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NPJ Genomic Medicine|December 22, 2017
Preparing for genomic medicine: a real world demonstration of health system changeClara L Gaff, Ingrid M Winship, Susan M Forrest, et al.BMC Medical Genetics|March 28, 2008
SNP selection for genes of iron metabolism in a study of genetic modifiers of hemochromatosisClare C Constantine, Lyle C Gurrin, Christine E McLaren, et al.Neurobiology of Disease|June 28, 2003
Spinocerebellar ataxia type 15 (sca15) maps to 3p24.2-3pter: exclusion of the ITPR1 gene, the human orthologue of an ataxic mouse mutantMelanie A Knight, Marina L Kennerson, Richard J Anney, et al.Human Molecular Genetics|September 20, 2008
A duplication at chromosome 11q12.2-11q12.3 is associated with spinocerebellar ataxia type 20Melanie A Knight, Dena Hernandez, Scott J Diede, et al.Plos Genetics|June 26, 2007
Deletion at ITPR1 underlies ataxia in mice and spinocerebellar ataxia 15 in humansJoyce van de Leemput, Jayanth Chandran, Melanie A Knight, et al.Genome Biology|August 23, 2011
Genome sequence of an Australian kangaroo, Macropus eugenii, provides insight into the evolution of mammalian reproduction and developmentMarilyn B Renfree, Anthony T Papenfuss, Janine E Deakin, et al.Pageof 2