Framework for the analysis of genetic variations across multiple DNA copy number samples. - Abdullah K. Alqallaf; Ahmed H. Tewfik; Scott B. Selleck; Rebecca Johnson (ICASSP, 2008)

Identifying patterns of copy number variants in case-control studies of human genetic disorders. - Abdullah K. Alqallaf; Ahmed H. Tewfik; Paula Krakowiak; Flora Tassone; Ryan Davis; Robin Hansen; Irva Hertz-Picciotto; Isaac Pessah; Jeff Gregg; Scott B. Selleck (GENSiPS, 2009)

Genetic variation detection using maximum likelihood estimator. - Abdullah K. Alqallaf; Ahmed H. Tewfik; Scott B. Selleck (GENSiPS, 2009)

Uncovering the Etiology of Autism Spectrum Disorders: Genomics, Bioinformatics, Environment, Data Collection and Exploration, and Future Possibilities. - Sarah A. Pendergrass; Santhosh Girirajan; Scott B. Selleck (Pacific Symposium on Biocomputing, 2014)

Diverse convergent evidence in the genetic analysis of complex disease: coordinating omic, informatic, and experimental evidence to better identify and validate risk factors. - Timothy H. Ciesielski; Sarah A. Pendergrass; Marquitta J. White; Nuri Kodaman; Rafal S. Sobota; Minjun Huang; Jacquelaine Bartlett; Jing Li; Qinxin Pan; Jiang Gui; Scott B. Selleck; Christopher I. Amos; et al. (BioData Min., 2014)