Ngo KJ - Search Results

1

Lack of Association Between GBA Mutations and Motor Complications in European and American Parkinson's Disease Cohorts.

Maple-Grødem J, Paul KC, Dalen I, Ngo KJ, Wong D, Macleod AD, Counsell CE, Bäckström D, Forsgren L, Tysnes OB, Kusters CDJ, Fogel BL, Bronstein JM, Ritz B, Alves G. Maple-Grødem J, et al. Among authors: ngo kj. J Parkinsons Dis. 2021;11(4):1569-1578. doi: 10.3233/JPD-212657. J Parkinsons Dis. 2021. PMID: 34275908 Free PMC article.

2

Expanding the global prevalence of spinocerebellar ataxia type 42.

Ngo K, Aker M, Petty LE, Chen J, Cavalcanti F, Nelson AB, Hassin-Baer S, Geschwind MD, Perlman S, Italiano D, Laganà A, Cavallaro S, Coppola G, Below JE, Fogel BL. Ngo K, et al. Neurol Genet. 2018 Apr 5;4(3):e232. doi: 10.1212/NXG.0000000000000232. eCollection 2018 Jun. Neurol Genet. 2018. PMID: 29629410 Free PMC article. No abstract available.

3

Spinocerebellar Ataxia type 29 in a family of Māori descent.

Ngo KJ, Poke G, Neas K, Fogel BL. Ngo KJ, et al. Cerebellum Ataxias. 2019 Oct 12;6:14. doi: 10.1186/s40673-019-0108-3. eCollection 2019. Cerebellum Ataxias. 2019. PMID: 31632679 Free PMC article.

4

A diagnostic ceiling for exome sequencing in cerebellar ataxia and related neurological disorders.

Ngo KJ, Rexach JE, Lee H, Petty LE, Perlman S, Valera JM, Deignan JL, Mao Y, Aker M, Posey JE, Jhangiani SN, Coban-Akdemir ZH, Boerwinkle E, Muzny D, Nelson AB, Hassin-Baer S, Poke G, Neas K, Geschwind MD, Grody WW, Gibbs R, Geschwind DH, Lupski JR, Below JE, Nelson SF, Fogel BL. Ngo KJ, et al. Hum Mutat. 2020 Feb;41(2):487-501. doi: 10.1002/humu.23946. Epub 2019 Nov 25. Hum Mutat. 2020. PMID: 31692161 Free PMC article.

5

miR-142-3p regulates cortical oligodendrocyte gene co-expression networks associated with tauopathy.

Hinman JD, Ngo KJ, Kim D, Chen C, Abraham CR, Ghanbari M, Ikram MA, Kushner SA, Kawaguchi R, Coppola G, Goth K, Bellusci S, Hernandez I, Kosik KS, Fogel BL. Hinman JD, et al. Among authors: ngo kj. Hum Mol Genet. 2021 Mar 25;30(1):103-118. doi: 10.1093/hmg/ddaa252. Hum Mol Genet. 2021. PMID: 33555315 Free PMC article.

6

De novo pathogenic variant in SETX causes a rapidly progressive neurodegenerative disorder of early childhood-onset with severe axonal polyneuropathy.

Hadjinicolaou A, Ngo KJ, Conway DY, Provias JP, Baker SK, Brady LI, Bennett CL, La Spada AR, Fogel BL, Yoon G. Hadjinicolaou A, et al. Among authors: ngo kj. Acta Neuropathol Commun. 2021 Dec 18;9(1):194. doi: 10.1186/s40478-021-01277-5. Acta Neuropathol Commun. 2021. PMID: 34922620 Free PMC article.

7

Alterations in oligodendrocyte transcriptional networks reveal region-specific vulnerabilities to neurological disease.

Tommasini D, Fox R, Ngo KJ, Hinman JD, Fogel BL. Tommasini D, et al. Among authors: ngo kj. iScience. 2023 Mar 8;26(4):106358. doi: 10.1016/j.isci.2023.106358. eCollection 2023 Apr 21. iScience. 2023. PMID: 36994077 Free PMC article.

8

Spinocerebellar ataxia type 14 (SCA14) in an Argentinian family: a case report.

Duggirala N, Ngo KJ, Pagnoni SM, Rosa AL, Fogel BL. Duggirala N, et al. Among authors: ngo kj. J Med Case Rep. 2023 Apr 27;17(1):168. doi: 10.1186/s13256-023-03897-y. J Med Case Rep. 2023. PMID: 37101238 Free PMC article.

9

Cross-Sectional Analysis of Exome Sequencing Diagnosis in Patients With Neurologic Phenotypes Facing Barriers to Clinical Testing.

Watson S, Ngo KJ, Stevens HA, Wong DY, Kim J, Song Y, Han B, Hyun SI, Khang R, Ryu SW, Lee E, Seo G, Lee H, Lajonchere C, Fogel BL. Watson S, et al. Among authors: ngo kj. Neurol Genet. 2024 Apr 9;10(3):e200133. doi: 10.1212/NXG.0000000000200133. eCollection 2024 Jun. Neurol Genet. 2024. PMID: 38617022 Free PMC article.

10

Lysosomal genes contribute to Parkinson's disease near agriculture with high intensity pesticide use.

Ngo KJ, Paul KC, Wong D, Kusters CDJ, Bronstein JM, Ritz B, Fogel BL. Ngo KJ, et al. NPJ Parkinsons Dis. 2024 Apr 25;10(1):87. doi: 10.1038/s41531-024-00703-4. NPJ Parkinsons Dis. 2024. PMID: 38664407 Free PMC article.

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