Shen Y - Search Results

1

TBX6-associated congenital scoliosis (TACS) as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage model.

Liu J, Wu N; Deciphering Disorders Involving Scoliosis and COmorbidities (DISCO) study; Yang N, Takeda K, Chen W, Li W, Du R, Liu S, Zhou Y, Zhang L, Liu Z, Zuo Y, Zhao S, Blank R, Pehlivan D, Dong S, Zhang J, Shen J, Si N, Wang Y, Liu G, Li S, Zhao Y, Zhao H, Chen Y, Zhao Y, Song X, Hu J, Lin M, Tian Y, Yuan B, Yu K, Niu Y, Yu B, Li X, Chen J, Yan Z, Zhu Q, Meng X, Chen X, Su J, Zhao X, Wang X, Ming Y, Li X, Raggio CL, Zhang B, Weng X, Zhang S, Zhang X, Watanabe K, Matsumoto M; Japan Early Onset Scoliosis Research Group; Jin L, Shen Y, Sobreira NL, Posey JE, Giampietro PF, Valle D; Baylor-Hopkins Center for Mendelian Genomics; Liu P, Wu Z, Ikegawa S, Lupski JR, Zhang F, Qiu G. Liu J, et al. Among authors: shen y, shen j. Genet Med. 2019 Jul;21(7):1548-1558. doi: 10.1038/s41436-018-0377-x. Epub 2019 Jan 14. Genet Med. 2019. PMID: 30636772 Free PMC article.

2

Genomic dissection of population substructure of Han Chinese and its implication in association studies.

Xu S, Yin X, Li S, Jin W, Lou H, Yang L, Gong X, Wang H, Shen Y, Pan X, He Y, Yang Y, Wang Y, Fu W, An Y, Wang J, Tan J, Qian J, Chen X, Zhang X, Sun Y, Zhang X, Wu B, Jin L. Xu S, et al. Among authors: shen y. Am J Hum Genet. 2009 Dec;85(6):762-74. doi: 10.1016/j.ajhg.2009.10.015. Am J Hum Genet. 2009. PMID: 19944404 Free PMC article.

3

Interstitial microduplication of Xp22.31: Causative of intellectual disability or benign copy number variant?

Li F, Shen Y, Köhler U, Sharkey FH, Menon D, Coulleaux L, Malan V, Rio M, McMullan DJ, Cox H, Fagan KA, Gaunt L, Metcalfe K, Heinrich U, Hislop G, Maye U, Sutcliffe M, Wu BL, Thiel BD, Mulchandani S, Conlin LK, Spinner NB, Murphy KM, Batista DA. Li F, et al. Among authors: shen y. Eur J Med Genet. 2010 Mar-Apr;53(2):93-9. doi: 10.1016/j.ejmg.2010.01.004. Epub 2010 Feb 2. Eur J Med Genet. 2010. PMID: 20132918

4

Intra-family phenotypic heterogeneity of 16p11.2 deletion carriers in a three-generation Chinese family.

Shen Y, Chen X, Wang L, Guo J, Shen J, An Y, Zhu H, Zhu Y, Xin R, Bao Y, Gusella JF, Zhang T, Wu BL. Shen Y, et al. Among authors: shen j. Am J Med Genet B Neuropsychiatr Genet. 2011 Mar;156(2):225-32. doi: 10.1002/ajmg.b.31147. Epub 2010 Dec 28. Am J Med Genet B Neuropsychiatr Genet. 2011. PMID: 21302351

5

Genome-wide detection of natural selection in African Americans pre- and post-admixture.

Jin W, Xu S, Wang H, Yu Y, Shen Y, Wu B, Jin L. Jin W, et al. Among authors: shen y. Genome Res. 2012 Mar;22(3):519-27. doi: 10.1101/gr.124784.111. Epub 2011 Nov 29. Genome Res. 2012. PMID: 22128132 Free PMC article.

6

Molecular analysis of a deletion hotspot in the NRXN1 region reveals the involvement of short inverted repeats in deletion CNVs.

Chen X, Shen Y, Zhang F, Chiang C, Pillalamarri V, Blumenthal I, Talkowski M, Wu BL, Gusella JF. Chen X, et al. Among authors: shen y. Am J Hum Genet. 2013 Mar 7;92(3):375-86. doi: 10.1016/j.ajhg.2013.02.006. Am J Hum Genet. 2013. PMID: 23472757 Free PMC article.

7

Increased genome instability in human DNA segments with self-chains: homology-induced structural variations via replicative mechanisms.

Zhou W, Zhang F, Chen X, Shen Y, Lupski JR, Jin L. Zhou W, et al. Among authors: shen y. Hum Mol Genet. 2013 Jul 1;22(13):2642-51. doi: 10.1093/hmg/ddt113. Epub 2013 Mar 7. Hum Mol Genet. 2013. PMID: 23474816 Free PMC article.

8

Genome-wide copy number variant analysis for congenital ventricular septal defects in Chinese Han population.

An Y, Duan W, Huang G, Chen X, Li L, Nie C, Hou J, Gui Y, Wu Y, Zhang F, Shen Y, Wu B, Wang H. An Y, et al. Among authors: shen y. BMC Med Genomics. 2016 Jan 8;9:2. doi: 10.1186/s12920-015-0163-4. BMC Med Genomics. 2016. PMID: 26742958 Free PMC article.

9

Further defining the critical genes for the 4q21 microdeletion disorder.

Hu X, Chen X, Wu B, Soler IM, Chen S, Shen Y. Hu X, et al. Among authors: shen y. Am J Med Genet A. 2017 Jan;173(1):120-125. doi: 10.1002/ajmg.a.37965. Epub 2016 Sep 8. Am J Med Genet A. 2017. PMID: 27604828

10

CNVbase: Batch identification of novel and rare copy number variations based on multi-ethnic population data.

Zhang C, Lu J, Lou H, Du R, Xu S, Shen Y, Zhang F, Jin L. Zhang C, et al. Among authors: shen y. J Genet Genomics. 2017 Jul 20;44(7):367-370. doi: 10.1016/j.jgg.2017.07.001. Epub 2017 Jul 11. J Genet Genomics. 2017. PMID: 28739046 No abstract available.

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