Lamei Yuan

ResearcherID Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2018-2021
Publications (10 Years): 8

Top Venues

Molecular genetics & genomic medicine

Journal of ophthalmology

Bioscience reports

Journal of neurology

The Third Xiangya Hospital, Central South University (PHD)

This page only lists publications with an associated author ORCID identifier.

Education History

The Third Xiangya Hospital, Central South University Sep 6o 2012 - May 19o 2017

China

PHD :: Center for Experimental Medicine

Publications

Qin Xiang, Yanna Cao, Hongbo Xu, Zhijian Yang, Liang Tang, Ju Xiang, Jianming Li, Hao Deng, Lamei Yuan
Novel MFSD8 Variants in a Chinese Family with Nonsyndromic Macular Dystrophy. Journal of ophthalmology 2021 (2021)
Yuan Wu, Yi Guo, Junhui Yi, Hongbo Xu, Lamei Yuan, Zhijian Yang, Hao Deng
Heterozygous RHO p.R135W missense mutation in a large Han-Chinese family with retinitis pigmentosa and different refractive errors. Bioscience reports 39 (7) (2019)
Qin Xiang, Lamei Yuan, Yanna Cao, Hongbo Xu, Yunfeiyang Li, Hao Deng
Identification of a Heterozygous Mutation in the TGFBI Gene in a Hui-Chinese Family with Corneal Dystrophy. Journal of ophthalmology 2019 (2019)
Mingyuan Wang, Yi Guo, Pengfei Rong, Hongbo Xu, Lina Gong, Hao Deng, Lamei Yuan
COL1A2 p.Gly1066Val variant identified in a Han Chinese family with osteogenesis imperfecta type I. Molecular genetics & genomic medicine 7 (5) (2019)
Yi Guo, Peng Wang, Xiaorong Li, Shaihong Zhu, Hongbo Xu, Shizhou Li, Hao Deng, Lamei Yuan
Identifying a BRCA2 c.5722_5723del mutation in a Han-Chinese family with breast cancer. Bioscience reports 39 (4) (2019)
Shan Wu, Sheng Deng, Zhi Song, Hongbo Xu, Zhijian Yang, Xin Liu, Li Qi, Hao Deng, Lamei Yuan
A Disease-Causing FRMD7 Variant in a Chinese Family with Infantile Nystagmus. Journal of molecular neuroscience : MN 67 (3) (2019)
Xiangjun Huang, Yi Guo, Hongbo Xu, Zhijian Yang, Xiong Deng, Hao Deng, Lamei Yuan
Identification of a novel EVC variant in a Han-Chinese family with Ellis-van Creveld syndrome. Molecular genetics & genomic medicine 7 (9) (2019)
Kuan Fan, Haixia Zhu, Hongbo Xu, Ping Mao, Lamei Yuan, Hao Deng
The identification of a transthyretin variant p.D38G in a Chinese family with early-onset leptomeningeal amyloidosis. Journal of neurology 266 (1) (2018)

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Publication Activity (10 Years)

Top Topics

Top Venues

Lamei Yuan