Copy number expansion of the <it>STX17</it> duplication in melanoma tissue from Grey horses by Sundström Elisabeth, Imsland Freyja, Mikko Sofia, Wade Claire, Sigurdsson Snaevar, Pielberg Gerli, Golovko Anna, Curik Ino, Seltenhammer Monika H, Sölkner Johann, Lindblad-Toh Kerstin, Andersson Leif

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Candidate genes and functional noncoding variants identified in a canine model of obsessive-compulsive disorder by Tang, Ruqi, Noh, Hyun Ji, Wang, Dongqing, Sigurdsson, Snaevar, Swofford, Ross, Perloski, Michele, Duxbury, Margaret, Patterson, Edward E., Albright, Julie, Castelhano, Marta, Auton, Adam, Boyko, Adam R., Feng, Guoping, Lindblad-Toh, Kerstin, Karlsson, Elinor K.

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Canine Hereditary Ataxia in Old English Sheepdogs and Gordon Setters Is Associated with a Defect in the Autophagy Gene Encoding RAB24 by Agler, Caryline, Nielsen, Dahlia M., Urkasemsin, Ganokon, Singleton, Andrew, Tonomura, Noriko, Sigurdsson, Snaevar, Tang, Ruqi, Linder, Keith, Arepalli, Sampath, Hernandez, Dena, Lindblad-Toh, Kerstin, van de Leemput, Joyce, Motsinger-Reif, Alison, O'Brien, Dennis P., Bell, Jerold, Harris, Tonya, Steinberg, Steven, Olby, Natasha J.

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Identification of Genomic Regions Associated with Phenotypic Variation between Dog Breeds using Selection Mapping by Vaysse, Amaury, Ratnakumar, Abhirami, Derrien, Thomas, Axelsson, Erik, Pielberg, Gerli Rosengren, Fall, Tove, Seppälä, Eija H., Hansen, Mark S. T., Lawley, Cindy T., Bannasch, Danika L., Vilà, Carles, Lohi, Hannes, Galibert, Francis, Fredholm, Merete, Häggström, Jens, Hedhammar, Åke, André, Catherine, Hitte, Christophe, Webster, Matthew T., Sigurdsson, Snaevar, Karlsson, Elinor K., Lindblad-Toh, Kerstin

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Genome-wide analyses implicate 33 loci in heritable dog osteosarcoma, including regulatory variants near CDKN2A/B by Karlsson, Elinor K., Sigurdsson, Snaevar, Ivansson, Emma, Thomas, Rachael, Elvers, Ingegerd, Wright, Jason, Howald, Cedric, Tonomura, Noriko, Perloski, Michele, Swofford, Ross, Biagi, Tara, Fryc, Sarah, Anderson, Nathan, Courtay-Cahen, Celine, Youell, Lisa, Ricketts, Sally L., Mandlebaum, Sarah, Rivera, Patricio, von Euler, Henrik, Kisseberth, William C., London, Cheryl A., Couto, Guillermo, Starkey, Mike P. Comstock, Kenine, Starkey, Mike P., Modiano, Jaime F., Breen, Matthew, Lindblad-Toh, Kerstin, Lander, Eric Steven

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Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing by Kirby, Andrew, Gnirke, Andreas, Jaffe, David B., Baresova, Veronika, Pochet, Nathalie, Blumenstiel, Brendan, Ye, Chun, Aird, Daniel, Stevens, Christine, Robinson, James T., Cabili, Moran N., Gat-Viks, Irit, Kelliher, Edward, Daza, Riza, DeFelice, Matthew, Hulkova, Helena, Sovova, Jana, Vylet'al, Petr, Antignac, Corinne, Guttman, Mitchell, Handsaker, Robert E., Perrin, Danielle, Steelman, Scott, Sigurdsson, Snaevar, Scheinman, Steven J., Sougnez, Carrie, Cibulskis, Kristian, Parkin, Melissa, Green, Todd, Rossin, Elizabeth, Zody, Michael C., Xavier, Ramnik J., Pollak, Martin R., Alper, Seth L., Lindblad-Toh, Kerstin, Gabriel, Stacey B., Hart, P. Suzanne, Regev, Aviv, Nusbaum, Chad, Kmoch, Stanislav, Bleyer, Anthony J., Daly, Mark J., Lander, Eric Steven

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