Privacy in the age of medical big data
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W. Price | I. Cohen | I. Cohen | W. N. Price | I. G. Cohen | I. G. Cohen
[1] D. Stone. The struggle for the soul of health insurance. , 1993, Journal of health politics, policy and law.
[2] Richard A Epstein,et al. The legal regulation of genetic discrimination: old responses to new technology. , 1994, Boston University law review. Boston University. School of Law.
[3] Workshop conclusions , 1996, Environmental monitoring and assessment.
[4] E. Jacobsohn,et al. Ethical and practical considerations of with , 1999 .
[5] A. Wall,et al. Book ReviewTo Err is Human: building a safer health system Kohn L T Corrigan J M Donaldson M S Washington DC USA: Institute of Medicine/National Academy Press ISBN 0 309 06837 1 $34.95 , 2000 .
[6] D. Winickoff,et al. The charitable trust as a model for genomic biobanks. , 2003, The New England journal of medicine.
[7] H. Morreim. Research versus Innovation: Real Differences , 2005, The American journal of bioethics : AJOB.
[8] H. Greely. The uneasy ethical and legal underpinnings of large-scale genomic biobanks. , 2007, Annual review of genomics and human genetics.
[9] Vitaly Shmatikov,et al. Robust De-anonymization of Large Sparse Datasets , 2008, 2008 IEEE Symposium on Security and Privacy (sp 2008).
[10] E. Emanuel,et al. Quality-improvement research and informed consent. , 2008, The New England journal of medicine.
[11] Helen Nissenbaum,et al. Privacy in Context , 2009 .
[12] Paul Ohm. Broken Promises of Privacy: Responding to the Surprising Failure of Anonymization , 2009 .
[13] Helen Nissenbaum,et al. Privacy in Context - Technology, Policy, and the Integrity of Social Life , 2009 .
[14] M. Calo. The Boundaries of Privacy Harm , 2010 .
[15] D. Blumenthal,et al. Achieving a Nationwide Learning Health System , 2010, Science Translational Medicine.
[16] R. Platt,et al. Developing the Sentinel System--a national resource for evidence development. , 2011, The New England journal of medicine.
[17] I. Kohane. Using electronic health records to drive discovery in disease genomics , 2011, Nature Reviews Genetics.
[18] Three Models of Health Insurance: The Conceptual Pluralism of the Patient Protection and Affordable Care Act , 2011 .
[19] Nicolas P. Terry,et al. Protecting Patient Privacy in the Age of Big Data , 2012 .
[20] Steven N Goodman,et al. The research-treatment distinction: a problematic approach for determining which activities should have ethical oversight. , 2013, The Hastings Center report.
[21] Nandita Mitra,et al. Public preferences about secondary uses of electronic health information. , 2013, JAMA internal medicine.
[22] K. Crawford,et al. Big Data and Due Process: Toward a Framework to Redress Predictive Privacy Harms , 2013 .
[23] Leopoldo C. Cancio,et al. Development and validation of a machine learning algorithm and hybrid system to predict the need for life-saving interventions in trauma patients , 2013, Medical & Biological Engineering & Computing.
[24] Eran Halperin,et al. Identifying Personal Genomes by Surname Inference , 2013, Science.
[25] Steven N Goodman,et al. An ethics framework for a learning health care system: a departure from traditional research ethics and clinical ethics. , 2013, The Hastings Center report.
[26] Daniel B. Vorhaus,et al. The next controversy in genetic testing: clinical data as trade secrets? , 2012, European Journal of Human Genetics.
[27] Aaron Roth,et al. The Algorithmic Foundations of Differential Privacy , 2014, Found. Trends Theor. Comput. Sci..
[28] W. Nicholson Price,et al. Black-Box Medicine , 2014 .
[29] Distinguishing QI projects from human subjects research: ethical and practical considerations. , 2014, Bulletin of the American College of Surgeons.
[30] S. Hoffman. Citizen Science: The Law and Ethics of Public Access to Medical Big Data , 2014 .
[31] Robert A Philibert,et al. Methylation array data can simultaneously identify individuals and convey protected health information: an unrecognized ethical concern , 2014, Clinical Epigenetics.
[32] Ruben Amarasingham,et al. The legal and ethical concerns that arise from using complex predictive analytics in health care. , 2014, Health affairs.
[33] Ben Goldacre,et al. How to Get All Trials Reported: Audit, Better Data, and Individual Accountability , 2015, PLoS medicine.
[34] Michael Morrison,et al. Dynamic consent: a patient interface for twenty-first century research networks , 2014, European Journal of Human Genetics.
[35] W. Nicholson Price,et al. Big Data, Patents, and the Future of Medicine , 2015 .
[36] Robert Cook-Deegan,et al. Broad Consent for Research With Biological Samples: Workshop Conclusions , 2015, The American journal of bioethics : AJOB.
[37] Andrew D. Selbst,et al. Big Data's Disparate Impact , 2016 .
[38] Frank Rockhold,et al. Data Sharing at a Crossroads. , 2016, The New England journal of medicine.
[39] Roger Allan Ford,et al. Privacy and Accountability in Black-Box Medicine , 2016 .
[40] S. Hoffman. Big Data's New Discrimination Threats: Amending the Americans with Disabilities Act to Cover Discrimination Based on Data-Driven Predictions of Future Disease , 2016 .
[41] After a prominent gene-testing firm declined to give patients their complete data, ACLU filed a legal complaint , 2016 .
[42] K. Spector-Bagdady,et al. "The Google of Healthcare": enabling the privatization of genetic bio/databanking. , 2016, Annals of epidemiology.
[43] Steven A. Demurjian,et al. Differential Privacy Approach for Big Data Privacy in Healthcare , 2017 .
[44] R. Eisenberg,et al. Promoting healthcare innovation on the demand side , 2016, Journal of law and the biosciences.
[45] An Expressive Theory of Privacy Intrusions , 2017 .
[46] N. Terry. Existential challenges for healthcare data protection in the United States , 2017 .
[47] Sebastian Thrun,et al. Dermatologist-level classification of skin cancer with deep neural networks , 2017, Nature.
[48] Jon M. Kleinberg,et al. Inherent Trade-Offs in the Fair Determination of Risk Scores , 2016, ITCS.
[49] W Nicholson Price,et al. Regulating Black-Box Medicine. , 2017, Michigan law review.
[50] A. Shuman,et al. Reg-ent within the Learning Health System , 2018, Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery.
[51] Urs Gasser,et al. Big Data, Health Law, and Bioethics , 2018 .
[52] Drug Approval in a Learning Health System , 2018 .
[53] C. Robertson,et al. Who's left out of Big Data?: How Big Data collection, analysis, and use neglect populations most in need of medical and public health research and interventions , 2018 .
[54] Thomas May. Sociogenetic Risks - Ancestry DNA Testing, Third-Party Identity, and Protection of Privacy. , 2018, The New England journal of medicine.
[55] Andrew Y. Ng,et al. Improving palliative care with deep learning , 2017, 2017 IEEE International Conference on Bioinformatics and Biomedicine (BIBM).
[56] Big Data’s Epistemology and Its Implications for Precision Medicine and Privacy , 2018 .
[57] E. Ingelsson,et al. Big Data and medicine: a big deal? , 2018, Journal of internal medicine.
[58] I. Cohen. Is There a Duty to Share Healthcare Data , 2018 .
[59] Margaret Foster Riley. Big Data, HIPAA, and the Common Rule , 2018 .
[60] Regulatory Disruption and Arbitrage in Health-Care Data Protection. , 2016, Yale journal of health policy, law, and ethics.
[61] S. Goodman,et al. Clinical Trial Participants’ Views of the Risks and Benefits of Data Sharing , 2018, The New England journal of medicine.
[62] P. Appelbaum,et al. Analysis of state laws on informed consent for clinical genetic testing in the era of genomic sequencing , 2018, American journal of medical genetics. Part C, Seminars in medical genetics.
[63] Nicolas P. Terry,et al. Appification, AI, and Healthcare's New Iron Triangle , 2018 .
[64] David Sontag,et al. Why Is My Classifier Discriminatory? , 2018, NeurIPS.
[65] Zhiwei Steven Wu,et al. Privacy-Preserving Generative Deep Neural Networks Support Clinical Data Sharing , 2017, bioRxiv.
[66] M. Lungren,et al. Preparing Medical Imaging Data for Machine Learning. , 2020, Radiology.
[67] Mariarosaria Taddeo,et al. How to Design AI for Social Good: Seven Essential Factors , 2020, Science and Engineering Ethics.
[69] G. Falcone,et al. Genetic Variation and Response to Neurocritical Illness: a Powerful Approach to Identify Novel Pathophysiological Mechanisms and Therapeutic Targets , 2020, Neurotherapeutics.
[70] B. Knoppers,et al. Genomic Sequencing Capacity, Data Retention, and Personal Access to Raw Data in Europe , 2020, Frontiers in Genetics.