Zhang F - Search Results

1

Association of polymorphisms in four bilirubin metabolism genes with serum bilirubin in three Asian populations.

Lin R, Wang X, Wang Y, Zhang F, Wang Y, Fu W, Yu T, Li S, Xiong M, Huang W, Jin L. Lin R, et al. Among authors: zhang f. Hum Mutat. 2009 Apr;30(4):609-15. doi: 10.1002/humu.20895. Hum Mutat. 2009. PMID: 19243019

2

The association of Y chromosome haplogroups with spermatogenic failure in the Han Chinese.

Lu C, Zhang F, Xia Y, Wu B, Gu A, Lu N, Wang S, Shen H, Jin L, Wang X. Lu C, et al. Among authors: zhang f. J Hum Genet. 2007;52(8):659-663. doi: 10.1007/s10038-007-0160-3. Epub 2007 Jun 9. J Hum Genet. 2007. PMID: 17558462

3

A spatial analysis of genetic structure of human populations in China reveals distinct difference between maternal and paternal lineages.

Xue F, Wang Y, Xu S, Zhang F, Wen B, Wu X, Lu M, Deka R, Qian J, Jin L. Xue F, et al. Among authors: zhang f. Eur J Hum Genet. 2008 Jun;16(6):705-17. doi: 10.1038/sj.ejhg.5201998. Epub 2008 Jan 23. Eur J Hum Genet. 2008. PMID: 18212820

4

Identification of copy number variation hotspots in human populations.

Fu W, Zhang F, Wang Y, Gu X, Jin L. Fu W, et al. Among authors: zhang f. Am J Hum Genet. 2010 Oct 8;87(4):494-504. doi: 10.1016/j.ajhg.2010.09.006. Am J Hum Genet. 2010. PMID: 20920665 Free PMC article.

5

Correlation between frequency of non-allelic homologous recombination and homology properties: evidence from homology-mediated CNV mutations in the human genome.

Peng Z, Zhou W, Fu W, Du R, Jin L, Zhang F. Peng Z, et al. Among authors: zhang f. Hum Mol Genet. 2015 Mar 1;24(5):1225-33. doi: 10.1093/hmg/ddu533. Epub 2014 Oct 16. Hum Mol Genet. 2015. PMID: 25324539

6

[Copy number variations in the human genome: their mutational mechanisms and roles in diseases].

Du RQ, Jin L, Zhang F. Du RQ, et al. Among authors: zhang f. Yi Chuan. 2011 Aug;33(8):857-69. doi: 10.3724/sp.j.1005.2011.00857. Yi Chuan. 2011. PMID: 21831802 Review. Chinese.

7

Evaluation of copy number variation detection for a SNP array platform.

Zhang X, Du R, Li S, Zhang F, Jin L, Wang H. Zhang X, et al. Among authors: zhang f. BMC Bioinformatics. 2014 Feb 21;15:50. doi: 10.1186/1471-2105-15-50. BMC Bioinformatics. 2014. PMID: 24555668 Free PMC article.

8

Copy Number Variation of HLA-DQA1 and APOBEC3A/3B Contribute to the Susceptibility of Systemic Sclerosis in the Chinese Han Population.

Guo S, Li Y, Wang Y, Chu H, Chen Y, Liu Q, Guo G, Tu W, Wu W, Zou H, Yang L, Xiao R, Ma Y, Zhang F, Xiong M, Jin L, Zhou X, Wang J. Guo S, et al. Among authors: zhang f. J Rheumatol. 2016 May;43(5):880-6. doi: 10.3899/jrheum.150945. Epub 2016 Apr 1. J Rheumatol. 2016. PMID: 27036383

9

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: zhang f. 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

10

Replicative mechanisms of CNV formation preferentially occur as intrachromosomal events: evidence from Potocki-Lupski duplication syndrome.

Sun Z, Liu P, Jia X, Withers MA, Jin L, Lupski JR, Zhang F. Sun Z, et al. Among authors: zhang f. Hum Mol Genet. 2013 Feb 15;22(4):749-56. doi: 10.1093/hmg/dds482. Epub 2012 Nov 16. Hum Mol Genet. 2013. PMID: 23161748 Free PMC article.

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