AASCIT - Journal -Reviewers

Individual Information

Lamei Yuan
Associate Professor
Center for Experimental Medicine, the Third Xiangya Hospital, Central South University

Research Interests
Medicine (Human Genetics)
Molecular Biology
Work Experience
From 07/2017 to present, Associate Professor , The Third Xiangya Hospital, Central South University
Selected Publications

Journal Articles

1.	Yuan L, Zheng W, Yang Z, Deng X, Song Z, Deng H. Association of the AADAC gene and Tourette syndrome in a Han Chinese cohort. Neurosci Lett. 2018;666:24-27.
2.	Yuan L, Song Z, Deng X, Yang Z, Yang Y, Guo Y, Lu H, Deng H. Genetic analysis of FBXO2, FBXO6, FBXO12 and FBXO41 variants in Han Chinese patients with sporadic Parkinson’s disease. Neurosci Bull. 2017;33(5):510-514.
3.	Lu Q, Yuan L (Co-first author), Xu H, Huang X, Yang Z, Yi J, Ni B, Chen Y, Deng H. Identification of a missense mutation in the TYR gene in a Chinese family with oculocutaneous albinism type 1. Molecular Medicine Reports. 2017;15(3):1426-1430.
4.	Yuan L, Song Z, Deng X, Zheng W, Guo Y, Yang Z, Deng H. Systematic analysis of genetic variants in Han Chinese patients with sporadic Parkinson's disease. Sci Rep. 2016;6:33850.
5.	Yuan L, Yi J, Lin Q, Xu H, Deng X, Xiong W, Xiao J, Jiang C, Yuan X, Chen Y, Deng H. Identification of a PRX variant in a Chinese family with congenital cataract by exome sequencing. QJM. 2016;109(11):731-735.
6.	Yuan L, Xu H, Yuan J, Deng X, Xiong W, Yang Z, Huang Y, Deng H. A novel FN1 variant associated with familial hematuria: TBMN? Clin Biochem. 2016;49(10-11):816-20.
7.	Yuan L, Song Z, Deng X, Zheng W, Yang Z, Yang Y, Deng H. Genetic analysis of FGF20 variants in Chinese Han patients with essential tremor. Neurosci Lett. 2016;620:159-162.
8.	Yuan L, Song Z, Deng X, Xiong W, Yang Z, Deng H. Association of the MTHFR rs1801131 and rs1801133 variants in sporadic Parkinson's disease patients. Neurosci Lett. 2016;616:26-31.
9.	Yuan L (Co-first author), Deng X, Song Z, Yang Z, Ni B, Chen Y, Deng H. Genetic analysis of the RAB39B gene in Chinese Han patients with Parkinson’s disease. Neurobiol Aging. 2015;36(10):2907.e11-2.
10.	Deng H, Yuan L (Co-first author). Genetic variants and animal models in SNCA and Parkinson disease. Ageing Res Rev. 2014;15:161-176.
11.	Yuan L, Wu S, Xu H, Xiao J, Yang Z, Xia H, Liu A, Hu P, Lu A, Shen Y, Xu F, Deng H. Identification of a novel PHEX mutation in a Chinese family with X-linked hypophosphatemic rickets using exome sequencing. Biol Chem. 2015;396 (1):27-33.
12.	Yuan L, Guo Y, Yi J, Xiao J, Yuan J, Xiong W, Xu H, Yang Z, Zhang J, Deng H. Identification of a novel GJA3 mutation in congenital nuclear cataract. Optom Vis Sci. 2015;92(3):337-342.
13.	Deng H, Yuan L (Co-first author). Molecular genetics of congenital nuclear cataract. Eur J Med Genet. 2014;57:113-122.
14.	Yuan L, Song Z, Xu H, Gu S, Zhu A, Gong L, Zhao Y, Deng H. EIF4G1 Ala502Val and Arg1205His variants in Chinese patients with Parkinson disease. Neurosci Lett. 2013; 543:69-71.
15.	Guo Y, Yuan L (Co-first author), Yi J, Xiao J, Xu H, Lv H, Xiong W, Zheng W, Guan L, Zhang J, Xiang H, Qi Y, Deng H. Identification of a GJA3 mutation in a Chinese family with congenital nuclear cataract using exome sequencing. Indian J Biochem Biophys. 2013; 50:253-258.
16.	Yuan L, Guo Y, Deng H. Genetic Research of von Hippel-Lindau Syndrome. Life Sci Res. 2012;16(2):181-185. (in Chinese)
17.	Chen Q, Yuan L, Deng X, Yang Z, Zhang S, Deng S, Lu H, Deng H. A missense variant p.Ala117Ser in the transthyretin gene of a Han Chinese family with familial amyloid polyneuropathy. Mol Neurobiol. 2017, doi: 10.1007/s12035-017-0694-0. PubMed PMID: 28762097.
18.	He D, Hu P, Deng X, Song Z, Yuan L, Yuan X, Deng H. Genetic analysis of the RIC3 gene in Han Chinese patients with Parkinson's disease. Neurosci Lett. 2017;653:351-354.
19.	Hu P, Wu S, Yuan L, Lin Q, Zheng W, Xia H, Xu H, Guan L, Deng H. Compound heterozygous POMT1 mutations in a Chinese family with autosomal recessive muscular dystrophy-dystroglycanopathy C1. J Cell Mol Med. 2017;21(7):1388-1393.
20.	Wu Y, Hu P, Xu H, Yuan J, Yuan L, Xiong W, Deng X, Deng H. A novel heterozygous COL4A4 missense mutation in a Chinese family with focal segmental glomerulosclerosis. J Cell Mol Med. 2016;20(12):2328-2332.
21.	Deng H, He D, Rong P, Xu H, Yuan L, Li L, Lu Q, Guo Y. Novel CLCN7 mutation identified in a Han Chinese family with autosomal dominant osteopetrosis-2. Mol Pain. 2016;12.
22.	Deng H, Lu Q, Xu H, Deng X, Yuan L, Yang Z, Guo Y, Lin Q, Xiao J, Guan L, Song Z. Identification of a novel missense FBN2 mutation in a Chinese family with congenital contractural arachnodactyly using exome sequencing. PLoS One. 2016;11(5):e0155908.
23.	Chen H, Huang X, Yuan L, Xia H, Xu H, Yang Y, Zheng W, Deng H. A homozygous parkin p.G284R mutation in a Chinese family with autosomal recessive juvenile parkinsonism. Neurosci Lett. 2016;624:100-104.
24.	Deng H, Deng S, Xu H, Deng HX, Chen Y, Yuan L, Deng X, Yang S, Guan L, Zhang J, Yuan H, Guo Y. Exome sequencing of a pedigree reveals S339L mutation in the TLN2 gene as a cause of fifth finger camptodactyly. PLoS One. 2016;11(5):e0155180.
25.	Chen H, Song Z, Yuan L, Xiong W, Yang Z, Gong L, Deng H. Genetic analysis of PITX3 variants in patients with essential tremor. Acta Neurol Scand. 2017;135(3):373-376.
26.	Xia H, Hu P, Yuan L, Xiong W, Xu H, Yi J, Yang Z, Deng X, Guo Y, Deng H. A homozygous MYO7A mutation associated to Usher syndrome and unilateral auditory neuropathy spectrum disorder. Mol Med Rep. 2017;16(4):4241-4246.
27.	Xia H, Xu H, Deng X, Yuan L, Xiong W, Yang Z, Deng H. Compound heterozygous GJB2 mutations associated with a consanguineous Chinese family with autosomal recessive nonsyndromic hearing loss. Acta Otolaryngol. 2016;136(8):782-5.
28.	Deng H, Huang X, Yuan L. Molecular genetics of the COL2A1-related disorders. Mutat Res Rev Mutat Res. 2016;768:1-13.
29.	Tan T, Song Z, Yuan L, Xiong W, Deng X, Ni B, Chen Y, Deng H. Genetic analysis of TREM2 variants in Chinese Han patients with sporadic Parkinson’s disease. Neurosci Lett. 2016;612:189-192.
30.	He S, Tan T, Song Z, Yuan L, Deng X, Ni B, Chen Y, Deng H. Genetic analysis of MC1R variants in Chinese Han patients with sporadic Parkinson’s disease. Neurosci Lett. 2016;611:101-105.
31.	Deng H, Tan T, Yuan L. Advances in the molecular genetics of non-syndromic polydactyly. Expert Rev Mol Med. 2015;17:e18.
32.	Zheng W, Chen H, Deng X, Yuan L, Yang Y, Song Z, Yang Z, Wu Y, Deng H. Identification of a novel mutation in the Titin gene in a Chinese family with limb-girdle muscular dystrophy 2J. Mol Neurobiol. 2016;53(8):5097-102.
33.	Zheng W, Zhang J, Deng X, Xiao J, Yuan L, Yang Y, Guan L, Song Z, Yang Z, Deng H. Identification of a premature termination mutation in the proline-rich transmembrane protein 2 gene in a Chinese family with febrile seizures. Mol Neurobiol. 2016;53(2):835-41.
34.	Huang X, Deng X, Xu H, Wu S, Yuan L, Yang Z, Yang Y, Deng H. Identification of a novel mutation in the COL2A1 gene in a Chinese family with spondyloepiphyseal dysplasia congenita. PLoS One. 2015;10(6):e0127529.
35.	Deng S, Xu H, Yuan J, Xiao J, Yuan L, Deng X, Guan L, Zhu A, Rong P, Zhang J, Deng H. Identification of a novel COL4A4 mutation in a Chinese family with autosomal dominant Alport syndrome using exome sequencing. Indian J Med Res. 2016;144(2):200-205.
36.	Deng S, Deng X, Yuan L, Song Z, Yang Z, Xiong W, Deng H. Genetic analysis of SNCA coding mutation in Chinese Han patients with Parkinson disease. Acta Neurologica Belgica. 2015;115(3):267-71.
37.	Guo Y, Yuan J, Liang H, Xiao J, Xu H, Yuan L, Gao K, Wu B, Tang Y, Li X, Deng H. Identification of a novel COL4A5 mutation in a Chinese family with X-linked Alport syndrome using exome sequencing. Mol Biol Rep. 2014;41:3631-3635.
38.	Guo Y, Yang H, Deng X, Song Z, Yang Z, Xiong W, Yuan L, Xu H, Deng S, Deng H. Genetic analysis of the S100B gene in Chinese patients with Parkinson disease. Neurosci Lett. 2013;555:134-136.