Yu Lin

Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia

Wan‐Jin Chen, Yu Lin, Zhi‐Qi Xiong et al. · Nature Genetics · 2011 · 477 citations

Transcriptional Regulation, Mendelian Disorder, Genetic Disorder +6

Analysis of TGFBI gene mutations in Chinese patients with corneal dystrophies and review of the literature.

Juhua Yang, Xiaoli Han, Dinggou Huang et al. · PubMed · 2010 · 51 citations · Full text

A frameshift mutation in HTRA1 expands CARASIL syndrome and peripheral small arterial disease to the Chinese population

Bin Cai, Jiabin Zeng, Yi Lin et al. · Neurological Sciences · 2015 · 21 citations

Carasil Syndrome, Vascular Disease, Cardiovascular Disease +8

Six Visual Rating Scales as A Biomarker for Monitoring Atrophied Brain Volume in Parkinson’s Disease

Yu Lin, Ying Fu, Yi‐Fang Zeng et al. · Aging and Disease · 2020 · 12 citations · Full text