Connection

AMY MCGUIRE to Genome, Human

This is a "connection" page, showing publications AMY MCGUIRE has written about Genome, Human.
Connection Strength

4.297
  1. The road ahead in genetics and genomics. Nat Rev Genet. 2020 10; 21(10):581-596.
    View in: PubMed
    Score: 0.438
  2. Moving beyond Bermuda: sharing data to build a medical information commons. Genome Res. 2017 06; 27(6):897-901.
    View in: PubMed
    Score: 0.346
  3. When bins blur: Patient perspectives on categories of results from clinical whole genome sequencing. AJOB Empir Bioeth. 2017 Apr-Jun; 8(2):82-88.
    View in: PubMed
    Score: 0.342
  4. Clinical integration of next generation sequencing: a policy analysis. J Law Med Ethics. 2014; 42 Suppl 1:5-8.
    View in: PubMed
    Score: 0.276
  5. The indispensable role of professional judgment in genomic medicine. JAMA. 2013 Apr 10; 309(14):1465-6.
    View in: PubMed
    Score: 0.263
  6. Balancing the risks and benefits of genomic data sharing: genome research participants' perspectives. Public Health Genomics. 2012; 15(2):106-14.
    View in: PubMed
    Score: 0.240
  7. Health system implications of direct-to-consumer personal genome testing. Public Health Genomics. 2011; 14(1):53-8.
    View in: PubMed
    Score: 0.222
  8. Science and regulation. Regulating direct-to-consumer personal genome testing. Science. 2010 Oct 08; 330(6001):181-2.
    View in: PubMed
    Score: 0.221
  9. Personal genome research : what should the participant be told? Trends Genet. 2010 May; 26(5):199-201.
    View in: PubMed
    Score: 0.213
  10. Research ethics and the challenge of whole-genome sequencing. Nat Rev Genet. 2008 02; 9(2):152-6.
    View in: PubMed
    Score: 0.183
  11. Medicine. The future of personal genomics. Science. 2007 Sep 21; 317(5845):1687.
    View in: PubMed
    Score: 0.179
  12. Actionability of unanticipated monogenic disease risks in newborn genomic screening: Findings from the BabySeq Project. Am J Hum Genet. 2023 07 06; 110(7):1034-1045.
    View in: PubMed
    Score: 0.133
  13. Toward better governance of human genomic data. Nat Genet. 2021 01; 53(1):2-8.
    View in: PubMed
    Score: 0.112
  14. Interpretation of Genomic Sequencing Results in Healthy and Ill Newborns: Results from the BabySeq Project. Am J Hum Genet. 2019 01 03; 104(1):76-93.
    View in: PubMed
    Score: 0.098
  15. The Clinical Sequencing Evidence-Generating Research Consortium: Integrating Genomic Sequencing in Diverse and Medically Underserved Populations. Am J Hum Genet. 2018 09 06; 103(3):319-327.
    View in: PubMed
    Score: 0.095
  16. Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine. Am J Hum Genet. 2016 06 02; 98(6):1051-1066.
    View in: PubMed
    Score: 0.081
  17. An open access pilot freely sharing cancer genomic data from participants in Texas. Sci Data. 2016 Feb 16; 3:160010.
    View in: PubMed
    Score: 0.080
  18. Potential Psychosocial Risks of Sequencing Newborns. Pediatrics. 2016 Jan; 137 Suppl 1:S24-9.
    View in: PubMed
    Score: 0.079
  19. Are physicians prepared for whole genome sequencing? a qualitative analysis. Clin Genet. 2016 Feb; 89(2):228-34.
    View in: PubMed
    Score: 0.077
  20. The MedSeq Project: a randomized trial of integrating whole genome sequencing into clinical medicine. Trials. 2014 Mar 20; 15:85.
    View in: PubMed
    Score: 0.070
  21. Identifying personal genomes by surname inference. Science. 2013 Jan 18; 339(6117):321-4.
    View in: PubMed
    Score: 0.065
  22. To share or not to share: a randomized trial of consent for data sharing in genome research. Genet Med. 2011 Nov; 13(11):948-55.
    View in: PubMed
    Score: 0.059
  23. Whole-genome sequencing in a patient with Charcot-Marie-Tooth neuropathy. N Engl J Med. 2010 Apr 01; 362(13):1181-91.
    View in: PubMed
    Score: 0.053
  24. Personalized genomic information: preparing for the future of genetic medicine. Nat Rev Genet. 2010 02; 11(2):161-5.
    View in: PubMed
    Score: 0.052
  25. Social networkers' attitudes toward direct-to-consumer personal genome testing. Am J Bioeth. 2009; 9(6-7):3-10.
    View in: PubMed
    Score: 0.049
  26. Don't throw the baby out with the bathwater: enabling a bottom-up approach in genome-wide association studies. Genome Res. 2008 Nov; 18(11):1683-5.
    View in: PubMed
    Score: 0.048
  27. The complete genome of an individual by massively parallel DNA sequencing. Nature. 2008 Apr 17; 452(7189):872-6.
    View in: PubMed
    Score: 0.046
  28. Research ethics recommendations for whole-genome research: consensus statement. PLoS Biol. 2008 Mar 25; 6(3):e73.
    View in: PubMed
    Score: 0.046
  29. The BabySeq Project: A clinical trial of genome sequencing in a diverse cohort of infants. Am J Hum Genet. 2024 Oct 03; 111(10):2094-2106.
    View in: PubMed
    Score: 0.036
  30. Patient understanding of, satisfaction with, and perceived utility of whole-genome sequencing: findings from the MedSeq Project. Genet Med. 2018 09; 20(9):1069-1076.
    View in: PubMed
    Score: 0.023
  31. A curated gene list for reporting results of newborn genomic sequencing. Genet Med. 2017 07; 19(7):809-818.
    View in: PubMed
    Score: 0.021
  32. Reflections on the cost of "low-cost" whole genome sequencing: framing the health policy debate. PLoS Biol. 2013 Nov; 11(11):e1001699.
    View in: PubMed
    Score: 0.017
  33. ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing. Genet Med. 2013 Jul; 15(7):565-74.
    View in: PubMed
    Score: 0.017
  34. Exploring concordance and discordance for return of incidental findings from clinical sequencing. Genet Med. 2012 Apr; 14(4):405-10.
    View in: PubMed
    Score: 0.015
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.