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Beggs, AH, Miner, and Scangos. 1990. “Cell Type-Specific Expression of JC Virus T Antigen in Primary and Established Cell Lines from Transgenic Mice.”. J Gen Virol 71 ( Pt 1): 151-64.

Koenig, AH Beggs, Moyer, Scherpf, Heindrich, Bettecken, Meng, Müller, Lindlöf, and Kaariainen. 1989. “The Molecular Basis for Duchenne versus Becker Muscular Dystrophy: Correlation of Severity With Type of Deletion.”. Am J Hum Genet 45 (4): 498-506.

Beggs, AH, and Scangos. 1986. “Serum-Free Selection of Onc Genes.”. Gene Amplif Anal 4: 177-95.

Brownstein, Catherine, Alan Beggs, Nils Homer, Barry Merriman, Timothy Yu, Katherine Flannery, Elizabeth Dechene, et al. 2014. “An International Effort towards Developing Standards for Best Practices in Analysis, Interpretation and Reporting of Clinical Genome Sequencing Results in the CLARITY Challenge.”. Genome Biol 15 (3): R53.

Joshi, Mugdha, Jacqueline Eagan, Nirav Desai, Stephanie Newton, Meghan Towne, Nicholas Marinakis, Kristyn Esteves, et al. 2014. “A Compound Heterozygous Mutation in GPD1 Causes Hepatomegaly, Steatohepatitis, and Hypertriglyceridemia.”. Eur J Hum Genet.

Landowski, Michael, Marie-Françoise O’Donohue, Christopher Buros, Roxanne Ghazvinian, Nathalie Montel-Lehry, Adrianna Vlachos, Colin Sieff, et al. 2013. “Novel Deletion of RPL15 Identified by Array-Comparative Genomic Hybridization in Diamond-Blackfan Anemia.”. Hum Genet 132 (11): 1265-74.

Manzini, Chiara, Dimira Tambunan, Sean Hill, Tim Yu, Thomas Maynard, Erin Heinzen, Kevin Shianna, et al. 2012. “Exome Sequencing and Functional Validation in Zebrafish Identify GTDC2 Mutations As a Cause of Walker-Warburg Syndrome.”. Am J Hum Genet 91 (3): 541-7.

Majczenko, Karen, Ann Davidson, Sandra Camelo-Piragua, Pankaj Agrawal, Richard Manfready, Xingli Li, Sucheta Joshi, et al. 2012. “Dominant Mutation of CCDC78 in a Unique Congenital Myopathy With Prominent Internal Nuclei and Atypical Cores.”. Am J Hum Genet 91 (2): 365-71.

Winter, Josine, Barbara Joureau, Vasco Sequeira, Nigel Clarke, Jolanda Velden, Ger Stienen, Henk Granzier, Alan Beggs, and Coen Ottenheijm. 2015. “Effect of Levosimendan on the Contractility of Muscle Fibers from Nemaline Myopathy Patients With Mutations in the Nebulin Gene.”. Skelet Muscle 5: 12.

Sarwal, Aarti, Michael Cartwright, Francis Walker, Erin Mitchell, Anna Buj-Bello, Alan Beggs, and Martin Childers. 2014. “Ultrasound Assessment of the Diaphragm: Preliminary Study of a Canine Model of X-Linked Myotubular Myopathy.”. Muscle Nerve 50 (4): 607-9.