Area of research
Genetics · Public Health, Environmental and Occupational Health
Research interest
Research interests include Genomics and Rare Diseases, Ethics in Clinical Research, BRCA gene mutations in cancer, and Biomedical Ethics and Regulation.
The BabySeq Project: A clinical trial of genome sequencing in a diverse cohort of infants
Measuring perceived utility of genomic sequencing: Development and validation of the GENEtic Utility (GENE-U) scale for adult screening
Actionability of unanticipated monogenic disease risks in newborn genomic screening: Findings from the BabySeq Project
Post-trial access in implanted neural device research: Device maintenance, abandonment, and cost
Toward better governance of human genomic data
Perceived Utility of Genomic Sequencing: Qualitative Analysis and Synthesis of a Conceptual Model to Inform Patient-Centered Instrument Development
The road ahead in genetics and genomics
Ventilator Triage Policies During the COVID-19 Pandemic at U.S. Hospitals Associated With Members of the Association of Bioethics Program Directors
Ethical Challenges Arising in the COVID-19 Pandemic: An Overview from the Association of Bioethics Program Directors (ABPD) Task Force
Interpretation of Genomic Sequencing Results in Healthy and Ill Newborns: Results from the BabySeq Project
Perceived Benefits, Risks, and Utility of Newborn Genomic Sequencing in the BabySeq Project
Clarify the HIPAA right of access to individuals’ research data
Returning a Genomic Result for an Adult-Onset Condition to the Parents of a Newborn: Insights From the BabySeq Project
Predispositional genome sequencing in healthy adults: design, participant characteristics, and early outcomes of the PeopleSeq Consortium
The Genomic Medicine Integrative Research Framework: A Conceptual Framework for Conducting Genomic Medicine Research
In support of mitochondrial replacement therapy
The BabySeq project: implementing genomic sequencing in newborns
The Clinical Sequencing Evidence-Generating Research Consortium: Integrating Genomic Sequencing in Diverse and Medically Underserved Populations
Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study
Citizen science, public policy
Should police have access to genetic genealogy databases? Capturing the Golden State Killer and other criminals using a controversial new forensic technique
Genealogy databases and the future of criminal investigation
Automated typing of red blood cell and platelet antigens: a whole-genome sequencing study
Newborn Sequencing in Genomic Medicine and Public Health
The Impact of Whole-Genome Sequencing on the Primary Care and Outcomes of Healthy Adult Patients
A curated gene list for reporting results of newborn genomic sequencing
Creating a data resource: what will it take to build a medical information commons?
Diagnostic Yield of Clinical Tumor and Germline Whole-Exome Sequencing for Children With Solid Tumors
Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine
GINA, Genetic Discrimination, and Genomic Medicine