Lista de obras - Megan Doerr - Dominio Público Uruguay

An Open Toolkit for Tracking Open Science Partnership Implementation and Impact

An open toolkit for tracking open science partnership implementation and impact

artículo científico publicado en 2019

An open toolkit for tracking open science partnership implementation and impact.

artículo científico publicado en 2019

Assessment of the <i>All of Us</i> research program's informed consent process

artículo científico publicado en 2020

Bringing Code to Data: Don't Forget Governance

artículo científico publicado en 2020

Cleveland Clinic's Center for personalized healthcare: setting the stage for value-based care

artículo científico publicado en 2014

Connected Medical Technology and Cybersecurity Informed Consent: A New Paradigm

artículo científico publicado en 2020

Consent Processes for Mobile App Mediated Research: Systematic Review

artículo científico

Developing pathways for community-led research with big data: a content analysis of stakeholder interviews

artículo científico publicado en 2020

Engaging populations underrepresented in research through novel approaches to consent.

artículo científico publicado en 2018

Family history: still relevant in the genomics era.

artículo científico

Formative Evaluation of Participant Experience With Mobile eConsent in the App-Mediated Parkinson mPower Study: A Mixed Methods Study.

artículo científico publicado en 2017

Formative evaluation of clinician experience with integrating family history-based clinical decision support into clinical practice.

artículo científico publicado en 2014

GA4GH: International policies and standards for data sharing across genomic research and healthcare

artículo científico publicado en 2021

Implementing a universal informed consent process for the Research Program

artículo científico publicado en 2019

Introduction to the "Technology in Practice" Special Issue

artículo científico publicado en 2018

Navigating ethical quandaries with the privacy dilemma of biomedical datasets

artículo científico publicado en 2020

Personalised care and the genome

artículo científico publicado en 2012

Physical activity, sleep and cardiovascular health data for 50,000 individuals from the MyHeart Counts Study

article

Review and Comparison of Electronic Patient-Facing Family Health History Tools.

artículo científico publicado en 2018

The Healthy Pregnancy Research Program: Transforming Pregnancy Research Through a ResearchKit App

article published in 2018

The Mole Mapper Study, mobile phone skin imaging and melanoma risk data collected using ResearchKit

artículo científico publicado en 2017

The mPower study, Parkinson disease mobile data collected using ResearchKit

artículo científico publicado en 2016

U.S. Adult Perspectives on Facial Images, DNA, and Other Biometrics

Understanding the contribution of family history to colorectal cancer risk and its clinical implications: A state-of-the-science review

artículo científico publicado en 2016

Unregulated Health Research Using Mobile Devices: Ethical Considerations and Policy Recommendations

artículo científico publicado en 2020

Lista de obras de Megan Doerr

An Open Toolkit for Tracking Open Science Partnership Implementation and Impact

An open toolkit for tracking open science partnership implementation and impact

An open toolkit for tracking open science partnership implementation and impact.

Assessment of the <i>All of Us</i> research program's informed consent process

Bringing Code to Data: Don't Forget Governance

Cleveland Clinic's Center for personalized healthcare: setting the stage for value-based care

Connected Medical Technology and Cybersecurity Informed Consent: A New Paradigm

Consent Processes for Mobile App Mediated Research: Systematic Review

Developing pathways for community-led research with big data: a content analysis of stakeholder interviews

Engaging populations underrepresented in research through novel approaches to consent.

Family history: still relevant in the genomics era.

Formative Evaluation of Participant Experience With Mobile eConsent in the App-Mediated Parkinson mPower Study: A Mixed Methods Study.

Formative evaluation of clinician experience with integrating family history-based clinical decision support into clinical practice.

GA4GH: International policies and standards for data sharing across genomic research and healthcare

Implementing a universal informed consent process for the Research Program

Introduction to the "Technology in Practice" Special Issue

Navigating ethical quandaries with the privacy dilemma of biomedical datasets

Personalised care and the genome

Physical activity, sleep and cardiovascular health data for 50,000 individuals from the MyHeart Counts Study

Review and Comparison of Electronic Patient-Facing Family Health History Tools.

The Healthy Pregnancy Research Program: Transforming Pregnancy Research Through a ResearchKit App

The Mole Mapper Study, mobile phone skin imaging and melanoma risk data collected using ResearchKit

The mPower study, Parkinson disease mobile data collected using ResearchKit

U.S. Adult Perspectives on Facial Images, DNA, and Other Biometrics

Understanding the contribution of family history to colorectal cancer risk and its clinical implications: A state-of-the-science review

Unregulated Health Research Using Mobile Devices: Ethical Considerations and Policy Recommendations

Young people’s data governance preferences for their mental health data: MindKind Study findings from India, South Africa, and the United Kingdom