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Cox Lab: Craniofacial Development & Dysmorphology

Research in the Cox lab is aimed at understanding the genetic and epigenetic contributions that govern normal facial development and determine an individual’s susceptibility to common craniofacial malformations, such as cleft lip/palate and craniofacial microsomia.

Rare Genetic Variants in Human APC Are Implicated in Mesiodens and Isolated Supernumerary Teeth.

Publication: Journal Article

Panyarat, Chomchanok, Siriruk Nakornchai, Kanoknart Chintakanon, Niramol Leelaadisorn, Worrachet Intachai, Bjorn Olsen, Sissades Tongsima, et al. 2023. “Rare Genetic Variants in Human APC Are Implicated in Mesiodens and Isolated Supernumerary Teeth.”. International Journal of Molecular Sciences 24 (5).

Mutations in GDF11 and the extracellular antagonist, Follistatin, as a likely cause of Mendelian forms of orofacial clefting in humans.

Publication: Journal Article

Cox, Timothy C, Andrew C Lidral, Jason C McCoy, Huan Liu, Liza L Cox, Ying Zhu, Ryan D Anderson, et al. 2019. “Mutations in GDF11 and the Extracellular Antagonist, Follistatin, As a Likely Cause of Mendelian Forms of Orofacial Clefting in Humans.”. Human Mutation 40 (10): 1813-25.

The Society for Craniofacial Genetics and Developmental Biology 42nd Annual Meeting.

Publication: Journal Article

Eisenhoffer, George T, David Clouthier, Timothy Cox, Jean-Pierre Saint-Jeannet, Lisa A Taneyhill, Paul A Trainor, and Sally A Moody. 2020. “The Society for Craniofacial Genetics and Developmental Biology 42nd Annual Meeting.”. American Journal of Medical Genetics. Part A 182 (7): 1555-61.

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Soumya Rao

Person: Postdoctoral Fellow

Soumya’s research focuses on using genomics technologies to gain actionable insights into biological questions using molecular biology, bioinformatics, and genomics. She completed her bachelor’s degree in Science (Biotechnology) in 2007 from Barkatullah University, and her master’s in science...