Lin MW - Search Results

1

Association of brain-derived neurotrophic factor gene Val66Met polymorphism with primary dysmenorrhea.

Lee LC, Tu CH, Chen LF, Shen HD, Chao HT, Lin MW, Hsieh JC. Lee LC, et al. Among authors: lin mw. PLoS One. 2014 Nov 10;9(11):e112766. doi: 10.1371/journal.pone.0112766. eCollection 2014. PLoS One. 2014. PMID: 25383981 Free PMC article.

2

Association analysis of the dopamine D3 receptor gene ser9gly and brain-derived neurotrophic factor gene val66met polymorphisms with antipsychotic-induced persistent tardive dyskinesia and clinical expression in Chinese schizophrenic patients.

Liou YJ, Liao DL, Chen JY, Wang YC, Lin CC, Bai YM, Yu SC, Lin MW, Lai IC. Liou YJ, et al. Among authors: lin cc, lin mw. Neuromolecular Med. 2004;5(3):243-51. doi: 10.1385/NMM:5:3:243. Neuromolecular Med. 2004. PMID: 15626824

3

Keloid-derived fibroblasts have a diminished capacity to produce prostaglandin E2.

Yeh FL, Shen HD, Lin MW, Chang CY, Tai HY, Huang MH. Yeh FL, et al. Among authors: lin mw. Burns. 2006 May;32(3):299-304. doi: 10.1016/j.burns.2005.10.009. Epub 2006 Feb 17. Burns. 2006. PMID: 16487663

4

Association of the Y402H polymorphism in complement factor H gene and neovascular age-related macular degeneration in Chinese patients.

Lau LI, Chen SJ, Cheng CY, Yen MY, Lee FL, Lin MW, Hsu WM, Wei YH. Lau LI, et al. Among authors: lin mw. Invest Ophthalmol Vis Sci. 2006 Aug;47(8):3242-6. doi: 10.1167/iovs.05-1532. Invest Ophthalmol Vis Sci. 2006. PMID: 16877387

5

Evidence for association between genetic variants of p75 neurotrophin receptor (p75NTR) gene and antidepressant treatment response in Chinese major depressive disorder.

Gau YT, Liou YJ, Yu YW, Chen TJ, Lin MW, Tsai SJ, Hong CJ. Gau YT, et al. Among authors: lin mw. Am J Med Genet B Neuropsychiatr Genet. 2008 Jul 5;147B(5):594-9. doi: 10.1002/ajmg.b.30646. Am J Med Genet B Neuropsychiatr Genet. 2008. PMID: 18081157

6

Association of brain serotonin transporter availability and brain-derived neurotrophic factor in models of serotonin transporter genotypes in healthy subjects.

Chou YH, Chen CK, Wang SJ, Tsai SJ, Lirng JF, Liou YJ, Lin CL, Yang KC, Lin MW, Lo WC, Liao MH, Chen CC. Chou YH, et al. Among authors: lin mw, lin cl. J Clin Psychopharmacol. 2013 Jun;33(3):432-5. doi: 10.1097/JCP.0b013e3182904a80. J Clin Psychopharmacol. 2013. PMID: 23609403

7

Effect of Common Genetic Variants of Growth Arrest-Specific 6 Gene on Insulin Resistance, Obesity and Type 2 Diabetes in an Asian Population.

Hsieh CH, Chung RH, Lee WJ, Lin MW, Chuang LM, Quertermous T, Assimes T, Hung YJ, Yu YW. Hsieh CH, et al. Among authors: lin mw. PLoS One. 2015 Aug 18;10(8):e0135681. doi: 10.1371/journal.pone.0135681. eCollection 2015. PLoS One. 2015. PMID: 26284522 Free PMC article.

8

The BDNF Val66Met polymorphism is associated with the functional connectivity dynamics of pain modulatory systems in primary dysmenorrhea.

Wei SY, Chao HT, Tu CH, Lin MW, Li WC, Low I, Shen HD, Chen LF, Hsieh JC. Wei SY, et al. Among authors: lin mw. Sci Rep. 2016 Mar 24;6:23639. doi: 10.1038/srep23639. Sci Rep. 2016. PMID: 27010666 Free PMC article.

9

The OPRM1 A118G polymorphism modulates the descending pain modulatory system for individual pain experience in young women with primary dysmenorrhea.

Wei SY, Chen LF, Lin MW, Li WC, Low I, Yang CJ, Chao HT, Hsieh JC. Wei SY, et al. Among authors: lin mw. Sci Rep. 2017 Jan 6;7:39906. doi: 10.1038/srep39906. Sci Rep. 2017. PMID: 28057931 Free PMC article.

10

Genome-wide association study identifies novel susceptibility loci for migraine in Han Chinese resided in Taiwan.

Chen SP, Fuh JL, Chung MY, Lin YC, Liao YC, Wang YF, Hsu CL, Yang UC, Lin MW, Chiou JJ, Wang PJ, Chen PK, Fan PC, Wu JY, Chen YT, Kao LS, Shen-Jang Fann C, Wang SJ. Chen SP, et al. Among authors: lin yc, lin mw. Cephalalgia. 2018 Mar;38(3):466-475. doi: 10.1177/0333102417695105. Epub 2017 Feb 17. Cephalalgia. 2018. PMID: 28952330

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