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Barnés, Carmen, Sui Huang, Arja Kaipainen, Despina Sanoudou, Emy Chen, Gabriel Eichler, Yuchun Guo, et al. 2005. “Evidence by Molecular Profiling for a Placental Origin of Infantile Hemangioma.”. Proc Natl Acad Sci U S A 102 (52): 19097-102.

Haslett, Judith, Peter Kang, Mei Han, Alvin Kho, Despina Sanoudou, Jay Volinski, Alan Beggs, Isaac Kohane, and Louis Kunkel. 2005. “The Influence of Muscle Type and Dystrophin Deficiency on Murine Expression Profiles.”. Mamm Genome 16 (10): 739-48.

Sparrow, John, Kristen Nowak, Hayley Durling, Alan Beggs, Carina Wallgren-Pettersson, Norma Romero, Ikuya Nonaka, and Nigel Laing. 2003. “Muscle Disease Caused by Mutations in the Skeletal Muscle Alpha-Actin Gene (ACTA1).”. Neuromuscul Disord 13 (7-8): 519-31.

Gurgel-Giannetti, Juliana, Umbertina Reed, Sueli Marie, Edmar Zanoteli, Moacir Fireman, Acary Oliveira, Lineu Werneck, Alan Beggs, Mayana Zatz, and Mariz Vainzof. 2003. “Rod Distribution and Muscle Fiber Type Modification in the Progression of Nemaline Myopathy.”. J Child Neurol 18 (3): 235-40.

Bönnemann, Thompson, Ven, Goebel, Warlo, Vollmers, Reimann, et al. 2003. “Filamin C Accumulation Is a Strong But Nonspecific Immunohistochemical Marker of Core Formation in Muscle.”. J Neurol Sci 206 (1): 71-8.

Vainzof, Mariz, Eloisa Moreira, Oscar Suzuki, Georgine Faulkner, Georgio Valle, Alan Beggs, Olli Carpen, et al. 2002. “Telethonin Protein Expression in Neuromuscular Disorders.”. Biochim Biophys Acta 1588 (1): 33-40.

Mizuno, Puca, O’Brien, AH Beggs, and Kunkel. 2001. “Genomic Organization and Single-Nucleotide Polymorphism Map of Desmuslin, a Novel Intermediate Filament Protein on Chromosome 15q26.3.”. BMC Genet 2: 8.

Takada, Vander Woude, Tong, Thompson, Watkins, Kunkel, and AH Beggs. 2001. “Myozenin: an Alpha-Actinin- and Gamma-Filamin-Binding Protein of Skeletal Muscle Z Lines.”. Proc Natl Acad Sci U S A 98 (4): 1595-600.

Wattanasirichaigoon, Vesely, Duggal, Levine, Blume, Wolff, Edwards, and AH Beggs. 1999. “Sodium Channel Abnormalities Are Infrequent in Patients With Long QT Syndrome: Identification of Two Novel SCN5A Mutations.”. Am J Med Genet 86 (5): 470-6.

Pelin, Hilpelä, Donner, Sewry, Akkari, Wilton, Wattanasirichaigoon, et al. 1999. “Mutations in the Nebulin Gene Associated With Autosomal Recessive Nemaline Myopathy.”. Proc Natl Acad Sci U S A 96 (5): 2305-10.