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Ottenheijm, Coen, Christian Witt, Ger Stienen, Siegfried Labeit, Alan Beggs, and Henk Granzier. 2009. “Thin Filament Length Dysregulation Contributes to Muscle Weakness in Nemaline Myopathy Patients With Nebulin Deficiency.”. Hum Mol Genet 18 (13): 2359-69.

Farrar, Jason, Michelle Nater, Emi Caywood, Michael McDevitt, Jeanne Kowalski, Clifford Takemoto, Conover Talbot, et al. 2008. “Abnormalities of the Large Ribosomal Subunit Protein, Rpl35a, in Diamond-Blackfan Anemia.”. Blood 112 (5): 1582-92.

Keller, Christian, Arthur Hays, Lewis Rowland, Behzad Moghadaszadeh, Alan Beggs, and Govind Bhagat. 2006. “Adult-Onset Nemaline Myopathy and Monoclonal Gammopathy.”. Arch Neurol 63 (1): 132-4.

Liadaki, Kho, Sanoudou, Schienda, Flint, AH Beggs, Kohane, and Kunkel. 2005. “Side Population Cells Isolated from Different Tissues Share Transcriptome Signatures and Express Tissue-Specific Markers.”. Exp Cell Res 303 (2): 360-74.

Sanoudou, Despina, Judith Haslett, Alvin Kho, Shaoqiang Guo, Hanna Gazda, Steven Greenberg, Hart Lidov, Isaac Kohane, Louis Kunkel, and Alan Beggs. 2003. “Expression Profiling Reveals Altered Satellite Cell Numbers and Glycolytic Enzyme Transcription in Nemaline Myopathy Muscle.”. Proc Natl Acad Sci U S A 100 (8): 4666-71.

Zervos, Hunt, Tong, Avallone, Morales, Friedman, Cohen, et al. 2002. “Clinical, Genetic and Histopathologic Findings in Two Siblings With Muscle-Eye-Brain Disease.”. Eur J Ophthalmol 12 (4): 253-61.

Splawski, Igor, Katherine Timothy, Michihiro Tateyama, Colleen Clancy, Alka Malhotra, Alan Beggs, Francesco Cappuccio, Giuseppe Sagnella, Robert Kass, and Mark Keating. 2002. “Variant of SCN5A Sodium Channel Implicated in Risk of Cardiac Arrhythmia.”. Science 297 (5585): 1333-6.

Gazda, Lipton, Willig, Ball, Niemeyer, Tchernia, Mohandas, et al. 2001. “Evidence for Linkage of Familial Diamond-Blackfan Anemia to Chromosome 8p23.3-P22 and for Non-19q Non-8p Disease.”. Blood 97 (7): 2145-50.

Kaplan, Kim, North, Rennke, Correia, Tong, Mathis, et al. 2000. “Mutations in ACTN4, Encoding Alpha-Actinin-4, Cause Familial Focal Segmental Glomerulosclerosis.”. Nat Genet 24 (3): 251-6.

Chan, Tong, AH Beggs, and Kunkel. 1998. “Human Skeletal Muscle-Specific Alpha-Actinin-2 and -3 Isoforms Form Homodimers and Heterodimers in Vitro and in Vivo.”. Biochem Biophys Res Commun 248 (1): 134-9.