Shao L - Search Results

1

Observation and prediction of recurrent human translocations mediated by NAHR between nonhomologous chromosomes.

Ou Z, Stankiewicz P, Xia Z, Breman AM, Dawson B, Wiszniewska J, Szafranski P, Cooper ML, Rao M, Shao L, South ST, Coleman K, Fernhoff PM, Deray MJ, Rosengren S, Roeder ER, Enciso VB, Chinault AC, Patel A, Kang SH, Shaw CA, Lupski JR, Cheung SW. Ou Z, et al. Among authors: shao l. Genome Res. 2011 Jan;21(1):33-46. doi: 10.1101/gr.111609.110. Genome Res. 2011. PMID: 21205869 Free PMC article.

2

Identification of chromosome abnormalities in subtelomeric regions by microarray analysis: a study of 5,380 cases.

Shao L, Shaw CA, Lu XY, Sahoo T, Bacino CA, Lalani SR, Stankiewicz P, Yatsenko SA, Li Y, Neill S, Pursley AN, Chinault AC, Patel A, Beaudet AL, Lupski JR, Cheung SW. Shao L, et al. Am J Med Genet A. 2008 Sep 1;146A(17):2242-51. doi: 10.1002/ajmg.a.32399. Am J Med Genet A. 2008. PMID: 18663743 Free PMC article.

3

Array comparative genomic hybridization detects chromosomal abnormalities in hematological cancers that are not detected by conventional cytogenetics.

Shao L, Kang SH, Li J, Hixson P, Taylor J, Yatsenko SA, Shaw CA, Milosavljevic A, Chang CC, Cheung SW, Patel A. Shao L, et al. J Mol Diagn. 2010 Sep;12(5):670-9. doi: 10.2353/jmoldx.2010.090192. Epub 2010 Aug 19. J Mol Diagn. 2010. PMID: 20724749 Free PMC article.

4

Low-level mosaicism of trisomy 14: phenotypic and molecular characterization.

Shinawi M, Shao L, Jeng LJ, Shaw CA, Patel A, Bacino C, Sutton VR, Belmont J, Cheung SW. Shinawi M, et al. Among authors: shao l. Am J Med Genet A. 2008 Jun 1;146A(11):1395-405. doi: 10.1002/ajmg.a.32287. Am J Med Genet A. 2008. PMID: 18412278

5

Matrix metalloproteinase polymorphisms and bladder cancer risk.

Kader AK, Shao L, Dinney CP, Schabath MB, Wang Y, Liu J, Gu J, Grossman HB, Wu X. Kader AK, et al. Among authors: shao l. Cancer Res. 2006 Dec 15;66(24):11644-8. doi: 10.1158/0008-5472.CAN-06-1212. Cancer Res. 2006. PMID: 17178858

6

Specific chromosome aberrations in peripheral blood lymphocytes are associated with risk of bladder cancer.

Shao L, Lerner SL, Bondaruk J, Czerniak BA, Zeng X, Grossman HB, Spitz MR, Wu X. Shao L, et al. Genes Chromosomes Cancer. 2004 Dec;41(4):379-89. doi: 10.1002/gcc.20095. Genes Chromosomes Cancer. 2004. PMID: 15390184

7

Mutagen sensitivity has high heritability: evidence from a twin study.

Wu X, Spitz MR, Amos CI, Lin J, Shao L, Gu J, de Andrade M, Benowitz NL, Shields PG, Swan GE. Wu X, et al. Among authors: shao l. Cancer Res. 2006 Jun 15;66(12):5993-6. doi: 10.1158/0008-5472.CAN-06-1007. Cancer Res. 2006. PMID: 16778168

8

An association between a NQO1 genetic polymorphism and risk of lung cancer.

Saldivar SJ, Wang Y, Zhao H, Shao L, Lin J, Spitz MR, Wu X. Saldivar SJ, et al. Among authors: shao l. Mutat Res. 2005 Apr 4;582(1-2):71-8. doi: 10.1016/j.mrgentox.2004.12.010. Mutat Res. 2005. PMID: 15781212

9

Comprehensive Pan-Genomic Characterization of Adrenocortical Carcinoma.

Zheng S, Cherniack AD, Dewal N, Moffitt RA, Danilova L, Murray BA, Lerario AM, Else T, Knijnenburg TA, Ciriello G, Kim S, Assie G, Morozova O, Akbani R, Shih J, Hoadley KA, Choueiri TK, Waldmann J, Mete O, Robertson AG, Wu HT, Raphael BJ, Shao L, Meyerson M, Demeure MJ, Beuschlein F, Gill AJ, Sidhu SB, Almeida MQ, Fragoso MCBV, Cope LM, Kebebew E, Habra MA, Whitsett TG, Bussey KJ, Rainey WE, Asa SL, Bertherat J, Fassnacht M, Wheeler DA; Cancer Genome Atlas Research Network; Hammer GD, Giordano TJ, Verhaak RGW. Zheng S, et al. Among authors: shao l. Cancer Cell. 2016 May 9;29(5):723-736. doi: 10.1016/j.ccell.2016.04.002. Cancer Cell. 2016. PMID: 27165744 Free PMC article.

10

Deficiency of cell cycle checkpoints and DNA repair system predispose individuals to esophageal cancer.

Shao L, Hittelman WN, Lin J, Yang H, Ajani JA, Wu X. Shao L, et al. Mutat Res. 2006 Dec 1;602(1-2):143-50. doi: 10.1016/j.mrfmmm.2006.08.011. Epub 2006 Oct 2. Mutat Res. 2006. PMID: 17011594

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