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Proceedings of the National Academy of Sciences of the United States of America|March 21, 2018
Precision medicine screening using whole-genome sequencing and advanced imaging to identify disease risk in adultsBradley A Perkins, C Thomas Caskey, Pamila Brar, et al.
Nature Medicine|July 3, 2019
ARAF recurrent mutation causes central conducting lymphatic anomaly treatable with a MEK inhibitorDong Li, Michael E March, Alvaro Gutierrez-Uzquiza, et al.
Autism Research : Official Journal of the International Society for Autism Research|January 21, 2020
Autism Heterogeneity in a Densely Sampled U.S. Population: Results From the First 1,000 Participants in the RI-CART StudyCarolyn E B McCormick, Brian C Kavanaugh, Danielle Sipsock, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 26, 2020
Precision medicine integrating whole-genome sequencing, comprehensive metabolomics, and advanced imagingYing-Chen Claire Hou, Hung-Chun Yu, Rick Martin, et al.
The American Journal of Sports Medicine|January 28, 2025
Descriptive Epidemiology of Complete ACL Tears in the Skeletally Immature Population: A Prospective Multicenter PLUTO StudyMelissa A Christino, Lauren E Hutchinson, Andrew T Pennock, et al.
The Journal of Clinical Investigation|October 5, 2013
Integrins protect cardiomyocytes from ischemia/reperfusion injuryHideshi Okada, N Chin Lai, Yoshitaka Kawaraguchi, et al.
The Lancet. Diabetes & Endocrinology|December 11, 2025
Continuous ketone monitoring for people with diabetes: international expert recommendations on the application of a new technologyKetan Dhatariya, Richard M Bergenstal, Mohammed Al-Sofiani, et al.
The American Journal of Sports Medicine|May 13, 2021
Assessment of Skeletal Maturity and Postoperative Growth Disturbance After Anterior Cruciate Ligament Reconstruction in Skeletally Immature Patients: A Systematic ReviewMatthew S Fury, Nikolaos K Paschos, Peter D Fabricant, et al.
The Journal of Pediatrics|February 15, 2015
Lymphatic and other vascular malformative/overgrowth disorders are caused by somatic mutations in PIK3CAValerie L Luks, Nolan Kamitaki, Matthew P Vivero, et al.
American Journal of Medical Genetics. Part A|June 6, 2020
Activating variants in PDGFRB result in a spectrum of disorders responsive to imatinib monotherapyTara L Wenger, Randall A Bly, Natalie Wu, et al.
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