Libin Mei

1.2k total citations
33 papers, 872 citations indexed

About

Libin Mei is a scholar working on Genetics, Reproductive Medicine and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Libin Mei has authored 33 papers receiving a total of 872 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Genetics, 19 papers in Reproductive Medicine and 17 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Libin Mei's work include Sperm and Testicular Function (18 papers), Reproductive Biology and Fertility (17 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (10 papers). Libin Mei is often cited by papers focused on Sperm and Testicular Function (18 papers), Reproductive Biology and Fertility (17 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (10 papers). Libin Mei collaborates with scholars based in China and Italy. Libin Mei's co-authors include Zhiyong Ji, Yan-Wei Sha, Zhiying Su, Lu Ding, Yanwei Sha, Ping Li, Lin Li, Xiaohui Xu, Xianjing Huang and Pingping Qiu and has published in prestigious journals such as Gene, Fertility and Sterility and Clinica Chimica Acta.

In The Last Decade

Libin Mei

31 papers receiving 867 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Libin Mei China 17 611 562 475 322 97 33 872
Yanwei Sha China 18 608 1.0× 554 1.0× 468 1.0× 323 1.0× 123 1.3× 43 911
Zine‐Eddine Kherraf France 14 536 0.9× 409 0.7× 477 1.0× 311 1.0× 78 0.8× 28 809
Zhiyong Ji China 15 491 0.8× 439 0.8× 360 0.8× 290 0.9× 73 0.8× 40 730
Thomas Karaouzène France 9 572 0.9× 346 0.6× 519 1.1× 285 0.9× 73 0.8× 10 790
Yan-Wei Sha China 13 385 0.6× 353 0.6× 283 0.6× 213 0.7× 69 0.7× 29 570
Xiuhong Cui China 15 280 0.5× 281 0.5× 279 0.6× 487 1.5× 73 0.8× 27 749
Caroline Cazin France 10 312 0.5× 278 0.5× 258 0.5× 190 0.6× 51 0.5× 20 481
Fuxi Zhu China 13 407 0.7× 300 0.5× 333 0.7× 259 0.8× 70 0.7× 25 593
Isabelle Koscinski France 13 436 0.7× 280 0.5× 321 0.7× 219 0.7× 74 0.8× 29 675
Shoji Kuretake Japan 8 548 0.9× 321 0.6× 591 1.2× 274 0.9× 68 0.7× 9 784

Countries citing papers authored by Libin Mei

Since Specialization
Citations

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

Fields of papers citing papers by Libin Mei

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Libin Mei

This figure shows the co-authorship network connecting the top 25 collaborators of Libin Mei. A scholar is included among the top collaborators of Libin Mei 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 Libin Mei. Libin Mei 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.
He, Xuemei, Xianjing Huang, Pingping Qiu, et al.. (2025). Preimplantation Genetic Testing in a Family with Neurofibromatosis Type 1. Genetic Testing and Molecular Biomarkers. 29(3). 54–62.
2.
Li, Mingjie, et al.. (2022). Congenital Short-Bowel Syndrome Is Associated With a Novel Deletion Mutation in the CLMP Gene: Mutations in CLMP Caused CSBS. Frontiers in Pediatrics. 9. 778859–778859. 3 indexed citations
3.
Huang, Yanru, Libin Mei, Huiming Ye, et al.. (2021). A Novel de novo Mutation in EBF3 Associated With Hypotonia, Ataxia, and Delayed Development Syndrome in a Chinese Boy. Frontiers in Genetics. 12. 676832–676832. 3 indexed citations
4.
Mei, Libin, Yanru Huang, Xiaoling Wu, et al.. (2021). Mutations in FIGLA Associated With Premature Ovarian Insufficiency in a Chinese Population. Frontiers in Medicine. 8. 714306–714306. 4 indexed citations
5.
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
6.
Li, Yang, Yanwei Sha, Xiong Wang, et al.. (2019). DNAH2 is a novel candidate gene associated with multiple morphological abnormalities of the sperm flagella. Clinical Genetics. 95(5). 590–600. 71 indexed citations
7.
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
8.
Mei, Libin, Yanru Huang, Jing Chen, et al.. (2019). Exome sequencing identifies compound heterozygous KCTD7 mutations in a girl with progressivemyoclonus epilepsy. Clinica Chimica Acta. 493. 87–91. 6 indexed citations
9.
Sha, Yanwei, Xiaoli Wei, Lu Ding, et al.. (2019). DNAH17 is associated with asthenozoospermia and multiple morphological abnormalities of sperm flagella. Annals of Human Genetics. 84(3). 271–279. 30 indexed citations
10.
Liu, Wensheng, Yanwei Sha, Yang Li, et al.. (2019). Loss-of-function mutations in SPEF2 cause multiple morphological abnormalities of the sperm flagella (MMAF). Journal of Medical Genetics. 56(10). 678–684. 62 indexed citations
11.
Sha, Yanwei, Xiong Wang, Xiaohui Xu, et al.. (2018). Biallelic mutations in PMFBP1 cause acephalic spermatozoa. Clinical Genetics. 95(2). 277–286. 47 indexed citations
12.
Sha, Yan-Wei, Libin Mei, Zhiyong Ji, et al.. (2018). Two cases of complex balanced autosomal translocations associated with severe oligozoospermia. Gene. 663. 126–130. 3 indexed citations
13.
Sha, Yan-Wei, Xiong Wang, Zhiying Su, et al.. (2018). TDRD6 is associated with oligoasthenoteratozoospermia by sequencing the patient from a consanguineous family. Gene. 659. 84–88. 28 indexed citations
14.
Jin, Baofang, Zhiying Su, Libin Mei, et al.. (2018). Identification of a novel mutation in FGFR1 gene in patients with Kallmann syndrome by high throughput sequencing. Systems Biology in Reproductive Medicine. 64(3). 202–206. 4 indexed citations
15.
16.
Sha, Yan-Wei, Xiaohui Xu, Zhiyong Ji, et al.. (2018). Genetic contribution of SUN5 mutations to acephalic spermatozoa in Fujian China. Gene. 647. 221–225. 34 indexed citations
17.
Li, Lin, Yan-Wei Sha, Zhiying Su, et al.. (2017). A novel mutation in HAUS7 results in severe oligozoospermia in two brothers. Gene. 639. 106–110. 16 indexed citations
18.
Sha, Yan-Wei, Libin Mei, Xianjing Huang, et al.. (2017). Use of targeted sequence capture and high-throughput sequencing identifies a novel PKD1 mutation involved in adult polycystic kidney disease. Gene. 634. 1–4. 4 indexed citations
19.
Sha, Yanwei, Xiaoyu Yang, Libin Mei, et al.. (2017). DNAH1 gene mutations and their potential association with dysplasia of the sperm fibrous sheath and infertility in the Han Chinese population. Fertility and Sterility. 107(6). 1312–1318.e2. 62 indexed citations
20.
Sha, Yan-Wei, Xiaohui Xu, Libin Mei, et al.. (2017). A homozygous CEP135 mutation is associated with multiple morphological abnormalities of the sperm flagella (MMAF). Gene. 633. 48–53. 100 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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