jasonbobe's Top Recommendations

These recommendations were last updated about 9 hours ago.

	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls [My Copy] Nature, Vol. 447, No. 7145. (07 June 2007), pp. 661-678. posted by 40 people ajbattle joseph_x_zhou rdiaz psique zufar mattwa daforerog ilyashl ekostem cchurc1 gruberjd Hans45 lkolodziej xingxu raistrick guhjy jfr yas hpiwowar larios vplagnol jandot frohike qmwwallace joepickrell massivemayhem Garamonfok PredictER hms jo_davies Bioinformatics T_lab caseybrown mcgannd parkinson's disease references raiyar ramensky wenhui balicea mfm11
	Potential harms, anonymization, and the right to withdraw consent to biobank research [My Copy] European Journal of Human Genetics, Vol. aop, No. current. by Stefan Eriksson, Gert Helgesson, posted by 7 people 8_01 lilith bwgoodman ladygoat cgreal PredictER CGREL
	Research with stored biological samples: what do research participants want? [My Copy] Arch Intern Med, Vol. 165, No. 6. (28 March 2005), pp. 652-655. by D. T. Chen, D. L. Rosenstein, P. Muthappan, et al.S. G. Hilsenbeck, F. G. Miller, E. J. Emanuel, D. Wendler posted by 3 people ladygoat PredictER CGREL
	Coding and consent: moral challenges of the database project in Iceland. [My Copy] Bioethics, Vol. 18, No. 1. (2004), pp. 27-49. by V. Arnason posted by 3 people ladygoat PredictER CGREL
	DNA databanks and consent: a suggested policy option involving an authorization model. [My Copy] BMC Med Ethics, Vol. 4, No. 1. (3 January 2003) by T. Caulfield, R. E. Upshur, A. Daar posted by 3 people ladygoat PredictER CGREL
	MEDICINE: Enhanced: Race and Reification in Science [My Copy] Science, Vol. 307, No. 5712. (18 February 2005), pp. 1050-1051. by Troy Duster posted by 8 people ladygoat PredictER kaniko CGREL Neuroscience STS feminist_technoscience triggr
	Ethical issues in psychiatric genetics. [My Copy] J Psychiatr Pract, Vol. 10, No. 6. (November 2004), pp. 343-351. by P. S. Appelbaum posted by 3 people ladygoat PredictER CGREL
	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 by 3 people ladygoat PredictER CGREL
	Creating needs? A review of survey data and concerns relevant to the commercialization of genetic testing. [My Copy] Community Genet, Vol. 4, No. 2. (2001), pp. 68-76. by T. Caulfield, D. Wertz posted by 3 people ladygoat PredictER CGREL
	The ethics of research using biobanks: reason to question the importance attributed to informed consent. [My Copy] Arch Intern Med, Vol. 165, No. 1. (10 January 2005), pp. 97-100. by K. Hoeyer, B. O. Olofsson, T. Mjörndal, N. Lynöe posted by 7 people 8_01 lilith bwgoodman ladygoat cgreal PredictER CGREL
	The debate over research on stored biological samples: what do sources think? [My Copy] Arch Intern Med, Vol. 162, No. 13. (8 July 2002), pp. 1457-1462. by D. Wendler, E. Emanuel posted by 3 people ladygoat PredictER CGREL
	Integrating ethics and science in the International HapMap Project. [My Copy] Nat Rev Genet, Vol. 5, No. 6. (June 2004), pp. 467-475. by posted by 4 people ladygoat evoltropia PredictER CGREL
	Science and society: Human genetic research: emerging trends in ethics [My Copy] Nature Reviews Genetics, Vol. 6, No. 1. (01 January 2005), pp. 75-79. by Bartha M. Knoppers, Ruth Chadwick posted by 4 people ladygoat evoltropia PredictER CGREL
	Parents' and children's attitudes toward the enrollment of minors in genetic susceptibility research: implications for informed consent. [My Copy] Am J Med Genet A, Vol. 116, No. 4. (1 February 2003), pp. 315-323. by B. A. Bernhardt, E. S. Tambor, G. Fraser, L. S. Wissow, G. Geller posted by 5 people ladygoat evoltropia elsiatcase PredictER CGREL
	Legal aspects of genetic information. [My Copy] Yale J Biol Med, Vol. 64, No. 1. (b 1991), pp. 29-40. by L. B. Andrews posted by 3 people ladygoat PredictER CGREL
	Human subject protections in genetic research. [My Copy] Genet Test, Vol. 8, No. 2. (2004), pp. 209-213. by M. J. Coffey, L. Ross posted by 3 people ladygoat PredictER CGREL
	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 by 2 people PredictER 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 by 1 person PredictER
	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 by 1 person PredictER
	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 by 1 person PredictER
	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 by 1 person PredictER
	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 by 1 person PredictER
	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 by 1 person PredictER
	Preimplantation Genetic Diagnosis, Reproductive Freedom, and Deliberative Democracy. [My Copy] The Journal of medicine and philosophy (27 February 2009) by Colin Farrelly posted by 1 person PredictER
	Egalitarianism and Responsibility in the Genetic Future. [My Copy] The Journal of medicine and philosophy (25 February 2009) by Linda Barclay posted by 1 person PredictER
	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 by 1 person PredictER
	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 by 1 person PredictER
	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 by 2 people PredictER cntbioet
	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 by 1 person PredictER
	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 by 4 people ricmilne 8_01 lilith PredictER
	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 by 1 person PredictER
	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 by 1 person PredictER
	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 by 1 person PredictER
	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 Chandros C. Hull, Benjamin S. Wilfond posted by 2 people bwgoodman PredictER
	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 by 1 person PredictER
	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 by 1 person PredictER
	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 by 1 person PredictER
	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 by 1 person PredictER
	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 by 1 person PredictER
	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 by 1 person PredictER
	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 by 2 people JenniferSemotok PredictER
	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 by 1 person PredictER
	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 by 7 people tnhh klo williamgunn PredictER psique sg45653 pkonings
	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 by 1 person PredictER
	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 by 1 person PredictER
	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 by 1 person PredictER
	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 by 1 person PredictER
	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 by 1 person PredictER
	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 by 1 person PredictER
	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 by 1 person PredictER
	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 by 4 people Scis0000002 Roswell Cancer Crosstalk Zephyrus PredictER
	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 by 2 people balshemh PredictER
	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 by 1 person PredictER
	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 by 2 people annaszuto PredictER
	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 by 1 person PredictER
	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 by 1 person PredictER
	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 by 1 person PredictER
	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 by 1 person PredictER
	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 by 1 person PredictER
	Genetics and Society Project. [My Copy] Community genetics, Vol. 3, No. 3. (2000), pp. 102-104. by D. Avard, B. M. Knoppers posted by 1 person PredictER
	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 by 1 person PredictER
	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 by 2 people PredictER 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 by 1 person PredictER
	Genetic databases and pharmacogenetics: introduction. [My Copy] Studies in history and philosophy of biological and biomedical sciences, Vol. 37, No. 3. (September 2006), pp. 499-502. by R. E. Ashcroft, A. M. Hedgecoe posted by 2 people Scis0000002 PredictER
	Focus group interviews examining attitudes toward medical research among the Japanese: a qualitative study. [My Copy] Bioethics, Vol. 18, No. 5. (September 2004), pp. 448-470. by A. Asai, M. Ohnishi, E. Nishigaki, M. Sekimoto, S. Fukuhara, T. Fukui posted by 1 person PredictER
	The implications of genetic testing for deafness. [My Copy] Ear and hearing, Vol. 24, No. 4. (August 2003), pp. 324-331. by K. S. Arnos posted by 1 person PredictER
	Potential impact of the HIPAA privacy rule on data collection in a registry of patients with acute coronary syndrome. [My Copy] Archives of internal medicine, Vol. 165, No. 10. (23 May 2005), pp. 1125-1129. by D. Armstrong, E. Kline-Rogers, S. M. Jani, et al.E. B. Goldman, J. Fang, D. Mukherjee, B. K. Nallamothu, K. A. Eagle posted by 1 person PredictER
	Motivations and concerns of patients with access to genetic testing for hereditary pancreatitis. [My Copy] The American journal of gastroenterology, Vol. 96, No. 5. (May 2001), pp. 1610-1617. by S. E. Applebaum-Shapiro, J. A. Peters, J. A. O'Connell, C. E. Aston, D. C. Whitcomb posted by 1 person PredictER
	Privacy rules for DNA databanks. Protecting coded 'future diaries'. [My Copy] JAMA : the journal of the American Medical Association, Vol. 270, No. 19. (17 November 1993), pp. 2346-2350. by G. J. Annas posted by 1 person PredictER
	Hereditary cancer risk notification and testing: how interested is the general population? [My Copy] Journal of clinical oncology : official journal of the American Society of Clinical Oncology, Vol. 15, No. 5. (May 1997), pp. 2139-2148. by M. A. Andrykowski, R. Lightner, J. L. Studts, R. K. Munn posted by 1 person PredictER
	Biobanks and Biomarker Research in Cardiovascular Disease. [My Copy] The Journal of cardiovascular nursing, Vol. 23, No. 2. (l 2008), pp. 153-158. by Lorraine Frazier, Elizabeth Sparks, Jennifer E. Sanner, Maria Henderson posted by 2 people Scis0000002 PredictER
	How can we provide effective training for research ethics committee members? A European assessment. [My Copy] Journal of medical ethics, Vol. 34, No. 4. (July 2008), pp. 301-302. by H. Davies, F. Wells, C. Druml posted by 3 people Competition_Commission RS-CC PredictER
	Access to medical records for research purposes: varying perceptions across research ethics boards. [My Copy] J Med Ethics, Vol. 34, No. 4. (July 2008), pp. 308-314. by D J J. Willison, C Emerson, K V V. Szala-Meneok, et al.E Gibson, L Schwartz, K M M. Weisbaum, F Fournier, K Brazil, M D D. Coughlin posted by 5 people 8_01 lilith christiand PredictER exgxax
	Thinking ethically about genetic inheritance: liberal rights, communitarianism and the right to privacy for parents of donor insemination children. [My Copy] J Med Ethics, Vol. 34, No. 4. (July 2008), pp. 281-284. by J. Burr, P. Reynolds posted by 1 person PredictER
	Evaluating Online Direct-to-Consumer Marketing of Genetic Tests: Informed Choices or Buyers Beware? [My Copy] Genet Test, Vol. 12, No. 1. (2008), pp. 13-23. by R. Geransar, E. Einsiedel posted by 1 person PredictER
	How do we know that research ethics committees are really working? the neglected role of outcomes assessment in research ethics review [My Copy] BMC Medical Ethics, Vol. 9 (28 March 2008), 6. by Carl H. Coleman, Marie C. Bouesseau posted by 2 people lilith PredictER
	Increased genetic counseling support improves communication of genetic information in families. [My Copy] Genet Med, Vol. 10, No. 3. (March 2008), pp. 167-172. by L. E. Forrest, J. Burke, S. Bacic, D. J. Amor posted by 1 person PredictER
	Incorporating ethnicity into genetic risk assessment for Alzheimer disease: the REVEAL study experience. [My Copy] Genet Med, Vol. 10, No. 3. (March 2008), pp. 207-214. by K. D. Christensen, J. S. Roberts, C. D. Royal, et al.G. A. Fasaye, T. Obisesan, L. A. Cupples, P. J. Whitehouse, M. B. Butson, E. Linnenbringer, N. R. Relkin, L. Farrer, R. Cook-Deegan, R. C. Green posted by 1 person PredictER
	Twenty-first century brain banking: at the crossroads [My Copy] Acta Neuropathologica by Manuel Graeber posted by 1 person PredictER
	Genetic tests for common diseases: new insights, old concerns [My Copy] BMJ, Vol. 336, No. 7644. (15 March 2008), pp. 590-593. by David Melzer, Stuart Hogarth, Katherine Liddell, Tom Ling, Simon Sanderson, Ron L. Zimmern posted by 3 people faw3 PredictER omalbam
	National Ethical Consultative Committee for the Life and Health Sciences in France issues opinion entitled "Genetics and medicine: from prediction to prevention. [My Copy] Int Dig Health Legis, Vol. 47, No. 2. (1996), pp. 263-265. posted by 1 person PredictER
	Genetic research and ethics. [My Copy] Bull Med Ethics, Vol. No. 145 (February 1999), pp. 21-24. by posted by 3 people 8_01 lilith PredictER
	Genetic testing for cystic fibrosis. National Institutes of Health Consensus Development Conference Statement on genetic testing for cystic fibrosis. [My Copy] Arch Intern Med, Vol. 159, No. 14. (26 July 1999), pp. 1529-1539. posted by 1 person PredictER
	Research based on archived information and samples. Recommendations from the Royal College of Physicians Committee on Ethical Issues in Medicine. [My Copy] J R Coll Physicians Lond, Vol. 33, No. 3. (n 1999), pp. 264-266. posted by 3 people 8_01 lilith PredictER
	American Society of Clinical Oncology policy statement update: genetic testing for cancer susceptibility. [My Copy] J Clin Oncol, Vol. 21, No. 12. (15 June 2003), pp. 2397-2406. by posted by 1 person PredictER
	Statement on human genomic databases, December 2002. [My Copy] J Int Bioethique, Vol. 14, No. 3-4. (c 2003), pp. 207-210. by posted by 1 person PredictER
	The work of the Medical Research Council. [My Copy] Bull Med Ethics, No. 187. (April 2003) by posted by 1 person PredictER
	Nuffield Council on Bioethics issues consultation paper on personalized medicines. [My Copy] Pharmacogenomics, Vol. 4, No. 1. (January 2003) posted by 1 person PredictER
	International Declaration on Human Genetic Data. [My Copy] Eur J Health Law, Vol. 11, No. 1. (March 2004), pp. 93-107. by H. D. Abbing, posted by 1 person PredictER
	African Americans' opinions about human-genetics research. [My Copy] Politics Life Sci, Vol. 23, No. 1. (March 2004), pp. 60-66. by P. Achter, R. Parrott, K. Silk posted by 1 person PredictER
	Human genetic databases and liberty. [My Copy] Jurid Rev, Vol. 2004, No. 1. (2004), pp. 65-74. by R. Adalsteinsson posted by 1 person PredictER
	Confidentiality and Huntington's chorea. [My Copy] J Med Ethics, Vol. 16, No. 4. (December 1990), pp. 196-199. by J. Adams posted by 1 person PredictER
	Should we genetically test everyone for haemochromatosis? [My Copy] J Med Ethics, Vol. 25, No. 2. (April 1999), pp. 209-214. by K. Allen, R. Williamson posted by 1 person PredictER
	Commercial tissue repositories: HIPAA raises sponsors' fears. [My Copy] IRB, Vol. 26, No. 5. (t 2004), pp. 9-11. by M. D. Allen posted by 1 person PredictER
	Homozygosity in Huntington's disease: new ethical dilemma caused by molecular diagnosis. [My Copy] Clin Genet, Vol. 61, No. 6. (June 2002), pp. 437-442. by M. E. Alonso, P. Yescas, A. Rasmussen, et al.A. Ochoa, R. Macías, I. Ruiz, R. Suástegui posted by 1 person PredictER
	IRB triage of projects that involve medical record review. [My Copy] IRB, Vol. 22, No. 1. (January 2000), pp. 4-7. by R. Amdur, M. A. Speers, E. Bankert posted by 1 person PredictER
	Continuing IRB review when research activity is limited to routine follow-up evaluations. [My Copy] IRB, Vol. 19, No. 1. (b 1997), pp. 7-10. by R. J. Amdur, E. Bankert posted by 1 person PredictER
	Medicolegal and ethical issues in genetic cancer syndromes. [My Copy] Semin Surg Oncol, Vol. 18, No. 4. (June 2000), pp. 339-346. by M. R. Anderlik, E. A. Lisko posted by 1 person PredictER
	Privacy and confidentiality of genetic information: what rules for the new science? [My Copy] Annu Rev Genomics Hum Genet, Vol. 2 (2001), pp. 401-433. by M. R. Anderlik, M. A. Rothstein posted by 1 person PredictER
	Nondirectiveness in prenatal genetics: patients read between the lines. [My Copy] Nurs Ethics, Vol. 6, No. 2. (March 1999), pp. 126-136. by G. Anderson posted by 1 person PredictER