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Author Details
Full Name
E Clayton
Affiliation
Harvard Medical School, Vanderbilt University, Yale University Yale Law School
ORCID
0000-0002-0308-4110
Career Start Year
1985
Papers
200
H Index
43
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
35942903
Mapping parents' journey following prenatal diagnosis of CHD: a qualitative study.
Cardiol Young
2023
37555276
Pediatric Decision Making: Consensus Recommendations.
Pediatrics
2023
37155245
Ethical Conflicts for Clinicians under Tennessee Abortion Law.
N Engl J Med
2023
37117219
A game theoretic approach to balance privacy risks and familial benefits.
Sci Rep
2023
37343562
Studying the impact of translational genomic research: Lessons from eMERGE.
Am J Hum Genet
2023
37246632
Education and electronic medical records and genomics network, challenges, and lessons learned from a large-scale clinical trial using polygenic risk scores.
Genet Med
2023
37245625
Concordance of International Regulation of Pediatric Health Research.
J Pediatr
2023
37428775
Intellectual conflicts of interest among cardiology and pulmonology clinical practice guidelines.
PLoS One
2023
37128377
A Representativeness-informed Model for Research Record Selection from Electronic Medical Record Systems.
AMIA Annu Symp Proc
2023
36961506
Human-Centered Design to Address Biases in Artificial Intelligence.
J Med Internet Res
2023
36748709
Practical considerations for reinterpretation of individual genetic variants.
Genet Med
2023
36621880
Returning integrated genomic risk and clinical recommendations: The eMERGE study.
Genet Med
2023
36809550
Managing re-identification risks while providing access to the All of Us research program.
J Am Med Inform Assoc
2023
36630592
Avoiding Liability and Other Legal Land Mines in the Evolving Genomics Landscape.
Annu Rev Genomics Hum Genet
2023
34665896
Do research participants share genomic screening results with family members?
J Genet Couns
2022
35614288
LGBTQ+ Perspectives on Conducting Genomic Research on Sexual Orientation and Gender Identity.
Behav Genet
2022
37113452
Implicit Incentives Among Reddit Users to Prioritize Attention Over Privacy and Reveal Their Faces When Discussing Direct-to-Consumer Genetic Test Results: Topic and Attention Analysis.
JMIR Infodemiology
2022
36422086
Outcomes of Returning Medically Actionable Genomic Results in Pediatric Research.
J Pers Med
2022
36048014
Dobbs and the future of health data privacy for patients and healthcare organizations.
J Am Med Inform Assoc
2022
35253644
Stewardship of patient genomic data: A policy statement of the American College of Medical Genetics and Genomics (ACMG).
Genet Med
2022
35246669
Sociotechnical safeguards for genomic data privacy.
Nat Rev Genet
2022
35216901
The reckoning: The return of genomic results to 1444 participants across the eMERGE3 Network.
Genet Med
2022
35275077
The Public Perception of the #GeneEditedBabies Event Across Multiple Social Media Platforms: Observational Study.
J Med Internet Res
2022
35332247
Publisher Correction: Sociotechnical safeguards for genomic data privacy.
Nat Rev Genet
2022
34906493
Correspondence on "Exploring the motivations of research participants who chose not to learn medically actionable secondary findings about themselves" by Schupmann et al.
Genet Med
2022
35341654
Impact of returning unsolicited genomic results to nongenetic health care providers in the eMERGE III Network.
Genet Med
2022
33120418
Combatting human trafficking in the United States: how can medical informatics help?
J Am Med Inform Assoc
2021
33930893
Analysis of conflict of interest policies among organizations producing clinical practice guidelines.
PLoS One
2021
34890225
Using game theory to thwart multistage privacy intrusions when sharing data.
Sci Adv
2021
34524722
Patients with Ehlers-Danlos syndrome on the diagnostic odyssey: Rethinking complexity and difficulty as a hero's journey.
Am J Med Genet C Semin Med Genet
2021
34843533
Direct-to-consumer genetic testing: Prospective users' attitudes toward information about ancestry and biological relationships.
PLoS One
2021
34512997
Protecting research data of publicly revealing participants.
J Law Biosci
2021
34263019
Ethical Issues in Genetics and Infectious Diseases Research: An Interdisciplinary Expert Review.
Ethics Med Public Health
2021
34048695
ISSCR guidelines for the transfer of human pluripotent stem cells and their direct derivatives into animal hosts.
Stem Cell Reports
2021
34048692
ISSCR Guidelines for Stem Cell Research and Clinical Translation: The 2021 update.
Stem Cell Reports
2021
33448306
Enabling realistic health data re-identification risk assessment through adversarial modeling.
J Am Med Inform Assoc
2021
33420344
Does the law require reinterpretation and return of revised genomic results?
Genet Med
2021
31553110
Patients' willingness to reconsider cancer genetic testing after initially declining: Mention it again.
J Genet Couns
2020
31886846
Be Ready to Talk With Parents About Direct-to-Consumer Genetic Testing.
JAMA Pediatr
2020
32716799
From Ventilators to Vaccines: Reframing the Ethics of Resource Allocation.
Am J Bioeth
2020
32898148
Health and kinship matter: Learning about direct-to-consumer genetic testing user experiences via online discussions.
PLoS One
2020
32154515
Can Clinical Genetics Laboratories be Sued for Medical Malpractice?
Ann Health Law Life Sci
2020
32555418
Ethical conflicts in translational genetic research: lessons learned from the eMERGE-III experience.
Genet Med
2020
32365191
Balancing Expediency and Scientific Rigor in Severe Acute Respiratory Syndrome Coronavirus 2 Vaccine Development.
J Infect Dis
2020
32121581
What Results Should Be Returned from Opportunistic Screening in Translational Research?
J Pers Med
2020
32308873
Public Attitudes Toward Direct to Consumer Genetic Testing.
AMIA Annu Symp Proc
2020
32308855
Biomedical Research Cohort Membership Disclosure on Social Media.
AMIA Annu Symp Proc
2020
32329193
Patient perspectives on variant reclassification after cancer susceptibility testing.
Mol Genet Genomic Med
2020
32349224
Returning Results in the Genomic Era: Initial Experiences of the eMERGE Network.
J Pers Med
2020
32369178
Uncertainty of Prenatally Diagnosed Congenital Heart Disease: A Qualitative Study.
JAMA Netw Open
2020
1 - 50 of 200
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Barbara A Koenig
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Janet L Williams
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