Ng CC - Search Results

1

Whole exome sequencing identifies a novel SCN1A mutation in genetic (idiopathic) generalized epilepsy and juvenile myoclonic epilepsy subtypes.

Chan CK, Low JS, Lim KS, Low SK, Tan CT, Ng CC. Chan CK, et al. Among authors: ng cc. Neurol Sci. 2020 Mar;41(3):591-598. doi: 10.1007/s10072-019-04122-9. Epub 2019 Nov 13. Neurol Sci. 2020. PMID: 31720899

2

Slow carbamazepine clearance in a nonadherent Malay woman with epilepsy and thyrotoxicosis.

Yeap LL, Lim KS, Ng CC, Hui-Ping Khor A, Lo YL. Yeap LL, et al. Among authors: ng cc. Ther Drug Monit. 2014 Feb;36(1):3-9. doi: 10.1097/FTD.0000000000000024. Ther Drug Monit. 2014. PMID: 24342894

3

HLA-B*15:02 association with carbamazepine-induced Stevens-Johnson syndrome and toxic epidermal necrolysis in an Indian population: a pooled-data analysis and meta-analysis.

Khor AH, Lim KS, Tan CT, Wong SM, Ng CC. Khor AH, et al. Among authors: ng cc. Epilepsia. 2014 Nov;55(11):e120-4. doi: 10.1111/epi.12802. Epub 2014 Sep 29. Epilepsia. 2014. PMID: 25266342 Free article.

4

R54C Mutation of NOTCH3 Gene in the First Rungus Family with CADASIL.

Lim KS, Tan AH, Lim CS, Chua KH, Lee PC, Ramli N, Rajahram GS, Hussin FT, Wong KT, Bhattacharjee MB, Ng CC. Lim KS, et al. Among authors: ng cc. PLoS One. 2015 Aug 13;10(8):e0135470. doi: 10.1371/journal.pone.0135470. eCollection 2015. PLoS One. 2015. PMID: 26270344 Free PMC article.

5

A Genome Wide Study of Copy Number Variation Associated with Nasopharyngeal Carcinoma in Malaysian Chinese Identifies CNVs at 11q14.3 and 6p21.3 as Candidate Loci.

Low JS, Chin YM, Mushiroda T, Kubo M, Govindasamy GK, Pua KC, Yap YY, Yap LF, Subramaniam SK, Ong CA, Tan TY, Khoo AS; Malaysian NPC Study Group; Ng CC. Low JS, et al. Among authors: ng cc. PLoS One. 2016 Jan 5;11(1):e0145774. doi: 10.1371/journal.pone.0145774. eCollection 2016. PLoS One. 2016. PMID: 26730743 Free PMC article.

6

Ethnic variation of genetic (idiopathic) generalized epilepsy in Malaysia.

Lim KS, Ng CC, Chan CK, Foo WS, Low JS, Tan CT. Lim KS, et al. Among authors: ng cc. Seizure. 2017 Feb;45:24-27. doi: 10.1016/j.seizure.2016.11.011. Epub 2016 Nov 24. Seizure. 2017. PMID: 27912112 Free article.

7

HLA-A*31: 01 and HLA-B*15:02 association with Stevens-Johnson syndrome and toxic epidermal necrolysis to carbamazepine in a multiethnic Malaysian population.

Khor AH, Lim KS, Tan CT, Kwan Z, Tan WC, Wu DB, Ng CC. Khor AH, et al. Among authors: ng cc. Pharmacogenet Genomics. 2017 Jul;27(7):275-278. doi: 10.1097/FPC.0000000000000287. Pharmacogenet Genomics. 2017. PMID: 28570299

8

Molecular Genetic Characterization of Patients With Focal Epilepsy Using a Customized Targeted Resequencing Gene Panel.

Tsai MH, Chan CK, Chang YC, Lin CH, Liou CW, Chang WN, Ng CC, Lim KS, Hwang DY. Tsai MH, et al. Among authors: ng cc. Front Neurol. 2018 Jul 6;9:515. doi: 10.3389/fneur.2018.00515. eCollection 2018. Front Neurol. 2018. PMID: 30034362 Free PMC article.

9

Pathogenic Variants in CEP85L Cause Sporadic and Familial Posterior Predominant Lissencephaly.

Tsai MH, Muir AM, Wang WJ, Kang YN, Yang KC, Chao NH, Wu MF, Chang YC, Porter BE, Jansen LA, Sebire G, Deconinck N, Fan WL, Su SC, Chung WH, Almanza Fuerte EP, Mehaffey MG; University of Washington Center for Mendelian Genomics; Ng CC, Chan CK, Lim KS, Leventer RJ, Lockhart PJ, Riney K, Damiano JA, Hildebrand MS, Mirzaa GM, Dobyns WB, Berkovic SF, Scheffer IE, Tsai JW, Mefford HC. Tsai MH, et al. Among authors: ng cc. Neuron. 2020 Apr 22;106(2):237-245.e8. doi: 10.1016/j.neuron.2020.01.027. Epub 2020 Feb 24. Neuron. 2020. PMID: 32097630 Free PMC article.

10

Potential role of regulatory DNA variants in modifying the risk of severe cutaneous reactions induced by aromatic anti-seizure medications.

Mullan KA, Anderson A, Shi YW, Ding JH, Ng CC, Chen Z, Baum L, Cherny S, Petrovski S, Sham PC, Lim KS, Liao WP, Kwan P. Mullan KA, et al. Among authors: ng cc. Epilepsia. 2022 Apr;63(4):936-949. doi: 10.1111/epi.17182. Epub 2022 Feb 16. Epilepsia. 2022. PMID: 35170024 Free PMC article.

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