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ladygoat library [552 articles]

Статьи, недавно добавленные в библиотеку ladygoat .
  • On warning families about genetic risk: the ghost of Tarasoff.
    Am J Med, Vol. 109, No. 9. (15 December 2000), pp. 738-739.
    by DP Sulmasy
  • Duty to warn at-risk relatives for genetic disease: Genetic counselors' clinical experience
    American Journal of Medical Genetics Part C: Seminars in Medical Genetics, Vol. 119C, No. 1. (17 December 2002), pp. 27-34.
    by Beth B Dugan, Georgia L Wiesner, Eric T Juengst, Maryann O'Riordan, Anne L Matthews, Nathaniel H Robin
  • Potential harms, anonymization, and the right to withdraw consent to biobank research
    European Journal of Human Genetics, Vol. aop, No. current.
    by Stefan Eriksson, Gert Helgesson,
    posted to biobanks by ladygoat on 2005-07-05 20:47:35 as ** along with 2 people and 1 group cgreal PredictER CGREL
  • Building on relationships of trust in biobank research.
    J Med Ethics, Vol. 31, No. 7. (July 2005), pp. 415-418.
    by M G G Hansson
    posted to biobanks by ladygoat on 2005-07-05 20:45:07 as ** along with 1 group CGREL
  • Public health and the challenge of genomics.
    Aust N Z J Public Health, Vol. 29, No. 2. (April 2005), pp. 163-165.
    by M Kirkman
    posted to eugenics public-health by ladygoat on 2005-07-05 20:42:59 as ** along with 1 group CGREL
  • 'At the point at which you can do something about it, then it becomes more relevant': Informed consent in the pharmacogenetic clinic.
    Soc Sci Med, Vol. 61, No. 6. (September 2005), pp. 1201-1210.
  • Genetic databases and consent for use of medical records.
    Community Genet, Vol. 7, No. 4. (2004), pp. 173-175.
    by JK Gevers
    posted to consent by ladygoat on 2005-06-24 19:20:56 as ** along with 1 group CGREL
  • Unexpected findings in identifiable stored blood samples after analysis without consent: moral arguments for and against disclosure.
    Genet Couns, Vol. 13, No. 2. (2002), pp. 115-121.
    by MF Verweij, BC Hamel
  • notes The complex relationship of genetics, groups, and health: what it means for public health.
    J Law Med Ethics, Vol. 30, No. 2. (2002), pp. 290-297.
    by EW Clayton
    posted to public-health recontact by ladygoat on 2005-06-23 18:27:02 as ** along with 1 group CGREL
  • A model agreement for genetic research in socially identifiable populations.
    Am J Hum Genet, Vol. 63, No. 3. (September 1998), pp. 696-702.
    by MW Foster, D Bernsten, TH Carter
  • Disseminating the results of participant-focused research.
    J Transcult Nurs, Vol. 10, No. 4. (October 1999), pp. 340-349.
  • Protecting communities in research: current guidelines and limits of extrapolation.
    Nat Genet, Vol. 23, No. 3. (November 1999), pp. 275-280.
    by C Weijer, G Goldsand, EJ Emanuel
  • DO GENETIC CLINICS HAVE A LEGAL ETHICAL DUTY TO RECONTACT THEIR PATIENTS WHEN NEW INFORMATION ARISES
    AMERICAN JOURNAL OF HUMAN GENETICS, Vol. 57, No. 4., 1704.
    by Jp Cote, Ml Klimek, Cl Johnson
    posted to recontact by ladygoat on 2005-06-23 17:58:18 as ** along with 1 group CGREL
  • notes Staying informed and recontacting patients about research advances: a study of patient attitudes.
    Am J Hum Genet, Vol. 59, No. 4. (October 1996)
    by M Huggins, C Hahn, T Costa
  • notes Medical Geneticists' duty to warn at-risk relatives for genetic disease.
    Am J Med Genet A, Vol. 120, No. 3. (30 July 2003), pp. 374-380.
    by MJ Falk, RB Dugan, MA O'Riordan, AL Matthews, NH Robin
  • notes Duty to disclose in medical genetics: a legal perspective.
    Am J Med Genet, Vol. 39, No. 3. (1 June 1991), pp. 347-354.
    by MZ Pelias
  • Ethical, legal, and practical concerns about recontacting patients to inform them of new information: the case in medical genetics.
    Am J Med Genet, Vol. 103, No. 4. (1 November 2001), pp. 265-276.
    by AG Hunter, N Sharpe, M Mullen, WS Meschino
  • The duty to recontact: benefit and harm.
    Am J Hum Genet, Vol. 65, No. 4. (October 1999), pp. 1201-1204.
    by NF Sharpe
  • The duty to recontact: attitudes of genetics service providers.
    Am J Hum Genet, Vol. 61, No. 4. (October 1997)
  • The duty to recontact: attitudes of genetics service providers.
    Am J Hum Genet, Vol. 64, No. 3. (March 1999), pp. 852-860.
    by JL Fitzpatrick, C Hahn, T Costa, MJ Huggins
  • The Patterns of Natural Variation in Human Genes.
    Annu Rev Genomics Hum Genet (15 February 2005)
    by Dana C C Crawford, Dayna T T Akey, Deborah A A Nickerson
  • Opinions about new reproductive genetic technologies: Hopes and fears for our genetic future.
    Fertil Steril, Vol. 83, No. 6. (June 2005), pp. 1612-1621.
    by AL Kalfoglou, T Doksum, B Bernhardt, G Geller, L Leroy, DJ Mathews, JH Evans, DJ Doukas, N Reame, J Scott, K Hudson
  • One of These Things Is Not Like the Others: The Idea of Precedence in Health Technology Assessment and Coverage Decisions
    The Milbank Quarterly, Vol. 83, No. 2. (June 2005), pp. 193-223.
    by Mit Giacomini
    posted to insurance by ladygoat on 2005-06-20 19:53:12 as ** along with 1 group CGREL
  • Keeping genetic secrets.
    Med Ethics (Burlingt, Mass), Vol. 11, No. 1. (2004)
    by LH Glantz
    posted to privacy by ladygoat on 2005-06-20 19:51:13 as ** along with 1 group CGREL
  • Consent forms and the therapeutic misconception: the example of gene transfer research.
    IRB, Vol. 27, No. 1. (b 2005), pp. 1-8.
    by NM King, GE Henderson, LR Churchill, AM Davis, SC Hull, DK Nelson, PC Parham-Vetter, BB Rothschild, MM Easter, BS Wilfond
  • Germ-line enhancement of humans and non-humans.
    Kennedy Inst Ethics J, Vol. 15, No. 1. (March 2005), pp. 57-76.
    by JR Loftis
    posted to enhancement by ladygoat on 2005-06-20 19:47:35 as ** along with 1 group CGREL
  • Racism and human genome diversity research: the ethical limits of "population thinking".
    Philos Sci, Vol. 63, No. 3(Suppl.). (2001)
    by L Gannett
    posted to genetic-diversity race by ladygoat on 2005-06-20 19:45:42 as ** along with 1 group CGREL
  • The distribution of human genetic diversity: a comparison of mitochondrial, autosomal, and Y-chromosome data.
    Am J Hum Genet, Vol. 66, No. 3. (March 2000), pp. 979-988.
    by LB Jorde, WS Watkins, MJ Bamshad, ME Dixon, CE Ricker, MT Seielstad, MA Batzer
  • DNA studies challenge the meaning of race.
    Science, Vol. 282, No. 5389. (23 October 1998), pp. 654-655.
  • Research with stored biological samples: what do research participants want?
    Arch Intern Med, Vol. 165, No. 6. (28 March 2005), pp. 652-655.
    posted to stored-samples by ladygoat on 2005-06-17 16:05:17 as ** along with 1 person and 1 group PredictER CGREL
  • Publication visibility of sensitive public health data: when scientists bury their results.
    Sci Eng Ethics, Vol. 10, No. 4. (October 2004), pp. 597-613.
    by DA Rier
    posted to media by ladygoat on 2005-06-15 19:56:42 as ** along with 1 group CGREL
  • Scientists' and science writers' experiences reporting genetic discoveries: toward an ethic of trust in science journalism.
    Genet Med, Vol. 7, No. 3. (March 2005), pp. 198-205.
    posted to media by ladygoat on 2005-06-15 19:55:58 as ** along with 1 person and 1 group elsiatcase CGREL
  • Do the print media "hype" genetic research? A comparison of newspaper stories and peer-reviewed research papers.
    CMAJ, Vol. 170, No. 9. (27 April 2004), pp. 1399-1407.
    by TM Bubela, TA Caulfield
    posted to media by ladygoat on 2005-06-15 19:53:07 as ** along with 1 group CGREL
  • Science reporting to the public: does the message get twisted?
    CMAJ, Vol. 170, No. 9. (27 April 2004), pp. 1415-1416.
    by C Condit
    posted to media by ladygoat on 2005-06-15 19:51:39 as ** along with 1 group CGREL
  • Public health and genetics--a dangerous combination?
    Eur J Public Health, Vol. 15, No. 2. (April 2005), pp. 114-116.
    by A Brand
    posted to no-tag by ladygoat on 2005-06-13 20:16:06 as ** along with 1 group CGREL
  • Examining Population Stratification via Individual Ancestry Estimates versus Self-Reported Race.
    Cancer Epidemiol Biomarkers Prev, Vol. 14, No. 6. (June 2005), pp. 1545-1551.
    posted to no-tag by ladygoat on 2005-06-13 20:15:15 as ** along with 1 group CGREL
  • Genomic screening and replication using the same data set in family-based association testing.
    Nat Genet (5 June 2005)
    by Kristel Van Steen, Matthew B B McQueen, Alan Herbert, Benjamin Raby, Helen Lyon, Dawn L L Demeo, Amy Murphy, Jessica Su, Soma Datta, Carsten Rosenow, Michael Christman, Edwin K K Silverman, Nan M M Laird, Scott T T Weiss, Christoph Lange
    posted to no-tag by ladygoat on 2005-06-13 20:02:41 as ** along with 1 group CGREL
  • FDA pharmacogenomics guidance sends clear message to industry.
    Nat Rev Drug Discov, Vol. 4, No. 5. (May 2005)
    by M Ratner
    posted to no-tag by ladygoat on 2005-06-13 20:01:46 as ** along with 1 group CGREL
  • Genetic nondiscrimination
    Nature Genetics, Vol. 37, No. 6., pp. 559-560.
    by Paul R Billings
    posted to no-tag by ladygoat on 2005-06-13 19:59:38 as ** along with 1 person and 1 group cgreal CGREL
  • Biobanking: international norms.
    J Law Med Ethics, Vol. 33, No. 1. (2005), pp. 7-14.
    by BM Knoppers
    posted to biobanks by ladygoat on 2005-06-13 19:55:10 as ** along with 1 group CGREL
  • Informed consent and biobanks.
    J Law Med Ethics, Vol. 33, No. 1. (2005), pp. 15-21.
    by EW Clayton
    posted to biobanks by ladygoat on 2005-06-13 19:54:35 as ** along with 1 group CGREL
  • Harnessing the benefits of biobanks.
    J Law Med Ethics, Vol. 33, No. 1. (2005), pp. 22-30.
    by LB Andrews
    posted to biobanks by ladygoat on 2005-06-13 19:54:03 as ** along with 1 group CGREL
  • Accountability in population biobanking: comparative approaches.
    J Law Med Ethics, Vol. 33, No. 1. (2005), pp. 40-53.
    posted to biobanks by ladygoat on 2005-06-13 19:53:19 as ** along with 2 people and 1 group cgreal elsiatcase CGREL
  • Technology Transfer in biobanking: credits, debits, and population health futures.
    J Law Med Ethics, Vol. 33, No. 1. (2005), pp. 54-69.
    posted to biobanks by ladygoat on 2005-06-13 19:52:50 as ** along with 1 person and 1 group cgreal CGREL
  • Should liability play a role in social control of biobanks?
    J Law Med Ethics, Vol. 33, No. 1. (2005), pp. 70-78.
    by LI Palmer
    posted to biobanks by ladygoat on 2005-06-13 19:52:08 as ** along with 1 group CGREL
  • Expanding the ethical analysis of biobanks.
    J Law Med Ethics, Vol. 33, No. 1. (2005), pp. 89-101.
    by MA Rothstein
    posted to biobanks by ladygoat on 2005-06-13 19:51:26 as ** along with 1 group CGREL
  • The seduction of science to perfect an imperfect race.
    Int J Health Serv, Vol. 35, No. 2. (2005), pp. 399-404.
    posted to no-tag by ladygoat on 2005-06-13 19:47:44 as ** along with 1 group CGREL
  • The biography of psychiatric genetics: From early achievements to historical burden, from an anxious society to critical geneticists.
    Am J Med Genet B Neuropsychiatr Genet (27 May 2005)
    by Peter Propping
    posted to no-tag by ladygoat on 2005-06-13 19:45:17 as ** along with 1 group CGREL
  • Portrayal of genetic risk for breast cancer in ethnic and non-ethnic newspapers.
    Women Health, Vol. 40, No. 4. (2004), pp. 93-111.
    posted to no-tag by ladygoat on 2005-06-13 19:39:52 as ** along with 1 group CGREL
  • Democracy and genetic privacy: the value of bodily integrity.
    Med Health Care Philos, Vol. 8, No. 1. (2005), pp. 97-103.
    by L Beckman
    posted to no-tag by ladygoat on 2005-06-13 19:38:56 as ** along with 1 person and 1 group cgreal CGREL
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