Chaofeng Tu

2.1k total citations
49 papers, 1.2k citations indexed

About

Chaofeng Tu is a scholar working on Reproductive Medicine, Genetics and Molecular Biology. According to data from OpenAlex, Chaofeng Tu has authored 49 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Reproductive Medicine, 25 papers in Genetics and 23 papers in Molecular Biology. Recurrent topics in Chaofeng Tu's work include Sperm and Testicular Function (25 papers), Reproductive Biology and Fertility (20 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (17 papers). Chaofeng Tu is often cited by papers focused on Sperm and Testicular Function (25 papers), Reproductive Biology and Fertility (20 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (17 papers). Chaofeng Tu collaborates with scholars based in China, United States and Canada. Chaofeng Tu's co-authors include Yue‐Qiu Tan, Lanlan Meng, Ge Lin, Juan Du, Weili Wang, Guangxiu Lu, Shi‐Min Yuan, Hongchuan Nie, Guiyuan Li and Guangxiu Lu and has published in prestigious journals such as Journal of Virology, Scientific Reports and The American Journal of Human Genetics.

In The Last Decade

Chaofeng Tu

47 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Chaofeng Tu China 20 582 502 471 416 226 49 1.2k
Xichen Nie United States 11 706 1.2× 479 1.0× 287 0.6× 346 0.8× 145 0.6× 14 1.1k
Shoko Yamashita Japan 15 388 0.7× 468 0.9× 216 0.5× 822 2.0× 59 0.3× 45 1.1k
Naim Shabani Germany 16 449 0.8× 256 0.5× 179 0.4× 133 0.3× 69 0.3× 34 938
Richard M. Schultz United States 9 793 1.4× 329 0.7× 206 0.4× 705 1.7× 53 0.2× 11 1.3k
Toshihiko Shikone Japan 20 603 1.0× 572 1.1× 172 0.4× 442 1.1× 77 0.3× 26 1.4k
Jinhua Lu China 17 332 0.6× 312 0.6× 168 0.4× 203 0.5× 69 0.3× 46 845
Graeme Scobie United Kingdom 13 343 0.6× 400 0.8× 388 0.8× 187 0.4× 65 0.3× 22 922
Firdous Abdulwahab Saudi Arabia 14 412 0.7× 95 0.2× 238 0.5× 210 0.5× 46 0.2× 30 729
Tiangang Zhuang United States 16 495 0.9× 133 0.3× 132 0.3× 101 0.2× 100 0.4× 18 744
Mark Cranfield United Kingdom 15 683 1.2× 328 0.7× 254 0.5× 611 1.5× 27 0.1× 19 1.1k

Countries citing papers authored by Chaofeng Tu

Since Specialization
Citations

This map shows the geographic impact of Chaofeng Tu'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 Chaofeng Tu with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Chaofeng Tu more than expected).

Fields of papers citing papers by Chaofeng Tu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Chaofeng Tu. 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 Chaofeng Tu. The network helps show where Chaofeng Tu may publish in the future.

Co-authorship network of co-authors of Chaofeng Tu

This figure shows the co-authorship network connecting the top 25 collaborators of Chaofeng Tu. A scholar is included among the top collaborators of Chaofeng Tu 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 Chaofeng Tu. Chaofeng Tu is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Meng, Lanlan, Chen Tan, Juan Du, et al.. (2025). Novel mutations in ZMYND15 are associated with male infertility with oligozoospermia/azoospermia. Journal of Assisted Reproduction and Genetics. 42(5). 1601–1611. 1 indexed citations
2.
He, Jiaxin, Chen Tan, Yong Li, et al.. (2025). Molecular insights into sperm head shaping and its role in human male fertility. Human Reproduction Update. 31(4). 307–332. 2 indexed citations
3.
Meng, Lanlan, Chen Tan, Wenbin He, et al.. (2024). A hemizygous loss‐of‐function variant in BCORL1 is associated with male infertility and oligoasthenoteratozoospermia. Clinical Genetics. 106(1). 27–36. 1 indexed citations
4.
Wang, Yaling, Yong Li, Chen Tan, et al.. (2024). Bi-allelic variants in DNAH3 cause male infertility with asthenoteratozoospermia in humans and mice. Human Reproduction Open. 2024(1). hoae003–hoae003. 13 indexed citations
5.
Wang, Weili, Lanlan Meng, Jiaxin He, et al.. (2023). Biallelic variants in KCTD19 associated with male factor infertility and oligoasthenoteratozoospermia. Human Reproduction. 38(7). 1399–1411. 11 indexed citations
6.
Li, Yunhao, Yong Li, Ying Wang, et al.. (2022). Identification of novel biallelic LRRC6 variants in male Chinese patients with primary ciliary dyskinesia and infertility. Journal of Assisted Reproduction and Genetics. 40(1). 41–51. 7 indexed citations
7.
Guo, Ting, Chaofeng Tu, Danhui Yang, et al.. (2021). Bi-allelic BRWD1 variants cause male infertility with asthenoteratozoospermia and likely primary ciliary dyskinesia. Human Genetics. 140(5). 761–773. 26 indexed citations
8.
Tu, Chaofeng, Ying Wang, Hongchuan Nie, et al.. (2020). An M1AP homozygous splice‐site mutation associated with severe oligozoospermia in a consanguineous family. Clinical Genetics. 97(5). 741–746. 17 indexed citations
9.
Li, Yong, Weili Wang, Chaofeng Tu, et al.. (2020). A novel homozygous frameshift mutation in MNS1 associated with severe oligoasthenoteratozoospermia in humans. Asian Journal of Andrology. 23(2). 197–204. 18 indexed citations
10.
Wang, Ying, Chaofeng Tu, Hongchuan Nie, et al.. (2020). Novel DNAAF6 variants identified by whole-exome sequencing cause male infertility and primary ciliary dyskinesia. Journal of Assisted Reproduction and Genetics. 37(4). 811–820. 16 indexed citations
11.
Tu, Chaofeng, et al.. (2020). Genetic underpinnings of asthenozoospermia. Best Practice & Research Clinical Endocrinology & Metabolism. 34(6). 101472–101472. 55 indexed citations
12.
Tu, Chaofeng, Lanlan Meng, Hongchuan Nie, et al.. (2020). A homozygous RPL10L missense mutation associated with male factor infertility and severe oligozoospermia. Fertility and Sterility. 113(3). 561–568. 17 indexed citations
13.
Tu, Chaofeng, Hongchuan Nie, Lanlan Meng, et al.. (2020). Novel mutations in SPEF2 causing different defects between flagella and cilia bridge: the phenotypic link between MMAF and PCD. Human Genetics. 139(2). 257–271. 57 indexed citations
14.
Tu, Chaofeng, Hongchuan Nie, Lanlan Meng, et al.. (2019). Identification of DNAH6 mutations in infertile men with multiple morphological abnormalities of the sperm flagella. Scientific Reports. 9(1). 15864–15864. 51 indexed citations
15.
Tan, Yue‐Qiu, Weili Wang, & Chaofeng Tu. (2019). Insight on multiple morphological abnormalities of sperm flagella in male infertility: what is new?. Asian Journal of Andrology. 22(3). 236–236. 50 indexed citations
16.
Li, Haiyu, Juan Du, Wen Li, et al.. (2018). Rare partial octosomy and hexasomy of 15q11-q13 associated with intellectual impairment and development delay: report of two cases and review of literature. Molecular Cytogenetics. 11(1). 15–15. 7 indexed citations
17.
Liu, Changhong, Yingnan Sun, Xiaoling She, et al.. (2017). CASC2c as an unfavorable prognosis factor interacts with miR-101 to mediate astrocytoma tumorigenesis. Cell Death and Disease. 8(3). e2639–e2639. 29 indexed citations
18.
Tan, Yue‐Qiu, Chaofeng Tu, Lanlan Meng, et al.. (2017). Loss-of-function mutations in TDRD7 lead to a rare novel syndrome combining congenital cataract and nonobstructive azoospermia in humans. Genetics in Medicine. 21(5). 1209–1217. 81 indexed citations
19.
Yuan, Shi‐Min, Lanlan Meng, Chaofeng Tu, et al.. (2017). Genotype-phenotype correlation and identification of two novel SRD5A2 mutations in 33 Chinese patients with hypospadias. Steroids. 125. 61–66. 12 indexed citations
20.
Xiao, Lan, Chaofeng Tu, Zhibin Yu, et al.. (2014). LRRC4 haplotypes are associated with pituitary adenoma in a Chinese population. Medical Oncology. 31(4). 888–888. 6 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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