Gail P. Jarvik

Ph.D., M.D.
Professor and Head, Medicine (Medical Genetics); Professor, Genome Sciences; Adjunct Professor, Epidemiology

Institution(s):

University of Washington Medical Center
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Methods

Quantitative Methods
Survey Research
Electronic Health Records

Disciplines

Genetics/Genomics
Epidemiology

Areas of Expertise

statistical genetics
Complex disease
Adult Medical Genetics
Return of results

Publications

Ethical considerations related to return of results from genomic medicine projects: The eMERGE network (phase III) experience
A template for authoring and adapting genomic medicine content in the eMERGE Infobutton Project
Refining the structure and content of clinical genomic reports
Can next generation sequencing save lives and provide a good economic value in colon cancer prevention?
Insurance coverage does not predict outcomes of genetic testing: The search for meaning in payer decisions for germline cancer tests
Relationship between genetic knowledge and familial communication of CRC risk and intent to communicate CRCP genetic information: Insights from FamilyTalk eMERGE III
Return of results in the genomic medicine projects of the eMERGE network
Ethical and practical guidelines for reporting genetic research results to study participants: Updated guidelines from a National Heart, Lung, and Blood Institute working group
Ethical and practical guidelines for reporting genetic research results to study participants: Updated guidelines from an NHLBI working group
Returning results in the genomic era: Initial experiences of the eMERGE Network
Clinical sequencing exploratory research consortium: Accelerating evidence-based practice of genomic medicine
The clinical sequencing evidence-generating research consortium: Integrating genomic sequencing in diverse and medically underserved populations
Navigating the research–clinical interface in genomic medicine: Analysis from the CSER Consortium
Is ‘incidental finding’ the best term?: A study of patients’ preferences
Public attitudes toward consent and data sharing in biobank research: A large multi-site experimental survey in the U.S.
Parents’ attitudes toward consent and data sharing in biobanks: A multisite experimental survey
Approaches to carrier testing and results disclosure in translational genomics research: The clinical sequencing exploratory research consortium experience
The responsibility to recontact research participants after reinterpretation of genetic and genomic research results
The genomic medicine integrative research framework: A conceptual framework for conducting genomic medicine research
The Feelings About genomiC Testing Results (FACToR) Questionnaire: Development and preliminary validation
Patients' choices for return of exome sequencing results to relatives in the event of their death
The cost-effectiveness of returning incidental findings from next-generation genomic sequencing
Regulatory changes raise troubling questions for genomic testing
Return of incidental findings in genomic medicine: Measuring what patients value--development of an instrument to measure preferences for information from next-generation testing (IMPRINT)
Informed consent in genome-scale research: What do prospective participants think?
Genomic research and wide data sharing: Views of prospective participants
An accessible, relational, inclusive, and actionable (ARIA) model of genetic counseling compared with usual care: Results of a randomized controlled trial
Returning integrated genomic risk and clinical recommendations: The eMERGE study
Familial hypercholesterolemia in the electronic medical records and genomics network: Prevalence, penetrance, cardiovascular risk, and outcomes after return of results
Managing differential performance of polygenic risk scores across groups: Real-world experience of the eMERGE Network

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