Zhihua Yang

发表

Genetic analysis of the TMEM230 gene in Chinese Han patients with Parkinson’s disease

Yuan Cheng, Changhe Shi, Jing Yang, 2017, Scientific Reports.

Whole‐exome sequencing identified novel variants in three Chinese Leigh syndrome pedigrees

Yibing Chen, Yucen Song, Zhihua Yang, 2022, American journal of medical genetics. Part A.

Two Novel Mutations and a de novo Mutation in PSEN1 in Early-onset Alzheimer’s Disease

Changhe Shi, Jing Yang, Shu-yu Zhang, 2019, Aging and disease.

No biallelic intronic AAGGG repeat expansion in RFC1 was found in patients with late-onset ataxia and MSA.

Han Liu, Changhe Shi, Jing Yang, 2020, Parkinsonism & related disorders.

Association of variants in microRNA with Parkinson’s disease in Chinese Han population

Changhe Shi, Jing Yang, Yuming Xu, 2018, Neurological Sciences.

Novel compound heterozygous GFPT1 mutations in a family with limb-girdle myasthenia with tubular aggregates

Changhe Shi, Jing Yang, Chengyuan Mao, 2019, Neuromuscular Disorders.

Metabolic Profiling Reveals Biochemical Pathways and Potential Biomarkers of Spinocerebellar Ataxia 3

Changhe Shi, Jing Yang, Chengyuan Mao, 2019, Front. Mol. Neurosci..

Identification of a novel mutation in PLA2G6 gene and phenotypic heterogeneity analysis of PLA2G6-related neurodegeneration.

Changhe Shi, Jing Yang, Yusheng li, 2019, Parkinsonism & related disorders.

Association analysis of 15 GWAS-linked loci with Parkinson’s disease in Chinese Han population

Changhe Shi, Jing Yang, Chengyuan Mao, 2020, Neuroscience Letters.

DNAJC12 mutation is rare in Chinese Han population with Parkinson's disease

Changhe Shi, Jing Yang, Yu-ming Xu, 2018, Neurobiology of Aging.

Genetic Study of Cerebral Small Vessel Disease in Chinese Han Population

Changhe Shi, Chengyuan Mao, Sen Wei, 2022, Frontiers in Neurology.

Spinocerebellar Ataxia Type 10 with Atypical Clinical Manifestation in Han Chinese

Changhe Shi, Chengyuan Mao, Hai-yang Luo, 2022, The Cerebellum.

New Insights Into the Pathogenesis of Alzheimer's Disease

Changhe Shi, Jing Yang, Chengyuan Mao, 2020, Frontiers in Neurology.

CHCHD2 gene mutations in familial and sporadic Parkinson's disease

C. Zuo, Changhe Shi, Jing Yang, 2016, Neurobiology of Aging.

AQP4 Association with Amyloid Deposition and Astrocyte Pathology in the Tg-ArcSwe Mouse Model of Alzheimer's Disease.

Changhe Shi, Jing Yang, Chengyuan Mao, 2017, Journal of Alzheimer's disease : JAD.

Modeling Parkinson's Disease Using Induced Pluripotent Stem Cells

Changhe Shi, Jing Yang, Chengyuan Mao, 2020, Stem cells international.

A novel RAB39B gene mutation in X‐linked juvenile parkinsonism with basal ganglia calcification

Hao Liu, Changhe Shi, Jing Yang, 2016, Movement disorders : official journal of the Movement Disorder Society.

GIPC1 CGG Repeat Expansion Is Associated with Movement Disorders

Han Liu, Changhe Shi, B. Song, 2022, Annals of neurology.

Analysis of Single Nucleotide Polymorphisms of STK32B, PPARGC1A and CTNNA3 Gene With Sporadic Parkinson's Disease Susceptibility in Chinese Han Population

Yuan Cheng, Mi-bo Tang, Changhe Shi, 2018, Front. Neurol..

Exome capture sequencing identifies a novel CCM1 mutation in a Chinese family with multiple cerebral cavernous malformations

Changhe Shi, B. Song, Jing Yang, 2016, The International journal of neuroscience.

α-Synuclein in Parkinson’s Disease: Does a Prion-Like Mechanism of Propagation from Periphery to the Brain Play a Role?

Changhe Shi, Jing Yang, Chengyuan Mao, 2020, The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry.

Carboxyl Terminus of Hsp70-Interacting Protein Is Increased in Serum and Cerebrospinal Fluid of Patients With Spinocerebellar Ataxia Type 3

Changhe Shi, Jing Yang, Chengyuan Mao, 2019, Front. Neurol..

Identification of a novel PAFAH1B1 missense mutation as a cause of mild lissencephaly with basal ganglia calcification

Changhe Shi, Yu-ming Xu, Shuo Zhang, 2019, Brain and Development.

SNCA but not DNM3 and GAK modifies age at onset of LRRK2-related Parkinson’s disease in Chinese population

Changhe Shi, Jing Yang, Chengyuan Mao, 2019, Journal of Neurology.

Genetic analysis of the TMEM230 gene in Chinese Han patients with Parkinson’s disease

Yuan Cheng, Changhe Shi, Jing Yang, 2017, Scientific Reports.

SMPD1 variants in Chinese Han patients with sporadic Parkinson's disease.

Changhe Shi, Jing Yang, Chengyuan Mao, 2017, Parkinsonism & related disorders.

TGM6 gene mutations in undiagnosed cerebellar ataxia patients.

Changhe Shi, Hai-yang Luo, Yu-ming Xu, 2018, Parkinsonism & related disorders.

Novel compound heterozygous PANK2 gene mutations in a Chinese patient with atypical pantothenate kinase-associated neurodegeneration

Yuan Cheng, Changhe Shi, Jing Yang, 2018, The International journal of neuroscience.

Two Novel Mutations and a de novo Mutation in PSEN1 in Early-onset Alzheimer’s Disease

Changhe Shi, Jing Yang, Shu-yu Zhang, 2019, Aging and disease.