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Prenatal Diagnosis|April 3, 2012
Prenatal chromosomal microarray analysis in a diagnostic laboratory; experience with >1000 cases and review of the literatureAmy Breman, Amber N Pursley, Patricia Hixson, et al.Cell|May 23, 2006
A protein-protein interaction network for human inherited ataxias and disorders of Purkinje cell degenerationJanghoo Lim, Tong Hao, Chad Shaw, et al.Nature Medicine|November 13, 2013
Racial differences in human platelet PAR4 reactivity reflect expression of PCTP and miR-376cLeonard C Edelstein, Lukas M Simon, Raúl Teruel Montoya, et al.European Journal of Human Genetics : EJHG|January 9, 2014
Somatic mosaicism detected by exon-targeted, high-resolution aCGH in 10,362 consecutive casesJustin Pham, Chad Shaw, Amber Pursley, et al.American Journal of Medical Genetics. Part A|March 27, 2010
Insertional translocation detected using FISH confirmation of array-comparative genomic hybridization (aCGH) resultsSung-Hae L Kang, Chad Shaw, Zhishuo Ou, et al.Development (Cambridge, England)|March 30, 2002
A transcriptional profile of multicellular development in Dictyostelium discoideumNancy Van Driessche, Chad Shaw, Mariko Katoh, et al.Plos Genetics|May 23, 2012
Genomic hypomethylation in the human germline associates with selective structural mutability in the human genomeJian Li, R Alan Harris, Sau Wai Cheung, et al.Blood|March 19, 2011
Platelet microRNA-mRNA coexpression profiles correlate with platelet reactivitySrikanth Nagalla, Chad Shaw, Xianguo Kong, et al.Genome Medicine|September 30, 2022
Sequencing individual genomes with recurrent genomic disorder deletions: an approach to characterize genes for autosomal recessive rare disease traitsBo Yuan, Katharina V Schulze, Nurit Assia Batzir, et al.Clinical Chemistry|January 3, 2025
Detection of Clinically Relevant Monogenic Copy-Number Variants by a Comprehensive Genome-Wide Microarray with Exonic CoverageMatthew Hoi Kin Chau, Stephanie A Anderson, Rodger Song, et al.Pageof 6