D. Peiffer

发表

Mapping and sequencing of structural variation from eight human genomes

Joshua M. Korn, Nancy F. Hansen, D. Altshuler, 2008, Nature.

High-resolution genomic profiling of chromosomal aberrations using Infinium whole-genome genotyping.

K. Gunderson, F. Steemers, C. Shaw, 2006, Genome research.

Power to Detect Risk Alleles Using Genome-Wide Tag SNP Panels

Pauline C Ng, Michael A Eberle, Richard Shen, 2007, PLoS genetics.

Global gene expression profiling and cluster analysis in Xenopus laevis

Ken W. Y. Cho, R. Eils, D. Peiffer, 2005, Mechanisms of Development.

Microarray optimizations: increasing spot accuracy and automated identification of true microarray signals.

Ken W. Y. Cho, D. Peiffer, J. Brody, 2002, Nucleic acids research.

Integrated Molecular Analyses of Biological Samples on a Bead-Based Microarray Platform

Kenneth M. Kuhn, K. Gunderson, F. Steemers, 2007 .

1 SNP-based Genome-wide Chromosome Copy Change , LOH , and Aneuploidy in Barrett ’ s Esophagus Neoplastic Progression .

Patricia L. Blount, K. Gunderson, D. Peiffer, 2008 .

Characterization of de novo microdeletions involving 17q11.2q12 identified through chromosomal comparative genomic hybridization

K. Gunderson, Z. Ou, M. L. Cooper, 2007, Clinical genetics.

Identification of neural genes using Xenopus DNA microarrays

Ken W. Y. Cho, A. Liao, D. Peiffer, 2005, Developmental dynamics : an official publication of the American Association of Anatomists.

Single Nucleotide Polymorphism–Based Genome-Wide Chromosome Copy Change, Loss of Heterozygosity, and Aneuploidy in Barrett's Esophagus Neoplastic Progression

Patricia L. Blount, K. Gunderson, D. Peiffer, 2008, Cancer Prevention Research.

Speech delay and autism spectrum behaviors are frequently associated with duplication of the 7q11.23 Williams-Beuren syndrome region

K. Gunderson, Ankita Patel, J. Lupski, 2007, Genetics in Medicine.

Phylogenetic footprinting and genome scanning identify vertebrate BMP response elements and new target genes.

Ken W. Y. Cho, Q. Zeng, D. Peiffer, 2005, Developmental biology.

Deletion at Fragile Sites Is a Common and Early Event in Barrett's Esophagus

K. Gunderson, D. Peiffer, C. Maley, 2010, Molecular Cancer Research.

Increased LIS1 expression affects human and mouse brain development

K. Gunderson, J. Lupski, S. Cheung, 2009, Nature Genetics.

Identification of critical regions for clinical features of distal 10q deletion syndrome

Z. Ou, S. Cheung, D. Peiffer, 2009, Clinical genetics.

Design of tag SNP whole genome genotyping arrays.

K. Gunderson, D. Peiffer, 2009, Methods in molecular biology.

Identification of neural genes using Xenopus DNA microarrays

Ken W. Y. Cho, A. Liao, D. Peiffer, 2005 .

Xenopus DNA Microarrays

Ken W. Y. Cho, D. Peiffer, Yongchol Shin, 2003 .

Deletion of 7q31.1 supports involvement of FOXP2 in language impairment: Clinical report and review

K. Gunderson, M. L. Cooper, Ankita Patel, 2007, American journal of medical genetics. Part A.

Mosaic tetrasomy 12p with triplication of 12p detected by array‐based comparative genomic hybridization of peripheral blood DNA

K. Gunderson, M. L. Cooper, Ankita Patel, 2007, American journal of medical genetics. Part A.

A Xenopus DNA microarray approach to identify novel direct BMP target genes involved in early embryonic development

Ken W. Y. Cho, D. Peiffer, N. Ueno, 2005, Developmental dynamics : an official publication of the American Association of Anatomists.

Genomic profiling of 766 cancer‐related genes in archived esophageal normal and carcinoma tissues

Marina Bibikova, Wei Jiang, Jessica Wang-Rodriguez, 2008, International journal of cancer.

Delineation of the proximal 3q microdeletion syndrome

K. Gunderson, S. Cheung, D. Peiffer, 2008, American Journal of Medical Genetics. Part A.

Clinical Report Delineation of the Proximal 3q Microdeletion Syndrome

K. Gunderson, S. Cheung, D. Peiffer, 2008 .

Schnurri transcription factors from Drosophila and vertebrates can mediate Bmp signaling through a phylogenetically conserved mechanism

Ken W. Y. Cho, D. Peiffer, I. Blitz, 2006, Development.

SNP-CGH technologies for genomic profiling of LOH and copy number

K. Gunderson, D. Peiffer, D. A. Peiffer, 2006 .