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Maga AM. Postnatal Development of the Craniofacial Skeleton in Male C57BL/6J Mice. Journal of the American Association for Laboratory Animal Science : JAALAS. 2016;55(2):131-136. PMCID: PMC4783629.

Vissers LE, Cox TC, Maga AM, Short KM, Wiradjaja F, Janssen IM, Jehee F, Bertola D, Liu J, Yagnik G, Sekiguchi K, Kiyozumi D, van Bokhoven H, Marcelis C, Cunningham ML, Anderson PJ, Boyadjiev SA, Passos-Bueno MR, Veltman JA, Smyth I, Buckley MF, Roscioli T. Heterozygous Mutations of FREM1 Are Associated with an Increased Risk of Isolated Metopic Craniosynostosis in Humans and Mice. van Heyningen V, ed. PLoS Genetics. 2011;7(9):e1002278. doi:10.1371/journal.pgen.1002278. PMCID: PMC3169541.

Purushothaman R, Cox TC, Muga AM, Cunningham ML. Facial suture synostosis of newborn Fgfr1(P250R/+) and Fgfr2(S252W/+) mouse models of Pfeiffer and Apert syndromes. Birth defects research. Part A, Clinical and molecular teratology. 2011;91(7)603-9. PMID: 21538817.

Slavotinek AM, Baranzini SE, Schanze D, Labelle-Dumais C, Short KM, Chao R, Yahyavi M, Bijlsma EK, Chu C, Musone S, Wheatley A, Kwok PY, Marles S, Fryns JP, Maga AM, Hassan MG, Gould DB, Madireddy L, Li C, Cox TC, Smyth I, Chudley AE, Zenker M. Manitoba-oculo-tricho-anal (MOTA) syndrome is caused by mutations in FREM1. Journal of medical genetics. 2011;48(6)375-82. PMID: 21507892.

Rolfe SM, Shapiro LG, Cox TC, Maga AM, Cox LL. A landmark-free framework for the detection and description of shape differences in embryos. Conference proceedings : … Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Conference. 2011;20115153-6 PMCID: PMC3261520.

Kaminen-Ahola N, Ahola A, Maga M, Mallitt KA, Fahey P, Cox TC, Whitelaw E, Chong S. Maternal ethanol consumption alters the epigenotype and the phenotype of offspring in a mouse model. PLoS genetics. 2010;6(1) e1000811 PMCID: PMC2797299.