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Public Health Genomics and Precision Health Knowledge Base (v6.9)
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Genomics and Precision Health Database
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Last data update: Jan 24, 2021
. (Total: 38387 Documents since 2012)
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Informed consent [original query]>>Reviews/Commentaries[Product Type]
Publication
Ethical and Psychosocial Implications of Genomic Newborn Screening.
Levy Harvey L et al. International journal of neonatal screening 2021 Jan 7(1)
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Organoids for personalized treatment of Cystic Fibrosis: Professional perspectives on the ethics and governance of organoid biobanking.
Lensink Michael A et al. Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society 2020 Dec
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How to Develop a Risk Prediction Smartphone App.
Mauch Jaclyn T et al. Surgical innovation 2020 Dec 1553350620974827
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Explainability for artificial intelligence in healthcare: a multidisciplinary perspective.
Amann Julia et al. BMC medical informatics and decision making 2020 Nov 20(1) 310
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Informed consent for genetic testing in hematology.
Marron Jonathan M et al. Hematology. American Society of Hematology. Education Program 2020 2020(1) 213-218
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Reflections on dynamic consent in biomedical research: the story so far.
Teare Harriet J A et al. European journal of human genetics : EJHG 2020 Nov
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Ethical Considerations about Genomic Medicine Implementation: Lessons Learned from the eMERGE III Study.
Inamura Kentaro et al. Journal of personalized medicine 2020 Oct 10(4)
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Should You Recommend Direct-to-Consumer Genetic Testing for This Patient? : Grand Rounds Discussion From Beth Israel Deaconess Medical Center.
Smetana Gerald W et al. Annals of internal medicine 2020 Oct 173(7) 563-571
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As genome-editing trials become more common, informed consent is changing
Science Daily, October 12, 2020
Contributory factors to the evolution of the concept and practice of informed consent in clinical research: A narrative review.
O'Sullivan Lydia et al. Contemporary clinical trials communications 2020 Sep 19100634
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Role of a regulatory and governance framework in human biological materials and data sharing in National Biobanks: Case studies from Biobank Integrating Platform, Taiwan and the National Biorepository, Uganda.
Nansumba Hellen et al. Wellcome open research 2019 4171
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Public engagement with genomic medicine: a summary of town hall discussions.
Etchegary Holly et al. Journal of community genetics 2020 Aug
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Digitizing clinical trials.
Inan O T et al. NPJ digital medicine 2020 3101
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Trust in and Ethical Design of Carebots: The Case for Ethics of Care.
Yew Gary Chan Kok et al. International journal of social robotics 2020 May 1-17
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Ethical Questions Concerning Newborn Genetic Screening.
Esquerda Montse et al. Clinical genetics 2020 Aug
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The generic Informed Consent Service gICS ® : implementation and benefits of a modular consent software tool to master the challenge of electronic consent management in research.
Rau Henriette et al. Journal of translational medicine 2020 Jul 18(1) 287
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A call for an ethical framework when using social media data for artificial intelligence applications in public health research.
Gilbert Jean-Philippe et al. Canada communicable disease report = Releve des maladies transmissibles au Canada 2020 Jun 46(6) 169-173
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The ethics of deferred consent in times of pandemics
RVD Graaf et al, Nature Medicine, July 10, 2020
Biobanking in health care: evolution and future directions.
Coppola Luigi et al. Journal of translational medicine 2019 17(1) 172
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[Challenges of screening germline predispositions in children].
Manabe Atsushi et al. [Rinsho ketsueki] The Japanese journal of clinical hematology 2020 61(6) 682-686
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Dynamic-informed consent: A potential solution for ethical dilemmas in population sequencing initiatives.
Dankar Fida K et al. Computational and structural biotechnology journal 2020 18913-921
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Genetic testing for neurodegenerative diseases: Ethical and health communication challenges.
Roberts J Scott et al. Neurobiology of disease 2020 Apr 104871
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Budgets versus Bans: How U.S. Law Restricts Germline Gene Editing.
Johnston Josephine et al. The Hastings Center report 2020 Mar 50(2) 4-5
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Why NIPT should be publicly funded.
Bunnik Eline Maria et al. Journal of medical ethics 2020 Apr
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[A consensus on the standardization of the next generation sequencing process for the diagnosis of genetic diseases (1) - Procedures prior to genetic testing].
Wang Jian et al. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2020 Mar 37(3) 334-338
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[A consensus on the standardization of the next generation sequencing process for the diagnosis of genetic diseases (4) - Report interpretation and genetic counseling].
Huang Hui et al. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2020 Mar 37(3) 352-357
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User-focused data sharing agreements: a foundation for the genomic future.
Petersen Carolyn et al. JAMIA open 2019 Dec 2(4) 402-406
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User-focused data sharing agreements: a foundation for the genomic future.
Petersen Carolyn et al. JAMIA open 2019 Dec 2(4) 402-406
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User-focused data sharing agreements: a foundation for the genomic future.
Petersen Carolyn et al. JAMIA open 2019 Dec 2(4) 402-406
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User-focused data sharing agreements: a foundation for the genomic future.
Petersen Carolyn et al. JAMIA open 2019 Dec 2(4) 402-406
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Page last reviewed:
Oct 1, 2020
Page last updated:
Jan 24, 2021
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