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Connection

Lainie Ross to Genetic Testing

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

7.567
  1. Ethical Issues in Newborn Sequencing Research: The Case Study of BabySeq. Pediatrics. 2019 12; 144(6).
    View in: PubMed
    Score: 0.469
  2. Introducing Genetic Tests With Uncertain Implications in Living Donor Kidney Transplantation: ApoL1 as a Case Study. Prog Transplant. 2016 Sep; 26(3):203-6.
    View in: PubMed
    Score: 0.370
  3. Ethical and policy issues in newborn screening of children for neurologic and developmental disorders. Pediatr Clin North Am. 2015 Jun; 62(3):787-98.
    View in: PubMed
    Score: 0.341
  4. Pediatric DTC Genetic Testing for Adult-Onset Inherited Cancer Risk: The Perspectives of High-Risk Parents. Public Health Genomics. 2025; 28(1):102-112.
    View in: PubMed
    Score: 0.337
  5. 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: 0.303
  6. Technical report: Ethical and policy issues in genetic testing and screening of children. Genet Med. 2013 Mar; 15(3):234-45.
    View in: PubMed
    Score: 0.294
  7. A pilot study to evaluate awareness of and attitudes about prenatal and neonatal genetic testing in postpartum African American women. J Natl Med Assoc. 2013; 105(1):85-91.
    View in: PubMed
    Score: 0.291
  8. Predictive genetic testing of children and the role of the best interest standard. J Law Med Ethics. 2013; 41(4):899-906, Table of Contents.
    View in: PubMed
    Score: 0.291
  9. A re-examination of the use of ethnicity in prenatal carrier testing. Am J Med Genet A. 2012 Jan; 158A(1):19-23.
    View in: PubMed
    Score: 0.270
  10. Ethical and policy issues raised by heterozygote carrier identification and predictive genetic testing of adolescents. Adolesc Med State Art Rev. 2011 Aug; 22(2):251-64, ix.
    View in: PubMed
    Score: 0.264
  11. Clinical and ethical considerations in managing carrier detection. Am J Public Health. 2009 Aug; 99(8):1348-9.
    View in: PubMed
    Score: 0.228
  12. Fragile X screening: attitudes of genetic health professionals. Am J Med Genet A. 2009 Feb 15; 149A(4):626-32.
    View in: PubMed
    Score: 0.223
  13. Policy considerations in designing a fragile X population screening program. Genet Med. 2008 Oct; 10(10):711-3.
    View in: PubMed
    Score: 0.217
  14. From genetics to genomics: ethics, policy, and parental decision-making. J Pediatr Psychol. 2009 Jul; 34(6):639-47.
    View in: PubMed
    Score: 0.214
  15. 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: 0.208
  16. Methodology matters. Am J Public Health. 2007 Apr; 97(4):589; author reply 589-90.
    View in: PubMed
    Score: 0.194
  17. Attitudes of genetic counselors towards expanding newborn screening and offering predictive genetic testing to children. Am J Med Genet A. 2006 Nov 01; 140(21):2312-9.
    View in: PubMed
    Score: 0.190
  18. Screening for conditions that do not meet the Wilson and Jungner criteria: the case of Duchenne muscular dystrophy. Am J Med Genet A. 2006 Apr 15; 140(8):914-22.
    View in: PubMed
    Score: 0.183
  19. 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: 0.179
  20. Parental Communication With their Children about Cancer Risk and DTC Cascade Genetic Testing: Implications for Genetic Education and Counseling. Am J Med Genet A. 2025 Sep; 197(9):e64115.
    View in: PubMed
    Score: 0.172
  21. Parental attitudes and beliefs regarding the genetic testing of children. Community Genet. 2005; 8(2):94-102.
    View in: PubMed
    Score: 0.167
  22. Attitudes of healthcare professionals and parents regarding genetic testing for violent traits in childhood. J Med Ethics. 2004 Dec; 30(6):580-6.
    View in: PubMed
    Score: 0.166
  23. Should children and adolescents undergo genetic testing? Pediatr Ann. 2004 Nov; 33(11):762-9.
    View in: PubMed
    Score: 0.165
  24. Newborn Screening for Neurodevelopmental Disorders May Exacerbate Health Disparities. Pediatrics. 2023 10 01; 152(4).
    View in: PubMed
    Score: 0.153
  25. 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: 0.151
  26. Diagnosis, treatment and disclosure: A qualitative exploration of participant challenges in a Monogenic Diabetes Registry. Genet Med. 2023 04; 25(4):100019.
    View in: PubMed
    Score: 0.146
  27. Professional and personal attitudes about access and confidentiality in the genetic testing of children: a pilot study. Genet Test. 2003; 7(2):123-30.
    View in: PubMed
    Score: 0.146
  28. Predictive genetic testing for conditions that present in childhood. Kennedy Inst Ethics J. 2002 Sep; 12(3):225-44.
    View in: PubMed
    Score: 0.142
  29. The ethics of preadoption genetic testing. Am J Med Genet. 2001 Dec 01; 104(3):214-20.
    View in: PubMed
    Score: 0.135
  30. Genetic exceptionalism vs. paradigm shift: lessons from HIV. J Law Med Ethics. 2001; 29(2):141-8.
    View in: PubMed
    Score: 0.127
  31. Ethical and policy issues in genetic testing. Pancreatology. 2001; 1(6):576-80.
    View in: PubMed
    Score: 0.127
  32. Ethical issues in genetic testing of children. Arch Pediatr Adolesc Med. 2000 Sep; 154(9):873-9.
    View in: PubMed
    Score: 0.124
  33. Genetic testing of adolescents: is it in their best interest? Arch Pediatr Adolesc Med. 2000 Aug; 154(8):850-2.
    View in: PubMed
    Score: 0.123
  34. Addressing the ethical challenges in genetic testing and sequencing of children. Am J Bioeth. 2014; 14(3):3-9.
    View in: PubMed
    Score: 0.078
  35. Recommendations for returning genomic incidental findings? We need to talk! Genet Med. 2013 Nov; 15(11):854-9.
    View in: PubMed
    Score: 0.076
  36. A pilot study to evaluate knowledge and attitudes of Illinois pediatricians toward newborn screening for sickle cell disease and cystic fibrosis. Am J Perinatol. 2011 Mar; 28(3):169-76.
    View in: PubMed
    Score: 0.062
  37. Population screening for genetic disorders in the 21st century: evidence, economics, and ethics. Public Health Genomics. 2010; 13(2):106-15.
    View in: PubMed
    Score: 0.057
  38. 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: 0.047
  39. 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: 0.041
  40. Correspondence on "Exploring the motivations of research participants who chose not to learn medically actionable secondary findings about themselves" by Schupmann et al. Genet Med. 2022 02; 24(2):499-500.
    View in: PubMed
    Score: 0.034
  41. Consent for clinical research. N Engl J Med. 1997 Jul 24; 337(4):282.
    View in: PubMed
    Score: 0.025
  42. Disclosing misattributed paternity. Bioethics. 1996 Apr; 10(2):114-30.
    View in: PubMed
    Score: 0.023
  43. Ethical issues in haemophilia. Haemophilia. 2006 Jul; 12 Suppl 3:30-5.
    View in: PubMed
    Score: 0.012
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.