Zhou X - Search Results

1

Trans-Ethnic Polygenic Analysis Supports Genetic Overlaps of Lumbar Disc Degeneration With Height, Body Mass Index, and Bone Mineral Density.

Zhou X, Cheung CL, Karasugi T, Karppinen J, Samartzis D, Hsu YH, Mak TS, Song YQ, Chiba K, Kawaguchi Y, Li Y, Chan D, Cheung KM, Ikegawa S, Cheah KS, Sham PC. Zhou X, et al. Front Genet. 2018 Aug 3;9:267. doi: 10.3389/fgene.2018.00267. eCollection 2018. Front Genet. 2018. PMID: 30127800 Free PMC article.

2

Polygenic scores via penalized regression on summary statistics.

Mak TSH, Porsch RM, Choi SW, Zhou X, Sham PC. Mak TSH, et al. Among authors: zhou x. Genet Epidemiol. 2017 Sep;41(6):469-480. doi: 10.1002/gepi.22050. Epub 2017 May 8. Genet Epidemiol. 2017. PMID: 28480976 Free article.

3

Exome sequencing identifies a novel frameshift mutation of MYO6 as the cause of autosomal dominant nonsyndromic hearing loss in a Chinese family.

Cheng J, Zhou X, Lu Y, Chen J, Han B, Zhu Y, Liu L, Choy KW, Han D, Sham PC, Zhang MQ, Zhang X, Yuan H. Cheng J, et al. Among authors: zhou x. Ann Hum Genet. 2014 Nov;78(6):410-23. doi: 10.1111/ahg.12084. Epub 2014 Sep 17. Ann Hum Genet. 2014. PMID: 25227905

4

CNV analysis in Chinese children of mental retardation highlights a sex differentiation in parental contribution to de novo and inherited mutational burdens.

Wang B, Ji T, Zhou X, Wang J, Wang X, Wang J, Zhu D, Zhang X, Sham PC, Zhang X, Ma X, Jiang Y. Wang B, et al. Among authors: zhou x. Sci Rep. 2016 Jun 3;6:25954. doi: 10.1038/srep25954. Sci Rep. 2016. PMID: 27257017 Free PMC article.

5

Exome Sequencing and Gene Prioritization Correct Misdiagnosis in a Chinese Kindred with Familial Amyloid Polyneuropathy.

Chen H, Zhou X, Wang J, Wang X, Liu L, Wu S, Li T, Chen S, Yang J, Sham PC, Zhu G, Zhang X, Wang B. Chen H, et al. Among authors: zhou x. Sci Rep. 2016 May 23;6:26362. doi: 10.1038/srep26362. Sci Rep. 2016. PMID: 27212199 Free PMC article.

6

Prioritizing genes responsible for host resistance to influenza using network approaches.

Bao S, Zhou X, Zhang L, Zhou J, To KK, Wang B, Wang L, Zhang X, Song YQ. Bao S, et al. Among authors: zhou x, zhou j. BMC Genomics. 2013 Nov 21;14(1):816. doi: 10.1186/1471-2164-14-816. BMC Genomics. 2013. PMID: 24261899 Free PMC article.

7

Mutations in Hnrnpa1 cause congenital heart defects.

Yu Z, Tang PL, Wang J, Bao S, Shieh JT, Leung AW, Zhang Z, Gao F, Wong SY, Hui AL, Gao Y, Dung N, Zhang ZG, Fan Y, Zhou X, Zhang Y, Wong DS, Sham PC, Azhar A, Kwok PY, Tam PP, Lian Q, Cheah KS, Wang B, Song YQ. Yu Z, et al. Among authors: zhou x. JCI Insight. 2018 Jan 25;3(2):e98555. doi: 10.1172/jci.insight.98555. eCollection 2018 Jan 25. JCI Insight. 2018. PMID: 29367466 Free PMC article.

8

A rare variant in MLKL confers susceptibility to ApoE ɛ4-negative Alzheimer's disease in Hong Kong Chinese population.

Wang B, Bao S, Zhang Z, Zhou X, Wang J, Fan Y, Zhang Y, Li Y, Chen L, Jia Y, Li J, Li M, Zheng W, Mu N, Wang L, Yu Z, Wong DSM, Zhang Y, Kwan J, Ka-Fung Mak H, Ambalavanan A, Zhou S, Cai W, Zheng J, Huang S, Rouleau GA, Yang W, Rogaeva E, Ma X, St George-Hyslop P, Chu LW, Song YQ. Wang B, et al. Among authors: zhou x, zhou s. Neurobiol Aging. 2018 Aug;68:160.e1-160.e7. doi: 10.1016/j.neurobiolaging.2018.03.006. Epub 2018 Mar 10. Neurobiol Aging. 2018. PMID: 29656768

9

Integrated analysis of mRNA-seq and miRNA-seq for host susceptibilities to influenza A (H7N9) infection in inbred mouse lines.

Bao S, Jia L, Zhou X, Zhang ZG, Wu HWL, Yu Z, Ng G, Fan Y, Wong DSM, Huang S, Wang To KK, Yuen KY, Yeung ML, Song YQ. Bao S, et al. Among authors: zhou x. Funct Integr Genomics. 2018 Jul;18(4):411-424. doi: 10.1007/s10142-018-0602-3. Epub 2018 Mar 21. Funct Integr Genomics. 2018. PMID: 29564647

10

Short read mapping for exome sequencing.

Zhou X, Bao S, Wang B, Zhang X, Song YQ. Zhou X, et al. Methods Mol Biol. 2013;1038:93-111. doi: 10.1007/978-1-62703-514-9_6. Methods Mol Biol. 2013. PMID: 23872971

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