PredictER's library 382 articles Export

	Disclosure and rationality: comparative risk information and decision-making about prevention. [My Copy] Theoretical medicine and bioethics, Vol. 30, No. 3. (2009), pp. 199-213. by Peter H. Schwartz posted to risk-and-behavior risk disclosure decision-making by PredictER on 2009-09-11 17:24:13 as
	The Scientific Foundation for personal genomics: recommendations from a National Institutes of Health-Centers for Disease Control and Prevention multidisciplinary workshop. [My Copy] Genetics in medicine : official journal of the American College of Medical Genetics, Vol. 11, No. 8. (16 August 2009), pp. 559-567. by Muin J. Khoury, Colleen M. McBride, Sheri D. Schully, et al.John P. Ioannidis, W. Gregory Feero, A. Cecile Janssens, Marta Gwinn, Denise G. Simons-Morton, Jay M. Bernhardt, Michele Cargill, Stephen J. Chanock, George M. Church, Ralph J. Coates, Francis S. Collins, Robert T. Croyle, Barry R. Davis, Gregory J. Downing, Amy Duross, Susan Friedman, Mitchell H. Gail, Geoffrey S. Ginsburg, Robert C. Green, Mark H. Greene, Philip Greenland, Jeffrey R. Gulcher, Andro Hsu, Kathy L. Hudson, Sharon L. Kardia, Paul L. Kimmel, Michael S. Lauer, Amy M. Miller, Kenneth Offit, David F. Ransohoff, J. Scott Roberts, Rebekah S. Rasooly, Kari Stefansson, Sharon F. Terry, Steven M. Teutsch, Angela Trepanier, Kay L. Wanke, John S. Witte, Jianfeng Xu posted to personalized-medicine nih genomics cdc by PredictER on 2009-09-08 14:50:10 as along with 1 person brianb
	Health information privacy and syndromic surveillance systems. [My Copy] MMWR. Morbidity and mortality weekly report, Vol. 53 Suppl (24 September 2004), pp. 221-225. by D. Drociuk, J. Gibson, J. Hodge posted to health-information hipaa privacy by PredictER on 2009-07-09 14:23:40 as
	Ethical, legal, and social implications of genomic medicine. [My Copy] The New England journal of medicine, Vol. 349, No. 6. (7 August 2003), pp. 562-569. by E. W. Clayton posted to elsi ethical-issues genomics personalized-medicine by PredictER on 2009-06-03 16:24:49 as
	Pharmacogenomics, ethics, and public policy. [My Copy] Kennedy Institute of Ethics journal, Vol. 18, No. 1. (March 2008), pp. 35-56. by K. Peterson-Iyer posted to elsi personalized-medicine pharmacogenomics policy by PredictER on 2009-06-03 16:21:44 as
	Is it ethical to deny genetic research participants individualised results? [My Copy] Journal of medical ethics, Vol. 35, No. 4. (April 2009), pp. 209-213. by P. Affleck posted to communication disclosure genetic-research by PredictER on 2009-04-06 14:14:31 as
	Researchers' preferences and attitudes on ethical aspects of genomics research: a comparative study between the USA and Spain. [My Copy] Journal of medical ethics, Vol. 35, No. 4. (April 2009), pp. 251-257. by M. Ruiz-Canela, J. I. Valle-Mansilla, D. P. Sulmasy posted to attitudes genomics informed-consent by PredictER on 2009-04-06 14:12:37 as
	Preimplantation Genetic Diagnosis, Reproductive Freedom, and Deliberative Democracy. [My Copy] The Journal of medicine and philosophy (27 February 2009) by Colin Farrelly posted to eugenics genetic-testing pgd reproductive-technologies by PredictER on 2009-03-09 12:28:37 as
	Egalitarianism and Responsibility in the Genetic Future. [My Copy] The Journal of medicine and philosophy (25 February 2009) by Linda Barclay posted to enhancement future genetic-enhancement justice by PredictER on 2009-03-09 12:22:23 as
	Silence about screening. [My Copy] The American journal of bioethics : AJOB, Vol. 7, No. 7. (July 2007), pp. 46-48. by P. H. Schwartz posted to comment screening by PredictER on 2009-02-05 21:33:20 as
	Helsinki discords: FDA, ethics, and international drug trials. [My Copy] Lancet, Vol. 373, No. 9657. (3 January 2009), pp. 13-14. by J. Kimmelman, C. Weijer, E. M. Meslin posted to fda helsinki international-research research-ethics by PredictER on 2009-02-05 00:48:32 as along with 1 person cntbioet
	Factors that influence characteristics of genetic biobanks. [My Copy] Journal of nursing scholarship : an official publication of Sigma Theta Tau International Honor Society of Nursing / Sigma Theta Tau, Vol. 39, No. 1. (2007), pp. 25-29. by J. E. Sanner, L. Frazier posted to attitudes biobanks demographics genetic-research participants by PredictER on 2009-01-23 00:55:24 as
	Personal Genomes: When consent gets in the way [My Copy] Nature, Vol. 456, No. 7218. (6 November 2008), pp. 32-33. by Patrick Taylor posted to autonomy comment genomics informed-consent personal-genomics by PredictER on 2008-12-01 13:17:39 as along with 6 people tnhh klo williamgunn psique sg45653 pkonings
	Alternatives to project-specific consent for access to personal information for health research: Insights from a public dialogue [My Copy] BMC Medical Ethics, Vol. 9 (19 November 2008), 18. by Donald, Lehana Thabane posted to health-information informed-consent medical-records public-engagement by PredictER on 2008-11-24 21:39:46 as
	Who's minding the shop? The role of Canadian research ethics boards in the creation and uses of registries and biobanks [My Copy] BMC Medical Ethics, Vol. 9 (14 November 2008), 17. by Elaine, Donald J. Willison posted to biobanks canada irb research-ethics by PredictER on 2008-11-24 21:37:35 as along with 1 person JenniferSemotok
	What does it mean to be identifiable? [My Copy] The American journal of bioethics : AJOB, Vol. 8, No. 10. (October 2008), pp. 7-8. by Sara C. Hull, Benjamin Wilfond posted to anonymized-research genetic-information genetic-research privacy by PredictER on 2008-11-24 21:35:44 as along with 1 person bwgoodman
	Participation in Research and Social Context: The Case of Population-Based Cancer Registration, Surveillance, and Research [My Copy] American Journal of Bioethics, Vol. 8, No. 10. (October 2008), pp. 41-42. by Robert Mclaughlin posted to cancer population-research research-participants by PredictER on 2008-11-24 21:33:43 as
	Patients' Views on Identifiability of Samples and Informed Consent for Genetic Research [My Copy] American Journal of Bioethics, Vol. 8, No. 10. (October 2008), pp. 62-70. by Sara Chandros C. Hull, Richard Sharp, Jeffrey Botkin, et al.Mark Brown, Mark Hughes, Jeremy Sugarman, Debra Schwinn, Pamela Sankar, Dragana Bolcic-Jankovic, Brian Clarridge, Benjamin Wilfond posted to attitudes biobanks genetic-information informed-consent privacy by PredictER on 2008-11-24 21:30:28 as
	Genomic Anonymity: Have We Already Lost It? [My Copy] American Journal of Bioethics, Vol. 8, No. 10. (October 2008), pp. 71-74. by Dov Greenbaum, Jiang Du, Mark Gerstein posted to anonymized-research genetic-information privacy by PredictER on 2008-11-24 21:28:37 as
	Identifiability of DNA Data: The Need for Consistent Federal Policy [My Copy] American Journal of Bioethics, Vol. 8, No. 10. (October 2008), pp. 75-76. by Amy Mcguire posted to databases dna genetic-information policy privacy by PredictER on 2008-11-24 21:26:32 as
	Directives for Retained DNA: Preferences of Adolescent Patients with Substance and Conduct Problems and Their Siblings [My Copy] American Journal of Bioethics, Vol. 8, No. 10. (October 2008), pp. 77-79. by Marilyn Coors, Susan Mikulich-Gilbertson, Kristen Raymond, et al.Shannon Stover, Thomas Crowley, Sandra Brown, Susan Tapert posted to addiction attitudes biobanks dna pediatrics by PredictER on 2008-11-24 21:18:37 as
	Ethical rhetoric: genomics and the moral content of UNESCO's "universal" declarations. [My Copy] Journal of medical ethics, Vol. 34, No. 11. (November 2008) by S. H. Harmon posted to genomics international-research unesco by PredictER on 2008-11-24 19:14:07 as
	The Genetic Privacy of Presidential Candidates. [My Copy] The New England journal of medicine, Vol. 359, No. 21. (20 November 2008), pp. 2192-2193. by Robert C. C. Green, George J. J. Annas posted to genetic-information politics privacy by PredictER on 2008-11-24 17:51:27 as along with 2 people and 1 group ricmilne lilith 8_01
	The health benefits of genomics: out with the old, in with the new. [My Copy] Health affairs (Project Hope), Vol. 27, No. 6. (c 2008), pp. 1612-1615. by K. Hudson posted to evidence-based-medicine genomics oversight public-health by PredictER on 2008-11-24 17:49:44 as
	The brave new era of human genetic testing. [My Copy] BioEssays : news and reviews in molecular, cellular and developmental biology, Vol. 30, No. 11-12. (November 2008), pp. 1246-1251. by H. J. Bandelt, Y. G. Yao, M. B. Richards, A. Salas posted to commerce direct-to-consumer genetic-testing by PredictER on 2008-11-24 16:46:56 as
	Subjects matter: a survey of public opinions about a large genetic cohort study. [My Copy] Genetics in medicine : official journal of the American College of Medical Genetics, Vol. 10, No. 11. (November 2008), pp. 831-839. by D. Kaufman, J. Murphy, J. Scott, K. Hudson posted to attitudes genetic-research survey-research by PredictER on 2008-11-24 16:36:13 as
	Patient attitudes toward genotyping in an urban women's health clinic. [My Copy] Obstetrics and gynecology, Vol. 112, No. 5. (November 2008), pp. 1023-1028. by D. M. Haas, J. L. Renbarger, E. M. Meslin, K. Drabiak, D. Flockhart posted to attitudes dna genetic-research genetic-testing indiana-university predicter women by PredictER on 2008-11-13 18:14:38 as
	Governance mechanisms and population biobanks: building a framework for trust. [My Copy] GenEdit, Vol. 6, No. 2. (2008) by S. Wallace, K. Bedard, A. Kent, B. M. Knoppers posted to biobanks genetics governance population-genetics by PredictER on 2008-10-14 19:05:56 as
	Trends in U.S. Attitudes Toward Genetic Testing, 1990-2004 [My Copy] Public Opin Q, Vol. 72, No. 3. (1 September 2008), pp. 446-458. by Eleanor Singer, Mick P. Couper, Trivellore E. Raghunathan, John Van Hoewyk, Toni C. Antonucci posted to attitudes genetic-testing by PredictER on 2008-10-10 17:47:00 as
	Bioethics, business ethics, and science: bioinformatics and the future of healthcare. [My Copy] Cambridge quarterly of healthcare ethics : CQ : the international journal of healthcare ethics committees, Vol. 17, No. 4. (2008), pp. 361-372. by K. W. Goodman, A. Cava posted to bioinformatics business-ethics ethics by PredictER on 2008-10-09 20:03:02 as
	Race as a variable in pharmacogenomics science: from empirical ethics to publication standards. [My Copy] Pharmacogenetics and genomics, Vol. 18, No. 10. (October 2008), pp. 837-841. by V. Ozdemir, J. E. Graham, B. Godard posted to academic-literature empirical-ethics pharmacogenomics race by PredictER on 2008-09-18 19:12:10 as
	Stroke Genetic Research and Adults With Impaired Decision-Making Capacity. A Survey of IRB and Investigator Practices. [My Copy] Stroke; a journal of cerebral circulation (24 July 2008) by Donna T T. Chen, James F F. Meschia, Thomas G G. Brott, Robert D D. Brown, Bradford B B. Worrall, posted to attitudes genetic-research irb research-ethics by PredictER on 2008-08-06 22:26:11 as
	Race-specific drugs: regulatory trends and public policy. [My Copy] Trends in pharmacological sciences, Vol. 29, No. 6. (June 2008), pp. 277-279. by D. E. Winickoff, O. K. Obasogie posted to clinical-trials personalized-medicine pharmacogenomics public-policy race by PredictER on 2008-06-27 17:47:02 as
	Long-term follow-up after diagnosis resulting from newborn screening: statement of the US Secretary of Health and Human Services' Advisory Committee on Heritable Disorders and Genetic Diseases in Newborns and Children. [My Copy] Genetics in medicine : official journal of the American College of Medical Genetics, Vol. 10, No. 4. (April 2008), pp. 259-261. by A. R. Kemper, C. A. Boyle, J. Aceves, et al.D. Dougherty, J. Figge, J. L. Fisch, A. R. Hinman, C. L. Greene, C. A. Kus, J. Miller, D. Robertson, B. Therrell, M. Lloyd-Puryear, P. C. van Dyck, R. R. Howell posted to advisory genetic-testing newborn-screening by PredictER on 2008-06-05 18:01:34 as
	Pharmacogenetic testing: not as simple as it seems. [My Copy] Genetics in medicine : official journal of the American College of Medical Genetics (16 May 2008) by Susanne B. Haga, Wylie Burke posted to ethical-issues genetic-testing pharmacogenetics by PredictER on 2008-06-05 17:58:52 as
	From human genetics and genomics to pharmacogenetics and pharmacogenomics: past lessons, future directions. [My Copy] Drug metabolism reviews, Vol. 40, No. 2. (2008), pp. 187-224. by D. W. Nebert, G. Zhang, E. S. Vesell posted to personalized-medicine pharmacogenetics pharmacogenomics by PredictER on 2008-06-05 17:51:55 as along with 2 people and 1 group Scis0000002 Zephyrus Roswell Cancer Crosstalk
	The Ethics of Information: Absolute Risk Reduction and Patient Understanding of Screening. [My Copy] Journal of general internal medicine : official journal of the Society for Research and Education in Primary Care Internal Medicine (18 April 2008) by Peter H. Schwartz, Eric M. Meslin posted to genetic-testing patients risk by PredictER on 2008-05-14 16:51:42 as along with 1 person balshemh
	Assessment of parental understanding by pediatric residents during counseling after newborn genetic screening. [My Copy] Archives of pediatrics & adolescent medicine, Vol. 162, No. 3. (March 2008), pp. 199-204. by M. H. Farrell, P. Kuruvilla posted to genetic-counseling genetic-testing newborn-screening pediatrics by PredictER on 2008-04-15 19:19:26 as
	Communicating genetic information in the family: enriching the debate through the notion of integrity [My Copy] Medicine, Health Care and Philosophy by Paula Boddington, Maggie Gregory posted to disclosure ethical-issues genetic-information integrity by PredictER on 2008-04-13 21:58:51 as along with 1 person annaszuto
	An open future? The principle of autonomy within medical ‘codes of conduct’ versus the heteronomy effects of predictive medicine [My Copy] Central European Journal of Medicine, Vol. 3, No. 2. (10 June 2008), pp. 141-148. by Ignaas Devisch posted to autonomy ethical-issues predictive-health by PredictER on 2008-04-13 21:54:55 as
	REASSESSING INSURERS' ACCESS TO GENETIC INFORMATION: GENETIC PRIVACY, IGNORANCE, AND INJUSTICE [My Copy] Bioethics, Vol. 0, No. 0. (0), pp. ???-???. by E. L. I. Feiring posted to genetic-information insurance privacy by PredictER on 2008-04-13 21:53:56 as
	A pilot study for human tumor/DNA banking: returned more questions than answers. [My Copy] Medical oncology (Northwood, London, England) (8 April 2008) by A C. Cavuşoğlu, S Saydam, M Alakavuklar, et al.T Canda, A Sevinç, Y Kılıç, O Harmancıoğlu, M A. Koçdor, M Kınay, H Alanyalı, I Görken, P Balcı, B Demirkan, M Sakızlı, G Güner posted to biobanks cancer ethical-issues turkey by PredictER on 2008-04-13 21:20:44 as
	Diffusion of information about genetic risk within families. [My Copy] Neuromuscular disorders : NMD, Vol. 3, No. 5-6. (v 1993), pp. 571-574. by S. Ayme, G. Macquart-Moulin, C. Julian-Reynier, F. Chabal, F. Giraud posted to disclosure genetic-information genetic-testing by PredictER on 2008-04-08 22:39:49 as
	Psychological impact of population-based carrier testing for cystic fibrosis: 3-year follow-up. UK Cystic Fibrosis Follow-Up Study Group. [My Copy] Lancet, Vol. 347, No. 9013. (25 May 1996), pp. 1443-1446. by D. Axworthy, D. J. Brock, M. Bobrow, T. M. Marteau posted to cystic-fibrosis ethical-issues genetic-testing by PredictER on 2008-04-08 22:36:38 as
	Ethical dimensions of genetics in pediatric neurology: a look into the future. [My Copy] Semin Pediatr Neurol, Vol. 9, No. 1. (March 2002), pp. 53-61. by D. M. Avard, B. M. Knoppers posted to ethical-issues neurology ped pediatric-research pediatrics by PredictER on 2008-04-08 22:34:58 as along with 1 person and 1 group ladygoat CGREL
	Genetics and Society Project. [My Copy] Community genetics, Vol. 3, No. 3. (2000), pp. 102-104. by D. Avard, B. M. Knoppers posted to ethical-issues genetic-research by PredictER on 2008-04-08 22:33:08 as
	Partnering in Oncogenetic Research The INHERIT BRCAs Experience: Opportunities and Challenges [My Copy] Familial Cancer, Vol. 5, No. 1. (March 2006), pp. 3-13. by Denise Avard, Peter Bridge, Lucie Bucci, et al.Jocelyne Chiquette, Michel Dorval, Francine Durocher, Doug Easton, Beatrice Godard, David Goldgar, Bartha Knoppers, Rachel Laframboise, Bernard Lesperance, Marie Plante, Sean Tavtigian, Helene Vezina, Brenda Wilson, Jacques Simard posted to brca cancer ethical-issues genetic-research by PredictER on 2008-04-08 22:31:27 as
	Monitoring ethical, legal, and social issues in developing population genetic databases. [My Copy] Genetics in medicine : official journal of the American College of Medical Genetics, Vol. 5, No. 6. (c 2003), pp. 451-457. by M. A. Austin, S. E. Harding, C. E. McElroy posted to biobanks ethical-issues by PredictER on 2008-04-08 22:29:30 as
	Ethical issues in human genome epidemiology: a case study based on the Japanese American Family Study in Seattle, Washington. [My Copy] American journal of epidemiology, Vol. 155, No. 7. (1 April 2002), pp. 585-592. by M. A. Austin posted to biobanks ethical-issues genomics by PredictER on 2008-04-08 22:27:22 as along with 1 person Daintry
	Ethnicity and the politics of the new genetics: principles and engagement. [My Copy] Ethnicity & health, Vol. 8, No. 2. (May 2003), pp. 91-109. by K. Atkin posted to ethical-issues ethnicity genetic-medicine by PredictER on 2008-04-08 22:23:55 as

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PredictER's library 382 articles Export

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