Hsu YA - Search Results

1

A novel nonsense mutation of the sedlin gene in a family with spondyloepiphyseal dysplasia tarda.

Shi YR, Lee CC, Hsu YA, Wang CH, Tsai FJ. Shi YR, et al. Among authors: hsu ya. Hum Hered. 2002;54(1):54-6. doi: 10.1159/000066694. Hum Hered. 2002. PMID: 12446987

2

Polymorphisms for interleukin-4 (IL-4) -590 promoter, IL-4 intron3, and tumor necrosis factor alpha -308 promoter: non-association with endometriosis.

Hsieh YY, Chang CC, Tsai FJ, Hsu Y, Tsai HD, Tsai CH. Hsieh YY, et al. J Clin Lab Anal. 2002;16(3):121-6. doi: 10.1002/jcla.10021. J Clin Lab Anal. 2002. PMID: 11968047 Free PMC article.

3

Lack of association between transforming growth factor-beta1 gene polymorphisms and mitral valve prolapse in Taiwan Chinese.

Chou HT, Shi YR, Hsu Y, Tsai FJ. Chou HT, et al. J Heart Valve Dis. 2002 Jul;11(4):478-84. J Heart Valve Dis. 2002. PMID: 12150293

4

Mutation screening of the EXT genes in patients with hereditary multiple exostoses in Taiwan.

Shi YR, Wu JY, Hsu YA, Lee CC, Tsai CH, Tsai FJ. Shi YR, et al. Among authors: hsu ya. Genet Test. 2002 Fall;6(3):237-43. doi: 10.1089/109065702761403441. Genet Test. 2002. PMID: 12490068

5

Lack of association of genetic polymorphisms in the interleukin-1beta, interleukin-1 receptor antagonist, interleukin-4 and interleukin-10 genes with mitral valve prolapse in Taiwan Chinese.

Chou HT, Shi YR, Hsu Y, Tsai FJ. Chou HT, et al. J Heart Valve Dis. 2003 Jan;12(1):38-44. J Heart Valve Dis. 2003. PMID: 12578333

6

Association between fibrillin-1 gene exon 15 and 27 polymorphisms and risk of mitral valve prolapse.

Chou HT, Shi YR, Hsu Y, Tsai FJ. Chou HT, et al. J Heart Valve Dis. 2003 Jul;12(4):475-81. J Heart Valve Dis. 2003. PMID: 12918850

7

Association of the nicotinic receptor beta 2 subunit and febrile seizures.

Peng CT, Chou IC, Li CI, Hsu YA, Tsai CH, Tsai FJ. Peng CT, et al. Among authors: hsu ya. Pediatr Neurol. 2004 Mar;30(3):186-9. doi: 10.1016/j.pediatrneurol.2003.08.001. Pediatr Neurol. 2004. PMID: 15033200

8

Association analysis between Tourette's syndrome and dopamine D1 receptor gene in Taiwanese children.

Chou IC, Tsai CH, Lee CC, Kuo HT, Hsu YA, Li CI, Tsai FJ. Chou IC, et al. Among authors: hsu ya. Psychiatr Genet. 2004 Dec;14(4):219-21. doi: 10.1097/00041444-200412000-00010. Psychiatr Genet. 2004. PMID: 15564897

9

Association of GABRG2 polymorphisms with idiopathic generalized epilepsy.

Chou IC, Lee CC, Tsai CH, Tsai Y, Wan L, Hsu YA, Li TC, Tsai FJ. Chou IC, et al. Among authors: hsu ya. Pediatr Neurol. 2007 Jan;36(1):40-4. doi: 10.1016/j.pediatrneurol.2006.09.011. Pediatr Neurol. 2007. PMID: 17162195

10

Association study between Tourette's syndrome and polymorphisms of noradrenergic genes (ADRA2A, ADRA2C).

Chou IC, Tsai CH, Wan L, Hsu YA, Tsai FJ. Chou IC, et al. Among authors: hsu ya. Psychiatr Genet. 2007 Dec;17(6):359. doi: 10.1097/YPG.0b013e3281ac2358. Psychiatr Genet. 2007. PMID: 18075481 No abstract available.

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