variants for possible roles in congenital heart diseases Bioscience Reports ·Yongsheng Hou, Jingzhi Wang, Shuai Shi, Ying Han, Yue Zhang, Jixin Zhi, Chao Xu, Fei-Feng Li, Guiyu Wang, Shu‐Lin Liu	2020	13
15	Characterization of Transcriptional Repressor Gene MSX1 Variations for Possible Associations with Congenital Heart Diseases PLoS ONE ·Fei-Feng Li, Ying Han, Shuai Shi, Xia Li, Xidong Zhu, Jing Zhou, Qingliang Shao, Xueqi Li, Shu‐Lin Liu	2015	12
16	Inherited neurovascular diseases affecting cerebral blood vessels and smooth muscle Metabolic Brain Disease ·Christine Sam, Fei-Feng Li, Shu‐Lin Liu	2015	12
17	Identification of a novel mutation associated with familial adenomatous polyposis and colorectal cancer International Journal of Molecular Medicine ·Fei-Feng Li, Zheng Liu, Peng Yan, Xin Shao, Xia Deng, Christine Sam, Yinggang Chen, Yongpeng Xu, Xishan Wang, Guiyu Wang, Shu‐Lin Liu	2015	11
18	Combined effects of age and polymorphisms in Notch3 in the pathogenesis of cerebral infarction disease Metabolic Brain Disease ·Chunyu Zhu, Yue Wang, Qingxuan Zeng, Yu Qian, Huan Li, Zixia Yang, Yamei Yang, Qiong Zhang, Fei-Feng Li, Shu‐Lin Liu	2016	10
19	Isobaric Tags for Relative and Absolute Quantitation in Proteomic Analysis of Potential Biomarkers in Invasive Cancer, Ductal Carcinoma In Situ, and Mammary Fibroadenoma Frontiers in Oncology ·Hao Wu, Xianyu Zhang, Ming Niu, Fei-Feng Li, Song Gao, Wei Wei, Siwei Li, Xing-Da Zhang, Shu‐Lin Liu, Da Pang	2020	6
20	Characterization of soluble N-ethylmaleimide-sensitive factor attachment protein receptor gene STX18 variations for possible roles in congenital heart diseases Gene ·Xia Li, Shuai Shi, Fei-Feng Li, Rui Cheng, Ying Han, Liwei Diao, Qiong Zhang, Jixin Zhi, Shu‐Lin Liu	2016	6

About Fei-Feng Li

Fei-Feng Li is a scholar working on Molecular Biology, Oncology, Epidemiology, Neurology and Rheumatology, having authored 29 papers that have together received 377 indexed citations. Recurring topics across this work include Congenital heart defects research (6 papers), Congenital Heart Disease Studies (5 papers), Connexins and lens biology (4 papers), Cerebrovascular and genetic disorders (4 papers), Moyamoya disease diagnosis and treatment (3 papers), Intraocular Surgery and Lenses (3 papers), Nonlinear Photonic Systems (2 papers) and Yersinia bacterium, plague, ectoparasites research (2 papers). The work is most often cited by research in Cancer Research (73 citations), Molecular Biology (256 citations), Ophthalmology (33 citations), Neurology (24 citations) and Genetics (77 citations). Fei-Feng Li has collaborated with scholars based in China and Canada. Frequent co-authors include Shu‐Lin Liu, Xu Ma, Meng Zhang, Shuzhen Wang, Peng Yan, Yi Cui, Yi Hu, Xiaochen Han, Hong-Fei Xia and Chang Gao. Their work appears in journals such as PLoS ONE, Oncotarget, Bioscience Reports, Gene and The European Physical Journal D.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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Fei-Feng Li

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Fei-Feng Li

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About Fei-Feng Li

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