DNA methylation aging and transcriptomic studies in horses von Horvath, Steve, Haghani, Amin, Peng, Sichong, Hales, Erin N., Zoller, Joseph A., Raj, Ken, Larison, Brenda, Robeck, Todd R., Petersen, Jessica L., Bellone, Rebecca R., Finno, Carrie J.

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Investigation of high gamma‐glutamyltransferase syndrome in California Thoroughbred racehorses von Peng, Sichong, Magdesian, K. Gary, Dowd, Joseph, Blea, Jeffrey, Carpenter, Ryan, Ho, Wayne, Finno, Carrie J.

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Genetic polymorphisms in vitamin E transport genes as determinants for risk of equine neuroaxonal dystrophy von Ma, Yunzhuo, Peng, Sichong, Donnelly, Callum G., Ghosh, Sharmila, Miller, Andrew D., Woolard, Kevin, Finno, Carrie J.

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Functional annotation of the animal genomes: An integrated annotation resource for the horse von Peng, Sichong, Dahlgren, Anna R, Donnelly, Callum G, Hales, Erin N, Petersen, Jessica L, Bellone, Rebecca R, Kalbfleisch, Ted, Finno, Carrie J

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Successful ATAC-Seq From Snap-Frozen Equine Tissues von Peng, Sichong, Bellone, Rebecca, Petersen, Jessica L., Kalbfleisch, Theodore S., Finno, Carrie J.

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A nonsense variant in Rap Guanine Nucleotide Exchange Factor 5 (RAPGEF5) is associated with equine familial isolated hypoparathyroidism in Thoroughbred Foals von Rivas, Victor N., Magdesian, K. Gary, Fagan, Sophia, Slovis, Nathan M., Luethy, Daniela, Javsicas, Laura H., Caserto, Brian G., Miller, Andrew D., Dahlgren, Anna R., Peterson, Janel, Hales, Erin N., Peng, Sichong, Watson, Katherine D., Khokha, Mustafa K., Finno, Carrie J.

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Increased α‐tocopherol metabolism in horses with equine neuroaxonal dystrophy von Hales, Erin N., Habib, Hadi, Favro, Gianna, Katzman, Scott, Sakai, R. Russell, Marquardt, Sabin, Bordbari, Matthew H., Ming‐Whitfield, Brittni, Peterson, Janel, Dahlgren, Anna R., Rivas, Victor, Ramirez, Carolina Alanis, Peng, Sichong, Donnelly, Callum G., Dizmang, Bobbi‐Sue, Kallenberg, Angelica, Grahn, Robert, Miller, Andrew D., Woolard, Kevin, Moeller, Benjamin, Puschner, Birgit, Finno, Carrie J.

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A missense mutation in MYH1 is associated with susceptibility to immune-mediated myositis in Quarter Horses von Finno, Carrie J, Gianino, Giuliana, Perumbakkam, Sudeep, Williams, Zoë J, Bordbari, Matthew H, Gardner, Keri L, Burns, Erin, Peng, Sichong, Durward-Akhurst, Sian A, Valberg, Stephanie J

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Generation of a Biobank From Two Adult Thoroughbred Stallions for the Functional Annotation of Animal Genomes Initiative von Donnelly, Callum G., Bellone, Rebecca R., Hales, Erin N., Nguyen, Annee, Katzman, Scott A., Dujovne, Ghislaine A., Knickelbein, Kelly E., Avila, Felipe, Kalbfleisch, Ted S., Giulotto, Elena, Kingsley, Nicole B., Tanaka, Jocelyn, Esdaile, Elizabeth, Peng, Sichong, Dahlgren, Anna, Fuller, Anna, Mienaltowski, Michael J., Raudsepp, Terje, Affolter, Verena K., Petersen, Jessica L., Finno, Carrie J.

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The localization of centromere protein A is conserved among tissues von Cappelletti, Eleonora, Piras, Francesca M., Sola, Lorenzo, Santagostino, Marco, Petersen, Jessica L., Bellone, Rebecca R., Finno, Carrie J., Peng, Sichong, Kalbfleisch, Ted S., Bailey, Ernest, Nergadze, Solomon G., Giulotto, Elena

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176 Functional Annotation of the Equine Genome: from Sample Collection to Fair Data von Petersen, Jessica L, Barber, Alexa, Finno, Carrie J, Bellone, Rebecca R, Peng, Sichong, Kingsley, Nicole B, Capelletti, Eleonora, Piras, Francesca M, Giulotto, Elena, Kalbfleisch, Ted

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17 A De novo Recessive Mutation Causative of Mandibulofacial Dysostosis in Hereford Cattle von Sieck, Renae L, Fuller, Anna M, Bedwell, Patrick, Ward, Jack, Sanders, Stacy, Xiang, Shi-Hua, Peng, Sichong, Steffen, David, Petersen, Jessica L

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A nonsense variant in Rap Guanine Nucleotide Exchange Factor 5 von Rivas, Victor N, Magdesian, K. Gary, Fagan, Sophia, Slovis, Nathan M, Luethy, Daniela, Javsicas, Laura H, Caserto, Brian G, Miller, Andrew D, Dahlgren, Anna R, Peterson, Janel, Hales, Erin N, Peng, Sichong, Watson, Katherine D, Khokha, Mustafa K, Finno, Carrie J

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Commercial genetic testing for type 2 polysaccharide storage myopathy and myofibrillar myopathy does not correspond to a histopathological diagnosis von Valberg, Stephanie J., Finno, Carrie J., Henry, Marisa L., Schott, Melissa, Velez‐Irizarry, Deborah, Peng, Sichong, McKenzie, Erica C., Petersen, Jessica L.

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Decoding the Equine Genome: Lessons from ENCODE von Peng, Sichong, Petersen, Jessica L., Bellone, Rebecca R., Kalbfleisch, Ted, Kingsley, N. B., Barber, Alexa M., Cappelletti, Eleonora, Giulotto, Elena, Finno, Carrie J.

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Mandibulofacial Dysostosis Attributed to a Recessive Mutation of CYP26C1 in Hereford Cattle von Sieck, Renae L., Fuller, Anna M., Bedwell, Patrick S., Ward, Jack A., Sanders, Stacy K., Xiang, Shi-Hua, Peng, Sichong, Petersen, Jessica L., Steffen, David J.

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Genome-Wide Association Study and Subsequent Exclusion of ATCAY as a Candidate Gene Involved in Equine Neuroaxonal Dystrophy Using Two Animal Models von Hales, Erin N., Esparza, Christina, Peng, Sichong, Dahlgren, Anna R., Peterson, Janel M., Miller, Andrew D., Finno, Carrie J.

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Generation of a Biobank from Two Adult Thoroughbred Stallions for the Functional Annotation of Animal Genomes Initiative von Bellone, Rebecca R, Kalbfleisch, Ted S, Giulotto, Elena, Tanaka, Jocelyn, Knickelbein, Kelly E, Esdaile, Elizabeth, Raudsepp, Terje, Nguyen, Annee, Dujovne, Ghislaine A, Petersen, Jessica L, Donnelly, Callum G, Fuller, Anna, Affolter, Verena K, Peng, Sichong, Katzman, Scott A, Hales, Erin N, Dahlgren, Anna, Avila, Felipe, Kingsley, Nicole B, Mienaltowski, Michael J, Finno, Carrie J

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Additional file 2: of A missense mutation in MYH1 is associated with susceptibility to immune-mediated myositis in Quarter Horses von Finno, Carrie, Gianino, Giuliana, Sudeep Perumbakkam, Williams, Zoë, Bordbari, Matthew, Gardner, Keri, Burns, Erin, Sichong Peng, Durward-Akhurst, Sian, Valberg, Stephanie

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Additional file 3: of A missense mutation in MYH1 is associated with susceptibility to immune-mediated myositis in Quarter Horses von Finno, Carrie, Gianino, Giuliana, Sudeep Perumbakkam, ZoĂŤ Williams, Bordbari, Matthew, Gardner, Keri, Burns, Erin, Sichong Peng, Durward-Akhurst, Sian, Valberg, Stephanie

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