Xiaoli Wei

791 total citations
37 papers, 603 citations indexed

About

Xiaoli Wei is a scholar working on Reproductive Medicine, Genetics and Molecular Biology. According to data from OpenAlex, Xiaoli Wei has authored 37 papers receiving a total of 603 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Reproductive Medicine, 13 papers in Genetics and 11 papers in Molecular Biology. Recurrent topics in Xiaoli Wei's work include Sperm and Testicular Function (14 papers), Reproductive Biology and Fertility (10 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (9 papers). Xiaoli Wei is often cited by papers focused on Sperm and Testicular Function (14 papers), Reproductive Biology and Fertility (10 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (9 papers). Xiaoli Wei collaborates with scholars based in China, Germany and United States. Xiaoli Wei's co-authors include Yanwei Sha, Zhiying Su, Wensheng Liu, Quanhong Xue, Wensheng Liu, Zhongxian Lu, Zhiyong Ji, Libin Mei, Jianguo Liu and Yifeng Wang and has published in prestigious journals such as Brain, International Journal of Molecular Sciences and Journal of Ethnopharmacology.

In The Last Decade

Xiaoli Wei

36 papers receiving 591 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Xiaoli Wei China 16 220 213 202 200 73 37 603
Xixia Li China 12 190 0.9× 89 0.4× 289 1.4× 141 0.7× 49 0.7× 30 651
Debby Ickowicz Israel 15 301 1.4× 96 0.5× 305 1.5× 256 1.3× 27 0.4× 19 846
Sarah E. Fiedler United States 12 187 0.8× 125 0.6× 219 1.1× 185 0.9× 19 0.3× 16 522
Gladis Sánchez United States 16 371 1.7× 133 0.6× 521 2.6× 275 1.4× 34 0.5× 27 936
Kanako Morohaku Japan 10 171 0.8× 93 0.4× 433 2.1× 226 1.1× 13 0.2× 18 767
Syed G. Haider Germany 10 295 1.3× 135 0.6× 163 0.8× 108 0.5× 22 0.3× 35 606
Seiji Kito Japan 17 337 1.5× 138 0.6× 360 1.8× 480 2.4× 19 0.3× 30 848
D. F. Cameron United States 15 178 0.8× 98 0.5× 166 0.8× 83 0.4× 119 1.6× 29 554
Christian Lessard United States 12 133 0.6× 71 0.3× 270 1.3× 142 0.7× 24 0.3× 19 694
Stéphanie Chauvin France 15 218 1.0× 159 0.7× 552 2.7× 72 0.4× 226 3.1× 24 888

Countries citing papers authored by Xiaoli Wei

Since Specialization
Citations

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

Fields of papers citing papers by Xiaoli Wei

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Xiaoli Wei

This figure shows the co-authorship network connecting the top 25 collaborators of Xiaoli Wei. A scholar is included among the top collaborators of Xiaoli Wei 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 Xiaoli Wei. Xiaoli Wei 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.
2.
Feng, Yu, Wensheng Liu, Jing Dong, et al.. (2025). Genetic Underpinnings of Oligoasthenoteratozoospermia. Clinical Genetics. 107(3). 243–260. 1 indexed citations
3.
Sha, Yanwei, et al.. (2023). TENT5D disruption causes oligoasthenoteratozoospermia and male infertility. Andrology. 11(6). 1121–1131. 15 indexed citations
4.
Sha, Yanwei, Wensheng Liu, Lu Han, et al.. (2023). Homozygous mutation in DNALI1 leads to asthenoteratozoospermia by affecting the inner dynein arms. Frontiers in Endocrinology. 13. 1058651–1058651. 8 indexed citations
5.
Wei, Xiaoli, Haibin Wang, You‐Qiang Su, et al.. (2022). Tyrosine phosphatase SHP2 in ovarian granulosa cells balances follicular development by inhibiting PI3K/AKT signaling. Journal of Molecular Cell Biology. 14(7). 12 indexed citations
6.
Li, Na, Wensheng Liu, Yan-Wei Sha, et al.. (2022). Biallelic mutations in spermatogenesis and centriole-associated 1 like (SPATC1L) cause acephalic spermatozoa syndrome and male infertility. Asian Journal of Andrology. 24(1). 67–72. 13 indexed citations
7.
Zhou, Xufeng, et al.. (2022). Efficacy and safety of ambroxol hydrochloride in the treatment of secretory otitis media: a systematic review and meta-analysis. Annals of Translational Medicine. 10(3). 142–142. 2 indexed citations
8.
Wei, Xiaoli, Qicai Liu, Wensheng Liu, et al.. (2021). Mutations in ZP4 are associated with abnormal zona pellucida and female infertility. Journal of Clinical Pathology. 75(3). 201–204. 17 indexed citations
9.
Wei, Xiaoli, Wensheng Liu, Xiaoya Zhang, et al.. (2021). Biallelic mutations in KATNAL2 cause male infertility due to oligo‐astheno‐teratozoospermia. Clinical Genetics. 100(4). 376–385. 15 indexed citations
10.
Sha, Yanwei, Wensheng Liu, Xiaoli Wei, et al.. (2021). Pathogenic variants of ATG4D in infertile men with non‐obstructive azoospermia identified using whole‐exome sequencing. Clinical Genetics. 100(3). 280–291. 5 indexed citations
11.
Sha, Yanwei, Wensheng Liu, Lin Li, et al.. (2021). Pathogenic Variants in ACTRT1 Cause Acephalic Spermatozoa Syndrome. Frontiers in Cell and Developmental Biology. 9. 676246–676246. 13 indexed citations
12.
Sha, Yanwei, Xiaoli Wei, Lu Ding, et al.. (2020). Biallelic mutations of CFAP74 may cause human primary ciliary dyskinesia and MMAF phenotype. Journal of Human Genetics. 65(11). 961–969. 43 indexed citations
13.
Liu, Hongli, Xiaoli Wei, Yanwei Sha, et al.. (2020). Whole-exome sequencing in patients with premature ovarian insufficiency: early detection and early intervention. Journal of Ovarian Research. 13(1). 114–114. 41 indexed citations
14.
Wei, Xiaoli, et al.. (2020). Contribution of salidroside to the relieve of symptom and sign in the early acute stage of osteoarthritis in rat model. Journal of Ethnopharmacology. 259. 112883–112883. 14 indexed citations
15.
Sha, Yanwei, Ding Ma, Ning Zhang, et al.. (2019). Novel NOG (p.P42S) mutation causes proximal symphalangism in a four-generation Chinese family. BMC Medical Genetics. 20(1). 133–133. 4 indexed citations
16.
Sha, Yanwei, Xiaoli Wei, Wensheng Liu, et al.. (2019). CCDC9 is identified as a novel candidate gene of severe asthenozoospermia. Systems Biology in Reproductive Medicine. 65(6). 465–473. 14 indexed citations
17.
Huang, Yuqi, Zhe Zhao, Xiaoli Wei, et al.. (2016). Long-term trihexyphenidyl exposure alters neuroimmune response and inflammation in aging rat: relevance to age and Alzheimer’s disease. Journal of Neuroinflammation. 13(1). 175–175. 10 indexed citations
18.
Wang, Dongsheng, et al.. (2014). Oligotrophy is Helpful for the Isolation of Bioactive Actinomycetes. Indian Journal of Microbiology. 54(2). 178–184. 20 indexed citations
19.
Zhang, Xiaoli, et al.. (2007). Impact of astaxanthin-enriched algal powder of Haematococcus pluvialis on memory improvement in BALB/c mice. Environmental Geochemistry and Health. 29(6). 483–489. 40 indexed citations
20.
Wei, Xiaoli, James N. Scott, Christopher Wallace, et al.. (2004). Posterior fossa lesion volume and slowed information processing in multiple sclerosis. Brain. 127(7). 1526–1534. 35 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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Breakdown of academic impact, for papers by Xixia Li Breakdown of academic impact, for papers by Debby Ickowicz Breakdown of academic impact, for papers by Sarah E. Fiedler Breakdown of academic impact, for papers by Gladis Sánchez Breakdown of academic impact, for papers by Kanako Morohaku Breakdown of academic impact, for papers by Syed G. Haider Breakdown of academic impact, for papers by Seiji Kito Breakdown of academic impact, for papers by D. F. Cameron Breakdown of academic impact, for papers by Christian Lessard Breakdown of academic impact, for papers by Stéphanie Chauvin
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