Lamei Yuan

1.4k total citations
83 papers, 1.0k citations indexed

About

Lamei Yuan is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Lamei Yuan has authored 83 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Molecular Biology, 25 papers in Genetics and 21 papers in Neurology. Recurrent topics in Lamei Yuan's work include Parkinson's Disease Mechanisms and Treatments (13 papers), RNA regulation and disease (10 papers) and Connective tissue disorders research (9 papers). Lamei Yuan is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (13 papers), RNA regulation and disease (10 papers) and Connective tissue disorders research (9 papers). Lamei Yuan collaborates with scholars based in China, United States and Slovakia. Lamei Yuan's co-authors include Hao Deng, Hongbo Xu, Zhijian Yang, Xiong Deng, Zhi Song, Yi Guo, Yan Yang, Sheng Deng, Wen Zheng and Xia Hong and has published in prestigious journals such as PLoS ONE, Scientific Reports and Neurobiology of Aging.

In The Last Decade

Lamei Yuan

78 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lamei Yuan China 19 551 268 249 133 106 83 1.0k
Sebahattin Çırak Germany 20 538 1.0× 170 0.6× 119 0.5× 106 0.8× 51 0.5× 62 943
Jason Gibson United States 14 467 0.8× 81 0.3× 118 0.5× 80 0.6× 63 0.6× 22 1.1k
Claudio Graziano Italy 20 695 1.3× 325 1.2× 62 0.2× 104 0.8× 73 0.7× 77 1.2k
Zhijian Yang China 15 319 0.6× 129 0.5× 102 0.4× 61 0.5× 52 0.5× 52 585
Toru Kurokawa Japan 20 589 1.1× 97 0.4× 178 0.7× 267 2.0× 92 0.9× 62 1.4k
Maila Penttinen Finland 19 383 0.7× 173 0.6× 219 0.9× 114 0.9× 29 0.3× 31 920
Davide Tonduti Italy 19 728 1.3× 183 0.7× 89 0.4× 83 0.6× 87 0.8× 64 1.1k
Göknur Haliloğlu Türkiye 23 922 1.7× 259 1.0× 210 0.8× 224 1.7× 68 0.6× 116 1.7k
Andrea Accogli Italy 17 322 0.6× 217 0.8× 83 0.3× 85 0.6× 29 0.3× 65 771
Julien Ratelade United States 26 629 1.1× 73 0.3× 685 2.8× 146 1.1× 347 3.3× 30 1.6k

Countries citing papers authored by Lamei Yuan

Since Specialization
Citations

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

Fields of papers citing papers by Lamei Yuan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lamei Yuan

This figure shows the co-authorship network connecting the top 25 collaborators of Lamei Yuan. A scholar is included among the top collaborators of Lamei Yuan 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 Lamei Yuan. Lamei Yuan 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.
Yuan, Lamei, et al.. (2025). Genetic architecture of amyotrophic lateral sclerosis: a comprehensive review. Journal of genetics and genomics. 52(10). 1155–1176.
2.
Deng, Xinyue, Shan Wu, Hao Deng, & Lamei Yuan. (2024). A TSC2 recurrent variant c.5126C>T in a Han-Chinese family with tuberous sclerosis complex. Pakistan Journal of Medical Sciences. 41(1). 263–268. 1 indexed citations
3.
Deng, Hao, et al.. (2024). Unraveling ptosis: A comprehensive review of clinical manifestations, genetics, and treatment. Progress in Retinal and Eye Research. 105. 101327–101327.
4.
Yuan, Lamei, Hanlin Yang, Yadong Guo, et al.. (2023). Analysis ofSOD1variants in Chinese patients with familial amyotrophic lateral sclerosis. QJM. 116(5). 365–374. 5 indexed citations
5.
Huang, Yanxia, et al.. (2023). Novel compound heterozygous variants in the USH2A gene associated with autosomal recessive retinitis pigmentosa without hearing loss. Frontiers in Cell and Developmental Biology. 11. 1129862–1129862.
6.
Qin, Xiang, Hongbo Xu, Zhijian Yang, et al.. (2021). Novel MFSD8 Variants in a Chinese Family with Nonsyndromic Macular Dystrophy. Journal of Ophthalmology. 2021. 1–5. 12 indexed citations
7.
Xiong, Ying, et al.. (2021). Identification of compound heterozygous DNAH11 variants in a Han‐Chinese family with primary ciliary dyskinesia. Journal of Cellular and Molecular Medicine. 25(18). 9028–9037. 8 indexed citations
8.
Yuan, Meng, Yi Guo, Xia Hong, et al.. (2021). Novel SCN5A and GPD1L Variants Identified in Two Unrelated Han-Chinese Patients With Clinically Suspected Brugada Syndrome. Frontiers in Cardiovascular Medicine. 8. 758903–758903. 6 indexed citations
9.
Yuan, Lamei, Xiangyu Chen, Zhi Song, et al.. (2020). Extended Study of NUS1 Gene Variants in Parkinson's Disease. Frontiers in Neurology. 11. 583182–583182. 6 indexed citations
10.
Qin, Xiang, et al.. (2019). Identification of a Heterozygous Mutation in the TGFBI Gene in a Hui-Chinese Family with Corneal Dystrophy. Journal of Ophthalmology. 2019. 1–7. 7 indexed citations
11.
Deng, Sheng, Hongbo Xu, Deren Hou, et al.. (2019). Novel and Recurring <b><i>NOTCH3</i></b> Mutations in Two Chinese Patients with CADASIL. Neurodegenerative Diseases. 19(1). 35–42. 9 indexed citations
12.
Chen, Han, Lamei Yuan, Zhi Song, et al.. (2018). Genetic Analysis of LRRK1 and LRRK2 Variants in Essential Tremor Patients. Genetic Testing and Molecular Biomarkers. 22(6). 398–402. 8 indexed citations
13.
Guo, Yi, Xia Hong, Hongbo Xu, et al.. (2018). Identification of a Novel Keratin 9 Missense Mutation in a Chinese Family with Epidermolytic Palmoplantar Keratoderma. Cellular Physiology and Biochemistry. 46(5). 1919–1929. 13 indexed citations
14.
Chen, Qian, Lamei Yuan, Xiong Deng, et al.. (2017). A Missense Variant p.Ala117Ser in the Transthyretin Gene of a Han Chinese Family with Familial Amyloid Polyneuropathy. Molecular Neurobiology. 55(6). 4911–4917. 18 indexed citations
15.
Deng, Hao, Sheng Deng, Hongbo Xu, et al.. (2016). Exome Sequencing of a Pedigree Reveals S339L Mutation in the TLN2 Gene as a Cause of Fifth Finger Camptodactyly. PLoS ONE. 11(5). e0155180–e0155180. 8 indexed citations
16.
Deng, Hao, Qian Lü, Hongbo Xu, et al.. (2016). Identification of a Novel Missense FBN2 Mutation in a Chinese Family with Congenital Contractural Arachnodactyly Using Exome Sequencing. PLoS ONE. 11(5). e0155908–e0155908. 12 indexed citations
17.
Yuan, Lamei, et al.. (2016). Association of the MTHFR rs1801131 and rs1801133 variants in sporadic Parkinson’s disease patients. Neuroscience Letters. 616. 26–31. 21 indexed citations
18.
Yuan, Lamei, Yi Guo, Jingjing Xiao, et al.. (2015). Identification of a Novel GJA3 Mutation in Congenital Nuclear Cataract. Optometry and Vision Science. 92(3). 337–342. 21 indexed citations
19.
20.
Deng, Hao & Lamei Yuan. (2014). Molecular genetics of congenital nuclear cataract. European Journal of Medical Genetics. 57(2-3). 113–122. 47 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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