M.D., University of Washington, 1978.
Ph.D., University of Washington, 1974.
Dr. Burke is an expert in the implications and appropriate use of genetic information in clinical and public health practice. Her research addresses the bioethical and health policy implications of genetic technology.
American Public Health Association
American Society of Human Genetics
Association for Prevention Teaching and Research
Society of General Internal Medicine
Actionable, pathogenic incidental findings in 1,000 participants' exomes.. American journal of human genetics. 93(4):631-40.. 2013.
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).. Genetics in medicine : official journal of the American College of Medical Genetics.. 2013.
The OHRP and SUPPORT.. The New England journal of medicine. 368(25):e36.. 2013.
Primary-care physicians' access to genetic specialists: an impediment to the routine use of genomic medicine? Genetics in medicine : official journal of the American College of Medical Genetics.. 2013.
Maternal perspectives on the return of genetic results: context matters.. American journal of medical genetics. Part A. 161A(1):38-47.. 2013.
Managing incidental genomic findings: legal obligations of clinicians.. Genetics in medicine : official journal of the American College of Medical Genetics.. 2013.
Recommendations for returning genomic incidental findings? We need to talk! Genetics in medicine : official journal of the American College of Medical Genetics.. 2013.
Building Partnerships in Community-Based Participatory Research: Budgetary and Other Cost Considerations.. Health promotion practice.. 2013.
From leaky pipeline to irrigation system: minority education through the lens of community-based participatory research.. Progress in community health partnerships : research, education, and action. 6(4):471-9.. 2012.
Next-generation sequencing in the clinic: are we ready? Nature reviews. Genetics. 13(11):818-24.. 2012.
Informed Consent in Genome-Scale Research: What Do Prospective Participants Think? AJOB primary research. 3(3):3-11.. 2012.
Predictors of recruited melanoma families into a behavioral intervention project.. Contemporary clinical trials. 33(1):85-92.. 2012.
Return of individual research results from genome-wide association studies: experience of the Electronic Medical Records and Genomics (eMERGE) Network.. Genetics in medicine : official journal of the American College of Medical Genetics.. 2012.
Beneficence, clinical urgency, and the return of individual research results to relatives.. The American journal of bioethics : AJOB. 12(10):9-10.. 2012.
Stakeholder perspectives on a risk-benefit framework for genetic testing.. Public health genomics. 14(2):59-67.. 2011.
Offering individual genetic research results: context matters.. Science translational medicine. 2(38):38cm20.. 2010.
Will Knowledge of Gene-based Colorectal Cancer Disease Risk Influence Quality of Life and Screening Behavior? Findings from a Population-based Study. Public health genomics. 13(1):nihpa102310.. 2010.
Breast cancer risk communication: assessment of primary care physicians by standardized patients.. Genetics in medicine : official journal of the American College of Medical Genetics. 11(10):735-41.. 2009.
Genetic assessment of breast cancer risk in primary care practice.. American journal of medical genetics. Part A. 149A(3):349-56.. 2009.