Assistant Professor
Department of Molecular and Human Genetics
Baylor College of Medicine
One Baylor Plaza, MS BCM227
Houston, TX 77030
http://www.bcm.edu/genetics/?pmid=11041
Dr. Scott earned his MD/PhD at the University of Iowa and completed his pediatric residency at the University of Utah/Primary Children's Medical Center and a fellowship in Clinical Genetics at Baylor College of Medicine, where he is now on faculty.
His laboratory is working to identify and characterize the genes that cause common birth defects, including congenital diaphragmatic hernia and esophageal atresia/trancheoesophageal fistula.
Scott DA, Cooper ML, Stankiewicz P, Patel A, Potocki L, Cheung SW.
Congenital diaphragmatic hernia in WAGR syndrome.
Am J Med Genet A.
2005;134(4):430-3.
PubMed abstract
Scott DA, Klaassens M, Holder AM, Lally KP, Fernandes CJ, Galjaard RJ, Tibboel D, de Klein A, Lee B.
Genome-wide oligonucleotide-based array comparative genome hybridization analysis of non-isolated congenital diaphragmatic
hernia.
Hum Mol Genet.
2007;16(4):424-30.
PubMed abstract
Qidwai K, Pearson DM, Patel GS, Pober BR, Immken LL, Cheung SW, Scott DA.
Deletions of Xp provide evidence for the role of holocytochrome C-type synthase (HCCS) in congenital diaphragmatic hernia.
Am J Med Genet A.
2010;152A(6):1588-90.
PubMed abstract / Full Text
Schaaf CP, Scott DA, Wiszniewska J, Beaudet AL.
Identification of incestuous parental relationships by SNP-based DNA microarrays.
Lancet.
2011;377(9765):555-6.
PubMed abstract
Wat MJ, Veenma D, Hogue J, Holder AM, Yu Z, Wat JJ, Hanchard N, Shchelochkov OA, Fernandes CJ, Johnson A, Lally KP, Slavotinek
A, Danhaive O, Schaible T, Cheung SW, Rauen KA, Tonk VS, Tibboel D, de Klein A, Scott DA.
Genomic alterations that contribute to the development of isolated and non-isolated congenital diaphragmatic hernia.
J Med Genet.
2011;48(5):299-307.
PubMed abstract / Full Text