Zhang J - Search Results

1

Whole exome sequencing identifies novel variant underlying hereditary spastic paraplegia in consanguineous Pakistani families.

Zulfiqar S, Tariq M, Ali Z, Fatima A, Klar J, Abdullah U, Ali A, Ramzan S, He S, Zhang J, Khan A, Shah S, Khan S, Makhdoom EH, Schuster J, Dahl N, Baig SM. Zulfiqar S, et al. Among authors: zhang j. J Clin Neurosci. 2019 Sep;67:19-23. doi: 10.1016/j.jocn.2019.06.039. Epub 2019 Jul 4. J Clin Neurosci. 2019. PMID: 31281085

2

A bioinformatic study revealed serotonergic neurons are involved in the etiology and therapygenetics of anxiety disorders.

Liu HK, He SJ, Zhang JG. Liu HK, et al. Transl Psychiatry. 2021 May 20;11(1):297. doi: 10.1038/s41398-021-01432-5. Transl Psychiatry. 2021. PMID: 34011923 Free PMC article.

3

Whole exome sequencing identified a homozygous novel variant in DOP1A gene in the Pakistan family with neurodevelopmental disabilities: case report and literature review.

Zhang W, Tariq M, Roy B, Shen J, Khan A, Altaf Malik N, He S, Baig SM, Fang X, Zhang J. Zhang W, et al. Among authors: zhang j. Front Genet. 2024 May 16;15:1351710. doi: 10.3389/fgene.2024.1351710. eCollection 2024. Front Genet. 2024. PMID: 38818041 Free PMC article.

4

Attractin Participates in Schizophrenia by Affecting Testosterone Levels.

Li N, Gao S, Wang S, He S, Wang J, He L, Jiang D, Shi YS, Zhang J, Gu Y, Chen T, Kong M, Xu X, Zhao Q. Li N, et al. Among authors: zhang j. Front Cell Dev Biol. 2021 Nov 11;9:755165. doi: 10.3389/fcell.2021.755165. eCollection 2021. Front Cell Dev Biol. 2021. PMID: 34869343 Free PMC article.

5

A Cysteinyl-tRNA Synthetase Mutation Causes Novel Autosomal-Dominant Inheritance of a Parkinsonism/Spinocerebellar-Ataxia Complex.

Liu HK, Hao HL, You H, Feng F, Qi XH, Huang XY, Hou B, Tian CG, Wang H, Yang HM, Wang J, Wu R, Fang H, Zhou JN, Zhang JG, Zhang ZX. Liu HK, et al. Among authors: zhang zx, zhang jg. Neurosci Bull. 2024 Oct;40(10):1489-1501. doi: 10.1007/s12264-024-01231-0. Epub 2024 Jun 13. Neurosci Bull. 2024. PMID: 38869703 Free PMC article.

6

Integrative genetic and single cell RNA sequencing analysis provides new clues to the amyotrophic lateral sclerosis neurodegeneration.

Liu H, Guan L, Deng M, Bolund L, Kristiansen K, Zhang J, Luo Y, Zhang Z. Liu H, et al. Among authors: zhang j, zhang z. Front Neurosci. 2023 Feb 17;17:1116087. doi: 10.3389/fnins.2023.1116087. eCollection 2023. Front Neurosci. 2023. PMID: 36875658 Free PMC article.

7

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

Wang C, Liu H, Li XY, Ma J, Gu Z, Feng X, Xie S, Tang BS, Chen S, Wang W, Wang J, Zhang J, Chan P. Wang C, et al. Among authors: zhang j. NPJ Parkinsons Dis. 2024 Jul 23;10(1):134. doi: 10.1038/s41531-024-00722-1. NPJ Parkinsons Dis. 2024. PMID: 39043730 Free PMC article.

8

Non-Invasive Prenatal Diagnosis of Monogenic Disorders Through Bayesian- and Haplotype-Based Prediction of Fetal Genotype.

Li J, Lu J, Su F, Yang J, Ju J, Lin Y, Xu J, Qi Y, Hou Y, Wu J, He W, Yang Z, Wu Y, Tang Z, Huang Y, Zhang G, Yang Y, Long Z, Cheng X, Liu P, Xia J, Zhang Y, Wang Y, Chen F, Zhang J, Zhao L, Jin X, Gao Y, Yin A. Li J, et al. Among authors: zhang g, zhang j, zhang y. Front Genet. 2022 Jul 1;13:911369. doi: 10.3389/fgene.2022.911369. eCollection 2022. Front Genet. 2022. PMID: 35846127 Free PMC article.

9

Populational pan-ethnic screening panel enabled by deep whole genome sequencing.

Yang L, Lin Z, Gao Y, Zhang J, Peng H, Li Y, Che J, Zhao L, Zhang J. Yang L, et al. Among authors: zhang j. NPJ Genom Med. 2023 Nov 20;8(1):38. doi: 10.1038/s41525-023-00383-8. NPJ Genom Med. 2023. PMID: 37985665 Free PMC article.

10

New Gene Variants Associated with the Risk of Chronic HBV Infection.

Fan M, Wang J, Wang S, Li T, Pan H, Liu H, Xu H, Zhernakova DV, O'Brien SJ, Feng Z, Chang L, Dai E, Lu J, Xi H, Yu Y, Zhang J, Wang B, Zeng Z. Fan M, et al. Among authors: zhang j. Virol Sin. 2020 Aug;35(4):378-387. doi: 10.1007/s12250-020-00200-x. Epub 2020 Apr 15. Virol Sin. 2020. PMID: 32297155 Free PMC article.

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