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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

7.895
  1. Newborn Sequencing: The Promise and Perils. Annu Rev Genomics Hum Genet. 2025 Aug; 26(1):401-423.
    View in: PubMed
    Score: 0.666
  2. Ethical Issues in Newborn Sequencing Research: The Case Study of BabySeq. Pediatrics. 2019 12; 144(6).
    View in: PubMed
    Score: 0.448
  3. 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: 0.354
  4. 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: 0.326
  5. 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: 0.322
  6. 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: 0.289
  7. 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: 0.281
  8. 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: 0.278
  9. 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: 0.278
  10. 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: 0.258
  11. 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: 0.252
  12. Clinical and ethical considerations in managing carrier detection. Am J Public Health. 2009 Aug; 99(8):1348-9.
    View in: PubMed
    Score: 0.218
  13. Fragile X screening: attitudes of genetic health professionals. Am J Med Genet A. 2009 Feb 15; 149A(4):626-32.
    View in: PubMed
    Score: 0.213
  14. Policy considerations in designing a fragile X population screening program. Genet Med. 2008 Oct; 10(10):711-3.
    View in: PubMed
    Score: 0.207
  15. From genetics to genomics: ethics, policy, and parental decision-making. J Pediatr Psychol. 2009 Jul; 34(6):639-47.
    View in: PubMed
    Score: 0.205
  16. 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: 0.199
  17. Methodology matters. Am J Public Health. 2007 Apr; 97(4):589; author reply 589-90.
    View in: PubMed
    Score: 0.186
  18. 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: 0.182
  19. 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: 0.175
  20. 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: 0.171
  21. 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 09; 197(9):e64115.
    View in: PubMed
    Score: 0.164
  22. Parental attitudes and beliefs regarding the genetic testing of children. Community Genet. 2005; 8(2):94-102.
    View in: PubMed
    Score: 0.160
  23. 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: 0.159
  24. Should children and adolescents undergo genetic testing? Pediatr Ann. 2004 Nov; 33(11):762-9.
    View in: PubMed
    Score: 0.158
  25. Newborn Screening for Neurodevelopmental Disorders May Exacerbate Health Disparities. Pediatrics. 2023 10 01; 152(4).
    View in: PubMed
    Score: 0.147
  26. 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: 0.144
  27. 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: 0.140
  28. 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: 0.139
  29. Predictive genetic testing for conditions that present in childhood. Kennedy Inst Ethics J. 2002 Sep; 12(3):225-44.
    View in: PubMed
    Score: 0.136
  30. The ethics of preadoption genetic testing. Am J Med Genet. 2001 Dec 01; 104(3):214-20.
    View in: PubMed
    Score: 0.129
  31. Genetic exceptionalism vs. paradigm shift: lessons from HIV. J Law Med Ethics. 2001; 29(2):141-8.
    View in: PubMed
    Score: 0.121
  32. Ethical and policy issues in genetic testing. Pancreatology. 2001; 1(6):576-80.
    View in: PubMed
    Score: 0.121
  33. Ethical issues in genetic testing of children. Arch Pediatr Adolesc Med. 2000 Sep; 154(9):873-9.
    View in: PubMed
    Score: 0.118
  34. Genetic testing of adolescents: is it in their best interest? Arch Pediatr Adolesc Med. 2000 Aug; 154(8):850-2.
    View in: PubMed
    Score: 0.118
  35. Addressing the ethical challenges in genetic testing and sequencing of children. Am J Bioeth. 2014; 14(3):3-9.
    View in: PubMed
    Score: 0.075
  36. Recommendations for returning genomic incidental findings? We need to talk! Genet Med. 2013 Nov; 15(11):854-9.
    View in: PubMed
    Score: 0.072
  37. 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: 0.059
  38. 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: 0.055
  39. 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: 0.045
  40. 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: 0.040
  41. 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: 0.032
  42. Consent for clinical research. N Engl J Med. 1997 Jul 24; 337(4):282.
    View in: PubMed
    Score: 0.024
  43. Disclosing misattributed paternity. Bioethics. 1996 Apr; 10(2):114-30.
    View in: PubMed
    Score: 0.022
  44. Ethical issues in haemophilia. Haemophilia. 2006 Jul; 12 Suppl 3:30-5.
    View in: PubMed
    Score: 0.011
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.