Lanlan Meng

1.8k total citations
56 papers, 938 citations indexed

About

Lanlan Meng is a scholar working on Genetics, Reproductive Medicine and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Lanlan Meng has authored 56 papers receiving a total of 938 indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Genetics, 27 papers in Reproductive Medicine and 26 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Lanlan Meng's work include Sperm and Testicular Function (25 papers), Reproductive Biology and Fertility (22 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (21 papers). Lanlan Meng is often cited by papers focused on Sperm and Testicular Function (25 papers), Reproductive Biology and Fertility (22 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (21 papers). Lanlan Meng collaborates with scholars based in China, United States and Canada. Lanlan Meng's co-authors include Yue‐Qiu Tan, Chaofeng Tu, Juan Du, Guangxiu Lu, Ge Lin, Shi‐Min Yuan, Wenbin He, Hongchuan Nie, Weili Wang and Aixiang Luo and has published in prestigious journals such as Nature Communications, Scientific Reports and The FASEB Journal.

In The Last Decade

Lanlan Meng

52 papers receiving 925 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lanlan Meng China 18 472 471 415 393 127 56 938
Zhiying Su China 15 306 0.6× 354 0.8× 290 0.7× 246 0.6× 80 0.6× 43 659
Kaoru Yanagida Japan 18 275 0.6× 786 1.7× 734 1.8× 212 0.5× 140 1.1× 52 1.1k
Jing Fu China 17 286 0.6× 368 0.8× 749 1.8× 505 1.3× 419 3.3× 43 1.1k
Hatem Elghezal Tunisia 20 412 0.9× 397 0.8× 463 1.1× 204 0.5× 281 2.2× 57 992
Jinhua Lu China 17 168 0.4× 312 0.7× 203 0.5× 332 0.8× 123 1.0× 46 845
Anahita Mohseni Meybodi Iran 15 250 0.5× 248 0.5× 140 0.3× 267 0.7× 67 0.5× 66 582
Debbie Montjean France 17 300 0.6× 614 1.3× 529 1.3× 436 1.1× 296 2.3× 41 1.1k
Mingrong Lv China 16 231 0.5× 336 0.7× 299 0.7× 239 0.6× 100 0.8× 37 587
Tugce Pehlivan United States 17 371 0.8× 177 0.4× 371 0.9× 308 0.8× 666 5.2× 20 1.1k

Countries citing papers authored by Lanlan Meng

Since Specialization
Citations

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

Fields of papers citing papers by Lanlan Meng

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lanlan Meng

This figure shows the co-authorship network connecting the top 25 collaborators of Lanlan Meng. A scholar is included among the top collaborators of Lanlan Meng 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 Lanlan Meng. Lanlan Meng 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, Juan Du, et al.. (2025). Novel mutations in ZMYND15 are associated with male infertility with oligozoospermia/azoospermia. Journal of Assisted Reproduction and Genetics. 42(5). 1601–1611. 1 indexed citations
2.
Jin, Hao, et al.. (2025). YTHDC2 manipulates anti-tumoral macrophage polarization and predicts favorable outcomes in triple negative breast cancer. npj Precision Oncology. 9(1). 119–119. 2 indexed citations
3.
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
4.
Zhang, Xueguang, Lanlan Meng, Tongtong Li, et al.. (2024). CEP112 coordinates translational regulation of essential fertility genes during spermiogenesis through phase separation in humans and mice. Nature Communications. 15(1). 8465–8465. 9 indexed citations
5.
Wang, Yaling, Yong Li, Chen Tan, et al.. (2024). Bi-allelic variants in DNAH3 cause male infertility with asthenoteratozoospermia in humans and mice. Human Reproduction Open. 2024(1). hoae003–hoae003. 13 indexed citations
6.
7.
Wang, Weili, Lanlan Meng, Jiaxin He, et al.. (2023). Biallelic variants in KCTD19 associated with male factor infertility and oligoasthenoteratozoospermia. Human Reproduction. 38(7). 1399–1411. 11 indexed citations
8.
Li, Yunhao, Yong Li, Ying Wang, et al.. (2022). Identification of novel biallelic LRRC6 variants in male Chinese patients with primary ciliary dyskinesia and infertility. Journal of Assisted Reproduction and Genetics. 40(1). 41–51. 7 indexed citations
9.
Wang, Yurong, Ling Liu, Chen Tan, et al.. (2022). Novel MEIOB variants cause primary ovarian insufficiency and non-obstructive azoospermia. Frontiers in Genetics. 13. 936264–936264. 13 indexed citations
10.
Lü, Shuai, Yayun Gu, Yifei Wu, et al.. (2021). Bi-allelic variants in human WDR63 cause male infertility via abnormal inner dynein arms assembly. Cell Discovery. 7(1). 110–110. 25 indexed citations
11.
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
12.
Li, Yong, Weili Wang, Chaofeng Tu, et al.. (2020). A novel homozygous frameshift mutation in MNS1 associated with severe oligoasthenoteratozoospermia in humans. Asian Journal of Andrology. 23(2). 197–204. 18 indexed citations
13.
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
14.
Tu, Chaofeng, Lanlan Meng, Hongchuan Nie, et al.. (2020). A homozygous RPL10L missense mutation associated with male factor infertility and severe oligozoospermia. Fertility and Sterility. 113(3). 561–568. 17 indexed citations
15.
Yang, Lijun, et al.. (2020). Inhibition of miR-200b-3p alleviates hypoxia-ischemic brain damage via targeting Slit2 in neonatal rats. Biochemical and Biophysical Research Communications. 523(4). 931–938. 9 indexed citations
16.
Tu, Chaofeng, Hongchuan Nie, Lanlan Meng, et al.. (2020). Novel mutations in SPEF2 causing different defects between flagella and cilia bridge: the phenotypic link between MMAF and PCD. Human Genetics. 139(2). 257–271. 57 indexed citations
17.
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
18.
Li, Haiyu, Juan Du, Wen Li, et al.. (2018). Rare partial octosomy and hexasomy of 15q11-q13 associated with intellectual impairment and development delay: report of two cases and review of literature. Molecular Cytogenetics. 11(1). 15–15. 7 indexed citations
19.
Tan, Yue‐Qiu, Chaofeng Tu, Lanlan Meng, et al.. (2017). Loss-of-function mutations in TDRD7 lead to a rare novel syndrome combining congenital cataract and nonobstructive azoospermia in humans. Genetics in Medicine. 21(5). 1209–1217. 81 indexed citations
20.
Yuan, Shi‐Min, Lanlan Meng, Chaofeng Tu, et al.. (2017). Genotype-phenotype correlation and identification of two novel SRD5A2 mutations in 33 Chinese patients with hypospadias. Steroids. 125. 61–66. 12 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Zhiying Su Breakdown of academic impact, for papers by Kaoru Yanagida Breakdown of academic impact, for papers by Jing Fu Breakdown of academic impact, for papers by Hatem Elghezal Breakdown of academic impact, for papers by Jinhua Lu Breakdown of academic impact, for papers by Anahita Mohseni Meybodi Breakdown of academic impact, for papers by Debbie Montjean Breakdown of academic impact, for papers by Mingrong Lv Breakdown of academic impact, for papers by Tugce Pehlivan
Rankless by CCL
2026