Kwan P - Search Results

1

ELF1 is associated with systemic lupus erythematosus in Asian populations.

Yang J, Yang W, Hirankarn N, Ye DQ, Zhang Y, Pan HF, Mok CC, Chan TM, Wong RW, Mok MY, Lee KW, Wong SN, Leung AM, Li XP, Avihingsanon Y, Rianthavorn P, Deekajorndej T, Suphapeetiporn K, Shotelersuk V, Baum L, Kwan P, Lee TL, Ho MH, Lee PP, Wong WH, Zeng S, Zhang J, Wong CM, Ng IO, Garcia-Barceló MM, Cherny SS, Tam PK, Sham PC, Lau CS, Lau YL. Yang J, et al. Among authors: kwan p. Hum Mol Genet. 2011 Feb 1;20(3):601-7. doi: 10.1093/hmg/ddq474. Epub 2010 Nov 2. Hum Mol Genet. 2011. PMID: 21044949

2

Two-stage genome-wide association study identifies variants in CAMSAP1L1 as susceptibility loci for epilepsy in Chinese.

Guo Y, Baum LW, Sham PC, Wong V, Ng PW, Lui CH, Sin NC, Tsoi TH, Tang CS, Kwan JS, Yip BH, Xiao SM, Thomas GN, Lau YL, Yang W, Cherny SS, Kwan P. Guo Y, et al. Among authors: kwan js, kwan p. Hum Mol Genet. 2012 Mar 1;21(5):1184-9. doi: 10.1093/hmg/ddr550. Epub 2011 Nov 24. Hum Mol Genet. 2012. PMID: 22116939

3

Genome-wide copy number variation study in anorectal malformations.

Wong EH, Cui L, Ng CL, Tang CS, Liu XL, So MT, Yip BH, Cheng G, Zhang R, Tang WK, Yang W, Lau YL, Baum L, Kwan P, Sun LD, Zuo XB, Ren YQ, Yin XY, Miao XP, Liu J, Lui VC, Ngan ES, Yuan ZW, Zhang SW, Xia J, Wang H, Sun XB, Wang R, Chang T, Chan IH, Chung PH, Zhang XJ, Wong KK, Cherny SS, Sham PC, Tam PK, Garcia-Barcelo MM. Wong EH, et al. Among authors: kwan p. Hum Mol Genet. 2013 Feb 1;22(3):621-31. doi: 10.1093/hmg/dds451. Epub 2012 Oct 29. Hum Mol Genet. 2013. PMID: 23108157

4

The potential role of CAMSAP1L1 in symptomatic epilepsy.

Zhang S, Kwan P, Baum L. Zhang S, et al. Among authors: kwan p. Neurosci Lett. 2013 Nov 27;556:146-51. doi: 10.1016/j.neulet.2013.10.020. Epub 2013 Oct 20. Neurosci Lett. 2013. PMID: 24148305

5

Association of BDNF Polymorphisms with the Risk of Epilepsy: a Multicenter Study.

Sha'ari HM, Haerian BS, Baum L, Tan HJ, Rafia MH, Kwan P, Cherny SS, Sham PC, Gui H, Raymond AA, Lim KS, Mohamed Z. Sha'ari HM, et al. Among authors: kwan p. Mol Neurobiol. 2016 Jul;53(5):2869-2877. doi: 10.1007/s12035-015-9150-1. Epub 2015 Apr 16. Mol Neurobiol. 2016. PMID: 25876511

6

Genetic overlap between epilepsy and schizophrenia: Evidence from cross phenotype analysis in Hong Kong Chinese population.

Gui H, Li M, Sham PC, Baum L; International League Against Epilepsy Consortium on Complex Epilepsies; Kwan P, Cherny SS. Gui H, et al. Among authors: kwan p. Am J Med Genet B Neuropsychiatr Genet. 2018 Jan;177(1):86-92. doi: 10.1002/ajmg.b.32607. Epub 2017 Nov 17. Am J Med Genet B Neuropsychiatr Genet. 2018. PMID: 29150900

7

Case-control association study of polymorphisms in the voltage-gated sodium channel genes SCN1A, SCN2A, SCN3A, SCN1B, and SCN2B and epilepsy.

Baum L, Haerian BS, Ng HK, Wong VC, Ng PW, Lui CH, Sin NC, Zhang C, Tomlinson B, Wong GW, Tan HJ, Raymond AA, Mohamed Z, Kwan P. Baum L, et al. Among authors: kwan p. Hum Genet. 2014 May;133(5):651-9. doi: 10.1007/s00439-013-1405-1. Epub 2013 Dec 13. Hum Genet. 2014. PMID: 24337656

8

Contribution of GABRG2 Polymorphisms to Risk of Epilepsy and Febrile Seizure: a Multicenter Cohort Study and Meta-analysis.

Haerian BS, Baum L, Kwan P, Cherny SS, Shin JG, Kim SE, Han BG, Tan HJ, Raymond AA, Tan CT, Mohamed Z. Haerian BS, et al. Among authors: kwan p. Mol Neurobiol. 2016 Oct;53(8):5457-67. doi: 10.1007/s12035-015-9457-y. Epub 2015 Oct 9. Mol Neurobiol. 2016. PMID: 26452361

9

Failure to detect association between polymorphisms of the sodium channel gene SCN1A and febrile seizures in Chinese patients with epilepsy.

Zhang C, Wong V, Ng PW, Lui CH, Sin NC, Wong KS, Baum L, Kwan P. Zhang C, et al. Among authors: kwan p. Epilepsia. 2010 Sep;51(9):1878-81. doi: 10.1111/j.1528-1167.2010.02587.x. Epilepsia. 2010. PMID: 20477842 Free article.

10

Rare variants and de novo variants in mesial temporal lobe epilepsy with hippocampal sclerosis.

Wong JKL, Gui H, Kwok M, Ng PW, Lui CHT, Baum L, Sham PC, Kwan P, Cherny SS. Wong JKL, et al. Among authors: kwan p. Neurol Genet. 2018 Jun 11;4(3):e245. doi: 10.1212/NXG.0000000000000245. eCollection 2018 Jun. Neurol Genet. 2018. PMID: 29904720 Free PMC article.

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