1. Cox, T.C. (2004) Taking it to the max: the genetic and developmental mechanisms coordinating midfacial morphogenesis and dysmorphology. (Review) Clinical Genetics 65:163-176. PMID: 14756664.
  2. Drenckhahn, J.D., Schwarz, Q.P. Gray, S., Laskowski, A., Kiriazis, H., Ming, Z., Harvey, R.P., Du, X.J., Thorburn, D.R. & Cox, T.C. (2008) Compensatory growth of healthy cardiac cells in the presence of diseased cells restores tissue homeostasis during heart development. Developmental Cell. 15:521-533. PMID: 18854137.
  3. Kaminen-Ahola, N., Ahola, A., Maga, M., Mallitt, K-A., Fahey, P., Cox, T.C., Whitelaw, E., & Chong, S. (2010) Maternal ethanol consumption alters the epigenotype and the phenotype of offspring in a mouse model. PLoS Genetics 6 (1) e1000811. doi:10.1371/journal.pgen.1000811. PMID: 20084100. [also included in the PLoS Genetics: Epigenetics 2010 Collection]
  4. Purushothaman, R., Cox, T.C., Maga, A.M. & Cunningham, M.L. (2011) Midfacial abnormalities of newborn Fgfr1 P250R/+ and Fgfr2 S252W/+ mouse models of Pfeiffer and Apert syndromes. Birth Defects Research Part A: Clinical and Molecular Teratology. 91 (7):603-609. PMID: 21538817.
  5. *Vissers, L.E.L.M., *Cox, T.C., *Maga, A.M., Short, K.M., Wirdajaja, F., Janssen, I.M., Jehee, F., Bertola, D., Liu, J., Yagnik, G., Sekiguchi, K., Kiyozumi, D., van Bokhoven, H., Marcelis, C., Cunningham, M.L., Anderson, P.J., Boyadjiev, S., Passos-Buenos, M-R., Veltman, J.A., Smyth, I., Buckley, M.F., & Roscioli, T. (2011) Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and mice. PLoS Genetics. 7 (9): e1002278. doi:10.1371/journal.pgen.1002278. PMID: 21931569.
  6. Fairfield, H., Gilbert, G., Barter, M., Corrigan, R., Curtain, M., Ding, Y., D'Ascenzo, M., Gerhardt, D., He, C., Huang, W., Richmond, T., Rowe, L., Probst, F.J., Bergstrom, D., Murray, S., Bult, C., Richardson, J., Cunningham, M.L., Cox, T.C., Justice, M., Spector, M.S., Lowe, S.W., Albert, T., Kile, B., Gut, I., Hager, J., Donahue, L-R., Jeddeloh, J., Shendure, J., Reinholdt, L.G. (2011) Mutation discovery in mice by whole exome sequencing. Genome Biology [Exome Sequencing Special Issue] 12:R86 doi:10.1186/gb-2011-12-9-r86. PMID: 21917142.
  7. Rolfe, S.M., Shapiro, L.G., Cox, T.C., Maga, A.M., Cox, L.L. (2011) A landmark-free framework for the detection and description of shape differences in embryos. Conference Proceedings of the 2011 Annual International Conference of the IEEE Engineering in Medicine and Biology Society. pp5153-5156. doi:10.1109/IEMBS.2011.6091276. PMID: 22255499.
  8. Rieder, M.J., Green, G.E., Park, S.S., Stamper, B.D., Gordon, C., Johnson, J.M., Cunniff, C.M., Smith, J.D., Emery, S.B., Lyonnet, S., Amiel, J., Holder, M., Bamshad, M.J., Nickerson, D.A., Cox, T.C., Hing, A.V., Horst, J.A., & Cunningham, M.L. (2012) A human homeotic transformation resulting from mutations in PLCB4 and GNAI3 causes auriculocondylar syndrome. American Journal of Human Genetics 90:907-914. doi: 10.1016/j.ajhg.2012.04.002. PMID: 22560091.
  9. Quina, L., Kuramoto, T., Luquetti, D.V., Cox, T.C., Serikawa, T. & Turner, E.E. (2012) Deletion of a conserved regulatory element required for Hmx1 expression in craniofacial mesenchyme in the dumbo rat: a novel cause of congenital ear malformation. Disease Models & Mechanisms 5:812-822. doi:10.1242/dmm.009910. PMID: 22736458.
  10. Du, H., Huang, Y., Zaghlula, M., Walters, E., Cox, T.C. & Massiah, M.A. (2013) The MID1 E3 ligase catalyzes the polyubiquitination of Alpha4, a regulatory subunit of Protein Phosphatase 2A (PP2A): Novel insights into MID1-mediated regulation of PP2A. Journal of Biological Chemistry 288 (29):21341-21350. doi:10.1074/jbc.M113.481093. PMID: 23740247.
  11. Siebert, J.R., Smith, K.J., Cox, L.L., Glass, I.A. & Cox, T.C. (2013) Microtomographic analysis of lower urinary tract obstruction. Pediatric and Developmental Pathology Aug 26 [Epub ahead of print]. PMID 23977847.
  12. Cox, T.C., Horst, J.A., Hing, A. & Cunningham, M.L. (2014) Molecular genetics and biology of craniofacial synostoses. In: Stem Cell Biology and Tissue Engineering in Dental Sciences (eds. A Vishwakarma, P Sharpe, S Shi, X-P Wang and M Ramalingam). in press.
  13. Cox, T.C., Luquetti, D.V. & Cunningham, M.L. (2013) Perspectives and challenges in advancing research into craniofacial anomalies. American Journal of Medical Genetics Part C (Seminars in Medical Genetics): Craniofacial Anomalies - Models, Mechanisms, and Management 163C:213-217. doi: 10.1002/ajmg.c.31383. PMID: 24142870.
  14. Turner, E.E. & Cox, T.C. Genetic evidence for conserved non-coding element function across species – the ears have it. Frontiers in Physiology (Craniofacial Biology). 5:7. doi: 10.3389/fphys.2014.00007

* Authors contributed equally to this work.