Xu-Ying Li

High-depth whole-genome sequencing identifies structure variants, copy number variants and short tandem repeats associated with Parkinson’s disease

Z. Gu, Shu Xie, Jinghong Ma, 2024, NPJ Parkinson's disease.

Identification of TARDBP Gly298Ser as a founder mutation for amyotrophic lateral sclerosis in Southern China

Xusheng Huang, Yan-ming Xu, Xiuli Feng, 2022, BMC Medical Genomics.