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High-resolution analysis of DNA copy number using oligonucleotide microarrays.
Bignell GR, Huang J, Greshock J, Watt S, Butler A, West S, Grigorova M, Jones KW, Wei W, Stratton MR, Futreal PA, Weber B, Shapero MH, Wooster R. Bignell GR, et al. Among authors: wooster r. Genome Res. 2004 Feb;14(2):287-95. doi: 10.1101/gr.2012304. Genome Res. 2004. PMID: 14762065 Free PMC article.
High throughput DNA sequence variant detection by conformation sensitive capillary electrophoresis and automated peak comparison.
Davies H, Dicks E, Stephens P, Cox C, Teague J, Greenman C, Bignell G, O'meara S, Edkins S, Parker A, Stevens C, Menzies A, Blow M, Bottomley B, Dronsfield M, Futreal PA, Stratton MR, Wooster R. Davies H, et al. Among authors: wooster r. Genomics. 2006 Mar;87(3):427-32. doi: 10.1016/j.ygeno.2005.11.008. Epub 2006 Jan 9. Genomics. 2006. PMID: 16406726 Free article.
A survey of RNA editing in human brain.
Blow M, Futreal PA, Wooster R, Stratton MR. Blow M, et al. Among authors: wooster r. Genome Res. 2004 Dec;14(12):2379-87. doi: 10.1101/gr.2951204. Epub 2004 Nov 15. Genome Res. 2004. PMID: 15545495 Free PMC article.
A survey of homozygous deletions in human cancer genomes.
Cox C, Bignell G, Greenman C, Stabenau A, Warren W, Stephens P, Davies H, Watt S, Teague J, Edkins S, Birney E, Easton DF, Wooster R, Futreal PA, Stratton MR. Cox C, et al. Among authors: wooster r. Proc Natl Acad Sci U S A. 2005 Mar 22;102(12):4542-7. doi: 10.1073/pnas.0408593102. Epub 2005 Mar 10. Proc Natl Acad Sci U S A. 2005. PMID: 15761058 Free PMC article.
Architectures of somatic genomic rearrangement in human cancer amplicons at sequence-level resolution.
Bignell GR, Santarius T, Pole JC, Butler AP, Perry J, Pleasance E, Greenman C, Menzies A, Taylor S, Edkins S, Campbell P, Quail M, Plumb B, Matthews L, McLay K, Edwards PA, Rogers J, Wooster R, Futreal PA, Stratton MR. Bignell GR, et al. Among authors: wooster r. Genome Res. 2007 Sep;17(9):1296-303. doi: 10.1101/gr.6522707. Epub 2007 Aug 3. Genome Res. 2007. PMID: 17675364 Free PMC article.
Mutations in the DLG3 gene cause nonsyndromic X-linked mental retardation.
Tarpey P, Parnau J, Blow M, Woffendin H, Bignell G, Cox C, Cox J, Davies H, Edkins S, Holden S, Korny A, Mallya U, Moon J, O'Meara S, Parker A, Stephens P, Stevens C, Teague J, Donnelly A, Mangelsdorf M, Mulley J, Partington M, Turner G, Stevenson R, Schwartz C, Young I, Easton D, Bobrow M, Futreal PA, Stratton MR, Gecz J, Wooster R, Raymond FL. Tarpey P, et al. Among authors: wooster r. Am J Hum Genet. 2004 Aug;75(2):318-24. doi: 10.1086/422703. Epub 2004 Jun 7. Am J Hum Genet. 2004. PMID: 15185169 Free PMC article.
114 results