Huiru Cheng

926 total citations
25 papers, 273 citations indexed

About

Huiru Cheng is a scholar working on Molecular Biology, Public Health, Environmental and Occupational Health and Genetics. According to data from OpenAlex, Huiru Cheng has authored 25 papers receiving a total of 273 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 9 papers in Public Health, Environmental and Occupational Health and 9 papers in Genetics. Recurrent topics in Huiru Cheng's work include Reproductive Biology and Fertility (8 papers), Sperm and Testicular Function (7 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers). Huiru Cheng is often cited by papers focused on Reproductive Biology and Fertility (8 papers), Sperm and Testicular Function (7 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers). Huiru Cheng collaborates with scholars based in China. Huiru Cheng's co-authors include Yunxia Cao, Xiaojin He, Yang Gao, Dongdong Tang, Hao Geng, Huan Wu, Xiaoqing Ni, Chuan Xu, Zhaolian Wei and Mingrong Lv and has published in prestigious journals such as Human Molecular Genetics, Food and Chemical Toxicology and Ecotoxicology and Environmental Safety.

In The Last Decade

Huiru Cheng

24 papers receiving 270 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Huiru Cheng China 9 119 109 97 82 42 25 273
Shaobin Lin China 9 99 0.8× 168 1.5× 152 1.6× 122 1.5× 38 0.9× 11 296
Qunshan Shen China 11 76 0.6× 57 0.5× 97 1.0× 71 0.9× 28 0.7× 24 219
Jitu W. George United States 10 136 1.1× 57 0.5× 136 1.4× 110 1.3× 20 0.5× 19 378
Ilona Kopera Poland 10 132 1.1× 85 0.8× 214 2.2× 113 1.4× 16 0.4× 11 357
Jann‐Frederik Cremers Germany 9 136 1.1× 62 0.6× 136 1.4× 56 0.7× 33 0.8× 18 250
Margot J. Wyrwoll Germany 10 232 1.9× 197 1.8× 228 2.4× 143 1.7× 47 1.1× 22 452
Dorte L Egeberg Denmark 5 117 1.0× 81 0.7× 134 1.4× 97 1.2× 18 0.4× 8 332
Zeng‐Ming Yang China 11 77 0.6× 55 0.5× 138 1.4× 72 0.9× 21 0.5× 22 323
Y. Sangeeta Devi United States 11 113 0.9× 105 1.0× 91 0.9× 64 0.8× 11 0.3× 14 348

Countries citing papers authored by Huiru Cheng

Since Specialization
Citations

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

Fields of papers citing papers by Huiru Cheng

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Huiru Cheng

This figure shows the co-authorship network connecting the top 25 collaborators of Huiru Cheng. A scholar is included among the top collaborators of Huiru Cheng 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 Huiru Cheng. Huiru Cheng 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.
Yang, Fan, Huiru Cheng, Kuokuo Li, et al.. (2025). Novel homozygous variants in piRNA pathway factors lead to male infertility in humans. Reproductive BioMedicine Online. 51(3). 104974–104974. 1 indexed citations
2.
Wang, Peiwen, Mengyao Wang, Yaxin Chen, et al.. (2025). Melatonin alleviates oxidative stress induced damage in human iPSCs harboring mtDNA 3243A>G mutation via MAPK pathway. Stem Cell Research & Therapy. 16(1). 554–554. 1 indexed citations
3.
Wang, Mengyao, Yaxin Chen, Yating Zhu, et al.. (2025). Melatonin mediates the BMP4/MAPK signaling pathway to alleviate zearalenone-induced abnormal embryonic development in mice. Ecotoxicology and Environmental Safety. 294. 118068–118068. 1 indexed citations
4.
5.
Ding, Zhi‐Ming, H. Chen, Huiru Cheng, et al.. (2025). BPZ inhibits early mouse embryonic development by disrupting maternal-to-zygotic transition and mitochondrial function. Ecotoxicology and Environmental Safety. 289. 117693–117693. 3 indexed citations
6.
Liu, Yunyun, Mengyao Wang, Shuangshuang Cui, et al.. (2024). HTR1B regulates mitochondrial homeostasis and mitophagy by activating the ERK/ MAPK signalling pathway during human embryonic arrest. Heliyon. 10(12). e33132–e33132. 4 indexed citations
7.
Cui, Shuangshuang, Huiru Cheng, Yang Liu, et al.. (2024). Melatonin Protects Against Mitochondrial Dyshomeostasis and Ovarian Damage Caused by Chronic Unpredictable Mild Stress Through the eIF2α-AFT4 Signaling Pathway in Mice. Reproductive Sciences. 31(10). 3191–3201. 7 indexed citations
8.
Yu, Zhen, Changyuan Yu, Xuan Li, et al.. (2024). Cadmium exposure activates mitophagy through downregulating thyroid hormone receptor/PGC1α signal in preeclampsia. Ecotoxicology and Environmental Safety. 276. 116259–116259. 2 indexed citations
9.
Zhu, Xiaoyu, Huiru Cheng, Huan Wu, et al.. (2023). Novel MEIOB pathogenic variants including a homozygous non‐canonical splicing variant, cause meiotic arrest and human non‐obstructive azoospermia. Clinical Genetics. 105(1). 99–105. 7 indexed citations
10.
Fang, Yuan, et al.. (2023). MANF Promotes Unexplained Recurrent Miscarriages by Interacting with NPM1 and Downregulating Trophoblast Cell Migration and Invasion. International Journal of Biological Sciences. 20(1). 296–311. 1 indexed citations
11.
Zhang, Shouxin, Siyuan Wang, Huiru Cheng, et al.. (2023). Carbendazim exposure inhibits mouse oocytes meiotic maturation in vitro by destroying spindle assembly. Food and Chemical Toxicology. 179. 113966–113966. 5 indexed citations
12.
Tang, Fei, Yang Gao, Kuokuo Li, et al.. (2023). Novel deleterious splicing variant in HFM1 causes gametogenesis defect and recurrent implantation failure: concerning the risk of chromosomal abnormalities in embryos. Journal of Assisted Reproduction and Genetics. 40(7). 1689–1702. 5 indexed citations
13.
Yu, Zhen, et al.. (2023). Thyroid hormone transport and metabolism are disturbed in the placental villi of miscarriage. Reproductive Biology and Endocrinology. 21(1). 108–108. 6 indexed citations
14.
Li, Xuan, Changyuan Yu, Huiru Cheng, et al.. (2022). Maternal cadmium exposure impairs placental angiogenesis in preeclampsia through disturbing thyroid hormone receptor signaling. Ecotoxicology and Environmental Safety. 244. 114055–114055. 15 indexed citations
15.
Tang, Dongdong, Kuokuo Li, Mingrong Lv, et al.. (2022). Altered mRNAs Profiles in the Testis of Patients With “Secondary Idiopathic Non-Obstructive Azoospermia”. Frontiers in Cell and Developmental Biology. 10. 824596–824596. 6 indexed citations
16.
Wu, Huan, Ying Wang, Qunshan Shen, et al.. (2021). Bi‐allelic mutations in MCIDA S and CCNO cause human infertility associated with abnormal gamete transport. Clinical Genetics. 100(6). 731–742. 9 indexed citations
17.
Tang, Dongdong, Yanwei Sha, Yang Gao, et al.. (2021). Novel variants in DNAH9 lead to nonsyndromic severe asthenozoospermia. Reproductive Biology and Endocrinology. 19(1). 27–27. 26 indexed citations
18.
Tang, Dongdong, Mingrong Lv, Yang Gao, et al.. (2021). Novel variants in helicase for meiosis 1 lead to male infertility due to non-obstructive azoospermia. Reproductive Biology and Endocrinology. 19(1). 129–129. 21 indexed citations
19.
Ni, Xiaoqing, Jiajia Wang, Mingrong Lv, et al.. (2020). A novel homozygous mutation in WDR19 induces disorganization of microtubules in sperm flagella and nonsyndromic asthenoteratospermia. Journal of Assisted Reproduction and Genetics. 37(6). 1431–1439. 38 indexed citations
20.
Wu, Huan, Yang Gao, Qunshan Shen, et al.. (2020). A novel hemizygous loss-of-function mutation in ADGRG2 causes male infertility with congenital bilateral absence of the vas deferens. Journal of Assisted Reproduction and Genetics. 37(6). 1421–1429. 15 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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