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Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome.
Sharp AJ, Hansen S, Selzer RR, Cheng Z, Regan R, Hurst JA, Stewart H, Price SM, Blair E, Hennekam RC, Fitzpatrick CA, Segraves R, Richmond TA, Guiver C, Albertson DG, Pinkel D, Eis PS, Schwartz S, Knight SJ, Eichler EE. Sharp AJ, et al. Among authors: segraves r. Nat Genet. 2006 Sep;38(9):1038-42. doi: 10.1038/ng1862. Epub 2006 Aug 13. Nat Genet. 2006. PMID: 16906162
Segmental duplications and copy-number variation in the human genome.
Sharp AJ, Locke DP, McGrath SD, Cheng Z, Bailey JA, Vallente RU, Pertz LM, Clark RA, Schwartz S, Segraves R, Oseroff VV, Albertson DG, Pinkel D, Eichler EE. Sharp AJ, et al. Among authors: segraves r. Am J Hum Genet. 2005 Jul;77(1):78-88. doi: 10.1086/431652. Epub 2005 May 25. Am J Hum Genet. 2005. PMID: 15918152 Free PMC article.
Regional copy number-independent deregulation of transcription in cancer.
Stransky N, Vallot C, Reyal F, Bernard-Pierrot I, de Medina SG, Segraves R, de Rycke Y, Elvin P, Cassidy A, Spraggon C, Graham A, Southgate J, Asselain B, Allory Y, Abbou CC, Albertson DG, Thiery JP, Chopin DK, Pinkel D, Radvanyi F. Stransky N, et al. Among authors: segraves r. Nat Genet. 2006 Dec;38(12):1386-96. doi: 10.1038/ng1923. Epub 2006 Nov 12. Nat Genet. 2006. PMID: 17099711
Assembly of microarrays for genome-wide measurement of DNA copy number.
Snijders AM, Nowak N, Segraves R, Blackwood S, Brown N, Conroy J, Hamilton G, Hindle AK, Huey B, Kimura K, Law S, Myambo K, Palmer J, Ylstra B, Yue JP, Gray JW, Jain AN, Pinkel D, Albertson DG. Snijders AM, et al. Among authors: segraves r. Nat Genet. 2001 Nov;29(3):263-4. doi: 10.1038/ng754. Nat Genet. 2001. PMID: 11687795
BAC microarray-based comparative genomic hybridization.
Snijders AM, Segraves R, Blackwood S, Pinkel D, Albertson DG. Snijders AM, et al. Among authors: segraves r. Methods Mol Biol. 2004;256:39-56. doi: 10.1385/1-59259-753-X:039. Methods Mol Biol. 2004. PMID: 15024158 No abstract available.
121 results