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European Journal of Medical Genetics|January 4, 2014
Molecular genetics of congenital nuclear cataractHao Deng, Lamei YuanAgeing Research Reviews|April 29, 2014
Genetic variants and animal models in SNCA and Parkinson diseaseHao Deng, Lamei YuanSignal Transduction and Targeted Therapy|September 21, 2021
Human genetic basis of coronavirus disease 2019Hao Deng, Xue Yan, Lamei YuanExpert Reviews in Molecular Medicine|October 31, 2015
Advances in the molecular genetics of non-syndromic polydactylyHao Deng, Ting Tan, Lamei YuanMutation Research. Reviews in Mutation Research|November 21, 2018
Molecular genetics of the POMT1-related muscular dystrophy-dystroglycanopathiesPengzhi Hu, Lamei Yuan, Hao DengJournal of Molecular Medicine (Berlin, Germany)|July 17, 2023
Auricular fistula: a review of its clinical manifestations, genetics, and treatmentsLamei Yuan, Ruikang Yang, Hao DengMutation Research. Reviews in Mutation Research|May 29, 2016
Molecular genetics of the COL2A1-related disordersHao Deng, Xiangjun Huang, Lamei YuanProgress in Retinal and Eye Research|December 26, 2024
Unraveling ptosis: A comprehensive review of clinical manifestations, genetics, and treatmentHao Deng, Qianling Zhang, Junhui Yi, et al.Ageing Research Reviews|May 26, 2023
The role of the PLA2G6 gene in neurodegenerative diseasesXinyue Deng, Lamei Yuan, Joseph Jankovic, et al.Journal of Advanced Research|January 4, 2024
CADASIL: A NOTCH3-associated cerebral small vessel diseaseLamei Yuan, Xiangyu Chen, Joseph Jankovic, et al.Pageof 9