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Journal of the American Geriatrics Society|May 7, 2026
Designing Consent Processes for Research With Older Adults Who May Lack Decisional Capacity: A Guide for InvestigatorsEmily A Largent, Stephanie R Morain, Jason KarlawishJournal of the National Cancer Institute|May 12, 2019
Recruitment and Trial-Finding Apps-Time for Rules of the RoadStephanie R Morain, Emily A LargentThe Hastings Center Report|April 11, 2021
Public Attitudes toward Consent When Research Is Integrated into Care-Any "Ought" from All the "Is"?Stephanie R Morain, Emily A LargentThe American Journal of Bioethics : AJOB|April 18, 2019
When Is It Ethical for Physician-Investigators to Seek Consent From Their Own Patients?Stephanie R Morain, Steven Joffe, Emily A LargentThe American Journal of Bioethics : AJOB|May 21, 2025
Mind Care: The Moral Significance of the Dementia Caregiving DyadAndrew Peterson, Emily A Largent, Jason KarlawishJournal of the American Geriatrics Society|September 12, 2023
Supported decision making: Facilitating the self-determination of persons living with Alzheimer's and related diseasesEmily A Largent, Andrew Peterson, Jason KarlawishBMC Digital Health|August 12, 2024
From an idea to the marketplace: Identifying and addressing ethical and regulatory considerations across the digital health product-development lifecycleEmily A Largent, Jason Karlawish, Anna WexlerAlzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 31, 2024
Applying recommendations for diagnostic disclosure of mild cognitive impairment and dementia: Practical guidance for cliniciansKyra O'Brien, Emily A Largent, Jason KarlawishPharmaceutical Medicine|April 1, 2025
The Importance of Including Underserved Populations in ResearchKayla R Mehl, Stephanie R Morain, Emily A LargentAlzheimer'S Research & Therapy|September 29, 2018
Study partners: essential collaborators in discovering treatments for Alzheimer's diseaseEmily A Largent, Jason Karlawish, Joshua D GrillPageof 30