Postnatal Development of the Craniofacial Skeleton in Male C57BL/6J Mice

Por Maga, A Murat
Publicado no J Am Assoc Lab Anim Sci (2016)

A Novel Procedure for Rapid Imaging of Adult Mouse Brains with MicroCT Using Iodine-Based Contrast

Por Anderson, Ryan, Maga, A. Murat
Publicado no PLoS One (2015)

Performance of single and multi-atlas based automated landmarking methods compared to expert annotations in volumetric microCT datasets of mouse mandibles

Por Young, Ryan, Maga, A. Murat
Publicado no Front Zool (2015)

Does 3D Phenotyping Yield Substantial Insights in the Genetics of the Mouse Mandible Shape?

Por Navarro, Nicolas, Maga, A. Murat
Publicado no G3 (Bethesda) (2016)

Skeleton of an unusual, cat-sized marsupial relative (Metatheria: Marsupialiformes) from the middle Eocene (Lutetian: 44-43 million years ago) of Turkey

Por Maga, A. Murat, Beck, Robin M. D.
Publicado no PLoS One (2017)

Correction: Skeleton of an unusual, cat-sized marsupial relative (Metatheria: Marsupialiformes) from the middle Eocene (Lutetian: 44-43 million years ago) of Turkey

Por Maga, A. Murat, Beck, Robin M. D.
Publicado no PLoS One (2017)

A population level atlas of Mus musculus craniofacial skeleton and automated image‐based shape analysis

Por Maga, A. Murat, Tustison, Nicholas J., Avants, Brian B.
Publicado no J Anat (2017)

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

Por Maga, A. Murat, Navarro, Nicolas, Cunningham, Michael L., Cox, Timothy C.
Publicado no Front Physiol (2015)

A new mammal skull from the Lower Cretaceous of China with implications for the evolution of obtuse-angled molars and ‘amphilestid’ eutriconodonts

Por Gao, Chun-Ling, Wilson, Gregory P., Luo, Zhe-Xi, Maga, A. Murat, Meng, Qingjin, Wang, Xuri
Publicado em 2010

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

Por 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
Publicado em 2011

Manitoba-oculo-tricho-anal (MOTA) syndrome is caused by mutations in FREM1

Por Slavotinek, Anne M, Baranzini, Sergio E, Schanze, Denny, Labelle-Dumais, Cassandre, Short, Kieran M, Chao, Ryan, Yahyavi, Mani, Bijlsma, Emilia K, Chu, Catherine, Musone, Stacey, Wheatley, Ashleigh, Kwok, Pui-Yan, Marles, Sandra, Fryns, Jean-Pierre, Maga, A Murat, Hassan, Mohamed G, Gould, Douglas B, Madireddy, Lohith, Li, Chumei, Cox, Timothy C, Smyth, Ian, Chudley, Albert E, Zenker, Martin
Publicado no J Med Genet (2011)

Mutations in CRADD Result in Reduced Caspase-2-Mediated Neuronal Apoptosis and Cause Megalencephaly with a Rare Lissencephaly Variant

Por Di Donato, Nataliya, Jean, Ying Y., Maga, A. Murat, Krewson, Briana D., Shupp, Alison B., Avrutsky, Maria I., Roy, Achira, Collins, Sarah, Olds, Carissa, Willert, Rebecca A., Czaja, Agnieszka M., Johnson, Rachel, Stover, Jessi A., Gottlieb, Steven, Bartholdi, Deborah, Rauch, Anita, Goldstein, Amy, Boyd-Kyle, Victoria, Aldinger, Kimberly A., Mirzaa, Ghayda M., Nissen, Anke, Brigatti, Karlla W., Puffenberger, Erik G., Millen, Kathleen J., Strauss, Kevin A., Dobyns, William B., Troy, Carol M., Jinks, Robert N.
Publicado no Am J Hum Genet (2016)