Jin L - Search Results

1

A homozygous mutation in CMAS causes autosomal recessive intellectual disability in a Kazakh family.

Qu R, Sang Q, Wang X, Xu Y, Chen B, Mu J, Zhang Z, Jin L, He L, Wang L. Qu R, et al. Among authors: jin l. Ann Hum Genet. 2020 Jan;84(1):46-53. doi: 10.1111/ahg.12349. Epub 2019 Sep 8. Ann Hum Genet. 2020. PMID: 31495922

2

Association of polymorphisms in the solute carrier organic anion transporter family member 1B1 gene with essential hypertension in the Uyghur population.

Lin R, Wang X, Zhou W, Fu W, Wang Y, Huang W, Jin L. Lin R, et al. Among authors: jin l. Ann Hum Genet. 2011 Mar;75(2):305-11. doi: 10.1111/j.1469-1809.2010.00622.x. Epub 2010 Dec 1. Ann Hum Genet. 2011. PMID: 21309757

3

Y-chromosome O3 haplogroup diversity in Sino-Tibetan populations reveals two migration routes into the eastern Himalayas.

Kang L, Lu Y, Wang C, Hu K, Chen F, Liu K, Li S, Jin L, Li H; Genographic Consortium. Kang L, et al. Among authors: jin l. Ann Hum Genet. 2012 Jan;76(1):92-9. doi: 10.1111/j.1469-1809.2011.00690.x. Epub 2011 Nov 23. Ann Hum Genet. 2012. PMID: 22111786

4

Efficient typing of copy number variations in a segmental duplication-mediated rearrangement hotspot using multiplex competitive amplification.

Du R, Lu C, Jiang Z, Li S, Ma R, An H, Xu M, An Y, Xia Y, Jin L, Wang X, Zhang F. Du R, et al. Among authors: jin l. J Hum Genet. 2012 Aug;57(8):545-51. doi: 10.1038/jhg.2012.66. Epub 2012 Jun 7. J Hum Genet. 2012. PMID: 22673690

5

Predictive value of XRCC1 gene polymorphisms on platinum-based chemotherapy in advanced non-small cell lung cancer patients: a systematic review and meta-analysis.

Wu J, Liu J, Zhou Y, Ying J, Zou H, Guo S, Wang L, Zhao N, Hu J, Lu D, Jin L, Li Q, Wang JC. Wu J, et al. Among authors: jin l. Clin Cancer Res. 2012 Jul 15;18(14):3972-81. doi: 10.1158/1078-0432.CCR-11-1531. Epub 2012 Jun 15. Clin Cancer Res. 2012. PMID: 22705987

6

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: jin l. 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

7

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: jin l. 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

8

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: jin l. PLoS One. 2013;8(1):e55178. doi: 10.1371/journal.pone.0055178. Epub 2013 Jan 29. PLoS One. 2013. PMID: 23383098 Free PMC article.

9

Identification of microRNAs in human follicular fluid: characterization of microRNAs that govern steroidogenesis in vitro and are associated with polycystic ovary syndrome in vivo.

Sang Q, Yao Z, Wang H, Feng R, Wang H, Zhao X, Xing Q, Jin L, He L, Wu L, Wang L. Sang Q, et al. Among authors: jin l. J Clin Endocrinol Metab. 2013 Jul;98(7):3068-79. doi: 10.1210/jc.2013-1715. Epub 2013 May 10. J Clin Endocrinol Metab. 2013. PMID: 23666971

10

The adaptive variant EDARV370A is associated with straight hair in East Asians.

Tan J, Yang Y, Tang K, Sabeti PC, Jin L, Wang S. Tan J, et al. Among authors: jin l. Hum Genet. 2013 Oct;132(10):1187-91. doi: 10.1007/s00439-013-1324-1. Epub 2013 Jun 23. Hum Genet. 2013. PMID: 23793515

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