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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: cheng z. 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: cheng z. 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.
Structural variation of the human genome.
Sharp AJ, Cheng Z, Eichler EE. Sharp AJ, et al. Among authors: cheng z. Annu Rev Genomics Hum Genet. 2006;7:407-42. doi: 10.1146/annurev.genom.7.080505.115618. Annu Rev Genomics Hum Genet. 2006. PMID: 16780417 Review.
Mouse segmental duplication and copy number variation.
She X, Cheng Z, Zöllner S, Church DM, Eichler EE. She X, et al. Among authors: cheng z. Nat Genet. 2008 Jul;40(7):909-14. doi: 10.1038/ng.172. Epub 2008 May 22. Nat Genet. 2008. PMID: 18500340 Free PMC article.
Recurrent duplication-driven transposition of DNA during hominoid evolution.
Johnson ME; National Institute of Health Intramural Sequencing Center Comparative Sequencing Program; Cheng Z, Morrison VA, Scherer S, Ventura M, Gibbs RA, Green ED, Eichler EE. Johnson ME, et al. Among authors: cheng z. Proc Natl Acad Sci U S A. 2006 Nov 21;103(47):17626-31. doi: 10.1073/pnas.0605426103. Epub 2006 Nov 13. Proc Natl Acad Sci U S A. 2006. PMID: 17101969 Free PMC article.
9,325 results