Jin Zhang

Spinocerebellar ataxia 17: Inconsistency between phenotype and neuroimage findings

W. Gu, Y. Hao, Jin Zhang, 2013, Annals of Indian Academy of Neurology.

Clinical phenotype and genetic mutation of one case with head tremor and cerebellar atrophy

Kunpeng Xie, W. Gu, Y. Hao, 2017 .

Autosomal Recessive Cerebellar Ataxia Type 1: Phenotypic and Genetic Correlation in a Cohort of Chinese Patients with SYNE1 Variants

X. Duan, Ren-bin Wang, W. Gu, 2020, The Cerebellum.

Autosomal Recessive Cerebellar Ataxia Type 1: Phenotypic and Genetic Correlation in a Cohort of Chinese Patients with SYNE1 Variants

X. Duan, Ren-bin Wang, W. Gu, 2020, The Cerebellum.

Identification of a Splicing Mutation in ITPR1 via WES in a Chinese Early-Onset Spinocerebellar Ataxia Family

W. Gu, Y. Hao, Zhenhua Cao, 2017, The Cerebellum.

Identification of a Splicing Mutation in ITPR1 via WES in a Chinese Early-Onset Spinocerebellar Ataxia Family

Peng Yu, W. Gu, Y. Hao, 2017, The Cerebellum.

Genome-wide association study identifies a new susceptibility locus in PLA2G4C for Multiple System Atrophy.

Sonja W. Scholz, A. Singleton, Y. Kusakabe, 2023, medRxiv.