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The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 12, 2010
Postnatal Sim1 deficiency causes hyperphagic obesity and reduced Mc4r and oxytocin expressionKristen P Tolson, Terry Gemelli, Laurent Gautron, et al.
Human Heredity|January 28, 2009
When a case is not a case: effects of phenotype misclassification on power and sample size requirements for the transmission disequilibrium test with affected child triosSteven Buyske, Guang Yang, Tara C Matise, et al.
The Journal of Clinical Endocrinology and Metabolism|June 16, 2005
Androgen receptor CAGn repeat length influences phenotype of 47,XXY (Klinefelter) syndromeAndrew R Zinn, Purita Ramos, Frederick F Elder, et al.
Human Genetics|January 24, 2007
The physical phenotype of girls and women with Turner syndrome is not X-imprintedCarolyn A Bondy, Lea Ann Matura, Nicole Wooten, et al.
Molecular Cytogenetics|February 17, 2009
MODY-like diabetes associated with an apparently balanced translocation: possible involvement of MPP7 gene and cell polarity in the pathogenesis of diabetesElizabeth J Bhoj, Stefano Romeo, Marco G Baroni, et al.
Plos One|April 11, 2025
Developmental trajectory of voluntary alcohol consumption in adolescent mice using finite mixture modeling and Bayesian posterior probability analysisNathan Yu, Derek Gordon, Hong Zou, et al.
Human Heredity|April 7, 2005
Quantifying the percent increase in minimum sample size for SNP genotyping errors in genetic model-based association studiesSun Jung Kang, Stephen J Finch, Chad Haynes, et al.
Human Heredity|May 19, 2006
Increase in linkage information by stratification of pedigree data into gold-standard and standard diagnoses: application to the NIMH Alzheimer Disease Genetics Initiative DatasetDerek Gordon, Chad Haynes, Stephen J Finch, et al.
Human Heredity|April 3, 2008
A family-based likelihood ratio test for general pedigree structures that allows for genotyping error and missing dataYang Yang, Carol A Wise, Derek Gordon, et al.
American Journal of Medical Genetics|July 13, 2002
Complete SHOX deficiency causes Langer mesomelic dysplasiaAndrew R Zinn, Fanglin Wei, Ling Zhang, et al.
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