Yingying Qin

9.7k total citations · 2 hit papers
136 papers, 4.0k citations indexed

About

Yingying Qin is a scholar working on Public Health, Environmental and Occupational Health, Molecular Biology and Reproductive Medicine. According to data from OpenAlex, Yingying Qin has authored 136 papers receiving a total of 4.0k indexed citations (citations by other indexed papers that have themselves been cited), including 76 papers in Public Health, Environmental and Occupational Health, 62 papers in Molecular Biology and 41 papers in Reproductive Medicine. Recurrent topics in Yingying Qin's work include Reproductive Biology and Fertility (69 papers), Ovarian function and disorders (25 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (24 papers). Yingying Qin is often cited by papers focused on Reproductive Biology and Fertility (69 papers), Ovarian function and disorders (25 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (24 papers). Yingying Qin collaborates with scholars based in China, United States and Hong Kong. Yingying Qin's co-authors include Zi‐Jiang Chen, Xue Jiao, Joe Leigh Simpson, Shidou Zhao, Hanni Ke, Han Zhao, Aleksandar Rajkovic, Ting Guo, Youngsok Choi and Yujie Dang and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Yingying Qin

129 papers receiving 3.9k citations

Hit Papers

Genetics of primary ovarian insufficiency: new developmen... 2015 2026 2018 2022 2015 2023 100 200 300

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yingying Qin China 34 2.2k 1.6k 1.4k 1.2k 619 136 4.0k
Yingpu Sun China 35 1.9k 0.8× 1.2k 0.7× 1.8k 1.3× 340 0.3× 506 0.8× 203 3.8k
Hsun‐Ming Chang Canada 34 1.2k 0.5× 1.6k 1.0× 1.3k 0.9× 294 0.3× 700 1.1× 131 3.5k
Zhaolian Wei China 27 1.3k 0.6× 772 0.5× 1.5k 1.0× 391 0.3× 362 0.6× 140 2.7k
Geri Méduri France 40 1.1k 0.5× 1.5k 0.9× 1.7k 1.2× 1.1k 0.9× 531 0.9× 93 4.2k
Yanping Kuang China 36 3.1k 1.4× 960 0.6× 2.8k 2.0× 482 0.4× 437 0.7× 180 4.5k
Toshifumi Takahashi Japan 27 1.0k 0.5× 786 0.5× 987 0.7× 289 0.3× 278 0.4× 116 2.4k
Takashi Minegishi Japan 32 847 0.4× 1.6k 1.0× 1.2k 0.8× 733 0.6× 444 0.7× 141 3.6k
Masataka Kudo Japan 40 1.1k 0.5× 1.8k 1.2× 1.0k 0.7× 521 0.5× 221 0.4× 128 4.9k
Aritro Sen United States 24 865 0.4× 518 0.3× 852 0.6× 341 0.3× 275 0.4× 53 2.0k
Akira Iwase Japan 34 1.1k 0.5× 656 0.4× 1.7k 1.2× 171 0.1× 521 0.8× 146 3.1k

Countries citing papers authored by Yingying Qin

Since Specialization
Citations

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

Fields of papers citing papers by Yingying Qin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yingying Qin

This figure shows the co-authorship network connecting the top 25 collaborators of Yingying Qin. A scholar is included among the top collaborators of Yingying Qin 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 Yingying Qin. Yingying Qin 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.
Guo, Ting, Hongyuan Liu, Bingying Xu, et al.. (2025). Epidemiology, Genetic Etiology, and Intervention of Premature Ovarian Insufficiency. Endocrine Reviews. 46(5). 621–651. 3 indexed citations
2.
Zhu, C. G., Dunfang Zhang, Shan Meng, et al.. (2025). CCR8 + decidual regulatory T cells maintain maternal-fetal immune tolerance during early pregnancy. Science Immunology. 10(106). eado2463–eado2463. 4 indexed citations
3.
Zhang, Shan, Shuya Liu, Yingying Qin, Shidou Zhao, & Hong Liu. (2025). Regulation of cell reprogramming by engineered biomaterial-based biophysical cues for next-generation cell therapies. Coordination Chemistry Reviews. 549. 217309–217309.
4.
Liu, Chong, Jiarui Chen, Jiang Xue, et al.. (2024). CT imaging analysis of the C7 pedicle and lateral mass in children aged 0–14 years. Annals of Anatomy - Anatomischer Anzeiger. 257. 152349–152349.
5.
Chen, Jiarui, Yingying Qin, Jiang Xue, et al.. (2024). Anatomical study of the C6 pedicle and lateral mass in children aged 0–14 years based on CT imaging. Journal of Orthopaedic Surgery and Research. 19(1). 468–468. 1 indexed citations
6.
Cao, Lili, Shuhan Wang, Simin Zhao, et al.. (2024). MCM8 interacts with DDX5 to promote R-loop resolution. The EMBO Journal. 43(14). 3044–3071. 8 indexed citations
7.
Zhang, Wenzhe, Xinyi Wu, Hanni Ke, et al.. (2023). Homozygous missense variant in MEIOSIN causes premature ovarian insufficiency. Human Reproduction. 38(Supplement_2). ii47–ii56. 6 indexed citations
8.
Zhao, Simin, Yajuan Yang, Ting Guo, et al.. (2023). TP63 gain-of-function mutations cause premature ovarian insufficiency by inducing oocyte apoptosis. Journal of Clinical Investigation. 133(5). 22 indexed citations
9.
Qi, Yu, et al.. (2023). Pathogenic bi‐allelic variants of meiotic ZMM complex gene SPO16 in premature ovarian insufficiency. Clinical Genetics. 104(4). 486–490. 4 indexed citations
10.
Zhang, Jie, Tao Chen, Fang Ting Liang, et al.. (2023). PDCD4 deficiency improved 4-vinylcyclohexene dioxide-induced mouse premature ovarian insufficiency. Reproductive BioMedicine Online. 48(4). 103685–103685. 1 indexed citations
11.
Ke, Hanni, Shuyan Tang, Ting Guo, et al.. (2023). Landscape of pathogenic mutations in premature ovarian insufficiency. Nature Medicine. 29(2). 483–492. 100 indexed citations breakdown →
12.
Jiao, Wenlin, et al.. (2022). HGF Secreted by Mesenchymal Stromal Cells Promotes Primordial Follicle Activation by Increasing the Activity of the PI3K-AKT Signaling Pathway. Stem Cell Reviews and Reports. 18(5). 1834–1850. 31 indexed citations
13.
Guo, Ting, Hanni Ke, Qian Zhang, et al.. (2021). Pathogenic variants of meiotic double strand break (DSB) formation genes PRDM9 and ANKRD31 in premature ovarian insufficiency. Genetics in Medicine. 23(12). 2309–2315. 15 indexed citations
14.
Xu, Lan, Duan Li, Xiaoxia Yu, et al.. (2021). Correction: FANCI plays an essential role in spermatogenesis and regulates meiotic histone methylation. Cell Death and Disease. 12(9). 808–808. 1 indexed citations
15.
Jiao, Wenlin, et al.. (2020). Stem Cell Transplantation Improves Ovarian Function through Paracrine Mechanisms. Current Gene Therapy. 20(5). 347–355. 19 indexed citations
16.
Ning, Yunna, Wen Liu, Yingying Qin, et al.. (2020). Variation analysis of SOX8 gene in Chinese men with non‐obstructive azoospermia or oligozoospermia. Andrologia. 52(4). e13531–e13531. 3 indexed citations
17.
Xu, Xiaofei, Xinxia Chen, Xiruo Zhang, et al.. (2017). Impaired Telomere Length and Telomerase Activity in Peripheral Blood Leukocytes and Granulosa Cells in Patients With Biochemical Primary Ovarian Insufficiency. Obstetrical & Gynecological Survey. 72(3). 172–173. 30 indexed citations
18.
Zhao, Shidou, Guangyu Li, Raymond Dalgleish, et al.. (2014). Transcription factor SOHLH1 potentially associated with primary ovarian insufficiency. Fertility and Sterility. 103(2). 548–553.e5. 27 indexed citations
19.
Qin, Yingying, et al.. (2007). Novel non-synonymous mutation in the transforming growth factor beta binding protein-like (TB) domain of the fibrillin-1 (FBN1) gene in a Han Chinese family with Marfan syndrome (MFS).. PubMed. 28(5). 629–32. 3 indexed citations
20.
Qin, Yingying, Youngsok Choi, Han Zhao, et al.. (2007). NOBOX Homeobox Mutation Causes Premature Ovarian Failure. The American Journal of Human Genetics. 81(3). 576–581. 188 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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