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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.
BMC Bioinformatics|January 24, 2012
TDT-HET: a new transmission disequilibrium test that incorporates locus heterogeneity into the analysis of family-based association dataDouglas Londono, Steven Buyske, Stephen J Finch, et al.
The Journal of Clinical Investigation|June 3, 2005
Factors affecting statistical power in the detection of genetic associationDerek Gordon, Stephen J Finch
Statistical Applications in Genetics and Molecular Biology|June 5, 2009
Increase of rejection rate in case-control studies with the differential genotyping error ratesKwangmi Ahn, Derek Gordon, Stephen J Finch
Human Heredity|February 7, 2007
The impact of genotype misclassification errors on the power to detect a gene-environment interaction using cox proportional hazards modelingLin Tung, Derek Gordon, Stephen J Finch
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.
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.
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.
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