Wang Z - Search Results

1

Clinical testing panels for ALS: global distribution, consistency, and challenges.

Dilliott AA, Al Nasser A, Elnagheeb M, Fifita J, Henden L, Keseler IM, Lenz S, Marriott H, Mccann E, Mesaros M, Opie-Martin S, Owens E, Palus B, Ross J, Wang Z, White H, Al-Chalabi A, Andersen PM, Benatar M, Blair I, Cooper-Knock J, Harrington EA, Heckmann J, Landers J, Moreno C, Nel M, Rampersaud E, Roggenbuck J, Rouleau G, Traynor B, Van Blitterswijk M, Van Rheenen W, Veldink J, Weishaupt J, Drury L, Harms MB, Farhan SMK; Amyotrophic lateral sclerosis spectrum disorders Gene Curation Expert Panel. Dilliott AA, et al. Among authors: wang z. Amyotroph Lateral Scler Frontotemporal Degener. 2023 Aug;24(5-6):420-435. doi: 10.1080/21678421.2023.2173015. Epub 2023 Mar 10. Amyotroph Lateral Scler Frontotemporal Degener. 2023. PMID: 36896705 Review.

2

New mutation in the SOD1 (copper/zinc superoxide dismutase-1) gene in a Chinese amyotrophic lateral sclerosis (ALS) patient.

Cui F, Cai W, Wang Z, Ren Y, Li M, Sun Z, Huang X. Cui F, et al. Among authors: wang z. Amyotroph Lateral Scler Frontotemporal Degener. 2013 Dec;14(7-8):635-7. doi: 10.3109/21678421.2013.817589. Epub 2013 Jul 29. Amyotroph Lateral Scler Frontotemporal Degener. 2013. PMID: 23889606

3

Screening for possible oligogenic pathogenesis in Chinese sporadic ALS patients.

Zhang H, Cai W, Chen S, Liang J, Wang Z, Ren Y, Liu W, Zhang X, Sun Z, Huang X. Zhang H, et al. Among authors: wang z. Amyotroph Lateral Scler Frontotemporal Degener. 2018 Aug;19(5-6):419-425. doi: 10.1080/21678421.2018.1432659. Epub 2018 Feb 7. Amyotroph Lateral Scler Frontotemporal Degener. 2018. PMID: 29411640

4

Mutation Screening of the GLE1 Gene in a Large Chinese Cohort of Amyotrophic Lateral Sclerosis Patients.

Li Y, Sun B, Wang Z, He Z, Yang F, Wang H, Cui F, Chen Z, Ling L, Wang C, Huang X. Li Y, et al. Among authors: wang h, wang z, wang c. Front Neurosci. 2021 May 5;15:595775. doi: 10.3389/fnins.2021.595775. eCollection 2021. Front Neurosci. 2021. PMID: 34025336 Free PMC article.

5

Sequencing of neurofilament genes identified NEFH Ser787Arg as a novel risk variant of sporadic amyotrophic lateral sclerosis in Chinese subjects.

Lin F, Lin W, Zhu C, Lin J, Zhu J, Li XY, Wang Z, Wang C, Huang H. Lin F, et al. Among authors: wang z, wang c. BMC Med Genomics. 2021 Sep 11;14(1):222. doi: 10.1186/s12920-021-01073-z. BMC Med Genomics. 2021. PMID: 34511133 Free PMC article.

6

Identification of a novel missense (C7W) mutation of SOD1 in a large familial amyotrophic lateral sclerosis pedigree.

Wang Z, Cai W, Cui F, Cai T, Chen Z, Mao F, Teng H, Chen L, Wang J, Sun Z, Huang X, Yu P. Wang Z, et al. Among authors: wang j. Neurobiol Aging. 2014 Mar;35(3):725.e11-5. doi: 10.1016/j.neurobiolaging.2013.08.024. Epub 2013 Oct 1. Neurobiol Aging. 2014. PMID: 24094577

7

Novel mutations and molecular pathways identified in patients with brain iron accumulation disorders.

Si L, Wang Z, Li XY, Song Y, Yao T, Xu E, Wang X, Wang C. Si L, et al. Among authors: wang x, wang z, wang c. Neurogenetics. 2023 Oct;24(4):231-241. doi: 10.1007/s10048-023-00725-9. Epub 2023 Jul 15. Neurogenetics. 2023. PMID: 37453004

8

Multidisciplinary molecular consultation increases the diagnosis of pediatric epileptic encephalopathy and neurodevelopmental disorders.

Zhang L, Li XY, Xu F, Gao L, Wang Z, Wang X, Li X, Liu M, Zhu J, Yao T, Ye J, Qi XH, Wang Y, Zhao G, Wang C; Xuanwu Molecular Counselling Group for Neurogenetic Diseases. Zhang L, et al. Among authors: wang x, wang z, wang y, wang c. Mol Genet Genomic Med. 2023 Nov;11(11):e2243. doi: 10.1002/mgg3.2243. Epub 2023 Jul 24. Mol Genet Genomic Med. 2023. PMID: 37489029 Free PMC article.

9

Hartnup disease presenting as hereditary spastic paraplegia and severe peripheral neuropathy.

Wang X, Li XY, Piao Y, Yuan G, Lin Y, Chen H, Wang Z, Li C, Wang C. Wang X, et al. Among authors: wang z, wang c. Am J Med Genet A. 2022 Jan;188(1):237-242. doi: 10.1002/ajmg.a.62475. Epub 2021 Aug 30. Am J Med Genet A. 2022. PMID: 34459558

10

Heterozygous HTRA1 Mutations Cause Cerebral Small Vessel Diseases: Genetic, Clinical, and Pathologic Findings From 3 Chinese Pedigrees.

Yao T, Zhu J, Wu X, Li X, Fu Y, Wang Y, Wang Z, Xu F, Lai H, He A, Teng L, Wang C, Song H. Yao T, et al. Among authors: wang z, wang y, wang c. Neurol Genet. 2022 Dec 5;8(6):e200044. doi: 10.1212/NXG.0000000000200044. eCollection 2022 Dec. Neurol Genet. 2022. PMID: 36524103 Free PMC article.

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