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Splawski, Igor, Katherine Timothy, Niels Decher, Pradeep Kumar, Frank Sachse, Alan Beggs, Michael Sanguinetti, and Mark Keating. 2005. “Severe Arrhythmia Disorder Caused by Cardiac L-Type Calcium Channel Mutations.”. Proc Natl Acad Sci U S A 102 (23): 8089-96; discussion 8086.

Sanoudou, Despina, Leslie Frieden, Judith Haslett, Alvin Kho, Steven Greenberg, Isaac Kohane, Louis Kunkel, and Alan Beggs. 2004. “Molecular Classification of Nemaline Myopathies: ‘nontyping’ Specimens Exhibit Unique Patterns of Gene Expression.”. Neurobiol Dis 15 (3): 590-600.

Tomczak, Kinga, Voichita Marinescu, Marco Ramoni, Despina Sanoudou, Federica Montanaro, Mei Han, Louis Kunkel, Isaac Kohane, and Alan Beggs. 2004. “Expression Profiling and Identification of Novel Genes Involved in Myogenic Differentiation.”. FASEB J 18 (2): 403-5.

Haslett, Judith, Despina Sanoudou, Alvin Kho, Mei Han, Richard Bennett, Isaac Kohane, Alan Beggs, and Louis Kunkel. 2003. “Gene Expression Profiling of Duchenne Muscular Dystrophy Skeletal Muscle.”. Neurogenetics 4 (4): 163-71.

Zanoteli, Edmar, Renato Lotuffo, Acary Oliveira, Alan Beggs, Marta Canovas, Mayana Zatz, and Mariz Vainzof. 2003. “Deficiency of Muscle Alpha-Actinin-3 Is Compatible With High Muscle Performance.”. J Mol Neurosci 20 (1): 39-42.

Greenberg, Sanoudou, Haslett, Kohane, Kunkel, AH Beggs, and Amato. 2002. “Molecular Profiles of Inflammatory Myopathies.”. Neurology 59 (8): 1170-82.

Ryan, Schnell, Strickland, Shield, Morgan, Iannaccone, Laing, AH Beggs, and North. 2001. “Nemaline Myopathy: A Clinical Study of 143 Cases.”. Ann Neurol 50 (3): 312-20.

Sanoudou, and AH Beggs. 2001. “Clinical and Genetic Heterogeneity in Nemaline Myopathy--a Disease of Skeletal Muscle Thin Filaments.”. Trends Mol Med 7 (8): 362-8.

Mills, Yang, Weinberger, Vander Woude, AH Beggs, Easteal, and North. 2001. “Differential Expression of the Actin-Binding Proteins, Alpha-Actinin-2 and -3, in Different Species: Implications for the Evolution of Functional Redundancy.”. Hum Mol Genet 10 (13): 1335-46.

Schwartz, Priori, Spazzolini, Moss, Vincent, Napolitano, Denjoy, et al. 2001. “Genotype-Phenotype Correlation in the Long-QT Syndrome: Gene-Specific Triggers for Life-Threatening Arrhythmias.”. Circulation 103 (1): 89-95.