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American Journal of Physiology. Endocrinology and Metabolism|February 26, 2004
Sim1 gene dosage modulates the homeostatic feeding response to increased dietary fat in miceJ Lloyd Holder, Ling Zhang, Bassil M Kublaoui, et al.Pediatric Research|June 7, 2008
Cryptic chromosomal abnormalities identified in children with congenital heart diseaseAshleigh A Richards, Lane Jaeckle Santos, Haley A Nichols, 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 A|February 13, 2008
Cognitive and motor development during childhood in boys with Klinefelter syndromeJudith L Ross, David P Roeltgen, Gerry Stefanatos, et al.The Journal of Pediatrics|October 18, 2005
The phenotype of short stature homeobox gene (SHOX) deficiency in childhood: contrasting children with Leri-Weill dyschondrosteosis and Turner syndromeJudith L Ross, Karen Kowal, Charmian A Quigley, 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.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.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.Pageof 13