Li Q - Search Results

1

Lack of support for association between the copy number variants in the FCGR locus and schizophrenia: a case control study.

Zhao A, Xiang Y, Xu J, Li Q, Wang L, Xing Q, Zhang Z, Liu Y, Feng G, He L, Zhao X. Zhao A, et al. Among authors: li q. Neurosci Lett. 2012 Aug 1;522(2):85-91. doi: 10.1016/j.neulet.2012.04.037. Epub 2012 May 1. Neurosci Lett. 2012. PMID: 22580203

2

Promoter hypomethylation of COMT in human placenta is not associated with the development of pre-eclampsia.

Zhao A, Cheng Y, Li X, Li Q, Wang L, Xu J, Xiang Y, Xing Q, He L, Zhao X. Zhao A, et al. Among authors: li x, li q. Mol Hum Reprod. 2011 Mar;17(3):199-206. doi: 10.1093/molehr/gaq092. Epub 2010 Nov 3. Mol Hum Reprod. 2011. PMID: 21047975

3

Common genetic variation in the 3'-untranslated region of gonadotropin-releasing hormone receptor regulates gene expression in cella and is associated with thyroid function, insulin secretion as well as insulin sensitivity in polycystic ovary syndrome patients.

Li Q, Yang G, Wang Y, Zhang X, Sang Q, Wang H, Zhao X, Xing Q, He L, Wang L. Li Q, et al. Hum Genet. 2011 May;129(5):553-61. doi: 10.1007/s00439-011-0954-4. Epub 2011 Jan 28. Hum Genet. 2011. PMID: 21274726

4

A common polymorphism in the human aromatase gene alters the risk for polycystic ovary syndrome and modifies aromatase activity in vitro.

Wang H, Li Q, Wang T, Yang G, Wang Y, Zhang X, Sang Q, Wang H, Zhao X, Xing Q, Shi J, He L, Wang L. Wang H, et al. Among authors: li q. Mol Hum Reprod. 2011 Jun;17(6):386-91. doi: 10.1093/molehr/gar007. Epub 2011 Jan 31. Mol Hum Reprod. 2011. PMID: 21282199

5

Analysis of JAG1 gene variant in Chinese patients with Alagille syndrome.

Wang H, Wang X, Li Q, Chen S, Liu L, Wei Z, Wang L, Liu Y, Zhao X, He L, Wang J, Xing Q. Wang H, et al. Among authors: li q. Gene. 2012 May 10;499(1):191-3. doi: 10.1016/j.gene.2012.02.038. Epub 2012 Mar 2. Gene. 2012. PMID: 22405927

6

HLA-B*58:01 allele is associated with augmented risk for both mild and severe cutaneous adverse reactions induced by allopurinol in Han Chinese.

Cao ZH, Wei ZY, Zhu QY, Zhang JY, Yang L, Qin SY, Shao LY, Zhang YT, Xuan JK, Li QL, Xu JH, Xu F, Ma L, Huang HY, Xing QH, Luo XQ. Cao ZH, et al. Pharmacogenomics. 2012 Jul;13(10):1193-201. doi: 10.2217/pgs.12.89. Pharmacogenomics. 2012. PMID: 22909208

7

Promoter hypomethylation of TIMP3 is associated with pre-eclampsia in a Chinese population.

Xiang Y, Zhang X, Li Q, Xu J, Zhou X, Wang T, Xing Q, Liu Y, Wang L, He L, Zhao X. Xiang Y, et al. Among authors: li q. Mol Hum Reprod. 2013 Mar;19(3):153-9. doi: 10.1093/molehr/gas054. Epub 2012 Nov 19. Mol Hum Reprod. 2013. PMID: 23172037

8

Quantitative analysis of follistatin (FST) promoter methylation in peripheral blood of patients with polycystic ovary syndrome.

Sang Q, Zhang S, Zou S, Wang H, Feng R, Li Q, Jin L, He L, Xing Q, Wang L. Sang Q, et al. Among authors: li q. Reprod Biomed Online. 2013 Feb;26(2):157-63. doi: 10.1016/j.rbmo.2012.10.011. Epub 2012 Oct 23. Reprod Biomed Online. 2013. PMID: 23265961

9

Common genetic variation in CYP1B1 is associated with concentrations of T₄, FT₃ and FT₄ in the sera of polycystic ovary syndrome patients.

Zou S, Sang Q, Wang H, Feng R, Li Q, Zhao X, Xing Q, Jin L, He L, Wang L. Zou S, et al. Among authors: li q. Mol Biol Rep. 2013 Apr;40(4):3315-20. doi: 10.1007/s11033-012-2406-1. Epub 2013 Jan 3. Mol Biol Rep. 2013. PMID: 23283740

10

Identification and functional study of a new missense mutation in the motor head domain of myosin VIIA in a family with autosomal dominant hearing impairment (DFNA11).

Sang Q, Yan X, Wang H, Feng R, Fei X, Ma D, Xing Q, Li Q, Zhao X, Jin L, He L, Li H, Wang L. Sang Q, et al. Among authors: li h, li q. PLoS One. 2013;8(1):e55178. doi: 10.1371/journal.pone.0055178. Epub 2013 Jan 29. PLoS One. 2013. PMID: 23383098 Free PMC article.

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