19 found
Order:
Disambiguations:
Jane Kaye [9]J. Kaye [4]Joel Kaye [3]Jacqueline Kaye [2]
Jonathan D. Kaye [2]Julian B. Kaye [1]Joe Kaye [1]Jeffrey A. Kaye [1]

Not all matches are shown. Search with initial or firstname to single out others.

See also:
Profile: Jerry Kaye
Profile: Johsua Kaye (New School for Social Research)
Profile: Jennifer Kaye (University of Wisconsin, Milwaukee)
  1.  7
    Todd S. Braver, Deanna M. Barch, Beth A. Keys, Cameron S. Carter, Jonathan D. Cohen, Jeffrey A. Kaye, Jeri S. Janowsky, Stephan F. Taylor, Jerome A. Yesavage & Martin S. Mumenthaler (2001). Context Processing in Older Adults: Evidence for a Theory Relating Cognitive Control to Neurobiology in Healthy Aging. Journal of Experimental Psychology: General 130 (4):746.
    Direct download (3 more)  
     
    Export citation  
     
    My bibliography   14 citations  
  2.  5
    J. Patrick Woolley, Michelle L. McGowan, Harriet J. A. Teare, Victoria Coathup, Jennifer R. Fishman, Richard A. Settersten, Sigrid Sterckx, Jane Kaye & Eric T. Juengst (2016). Citizen science or scientific citizenship? Disentangling the uses of public engagement rhetoric in national research initiatives. BMC Medical Ethics 17 (1):1.
    The language of “participant-driven research,” “crowdsourcing” and “citizen science” is increasingly being used to encourage the public to become involved in research ventures as both subjects and scientists. Originally, these labels were invoked by volunteer research efforts propelled by amateurs outside of traditional research institutions and aimed at appealing to those looking for more “democratic,” “patient-centric,” or “lay” alternatives to the professional science establishment. As mainstream translational biomedical research requires increasingly larger participant pools, however, corporate, academic and governmental research programs (...)
    Translate
      Direct download (3 more)  
     
    Export citation  
     
    My bibliography  
  3.  3
    Don Chalmers, Dianne Nicol, Jane Kaye, Jessica Bell, Alastair V. Campbell, Calvin W. L. Ho, Kazuto Kato, Jusaku Minari, Chih-Hsing Ho, Colin Mitchell, Fruzsina Molnár-Gábor, Margaret Otlowski, Daniel Thiel, Stephanie M. Fullerton & Tess Whitton (2016). Has the biobank bubble burst? Withstanding the challenges for sustainable biobanking in the digital era. BMC Medical Ethics 17 (1):1.
    _BMC Medical Ethics_ is an open access journal publishing original peer-reviewed research articles in relation to the ethical aspects of biomedical research and clinical practice, including professional choices and conduct, medical technologies, healthcare systems and health policies. _BMC __Medical Ethics _is part of the _BMC_ series which publishes subject-specific journals focused on the needs of individual research communities across all areas of biology and medicine. We do not make editorial decisions on the basis of the interest of a study or (...)
    Translate
      Direct download (3 more)  
     
    Export citation  
     
    My bibliography  
  4.  3
    Jessica Bell, Mirko Ancillotti, Victoria Coathup, Sarah Coy, Tessel Rigter, Travis Tatum, Jasjote Grewal, Faruk Berat Akcesme, Jovana Brkić, Anida Causevic-Ramosevac, Goran Milovanovic, Marianna Nobile, Cristiana Pavlidis, Teresa Finlay & Jane Kaye (2016). Challenges and opportunities for ELSI early career researchers. BMC Medical Ethics 17 (1):1.
    Over the past 25 years, there has been growing recognition of the importance of studying the Ethical, Legal and Social Implications of genetic and genomic research. A large investment into ELSI research from the National Institutes of Health Human Genomic Project budget in 1990 stimulated the growth of this emerging field; ELSI research has continued to develop and is starting to emerge as a field in its own right. The evolving subject matter of ELSI research continues to raise new research (...)
    Translate
      Direct download (3 more)  
     
    Export citation  
     
    My bibliography  
  5.  64
    D. Chalmers, M. Burgess, K. Edwards, J. Kaye, E. M. Meslin & D. Nicol (2015). Marking Shifts in Human Research Ethics in the Development of Biobanking. Public Health Ethics 8 (1):63-71.
    Biobanks are increasingly being created specifically for research purposes. Concomitantly, we are seeing significant and evolving shifts in research ethics in relation to biobanking. Three discrete shifts are identified in this article. The first extends the ethical focus beyond the protection of human subjects to the promotion of broader community benefits of research utilizing biobanked resources, and an expectation that these benefits will be shared. The second involves the evolution of the traditional consent paradigm for future research uses of biobanks (...)
    Direct download (4 more)  
     
    Export citation  
     
    My bibliography  
  6.  84
    B. M. Knoppers, J. R. Harris, P. R. Burton, M. Murtagh, D. Cox, M. Deschenes, I. Fortier, T. J. Hudson, J. Kaye & K. Lindpaintner (2011). From Genomic Databases to Translation: A Call to Action. Journal of Medical Ethics 37 (8):515-516.
    The rapid rise of international collaborative science has enabled access to genomic data. In this article, it is argued that to move beyond mapping genomic variation to understanding its role in complex disease aetiology and treatment will require extending data sharing for the purposes of clinical research translation and implementation.
    Direct download (6 more)  
     
    Export citation  
     
    My bibliography   1 citation  
  7.  3
    Jane Kaye, Paula Boddington, Jantina de Vries, Naomi Hawkins & Karen Melham, Ethical Implications of the Use of Whole Genome Methods in Medical Research.
    The use of genome-wide association studies in medical research and the increased ability to share data give a new twist to some of the perennial ethical issues associated with genomic research. GWAS create particular challenges because they produce fine, detailed, genotype information at high resolution, and the results of more focused studies can potentially be used to determine genetic variation for a wide range of conditions and traits. The information from a GWA scan is derived from DNA that is a (...)
    Direct download  
     
    Export citation  
     
    My bibliography   2 citations  
  8.  1
    B. Elan Dresher & Jonathan D. Kaye (1990). A Computational Learning Model for Metrical Phonology. Cognition 34 (2):137-195.
    Direct download (3 more)  
     
    Export citation  
     
    My bibliography   6 citations  
  9.  1
    Victoria Coathup, Harriet J. A. Teare, Jusaku Minari, Go Yoshizawa, Jane Kaye, Masanori P. Takahashi & Kazuto Kato (2016). Using digital technologies to engage with medical research: views of myotonic dystrophy patients in Japan. BMC Medical Ethics 17 (1):51.
    _BMC Medical Ethics_ is an open access journal publishing original peer-reviewed research articles in relation to the ethical aspects of biomedical research and clinical practice, including professional choices and conduct, medical technologies, healthcare systems and health policies. _BMC __Medical Ethics _is part of the _BMC_ series which publishes subject-specific journals focused on the needs of individual research communities across all areas of biology and medicine. We do not make editorial decisions on the basis of the interest of a study or (...)
    Translate
      Direct download (3 more)  
     
    Export citation  
     
    My bibliography  
  10.  8
    Jacqueline Kaye (1996). The Implications of a Too‐Regular Form: The Muslim Woman and the European Mind. The European Legacy 1 (3):900-907.
    Direct download (4 more)  
     
    Export citation  
     
    My bibliography  
  11.  10
    A. Lucassen & J. Kaye (2006). Genetic Testing Without Consent: The Implications of the New Human Tissue Act 2004. Journal of Medical Ethics 32 (12):690-692.
    Despite its focus on consent the new Human Tissue Act 2004 allows for testing without consent where a relative could benefitIn recognition of the fact that genetic test results in people can have implications for close relatives, the new Human Tissue Act 2004 allows for a direction to access a person’s tissue so that testing can be carried out for the benefit of a relative, without the consent of that person. Clinical practice governed by common law and statute, before this (...)
    Direct download (4 more)  
     
    Export citation  
     
    My bibliography  
  12.  3
    J. Kaye (2007). Testing Times: What is the Legal Situation When an Adolescent Wants a Genetic Test? Clinical Ethics 2 (4):176-180.
    Clinicians, as well as other health-care professionals in genetics clinics, may find themselves in the position where they must consider whether it would be appropriate to offer a diagnostic genetic test to an adolescent. While a clinician's decision to offer a diagnostic genetic test may be straightforward in clinical terms, the dynamics of family interaction and circumstances may make the decision-making process more complicated. Disagreement between parent and child place clinicians in a difficult position and they must be clear about (...)
    Direct download (4 more)  
     
    Export citation  
     
    My bibliography  
  13.  1
    Joel Kaye (2000). Odd Langholm, The Legacy of Scholasticism in Economic Thought: Antecedents of Choice and Power.(Historical Perspectives on Modern Economics.) Cambridge, Eng.: Cambridge University Press, 1998. Pp. Xi, 215. $59.95. [REVIEW] Speculum 75 (3):705-708.
    No categories
    Direct download  
     
    Export citation  
     
    My bibliography  
  14. Jessica Bell, Karen Kennedy, Carol Smee, Dawn Muddyman & Jane Kaye (2015). ‘Pop-Up’ Governance: Developing Internal Governance Frameworks for Consortia: The Example of UK10K. Life Sciences, Society and Policy 11 (1):1-17.
    Innovations in information technologies have facilitated the development of new styles of research networks and forms of governance. This is evident in genomics where increasingly, research is carried out by large, interdisciplinary consortia focussing on a specific research endeavour. The UK10K project is an example of a human genomics consortium funded to provide insights into the genomics of rare conditions, and establish a community resource from generated sequence data. To achieve its objectives according to the agreed timetable, the UK10K project (...)
    No categories
    Direct download  
     
    Export citation  
     
    My bibliography  
  15. Sylvia Joseph Galambos, C. R. Gallistel, Rachel Gelman, Susan Goldin-Meadow, Trevor A. Harley, Annette Karmiloff-Smith, Jonathan D. Kaye, Stephen M. Kosslyn, Robert J. Melara & Elizabeth F. Shipley (1990). Fly~, Rex A., 203. Cognition 34 (303):303.
     
    Export citation  
     
    My bibliography  
  16. Mirko Ancillotti Jessica Bell, Sarah Coy Victoria Coathup, Travis Tatum Tessel Rigter, Faruk Berat Akcesme Jasjote Grewal, Anida Causevic-Ramosevac Jovana Brkić, Marianna Nobile Goran Milovanovic, Teresa Finlay Cristiana Pavlidis & Jane Kaye (forthcoming). Challenges and Opportunities for ELSI Early Career Researchers. Most Recent Articles: Bmc Medical Ethics.
    Over the past 25 years, there has been growing recognition of the importance of studying the Ethical, Legal and Social Implications of genetic and genomic research. A large investment into ELSI research...
    No categories
    Direct download  
     
    Export citation  
     
    My bibliography  
  17. Jane Kaye (ed.) (2012). Governing Biobanks: Understanding the Interplay Between Law and Practice. Hart Pub..
     
    Export citation  
     
    My bibliography  
  18. Joel Kaye (2000). The Legacy of Scholasticism in Economic Thought: Antecedents of Choice and PowerOdd Langholm. Speculum 75 (3):705-708.
    No categories
    Direct download (2 more)  
     
    Export citation  
     
    My bibliography  
  19. Mary Ellen Wolf, Jacqueline Kaye & Abdelhamid Zoubir (1992). The Ambiguous Compromise: Language, Literature and National Identity in Algeria and Morocco. Substance 21 (3):124.
    Direct download (2 more)  
     
    Export citation  
     
    My bibliography