Barbara A Koenig

Barbara A Koenig

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Barbara A Koenig

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Hospital Responses to the End of Life Option Act: Implementation of Aid in Dying in California.

JAMA Intern Med 2019 Apr 8. Epub 2019 Apr 8.

Division of General Internal Medicine and Health Services Research, University of California, Los Angeles, Los Angeles.

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http://dx.doi.org/10.1001/jamainternmed.2018.8690DOI Listing
April 2019

Importance of Participant-Centricity and Trust for a Sustainable Medical Information Commons.

J Law Med Ethics 2019 Mar;47(1):12-20

Amy L. McGuire, J.D., Ph.D., is the Leon Jaworski Professor of Biomedical Ethics and Director of the Center for Medical Ethics and Health Policy at Baylor College of Medicine. Dr. McGuire serves on the program committee for the Greenwall Foundation Faculty Scholars Program in Bioethics and is immediate past president of the Association of Bioethics Program Directors. Mary A. Majumder, J.D., Ph.D., is an Associate Professor of Medicine at the Center for Medical Ethics and Health Policy, Baylor College of Medicine. Angela G. Villanueva, M.P.H., is a Research Associate at the Center for Medical Ethics and Health Policy at Baylor College of Medicine. Jessica Bardill, Ph.D., is an Assistant Professor of Indigenous Canadian Literatures and Cultures at Concordia University in Montreal, Quebec. Juli M. Bollinger, M.S., is a Research Associate in the Center for Medical Ethics and Health Policy at the Baylor College of Medicine and a Research Associate and Associate Faculty at the Berman Institute of Bioethics at Johns Hopkins University. Eric Boerwinkle, Ph.D., is the Dean of the University of Texas Health Science Center at Houston, School of Public Health and the Associate Director, Human Genome Sequencing Center at Baylor College of Medicine. Tania Bubela, Ph.D., J.D., is the Dean of the Faculty of Health Sciences at Simon Fraser University and a Fellow of the Canadian Academy of Health Sciences. Patricia Deverka, M.D., M.S., M.B.E., is Director, Value Evidence and Outcomes at Geisinger National Precision Health, where she focuses Outcomes at Geisinger National Precision Health, where she focuses systems and policymakers. Barbara Evans, MS, Ph.D., J.D., LL.M., is the Mary Ann and Lawrence E. Faust Professor of Law and Director of the Center for Biotechnology & Law at the University of Houston Law Center and holds a joint appointment as Professor of Electrical and Computer Engineering at the UH Cullen College of Engineering. Nanibaa' A. Garrison, Ph.D. (Navajo), is an Assistant Professor at the Treuman Katz Center for Pediatric Bioethics at Seattle Children's Hospital and Research Institute and at the Department of Pediatrics at the University of Washington School of Medicine. David Glazer is an engineering director at Verily Life Sciences, where he helps life science organizations use cloud computing to accelerate and scale their work with big data. Melissa M. Goldstein, J.D., is an Associate Professor in the Department of Health Policy and Management at the Milken Institute School of Public Health at the George Washington University. Henry T. Greely, J.D., is the Deane F. and Kate Edelman Johnson Professor of Law and a professor (by courtesy) of Genetics at Stanford University, where he directs the Center for Law and the Biosciences. He is President of the International Neuroethics Society, co-chair of the Neuroethics Work Group of the NIH BRAIN Initiative, and a member of the National Academies' Committee on Science, Technology, and Law. Scott D. Kahn, Ph.D., is the Chief Information Officer at LunaDNA where he is responsible for all informatics and data science strategy. Bartha M. Knoppers, Ph.D., (Comparative Medical Law), is a Full Professor, Canada Research Chair in Law and Medicine and Director of the Centre of Genomics and Policy of the Faculty of Medicine at McGill University. Barbara A. Koenig, Ph.D., is Professor of Bioethics and Medical Anthropology, based at the Institute for Health & Aging, University of California, San Francisco. She also serve as Director of the UCSF Program in Bioethics. J. Mark Lambright, M.B.A., is the Chairman, Trident Advisors, LLC - CEO (Interim), Private Access, Inc. Mark Lambright has been a senior executive of a number of healthcare and technology companies ranging in size from startup to multi-billion in revenue. John Mattison, M.D., is Assistant Medical Director, KP, SCAL, Chief Health Information Officer. Founder of CDA/CCD (XML standard for healthcare interoperability). Co-Editor of Healthcare Information Technology (2017 McGraw Hill). Christopher J. O'Donnell, M.D., M.P.H., is Chief, Cardiology Section and Director, Center for Population Genomics, of the Boston VA Healthcare System and co-Principal Investigator (Chief Scientist) of the national VA Million Veteran Program; and is VA Contact Principal Investigator of the NIH All of Us Research Program. He is also a faculty member of the Department of Medicine, Brigham and Women's Hospital and Associate Professor of Medicine, Harvard Medical School. Arti K. Rai, J.D., is the Elvin R. Latty Professor of Law and co-Director of the Center for Innovation Policy at Duke Law. Laura L. Rodriguez, Ph.D., is the Director of the Division of Policy, Communications, and Education at the National Human Genome Research Institute. Tania Simoncelli, M.S., is the Director of Science Policy at the Chan Zuckerberg Initiative. Formerly Executive Director, Count Me In at the Broad Institute, Assistant Director of Forensic Science and Biomedical Innovation, White House Office of Science & Technology Policy, and Science Advisor to the American Civil Liberties Union. Sharon F. Terry, M.A., is the president and CEO of Genetic Alliance. Adrian Thorogood, B.C.L./LL.B., is a lawyer and Academic Associate at the Centre of Genomics and Policy at McGill University in Montreal, Canada. He manages the Regulatory and Ethics Work Stream of the Global Alliance for Genomics and Health. Michael S. Watson, M.S., Ph.D., is the Executive Director, American College of Medical Genetics and Genomics and ACMG Foundation for Genetic and Genomic Medicine and an Adjunct Professor of Pediatrics at Washington University School of Medicine. John T. Wilbanks is the Chief Commons Officer at Sage Bionetworks, and co-PI on awards for AllofUs Research Program, ELSI Issues in Unregulated Mobile Research, CTSA Center for Data To Health. Robert Cook-Deegan, M.D., is a Professor in the School for the Future of Innovation in Society at Arizona State University.

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http://dx.doi.org/10.1177/1073110519840480DOI Listing
March 2019

Characterizing the Biomedical Data-Sharing Landscape.

J Law Med Ethics 2019 Mar;47(1):21-30

Angela G. Villanueva, M.P.H., is a Research Associate at the Center for Medical Ethics and Health Policy at Baylor College of Medicine. Robert Cook-Deegan, M.D., is a Professor in the School for the Future of Innovation in Society at Arizona State University. Barbara A. Koenig, Ph.D., is Professor of Bioethics and Medical Anthropology, based at the Institute for Health & Aging, University of California, San Francisco. Patricia A. Deverka, M.D., M.S., M.B.E., is Director, Value Evidence and Outcomes at Geisinger National Precision Health, where she focuses on demonstrating the value of genomic sequencing for health systems and policy-makers.Erika Versalovic is a Ph.D. student in the philosophy department at the University of Washington and a neuroethics fellow with the Center for Neurotechnology in Seattle, WA. Amy L. McGuire, J.D., Ph.D., is the Leon Jaworski Professor of Biomedical Ethics and Director of the Center for Medical Ethics and Health Policy at Baylor College of Medicine. Mary A. Majumder, J.D., Ph.D., is an Associate Professor of Medicine at the Center for Medical Ethics and Health Policy, Baylor College of Medicine.

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http://dx.doi.org/10.1177/1073110519840481DOI Listing
March 2019

Hopeful and Concerned: Public Input on Building a Trustworthy Medical Information Commons.

J Law Med Ethics 2019 Mar;47(1):70-87

Patricia A. Deverka, M.D., M.S., M.B.E., is Director, Value Evidence and Outcomes at Geisinger National Precision Health, where she focuses on demonstrating the value of genomic sequencing for health systems and policymakers. Dierdre Gilmore, M.A., is a Senior Researcher at the American Institutes for Research. Gilmore earned a MA in Medical Anthropology at the University of London. Jennifer Richmond, M.S.P.H., is a Research Associate at the American Institutes for Research and a doctoral student in the Department of Health Behavior at the University of North Carolina at Chapel Hill (UNC-CH) Gillings School of Global Public Health. Zachary Smith is a Research Assistant at the American Institutes for Research. Rikki Mangrum, M.L.S., is a Senior Research Scientist at the American Institutes for Research. Barbara A. Koenig, Ph.D., is Professor of Bioethics and Medical Anthropology, based at the Institute for Health & Aging, University of California, San Francisco. She serves as Director of the UCSF Program in Bioethics. Robert Cook-Deegan, M.D., is a Professor in the School for the Future of Innovation in Society at Arizona State University. He is a physician and molecular biologist who turned to policy and then entered academe through Georgetown, Stanford, and Duke Universities before joining ASU. Angela G. Villanueva, M.P.H., is a Research Associate at the Center for Medical Ethics and Health Policy at Baylor College of Medicine. Mary A. Majumder, J.D., Ph.D., is an Associate Professor of Medicine at the Center for Medical Ethics and Health Policy, Baylor College of Medicine. Amy L. McGuire, J.D., Ph.D., is the Leon Jaworski Professor of Biomedical Ethics and Director of the Center for Medical Ethics and Health Policy at Baylor College of Medicine. Dr. McGuire serves on the program committee for the Greenwall Foundation Faculty Scholars Program in Bioethics and is immediate past president of the Association of Bioethics Program Directors.

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http://dx.doi.org/10.1177/1073110519840486DOI Listing
March 2019

The Role of Participants in a Medical Information Commons.

J Law Med Ethics 2019 Mar;47(1):51-61

Mary A. Majumder, J.D., Ph.D., is an Associate Professor of Medicine at the Center for Medical Ethics and Health Policy, Baylor College of Medicine. Juli M. Bollinger, M.S., is a Research Associate in the Center for Medical Ethics and Health Policy at the Baylor College of Medicine and a Research Associate and Associate Faculty at the Berman Institute of Bioethics at Johns Hopkins University. Angela G. Villanueva, M.P.H., is a Research Associate at the Center for Medical Ethics and Health Policy at Baylor College of Medicine. Patricia A. Deverka, M.D., M.S., M.B.E., is Director, Value Evidence and Outcomes at Geisinger National Precision Health, where she focuses on demonstrating the value of genomic sequencing for health systems and policymakers. Barbara A. Koenig, Ph.D., is Professor of Bioethics and Medical Anthropology, based at the Institute for Health & Aging, University of California, San Francisco. She serves as Director of the UCSF Program in Bioethics. Previously, Prof. Koenig was the founding executive director of the Center for Biomedical Ethics at Stanford University; she created and led the Bioethics Research Program at the Mayo Clinic in Rochester, Minn.

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http://dx.doi.org/10.1177/1073110519840484DOI Listing
March 2019

"Why did I get that part of you?" Understanding addiction genetics through family history.

Public Underst Sci 2019 01 27;28(1):53-67. Epub 2018 Jun 27.

The Pennsylvania State University, USA.

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http://dx.doi.org/10.1177/0963662518785350DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6342673PMC
January 2019

Understanding variations in secondary findings reporting practices across U.S. genome sequencing laboratories.

AJOB Empir Bioeth 2018 Jan-Mar;9(1):48-57. Epub 2017 Dec 21.

b Institute for Health and Aging, University of California , San Francisco.

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http://dx.doi.org/10.1080/23294515.2017.1405095DOI Listing
October 2018

Pragmatic Tools for Sharing Genomic Research Results with the Relatives of Living and Deceased Research Participants.

J Law Med Ethics 2018 Mar 27;46(1):87-109. Epub 2018 Mar 27.

Susan M. Wolf, J.D., is McKnight Presidential Professor of Law, Medicine & Public Policy; Faegre Baker Daniels Professor of Law; Professor of Medicine; and Chair of the Consortium on Law and Values in Health, Environment & the Life Sciences, University of Minnesota. She was one of three Principal Investigators on NIH/NCI/NHGRI grant 1R01CA154517 on return of genomic results to family members, including after the death of the proband. Emily Scholtes, J.D., is a graduate of the University of Minnesota Law School, where she served as a Research Assistant on the project on return of genomic results to family members. She then clerked for the U.S. Court of Appeals for the Eighth Circuit before going into private practice. The views expressed in this article are exclusively those of the authors. This article has been prepared for informational purposes only and does not constitute legal advice. Barbara A. Koenig, Ph.D., is Director of Bioethics and Professor of Bioethics and Medical Anthropology based at the Institute for Health & Aging, University of California, San Francisco. She was one of three Principal Investigators on NIH/NCI/NHGRI grant 1R01CA154517 on return of genomic results to family members, including after the death of the proband. Gloria M. Petersen, Ph.D., is Professor of Epidemiology, Department of Health Sciences Research, Mayo Clinic College of Medicine. She is a Founding Fellow of the American College of Medical Genetics and Genomics. She was one of three Principal Investigators on NIH/NCI/NHGRI grant 1R01CA154517 on return of genomic results to family members, including after the death of the proband. Susan A. Berry, M.D., is Professor of Pediatrics & Genetics and Division Director for Genetics and Metabolism in the Department of Pediatrics, University of Minnesota. She is a Fellow of the American Academy of Pediatrics and the American College of Medical Genetics. Laura M. Beskow, M.P.H., Ph.D., is Professor of Health Policy and Director of Research Ethics, Center for Biomedical Ethics & Society, Vanderbilt University. She received her M.P.H. with a concentration in health law from Boston University and her Ph.D. in Health Policy and Administration, with a minor in Epidemiology, at the University of North Carolina at Chapel Hill. Mary B. Daly, M.D., Ph.D., is a medical oncologist and epidemiologist who chairs the Department of Clinical Genetics at Fox Chase Cancer Center. Her research focuses on defining the best methods of communicating hereditary cancer risk information and on providing risk management strategies and coping skills to family members dealing with an increased risk for cancer. Conrad V. Fernandez, B.Sc., M.D., is Professor and Head of the Division of Pediatric Hematology/Oncology in the Department of Pediatrics, IWK Health Centre, Dalhousie University and is cross-appointed in Bioethics, Medicine, and Postgraduate Studies. He obtained his medical degree at McMaster University, specialist certification in Pediatrics as a Fellow of the Royal College of Physicians and Surgeons of Canada at Dalhousie University, and completed specialty training in Pediatric Hematology/Oncology at the University of British Columbia. Robert C. Green, M.D., M.P.H., is a medical geneticist and physician-scientist who directs the G2P Research Program in translational genomics and health outcomes in the Division of Genetics, Brigham and Women's Hospital and Harvard Medical School. He is also Associate Director for Research at Partners Personalized Medicine. Dr. Green leads and co-leads the MedSeq Project and the BabySeq Project respectively, two NIH-funded randomized trials designed to explore the medical, behavioral, and economic implications of integrating genome sequencing into the medical care of adults and newborns. Bonnie S. LeRoy, M.S., C.G.C., is Professor and Director of the Graduate Program in Genetic Counseling, University of Minnesota. Her work focuses on preparing graduate students to enter the profession of genetic counseling. Her research examines the ethical and social challenges associated with the genetic counseling profession. She served as the President of the American Board of Genetic Counseling from 2001-03. Noralane M. Lindor, M.D., is Professor of Medical Genetics in the Department of Health Sciences Research at Mayo Clinic in Scottsdale, Arizona. She received her medical degree from Mayo Medical School, and did her residencies at Bowman Gray School of Medicine in Winston-Salem, North Carolina, and at Mayo Clinic in Rochester. P. Pearl O'Rourke, M.D., is Director of Human Research Affairs at Partners HealthCare in Boston, and Associate Professor of Pediatrics at Harvard Medical School. She completed medical school at Dartmouth Medical School and the University of Minnesota Medical School. Carmen Radecki Breitkopf, Ph.D., is Professor of Health Services Research in the Department of Health Sciences Research at Mayo Clinic College of Medicine and Science in Rochester, Minnesota. She earned her Master's and Doctoral degrees in Psychology from the State University of New York at Albany. Mark A. Rothstein, J.D., is Herbert F. Boehl Chair of Law & Medicine and Director of the Institute for Bioethics, Health Policy & Law at the University of Louisville School of Medicine. He is past-President of the American Society of Law, Medicine & Ethics and serves as Public Health Ethics editor for the American Journal of Public Health. Brian Van Ness, Ph.D., is Professor of Genetics, Cell Biology and Development at the University of Minnesota. He earned his doctorate in Biochemistry from the University of Minnesota, completed a postdoctoral fellowship at Fox Chase Cancer Center, and has served as the Department Head and Director of the Institute of Human Genetics at the University of Minnesota. Benjamin S. Wilfond, M.D., is Director of the Treuman Katz Center for Pediatric Bioethics, Seattle Children's Hospital; Professor and Chief of the Division of Bioethics; Professor, Pulmonary and Sleep Medicine, Department of Pediatrics; and Adjunct Professor, Department of Bioethics and Humanities, University of Washington School of Medicine. He is past-President of the Association of Bioethics Program Directors, Chair for the Clinical Research Ethics Consultation Working Group for the Clinical and Translational Science Awards program, and a member of the Bioethics and Legal Working Group of the Newborn Screening Translational Research Network.

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http://dx.doi.org/10.1177/1073110518766024DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6040667PMC
March 2018

"I don't have to know why it snows, I just have to shovel it!": Addiction Recovery, Genetic Frameworks, and Biological Citizenship.

Biosocieties 2017 Dec 11;12(4):568-587. Epub 2017 Jul 11.

Pennsylvania State University, 1743C Humanities, Hershey Medical Center, Hershey, PA 17033

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http://dx.doi.org/10.1057/s41292-017-0045-4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5851475PMC
December 2017

How California Prepared for Implementation of Physician-Assisted Death: A Primer.

Am J Public Health 2017 06 20;107(6):883-888. Epub 2017 Apr 20.

Laura A. Petrillo is with the Division of Geriatrics, University of California, San Francisco (UCSF), and San Francisco Veterans Affairs. Elizabeth Dzeng is with the Division of Hospital Medicine, UCSF, and UCSF Bioethics. Krista L. Harrison is with the Division of Geriatrics, UCSF. Lindsay Forbes and Barbara A. Koenig are with the Institute for Health and Aging, UCSF, and UCSF Bioethics. Benjamin Scribner is with the School of Nursing, UCSF.

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http://dx.doi.org/10.2105/AJPH.2017.303755DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5425870PMC
June 2017

Returning Results in Biobank Research: Global Trends and Solutions.

Genet Test Mol Biomarkers 2017 Mar 1;21(3):128-131. Epub 2017 Feb 1.

1 Institute for Biomedical Ethics, University of Basel , Basel, Switzerland .

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http://dx.doi.org/10.1089/gtmb.2016.0394DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5367909PMC
March 2017

Ten simple rules for responsible big data research.

PLoS Comput Biol 2017 03 30;13(3):e1005399. Epub 2017 Mar 30.

Carey School of Law, University of Maryland, Baltimore, Maryland, United States of America.

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http://dx.doi.org/10.1371/journal.pcbi.1005399DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5373508PMC
March 2017

Returning a Research Participant's Genomic Results to Relatives: Analysis and Recommendations.

J Law Med Ethics 2015 ;43(3):440-63

Director of the Treuman Katz Center for Pediatric Bioethics, Seattle Children's Hospital; Professor and Chief of the Division of Bioethics; Professor, Pulmonary and Sleep Medicine, Department of Pediatrics; and Adjunct Professor, Department of Bioethics and Humanities, University of Washington School of Medicine. He is President of the Association of Bioethics Program Directors, Chair for the Clinical Research Ethics Consultation Working Group for the Clinical and Translational Science Awards program, and a member of the Bioethics and Legal Working Group of the Newborn Screening Translational Research Network.

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http://dx.doi.org/10.1111/jlme.12288DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4617203PMC
January 2017

Preferences Regarding Return of Genomic Results to Relatives of Research Participants, Including after Participant Death: Empirical Results from a Cancer Biobank.

J Law Med Ethics 2015 ;43(3):464-75

Professor of Bioethics and Medical Anthropology based at the Institute for Health & Aging, University of California, San Francisco. Currently, she co-directs a Center of Excellence in ELSI Research that focuses on translational genomics, co-leads an NCI/NHGRI R01 on return of results in genomic biobanks, and directs the ELSI component of a U19 award focused on newborn screening in an era of whole genome analysis.

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http://dx.doi.org/10.1111/jlme.12289DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4617194PMC
January 2017

Mapping the Ethics of Translational Genomics: Situating Return of Results and Navigating the Research-Clinical Divide.

J Law Med Ethics 2015 ;43(3):486-501

Professor of Bioethics and Medical Anthropology based at the Institute for Health & Aging, University of California, San Francisco. Currently, she co-directs a Center of Excellence in ELSI Research that focuses on translational genomics, co-leads an NCI/NHGRI R01 on return of results in genomic biobanks, and directs the ELSI component of a U19 award focused on newborn screening in an era of whole genome analysis.

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http://dx.doi.org/10.1111/jlme.12291DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4620583PMC
January 2017

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

BMC Med Ethics 2016 09 6;17(1):54. Epub 2016 Sep 6.

Institute of Health Policy Management and Evaluation | Joint Centre for Bioethics, University of Toronto, Toronto, Canada.

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http://dx.doi.org/10.1186/s12910-016-0137-xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5011895PMC
September 2016

Professionally Responsible Disclosure of Genomic Sequencing Results in Pediatric Practice.

Pediatrics 2015 Oct 14;136(4):e974-82. Epub 2015 Sep 14.

Department of Pediatrics, University of Washington, Seattle, Washington.

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http://dx.doi.org/10.1542/peds.2015-0624DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4586726PMC
October 2015

EngageUC: Developing an Efficient and Ethical Approach to Biobanking Research at the University of California.

Clin Transl Sci 2015 Aug 10;8(4):362-6. Epub 2015 Jan 10.

Philip R. Lee Institute for Health Policy Studies, University of California, San Francisco, California, USA.

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http://dx.doi.org/10.1111/cts.12259DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4499012PMC
August 2015

Unwarranted optimism in media portrayals of genetic research on addiction overshadows critical ethical and social concerns.

J Health Commun 2015 25;20(5):555-65. Epub 2015 Mar 25.

a Department of Health Behavior and Health Education , University of Michigan School of Public Health , Ann Arbor , Michigan , USA.

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http://dx.doi.org/10.1080/10810730.2014.999895DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4451206PMC
July 2015

The media and behavioral genetics: Alternatives coexisting with addiction genetics.

Sci Technol Human Values 2015 Jul;40(4):459-486

University of California, San Francisco, Institute for Health & Aging, San Francisco, CA, USA.

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http://dx.doi.org/10.1177/0162243914558491DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4574304PMC
July 2015

Challenges in translational research: the views of addiction scientists.

PLoS One 2014 4;9(4):e93482. Epub 2014 Apr 4.

Divisions of General Internal Medicine & Health Care Policy Research, and Biomedical Ethics Program, Mayo Clinic, Rochester, Minnesota, United States of America.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0093482PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3976268PMC
June 2015

Have we asked too much of consent?

Authors:
Barbara A Koenig

Hastings Cent Rep 2014 Jul-Aug;44(4):33-4

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http://dx.doi.org/10.1002/hast.329DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4249719PMC
September 2014

Ethical, legal, and social implications of incorporating genomic information into electronic health records.

Genet Med 2013 Oct 12;15(10):810-6. Epub 2013 Sep 12.

Department of Internal Medicine, Wayne State University School of Medicine, Detroit, Michigan, USA.

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http://dx.doi.org/10.1038/gim.2013.117DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3926430PMC
October 2013

Point-counterpoint. Ethics and genomic incidental findings.

Science 2013 May 16;340(6136):1047-8. Epub 2013 May 16.

Center for Medical Ethics and Health Policy, Baylor College of Medicine, Houston, TX 77030, USA.

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http://dx.doi.org/10.1126/science.1240156DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3772710PMC
May 2013

Addiction science, meet translational genomics.

Authors:
Barbara A Koenig

Addiction 2012 Dec;107(12):2079-80

University of California, San Francisco, CA, 94143, USA.

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http://dx.doi.org/10.1111/j.1360-0443.2012.04029.xDOI Listing
December 2012

"Just Because We Can Doesn't Mean We Should": views of nurses on deactivation of pacemakers and implantable cardioverter-defibrillators.

J Interv Card Electrophysiol 2011 Dec 30;32(3):243-52. Epub 2011 Jul 30.

Beth Israel Deaconess Medical Center, Harvard Medical School, 185 Pilgrim Road, Baker 4, Boston, MA, 02215, USA.

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http://dx.doi.org/10.1007/s10840-011-9596-7DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3733086PMC
December 2011

Ironic technology: Old age and the implantable cardioverter defibrillator in US health care.

Soc Sci Med 2011 Jan 11;72(1):6-14. Epub 2010 Nov 11.

University of California, Institute for Health and Aging, San Francisco, CA 94118, USA.

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http://dx.doi.org/10.1016/j.socscimed.2010.09.052DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3032945PMC
January 2011

Facing the challenges of influenza in healthcare settings: the ethical rationale for mandatory seasonal influenza vaccination and its implications for future pandemics.

Vaccine 2008 Sep;26 Suppl 4:D27-30

Division of General Internal Medicine, Mayo Clinic 200 1st. St. SW Rochester, MN 55905, USA.

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September 2008

Topics in transplant ethics.

Transplant Rev (Orlando) 2008 Jul;22(3):151-3

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http://dx.doi.org/10.1016/j.trre.2008.04.009DOI Listing
July 2008

Ethical issues in stopping randomized trials early because of apparent benefit.

Ann Intern Med 2007 Jun;146(12):878-81

Department of Medicine, Mayo Clinic College of Medicine, Rochester, Minnesota 55905, USA.

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June 2007

Family member involvement in hastened death.

Death Stud 2007 Feb;31(2):105-30

Department of Medical History and Ethics, University of Washington, Box 357120, Seattle, WA 98195-7240, USA.

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http://dx.doi.org/10.1080/07481180601100483DOI Listing
February 2007

Brain science and social policy.

Cerebrum 2002 ;4(3):59-62

Stanford University Center for Biomedical Ethics, USA.

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May 2006

Advertising, patient decision making, and self-referral for computed tomographic and magnetic resonance imaging.

Arch Intern Med 2004 Dec 13-27;164(22):2415-9

Stanford Center for Biomedical Ethics, Program in Human Biology, and Department of Radiology, Stanford University, Stanford, Calif, USA.

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http://archinte.jamanetwork.com/article.aspx?doi=10.1001/arc
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http://dx.doi.org/10.1001/archinte.164.22.2415DOI Listing
January 2005

Dead donors and the "shortage" of human organs: are we missing the point?

Authors:
Barbara A Koenig

Am J Bioeth 2003 ;3(1):26-7

Stanford University.

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http://dx.doi.org/10.1162/152651603766436388DOI Listing
December 2003

Self-referred whole-body CT imaging: current implications for health care consumers.

Radiology 2003 Aug;228(2):346-51

Department of Medicine, Stanford University Medical Center, 701 Welch Rd, Stanford, CA 94304-5748, USA.

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http://dx.doi.org/10.1148/radiol.2282021083DOI Listing
August 2003

Qualitative methods in end-of-life research: recommendations to enhance the protection of human subjects.

J Pain Symptom Manage 2003 Apr;25(4):S43-52

Stanford University Center for Biomedical Ethics, 701A Welch Road #1105, Palo Alto, CA 94304, USA.

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April 2003

"Choice" in end-of-life decision making: researching fact or fiction?

Gerontologist 2002 Oct;42 Spec No 3:114-28

Kaiser Permanente, Oakland, CA 94612, USA.

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http://dx.doi.org/10.1093/geront/42.suppl_3.114DOI Listing
October 2002

Strategies for culturally effective end-of-life care.

Ann Intern Med 2002 May;136(9):673-9

Stanford University Center for Biomedical Ethics, 701 Welch Road, Suite 1105, Palo Alto, CA 94304, USA.

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May 2002

AIDS and ethics.

Issues Sci Technol 1986 ;2(2):56-65

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April 1986