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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.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 5, 2010
A serotonin and melanocortin circuit mediates D-fenfluramine anorexiaYong Xu, Juli E Jones, Danielle A Lauzon, et al.
Statistical Applications in Genetics and Molecular Biology|May 2, 2006
Increasing power for tests of genetic association in the presence of phenotype and/or genotype error by use of double-samplingDerek Gordon, Yaning Yang, Chad Haynes, et al.
Addiction Biology|June 15, 2007
Prodynorphin gene promoter repeat associated with cocaine/alcohol codependenceTanya J Williams, K Steven LaForge, Derek Gordon, et al.
Journal of Pediatric Urology|May 4, 2007
DELETION MAPPING OF CRITICAL REGION FOR HYPOSPADIAS, PENOSCROTAL TRANSPOSITION AND IMPERFORATE ANUS ON HUMAN CHROMOSOME 13Nilda M Garcia, Jocelyn Allgood, Lane J Santos, et al.
Pharmacogenetics and Genomics|December 14, 2005
Association analysis of polymorphisms in serotonin 1B receptor (HTR1B) gene with heroin addiction: a comparison of molecular and statistically estimated haplotypesDmitri Proudnikov, K Steven LaForge, Heather Hofflich, et al.
Human Heredity|September 3, 2005
Power and sample size calculations for genetic case/control studies using gene-centric SNP maps: application to human chromosomes 6, 21, and 22 in three populationsFrancisco M De La Vega, Derek Gordon, Xiaoping Su, et al.
American Journal of Medical Genetics. Part A|August 7, 2013
Screening and familial characterization of copy-number variations in NR5A1 in 46,XY disorders of sex development and premature ovarian failureSteven M Harrison, Ian M Campbell, Melise Keays, et al.
European Archives of Psychiatry and Clinical Neuroscience|December 13, 2023
LD block disorder-specific pleiotropic roles of novel CRHR1 in type 2 diabetes and depression disorder comorbidityLaura Del Bosque-Plata, Mutaz Amin, Ricardo González-Ramírez, et al.
Human Reproduction (Oxford, England)|October 26, 2007
Sequence variation at the human FOXO3 locus: a study of premature ovarian failure and primary amenorrheaTeresa D Gallardo, George B John, Karen Bradshaw, et al.
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