Lanlan Meng

1.9k citations

56 papers · 1.0k · h-index 18

Impact in

Reproductive Medicine top 1%
- Sperm and Testicular Function
- Ovarian function and disorders
Genetics top 5%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetic and Kidney Cyst Diseases

Papers in

Reproductive Medicine 23
- Sperm and Testicular Function 22
Genetics 19
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 13
- Genetic and Kidney Cyst Diseases 3

Co-authors: Yue‐Qiu Tan (44 shared papers)Chaofeng Tu (34 shared papers)Juan Du (34 shared papers)Guangxiu Lu (28 shared papers)Ge Lin (20 shared papers)Shi‐Min Yuan (10 shared papers)Wenbin He (16 shared papers)Hongchuan Nie (16 shared papers)
Journals: Journal of Medical Genetics (6 papers)Journal of Assisted Reproduction and Genetics (5 papers)Asian Journal of Andrology (4 papers)Clinica Chimica Acta (3 papers)Human Molecular Genetics (3 papers)
Partner nations: China United States Hong Kong

In The Last Decade

Lanlan Meng

54 papers receiving 987 citations

Peers

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-authors

The 25 scholars most cited alongside Lanlan Meng, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Lanlan Meng Line = papers co-authored together Lanlan Meng links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 56 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	DMC1 mutation that causes human non-obstructive azoospermia and premature ovarian insufficiency identified by whole-exome sequencing Journal of Medical Genetics ·Wenbin He, Chaofeng Tu, Qiang Liu, Lanlan Meng, Shi‐Min Yuan, Aixiang Luo, Fu‐Sheng He, Juan Shen, Wen Li, Juan Du, Changgao Zhong, Guangxiu Lu, Ge Lin, Li-Qing Fan, Yue‐Qiu Tan	2018	95
2	Loss-of-function mutations in TDRD7 lead to a rare novel syndrome combining congenital cataract and nonobstructive azoospermia in humans Genetics in Medicine ·Yue‐Qiu Tan, Chaofeng Tu, Lanlan Meng, Shi‐Min Yuan, Calvin Sjaarda, Aixiang Luo, Juan Du, Wen Li, Fei Gong, Changgao Zhong, Han‐Xiang Deng, Guangxiu Lu, Ping Liang, Ge Lin	2017	84
3	Biallelic mutations in CFAP65 lead to severe asthenoteratospermia due to acrosome hypoplasia and flagellum malformations Journal of Medical Genetics ·Weili Wang, Chaofeng Tu, Hongchuan Nie, Lanlan Meng, Yong Li, Shi‐Min Yuan, (unknown), Juan Du, Junpu Wang, Fei Gong, Li-Qing Fan, Guangxiu Lu, Ge Lin, Yue‐Qiu Tan	2019	71
4	Novel mutations in SPEF2 causing different defects between flagella and cilia bridge: the phenotypic link between MMAF and PCD Human Genetics ·Chaofeng Tu, Hongchuan Nie, Lanlan Meng, Weili Wang, Haiyu Li, Shi‐Min Yuan, Dehua Cheng, Wenbin He, Gang Liu, Juan Du, Fei Gong, Guangxiu Lu, Ge Lin, (unknown), Yue‐Qiu Tan	2020	57
5	Identification of DNAH6 mutations in infertile men with multiple morphological abnormalities of the sperm flagella Scientific Reports ·Chaofeng Tu, Hongchuan Nie, Lanlan Meng, Shi‐Min Yuan, Wenbin He, Aixiang Luo, Haiyu Li, Wen Li, Juan Du, Guangxiu Lu, Ge Lin, Yue‐Qiu Tan	2019	52
6	Meiotic recombination: insights into its mechanisms and its role in human reproduction with a special focus on non-obstructive azoospermia Human Reproduction Update ·Chunbo Xie, Weili Wang, Chaofeng Tu, Lanlan Meng, Guangxiu Lu, Ge Lin, Lin‐Yu Lu, Yue‐Qiu Tan	2022	49
7	Establishment of trimester-specific reference intervals of serum lipids and the associations with pregnancy complications and adverse perinatal outcomes: a population-based prospective study Annals of Medicine ·Yifan Lu, Zhaoxia Jia, Shaofei Su, Lican Han, Lanlan Meng, Guodong Tang, Jing Wang, Chunhong Zhang, Xin Xie, Yi Zhang, Yue Zhang, Yanhong Zhai, Zheng Cao	2021	41
8	CFAP65 is required in the acrosome biogenesis and mitochondrial sheath assembly during spermiogenesis Human Molecular Genetics ·Weili Wang, Shixong Tian, Hongchuan Nie, Chaofeng Tu, Chunyu Liu, Yong Li, Dongyan Li, Xiaoxuan Yang, Lanlan Meng, Tongyao Hu, (unknown), Juan Du, Li-Qing Fan, Guangxiu Lu, Ge Lin, Feng Zhang, Yue‐Qiu Tan	2021	34
9	Bi-allelic variants in DNHD1 cause flagellar axoneme defects and asthenoteratozoospermia in humans and mice The American Journal of Human Genetics ·Chen Tan, Lanlan Meng, Mingrong Lv, Xiaojin He, Yanwei Sha, Dongdong Tang, Yaqi Tan, Tongyao Hu, Wenbin He, Chaofeng Tu, Hongchuan Nie, Huan Zhang, Juan Du, Guangxiu Lu, Liqing Fan, Yunxia Cao, Ge Lin, Yue‐Qiu Tan	2021	33
10	TDRD7 participates in lens development and spermiogenesis by mediating autophagosome maturation Autophagy ·Chaofeng Tu, Haiyu Li, Xuyang Liu, Ying Wang, Wei Li, Lanlan Meng, Weili Wang, Yong Li, Dongyan Li, Juan Du, Guangxiu Lu, Ge Lin, Yue‐Qiu Tan	2021	28
11	In-Frame Variants in STAG3 Gene Cause Premature Ovarian Insufficiency Frontiers in Genetics ·Wenjuan Xiao, Wenbin He, Yaxin Zhang, Lanlan Meng, Guangxiu Lu, Ge Lin, Yue‐Qiu Tan, Juan Du	2019	28
12	Loss-of-function missense variant ofAKAP4induced male infertility through reduced interaction with QRICH2 during sperm flagella development Human Molecular Genetics ·Guohui Zhang, Dongyan Li, Chaofeng Tu, Lanlan Meng, Yue‐Qiu Tan, Zhi‐Liang Ji, Jiao Cheng, Guangxiu Lu, Ge Lin, Huan Zhang, Jin‐Peng Sun, Ming‐Wei Wang, Juan Du, Wenming Xu	2021	27
13	Bi-allelic variants in human WDR63 cause male infertility via abnormal inner dynein arms assembly Cell Discovery ·Shuai Lü, Yayun Gu, Yifei Wu, Shenmin Yang, Chenmeijie Li, Lanlan Meng, Wenwen Yuan, Tao Jiang, Xin Zhang, Yang Li, Cheng Wang, Mingxi Liu, Lan Ye, Xuejiang Guo, Hongbing Shen, Xiaoyu Yang, Yue‐Qiu Tan, Zhibin Hu	2021	26
14	Novel loss‐of‐function mutation in MCM8 causes premature ovarian insufficiency Molecular Genetics & Genomic Medicine ·Ya‐Xin Zhang, Wenbin He, Wenjuan Xiao, Lanlan Meng, Chen Tan, Juan Du, Guangxiu Lu, Ge Lin, Yue‐Qiu Tan	2020	24
15	Biallelic CFAP61 variants cause male infertility in humans and mice with severe oligoasthenoteratozoospermia Journal of Medical Genetics ·Tongyao Hu, Lanlan Meng, Chen Tan, Chen Luo, Wenbin He, Chaofeng Tu, Huan Zhang, Juan Du, Hongchuan Nie, Guangxiu Lu, Ge Lin, Yue‐Qiu Tan	2022	21
16	Homozygous variants in SYCP2L cause premature ovarian insufficiency Journal of Medical Genetics ·Wenbin He, Chen Tan, Yaxin Zhang, Lanlan Meng, Fei Gong, Guangxiu Lu, Ge Lin, Juan Du, Yue‐Qiu Tan	2020	20
17	A novel homozygous frameshift mutation in MNS1 associated with severe oligoasthenoteratozoospermia in humans Asian Journal of Andrology ·Yong Li, Weili Wang, Chaofeng Tu, Lanlan Meng, Tongyao Hu, Juan Du, Ge Lin, Hongchuan Nie, Yue-Qiu Tan	2020	19
18	An M1AP homozygous splice‐site mutation associated with severe oligozoospermia in a consanguineous family Clinical Genetics ·Chaofeng Tu, Ying Wang, Hongchuan Nie, Lanlan Meng, Weili Wang, Yong Li, Dongyan Li, Huan Zhang, Guangxiu Lu, Ge Lin, Yue‐Qiu Tan, Juan Du	2020	17
19	Bi-allelic variants in DNAH3 cause male infertility with asthenoteratozoospermia in humans and mice Human Reproduction Open ·Guiquan Meng, Yaling Wang, Chen Luo, Yu‐Mei Tan, Yong Li, Chen Tan, Chaofeng Tu, (unknown), Liang Hu, Huan Zhang, Lanlan Meng, Chunyu Liu, Leiyu Deng, Guangxiu Lu, Ge Lin, Juan Du, Yue‐Qiu Tan, Yanwei Sha, Lingbo Wang, Wenbin He	2024	17
20	Sperm flagellar 2 (SPEF2) is essential for sperm flagellar assembly in humans Asian Journal of Andrology ·Dongyan Li, Xiaoxuan Yang, Chaofeng Tu, Weili Wang, Lanlan Meng, Guangxiu Lu, Yue‐Qiu Tan, (unknown), Juan Du	2021	17

About Lanlan Meng

Lanlan Meng is a scholar working on Reproductive Medicine, Genetics, Molecular Biology, Public Health, Environmental and Occupational Health and Pulmonary and Respiratory Medicine, having authored 56 papers that have together received 1.0k indexed citations. Recurring topics across this work include Sperm and Testicular Function (22 papers), Reproductive Biology and Fertility (14 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (13 papers), DNA Repair Mechanisms (4 papers), Renal and related cancers (4 papers), Sexual Differentiation and Disorders (4 papers), Cystic Fibrosis Research Advances (4 papers) and Genetic and Kidney Cyst Diseases (3 papers). The work is most often cited by research in Reproductive Medicine (450 citations), Genetics (362 citations), Public Health, Environmental and Occupational Health (306 citations), Obstetrics and Gynecology (35 citations) and Molecular Biology (328 citations). Lanlan Meng has collaborated with scholars based in China, United States and Hong Kong. Frequent 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. Their work appears in journals such as Journal of Medical Genetics, Journal of Assisted Reproduction and Genetics, Asian Journal of Andrology, Clinica Chimica Acta and Human Molecular Genetics.

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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Lanlan Meng

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About Lanlan Meng

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