Lista de obras - John Wilbanks - Dominio Público Uruguay

'Omics data sharing

artículo científico publicado en 2009

An Interoperability Principle for Knowledge Creation and Governance: The Role of Emerging Institutions

scholarly article

An open source pharma roadmap

artículo científico publicado en 2017

Another reason for opening access to research

artículo científico publicado en 2006

Assessing the consequences of decentralizing biomedical research

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

Citizen Science on Your Smartphone: An ELSI Research Agenda

artículo científico publicado en 2015

Collaborating to Compete: Blood Profiling Atlas in Cancer (BloodPAC) Consortium.

artículo científico publicado en 2017

Collaborative Computational Technologies for Biomedical Research

Cost of Freedom ⬇️

libro de Jon Phillips

Creating a data resource: what will it take to build a medical information commons?

artículo científico publicado en 2017

Custom-fit your journey to improved patient safety.

artículo científico

Design Issues in E-Consent

artículo científico publicado en 2018

Electronic Informed Consent in Mobile Applications Research

scientific article published on 01 March 2020

Empirical validation of an automated approach to data use oversight

scientific article published on 10 November 2021

First, design for data sharing

artículo científico publicado en 2016

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

artículo científico publicado en 2017

Implementing a universal informed consent process for the Research Program

artículo científico publicado en 2019

Importance of Participant-Centricity and Trust for a Sustainable Medical Information Commons

artículo científico publicado en 2019

Indicators of retention in remote digital health studies: a cross-study evaluation of 100,000 participants

scientific article published on 17 February 2020

Intellectual Property Aspects of Collaboration

Introduction: Unregulated Health Research Using Mobile Devices

scientific article published on 01 March 2020

Licence restrictions: A fool's errand

artículo científico publicado en 2013

Navigating ethical quandaries with the privacy dilemma of biomedical datasets

artículo científico publicado en 2020

Open Access, Public Access: Policies, Implementation, Developments, and the Future of U.S.-Published Research

Open letter to the Society for Neuroscience

Openness as infrastructure ⬇️

artículo científico publicado el 14 de octubre de 2011

Panton Principles

set of guidelines on how to share scientific data

Portable Approaches to Informed Consent and Open Data

Responsible sharing of biomedical data and biospecimens via the "Automatable Discovery and Access Matrix" (ADA-M)

Science, Open Communication and Sustainable Development

article

Stop the privatization of health data

artículo científico publicado en 2016

The Rise of Citizen Science in Health and Biomedical Research

artículo científico publicado en 2019

The Role of Government in Precision Medicine, Precision Public Health and the Intersection With Healthy Living

scientific article published on 07 December 2018

The mPower study, Parkinson disease mobile data collected using ResearchKit

artículo científico publicado en 2016

Transgenic mouse with human mutant p53 expression in the prostate epithelium

artículo científico publicado en 2004

Lista de obras de John Wilbanks

'Omics data sharing

An Interoperability Principle for Knowledge Creation and Governance: The Role of Emerging Institutions

An open source pharma roadmap

Another reason for opening access to research

Assessing the consequences of decentralizing biomedical research

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

Bringing Code to Data: Don't Forget Governance

Citizen Science on Your Smartphone: An ELSI Research Agenda

Collaborating to Compete: Blood Profiling Atlas in Cancer (BloodPAC) Consortium.

Collaborative Computational Technologies for Biomedical Research

Cost of Freedom ⬇️

Creating a data resource: what will it take to build a medical information commons?

Custom-fit your journey to improved patient safety.

Design Issues in E-Consent

Electronic Informed Consent in Mobile Applications Research

Empirical validation of an automated approach to data use oversight

First, design for data sharing

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

Implementing a universal informed consent process for the Research Program

Importance of Participant-Centricity and Trust for a Sustainable Medical Information Commons

Indicators of retention in remote digital health studies: a cross-study evaluation of 100,000 participants

Intellectual Property Aspects of Collaboration

Introduction: Unregulated Health Research Using Mobile Devices

Licence restrictions: A fool's errand

Navigating ethical quandaries with the privacy dilemma of biomedical datasets

Open Access, Public Access: Policies, Implementation, Developments, and the Future of U.S.-Published Research

Open letter to the Society for Neuroscience

Openness as infrastructure ⬇️

Panton Principles

Portable Approaches to Informed Consent and Open Data

Responsible sharing of biomedical data and biospecimens via the "Automatable Discovery and Access Matrix" (ADA-M)

Science, Open Communication and Sustainable Development

Stop the privatization of health data

The Rise of Citizen Science in Health and Biomedical Research

The Role of Government in Precision Medicine, Precision Public Health and the Intersection With Healthy Living

The mPower study, Parkinson disease mobile data collected using ResearchKit

Transgenic mouse with human mutant p53 expression in the prostate epithelium

US-EU Scientific Research Collaborations: Sage Bionetworks’ Experience Navigating the Complex Regulatory Landscape

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

We need a Web for data

What the semantic web could do for the life sciences

Why Open Drug Discovery Needs Four Simple Rules for Licensing Data and Models

Why open drug discovery needs four simple rules for licensing data and models

John Wilbanks: Hagamos un patrimonio común con nuestros datos médicos