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Search life-sciences literature (45,103,589 articles, preprints and more)

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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
Mol Cancer Res, 8(8):1084-1094, 20 Jul 2010
Cited by: 30 articles | PMID: 20647332 | PMCID: PMC3100793
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Identification of critical regions for clinical features of distal 10q deletion syndrome.
Yatsenko SA, Kruer MC, Bader PI, Corzo D, Schuette J, Keegan CE, Nowakowska B, Peacock S, Cai WW, Peiffer DA, Gunderson KL, Ou Z, Chinault AC, Cheung SW
Clin Genet, 76(1):54-62, 22 Jun 2009
Cited by: 38 articles | PMID: 19558528
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Design of tag SNP whole genome genotyping arrays.
Peiffer DA, Gunderson KL
Methods Mol Biol, 529:51-61, 01 Jan 2009
Cited by: 7 articles | PMID: 19381970
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Increased LIS1 expression affects human and mouse brain development.
Bi W, Sapir T, Shchelochkov OA, Zhang F, Withers MA, Hunter JV, Levy T, Shinder V, Peiffer DA, Gunderson KL, Nezarati MM, Shotts VA, Amato SS, Savage SK, Harris DJ, Day-Salvatore DL, Horner M, Lu XY, Sahoo T, [...] Reiner O
Nat Genet, 41(2):168-177, 11 Jan 2009
Cited by: 154 articles | PMID: 19136950 | PMCID: PMC4396744
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Single nucleotide polymorphism-based genome-wide chromosome copy change, loss of heterozygosity, and aneuploidy in Barrett's esophagus neoplastic progression.
Li X, Galipeau PC, Sanchez CA, Blount PL, Maley CC, Arnaudo J, Peiffer DA, Pokholok D, Gunderson KL, Reid BJ
Cancer Prev Res (Phila), 1(6):413-423, 01 Nov 2008
Cited by: 32 articles | PMID: 19138988 | PMCID: PMC2882787
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Characterization of de novo microdeletions involving 17q11.2q12 identified through chromosomal comparative genomic hybridization.
Brunetti-Pierri N, Grange DK, Ou Z, Peiffer DA, Peacock SK, Cooper ML, Eng PA, Lalani SR, Chinault AC, Gunderson KL, Craigen WJ, Cheung SW
Clin Genet, 72(5):411-419, 03 Oct 2007
Cited by: 10 articles | PMID: 17916097
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Delineation of the proximal 3q microdeletion syndrome.
Simovich MJ, Bland SD, Peiffer DA, Gunderson KL, Cheung SW, Yatsenko SA, Shinawi M
Am J Med Genet A, 146A(13):1729-1735, 01 Jul 2008
Cited by: 12 articles | PMID: 18536049
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Mapping and sequencing of structural variation from eight human genomes.
Kidd JM, Cooper GM, Donahue WF, Hayden HS, Sampas N, Graves T, Hansen N, Teague B, Alkan C, Antonacci F, Haugen E, Zerr T, Yamada NA, Tsang P, Newman TL, Tüzün E, Cheng Z, Ebling HM, Tusneem N, [...] Eichler EE
Nature, 453(7191):56-64, 01 May 2008
Cited by: 721 articles | PMID: 18451855 | PMCID: PMC2424287
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Genomic profiling of 766 cancer-related genes in archived esophageal normal and carcinoma tissues.
Chen J, Guo L, Peiffer DA, Zhou L, Chan OT, Bibikova M, Wickham-Garcia E, Lu SH, Zhan Q, Wang-Rodriguez J, Jiang W, Fan JB
Int J Cancer, 122(10):2249-2254, 01 May 2008
Cited by: 40 articles | PMID: 18241037
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Mosaic tetrasomy 12p with triplication of 12p detected by array-based comparative genomic hybridization of peripheral blood DNA.
Powis Z, Kang SH, Cooper ML, Patel A, Peiffer DA, Hawkins A, Heidenreich R, Gunderson KL, Cheung SW, Erickson RP
Am J Med Genet A, 143A(24):2910-2915, 01 Dec 2007
Cited by: 11 articles | PMID: 18000900
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Deletion of 7q31.1 supports involvement of FOXP2 in language impairment: clinical report and review.
Lennon PA, Cooper ML, Peiffer DA, Gunderson KL, Patel A, Peters S, Cheung SW, Bacino CA
Am J Med Genet A, 143A(8):791-798, 01 Apr 2007
Cited by: 48 articles | PMID: 17330859
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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
PLoS Genet, 3(10):1827-1837, 22 Aug 2007
Cited by: 61 articles | PMID: 17922574 | PMCID: PMC2000969
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This article is in the Europe PMC Open access subset. Refer to the copyright information in the article for licensing details.
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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, [...] Cheung SW
Genet Med, 9(7):427-441, 01 Jul 2007
Cited by: 129 articles | PMID: 17666889
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High-resolution genomic profiling of chromosomal aberrations using Infinium whole-genome genotyping.
Peiffer DA, Le JM, Steemers FJ, Chang W, Jenniges T, Garcia F, Haden K, Li J, Shaw CA, Belmont J, Cheung SW, Shen RM, Barker DL, Gunderson KL
Genome Res, 16(9):1136-1148, 09 Aug 2006
Cited by: 341 articles | PMID: 16899659 | PMCID: PMC1557768
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Schnurri transcription factors from Drosophila and vertebrates can mediate Bmp signaling through a phylogenetically conserved mechanism.
Yao LC, Blitz IL, Peiffer DA, Phin S, Wang Y, Ogata S, Cho KW, Arora K, Warrior R
Development, 133(20):4025-4034, 01 Oct 2006
Cited by: 47 articles | PMID: 17008448
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Identification of neural genes using Xenopus DNA microarrays.
Shin Y, Kitayama A, Koide T, Peiffer DA, Mochii M, Liao A, Ueno N, Cho KW
Dev Dyn, 232(2):432-444, 01 Feb 2005
Cited by: 21 articles | PMID: 15614765
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Phylogenetic footprinting and genome scanning identify vertebrate BMP response elements and new target genes.
von Bubnoff A, Peiffer DA, Blitz IL, Hayata T, Ogata S, Zeng Q, Trunnell M, Cho KW
Dev Biol, 281(2):210-226, 01 May 2005
Cited by: 44 articles | PMID: 15893974
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A Xenopus DNA microarray approach to identify novel direct BMP target genes involved in early embryonic development.
Peiffer DA, Von Bubnoff A, Shin Y, Kitayama A, Mochii M, Ueno N, Cho KW
Dev Dyn, 232(2):445-456, 01 Feb 2005
Cited by: 19 articles | PMID: 15614776
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Microarray optimizations: increasing spot accuracy and automated identification of true microarray signals.
Tran PH, Peiffer DA, Shin Y, Meek LM, Brody JP, Cho KW
Nucleic Acids Res, 30(12):e54, 01 Jun 2002
Cited by: 75 articles | PMID: 12060692 | PMCID: PMC117296
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