Beyond the MHC: A canine model of dermatomyositis shows a complex pattern of genetic risk involving novel loci von Evans, Jacquelyn M, Noorai, Rooksana E, Tsai, Kate L, Starr-Moss, Alison N, Hill, Cody M, Anderson, Kendall J, Famula, Thomas R, Clark, Leigh Anne

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A COLQ missense mutation in Labrador Retrievers having congenital myasthenic syndrome von Rinz, Caitlin J, Levine, Jonathan, Minor, Katie M, Humphries, Hammon D, Lara, Renee, Starr-Moss, Alison N, Guo, Ling T, Williams, D Colette, Shelton, G Diane, Clark, Leigh Anne

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Alleles of the major histocompatibility complex play a role in the pathogenesis of pancreatic acinar atrophy in dogs von Tsai, Kate L., Starr-Moss, Alison N., Venkataraman, Gopalakrishnan M., Robinson, Christopher, Kennedy, Lorna J., Steiner, Jörg M., Clark, Leigh Anne

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Exome sequencing reveals independent SGCD deletions causing limb girdle muscular dystrophy in Boston terriers von Cox, Melissa L, Evans, Jacquelyn M, Davis, Alexander G, Guo, Ling T, Levy, Jennifer R, Starr-Moss, Alison N, Salmela, Elina, Hytönen, Marjo K, Lohi, Hannes, Campbell, Kevin P, Clark, Leigh Anne, Shelton, G Diane

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A missense mutation in the 20S proteasome beta 2 subunit of Great Danes having harlequin coat patterning von Clark, Leigh Anne, Tsai, Kate L, Starr, Alison N, Nowend, Keri L, Murphy, Keith E

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A missense mutation in the 20S proteasome β2 subunit of Great Danes having harlequin coat patterning von Clark, Leigh Anne, Tsai, Kate L., Starr, Alison N., Nowend, Keri L., Murphy, Keith E.

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Novel Y Chromosome Retrocopies in Canids Revealed through a Genome-Wide Association Study for Sex von Tsai, Kate L, Evans, Jacquelyn M, Noorai, Rooksana E, Starr-Moss, Alison N, Clark, Leigh Anne

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A CHRNE frameshift mutation causes congenital myasthenic syndrome in young Jack Russell Terriers von Rinz, Caitlin J, Lennon, Vanda A, James, Fiona, Thoreson, James B, Tsai, Kate L, Starr-Moss, Alison N, Humphries, H. Dale, Guo, Ling T, Palmer, Anthony C, Clark, Leigh Anne, Shelton, G. Diane

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Genome-wide linkage scan localizes the harlequin locus in the Great Dane to chromosome 9 von Clark, Leigh Anne, Starr, Alison N., Tsai, Kate L., Murphy, Keith E.

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The function of dog models in developing gene therapy strategies for human health von Nowend, Keri L., Starr-Moss, Alison N., Murphy, Keith E.

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Genome-wide association studies for multiple diseases of the German Shepherd Dog von Tsai, Kate L, Noorai, Rooksana E, Starr-Moss, Alison N, Quignon, Pascale, Rinz, Caitlin J, Ostrander, Elaine A, Steiner, Jörg M, Murphy, Keith E, Clark, Leigh Anne

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Hereditary Evaluation of Multiple Developmental Abnormalities in the Havanese Dog Breed von Starr, Alison N, Famula, Thomas R, Markward, Nathan J, Baldwin, Joanne V, Fowler, Karon D, Klumb, Diane E, Simpson, Nancy L, Murphy, Keith E

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Exome sequencing reveals independent SGCD deletions causing limb girdle muscular dystrophy in Boston terriers von Cox, Melissa L, Evans, Jacquelyn M, Davis, Alexander G, Guo, Ling T, Levy, Jennifer R, Starr-Moss, Alison N, Salmela, Elina, Hytönen, Marjo K, Lohi, Hannes, Campbell, Kevin P, Clark, Leigh Anne, Shelton, G Diane

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A COLQ Missense Mutation in Labrador Retrievers Having Congenital Myasthenic Syndrome: e106425 von Rinz, Caitlin J, Levine, Jonathan, Minor, Katie M, Humphries, Hammon D, Lara, Renee, Starr-Moss, Alison N, Guo, Ling T, Williams, D Colette, Shelton, G Diane, Clark, Leigh Anne

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DNA methylation age of blood predicts all-cause mortality in later life von Marioni, Riccardo E, Shah, Sonia, McRae, Allan F, Chen, Brian H, Colicino, Elena, Harris, Sarah E, Gibson, Jude, Henders, Anjali K, Redmond, Paul, Cox, Simon R, Pattie, Alison, Corley, Janie, Murphy, Lee, Martin, Nicholas G, Montgomery, Grant W, Feinberg, Andrew P, Fallin, M Daniele, Multhaup, Michael L, Jaffe, Andrew E, Joehanes, Roby, Schwartz, Joel, Just, Allan C, Lunetta, Kathryn L, Murabito, Joanne M, Starr, John M, Horvath, Steve, Baccarelli, Andrea A, Levy, Daniel, Visscher, Peter M, Wray, Naomi R, Deary, Ian J

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Retinal microvascular network geometry and cognitive abilities in community-dwelling older people: The Lothian Birth Cohort 1936 study von McGrory, Sarah, Taylor, Adele M, Kirin, Mirna, Corley, Janie, Pattie, Alison, Cox, Simon R, Dhillon, Baljean, Wardlaw, Joanna M, Doubal, Fergus N, Starr, John M, Trucco, Emanuele, MacGillivray, Thomas J, Deary, Ian J

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ACTN3 genotype, athletic status, and life course physical capability: meta-analysis of the published literature and findings from nine studies von Alfred, Tamuno, Ben-Shlomo, Yoav, Cooper, Rachel, Hardy, Rebecca, Cooper, Cyrus, Deary, Ian J., Gunnell, David, Harris, Sarah E., Kumari, Meena, Martin, Richard M., Moran, Colin N., Pitsiladis, Yannis P., Ring, Susan M., Sayer, Avan Aihie, Smith, George Davey, Starr, John M., Kuh, Diana, Day, Ian N.M.

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A study of common Mendelian disease carriers across ageing British cohorts: meta-analyses reveal heterozygosity for alpha 1-antitrypsin deficiency increases respiratory capacity an... von North, Teri-Louise, Ben-Shlomo, Yoav, Cooper, Cyrus, Deary, Ian J, Gallacher, John, Kivimaki, Mika, Kumari, Meena, Martin, Richard M, Pattie, Alison, Sayer, Avan Aihie, Starr, John M, Wong, Andrew, Kuh, Diana, Rodriguez, Santiago, Day, Ian N M

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Effect of smoking on physical and cognitive capability in later life: a multicohort study using observational and genetic approaches von North, Teri-Louise, Palmer, Tom M, Lewis, Sarah J, Cooper, Rachel, Power, Chris, Pattie, Alison, Starr, John M, Deary, Ian J, Martin, Richard M, Aihie Sayer, Avan, Kumari, Meena, Cooper, Cyrus, Kivimaki, Mika, Kuh, Diana, Ben-Shlomo, Yoav, Day, Ian N M

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A multi-cohort study of polymorphisms in the GH/IGF axis and physical capability: the HALCyon programme von Alfred, Tamuno, Ben-Shlomo, Yoav, Cooper, Rachel, Hardy, Rebecca, Cooper, Cyrus, Deary, Ian J, Gaunt, Tom R, Gunnell, David, Harris, Sarah E, Kumari, Meena, Martin, Richard M, Sayer, Avan Aihie, Starr, John M, Kuh, Diana, Day, Ian N M

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