Qiaoli Li

1.1k total citations
26 papers, 640 citations indexed

About

Qiaoli Li is a scholar working on Molecular Biology, Public Health, Environmental and Occupational Health and Reproductive Medicine. According to data from OpenAlex, Qiaoli Li has authored 26 papers receiving a total of 640 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 11 papers in Public Health, Environmental and Occupational Health and 11 papers in Reproductive Medicine. Recurrent topics in Qiaoli Li's work include Reproductive Biology and Fertility (11 papers), Ovarian function and disorders (6 papers) and Epigenetics and DNA Methylation (4 papers). Qiaoli Li is often cited by papers focused on Reproductive Biology and Fertility (11 papers), Ovarian function and disorders (6 papers) and Epigenetics and DNA Methylation (4 papers). Qiaoli Li collaborates with scholars based in China. Qiaoli Li's co-authors include Lei Wang, Qing Sang, Jin Li, Lin He, Yanping Kuang, Jian Mu, Biaobang Chen, Xinzhi Zhao, Bin Li and Yao Xu and has published in prestigious journals such as Proceedings of the National Academy of Sciences, PLoS ONE and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Qiaoli Li

26 papers receiving 625 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Qiaoli Li China	12	340	281	244	153	149	26	640
Hazel L. Kinnell United Kingdom	14	547 1.6×	419 1.5×	313 1.3×	99 0.6×	215 1.4×	16	851
Michaël W. Pankhurst New Zealand	16	353 1.0×	144 0.5×	400 1.6×	52 0.3×	85 0.6×	36	643
Yan-Guang Wu United States	17	573 1.7×	255 0.9×	438 1.8×	137 0.9×	127 0.9×	27	788
Naohiro Tezuka Japan	9	321 0.9×	140 0.5×	219 0.9×	121 0.8×	35 0.2×	14	535
Hiroko Shiina Japan	12	177 0.5×	184 0.7×	188 0.8×	54 0.4×	167 1.1×	15	571
P Rodrigues Portugal	10	405 1.2×	214 0.8×	248 1.0×	94 0.6×	47 0.3×	23	551
Maria Lucia Scaldaferri Italy	10	174 0.5×	298 1.1×	143 0.6×	37 0.2×	90 0.6×	12	545
Xiu Lowe United States	21	433 1.3×	387 1.4×	401 1.6×	448 2.9×	416 2.8×	33	1.3k
Nancy Telford United States	6	515 1.5×	507 1.8×	161 0.7×	103 0.7×	300 2.0×	10	878
Signe M. Kilen United States	16	510 1.5×	436 1.6×	352 1.4×	53 0.3×	267 1.8×	18	917

Countries citing papers authored by Qiaoli Li

Since Specialization

Citations

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

Fields of papers citing papers by Qiaoli Li

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Qiaoli Li

This figure shows the co-authorship network connecting the top 25 collaborators of Qiaoli Li. A scholar is included among the top collaborators of Qiaoli Li 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 Qiaoli Li. Qiaoli Li is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Li, Xu, et al.. (2025). Deep eutectic solvent extraction and biological activity of polysaccharides from Tenebrio molitor. Heliyon. 11(2). e41790–e41790. 3 indexed citations

Zhang, Zhihua, Ran Yu, Zhi-Jing Wu, et al.. (2024). COX15 deficiency causes oocyte ferroptosis. Proceedings of the National Academy of Sciences. 121(45). e2406174121–e2406174121. 10 indexed citations

Li, Da, Xiangli Niu, Aimin Yang, et al.. (2024). Identification novel mutations and phenotypic spectrum expanding in PATL2 in infertile women with IVF/ICSI failure. Journal of Assisted Reproduction and Genetics. 41(5). 1233–1243. 6 indexed citations

Qu, Ronggui, Zhihua Zhang, Ling Wu, et al.. (2023). ADGB variants cause asthenozoospermia and male infertility. Human Genetics. 142(6). 735–748. 11 indexed citations

Wang, Wenjun, Qiaoli Li, Shuang Yang, et al.. (2023). High Expression of Microtubule-associated Protein TBCB Predicts Adverse Outcome and Immunosuppression in Acute Myeloid Leukemia. Journal of Cancer. 14(10). 1707–1724. 1 indexed citations

Zhou, Zhou, Xiaoyan Mao, Biaobang Chen, et al.. (2021). A novel splicing variant in DNAH8 causes asthenozoospermia. Journal of Assisted Reproduction and Genetics. 38(6). 1545–1550. 10 indexed citations

Mu, Jian, Wenjing Wang, Biaobang Chen, et al.. (2019). Mutations in NLRP2 and NLRP5 cause female infertility characterised by early embryonic arrest. Journal of Medical Genetics. 56(7). 471–480. 102 indexed citations

Chen, Biaobang, Zhihua Zhang, Xiaoxi Sun, et al.. (2017). Biallelic Mutations in PATL2 Cause Female Infertility Characterized by Oocyte Maturation Arrest. The American Journal of Human Genetics. 101(4). 609–615. 112 indexed citations

Zhang, Qiang, Tian Tian, Teng Wang, et al.. (2017). Detection of Turner syndrome using X-chromosome inactivation specific differentially methylated CpG sites: A pilot study. Clinica Chimica Acta. 468. 174–179. 3 indexed citations

10.

Chen, Biaobang, Bin Li, Da Li, et al.. (2016). Novel mutations and structural deletions inTUBB8: expanding mutational and phenotypic spectrum of patients with arrest in oocyte maturation, fertilization or early embryonic development. Human Reproduction. 32(2). 457–464. 84 indexed citations

11.

Li, Qiaoli, Zheng Yan, Yanping Kuang, et al.. (2016). Genetic variations in the 3′-untranslated region ofSLC18A2are associated with serum FSH concentration in polycystic ovary syndrome patients and regulate gene expressionin vitro. Human Reproduction. 31(9). 2150–2157. 8 indexed citations

12.

Xu, Jiawei, Guang He, Xinyao Zhou, et al.. (2015). Prenatal Nutritional Deficiency Reprogrammed Postnatal Gene Expression in Mammal Brains: Implications for Schizophrenia. The International Journal of Neuropsychopharmacology. 18(4). 34 indexed citations

13.

Sang, Qing, Xin Li, Haojue Wang, et al.. (2014). Quantitative Methylation Level of the EPHX1 Promoter in Peripheral Blood DNA Is Associated with Polycystic Ovary Syndrome. PLoS ONE. 9(2). e88013–e88013. 31 indexed citations

14.

Sang, Qing, Junyu Zhang, Ruizhi Feng, et al.. (2014). Ildr1b is essential for semicircular canal development, migration of the posterior lateral line primordium and hearing ability in zebrafish: implications for a role in the recessive hearing impairment DFNB42. Human Molecular Genetics. 23(23). 6201–6211. 12 indexed citations

15.

Sang, Qing, Huan Wang, Ruizhi Feng, et al.. (2013). Identification and Functional Study of a New Missense Mutation in the Motor Head Domain of Myosin VIIA in a Family with Autosomal Dominant Hearing Impairment (DFNA11). PLoS ONE. 8(1). e55178–e55178. 18 indexed citations

16.

Sang, Qing, Shaozhen Zhang, Shien Zou, et al.. (2012). Quantitative analysis of follistatin (FST) promoter methylation in peripheral blood of patients with polycystic ovary syndrome. Reproductive BioMedicine Online. 26(2). 157–163. 23 indexed citations

17.

Wang, Hui, Qiaoli Li, Ying Wang, et al.. (2011). A common polymorphism in the human aromatase gene alters the risk for polycystic ovary syndrome and modifies aromatase activity in vitro. Molecular Human Reproduction. 17(6). 386–391. 43 indexed citations

18.

Li, Qiaoli, Ying Wang, Xiaoping Zhang, et al.. (2011). Common genetic variation in the 3′-untranslated region of gonadotropin-releasing hormone receptor regulates gene expression in cella and is associated with thyroid function, insulin secretion as well as insulin sensitivity in polycystic ovary syndrome patients. Human Genetics. 129(5). 553–561. 22 indexed citations

19.

Cheng, Yan, Xiaotian Li, Qiaoli Li, et al.. (2010). Promoter hypomethylation of COMT in human placenta is not associated with the development of pre-eclampsia. Molecular Human Reproduction. 17(3). 199–206. 16 indexed citations

20.

Wang, Zhaoxia, Minghao Yin, Wangjie Xu, et al.. (2009). A study of Y chromosome gene mRNA in human ejaculated spermatozoa. Molecular Reproduction and Development. 77(2). 158–166. 10 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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