Ge Lin

3.0k total citations
89 papers, 1.6k citations indexed

About

Ge Lin is a scholar working on Public Health, Environmental and Occupational Health, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Ge Lin has authored 89 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Public Health, Environmental and Occupational Health, 31 papers in Pediatrics, Perinatology and Child Health and 29 papers in Molecular Biology. Recurrent topics in Ge Lin's work include Reproductive Biology and Fertility (32 papers), Prenatal Screening and Diagnostics (25 papers) and Sperm and Testicular Function (20 papers). Ge Lin is often cited by papers focused on Reproductive Biology and Fertility (32 papers), Prenatal Screening and Diagnostics (25 papers) and Sperm and Testicular Function (20 papers). Ge Lin collaborates with scholars based in China, United States and Hong Kong. Ge Lin's co-authors include Guangxiu Lu, Yue‐Qiu Tan, Chaofeng Tu, Lanlan Meng, Guangxiu Lu, Fei Gong, Juan Du, Xi Ran, Na Xu and Shuoping Zhang and has published in prestigious journals such as Nature Communications, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Ge Lin

83 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ge Lin China 25 685 555 553 469 366 89 1.6k
Xiaoyu Yang China 19 562 0.8× 587 1.1× 776 1.4× 556 1.2× 142 0.4× 73 1.5k
Marion S. Verp United States 19 217 0.3× 478 0.9× 248 0.4× 539 1.1× 454 1.2× 51 1.4k
Liqing Fan China 21 383 0.6× 460 0.8× 559 1.0× 205 0.4× 62 0.2× 96 1.4k
Suraksha Agrawal India 25 434 0.6× 593 1.1× 212 0.4× 642 1.4× 167 0.5× 136 2.5k
Ertuğ Kovanci United States 25 1.2k 1.8× 529 1.0× 1.4k 2.4× 451 1.0× 762 2.1× 60 2.7k
A. O’Doherty Ireland 20 274 0.4× 428 0.8× 223 0.4× 281 0.6× 168 0.5× 53 1.3k
Jean Parinaud France 23 1.1k 1.6× 210 0.4× 1.3k 2.3× 202 0.4× 363 1.0× 90 2.1k
Aafke P.A. van Montfoort Netherlands 29 1.3k 1.9× 675 1.2× 1.1k 2.1× 375 0.8× 2.0k 5.5× 57 2.8k
Federico Jensen Germany 25 465 0.7× 251 0.5× 278 0.5× 127 0.3× 151 0.4× 51 1.6k
Amy Winship Australia 23 634 0.9× 466 0.8× 617 1.1× 134 0.3× 185 0.5× 53 1.7k

Countries citing papers authored by Ge Lin

Since Specialization
Citations

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

Fields of papers citing papers by Ge Lin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ge Lin

This figure shows the co-authorship network connecting the top 25 collaborators of Ge Lin. A scholar is included among the top collaborators of Ge Lin 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 Ge Lin. Ge Lin 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.
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
2.
Chen, Huijun, Yvonne Liu, Liang Hu, et al.. (2024). Estradiol-to-follicle ratio on human chorionic gonadotropin day is a novel predictor of gestational diabetes mellitus in women receiving fresh embryo transfer. Frontiers in Endocrinology. 15. 1465069–1465069. 1 indexed citations
3.
Wang, Qian, Hui Chen, Fei Gong, et al.. (2024). Diagnosis and management of heterotopic intramural pregnancy after in vitro fertilization: an eight-case series. Ultraschall in der Medizin - European Journal of Ultrasound. 47(1). 51–60.
4.
Hu, Huiling, Jiaqi Sun, Fei Meng, et al.. (2024). Biallelic variants in α-tubulin isotypes cause female infertility characterised as recurrent preimplantation embryo arrest. Journal of Medical Genetics. 61(11). 1045–1052. 2 indexed citations
5.
Feng, Yanhui, Juan Xiong, Ge Lin, et al.. (2024). Exploring IAA biosynthesis and plant growth promotion mechanism for tomato root endophytes with incomplete IAA synthesis pathways. Chemical and Biological Technologies in Agriculture. 11(1). 7 indexed citations
6.
7.
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.
Liu, Gang, Xiaowei Xing, Huan Zhang, et al.. (2021). Patients with acephalic spermatozoa syndrome linked to novel TSGA10/PMFBP1 variants have favorable pregnancy outcomes from intracytoplasmic sperm injection. Clinical Genetics. 100(3). 334–339. 8 indexed citations
10.
Li, Yiqun, Yuding Fan, Yong Zhou, et al.. (2021). Bcl-xL Reduces Chinese Giant Salamander Iridovirus-Induced Mitochondrial Apoptosis by Interacting with Bak and Inhibiting the p53 Pathway. Viruses. 13(11). 2224–2224. 7 indexed citations
11.
Yuan, Shi‐Min, Dehua Cheng, Keli Luo, et al.. (2021). Reproductive risks and preimplantation genetic testing intervention for X–autosome translocation carriers. Reproductive BioMedicine Online. 43(1). 73–80. 2 indexed citations
12.
Tu, Chaofeng, Ying Wang, Hongchuan Nie, et al.. (2020). An M1AP homozygous splice‐site mutation associated with severe oligozoospermia in a consanguineous family. Clinical Genetics. 97(5). 741–746. 17 indexed citations
13.
Ouyang, Yan, Jiabi Qin, Ge Lin, Shuanglin Xiang, & Xihong Li. (2020). Reference intervals of gestational sac, yolk sac, embryonic length, embryonic heart rate at 6–10 weeks after in vitro fertilization-embryo transfer. BMC Pregnancy and Childbirth. 20(1). 533–533. 6 indexed citations
14.
Sha, Qian‐Qian, Wei Zheng, Feng Xie, et al.. (2020). Novel mutations in TUBB8 expand the mutational and phenotypic spectrum of patients with zygotes containing multiple pronuclei. Gene. 769. 145227–145227. 22 indexed citations
15.
Wang, Ying, Chaofeng Tu, Hongchuan Nie, et al.. (2020). Novel DNAAF6 variants identified by whole-exome sequencing cause male infertility and primary ciliary dyskinesia. Journal of Assisted Reproduction and Genetics. 37(4). 811–820. 16 indexed citations
16.
Tu, Chaofeng, et al.. (2020). Genetic underpinnings of asthenozoospermia. Best Practice & Research Clinical Endocrinology & Metabolism. 34(6). 101472–101472. 55 indexed citations
17.
Dai, Jing, Can Dai, Jing Guo, et al.. (2019). Novel homozygous variations in PLCZ1 lead to poor or failed fertilization characterized by abnormal localization patterns of PLCζ in sperm. Clinical Genetics. 97(2). 347–351. 40 indexed citations
18.
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
19.
Zhang, Tonglin & Ge Lin. (2013). On the limiting distribution of the spatial scan statistic. Journal of Multivariate Analysis. 122. 215–225. 3 indexed citations
20.

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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