Liu X - Search Results

1

PPARGC1B gene is associated with Kashin-Beck disease in Han Chinese.

Wen Y, Hao J, Xiao X, Wang W, Guo X, Lin W, Yang T, Liu X, Shen H, Tan L, Chen X, Tian Q, Deng HW, Zhang F. Wen Y, et al. Among authors: liu x. Funct Integr Genomics. 2016 Jul;16(4):459-63. doi: 10.1007/s10142-016-0496-x. Epub 2016 Apr 23. Funct Integr Genomics. 2016. PMID: 27108113

2

Exome sequencing identified FGF12 as a novel candidate gene for Kashin-Beck disease.

Zhang F, Dai L, Lin W, Wang W, Liu X, Zhang J, Yang T, Liu X, Shen H, Chen X, Tan L, Tian Q, Deng HW, Xu X, Guo X. Zhang F, et al. Among authors: liu x. Funct Integr Genomics. 2016 Jan;16(1):13-7. doi: 10.1007/s10142-015-0462-z. Epub 2015 Aug 20. Funct Integr Genomics. 2016. PMID: 26290467

3

A bivariate genome-wide association study identifies ADAM12 as a novel susceptibility gene for Kashin-Beck disease.

Hao J, Wang W, Wen Y, Xiao X, He A, Guo X, Yang T, Liu X, Shen H, Chen X, Tian Q, Deng HW, Zhang F. Hao J, et al. Among authors: liu x. Sci Rep. 2016 Aug 22;6:31792. doi: 10.1038/srep31792. Sci Rep. 2016. PMID: 27545300 Free PMC article.

4

Genome-wide association scan for stature in Chinese: evidence for ethnic specific loci.

Lei SF, Yang TL, Tan LJ, Chen XD, Guo Y, Guo YF, Zhang L, Liu XG, Yan H, Pan F, Zhang ZX, Peng YM, Zhou Q, He LN, Zhu XZ, Cheng J, Liu YZ, Papasian CJ, Deng HW. Lei SF, et al. Hum Genet. 2009 Feb;125(1):1-9. doi: 10.1007/s00439-008-0590-9. Epub 2008 Nov 23. Hum Genet. 2009. PMID: 19030899 Free PMC article.

5

Genome-wide association study identifies two novel loci containing FLNB and SBF2 genes underlying stature variation.

Lei SF, Tan LJ, Liu XG, Wang L, Yan H, Guo YF, Liu YZ, Xiong DH, Li J, Yang TL, Chen XD, Guo Y, Deng FY, Zhang YP, Zhu XZ, Levy S, Papasian CJ, Hamilton JJ, Recker RR, Deng HW. Lei SF, et al. Hum Mol Genet. 2009 May 1;18(9):1661-9. doi: 10.1093/hmg/ddn405. Epub 2008 Nov 27. Hum Mol Genet. 2009. PMID: 19039035 Free PMC article.

6

Genome-wide association and replication studies identified TRHR as an important gene for lean body mass.

Liu XG, Tan LJ, Lei SF, Liu YJ, Shen H, Wang L, Yan H, Guo YF, Xiong DH, Chen XD, Pan F, Yang TL, Zhang YP, Guo Y, Tang NL, Zhu XZ, Deng HY, Levy S, Recker RR, Papasian CJ, Deng HW. Liu XG, et al. Am J Hum Genet. 2009 Mar;84(3):418-23. doi: 10.1016/j.ajhg.2009.02.004. Epub 2009 Mar 5. Am J Hum Genet. 2009. PMID: 19268274 Free PMC article.

7

Copy number variations at the Prader-Willi syndrome region on chromosome 15 and associations with obesity in whites.

Chen Y, Liu YJ, Pei YF, Yang TL, Deng FY, Liu XG, Li DY, Deng HW. Chen Y, et al. Obesity (Silver Spring). 2011 Jun;19(6):1229-34. doi: 10.1038/oby.2010.323. Epub 2011 Jan 13. Obesity (Silver Spring). 2011. PMID: 21233802 Free PMC article.

8

Pathway-based association analyses identified TRAIL pathway for osteoporotic fractures.

Zhang YP, Liu YZ, Guo Y, Liu XG, Xu XH, Guo YF, Chen Y, Zhang F, Pan F, Zhu XZ, Deng HW. Zhang YP, et al. PLoS One. 2011;6(7):e21835. doi: 10.1371/journal.pone.0021835. Epub 2011 Jul 8. PLoS One. 2011. PMID: 21760914 Free PMC article.

9

Copy number variation in CNP267 region may be associated with hip bone size.

Liu SL, Lei SF, Yang F, Li X, Liu R, Nie S, Liu XG, Yang TL, Guo Y, Deng FY, Tian Q, Li J, Liu YZ, Liu YJ, Shen H, Deng HW. Liu SL, et al. Among authors: liu yz, liu yj, liu r, liu xg. PLoS One. 2011;6(7):e22035. doi: 10.1371/journal.pone.0022035. Epub 2011 Jul 15. PLoS One. 2011. PMID: 21789208 Free PMC article.

10

ANKRD7 and CYTL1 are novel risk genes for alcohol drinking behavior.

Chen XD, Xiong DH, Yang TL, Pei YF, Guo YF, Li J, Yang F, Pan F, Tan LJ, Yan H, Liu XG, Lei SF, Li X, Ning LL, Zhu XZ, Levy S, Kranzler HR, Farrer LA, Gelernter J, Recker RR, Deng HW. Chen XD, et al. Among authors: liu xg. Chin Med J (Engl). 2012 Mar;125(6):1127-34. Chin Med J (Engl). 2012. PMID: 22613542 Free PMC article.

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