Utility and limitations of animal models for the functional validation of human sequence variants

by Cox, Timothy C
Published 2015

Expression profiles of cIRF6, cLHX6 and cLHX7 in the facial primordia suggest specific roles during primary palatogenesis

by Washbourne, Belinda J, Cox, Timothy C
Published 2006

Genetic evidence for conserved non-coding element function across species–the ears have it

by Turner, Eric E., Cox, Timothy C.
Published 2014

MID1 and MID2 homo- and heterodimerise to tether the rapamycin-sensitive PP2A regulatory subunit, Alpha 4, to microtubules: implications for the clinical variability of X-linked Op...

by Short, Kieran M, Hopwood, Blair, Yi, Zou, Cox, Timothy C
Published 2002

Postnatal Ontogeny of the Cranial Base and Craniofacial Skeleton in Male C57BL/6J Mice: A Reference Standard for Quantitative Analysis

by Vora, Siddharth R., Camci, Esra D., Cox, Timothy C.
Published 2016

Deletion of a conserved regulatory element required for Hmx1 expression in craniofacial mesenchyme in the dumbo rat: a newly identified cause of congenital ear malformation

by Quina, Lely A., Kuramoto, Takashi, Luquetti, Daniela V., Cox, Timothy C., Serikawa, Tadao, Turner, Eric E.
Published 2012

Quantitative trait loci affecting the 3D skull shape and size in mouse and prioritization of candidate genes in-silico

by Maga, A. Murat, Navarro, Nicolas, Cunningham, Michael L., Cox, Timothy C.
Published 2015

Lack of association between the A118G polymorphism of the mu opioid receptor gene (OPRM1) and opioid dependence: A meta-analysis

by Coller, Janet K, Beardsley, Julia, Bignold, James, Li, Yibai, Merg, Florence, Sullivan, Thomas, Cox, Timothy C, Somogyi, Andrew A
Published 2009

Evaluation and integration of disparate classification systems for clefts of the lip

by Wang, Kathie H., Heike, Carrie L., Clarkson, Melissa D., Mejino, Jose L. V., Brinkley, James F., Tse, Raymond W., Birgfeld, Craig B., Fitzsimons, David A., Cox, Timothy C.
Published 2014

Effects of Cell Grafting on Coronary Remodeling After Myocardial Infarction

by Weyers, Jill J., Schwartz, Stephen M., Minami, Elina, Carlson, Dara D., Dupras, Sarah K., Weitz, Kevin, Simons, Michael, Cox, Timothy C., Murry, Charles E., Mahoney, William M.
Published 2013

Heterozygous Mutations of FREM1 Are Associated with an Increased Risk of Isolated Metopic Craniosynostosis in Humans and Mice

by Vissers, Lisenka E. L. M., Cox, Timothy C., Maga, A. Murat, Short, Kieran M., Wiradjaja, Fenny, Janssen, Irene M., Jehee, Fernanda, Bertola, Debora, Liu, Jia, Yagnik, Garima, Sekiguchi, Kiyotoshi, Kiyozumi, Daiji, van Bokhoven, Hans, Marcelis, Carlo, Cunningham, Michael L., Anderson, Peter J., Boyadjiev, Simeon A., Passos-Bueno, Maria Rita, Veltman, Joris A., Smyth, Ian, Buckley, Michael F., Roscioli, Tony
Published 2011

Genome-Wide Association Studies in Dogs and Humans Identify ADAMTS20 as a Risk Variant for Cleft Lip and Palate

by Wolf, Zena T., Brand, Harrison A., Shaffer, John R., Leslie, Elizabeth J., Arzi, Boaz, Willet, Cali E., Cox, Timothy C., McHenry, Toby, Narayan, Nicole, Feingold, Eleanor, Wang, Xioajing, Sliskovic, Saundra, Karmi, Nili, Safra, Noa, Sanchez, Carla, Deleyiannis, Frederic W. B., Murray, Jeffrey C., Wade, Claire M., Marazita, Mary L., Bannasch, Danika L.
Published 2015

Mutation discovery in mice by whole exome sequencing

by Fairfield, Heather, Gilbert, Griffith J, Barter, Mary, Corrigan, Rebecca R, Curtain, Michelle, Ding, Yueming, D'Ascenzo, Mark, Gerhardt, Daniel J, He, Chao, Huang, Wenhui, Richmond, Todd, Rowe, Lucy, Probst, Frank J, Bergstrom, David E, Murray, Stephen A, Bult, Carol, Richardson, Joel, Kile, Benjamin T, Gut, Ivo, Hager, Jorg, Sigurdsson, Snaevar, Mauceli, Evan, Di Palma, Federica, Lindblad-Toh, Kerstin, Cunningham, Michael L, Cox, Timothy C, Justice, Monica J, Spector, Mona S, Lowe, Scott W, Albert, Thomas, Donahue, Leah Rae, Jeddeloh, Jeffrey, Shendure, Jay, Reinholdt, Laura G
Published 2011