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Genetic Epidemiology|January 30, 2004
What SNP genotyping errors are most costly for genetic association studies?Sun Jung Kang, Derek Gordon, Stephen J Finch
Bioinformatics (Oxford, England)|August 27, 2005
PAWE-3D: visualizing power for association with error in case-control genetic studies of complex traitsDerek Gordon, Chad Haynes, Jon Blumenfeld, et al.
BMC Genetics|February 3, 2006
Precision and type I error rate in the presence of genotype errors and missing parental data: a comparison between the original transmission disequilibrium test (TDT) and TDTae statisticsSandra Barral, Chad Haynes, Mark A Levenstien, et al.
Annals of Human Genetics|April 7, 2009
The cost effectiveness of duplicate genotyping for testing genetic associationNathan Tintle, Derek Gordon, Dirk Van Bruggen, et al.
Human Heredity|November 26, 2002
Power and sample size calculations for case-control genetic association tests when errors are present: application to single nucleotide polymorphismsDerek Gordon, Stephen J Finch, Michael Nothnagel, et al.
BMJ Case Reports|June 15, 2012
Use of cetrorelix in the investigation of testosterone excess in a postmenopausal womanDonna J Chantler, Derek Gordon, David Millan, 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.
Archives of Ophthalmology (Chicago, Ill. : 1960)|April 12, 2006
Ophthalmologic findings in Cornelia de Lange syndrome: a genotype-phenotype correlation studySudha Nallasamy, Femida Kherani, Dinah Yaeger, et al.
Inflammatory Bowel Diseases|September 28, 2019
The Unique Disease Course of Children with Very Early onset-Inflammatory Bowel DiseaseJudith R Kelsen, Maire A Conrad, Noor Dawany, et al.
Human Molecular Genetics|February 2, 2002
Linkage analysis conditional on HLA status in a large North American pedigree supports the presence of a multiple sclerosis susceptibility locus on chromosome 12p12Emilia Vitale, Stuart Cook, Rong Sun, et al.
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