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个人简介
Stephanie Malia Fullerton, DPhil, is Professor of Bioethics and Humanities at the University of Washington School of Medicine. She is also Adjunct Professor in the UW Departments of Epidemiology, Genome Sciences, and Medicine (Medical Genetics), as well as an affiliate investigator with the Public Health Sciences division of the Fred Hutchinson Cancer Research Center.
Dr. Fullerton’s work focuses on the ethical and social implications of genomic research and its equitable and safe translation for clinical and public health benefit. She serves as the ELSI lead for the Clinical Sequencing Evidence-Generating Research (CSER2) Consortium coordinating center, co-chairs the TOPMed Consortium ELSI Committee, and chairs the Bioethics Advisory Board of the Kaiser Permanente national Research Bank. She contributes to a range of empirical projects focused on clinical genomics translation and precision medicine approaches to the treatment and prevention of cancer and kidney disease in diverse patient populations.
Dr. Fullerton’s work focuses on the ethical and social implications of genomic research and its equitable and safe translation for clinical and public health benefit. She serves as the ELSI lead for the Clinical Sequencing Evidence-Generating Research (CSER2) Consortium coordinating center, co-chairs the TOPMed Consortium ELSI Committee, and chairs the Bioethics Advisory Board of the Kaiser Permanente national Research Bank. She contributes to a range of empirical projects focused on clinical genomics translation and precision medicine approaches to the treatment and prevention of cancer and kidney disease in diverse patient populations.
研究兴趣
论文共 191 篇作者统计合作学者相似作者
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HUMAN GENETICS AND GENOMICS ADVANCESno. 1 (2024): 100243-100243
Genetics in Medicine Openno. 1 (2023): 100751-100751
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medRxiv (Cold Spring Harbor Laboratory) (2023)
Perspectives in biology and medicineno. 2 (2023): 225-248
PUBLIC HEALTH GENOMICSno. 1 (2023): 103-112
American journal of human geneticsno. 7 (2023): 1021-1033
AJOB empirical bioethicspp.1-12, (2023)
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Genetics in Medicine Openno. 1 (2023): 100426-100426
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