An Examination of Phonological Awareness Treatment Outcomes for Seventh-Grade Poor Readers From a Bilingual Community by Swanson, Teri J, Hodson, Barbara W, Schommer-Aikins, Marlene

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Mutations in the Kinesin-2 Motor KIF3B Cause an Autosomal-Dominant Ciliopathy by Cogné, Benjamin, Latypova, Xenia, Senaratne, Lokuliyanage Dona Samudita, Martin, Ludovic, Koboldt, Daniel C., Kellaris, Georgios, Fievet, Lorraine, Le Meur, Guylène, Caldari, Dominique, Debray, Dominique, Nizon, Mathilde, Frengen, Eirik, Bowne, Sara J., Buckley, Reuben M., Aberdein, Danielle, Alves, Paulo C., Barsh, Gregory S., Bellone, Rebecca R., Bergström, Tomas F., Boyko, Adam R., Brockman, Jeffrey A., Casal, Margret L., Castelhano, Marta G., Distl, Ottmar, Dodman, Nicholas H., Ellinwood, N. Matthew, Fogle, Jonathan E., Forman, Oliver P., Garrick, Dorian J., Ginns, Edward I., Häggström, Jens, Harvey, Robert J., Hasegawa, Daisuke, Haase, Bianca, Helps, Christopher R., Hernandez, Isabel, Hytönen, Marjo K., Kaukonen, Maria, Kaelin, Christopher B., Kosho, Tomoki, Leclerc, Emilie, Lear, Teri L., Leeb, Tosso, Li, Ronald H.L., Lohi, Hannes, Longeri, Maria, Magnuson, Mark A., Malik, Richard, Mane, Shrinivas P., Munday, John S., Murphy, William J., Pedersen, Niels C., Rothschild, Max F., Rusbridge, Clare, Shapiro, Beth, Stern, Joshua A., Swanson, William F., Terio, Karen A., Todhunter, Rory J., Warren, Wesley C., Wilcox, Elizabeth A., Wildschutte, Julia H., Yu, Yoshihiko, Cadena, Elizabeth L., Daiger, Stephen P., Bujakowska, Kinga M., Pierce, Eric A., Gorin, Michael, Katsanis, Nicholas, Bézieau, Stéphane, Petersen-Jones, Simon M., Occelli, Laurence M., Lyons, Leslie A., Legeai-Mallet, Laurence, Sullivan, Lori S., Davis, Erica E., Isidor, Bertrand

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Mining the 99 Lives Cat Genome Sequencing Consortium database implicates genes and variants for the Ticked locus in domestic cats (Felis catus) by Lyons, L. A., Buckley, R. M., Harvey, R. J., Abitbol, Marie, Aberdein, Danielle, Alves, Paulo C., Ohlsson Andersson, Asa, Bellone, Rebecca R., Bergström, Tomas F., Bilgen, Nuket, Boyko, Adam R., Brockman, Jeffrey A., Casal, Margret L., Castelhano, Marta G., Davis, Brian W., Davison, Lucy, Distl, Ottmar, Dodman, Nicholas H., Ellinwood, N. Matthew, Fogle, Jonathan E., Forman, Oliver P., Garrick, Dorian J., Ginns, Edward I., Häggström, Jens, Hasegawa, Daisuke, Haase, Bianca, Jagannathan, Vidhya, Lait, Philippa, Hernandez, Isabel, Hytönen, Marjo K., Kaukonen, Maria, Kosho, Tomoki, Leclerc, Emilie, Lear, Teri L., Leeb, Tosso, Li, Ronald H.L., Lohi, Hannes, Longeri, Maria, Magnuson, Mark A., Malik, Richard, Mane, Shrinivasrao P., Middleton, Rondo, Munday, John S., Murphy, William J., Myers, Alexandra N., Pedersen, Niels C., Peterson‐Jones, Simon M., Rothschild, Max F., Rusbridge, Clare, Schoenebeck, Jeffrey J., Shapiro, Beth, Stern, Joshua A., Swanson, William F., Terio, Karen A., Todhunter, Rory J., Warren, Wesley C., Wilcox, Elizabeth A., Wildschutte, Julia H., Yu, Yoshihiko

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Multi-omic analyses in Abyssinian cats with primary renal amyloid deposits by Genova, Francesca, Nonnis, Simona, Maffioli, Elisa, Tedeschi, Gabriella, Strillacci, Maria Giuseppina, Carisetti, Michela, Sironi, Giuseppe, Cupaioli, Francesca Anna, Di Nanni, Noemi, Mezzelani, Alessandra, Mosca, Ettore, Helps, Christopher R., Leegwater, Peter A. J., Dorso, Laetitia, Longeri, Maria

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First genome-wide CNV mapping in FELIS CATUS using next generation sequencing data by Genova, F, Longeri, M, Lyons, L A, Bagnato, A, Strillacci, M G

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Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed by Buckley, Reuben M, Gandolfi, Barbara, Creighton, Erica K, Pyne, Connor A, Bouhan, Delia M, LeRoy, Michelle L, Senter, David A, Gobble, Johnny R, Abitbol, Marie, Lyons, Leslie A

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A Deletion in GDF7 is Associated with a Heritable Forebrain Commissural Malformation Concurrent with Ventriculomegaly and Interhemispheric Cysts in Cats by Yu, Yoshihiko, Creighton, Erica K, Buckley, Reuben M, Lyons, Leslie A

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