Zhenwei Liu

发表

Identification of de novo germline mutations and causal genes for sporadic diseases using trio‐based whole‐exome/genome sequencing

Jinyu Wu, Zi-Bing Jin, Zhongshan Li, 2018, Biological reviews of the Cambridge Philosophical Society.

PRRT2 variants and effectiveness of various antiepileptic drugs in self-limited familial infantile epilepsy

Zhenwei Liu, Qianlei Zhao, Ying-chun Hu, 2021, Seizure.

Different experiences of two PRRT2-associated self-limited familial infantile epilepsy

Zhenwei Liu, Qianlei Zhao, Shiyu Fang, 2020, Acta Neurologica Belgica.

A de novo pathogenic CSNK1E mutation identified by exome sequencing in family trios with epileptic encephalopathy

Tao Zhang, N. Zhang, Jinyu Wu, 2018, Human mutation.

Identification of De Novo DNMT3A Mutations That Cause West Syndrome by Using Whole-Exome Sequencing

Jinyu Wu, Zhongshan Li, Zhenwei Liu, 2017, Molecular Neurobiology.

Whole-exome sequencing identifies a novel de novo mutation in DYNC1H1 in epileptic encephalopathies

Y. Liu, Zhenwei Liu, Zhen Wang, 2017, Scientific Reports.

mirVAFC: A Web Server for Prioritizations of Pathogenic Sequence Variants from Exome Sequencing Data via Classifications

Jinyu Wu, Zhongsheng Sun, Zhongshan Li, 2017, Human mutation.

mirDNMR: a gene-centered database of background de novo mutation rates in human

Wei Li, Yi Jiang, Denghui Chen, 2016, Nucleic Acids Res..

Integrative analyses of gene expression profile reveal potential crucial roles of mitotic cell cycle and microtubule cytoskeleton in pulmonary artery hypertension

Zhenwei Liu, Haiyan Li, Jing Guo, 2019, BMC Medical Genomics.

Microbiota dysbiosis in primary Sjögren's syndrome and the ameliorative effect of hydroxychloroquine.

Jinyu Wu, Zhenwei Liu, Jinfeng Wang, 2022, Cell reports.

Trio-based exome sequencing arrests de novo mutations in early-onset high myopia

Meixiao Shen, Ting Xie, Fan Lu, 2017, Proceedings of the National Academy of Sciences.

Nonrandom occurrence of multiple de novo coding variants in a proband indicates the existence of an oligogenic model in autism

N. Zhang, Jinyu Wu, Zhongshan Li, 2019, Genetics in Medicine.

De Novo Germline Mutations in SEMA5A Associated With Infantile Spasms

Y. Lou, Zhenwei Liu, Junzhao Zhao, 2019, Front. Genet..

Distinct genetic patterns of shared and unique genes across four neurodevelopmental disorders

Jinyu Wu, Zhongshan Li, Zhenwei Liu, 2020, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Whole Exome Sequencing Identified a Novel Biallelic SMARCAL1 Mutation in the Extremely Rare Disease SIOD

Zhen Wang, Zhenwei Liu, Shan Jiang, 2019, Front. Genet..

Whole-exome sequencing identifies a novel de novo mutation in DYNC1H1 in epileptic encephalopathies

Y. Liu, Zhenwei Liu, Zhen Wang, 2017, Scientific Reports.

Prioritized High-Confidence Risk Genes for Intellectual Disability Reveal Molecular Convergence During Brain Development

Jinyu Wu, Zhongshan Li, Zhenwei Liu, 2018, Front. Genet..

Circular RNA sequencing indicates circ-IQGAP2 and circ-ZC3H6 as noninvasive biomarkers of primary Sjögren's syndrome.

M. Brown, Jinyu Wu, Zhenwei Liu, 2020, Rheumatology.

Elevated CCL19/CCR7 Expression During the Disease Process of Primary Sjögren's Syndrome

M. Brown, Zhenwei Liu, Shan Jiang, 2019, Front. Immunol..

Metagenomic Analysis Reveals A Possible Association Between Respiratory Infection and Periodontitis

Jinyu Wu, T. Zhang, Zhongshan Li, 2020, medRxiv.

Increased RNA editing sites revealed as potential novel biomarkers for diagnosis in primary Sjögren's syndrome.

Huji Xu, Zhenwei Liu, Senhong Ying, 2023, Journal of autoimmunity.

Nonrandom occurrence of multiple de novo coding variants in a proband indicates the existence of an oligogenic model in autism

N. Zhang, Jinyu Wu, Zhongshan Li, 2019, Genetics in Medicine.