Connection

AMY MCGUIRE to Genomics

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

6.378
  1. The road ahead in genetics and genomics. Nat Rev Genet. 2020 10; 21(10):581-596.
    View in: PubMed
    Score: 0.398
  2. Donors, authors, and owners: how is genomic citizen science addressing interests in research outputs? BMC Med Ethics. 2019 11 21; 20(1):84.
    View in: PubMed
    Score: 0.377
  3. Moving beyond Bermuda: sharing data to build a medical information commons. Genome Res. 2017 06; 27(6):897-901.
    View in: PubMed
    Score: 0.314
  4. Persistent confusion and controversy surrounding gene patents. Nat Biotechnol. 2016 Feb; 34(2):145-7.
    View in: PubMed
    Score: 0.290
  5. Can I be sued for that? Liability risk and the disclosure of clinically significant genetic research findings. Genome Res. 2014 May; 24(5):719-23.
    View in: PubMed
    Score: 0.255
  6. Participants' recall and understanding of genomic research and large-scale data sharing. J Empir Res Hum Res Ethics. 2013 Oct; 8(4):42-52.
    View in: PubMed
    Score: 0.247
  7. Point-counterpoint. Ethics and genomic incidental findings. Science. 2013 May 31; 340(6136):1047-8.
    View in: PubMed
    Score: 0.240
  8. The indispensable role of professional judgment in genomic medicine. JAMA. 2013 Apr 10; 309(14):1465-6.
    View in: PubMed
    Score: 0.239
  9. The legal risks of returning results of genomics research. Genet Med. 2012 Apr; 14(4):473-7.
    View in: PubMed
    Score: 0.220
  10. 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: 0.218
  11. 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: 0.216
  12. Ethical and practical challenges of sharing data from genome-wide association studies: the eMERGE Consortium experience. Genome Res. 2011 Jul; 21(7):1001-7.
    View in: PubMed
    Score: 0.210
  13. The right to ignore genetic status of late onset genetic disease in the genomic era; Prenatal testing for Huntington disease as a paradigm. Am J Med Genet A. 2010 Jul; 152A(7):1774-80.
    View in: PubMed
    Score: 0.197
  14. The ethical use of existing samples for genome research. Genet Med. 2009 Oct; 11(10):712-5.
    View in: PubMed
    Score: 0.187
  15. Medicine. The future of personal genomics. Science. 2007 Sep 21; 317(5845):1687.
    View in: PubMed
    Score: 0.162
  16. Meeting the growing demands of genetic research. J Law Med Ethics. 2006; 34(4):809-12.
    View in: PubMed
    Score: 0.144
  17. Conceptualization of utility in translational clinical genomics research. Am J Hum Genet. 2021 11 04; 108(11):2027-2036.
    View in: PubMed
    Score: 0.108
  18. Perceived Utility of Genomic Sequencing: Qualitative Analysis and Synthesis of a Conceptual Model to Inform Patient-Centered Instrument Development. Patient. 2022 05; 15(3):317-328.
    View in: PubMed
    Score: 0.108
  19. Toward better governance of human genomic data. Nat Genet. 2021 01; 53(1):2-8.
    View in: PubMed
    Score: 0.102
  20. Airmen and health-care providers' attitudes toward the use of genomic sequencing in the US Air Force: findings from the MilSeq Project. Genet Med. 2020 12; 22(12):2003-2010.
    View in: PubMed
    Score: 0.099
  21. Integrating Rules for Genomic Research, Clinical Care, Public Health Screening and DTC Testing: Creating Translational Law for Translational Genomics. J Law Med Ethics. 2020 03; 48(1):69-86.
    View in: PubMed
    Score: 0.096
  22. Responsibility, culpability, and parental views on genomic testing for seriously ill children. Genet Med. 2019 12; 21(12):2791-2797.
    View in: PubMed
    Score: 0.091
  23. The Genomic Medicine Integrative Research Framework: A Conceptual Framework for Conducting Genomic Medicine Research. Am J Hum Genet. 2019 06 06; 104(6):1088-1096.
    View in: PubMed
    Score: 0.091
  24. 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: 0.089
  25. Agents of empathy: How medical interpreters bridge sociocultural gaps in genomic sequencing disclosures with Spanish-speaking families. Patient Educ Couns. 2019 05; 102(5):895-901.
    View in: PubMed
    Score: 0.088
  26. Portero versus portador: Spanish interpretation of genomic terminology during whole exome sequencing results disclosure. Per Med. 2017 11; 14(6):503-514.
    View in: PubMed
    Score: 0.082
  27. Navigating the research-clinical interface in genomic medicine: analysis from the CSER Consortium. Genet Med. 2018 04; 20(5):545-553.
    View in: PubMed
    Score: 0.081
  28. 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: 0.074
  29. GINA, genetic discrimination, and genomic medicine. N Engl J Med. 2015 Jan 29; 372(5):397-9.
    View in: PubMed
    Score: 0.068
  30. A one-page summary report of genome sequencing for the healthy adult. Public Health Genomics. 2015; 18(2):123-9.
    View in: PubMed
    Score: 0.067
  31. Pediatric Cancer Genetics Research and an Evolving Preventive Ethics Approach for Return of Results after Death of the Subject. J Law Med Ethics. 2015; 43(3):529-37.
    View in: PubMed
    Score: 0.067
  32. Development of the clinical next-generation sequencing industry in a shifting policy climate. Nat Biotechnol. 2014 Oct; 32(10):980-2.
    View in: PubMed
    Score: 0.066
  33. Social and behavioral research in genomic sequencing: approaches from the Clinical Sequencing Exploratory Research Consortium Outcomes and Measures Working Group. Genet Med. 2014 Oct; 16(10):727-35.
    View in: PubMed
    Score: 0.064
  34. Pediatric data sharing in genomic research: attitudes and preferences of parents. Pediatrics. 2014 Apr; 133(4):690-7.
    View in: PubMed
    Score: 0.064
  35. Guidelines for return of research results from pediatric genomic studies: deliberations of the Boston Children's Hospital Gene Partnership Informed Cohort Oversight Board. Genet Med. 2014 Jul; 16(7):547-52.
    View in: PubMed
    Score: 0.063
  36. 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: 0.062
  37. Adult genetic risk screening. Annu Rev Med. 2014; 65:1-17.
    View in: PubMed
    Score: 0.062
  38. Return of research results from genomic biobanks: a call for data. Genet Med. 2013 Feb; 15(2):159-60.
    View in: PubMed
    Score: 0.059
  39. Identifying personal genomes by surname inference. Science. 2013 Jan 18; 339(6117):321-4.
    View in: PubMed
    Score: 0.059
  40. Return of research results from genomic biobanks: cost matters. Genet Med. 2013 Feb; 15(2):103-5.
    View in: PubMed
    Score: 0.057
  41. The Human Microbiome Project: a community resource for the healthy human microbiome. PLoS Biol. 2012; 10(8):e1001377.
    View in: PubMed
    Score: 0.057
  42. Personalized genomic information: preparing for the future of genetic medicine. Nat Rev Genet. 2010 02; 11(2):161-5.
    View in: PubMed
    Score: 0.048
  43. The complete genome of an individual by massively parallel DNA sequencing. Nature. 2008 Apr 17; 452(7189):872-6.
    View in: PubMed
    Score: 0.042
  44. Research ethics recommendations for whole-genome research: consensus statement. PLoS Biol. 2008 Mar 25; 6(3):e73.
    View in: PubMed
    Score: 0.042
  45. "A Double-Edged Sword": A Brief History of Genomic Data Governance and Genetic Researcher Perspectives on Data Sharing. J Law Med Ethics. 2024; 52(2):399-411.
    View in: PubMed
    Score: 0.033
  46. Measuring perceived utility of genomic sequencing: Development and validation of the GENEtic Utility (GENE-U) scale for adult screening. Genet Med. 2024 Nov; 26(11):101240.
    View in: PubMed
    Score: 0.033
  47. Genomic sequencing research in pediatric cancer care: Decision making, attitudes, and perceived utility among adolescents and young adults and their parents. Genet Med. 2024 Aug; 26(8):101168.
    View in: PubMed
    Score: 0.032
  48. Measuring perceived utility of genomic sequencing: Development and validation of?the GENEtic Utility (GENE-U) scale for pediatric diagnostic testing. Genet Med. 2024 Aug; 26(8):101146.
    View in: PubMed
    Score: 0.032
  49. Families' experiences accessing care after genomic sequencing in the pediatric cancer context: "It's just been a big juggle". J Genet Couns. 2024 Dec; 33(6):1337-1350.
    View in: PubMed
    Score: 0.031
  50. 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: 0.030
  51. Views of Adolescents and Young Adults with Cancer and Their Oncologists Toward Patients' Participation in Genomic Research. J Adolesc Young Adult Oncol. 2023 10; 12(5):773-781.
    View in: PubMed
    Score: 0.029
  52. Key drivers of family-level utility of pediatric genomic sequencing: a qualitative analysis to support preference research. Eur J Hum Genet. 2023 04; 31(4):445-452.
    View in: PubMed
    Score: 0.029
  53. Effects of participation in a U.S. trial of newborn genomic sequencing on parents at risk for depression. J Genet Couns. 2022 02; 31(1):218-229.
    View in: PubMed
    Score: 0.026
  54. Psychological outcomes related to exome and genome sequencing result disclosure: a meta-analysis of seven Clinical Sequencing Exploratory Research (CSER) Consortium studies. Genet Med. 2019 12; 21(12):2781-2790.
    View in: PubMed
    Score: 0.023
  55. Improving recommendations for genomic medicine: building an evolutionary process from clinical practice advisory documents to guidelines. Genet Med. 2019 11; 21(11):2431-2438.
    View in: PubMed
    Score: 0.023
  56. Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study. Genet Med. 2019 05; 21(5):1100-1110.
    View in: PubMed
    Score: 0.022
  57. 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: 0.022
  58. A curated gene list for reporting results of newborn genomic sequencing. Genet Med. 2017 07; 19(7):809-818.
    View in: PubMed
    Score: 0.019
  59. Confronting real time ethical, legal, and social issues in the Electronic Medical Records and Genomics (eMERGE) Consortium. Genet Med. 2010 Oct; 12(10):616-20.
    View in: PubMed
    Score: 0.013
  60. Developing a tissue resource to characterize the genome of pancreatic cancer. World J Surg. 2009 Apr; 33(4):723-31.
    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.