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Power to detect risk alleles using genome-wide tag SNP panels.
Eberle MA, Ng PC, Kuhn K, Zhou L, Peiffer DA, Galver L, Viaud-Martinez KA, Lawley CT, Gunderson KL, Shen R, Murray SS. Eberle MA, et al. Among authors: peiffer da. PLoS Genet. 2007 Oct;3(10):1827-37. doi: 10.1371/journal.pgen.0030170. Epub 2007 Aug 22. PLoS Genet. 2007. PMID: 17922574 Free PMC article.
Deletion at fragile sites is a common and early event in Barrett's esophagus.
Lai LA, Kostadinov R, Barrett MT, Peiffer DA, Pokholok D, Odze R, Sanchez CA, Maley CC, Reid BJ, Gunderson KL, Rabinovitch PS. Lai LA, et al. Among authors: peiffer da. Mol Cancer Res. 2010 Aug;8(8):1084-94. doi: 10.1158/1541-7786.MCR-09-0529. Epub 2010 Jul 20. Mol Cancer Res. 2010. PMID: 20647332 Free PMC article.
Delineation of the proximal 3q microdeletion syndrome.
Simovich MJ, Bland SD, Peiffer DA, Gunderson KL, Cheung SW, Yatsenko SA, Shinawi M. Simovich MJ, et al. Among authors: peiffer da. Am J Med Genet A. 2008 Jul 1;146A(13):1729-35. doi: 10.1002/ajmg.a.32292. Am J Med Genet A. 2008. PMID: 18536049 Review.
Speech delay and autism spectrum behaviors are frequently associated with duplication of the 7q11.23 Williams-Beuren syndrome region.
Berg JS, Brunetti-Pierri N, Peters SU, Kang SH, Fong CT, Salamone J, Freedenberg D, Hannig VL, Prock LA, Miller DT, Raffalli P, Harris DJ, Erickson RP, Cunniff C, Clark GD, Blazo MA, Peiffer DA, Gunderson KL, Sahoo T, Patel A, Lupski JR, Beaudet AL, Cheung SW. Berg JS, et al. Among authors: peiffer da. Genet Med. 2007 Jul;9(7):427-41. doi: 10.1097/gim.0b013e3180986192. Genet Med. 2007. PMID: 17666889 Free article.
20 results