Wenbin He

1.5k total citations
58 papers, 917 citations indexed

About

Wenbin He is a scholar working on Genetics, Molecular Biology and Reproductive Medicine. According to data from OpenAlex, Wenbin He has authored 58 papers receiving a total of 917 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Genetics, 17 papers in Molecular Biology and 13 papers in Reproductive Medicine. Recurrent topics in Wenbin He's work include Reproductive Biology and Fertility (12 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (10 papers) and Sperm and Testicular Function (9 papers). Wenbin He is often cited by papers focused on Reproductive Biology and Fertility (12 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (10 papers) and Sperm and Testicular Function (9 papers). Wenbin He collaborates with scholars based in China, Australia and Italy. Wenbin He's co-authors include Nai‐Hong Chen, Yue‐Qiu Tan, Juan Du, Guangxiu Lu, Wei Zuo, Lanlan Meng, Xiaofeng Guo, Ge Lin, Cong‐Yuan Xia and Shuai Zhang and has published in prestigious journals such as Scientific Reports, European Heart Journal and The American Journal of Human Genetics.

In The Last Decade

Wenbin He

54 papers receiving 904 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Wenbin He China 16 335 293 257 250 112 58 917
Laura Chang United States 16 316 0.9× 109 0.4× 273 1.1× 195 0.8× 77 0.7× 22 1.2k
Yasuko Fujisawa Japan 21 338 1.0× 221 0.8× 28 0.1× 84 0.3× 63 0.6× 106 1.5k
Élisabeth Le Rumeur France 22 880 2.6× 127 0.4× 44 0.2× 17 0.1× 57 0.5× 73 1.6k
D. Lo Presti Italy 20 225 0.7× 121 0.4× 117 0.5× 26 0.1× 8 0.1× 109 1.3k
Marc-Étienne Meyer France 17 338 1.0× 415 1.4× 56 0.2× 57 0.2× 103 0.9× 42 1.7k
Giuseppe Di Caprio United States 17 462 1.4× 24 0.1× 63 0.2× 90 0.4× 54 0.5× 36 1.4k
Steven Wiltshire United Kingdom 22 1.0k 3.0× 551 1.9× 114 0.4× 125 0.5× 141 1.3× 39 1.8k
Sang Wook Yoo South Korea 15 138 0.4× 45 0.2× 78 0.3× 93 0.4× 68 0.6× 24 593
Ewa Gorczyńska Poland 17 173 0.5× 191 0.7× 186 0.7× 165 0.7× 123 1.1× 84 1.1k
Ikuko N. Motoike Japan 17 357 1.1× 101 0.3× 15 0.1× 21 0.1× 43 0.4× 50 824

Countries citing papers authored by Wenbin He

Since Specialization
Citations

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

Fields of papers citing papers by Wenbin He

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Wenbin He

This figure shows the co-authorship network connecting the top 25 collaborators of Wenbin He. A scholar is included among the top collaborators of Wenbin He 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 Wenbin He. Wenbin He 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.
Ma, Xiaoqin, et al.. (2025). Integration of serum pharmacochemistry, chromatographic fingerprint, and network pharmacology to identify chemical markers for quality makers of Di Huang Yin Zi. Journal of Pharmaceutical and Biomedical Analysis. 265. 117022–117022. 2 indexed citations
2.
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
3.
Yuan, Shi‐Min, Liang Hu, Jim Zhong, et al.. (2024). Genetic Analysis and Reproductive Interventions for Two Rare Families Affected by Severe Haemophilia A. Haemophilia. 31(1). 148–155. 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, Jie, et al.. (2023). Impact of Codonopsis decoction on cerebral blood flow and cognitive function in rats with chronic cerebral ischemia. Journal of Ethnopharmacology. 323. 117585–117585. 8 indexed citations
6.
Wang, Jie, et al.. (2023). A richer and more diverse future for microglia phenotypes. Heliyon. 9(4). e14713–e14713. 57 indexed citations
7.
Ji, Zhiyong, Jiaqiang Luo, Yuxiang Zhang, et al.. (2023). Identification of a missense variant of MND1 in meiotic arrest and non-obstructive azoospermia. Journal of Human Genetics. 68(11). 729–735. 2 indexed citations
8.
He, Wenbin, Xiurong Li, Liang Hu, et al.. (2022). Clinical Utility of Medical Exome Sequencing: Expanded Carrier Screening for Patients Seeking Assisted Reproductive Technology in China. Frontiers in Genetics. 13. 943058–943058. 10 indexed citations
9.
Wang, Yurong, Ling Liu, Chen Tan, et al.. (2022). Novel MEIOB variants cause primary ovarian insufficiency and non-obstructive azoospermia. Frontiers in Genetics. 13. 936264–936264. 13 indexed citations
10.
Chen, Yongzhe, Wenbin He, Juan Du, et al.. (2021). Case Report: A Novel Heterozygous ZP3 Deletion Associated With Empty Follicle Syndrome and Abnormal Follicular Development. Frontiers in Genetics. 12. 690070–690070. 12 indexed citations
11.
Tan, Chen, Lanlan Meng, Mingrong Lv, et al.. (2021). Bi-allelic variants in DNHD1 cause flagellar axoneme defects and asthenoteratozoospermia in humans and mice. The American Journal of Human Genetics. 109(1). 157–171. 32 indexed citations
12.
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
13.
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
14.
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
15.
He, Wenbin, Wenjuan Xiao, Yue‐Qiu Tan, et al.. (2018). Novel mutations of PKD genes in Chinese patients suffering from autosomal dominant polycystic kidney disease and seeking assisted reproduction. BMC Medical Genetics. 19(1). 186–186. 13 indexed citations
16.
He, Wenbin, Juan Du, Xiaowen Yang, et al.. (2018). Novel inactivating mutations in the FSH receptor cause premature ovarian insufficiency with resistant ovary syndrome. Reproductive BioMedicine Online. 38(3). 397–406. 27 indexed citations
17.
He, Wenbin, Yue‐Qiu Tan, Xiao Hu, et al.. (2018). Expanded carrier screening and preimplantation genetic diagnosis in a couple who delivered a baby affected with congenital factor VII deficiency. BMC Medical Genetics. 19(1). 15–15. 2 indexed citations
18.
19.
Zhang, Shuai, Wenbin He, & Nai‐Hong Chen. (2014). Causes of Death Among Persons Who Survive an Acute Ischemic Stroke. Current Neurology and Neuroscience Reports. 14(8). 467–467. 23 indexed citations
20.
Gao, Yan, et al.. (2014). Do glial cells play an anti-oxidative role in Huntington's disease?. Free Radical Research. 48(10). 1135–1144. 11 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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