Su‐Ren Chen

2.3k total citations
50 papers, 1.6k citations indexed

About

Su‐Ren Chen is a scholar working on Molecular Biology, Reproductive Medicine and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Su‐Ren Chen has authored 50 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 30 papers in Reproductive Medicine and 25 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Su‐Ren Chen's work include Sperm and Testicular Function (29 papers), Reproductive Biology and Fertility (24 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (14 papers). Su‐Ren Chen is often cited by papers focused on Sperm and Testicular Function (29 papers), Reproductive Biology and Fertility (24 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (14 papers). Su‐Ren Chen collaborates with scholars based in China, United States and Hong Kong. Su‐Ren Chen's co-authors include Yixun Liu, Aalia Batool, Yihong Yang, Xiaozhen Zhang, Shoulong Deng, Xiuxia Wang, Hao Liu, Yuqian Wang, Ji‐Xin Tang and Jinmei Cheng and has published in prestigious journals such as The Journal of Cell Biology, Development and The FASEB Journal.

In The Last Decade

Su‐Ren Chen

49 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Su‐Ren Chen China 23 775 737 582 415 229 50 1.6k
Francesca Gioia Klinger Italy 25 1.1k 1.4× 798 1.1× 1.3k 2.2× 245 0.6× 120 0.5× 70 2.3k
Makoto Orisaka Japan 23 568 0.7× 823 1.1× 815 1.4× 279 0.7× 124 0.5× 62 1.8k
Sha Peng China 22 719 0.9× 292 0.4× 302 0.5× 186 0.4× 353 1.5× 58 1.4k
Zhao‐Yuan Hu China 22 545 0.7× 654 0.9× 567 1.0× 231 0.6× 129 0.6× 46 1.3k
Meijia Zhang China 23 709 0.9× 892 1.2× 1.4k 2.4× 232 0.6× 102 0.4× 70 2.0k
Nathan C. Law United States 14 608 0.8× 448 0.6× 442 0.8× 280 0.7× 90 0.4× 22 1.0k
JoAnne S. Richards United States 17 731 0.9× 582 0.8× 754 1.3× 375 0.9× 123 0.5× 23 1.6k
Alex Tsafriri Israel 23 789 1.0× 1.1k 1.5× 1.6k 2.8× 346 0.8× 141 0.6× 29 2.4k
Xiang‐Hong Ou China 23 1.1k 1.5× 323 0.4× 742 1.3× 196 0.5× 175 0.8× 89 1.8k
Aiyue Luo China 23 531 0.7× 300 0.4× 476 0.8× 118 0.3× 186 0.8× 50 1.3k

Countries citing papers authored by Su‐Ren Chen

Since Specialization
Citations

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

Fields of papers citing papers by Su‐Ren Chen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Su‐Ren Chen. 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 Su‐Ren Chen. The network helps show where Su‐Ren Chen may publish in the future.

Co-authorship network of co-authors of Su‐Ren Chen

This figure shows the co-authorship network connecting the top 25 collaborators of Su‐Ren Chen. A scholar is included among the top collaborators of Su‐Ren Chen 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 Su‐Ren Chen. Su‐Ren Chen 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.
Zhu, Yun, Guangwen Yin, Linhua Tai, et al.. (2025). In situ structure of the mouse sperm central apparatus reveals mechanistic insights into asthenozoospermia. Cell Research. 35(8). 551–567. 4 indexed citations
2.
Yang, Xiaoyu, Yue Dong, Xiaozhen Zhang, et al.. (2024). Disruption in CYLC1 leads to acrosome detachment, sperm head deformity, and male in/subfertility in humans and mice. eLife. 13. 1 indexed citations
3.
Yang, Xiaoyu, Yue Dong, Xiaozhen Zhang, et al.. (2024). Disruption in CYLC1 leads to acrosome detachment, sperm head deformity, and male in/subfertility in humans and mice. eLife. 13. 3 indexed citations
4.
Li, Jiaxun, Weiwei Liu, Wei Han, et al.. (2024). Deletion of ACTRT1 is associated with male infertility as sperm acrosomal ultrastructural defects and fertilization failure in human. Human Reproduction. 39(5). 880–891. 3 indexed citations
5.
Zhou, Ruixi, et al.. (2024). Deficiency of IQCH causes male infertility in humans and mice. eLife. 12.
6.
Wang, Junli, et al.. (2023). CFAP70 is a solid and valuable target for the genetic diagnosis of oligo-astheno-teratozoospermia in infertile men. EBioMedicine. 93. 104675–104675. 20 indexed citations
8.
Zhang, Xueguang, Rui Zheng, Chen Liang, et al.. (2022). Loss-of-function mutations inCEP78cause male infertility in humans and mice. Science Advances. 8(40). eabn0968–eabn0968. 27 indexed citations
9.
Zhang, Xiaozhen, et al.. (2022). The perinuclear theca protein Calicin helps shape the sperm head and maintain the nuclear structure in mice. Cell Reports. 40(1). 111049–111049. 27 indexed citations
10.
Chen, Su‐Ren. (2019). Recent advances in the regulation of testicular germ cell tumors by microRNAs. Frontiers in bioscience. 24(4). 765–776. 10 indexed citations
11.
Batool, Aalia, et al.. (2019). Testicular germ cell tumor: a comprehensive review. Cellular and Molecular Life Sciences. 76(9). 1713–1727. 107 indexed citations
12.
Batool, Aalia, Yuqian Wang, Xiaoxia Hao, Su‐Ren Chen, & Yixun Liu. (2018). A miR-125b/CSF1-CX3CL1/tumor-associated macrophage recruitment axis controls testicular germ cell tumor growth. Cell Death and Disease. 9(10). 962–962. 40 indexed citations
13.
Deng, Shoulong, Zhipeng Wang, Cheng Jin, et al.. (2017). Melatonin promotes sheep Leydig cell testosterone secretion in a co-culture with Sertoli cells. Theriogenology. 106. 170–177. 56 indexed citations
14.
Cheng, Jinmei, Ji‐Xin Tang, Jian Li, et al.. (2017). Role of WNT signaling in epididymal sperm maturation. Journal of Assisted Reproduction and Genetics. 35(2). 229–236. 15 indexed citations
15.
Tang, Ji‐Xin, Jian Li, Jinmei Cheng, et al.. (2017). Requirement for CCNB1 in mouse spermatogenesis. Cell Death and Disease. 8(10). e3142–e3142. 37 indexed citations
16.
Chen, Su‐Ren, et al.. (2016). Does murine spermatogenesis require WNT signalling? A lesson from Gpr177 conditional knockout mouse models. Cell Death and Disease. 7(6). e2281–e2281. 15 indexed citations
17.
Chen, Su‐Ren & Yixun Liu. (2016). Testis Cord Maintenance in Mouse Embryos: Genes and Signaling1. Biology of Reproduction. 94(2). 42–42. 26 indexed citations
18.
Deng, Shoulong, Xiuxia Wang, Zhipeng Wang, et al.. (2016). In vitro production of functional haploid sperm cells from male germ cells of Saanen dairy goat. Theriogenology. 90. 120–128. 12 indexed citations
19.
Chen, Su‐Ren, et al.. (2016). Sodium–hydrogen exchanger NHA1 and NHA2 control sperm motility and male fertility. Cell Death and Disease. 7(3). e2152–e2152. 52 indexed citations
20.
Chen, Su‐Ren & Yixun Liu. (2014). Regulation of spermatogonial stem cell self-renewal and spermatocyte meiosis by Sertoli cell signaling. Reproduction. 149(4). R159–R167. 225 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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