Jianteng Zhou

827 total citations
23 papers, 222 citations indexed

About

Jianteng Zhou is a scholar working on Genetics, Public Health, Environmental and Occupational Health and Reproductive Medicine. According to data from OpenAlex, Jianteng Zhou has authored 23 papers receiving a total of 222 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 14 papers in Public Health, Environmental and Occupational Health and 13 papers in Reproductive Medicine. Recurrent topics in Jianteng Zhou's work include Reproductive Biology and Fertility (14 papers), Sperm and Testicular Function (13 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers). Jianteng Zhou is often cited by papers focused on Reproductive Biology and Fertility (14 papers), Sperm and Testicular Function (13 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers). Jianteng Zhou collaborates with scholars based in China, Pakistan and United States. Jianteng Zhou's co-authors include Qinghua Shi, Yuanwei Zhang, Hui Ma, Huan Zhang, Xiaohua Jiang, Yang Li, Muhammad Zubair, Ihsan Khan, Ranjha Khan and Wasim Shah and has published in prestigious journals such as International Journal of Molecular Sciences, Human Molecular Genetics and Science Advances.

In The Last Decade

Jianteng Zhou

22 papers receiving 220 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jianteng Zhou China 10 130 108 106 100 17 23 222
Denise R. Archambeault United States 8 109 0.8× 196 1.8× 99 0.9× 79 0.8× 11 0.6× 8 267
Manan Khan China 7 71 0.5× 98 0.9× 66 0.6× 56 0.6× 4 0.2× 10 172
Christiane Pleuger Germany 7 108 0.8× 66 0.6× 37 0.3× 66 0.7× 8 0.5× 12 192
Sélima Fourati Ben Mustapha France 7 239 1.8× 137 1.3× 184 1.7× 191 1.9× 9 0.5× 13 338
Özlem Okutman France 8 226 1.7× 179 1.7× 207 2.0× 161 1.6× 10 0.6× 18 353
Longfei Ma China 7 77 0.6× 105 1.0× 79 0.7× 54 0.5× 12 0.7× 9 179
Gaku Minase Japan 5 73 0.6× 66 0.6× 58 0.5× 45 0.5× 5 0.3× 11 128
Yamato Fukui Japan 11 218 1.7× 45 0.4× 34 0.3× 74 0.7× 5 0.3× 21 349
Capucine Hyon France 12 89 0.7× 210 1.9× 262 2.5× 64 0.6× 9 0.5× 21 376
Swapna S. Desai India 8 219 1.7× 146 1.4× 125 1.2× 203 2.0× 3 0.2× 9 365

Countries citing papers authored by Jianteng Zhou

Since Specialization
Citations

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

Fields of papers citing papers by Jianteng Zhou

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jianteng Zhou

This figure shows the co-authorship network connecting the top 25 collaborators of Jianteng Zhou. A scholar is included among the top collaborators of Jianteng Zhou 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 Jianteng Zhou. Jianteng Zhou 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.
Li, Ying, R. Kasturi Bai, Yao Zhu, et al.. (2025). Genetic variation in gut microbe as a key regulator of host social behavior in C. elegans. Gut Microbes. 17(1). 2490828–2490828. 2 indexed citations
2.
Li, Jingping, Xinhai Zhu, Huan Deng, et al.. (2024). CCDC157 is essential for sperm differentiation and shows oligoasthenoteratozoospermia‐related mutations in men. Journal of Cellular and Molecular Medicine. 28(7). e18215–e18215. 4 indexed citations
3.
Zhang, Xinrong, et al.. (2024). Pathogenic relationship between phenotypes of ARPKD and novel compound heterozygous mutations of PKHD1. Frontiers in Genetics. 15. 1429336–1429336.
4.
Zhang, Xiangjun, Jianteng Zhou, Jingwei Ye, et al.. (2024). CCDC181 is required for sperm flagellum biogenesis and male fertility in mice. 动物学研究. 45(5). 1061–1072. 3 indexed citations
5.
Ye, Jingwei, Tanveer Abbas, Jianteng Zhou, et al.. (2024). Homozygous <i>CCDC146</i> mutation causes oligoasthenoteratozoospermia in humans and mice. 动物学研究. 45(5). 1073–1087. 3 indexed citations
6.
Li, Ming, Yue Wang, Jianteng Zhou, et al.. (2024). A homozygous nonsense variant in HENMT1 causes male infertility in humans and mice. Andrology. 13(6). 1439–1450. 1 indexed citations
7.
Ahmad, Nisar, Aurang Zeb, Jianteng Zhou, et al.. (2024). A novel missense mutation of CCDC34 causes male infertility with oligoasthenoteratozoospermia in a consanguineous Pakistani family. Asian Journal of Andrology. 26(6). 605–609. 4 indexed citations
8.
Dil, Sobia, Jianteng Zhou, Huan Zhang, et al.. (2023). A homozygous KASH5 frameshift mutation causes diminished ovarian reserve, recurrent miscarriage, and non-obstructive azoospermia in humans. Frontiers in Endocrinology. 14. 1128362–1128362. 8 indexed citations
9.
Shah, Wasim, Li Liu, Jianteng Zhou, et al.. (2023). Biallelic mutations in RNA-binding protein ADAD2 cause spermiogenic failure and non-obstructive azoospermia in humans. Human Reproduction Open. 2023(3). hoad022–hoad022. 5 indexed citations
10.
Ma, Hui, Tao Li, Xuefeng Xie, et al.. (2022). RAD51AP2 is required for efficient meiotic recombination between X and Y chromosomes. Science Advances. 8(2). eabk1789–eabk1789. 15 indexed citations
11.
Li, Yang, Yufan Wu, Ihsan Khan, et al.. (2022). M1AP interacts with the mammalian ZZS complex and promotes male meiotic recombination. EMBO Reports. 24(2). e55778–e55778. 12 indexed citations
12.
Zubair, Muhammad, Ranjha Khan, Uzma Hameed, et al.. (2022). A recurrent homozygous missense mutation in CCDC103 causes asthenoteratozoospermia due to disorganized dynein arms. Asian Journal of Andrology. 24(3). 255–259. 12 indexed citations
13.
Xie, Xuefeng, Mazhar Khan, Muhammad Zubair, et al.. (2022). A homozygous missense variant in DND1 causes non-obstructive azoospermia in humans. Frontiers in Genetics. 13. 1017302–1017302. 4 indexed citations
14.
Khan, Asad, Beibei Zhang, Jianteng Zhou, et al.. (2022). Biallelic Variants in CFAP61 Cause Multiple Morphological Abnormalities of the Flagella and Male Infertility. Frontiers in Cell and Developmental Biology. 9. 803818–803818. 24 indexed citations
15.
Khan, Ranjha, Jing Chen, Manan Khan, et al.. (2021). Novel Loss-of-Function Mutations in DNAH1 Displayed Different Phenotypic Spectrum in Humans and Mice. Frontiers in Endocrinology. 12. 765639–765639. 11 indexed citations
16.
Khan, Ihsan, Sobia Dil, Huan Zhang, et al.. (2021). A novel stop-gain mutation in ARMC2 is associated with multiple morphological abnormalities of the sperm flagella. Reproductive BioMedicine Online. 43(5). 913–919. 8 indexed citations
17.
Dil, Sobia, Jianteng Zhou, Yuanwei Zhang, et al.. (2021). Novel biallelic loss-of-function mutations in CFAP43 cause multiple morphological abnormalities of the sperm flagellum in Pakistani families. Asian Journal of Andrology. 23(6). 627–632. 14 indexed citations
18.
Ma, Hui, Beibei Zhang, Asad Khan, et al.. (2021). Novel frameshift mutation in STK33 is associated with asthenozoospermia and multiple morphological abnormalities of the flagella. Human Molecular Genetics. 30(21). 1977–1984. 22 indexed citations
19.
Li, Yang, Yufan Wu, Jianteng Zhou, et al.. (2021). A recurrent ZSWIM7 mutation causes male infertility resulting from decreased meiotic recombination. Human Reproduction. 36(5). 1436–1445. 20 indexed citations
20.
Zhou, Jianteng, Jianing Gao, Huan Zhang, et al.. (2020). PedMiner: a tool for linkage analysis-based identification of disease-associated variants using family based whole-exome sequencing data. Briefings in Bioinformatics. 22(3). 7 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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