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Boutis, Komar, Jaramillo, Babyn, Alman, Snyder, Mandl, and Schuh. 2001. “Sensitivity of a Clinical Examination to Predict Need for Radiography in Children With Ankle Injuries: A Prospective Study”. Lancet 358: 2118-21.

Mandl, Homer, Harary, and Finkelstein. 2000. “Effect of a Reduced Postpartum Length of Stay Program on Primary Care Services Use by Mothers and Infants”. Pediatrics 106: 937-41.

Lawlor, Michael, Coen Ottenheijm, Vilma-Lotta Lehtokari, Kiyomi Cho, Katarina Pelin, Carina Wallgren-Pettersson, Henk Granzier, and Alan Beggs. 2011. “Novel Mutations in NEB Cause Abnormal Nebulin Expression and Markedly Impaired Muscle Force Generation in Severe Nemaline Myopathy.”. Skelet Muscle 1 (1): 23.

Ottenheijm, Coen, Michael Lawlor, Ger Stienen, Henk Granzier, and Alan Beggs. 2011. “Changes in Cross-Bridge Cycling Underlie Muscle Weakness in Patients With Tropomyosin 3-Based Myopathy.”. Hum Mol Genet 20 (10): 2015-25.

Gupta, Vandana, Genri Kawahara, Stacey Gundry, Aye Chen, Wayne Lencer, Yi Zhou, Leonard Zon, Louis Kunkel, and Alan Beggs. 2011. “The Zebrafish Dag1 Mutant: A Novel Genetic Model for Dystroglycanopathies.”. Hum Mol Genet 20 (9): 1712-25.

Lawlor, Michael, Elizabeth Dechene, Emily Roumm, Amelia Geggel, Behzad Moghadaszadeh, and Alan Beggs. 2010. “Mutations of Tropomyosin 3 (TPM3) Are Common and Associated With Type 1 Myofiber Hypotrophy in Congenital Fiber Type Disproportion.”. Hum Mutat 31 (2): 176-83.

Ziane, Rahima, Hai Huang, Behzad Moghadaszadeh, Alan Beggs, Georges Levesque, and Mohamed Chahine. 2010. “Cell Membrane Expression of Cardiac Sodium Channel Na(v)1.5 Is Modulated by Alpha-Actinin-2 Interaction.”. Biochemistry 49 (1): 166-78.

Al-Qusairi, Lama, Norbert Weiss, Anne Toussaint, Céline Berbey, Nadia Messaddeq, Christine Kretz, Despina Sanoudou, et al. 2009. “T-Tubule Disorganization and Defective Excitation-Contraction Coupling in Muscle Fibers Lacking Myotubularin Lipid Phosphatase.”. Proc Natl Acad Sci U S A 106 (44): 18763-8.

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.