Citation Impact
Citing Papers
Dynamic consent: a patient interface for twenty-first century research networks
2014
Diagnostic accuracy of deep learning in medical imaging: a systematic review and meta-analysis
2021 Standout
Big Data and discrimination: perils, promises and solutions. A systematic review
2019 Standout
The role of artificial intelligence in healthcare: a structured literature review
2021 Standout
Communicating new knowledge on previously reported genetic variants
2012
Major depressive disorder
2016 Standout
The Ethics of Big Data: Current and Foreseeable Issues in Biomedical Contexts
2015
Legal and Regulatory Considerations Associated with Use of Patient-Generated Health Data from Social Media and Mobile Health (mHealth) Devices
2015
Patient-Derived Xenograft Models: An Emerging Platform for Translational Cancer Research
2014 Standout
Charting a course for genomic medicine from base pairs to bedside
2011 Nature
Personalized Telehealth in the Future: A Global Research Agenda
2016
Opportunities and challenges for the integration of massively parallel genomic sequencing into clinical practice: lessons from the ClinSeq project
2012
Visualizing the intellectual structure and evolution of electronic health and telemedicine research
2019
Do Researchers Have an Obligation to Actively Look for Genetic Incidental Findings?
2013
Improving personal health records for patient-centered care
2010
Tectonic Shifts in the Health Information Economy
2008 Standout
Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology
2015 Standout
Using electronic health records to drive discovery in disease genomics
2011
WHO World Mental Health Surveys International College Student Project: Prevalence and distribution of mental disorders.
2018 Standout
An informatics approach to analyzing the incidentalome
2012
Understanding factors influencing the adoption of mHealth by the elderly: An extension of the UTAUT model
2017 Standout
Sharing Data for Public Health Research by Members of an International Online Diabetes Social Network
2011
Regenerative Endodontics: A Review of Current Status and a Call for Action
2007
Taxonomizing, sizing, and overcoming the incidentalome
2012
Getting personalized cancer genome analysis into the clinic: the challenges in bioinformatics
2012
Meaningful Use of a Confidential Adolescent Patient Portal
2016
No Small Change for the Health Information Economy
2009 Standout
A New Dimension of Health Care: Systematic Review of the Uses, Benefits, and Limitations of Social Media for Health Communication
2013 Standout
Broad Consent for Research With Biological Samples: Workshop Conclusions
2015
Privacy in the age of medical big data
2018 Standout
Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations
2018 Standout
Points to Consider: Ethical, Legal, and Psychosocial Implications of Genetic Testing in Children and Adolescents
2015 Standout
ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing
2013 Standout
Telehealth
2017 Standout
Standards for Health Information Technology to Ensure Adolescent Privacy
2012
Patenting human pluripotent cells: balancing commercial, academic and ethical interests
2009
Genetics professionals' perspectives on reporting incidental findings from clinical genome‐wide sequencing
2013
Instrumenting the health care enterprise for discovery research in the genomic era
2009
Sharing Medical Data for Health Research: The Early Personal Health Record Experience
2010
Mining electronic health records: towards better research applications and clinical care
2012 Standout
Return of individual research results from genome-wide association studies: experience of the Electronic Medical Records and Genomics (eMERGE) Network
2012
Personal genomes in progress: from the Human Genome Project to the Personal Genome Project
2010
Sexually Transmitted Infections Treatment Guidelines, 2021
2021 Standout
The ethics of algorithms: Mapping the debate
2016 Standout
What Is the Bioeconomy? A Review of the Literature
2016 Standout
Health 2050: The Realization of Personalized Medicine through Crowdsourcing, the Quantified Self, and the Participatory Biocitizen
2012
Open Notes: Doctors and Patients Signing On
2010 Standout
Sensor Mania! The Internet of Things, Wearable Computing, Objective Metrics, and the Quantified Self 2.0
2012 Standout
Public Participation in Scientific Research: a Framework for Deliberate Design
2012 Standout
Offering Individual Genetic Research Results: Context Matters
2010
Mesenchymal Stem Cells Derived from Dental Tissues vs. Those from Other Sources: Their Biology and Role in Regenerative Medicine
2009 Standout
Exploring the Role of Service Quality and Knowledge for Mobile Health Services
2016
Meaningful Citizen Engagement in Science and Technology
2008
Evaluating barriers to adopting telemedicine worldwide: A systematic review
2016 Standout
The Unintended Implications of Blurring the Line Between Research and Clinical Care in a Genomic Age
2014
The NIMH Research Domain Criteria (RDoC) Project: Precision Medicine for Psychiatry
2014
MeDShare: Trust-Less Medical Data Sharing Among Cloud Service Providers via Blockchain
2017 Standout
Standardization of sample collection, isolation and analysis methods in extracellular vesicle research
2013 Standout
The Ethics of Biomedical ‘Big Data’ Analytics
2019
Accurate proteome-wide missense variant effect prediction with AlphaMissense
2023 StandoutScienceNobel
Works of Patrick L. Taylor being referenced
Retroactive Ethics in Rapidly Developing Scientific Fields
2009
Research sharing, ethics and public benefit
2007
The gap between law and ethics in human embryonic stem cell research: Overcoming the effect of U.S. Federal policy on research advances and public benefit
2005
Disclosing pathogenic genetic variants to research participants: Quantifying an emerging ethical responsibility
2011
Rules of engagement
2007 Nature
The beliefs, motivations, and expectations of parents who have enrolled their children in a genetic biorepository
2012
From patients to partners: participant-centric initiatives in biomedical research
2012
Whose Personal Control? Creating Private, Personally Controlled Health Records for Pediatric and Adolescent Patients
2008
Multidimensional Results Reporting to Participants in Genomic Studies: Getting It Right
2010
Availability and quality of mobile health app privacy policies
2014
Reestablishing the Researcher-Patient Compact
2007 Science