Predicted genetic burden and frequency of phenotype-associated variants in the horse von Durward-Akhurst, S. A., Marlowe, J. L., Schaefer, R. J., Springer, K., Grantham, B., Carey, W. K., Bellone, R. R., Mickelson, J. R., McCue, M. E.

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Genome Sequence, Comparative Analysis, and Population Genetics of the Domestic Horse von Wade, C.M, Giulotto, E, Sigurdsson, S, Zoli, M, Gnerre, S, Imsland, F, Lear, T.L, Adelson, D.L, Bailey, E, Bellone, R.R, Blöcker, H, Distl, O, Edgar, R.C, Garber, M, Leeb, T, Mauceli, E, MacLeod, J.N, Penedo, M.C.T, Raison, J.M, Sharpe, T, Vogel, J, Andersson, L, Antczak, D.F, Biagi, T, Binns, M.M, Chowdhary, B.P, Coleman, S.J, Della Valle, G, Fryc, S, Guérin, G, Hasegawa, T, Hill, E.W, Jurka, J, Kiialainen, A, Lindgren, G, Liu, J, Magnani, E, Mickelson, J.R, Murray, J, Nergadze, S.G, Onofrio, R, Pedroni, S, Piras, M.F, Raudsepp, T, Rocchi, M, Røed, K.H, Ryder, O.A, Searle, S, Skow, L, Swinburne, J.E, Syvänen, A.C, Tozaki, T, Valberg, S.J, Vaudin, M, White, J.R, Zody, M.C, Lander, E.S, Lindblad-Toh, K

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Genetic Variation and the Distribution of Variant Types in the Horse von Durward-Akhurst, S A, Schaefer, R J, Grantham, B, Carey, W K, Mickelson, J R, McCue, M E

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Associations between endocrine disrupting chemicals and equine metabolic syndrome phenotypes von Durward-Akhurst, S.A., Schultz, N.E., Norton, E.M., Rendahl, A.K., Besselink, H., Behnisch, P.A., Brouwer, A., Geor, R.J., Mickelson, J.R., McCue, M.E.

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Malignant hyperthermia: excitation-contraction coupling, Ca2+ release channel, and cell Ca2+ regulation defects von Mickelson, J. R, Louis, C. F

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Heritability of metabolic traits associated with equine metabolic syndrome in Welsh ponies and Morgan horses von Norton, E. M., Schultz, N. E., Rendahl, A. K., Mcfarlane, D., Geor, R. J., Mickelson, J. R., McCue, M. E.

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Equine recombination map updated to EquCab3.0 von Beeson, S. K., Mickelson, J. R., McCue, M. E.

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A highly prevalent equine glycogen storage disease is explained by constitutive activation of a mutant glycogen synthase von Maile, C.A., Hingst, J.R., Mahalingan, K.K., O'Reilly, A.O., Cleasby, M.E., Mickelson, J.R., McCue, M.E., Anderson, S.M., Hurley, T.D., Wojtaszewski, J.F.P., Piercy, R.J.

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SNP‐based heritability and genetic architecture of tarsal osteochondrosis in North American Standardbred horses von McCoy, A. M., Norton, E. M., Kemper, A. M., Beeson, S. K., Mickelson, J. R., McCue, M. E.

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Assessment of the FAM174A 11G allele as a risk allele for equine metabolic syndrome von Roy, M. M., Norton, E. M., Rendahl, A. K., Schultz, N. E., McFarlane, D., Geor, R. J., Mickelson, J. R., McCue, M. E.

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Genetic risk factors for insidious equine recurrent uveitis in Appaloosa horses von Fritz, K. L., Kaese, H. J., Valberg, S. J., Hendrickson, J. A., Rendahl, A. K., Bellone, R. R., Dynes, K. M., Wagner, M. L., Lucio, M. A., Cuomo, F. M., Brinkmeyer-Langford, C. L., Skow, L. C., Mickelson, J. R., Rutherford, M. S., McCue, M. E.

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Canine NAPEPLD-associated models of human myelin disorders von Minor, K. M., Letko, A., Becker, D., Drögemüller, M., Mandigers, P. J. J., Bellekom, S. R., Leegwater, P. A. J., Stassen, Q. E. M., Putschbach, K., Fischer, A., Flegel, T., Matiasek, K., Ekenstedt, K. J., Furrow, E., Patterson, E. E., Platt, S. R., Kelly, P. A., Cassidy, J. P., Shelton, G. D., Lucot, K., Bannasch, D. L., Martineau, H., Muir, C. F., Priestnall, S. L., Henke, D., Oevermann, A., Jagannathan, V., Mickelson, J. R., Drögemüller, C.

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Role of ryanodine receptor channels in Ca2+ oscillations of porcine tracheal smooth muscle von Kannan, M. S, Prakash, Y. S, Brenner, T, Mickelson, J. R, Sieck, G. C

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Glycogen Synthase 1 (GYS1) Mutation in Diverse Breeds with Polysaccharide Storage Myopathy von McCue, M.E, Valberg, S.J, Lucio, M, Mickelson, J.R

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Microarray Analysis of Differentially Expressed Genes of Primary Tumors in the Canine Central Nervous System von Thomson, S. A. M, Kennerly, E, Olby, N, Mickelson, J. R, Hoffmann, D. E, Dickinson, P. J, Gibson, G, Breen, M

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Coat Color Genotypes and Risk and Severity of Melanoma in Gray Quarter Horses von Teixeira, R.B.C., Rendahl, A.K., Anderson, S.M., Mickelson, J.R., Sigler, D., Buchanan, B.R., Coleman, R.J., McCue, M.E.

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Genome‐wide association analysis of osteochondrosis of the tibiotarsal joint in Norwegian Standardbred trotters von Lykkjen, S, Dolvik, N.I, McCue, M.E, Rendahl, A.K, Mickelson, J.R, Roed, K.H

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glycogen synthase 1 mutation associated with equine polysaccharide storage myopathy and exertional rhabdomyolysis occurs in a variety of UK breeds von Stanley, R.L, McCue, M.E, Valberg, S.J, Mickelson, J.R, Mayhew, I.G, McGowan, C, Hahn, C.N, Patterson-Kane, J.C, Piercy, R.J

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Polysaccharide storage myopathy phenotype in quarter horse-related breeds is modified by the presence of an RYR1 mutation von McCue, M.E, Valberg, S.J, Jackson, M, Borgia, L, Lucio, M, Mickelson, J.R

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Comparative Skeletal Muscle Histopathologic and Ultrastructural Features in Two Forms of Polysaccharide Storage Myopathy in Horses von McCue, M.E, Armién, A.G, Lucio, M, Mickelson, J.R, Valberg, S.J

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