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Plos Genetics|August 29, 2006
Are molecular haplotypes worth the time and expense? A cost-effective method for applying molecular haplotypesMark A Levenstien, Jürg Ott, Derek GordonPlos One|June 18, 2025
Improved drug-screening tests of candidate anti-cancer drugs in patient-derived xenografts through use of numerous measures of tumor growth determined in multiple independent laboratoriesElizabeth Rosenzweig, David E Axelrod, Derek GordonHuman Heredity|February 7, 2007
The impact of genotype misclassification errors on the power to detect a gene-environment interaction using cox proportional hazards modelingLin Tung, Derek Gordon, Stephen J FinchCancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|February 8, 2022
Genetic Analysis in African American Children Supports Ancestry-Specific Neuroblastoma SusceptibilityAlessandro Testori, Zalman Vaksman, Sharon J Diskin, et al.Plos One|July 10, 2008
Variants of ST8SIA1 are associated with risk of developing multiple sclerosisSeema Husain, Cagri Yildirim-Toruner, Justin P Rubio, et al.Scientific Reports|February 19, 2020
Exome Sequencing in Individuals with Isolated Biliary AtresiaRamakrishnan Rajagopalan, Ellen A Tsai, Christopher M Grochowski, et al.American Journal of Medical Genetics. Part A|August 16, 2005
Precocious sister chromatid separation (PSCS) in Cornelia de Lange syndromeManinder Kaur, Cheryl DeScipio, Jennifer McCallum, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|May 30, 2013
Developmental dysplasia of the hip: linkage mapping and whole exome sequencing identify a shared variant in CX3CR1 in all affected members of a large multigeneration familyGeorge J Feldman, Javad Parvizi, Mark Levenstien, et al.Haematologica|January 25, 2012
Genetic modifiers of β-thalassemia and clinical severity as assessed by age at first transfusionFabrice Danjou, Franco Anni, Lucia Perseu, et al.BMC Genetics|May 13, 2006
LRTae: improving statistical power for genetic association with case/control data when phenotype and/or genotype misclassification errors are presentSandra Barral, Chad Haynes, Millicent Stone, et al.Pageof 21