W. Burke

Colin C Pritchard, Laura M Amendola, Gail P Jarvik, 2015, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

The cost-effectiveness of returning incidental findings from next-generation genomic sequencing

Gail P Jarvik, David L Veenstra, Wylie Burke, 2014, Genetics in Medicine.

Response to Phillips et al.

G. Jarvik, W. Burke, D. Veenstra, 2015, Genetics in Medicine.

Patient safety in genomic medicine: an exploratory study

Diane M. Korngiebel, S. Fullerton, A. Rubenstein, 2016, Genetics in Medicine.

Return of results: Ethical and legal distinctions between research and clinical care

Gail P Jarvik, Wylie Burke, Barbara J Evans, 2014, American journal of medical genetics. Part C, Seminars in medical genetics.

Comprar Achieving Justice in Genomic Translation Re-Thinking the Pathway to Benefit | Susan Brown Trinidad | 9780195390384 | Oxford University Press

W. Burke, S. B. Trinidad, K. Edwards, 2011 .

Achieving Justice in Genomic Translation: Re-Thinking the Pathway to Benefit

W. Burke, S. B. Trinidad, K. Edwards, 2011 .

The FDA and genomic tests--getting regulation right.

Gail P Jarvik, Wylie Burke, Barbara J Evans, 2015, The New England journal of medicine.

All in the family? Communication of cancer survivors with their families

D. Bowen, W. Burke, J. Hay, 2017, Familial Cancer.

Predictors of recruited melanoma families into a behavioral intervention project.

D. Bowen, W. Burke, M. Asgari, 2012, Contemporary clinical trials.

Communal Coping as a Strategy to Enhance Family Engagement in Dilated Cardiomyopathy

S. Hovick, W. Burke, D. Kinnamon, 2022, Circulation. Genomic and precision medicine.

Responsible Research With Urban American Indians and Alaska Natives.

W. Burke, Katrina G. Claw, M. Taualii, 2018, American journal of public health.

Partnership with the Confederated Salish and Kootenai Tribes: Establishing an Advisory Committee for Pharmacogenetic Research.

W. Burke, S. B. Trinidad, M. Pershouse, 2016, Progress in community health partnerships : research, education, and action.

Ethical Issues in Developing Pharmacogenetic Research Partnerships With American Indigenous Communities

W. Burke, B. Boyer, E. Woodahl, 2011, Clinical pharmacology and therapeutics.

Hereditary haemochromatosis: a realistic approach to prevention of iron overload disease in the population.

W. Burke, G. Imperatore, M. Reyes, 2002, Best practice & research. Clinical haematology.

Genetics and Public Health in the 21st Century

E. Thomson, M. Khoury, W. Burke, 2000 .

Native Hawaiian Views on Biobanking

M. Hudson, W. Burke, Kathryn L. Braun, 2014, Journal of Cancer Education.

Jewish identity and intentions to obtain breast cancer screening.

D. Bowen, E. Eng, W. Burke, 2003, Cultural diversity & ethnic minority psychology.

Diabetes and HFE mutations: cause or coincidence?

W. Burke, G. Imperatore, L. Pinsky, 2002, The Western journal of medicine.

Primary-care physicians’ access to genetic specialists: an impediment to the routine use of genomic medicine?

W. Burke, R. Agans, S. Haga, 2013, Genetics in Medicine.

neurofibromatosis 1 ( NF 1 ) Growth in North American white children with Foundation

W. Burke, R. Bennett, J. Friedman, 2000 .

What influences career choices among graduates of a primary care training program?

W. Burke, J. Curtis, D. Dewitt, 1998, Journal of general internal medicine.

Familial Aggregation of Early-Onset Myocardial Infarction

K. Greenlund, J. Croft, W. Burke, 2002, Public Health Genomics.

Erratum: Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine (American Journal of Human Genetics (2016) 98(6) (1067–1076) (S0002929716301069) (10.1016/j.ajhg.2016.04.011))

Sara Chandros Hull, Robert C. Green, Sean D. Mooney, 2016 .

The Asthma Consultative Process: A Collaborative Approach to Integrating Genomics Into Public Health Practice

W. Burke, T. Harrison, K. Edwards, 2005, Preventing chronic disease.

Temporal order in yeast chromosome replication

W. Burke, W. L. Fangman, 1975, Cell.

ASHG Statement* on Direct-to-Consumer Genetic Testing in the United States

Gail Javitt, Kathy Hudson, Wylie Burke, 2007, Obstetrics and gynecology.

Ethical Considerations in Precision Medicine and Genetic Testing in Internal Medicine Practice: A Position Paper From the American College of Physicians

W. Burke, L. Lehmann, Lois Snyder Sulmasy, 2022, Annals of Internal Medicine.

Genetic Research and Smoking Behavior—Reply

W. Burke, C. Carlsten, 2007 .

Recommendations for the care of individuals with an inherited predisposition to Lynch syndrome: a systematic review.

G. Petersen, W. Burke, N. Lindor, 2006, JAMA.

Hereditary diffuse gastric cancer: association with lobular breast cancer

Janine Senz, Henry T. Lynch, Wylie Burke, 2007, Familial Cancer.

Gene expression profiling and breast cancer care: What are the potential benefits and policy implications?

H. Linden, L. J. Veer, S. Ramsey, 2005, Genetics in Medicine.

Identifying “ownership” through role descriptions to support implementing universal colorectal cancer tumor screening for Lynch Syndrome

Diane M. Korngiebel, W. Burke, K. West, 2017, Genetics in Medicine.

Duty to warn at-risk family members of genetic disease.

W. Burke, A. Laberge, 2009, The virtual mentor : VM.

NIH State-of-the-Science Conference Statement: Role of active surveillance in the management of men with localized prostate cancer.

P. Corso, K. Viswanath, N. Col, 2011, NIH consensus and state-of-the-science statements.

Pharmacogenomic testing to prevent aminoglycoside-induced hearing loss in cystic fibrosis patients: potential impact on clinical, patient, and economic outcomes

R. Gibson, M. Rosenfeld, W. Burke, 2007, Genetics in Medicine.

Offering Individual Genetic Research Results: Context Matters

Laura M. Beskow, Wylie Burke, W. Burke, 2010, Science Translational Medicine.

Family History Assessment to Detect Increased Risk for Colorectal Cancer: Conceptual Considerations and a Preliminary Economic Analysis

M. Khoury, P. Newcomb, S. Ramsey, 2005, Cancer Epidemiology Biomarkers & Prevention.

Genetic risk in context: calculating the penetrance of BRCA1 and BRCA2 mutations.

Wylie Burke, W. Burke, M. Austin, 2002, Journal of the National Cancer Institute.

Recommendations for Follow-up Care of Individuals With an Inherited Predisposition to Cancer: I. Hereditary Nonpolyposis Colon Cancer

E. Thomson, K. Offit, A. McTiernan, 1997 .

Communicating Precision Medicine Research: Multidisciplinary Teams and Diverse Communities

P. Gaffney, P. Spicer, W. Burke, 2022, Public Health Genomics.

Incorporating Principles and Practical Wisdom in Research Ethics Education: A Preliminary Study

Julie O. Culver, Denise M. Dudzinski, L. Robins, 2007, Academic medicine : journal of the Association of American Medical Colleges.

Diverse Perceptions of the Informed Consent Process: Implications for the Recruitment and Participation of Diverse Communities in the National Children’s Study

Kimberley D. Lakes, J. Swanson, W. Burke, 2012, American journal of community psychology.

Extending the reach of public health genomics: What should be the agenda for public health in an era of genome-based and “personalized” medicine?

B. Knoppers, M. Khoury, F. Stanley, 2010, Genetics in Medicine.

Ethics Rounds: Death After Pediatric Dental Anesthesia: An Avoidable Tragedy?

W. Burke, C. Huebner, J. Lantos, 2017, Pediatrics.

Trends in death associated with pediatric dental sedation and general anesthesia

W. Burke, H. Starks, P. Milgrom, 2013, Paediatric anaesthesia.

Potential for genetics to promote public health: genetics research on smoking suggests caution about expectations.

W. Burke, C. Carlsten, 2006, JAMA.

Access and Management: Indigenous Perspectives on Genomic Data Sharing.

W. Burke, Krysta S. Barton, N. Garrison, 2019, Ethnicity & disease.

Genetics researchers’ and IRB professionals’ attitudes toward genetic research review: a comparative analysis

W. Burke, A. Lemke, G. Wiesner, 2012, Genetics in Medicine.

Carnitine palmitoyltransferase 1A P479L and infant death: policy implications of emerging data

W. Burke, M. Austin, N. Garrison, 2017, Genetics in Medicine.

Is Incidental Finding the Best Term? A Study of Patients’ Preferences

B. Wilfond, G. Henderson, Julianne M. O’Daniel, 2016, Genetics in Medicine.

Iron deficiency and iron overload: effects of diet and genes

W. Burke, G. Imperatore, M. Reyes, 2001, The Proceedings of the Nutrition Society.

Whole‐Genome Sequencing in Healthy People

Stephen N. Thibodeau, Wylie Burke, S. Thibodeau, 2017, Mayo Clinic proceedings.

Genetics as a tool to improve cancer outcomes: ethics and policy

W. Burke, N. Press, 2006, Nature Reviews Cancer.

Bioethics of Genetic Testing for Hereditary Breast Cancer

B. Peshkin, W. Burke, 2007 .

Pathways from Autism Spectrum Disorder (ASD) Diagnosis to Genetic Testing

H. Tabor, W. Burke, Krysta S. Barton, 2017, Genetics in Medicine.

Effects of counseling Ashkenazi Jewish women about breast cancer risk.

Julie O. Culver, D. Bowen, W. Burke, 2006, Cultural diversity & ethnic minority psychology.

Effects of risk counseling on interest in breast cancer genetic testing for lower risk women

D. Bowen, A. McTiernan, W. Burke, 2002, Genetics in Medicine.

Explaining the Black-White Disparity in Preterm Birth: A Consensus Statement From a Multi-Disciplinary Scientific Work Group Convened by the March of Dimes

Siobhan M. Dolan, G. Shaw, D. Stevenson, 2021, Frontiers in Reproductive Health.

Precision medicine and health disparities: The case of pediatric acute lymphoblastic leukemia.

W. Burke, K. Thummel, 2019, Nursing outlook.

A Formal Risk-benefit Framework for Genomic Tests: Facilitating the Appropriate Translation of Genomics into Clinical Practice

L. Garrison, S. Ramsey, W. Burke, 2022 .

Newborn Screening Technology: Proceed With Caution

Ellen Wright Clayton, Thomas H Murray, Alfred Berg, 2006, Pediatrics.

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)

S. Fullerton, D. Patrick, G. Jarvik, 2013, Genetics in Medicine.

Genetic Testing

W. Burke, Referral Worksheet, 2019, Definitions.

The complexities of predictive genetic testing

Wylie Burke, James P Evans, W. Burke, 2001, BMJ : British Medical Journal.

Managing incidental genomic findings: legal obligations of clinicians

Ellen Wright Clayton, Wylie Burke, Patricia C. Kuszler, 2013, Genetics in Medicine.

Design, implementation, and first-year outcomes of a value-based drug formulary.

John B. Watkins, L. Garrison, S. Ramsey, 2015, Journal of managed care & specialty pharmacy.

Practice Implications of Expanded Genetic Testing in Oncology

Diane M. Korngiebel, Jennifer M. Zech, S. Fullerton, 2019, Cancer investigation.

Population description and its role in the interpretation of genetic association

S. Fullerton, W. Burke, Kelly A Fryer-Edwards, 2010, Human Genetics.

Mammography American Cancer Society Guidelines for Breast Screening with MRI as an Adjunct to

E. Pisano, M. Schnall, E. Morris, 2008 .

Stakeholder Perspectives on Returning Nonactionable Apolipoprotein L1 (APOL1) Genetic Results to African American Research Participants

S. Fullerton, W. Burke, E. Blacksher, 2021, Journal of empirical research on human research ethics : JERHRE.

At the Research-Clinical Interface: Returning Individual Genetic Results to Research Participants.

S. Fullerton, W. Burke, B. Young, 2020, Clinical journal of the American Society of Nephrology : CJASN.

Discordance in selected designee for return of genomic findings in the event of participant death and estate executor

S. Fullerton, G. Jarvik, W. Burke, 2017, Molecular genetics & genomic medicine.

Community dissemination and genetic research: Moving beyond results reporting

W. Burke, E. Ludman, S. Hopkins, 2015, American Journal of Medical Genetics. Part A.

Deliberate deceit of family members: a challenge to providers of clinical genetics services.

M. Greene, B. Wilfond, W. Burke, 2006, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Application of population screening principles to genetic screening for adult-onset conditions.

M. Khoury, S. Coughlin, D. Weed, 2001, Genetic testing.

Pharmacogenomics in diverse practice settings: implementation beyond major metropolitan areas.

W. Burke, Susan Brown Trinidad, E. Woodahl, 2015, Pharmacogenomics.

Is there a duty to reinterpret genetic data? The ethical dimensions

W. Chung, E. Parens, P. Appelbaum, 2019, Genetics in Medicine.

Breast cancer risk communication: Assessment of primary care physicians by standardized patients

Julie O. Culver, D. Bowen, W. Burke, 2009, Genetics in Medicine.

A reality check for personalized medicine

M. Khoury, W. Burke, JamesT. Evans, 2010, Nature.

Improving recommendations for genomic medicine: building an evolutionary process from clinical practice advisory documents to guidelines

Ellen Wright Clayton, Susan M Wolf, Diane M. Korngiebel, 2019, Genetics in Medicine.

Genetics education for primary-care providers

Jon Emery, Wylie Burke, J. Emery, 2002, Nature reviews genetics.

Current priorities for public health practice in addressing the role of human genomics in improving population health.

M. Khoury, R. Coates, N. Dowling, 2011, American journal of preventive medicine.

Human Genome Epidemiology: A Scientific Foundation for Using Genetic Information to Improve Health and Prevent Disease

M. Khoury, J. Little, W. Burke, 2003 .

Effects of Individual and Family Functioning on Interest in Genetic Testing

Emily Bourcier, D. Bowen, W. Burke, 2004, Public Health Genomics.

Precision medicine research with American Indian and Alaska Native communities: Results of a deliberative engagement with tribal leaders.

W. Burke, S. Hopkins, B. Boyer, 2021, Genetics in medicine : official journal of the American College of Medical Genetics.

Exploring pathways to trust: a tribal perspective on data sharing

W. Burke, R. Whitener, Rosalina James, 2014, Genetics in Medicine.

Native Hawaiian Views on Biobanking

M. Hudson, W. Burke, Kathryn L. Braun, 2014, Journal of Cancer Education.

Measuring Attitudes About Alcohol Misuse and Dependence Among Alaska Native People Within a Tribal Health Care System.

W. Burke, E. Ludman, D. Donovan, 2022, Journal of addiction medicine.

Genomics as a probe for disease biology.

Wylie Burke, W. Burke, 2003, The New England journal of medicine.

Hereditary hemochromatosis: gene discovery and its implications for population-based screening.

F. Collins, E. Thomson, E. Clayton, 1998, JAMA.

Clinical and public health implications of emerging genetic technologies.

W. Burke, A. Laberge, 2010, Seminars in nephrology.

Familial pancreatic adenocarcinoma: association with diabetes and early molecular diagnosis.

M. Kimmey, D. Byrd, W. Burke, 1995, Journal of medical genetics.

ASHG Statement* on Direct-to-Consumer Genetic Testing in the United States

Gail Javitt, Peter Byers, Kathy Hudson, 2007, Obstetrics and gynecology.

Anticipating dissemination of cancer genomics in public health: A theoretical approach to psychosocial and behavioral challenges

D. Bowen, W. Burke, M. Asgari, 2007, Annals of behavioral medicine : a publication of the Society of Behavioral Medicine.

Differential use of available genetic tests among primary care physicians in the United States: results of a national survey

D. Levy, W. Burke, Alexandra E. Shields, 2008, Genetics in Medicine.

Ethical issues in identifying and recruiting participants for familial genetic research

Jeremy Sugarman, Wylie Burke, L. Ross, 2004, American journal of medical genetics. Part A.

Challenges in communicating genetics: A public health approach

James F. Thrasher, M. Khoury, W. Burke, 2000, Genetics in Medicine.

Research Practice and Participant Preferences: The Growing Gulf

Stephanie M. Fullerton, Gail P. Jarvik, Eric B. Larson, 2011, Science.

Dietary and genetic influences on hemostasis in a Yup’ik Alaska Native population

T. Thornton, W. Burke, A. Rettie, 2017, PloS one.

Pharmacogenetic testing: not as simple as it seems

W. Burke, S. Haga, 2008, Genetics in Medicine.

Pathways from autism spectrum disorder diagnosis to genetic testing

H. Tabor, W. Burke, Krysta S. Barton, 2017, Genetics in Medicine.

Primary care physicians' knowledge of and experience with pharmacogenetic testing

W Burke, G. Ginsburg, W. Burke, 2012, Clinical genetics.

Return of individual research results from genome-wide association studies: experience of the Electronic Medical Records and Genomics (eMERGE) Network

Marylyn D. Ritchie, Joshua C. Denny, Eugenia R. McPeek Hinz, 2012, Genetics in Medicine.

P450 Pharmacogenetics in Indigenous North American Populations

W. Burke, Katrina G. Claw, B. Boyer, 2018, Journal of personalized medicine.

Cytochrome P450 Enzyme Polymorphism Frequency in Indigenous and Native American Populations: A Systematic Review

David L. Veenstra, Wylie Burke, W. Burke, 2008, Public Health Genomics.

Long-term outcomes of the "Genetics in Primary Care" faculty development initiative.

Penny Kyler, Wylie Burke, Kelly Fryer-Edwards, 2009, Family medicine.

Genetic testing in primary care.

W. Burke, 2004, Annual review of genomics and human genetics.

Predictive and Precision Medicine with Genomic Data.

Robert C Green, Linnea M Baudhuin, Leslie G Biesecker, 2019, Clinical chemistry.

Clinical decisions. Screening an asymptomatic person for genetic risk.

W. Burke, D. Dimmock, 2014, The New England journal of medicine.

Patient safety in genomic medicine: an exploratory study

Diane M. Korngiebel, S. Fullerton, W. Burke, 2016, Genetics in Medicine.

Offering aggregate results to participants in genomic research: opportunities and challenges

Stephanie M. Fullerton, Richard R. Sharp, Laura M. Beskow, 2012, Genetics in Medicine.

Genetic screening.

W. Burke, B. Tarini, N. Press, 2003, Nursing standard (Royal College of Nursing (Great Britain) : 1987).

Randomized trial of a web-based survivor intervention on melanoma prevention behaviors of first-degree relatives

D. Bowen, W. Burke, J. Hay, 2018, Cancer Causes & Control.

Hereditary hemochromatosis: Perspectives of public health, medical genetics, and primary care

A. Motulsky, L. Bradley, W. Burke, 2003, Genetics in Medicine.

Closing the Gap between Knowledge and Clinical Application: Challenges for Genomic Translation

Diane M. Korngiebel, W. Burke, 2015, PLoS genetics.

Apolipoprotein L1 Testing in African Americans: Involving the Community in Policy Discussions

S. Fullerton, James G. Wilson, B. Freedman, 2019, American Journal of Nephrology.

If you build it, they will come: unintended future uses of organised health data collections

W. Burke, B. Koenig, N. Hallowell, 2016, BMC medical ethics.

Personalized Medicine and Tobacco-Related Health Disparities: Is There a Role for Genetics?

W. Burke, C. Carlsten, Abigail C. Halperin, 2011, The Annals of Family Medicine.

Stakeholder Perspectives on a Risk-Benefit Framework for Genetic Testing

S. Ramsey, W. Burke, J. Roth, 2010, Public Health Genomics.

The Genomic Applications in Practice and Prevention Network

Rebekah Rasooly, Muin J Khoury, Teri Manolio, 2009, Genetics in Medicine.

Participation in Breast Cancer Genetic Counseling: The Influence of Educational Level, Ethnic Background, and Risk Perception

Julie O. Culver, W. Burke, Y. Yasui, 2001, Journal of Genetic Counseling.

Genetic counseling for women with an intermediate family history of breast cancer.

Julie O. Culver, D. Bowen, A. McTiernan, 2000, American journal of medical genetics.

Family history as a predictor of asthma risk.

Wylie Burke, W. Burke, M. Fesinmeyer, 2003, American journal of preventive medicine.

Breast cancer risk counseling improves women's functioning.

D. Bowen, A. McTiernan, W. Burke, 2004, Patient education and counseling.

Predicting breast cancer screening intentions and behavior with emotion and cognition.

Wylie Burke, D. Bowen, A. McTiernan, 2003 .

The Challenge of Genetic Variants of Uncertain Clinical Significance

W. Chung, E. Parens, P. Appelbaum, 2022, Annals of Internal Medicine.

An economic viewpoint on alternative strategies for identifying persons with hereditary nonpolyposis colorectal cancer

S. Ramsey, W. Burke, L. Clarke, 2003, Genetics in Medicine.

The rules remain the same for genomic medicine: The case against “reverse genetic exceptionalism”

Wylie Burke, M. Khoury, James P Evans, 2010, Genetics in Medicine.

Effectiveness of the Family Heart Talk Communication Tool in Improving Family Member Screening for Dilated Cardiomyopathy: Results of a Randomized Trial

G. Ewald, M. Wheeler, S. Gottlieb, 2023, Circulation.

The advent of the ‘unpatients’

Albert R. Jonsen, Wylie Burke, Arno G. Motulsky, 1996, Nature Medicine.

Genetics in Primary Care: A USA Faculty Development Initiative

Jeffery R. Botkin, Linda E. Pinsky, Wylie Burke, 2002, Public Health Genomics.

Use of Factor V Leiden genetic testing in practice and impact on management

B. Psaty, L. Hindorff, W. Burke, 2009, Genetics in Medicine.

Systems medicine and the public's health

Wylie Burke, Susan Brown Trinidad, W. Burke, 2011, Genome Medicine.

Genetic assessment of breast cancer risk in primary care practice

Julie O. Culver, W. Burke, Y. Yasui, 2009, American journal of medical genetics. Part A.

Contributions of Public Health to Genetics Education for Health Care Professionals

W. Burke, 2005, Health education & behavior : the official publication of the Society for Public Health Education.

Risk, reward, and the double-edged sword: perspectives on pharmacogenetic research and clinical testing among Alaska Native people.

W. Burke, H. Starks, J. Shaw, 2013, American journal of public health.

Risk,Reward,andtheDouble-EdgedSword:Perspectives onPharmacogeneticResearchandClinicalTestingAmong AlaskaNativePeople

W. Burke, H. Starks, J. Shaw, 2013 .

Re: On the use of familial aggregation in population-based case probands for calculating penetrance.

W. Burke, M. Austin, 2003, Journal of the National Cancer Institute.

Pharmacogenetic research in partnership with American Indian and Alaska Native communities.

L. Lesko, W. Burke, S. Hopkins, 2014, Pharmacogenomics (London).

Defining purpose: a key step in genetic test evaluation

W. Burke, R. Zimmern, M. Kroese, 2007, Genetics in Medicine.

Can Precision Medicine Reduce the Burden of Diabetes?

W. Burke, David P. Schenck, S. Trinidad, 2019, Ethnicity & disease.

The human genome at ten

T. Golub, J. Venter, M. Khoury, 2010, Nature.

Prenatal Pharmacogenomics: A promising area for research

W. Burke, M. Hebert, K. Thummel, 2016, The Pharmacogenomics Journal.

Breast cancer and hormone replacement therapy

A. LaCroix, W. Burke, 1997, The Lancet.

Patients' Choices for Return of Exome Sequencing Results to Relatives in the Event of Their Death

S. Fullerton, B. Evans, G. Jarvik, 2015, Journal of Law, Medicine & Ethics.

Educational Needs in Genetic Medicine: Primary Care Perspectives

Penny Kyler, Susan B. Trinidad, Wylie Burke, 2008, Public Health Genomics.

The Precautionary Principle for Shift-Work Research and Decision-Making

W. Burke, C. Adams, E. Blacksher, 2018, Public health ethics.

Achieving utility with family history: colorectal cancer risk.

D. Bowen, W. Burke, E. Ludman, 2003, American journal of preventive medicine.

Breast carcinoma genetics from a primary care perspective

W. Burke, L. Pinsky, N. Press, 1997 .

Experiences of patients seeking to participate in variant of uncertain significance reclassification research

D. Bowen, W. Burke, Sukh Makhnoon, 2018, Journal of Community Genetics.

Ensuring the appropriate use of genetic tests

Wylie Burke, W. Burke, R. Zimmern, 2004, Nature Reviews Genetics.

Health System Implications of Direct-to-Consumer Personal Genome Testing

A. McGuire, W. Burke, 2010, Public Health Genomics.

Does genomic risk information motivate people to change their behavior?

Wylie Burke, D. Bowen, W. Burke, 2009, Genome Medicine.

Delivery of primary care to women

A. LaCroix, T. Koepsell, R. Deyo, 2007, Journal of General Internal Medicine.

From Leaky Pipeline to Irrigation System: Minority Education Through the Lens of Community-Based Participatory Research

W. Burke, H. Starks, Rosalina James, 2012, Progress in community health partnerships : research, education, and action.

Categorizing genetic tests to identify their ethical, legal, and social implications.

W Burke, W. Burke, L. Pinsky, 2001, American journal of medical genetics.

Motivating factors for physician ordering of factor V Leiden genetic tests.

T. Lumley, B. Psaty, L. Hindorff, 2009, Archives of internal medicine.

The Deceptive Appeal of Direct-to-Consumer Genetics

W. Burke, S. Trinidad, 2016, Annals of Internal Medicine.

Genetic screening.

W. Burke, B. Tarini, N. Press, 2011, Epidemiologic reviews.

Uncertainties in genetic testing for chronic disease.

H. Welch, W. Burke, Welch Hg, 1998, JAMA.

Ethical issues arising from the participation of children in genetic research.

W. Burke, D. Diekema, 2006, The Journal of pediatrics.

Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.

Matthew S. Lebo, Victoria A. Miller, Jeffrey W. Pennington, 2016, American journal of human genetics.

Building Partnerships in Community-Based Participatory Research

W. Burke, S. Hopkins, B. Boyer, 2014, Health promotion practice.

Handbook of professional ethics for psychologists : issues, questions, and controversies

Denise M. Dudzinski, L. Robins, W. Burke, 2003 .

The Aging Cystic Fibrosis Patient: Presentations and Problems

W. Burke, M. Aitken, 1994 .

Informed consent for population-based research involving genetics.

M Gwinn, M J Khoury, M. Khoury, 2001, JAMA.

Genetic information: Special or not? Responses from focus groups with members of a health maintenance organization

Julie O. Culver, D. Bowen, W. Burke, 2007, American journal of medical genetics. Part A.

Genetic Architecture of Dilated Cardiomyopathy in Individuals of African and European Ancestry.

G. Ewald, M. Wheeler, H. Rehm, 2023, JAMA.

Glutathione S-transferase M1 (GSTM1) polymorphisms and lung cancer: a literature-based systematic HuGE review and meta-analysis.

J. Higgins, W. Burke, W. Burke, 2008, American journal of epidemiology.

Finding a Place for Genomics in Health Disparities Research

S. Fullerton, W. Burke, S. Fullerton, 2012, Public Health Genomics.

Recommendations for follow-up care of individuals with an inherited predisposition to cancer. I. Hereditary nonpolyposis colon cancer. Cancer Genetics Studies Consortium.

E. Thomson, K. Offit, A. McTiernan, 1997, JAMA.

Cultural basis for differences between US and French clinical recommendations for women at increased risk of breast and ovarian cancer

N. Holtzman, G. Geller, W. Burke, 1999, The Lancet.

Women's interest in genetic testing for breast cancer susceptibility may be based on unrealistic expectations.

W. Burke, Y. Yasui, N. Press, 2001, American journal of medical genetics.

The Feelings About genomiC Testing Results (FACToR) Questionnaire: Development and Preliminary Validation.

S. Fullerton, P. Heagerty, D. Patrick, 2019, Journal of genetic counseling.

Seeking Genomic Knowledge: The Case for Clinical Restraint.

Ellen Wright Clayton, Wylie Burke, Susan Brown Trinidad, 2013, The Hastings law journal.

Looking for Trouble and Finding It

S. Fullerton, W. Burke, S. Trinidad, 2015, The American journal of bioethics : AJOB.

Recombinant human DNase inhalation in normal subjects and patients with cystic fibrosis. A phase 1 study.

S. Shak, W. Burke, A. Smith, 1992, JAMA.

Debating Clinical Utility

W. Burke, N. Press, W. Burke, 2010, Public Health Genomics.

Comparisons of two breast cancer risk estimates in women with a family history of breast cancer.

D. Bowen, A. McTiernan, Y. Yasui, 2001, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

Cases in Precision Medicine: Is There an Obligation to Return Reinterpreted Genetic Results to Former Patients?

E. Parens, P. Appelbaum, W. Burke, 2023, Annals of Internal Medicine.

Implementation outcomes of a multiinstitutional web-based ethical, legal, and social implications genetics curriculum for primary care residents in three specialties

Frank C. Day, M. Srinivasan, R. Pagon, 2011, Genetics in Medicine.

Re: "Invited commentary: genes, environment, and hybrid vigor".

W. Burke, C. Carlsten, 2010, American journal of epidemiology.

Genetics of Hypertension – An Overview

A. Motulsky, W. Burke, 1991 .

Assessing the Potential Success of Cystic Fibrosis Carrier Screening: Lessons Learned from Tay-Sachs Disease and β-Thalassemia

W. Burke, A. Laberge, C. Watts, 2009, Public Health Genomics.

Recommendations for follow-up care of individuals with an inherited predisposition to cancer. II. BRCA1 and BRCA2. Cancer Genetics Studies Consortium.

K Offit, C Varricchio, E. Thomson, 1997, JAMA.

Attitudes and interest in genetic testing for breast and ovarian cancer susceptibility in diverse groups of women in western Washington.

D. Bowen, A. McTiernan, W. Burke, 1999, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.

Joseph S. Salama, W. Chung, I. Krantz, 2016, American journal of human genetics.

Informed Consent in Translational Genomics: Insufficient Without Trustworthy Governance

Kathleen M. Brelsford, S. Fullerton, W. Burke, 2018, Journal of Law, Medicine & Ethics.

Offering Individual Genetic Research Results: Context Matters

W. Burke, L. Beskow, 2010, Science Translational Medicine.

Genomics, Health Disparities, and Missed Opportunities for the Nation's Research Agenda.

W. Burke, E. Blacksher, K. West, 2017, JAMA.

Educational Needs in Genetic Medicine: Primary Care Perspectives

W. Burke, Kelly A Fryer-Edwards, M. Lloyd-Puryear, 2008, Public Health Genomics.

Glad You Asked: Participants' Opinions of Re-Consent for DbGap Data Submission

S. Fullerton, E. Larson, G. Jarvik, 2010, Journal of empirical research on human research ethics : JERHRE.

Practical Ethics: Establishing a Pathway to Benefit for Complex Pharmacogenomic Tests

W. Burke, S. Haga, Wylie Burke, 2011, Clinical pharmacology and therapeutics.

Randomized trial of a web-based survivor intervention on melanoma prevention behaviors of first-degree relatives

D. Bowen, W. Burke, J. Hay, 2018, Cancer Causes & Control.

Communication Among Melanoma Family Members

D. Bowen, T. Albrecht, W. Burke, 2017, Journal of health communication.

Genetics, Health Care and Public Policy: Foreword

W. Burke, 2007 .

A formal risk-benefit framework for genomic tests: Facilitating the appropriate translation of genomics into clinical practice

L. Garrison, S. Ramsey, W. Burke, 2010, Genetics in Medicine.

Teaching with single nucleotide polymorphisms: Learning the right lessons

W. Burke, J. Evans, 2011, Genetics in Medicine.

Clinician-Stakeholders’ Perspectives on Using Patient Portals to Return Lynch Syndrome Screening Results

Diane M. Korngiebel, W. Burke, K. West, 2018, Journal of Genetic Counseling.

The effect of Mycoplasma contamination on the in vitro assay of pyruvate dehydrogenase activity in cultured fibroblasts.

W. Burke, D. Farrell, A. Clark, 1978, Clinica chimica acta; international journal of clinical chemistry.

Standardizing return of participant results

Suzanne Bakken, Jeffrey R. Botkin, James H. Nichols, 2018, Science.

Large de novo DNA deletion in a patient with sporadic neurofibromatosis 1, mental retardation, and dysmorphism.

W. Burke, R. Bennett, V. Riccardi, 1992, Journal of medical genetics.

Impact of Value-Based Benefits on Use of and Adherence to Drugs in 3 Disease Cohorts

John B. Watkins, L. Garrison, S. Ramsey, 2015 .

Proceedings from the 9th annual conference on the science of dissemination and implementation

Caitlin N. Dorsey, Robert D. Lieberthal, Julie E. Reed, 2017, Implementation Science.

Translational Genomics: Seeking a Shared Vision of Benefit

Patricia C. Kuszler, W. Burke, H. Starks, 2008, The American journal of bioethics : AJOB.

ERRATUM: Processes and preliminary outputs for identification of actionable genes as incidental findings in genomic sequence data in the Clinical Sequencing Exploratory Research Consortium

N. Spinner, R. Green, L. Garraway, 2014, Genetics in Medicine.