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Byers, Neumann, AH Beggs, and Kunkel. 1992. “ELISA Quantitation of Dystrophin for the Diagnosis of Duchenne and Becker Muscular Dystrophies.”. Neurology 42 (3 Pt 1): 570-6.

Beggs, AH, Koenig, Boyce, and Kunkel. 1990. “Detection of 98% of DMD/BMD Gene Deletions by Polymerase Chain Reaction.”. Hum Genet 86 (1): 45-8.

Angelini, AH Beggs, Hoffman, Fanin, and Kunkel. 1990. “Enormous Dystrophin in a Patient With Becker Muscular Dystrophy.”. Neurology 40 (5): 808-12.

Beggs, AH, and Kunkel. 1990. “Improved Diagnosis of Duchenne/Becker Muscular Dystrophy.”. J Clin Invest 85 (3): 613-9.

Hoffman, AH Beggs, Koenig, Kunkel, and Angelini. 1989. “Cross-Reactive Protein in Duchenne Muscle.”. Lancet 2 (8673): 1211-2.

Kunkel, AH Beggs, and Hoffman. 1989. “Molecular Genetics of Duchenne and Becker Muscular Dystrophy: Emphasis on Improved Diagnosis.”. Clin Chem 35 (7 Suppl): B21-4.

Ottenheijm, Coen, Danielle Buck, Josine Winter, Claudia Ferrara, Nicoletta Piroddi, Chiara Tesi, Jeffrey Jasper, et al. 2013. “Deleting Exon 55 from the Nebulin Gene Induces Severe Muscle Weakness in a Mouse Model for Nemaline Myopathy.”. Brain 136 (Pt 6): 1718-31.

Winter, Josine Marieke, Danielle Buck, Carlos Hidalgo, Jeffrey Jasper, Fady Malik, Nigel Clarke, Ger Stienen, et al. 2013. “Troponin Activator Augments Muscle Force in Nemaline Myopathy Patients With Nebulin Mutations.”. J Med Genet 50 (6): 383-92.

Moghadaszadeh, Behzad, Branden Rider, Michael Lawlor, Martin Childers, Robert Grange, Kushagra Gupta, Steve Boukedes, Caroline Owen, and Alan Beggs. 2013. “Selenoprotein N Deficiency in Mice Is Associated With Abnormal Lung Development.”. FASEB J 27 (4): 1585-99.

Lawlor, Michael, Dustin Armstrong, Marissa Viola, Jeffrey Widrick, Hui Meng, Robert Grange, Martin Childers, et al. 2013. “Enzyme Replacement Therapy Rescues Weakness and Improves Muscle Pathology in Mice With X-Linked Myotubular Myopathy.”. Hum Mol Genet 22 (8): 1525-38.