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BMC Proceedings|December 19, 2014
Mapping genes with longitudinal phenotypes via Bayesian posterior probabilitiesAnthony Musolf, Alejandro Q Nato, Douglas Londono, et al.BMC Gastroenterology|November 20, 2015
A de novo whole gene deletion of XIAP detected by exome sequencing analysis in very early onset inflammatory bowel disease: a case reportJudith R Kelsen, Noor Dawany, Alejandro Martinez, et al.International Journal of Molecular Sciences|September 9, 2022
Comorbidity of Novel CRHR2 Gene Variants in Type 2 Diabetes and DepressionMutaz Amin, Jurg Ott, Derek Gordon, et al.Nature Genetics|February 26, 2008
Disruption of P2RY5, an orphan G protein-coupled receptor, underlies autosomal recessive woolly hairYutaka Shimomura, Muhammad Wajid, Yoshiyuki Ishii, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|September 25, 2004
Association of the dihydrolipoamide dehydrogenase gene with Alzheimer's disease in an Ashkenazi Jewish populationAbraham M Brown, Derek Gordon, Hsinhwa Lee, et al.Journal of Molecular Medicine (Berlin, Germany)|December 16, 2004
Identification of a recurrent mutation in GALNT3 demonstrates that hyperostosis-hyperphosphatemia syndrome and familial tumoral calcinosis are allelic disordersYaacov Frishberg, Orit Topaz, Reuven Bergman, et al.Human Reproduction (Oxford, England)|April 5, 2018
Subphenotype meta-analysis of testicular cancer genome-wide association study data suggests a role for RBFOX family genes in cryptorchidism susceptibilityYanping Wang, Dione R Gray, Alan K Robbins, et al.Molecular Carcinogenesis|March 21, 2012
A keratin 15 containing stem cell population from the hair follicle contributes to squamous papilloma development in the mouseShulan Li, Heuijoon Park, Carol S Trempus, et al.The Journal of Investigative Dermatology|May 2, 2002
Multiple cutaneous and uterine leiomyomas: refinement of the genetic locus for multiple cutaneous and uterine leiomyomas on chromosome 1q42.3-43Amalia Martinez-Mir, Derek Gordon, Liran Horev, et al.Molecular Human Reproduction|May 22, 2015
Expression and characterization of three Aurora kinase C splice variants found in human oocytesJessica E Fellmeth, Derek Gordon, Christian E Robins, et al.Pageof 21