Fei-Feng Li

528 total citations
29 papers, 377 citations indexed

About

Fei-Feng Li is a scholar working on Molecular Biology, Oncology and Epidemiology. According to data from OpenAlex, Fei-Feng Li has authored 29 papers receiving a total of 377 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 6 papers in Oncology and 5 papers in Epidemiology. Recurrent topics in Fei-Feng Li's work include Congenital heart defects research (6 papers), Congenital Heart Disease Studies (5 papers) and Connexins and lens biology (4 papers). Fei-Feng Li is often cited by papers focused on Congenital heart defects research (6 papers), Congenital Heart Disease Studies (5 papers) and Connexins and lens biology (4 papers). Fei-Feng Li collaborates with scholars based in China and Canada. Fei-Feng Li's co-authors include Shu‐Lin Liu, Xu Ma, Meng Zhang, Shuzhen Wang, Peng Yan, Hong-Fei Xia, Rui Wang, Chang Gao, Yi Hu and Xiaochen Han and has published in prestigious journals such as PLoS ONE, Gene and Medicine.

In The Last Decade

Fei-Feng Li

27 papers receiving 374 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Fei-Feng Li China	14	256	77	73	47	39	29	377
Kerra Pearce United Kingdom	12	276 1.1×	105 1.4×	48 0.7×	29 0.6×	30 0.8×	15	444
Alfons Meindl Germany	11	332 1.3×	121 1.6×	32 0.4×	102 2.2×	27 0.7×	14	490
J.A.P. Hiel Netherlands	10	204 0.8×	23 0.3×	69 0.9×	52 1.1×	35 0.9×	13	350
Anne Senabouth Australia	13	459 1.8×	102 1.3×	99 1.4×	44 0.9×	38 1.0×	15	603
Kristin McDonald Gibson United States	8	272 1.1×	118 1.5×	44 0.6×	12 0.3×	13 0.3×	9	424
Pershang Farshi United States	10	320 1.3×	59 0.8×	36 0.5×	63 1.3×	31 0.8×	12	425
Jérémie Cosette France	10	302 1.2×	51 0.7×	19 0.3×	50 1.1×	29 0.7×	22	426
Christina Rudduck Australia	14	233 0.9×	111 1.4×	33 0.5×	96 2.0×	28 0.7×	26	442
G. Robinson United States	4	343 1.3×	40 0.5×	113 1.5×	88 1.9×	19 0.5×	4	598
Ami Wang Canada	9	104 0.4×	50 0.6×	35 0.5×	50 1.1×	35 0.9×	17	264

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-authorship network of co-authors of Fei-Feng Li

This figure shows the co-authorship network connecting the top 25 collaborators of Fei-Feng Li. A scholar is included among the top collaborators of Fei-Feng Li based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Fei-Feng Li. Fei-Feng Li is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Zhang, Qiong, et al.. (2022). Structural Genomic Analysis of SARS-CoV-2 and Other Coronaviruses. Frontiers in Genetics. 13. 801902–801902. 1 indexed citations

Li, Fei-Feng, et al.. (2020). Exciting rogue waves, breathers, and solitons in coherent atomic media. Communications in Theoretical Physics. 72(7). 75003–75003. 13 indexed citations

Wu, Hao, Xianyu Zhang, Ming Niu, et al.. (2020). 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. 10. 574552–574552. 6 indexed citations

Xu, Chao, Xinying Zhao, Xin Liu, et al.. (2020). Associations of CXCL1 gene 5’UTR variations with ovarian cancer. Journal of Ovarian Research. 13(1). 43–43. 3 indexed citations

Li, Fei-Feng, et al.. (2019). Manipulating rogue waves, breathers and solitons in several non-integrable nonlinear Schrödinger equations. The European Physical Journal D. 73(12).

Zhang, Qiong, Jie Zhou, Chunyu Zhu, et al.. (2018). RBPJ polymorphisms associated with cerebral infarction diseases in Chinese Han population. Medicine. 97(31). e11420–e11420. 2 indexed citations

Zeng, Wenjuan, Shengli An, Hao Huang, et al.. (2017). [Expectant therapy versus curettage for retained products of conception after second trimester termination of pregnancy: analysis of outcomes and complications].. PubMed. 37(5). 569–574.

Li, Xia, Shuai Shi, Fei-Feng Li, et al.. (2016). Characterization of soluble N-ethylmaleimide-sensitive factor attachment protein receptor gene STX18 variations for possible roles in congenital heart diseases. Gene. 598. 79–83. 6 indexed citations

Li, Fei-Feng, Xudong Wang, Minwei Zhu, et al.. (2015). 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. 30(6). 1387–1394. 17 indexed citations

10.

Li, Fei-Feng, Jing Zhou, Dandan Zhao, et al.. (2015). Characterization of SMAD3 Gene Variants for Possible Roles in Ventricular Septal Defects and Other Congenital Heart Diseases. PLoS ONE. 10(6). e0131542–e0131542. 16 indexed citations

11.

Sam, Christine, Fei-Feng Li, & Shu‐Lin Liu. (2015). Inherited neurovascular diseases affecting cerebral blood vessels and smooth muscle. Metabolic Brain Disease. 30(5). 1105–1116. 12 indexed citations

12.

Li, Fei-Feng, Ying Han, Shuai Shi, et al.. (2015). Characterization of Transcriptional Repressor Gene MSX1 Variations for Possible Associations with Congenital Heart Diseases. PLoS ONE. 10(11). e0142666–e0142666. 12 indexed citations

13.

Li, Fei-Feng, Zheng Liu, Peng Yan, et al.. (2015). Identification of a novel mutation associated with familial adenomatous polyposis and colorectal cancer. International Journal of Molecular Medicine. 36(4). 1049–1056. 11 indexed citations

14.

Deng, Xia, Jing Zhou, Fei-Feng Li, et al.. (2014). Characterization of Nodal/TGF-Lefty Signaling Pathway Gene Variants for Possible Roles in Congenital Heart Diseases. PLoS ONE. 9(8). e104535–e104535. 21 indexed citations

15.

Li, Fei-Feng. (2013). Identification of a Location at Chromosome 19p in a Big Chinese Family with Charcot-Marie-Tooth Disease. Journal of Molecular Biomarkers & Diagnosis. 4(2). 2 indexed citations

16.

Li, Fei-Feng, Youyang Qu, Ji Liu, et al.. (2012). Identification of a Known Mutation in Notch 3 in Familiar CADASIL in China. PLoS ONE. 7(5). e36590–e36590. 20 indexed citations

17.

Wang, Rui, Hongbin Wang, Yi Cui, et al.. (2012). MiR-101 Is Involved in Human Breast Carcinogenesis by Targeting Stathmin1. PLoS ONE. 7(10). e46173–e46173. 63 indexed citations

18.

Li, Fei-Feng, Qianqian Li, Siyao Zhang, et al.. (2011). A Novel Mutation in CACNA1S Gene Associated with Hypokalemic Periodic Paralysis Which has a Gender Difference in the Penetrance. Journal of Molecular Neuroscience. 46(2). 378–383. 24 indexed citations

19.

Zhang, Wang, Hongchen Cai, Fei-Feng Li, et al.. (2011). The Congenital Cataract-Linked G61C Mutation Destabilizes γD-Crystallin and Promotes Non-Native Aggregation. PLoS ONE. 6(5). e20564–e20564. 29 indexed citations

20.

Li, Fei-Feng, Min Yang, Xu Ma, et al.. (2010). Autosomal Dominant Congenital Nuclear Cataracts Caused by a CRYAA Gene Mutation. Current Eye Research. 35(6). 492–498. 14 indexed citations

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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