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BMJ (Clinical Research Ed.)|May 26, 2018
Postmarket studies required by the US Food and Drug Administration for new drugs and biologics approved between 2009 and 2012: cross sectional analysisJoshua D Wallach, Alexander C Egilman, Sanket S Dhruva, et al.BMJ Open|March 25, 2019
Submissions from the SPRINT Data Analysis Challenge on clinical risk prediction: a cross-sectional evaluationCynthia A Jackevicius, JaeJin An, Dennis T Ko, et al.The American Journal of Managed Care|March 16, 2019
Access to primary and dental care among adults newly enrolled in MedicaidKrisda H Chaiyachati, Jeffrey K Hom, Charlene Wong, et al.Polymers|January 17, 2024
Chitosan-Polyvinyl Alcohol Nanocomposites for Regenerative TherapyCarlos David Grande-Tovar, Jorge Ivan Castro, Diego López Tenorio, et al.Molecules (Basel, Switzerland)|January 25, 2025
Histology Assessment of Chitosan-Polyvinyl Alcohol Scaffolds Incorporated with CaO NanoparticlesCarlos David Grande-Tovar, Jorge Ivan Castro Castro, Lemy Vanessa Barba-Rosado, et al.Biomolecules|September 11, 2019
Chitosan Beads Incorporated with Essential Oil of Thymus capitatus: Stability Studies on Red Tilapia FilletsMayra Alejandra Valencia Junca, Cesar Valencia, Edwin Flórez López, et al.Polymers|June 26, 2026
Synergistic Coatings Based on Chitosan and Eugenia caryophyllata Essential Oil to Improve Postharvest Quality of Capsicum chinenseFanor David Reyes Pérez, Yeimmy Peralta-Ruiz, Domingo César Carrascal-Hernández, et al.Circulation. Cardiovascular Quality and Outcomes|May 18, 2013
Regional density of cardiologists and rates of mortality for acute myocardial infarction and heart failureVivek T Kulkarni, Joseph S Ross, Yongfei Wang, et al.Medrxiv : the Preprint Server for Health Sciences|December 8, 2025
Modeling In-Hospital Mortality Among Patients Undergoing Percutaneous Coronary Intervention with Acute Myocardial Infarction Complicated by Cardiogenic Shock Receiving Mechanical Circulatory SupportNathan C Hurley, Bobak J Mortazavi, Sanket S Dhruva, et al.Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|August 9, 2017
US Food and Drug Administration Clearance of Moderate-Risk Otolaryngologic Devices via the 510(k) Process, 1997-2016Vinay K Rathi, Shekhar K Gadkaree, Joseph S Ross, et al.Pageof 66