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Madden, Soumerai, Lieu, Mandl, Zhang, Ross-Degnan, and Health maintenance. 2002. “Effects of a Law Against Early Postpartum Discharge on Newborn Follow-Up, Adverse Events, and HMO Expenditures”. N Engl J Med 347: 2031-8.

Pena, Taylor, Fishman, and Mandl. 2002. “Effect of an Imaging Protocol on Clinical Outcomes Among Pediatric Patients With Appendicitis”. Pediatrics 110: 1088-93.

Smith, Laura, Alan Beggs, and Vandana Gupta. 2013. “Analysis of Skeletal Muscle Defects in Larval Zebrafish by Birefringence and Touch-Evoke Escape Response Assays.”. J Vis Exp, no. 82: e50925.

Brownstein, Catherine, Meghan Towne, Lovelace Luquette, David Harris, Nicholas Marinakis, Peter Meinecke, Kerstin Kutsche, et al. 2013. “Mutation of KCNJ8 in a Patient With Cantú Syndrome With Unique Vascular Abnormalities - Support for the Role of K(ATP) Channels in This Condition.”. Eur J Med Genet 56 (12): 678-82.

Mandl, and Jr. Lovejoy F. H. 1994. “Common Poisonings”. Pediatr Rev 15: 151-9.

Mandl, and Kohane. 1999. “Healthconnect: Clinical Grade Patient-Physician Communication”. Proc AMIA Symp, 849-53.

Soprano, Fleisher, and Mandl. 1999. “The Spontaneous Passage of Esophageal Coins in Children”. Arch Pediatr Adolesc Med 153: 1073-6.

Mandl, Stack, and Fleisher. 1997. “Incidence of Bacteremia in Infants and Children With Fever and Petechiae”. J Pediatr 131: 398-404.

Ockeloen, Gilhuis, Pfundt, Kamsteeg, PB Agrawal, AH Beggs, Dara Hama-Amin, et al. 2012. “Congenital Myopathy Caused by a Novel Missense Mutation in the CFL2 Gene.”. Neuromuscul Disord 22 (7): 632-9.

Agrawal, Pankaj, Mugdha Joshi, Talia Savic, Zoe Chen, and Alan Beggs. 2012. “Normal Myofibrillar Development Followed by Progressive Sarcomeric Disruption With Actin Accumulations in a Mouse Cfl2 Knockout Demonstrates Requirement of Cofilin-2 for Muscle Maintenance.”. Hum Mol Genet 21 (10): 2341-56.