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Health Affairs (Project Hope)|December 8, 2010
State-sponsored public reporting of hospital quality: results are hard to find and lack uniformityJoseph S Ross, Sameer Sheth, Harlan M KrumholzJournal of Clinical Epidemiology|January 29, 2016
Compliance with prospective trial registration guidance remained low in high-impact journals and has implications for primary end point reportingRafael Dal-Ré, Joseph S Ross, Ana MarušićClinical Trials (London, England)|June 7, 2018
The US Food and Drug Administration's expedited approval programs: Evidentiary standards, regulatory trade-offs, and potential improvementsJoshua D Wallach, Joseph S Ross, Huseyin NaciHealth Affairs (Project Hope)|April 8, 2015
Efficacy and safety concerns are important reasons why the FDA requires multiple reviews before approval of new drugsJoseph S Ross, Kristina Dzara, Nicholas S DowningResearch Integrity and Peer Review|January 9, 2020
Impact of US industry payment disclosure laws on payments to surgeons: a natural experimentTaeho Greg Rhee, Tijana Stanic, Joseph S RossJAMA Health Forum|June 20, 2025
Public Health Implications of Legal Challenges to the FDA's Regulation of Laboratory-Developed TestsKushal T Kadakia, Joseph S Ross, Reshma RamachandranJournal of General Internal Medicine|July 10, 2024
Unveiling the Adoption and Barriers of Telemedicine in US Hospitals: A Comprehensive Analysis (2017-2022)John Xuefeng Jiang, Joseph S Ross, Ge BaiHealth Affairs Scholar|January 15, 2026
Changes in pharmaceutical industry payments to physicians after New Jersey's 2018 restrictionNeeraj G Patel, Reshma Ramachandran, Joseph S RossClinical Pharmacology and Therapeutics|November 25, 2018
Generic Drugs in the United States: Policies to Address Pricing and CompetitionRavi Gupta, Nilay D Shah, Joseph S RossBMJ Open|November 14, 2015
Clinical trial registration, reporting, publication and FDAAA compliance: a cross-sectional analysis and ranking of new drugs approved by the FDA in 2012Jennifer E Miller, David Korn, Joseph S RossPageof 66