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Kho, Alvin, Peter Kang, Isaac Kohane, and Louis Kunkel. 2006. “Transcriptome-Scale Similarities Between Mouse and Human Skeletal Muscles With Normal and Myopathic Phenotypes.”. BMC Musculoskelet Disord 7: 23.

Gazda, Hanna, Alvin Kho, Despina Sanoudou, Jan Zaucha, Isaac Kohane, Colin Sieff, and Alan Beggs. 2006. “Defective Ribosomal Protein Gene Expression Alters Transcription, Translation, Apoptosis, and Oncogenic Pathways in Diamond-Blackfan Anemia.”. Stem Cells 24 (9): 2034-44.

Poland, Ager, Olson, and Sokol. 1990. “Quality of Prenatal Care; Selected Social, Behavioral, and Biomedical Factors; And Birth Weight”. Obstet GynecolObstet Gynecol 75: 607-12.

Mandl, and Kohane. 2015. “Federalist Principles for Healthcare Data Networks”. Nat Biotechnol 33: 360-3.

Ong, and Mandl. 2015. “National Expenditure for False-Positive Mammograms and Breast Cancer Overdiagnoses Estimated at $4 Billion a Year”. Health Aff (Millwood) 34: 576-83.

Mandl, Kenneth, Isaac Kohane, Douglas McFadden, Griffin Weber, Marc Natter, Joshua Mandel, Sebastian Schneeweiss, et al. 2014. “Scalable Collaborative Infrastructure for a Learning Healthcare System (SCILHS): Architecture.”. J Am Med Inform Assoc 21 (4): 615-20.

Lionetti, Geraldina, Yukiko Kimura, Laura Schanberg, Timothy Beukelman, Carol Wallace, Norman Ilowite, Jane Winsor, et al. 2013. “Using Registries to Identify Adverse Events in Rheumatic Diseases.”. Pediatrics 132 (5): e1384-94.

Zukosky, Kristen, Katherine Meilleur, Bryan Traynor, Jahannaz Dastgir, Livija Medne, Marcella Devoto, James Collins, et al. 2015. “Association of a Novel ACTA1 Mutation With a Dominant Progressive Scapuloperoneal Myopathy in an Extended Family.”. JAMA Neurol 72 (6): 689-98.

Thaker, Vidhu, Kristyn Esteves, Meghan Towne, Catherine Brownstein, Philip James, Laura Crowley, Joel Hirschhorn, et al. 2015. “Whole Exome Sequencing Identifies RAI1 Mutation in a Morbidly Obese Child Diagnosed With ROHHAD Syndrome.”. J Clin Endocrinol Metab 100 (5): 1723-30.

Shelton, Diane, Branden Rider, Georgina Child, Sophia Tzannes, Ling Guo, Behzad Moghadaszadeh, Emily Troiano, Bianca Haase, Claire Wade, and Alan Beggs. 2015. “X-Linked Myotubular Myopathy in Rottweiler Dogs Is Caused by a Missense Mutation in Exon 11 of the MTM1 Gene.”. Skelet Muscle 5 (1): 1.