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Connection

Lainie Ross to Informed Consent

This is a "connection" page, showing publications Lainie Ross has written about Informed Consent.
Connection Strength

6.637
  1. Developing an ethics framework for living donor transplantation. J Med Ethics. 2018 12; 44(12):843-850.
    View in: PubMed
    Score: 0.538
  2. Ethical Analysis and Policy Recommendations Regarding Domino Liver Transplantation. Transplantation. 2018 05; 102(5):803-808.
    View in: PubMed
    Score: 0.532
  3. Prisoners as Living Donors: A Vulnerabilities Analysis. Camb Q Healthc Ethics. 2018 Jan; 27(1):93-108.
    View in: PubMed
    Score: 0.520
  4. Pediatric Resident Preparedness and Educational Experiences With Informed Consent. Acad Pediatr. 2016 Apr; 16(3):298-304.
    View in: PubMed
    Score: 0.446
  5. Mandatory versus voluntary consent for newborn screening? Kennedy Inst Ethics J. 2010 Dec; 20(4):299-328.
    View in: PubMed
    Score: 0.318
  6. Against the tide: arguments against respecting a minor's refusal of efficacious life-saving treatment. Camb Q Healthc Ethics. 2009; 18(3):302-15; discussion 315-22.
    View in: PubMed
    Score: 0.279
  7. Arguments against respecting a minor's refusal of efficacious life-saving treatment redux, part II. Camb Q Healthc Ethics. 2009; 18(4):432-40; discussion 440-2.
    View in: PubMed
    Score: 0.279
  8. Informed consent for genetic research involving pleiotropic genes: an empirical study of ApoE research. IRB. 2006 Sep-Oct; 28(5):1-11.
    View in: PubMed
    Score: 0.237
  9. Adolescent autonomy in health care? APA Newsl Philos Med. 2003; 2(2):193-200.
    View in: PubMed
    Score: 0.184
  10. Ethical issues in pediatric trials. Am Heart J. 2001 Aug; 142(2):233-6.
    View in: PubMed
    Score: 0.167
  11. "Medical Benefit" and Therapeutic Misconception: The Ethical Conundrum of Phase 1 Pediatric Oncology Research. J Pediatr. 2021 11; 238:11-13.
    View in: PubMed
    Score: 0.166
  12. Attitudes and practices in postmortem organ procurement. JAMA. 2001 Apr 18; 285(15):1958; author reply 1959-60.
    View in: PubMed
    Score: 0.163
  13. Gender and race/ethnicity differences in living kidney donor demographics: Preference or disparity? Transplant Rev (Orlando). 2021 07; 35(3):100614.
    View in: PubMed
    Score: 0.163
  14. Genetic testing of adolescents: is it in their best interest? Arch Pediatr Adolesc Med. 2000 Aug; 154(8):850-2.
    View in: PubMed
    Score: 0.155
  15. The Ethical Limits of Children's Participation in Clinical Research. Hastings Cent Rep. 2020 Jul; 50(4):12-13.
    View in: PubMed
    Score: 0.155
  16. Patient confidentiality and the surrogate's right to know. J Law Med Ethics. 2000; 28(2):137-43.
    View in: PubMed
    Score: 0.149
  17. Delegating Decision-Making Authority To a Surrogate. Ann Thorac Surg. 2019 12; 108(6):1615-1616.
    View in: PubMed
    Score: 0.148
  18. Pediatric bioethics: reintroducing the parents. Responsive Community. 1999; 9(3):40-7.
    View in: PubMed
    Score: 0.139
  19. Consent for clinical research. N Engl J Med. 1997 Jul 24; 337(4):282.
    View in: PubMed
    Score: 0.126
  20. Adolescent sexuality and public policy: an unrepentant liberal approach. Politics Life Sci. 1996 Sep; 15(2):323-8.
    View in: PubMed
    Score: 0.118
  21. The 1966 Ciba Symposium on Transplantation Ethics: 50 Years Later. Transplantation. 2016 Jun; 100(6):1191-7.
    View in: PubMed
    Score: 0.116
  22. Adolescent sexuality and public policy: a liberal response. Politics Life Sci. 1996 Mar; 15(1):13-21.
    View in: PubMed
    Score: 0.114
  23. To tell or not to tell: attitudes of transplant surgeons and transplant nephrologists regarding the disclosure of recipient information to living kidney donors. Clin Transplant. 2015 Dec; 29(12):1203-12.
    View in: PubMed
    Score: 0.112
  24. Arguments against health care autonomy for minors. Bioethics Forum. 1995; 11(4):22-6.
    View in: PubMed
    Score: 0.106
  25. Mandatory extended searches in all genome sequencing: "incidental findings," patient autonomy, and shared decision making. JAMA. 2013 Jul 24; 310(4):367-8.
    View in: PubMed
    Score: 0.096
  26. The OHRP and SUPPORT. N Engl J Med. 2013 Jun 20; 368(25):e36.
    View in: PubMed
    Score: 0.095
  27. Attitudes of African-American parents about biobank participation and return of results for themselves and their children. J Med Ethics. 2012 Sep; 38(9):561-6.
    View in: PubMed
    Score: 0.088
  28. The challenges of collaboration for academic and community partners in a research partnership: points to consider. J Empir Res Hum Res Ethics. 2010 Mar; 5(1):19-31.
    View in: PubMed
    Score: 0.075
  29. Nine key functions for a human subjects protection program for community-engaged research: points to consider. J Empir Res Hum Res Ethics. 2010 Mar; 5(1):33-47.
    View in: PubMed
    Score: 0.075
  30. What the medical excuse teaches us about the potential living donor as patient. Am J Transplant. 2010 Apr; 10(4):731-736.
    View in: PubMed
    Score: 0.075
  31. Minors as living solid-organ donors. Pediatrics. 2008 Aug; 122(2):454-61.
    View in: PubMed
    Score: 0.068
  32. Ethical and policy issues in pediatric genetics. Am J Med Genet C Semin Med Genet. 2008 Feb 15; 148C(1):1-7.
    View in: PubMed
    Score: 0.066
  33. The participation of children in nontherapeutic diabetes research in the US. Nat Clin Pract Endocrinol Metab. 2007 May; 3(5):378-9.
    View in: PubMed
    Score: 0.062
  34. The ethical limits in expanding living donor transplantation. Kennedy Inst Ethics J. 2006 Jun; 16(2):151-72.
    View in: PubMed
    Score: 0.058
  35. A compounding of errors: the case of bone marrow donation between non-intimate siblings. J Clin Ethics. 2006; 17(3):220-6.
    View in: PubMed
    Score: 0.057
  36. Heterozygote carrier testing in high schools abroad: what are the lessons for the U.S.? J Law Med Ethics. 2006; 34(4):753-64.
    View in: PubMed
    Score: 0.057
  37. Certificates of confidentiality in research: rationale and usage. Genet Test. 2004; 8(2):214-20.
    View in: PubMed
    Score: 0.049
  38. Are minority children under- or overrepresented in pediatric research? Pediatrics. 2003 Oct; 112(4):890-5.
    View in: PubMed
    Score: 0.048
  39. Parental attitudes regarding newborn screening of PKU and DMD. Am J Med Genet A. 2003 Jul 15; 120A(2):209-14.
    View in: PubMed
    Score: 0.048
  40. Do healthy children deserve greater protection in medical research? J Pediatr. 2003 Feb; 142(2):108-12.
    View in: PubMed
    Score: 0.046
  41. Are research ethics standards satisfied in pediatric journal publications? Pediatrics. 2002 Aug; 110(2 Pt 1):364-70.
    View in: PubMed
    Score: 0.045
  42. Ethics of a paired-kidney-exchange program. N Engl J Med. 1997 Jun 12; 336(24):1752-5.
    View in: PubMed
    Score: 0.031
  43. Children as research subjects: a proposal to revise the current federal regulations using a moral framework. Stanford Law Pol Rev. 1997; 8(1):159-76.
    View in: PubMed
    Score: 0.030
  44. Justice for children: the child as organ donor. Bioethics. 1994 Apr; 8(2):105-26.
    View in: PubMed
    Score: 0.025
  45. Ethical issues in identifying and recruiting participants for familial genetic research. Am J Med Genet A. 2004 Nov 01; 130A(4):424-31.
    View in: PubMed
    Score: 0.013
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.