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Human Heredity|February 24, 2007
Genetic predisposition to familial neuroblastoma: identification of two novel genomic regions at 2p and 12pLuca Longo, Emanuele Panza, Francesca Schena, et al.
Diabetes|November 25, 2004
Heterogeneity in the magnitude of the insulin gene effect on HLA risk in type 1 diabetesCostantino Motzo, Daniela Contu, Heather J Cordell, et al.
Annals of the New York Academy of Sciences|July 4, 2002
Linkage analysis in families with recurrent neuroblastomaPatrizia Perri, Luca Longo, Carmel McConville, et al.
American Journal of Human Genetics|September 6, 2002
A rare haplotype of the RET proto-oncogene is a risk-modifying allele in hirschsprung diseasePaola Griseri, Barbara Pesce, Giovanna Patrone, 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.
Thrombosis and Haemostasis|November 13, 2002
Polymorphic changes in the 5' flanking region of factor VII have a combined effect on promoter strengthRama Kudaravalli, Theresa Tidd, Mirko Pinotti, et al.
Statistical Applications in Genetics and Molecular Biology|April 4, 2007
Using duplicate genotyped data in genetic analyses: testing association and estimating error ratesNathan L Tintle, Derek Gordon, Francis J McMahon, et al.
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