Davis S - Search Results

1

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia.

Walsh T, McClellan JM, McCarthy SE, Addington AM, Pierce SB, Cooper GM, Nord AS, Kusenda M, Malhotra D, Bhandari A, Stray SM, Rippey CF, Roccanova P, Makarov V, Lakshmi B, Findling RL, Sikich L, Stromberg T, Merriman B, Gogtay N, Butler P, Eckstrand K, Noory L, Gochman P, Long R, Chen Z, Davis S, Baker C, Eichler EE, Meltzer PS, Nelson SF, Singleton AB, Lee MK, Rapoport JL, King MC, Sebat J. Walsh T, et al. Among authors: davis s. Science. 2008 Apr 25;320(5875):539-43. doi: 10.1126/science.1155174. Epub 2008 Mar 27. Science. 2008. PMID: 18369103

2

GEOquery: a bridge between the Gene Expression Omnibus (GEO) and BioConductor.

Davis S, Meltzer PS. Davis S, et al. Bioinformatics. 2007 Jul 15;23(14):1846-7. doi: 10.1093/bioinformatics/btm254. Epub 2007 May 12. Bioinformatics. 2007. PMID: 17496320

3

Ewing's sarcoma: general insights from a rare model.

Davis S, Meltzer PS. Davis S, et al. Cancer Cell. 2006 May;9(5):331-2. doi: 10.1016/j.ccr.2006.05.003. Cancer Cell. 2006. PMID: 16697953 Free article.

4

Modeling synovial sarcoma: timing is everything.

Davis SR, Meltzer PS. Davis SR, et al. Cancer Cell. 2007 Apr;11(4):305-7. doi: 10.1016/j.ccr.2007.03.016. Cancer Cell. 2007. PMID: 17418406 Free article.

5

GEOmetadb: powerful alternative search engine for the Gene Expression Omnibus.

Zhu Y, Davis S, Stephens R, Meltzer PS, Chen Y. Zhu Y, et al. Among authors: davis s. Bioinformatics. 2008 Dec 1;24(23):2798-800. doi: 10.1093/bioinformatics/btn520. Epub 2008 Oct 7. Bioinformatics. 2008. PMID: 18842599 Free PMC article.

6

caOmicsV: an R package for visualizing multidimensional cancer genomic data.

Zhang H, Meltzer PS, Davis SR. Zhang H, et al. Among authors: davis sr. BMC Bioinformatics. 2016 Mar 22;17:141. doi: 10.1186/s12859-016-0989-6. BMC Bioinformatics. 2016. PMID: 27005934 Free PMC article.

7

RCircos: an R package for Circos 2D track plots.

Zhang H, Meltzer P, Davis S. Zhang H, et al. Among authors: davis s. BMC Bioinformatics. 2013 Aug 10;14:244. doi: 10.1186/1471-2105-14-244. BMC Bioinformatics. 2013. PMID: 23937229 Free PMC article.

8

SRAdb: query and use public next-generation sequencing data from within R.

Zhu Y, Stephens RM, Meltzer PS, Davis SR. Zhu Y, et al. Among authors: davis sr. BMC Bioinformatics. 2013 Jan 17;14:19. doi: 10.1186/1471-2105-14-19. BMC Bioinformatics. 2013. PMID: 23323543 Free PMC article.

9

Zoom-in comparative genomic hybridisation arrays for the characterisation of variable breakpoint contiguous gene syndromes.

Johnston JJ, Walker RL, Davis S, Facio F, Turner JT, Bick DP, Daentl DL, Ellison JW, Meltzer PS, Biesecker LG. Johnston JJ, et al. Among authors: davis s. J Med Genet. 2007 Jan;44(1):e59. doi: 10.1136/jmg.2006.042473. Epub 2006 Nov 10. J Med Genet. 2007. PMID: 17098889 Free PMC article.

10

Pan-cancer genome and transcriptome analyses of 1,699 paediatric leukaemias and solid tumours.

Ma X, Liu Y, Liu Y, Alexandrov LB, Edmonson MN, Gawad C, Zhou X, Li Y, Rusch MC, Easton J, Huether R, Gonzalez-Pena V, Wilkinson MR, Hermida LC, Davis S, Sioson E, Pounds S, Cao X, Ries RE, Wang Z, Chen X, Dong L, Diskin SJ, Smith MA, Guidry Auvil JM, Meltzer PS, Lau CC, Perlman EJ, Maris JM, Meshinchi S, Hunger SP, Gerhard DS, Zhang J. Ma X, et al. Among authors: davis s. Nature. 2018 Mar 15;555(7696):371-376. doi: 10.1038/nature25795. Epub 2018 Feb 28. Nature. 2018. PMID: 29489755 Free PMC article.

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