Connection

AMY MCGUIRE to Humans

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

1.280
  1. Large-scale genotype prediction from RNA sequence data necessitates a new ethical and policy framework. Nat Genet. 2024 Aug; 56(8):1537-1540.
    View in: PubMed
    Score: 0.019
  2. Developing an Ethics and Policy Framework for Psychedelic Clinical Care: A Consensus Statement. JAMA Netw Open. 2024 Jun 03; 7(6):e2414650.
    View in: PubMed
    Score: 0.018
  3. IGG in the trenches: Results of an in-depth interview study on the practice, politics, and future of investigative genetic genealogy. Forensic Sci Int. 2024 Mar; 356:111946.
    View in: PubMed
    Score: 0.018
  4. Bio-Psycho-Spiritual Perspectives on Psychedelics: Clinical and Ethical Implications. Perspect Biol Med. 2024; 67(1):117-142.
    View in: PubMed
    Score: 0.018
  5. Are Psychedelic Experiences Transformative? Can We Consent to Them? Perspect Biol Med. 2024; 67(1):143-154.
    View in: PubMed
    Score: 0.018
  6. Integrating Social Determinants of Health into Ethical Digital Simulations. Am J Bioeth. 2023 09; 23(9):57-60.
    View in: PubMed
    Score: 0.017
  7. Pressing regulatory challenges for psychedelic medicine. Science. 2023 04 28; 380(6643):347-350.
    View in: PubMed
    Score: 0.017
  8. Increasing physician participation as subjects in scientific and quality improvement research. BMC Med Ethics. 2022 08 13; 23(1):81.
    View in: PubMed
    Score: 0.016
  9. Family secrets: Experiences and outcomes of participating in direct-to-consumer genetic relative-finder services. Am J Hum Genet. 2022 03 03; 109(3):486-497.
    View in: PubMed
    Score: 0.016
  10. How NFTs could transform health information exchange. Science. 2022 02 04; 375(6580):500-502.
    View in: PubMed
    Score: 0.016
  11. Should Pediatricians Dismiss Families Who Refuse a COVID-19 Vaccine? Clin Pediatr (Phila). 2022 02; 61(2):99-103.
    View in: PubMed
    Score: 0.015
  12. 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: 0.015
  13. Direct-to-Consumer Drug Advertisement and Prescribing Practices: Evidence Review and Practical Guidance for Clinicians. J Gen Intern Med. 2021 05; 36(5):1390-1394.
    View in: PubMed
    Score: 0.014
  14. The road ahead in genetics and genomics. Nat Rev Genet. 2020 10; 21(10):581-596.
    View in: PubMed
    Score: 0.014
  15. 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: 0.014
  16. Direct-to-Consumer Genetic Testing: Value and Risk. Annu Rev Med. 2021 01 27; 72:151-166.
    View in: PubMed
    Score: 0.014
  17. Ethical Challenges Arising in the COVID-19 Pandemic: An Overview from the Association of Bioethics Program Directors (ABPD) Task Force. Am J Bioeth. 2020 07; 20(7):15-27.
    View in: PubMed
    Score: 0.014
  18. Physician Involvement in Promoting Gun Safety. Ann Fam Med. 2020 05; 18(3):262-264.
    View in: PubMed
    Score: 0.014
  19. Data Sharing in the Context of Health-Related Citizen Science. J Law Med Ethics. 2020 03; 48(1_suppl):167-177.
    View in: PubMed
    Score: 0.014
  20. A Right to Privacy and Confidentiality: Ethical Medical Care for Patients in United States Immigration Detention. J Law Med Ethics. 2020 03; 48(1):161-168.
    View in: PubMed
    Score: 0.014
  21. Essential, not peripheral: Addressing health care workers' mental health concerns during the COVID-19 pandemic. J Occup Health. 2020 Jan; 62(1):e12169.
    View in: PubMed
    Score: 0.014
  22. 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: 0.013
  23. Learning Health System - Moving from Ethical Frameworks to Practical Implementation. J Law Med Ethics. 2019 09; 47(3):454-458.
    View in: PubMed
    Score: 0.013
  24. Who's on third? Regulation of third-party genetic interpretation services. Genet Med. 2020 01; 22(1):4-11.
    View in: PubMed
    Score: 0.013
  25. Clarify the HIPAA right of access to individuals' research data. Nat Biotechnol. 2019 08; 37(8):850-852.
    View in: PubMed
    Score: 0.013
  26. Biomedical Citizen Science or Something Else? Reflections on Terms and Definitions. Am J Bioeth. 2019 Aug; 19(8):17-19.
    View in: PubMed
    Score: 0.013
  27. Responsibility, culpability, and parental views on genomic testing for seriously ill children. Genet Med. 2019 12; 21(12):2791-2797.
    View in: PubMed
    Score: 0.013
  28. Quantifying Tip60 (Kat5) stratifies breast cancer. Sci Rep. 2019 03 07; 9(1):3819.
    View in: PubMed
    Score: 0.013
  29. Introduction: Sharing Data in a Medical Information Commons. J Law Med Ethics. 2019 03; 47(1):7-11.
    View in: PubMed
    Score: 0.013
  30. Importance of Participant-Centricity and Trust for a Sustainable Medical Information Commons. J Law Med Ethics. 2019 03; 47(1):12-20.
    View in: PubMed
    Score: 0.013
  31. Hopeful and Concerned: Public Input on Building a Trustworthy Medical Information Commons. J Law Med Ethics. 2019 03; 47(1):70-87.
    View in: PubMed
    Score: 0.013
  32. Who Owns the Data in a Medical Information Commons? J Law Med Ethics. 2019 03; 47(1):62-69.
    View in: PubMed
    Score: 0.013
  33. 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: 0.013
  34. Should police have access to genetic genealogy databases? Capturing the Golden State Killer and other criminals using a controversial new forensic technique. PLoS Biol. 2018 10; 16(10):e2006906.
    View in: PubMed
    Score: 0.012
  35. Genealogy databases and the future of criminal investigation. Science. 2018 06 08; 360(6393):1078-1079.
    View in: PubMed
    Score: 0.012
  36. HEADS4: Social Media Screening in Adolescent Primary Care. Pediatrics. 2018 06; 141(6).
    View in: PubMed
    Score: 0.012
  37. Creating a data resource: what will it take to build a medical information commons? Genome Med. 2017 09 22; 9(1):84.
    View in: PubMed
    Score: 0.012
  38. Sharing data under the 21st Century Cures Act. Genet Med. 2017 12; 19(12):1289-1294.
    View in: PubMed
    Score: 0.011
  39. Moving beyond Bermuda: sharing data to build a medical information commons. Genome Res. 2017 06; 27(6):897-901.
    View in: PubMed
    Score: 0.011
  40. 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: 0.011
  41. Beyond Our Borders? Public Resistance to Global Genomic Data Sharing. PLoS Biol. 2016 Nov; 14(11):e2000206.
    View in: PubMed
    Score: 0.011
  42. The ethics of conducting molecular autopsies in cases of sudden death in the young. Genome Res. 2016 09; 26(9):1165-9.
    View in: PubMed
    Score: 0.011
  43. Return of individual genomic research results: what do consent forms tell participants? Eur J Hum Genet. 2016 11; 24(11):1524-1529.
    View in: PubMed
    Score: 0.011
  44. Ethical and Legal Challenges Associated with Public Molecular Autopsies. J Law Med Ethics. 2016 06; 44(2):309-18.
    View in: PubMed
    Score: 0.011
  45. Persistent confusion and controversy surrounding gene patents. Nat Biotechnol. 2016 Feb; 34(2):145-7.
    View in: PubMed
    Score: 0.010
  46. Potential Psychosocial Risks of Sequencing Newborns. Pediatrics. 2016 Jan; 137 Suppl 1:S24-9.
    View in: PubMed
    Score: 0.010
  47. Cultivating Administrative Support for a Clinical Ethics Consultation Service. J Clin Ethics. 2016; 27(4):341-351.
    View in: PubMed
    Score: 0.010
  48. GINA, genetic discrimination, and genomic medicine. N Engl J Med. 2015 Jan 29; 372(5):397-9.
    View in: PubMed
    Score: 0.010
  49. Overcoming the reimbursement barriers for clinical sequencing. JAMA. 2014 Nov 12; 312(18):1857-8.
    View in: PubMed
    Score: 0.009
  50. Responding to moderate breaches in professionalism: an intervention for medical students. Med Teach. 2015 Feb; 37(2):136-9.
    View in: PubMed
    Score: 0.009
  51. Clinical integration of next generation sequencing: a policy analysis. J Law Med Ethics. 2014; 42 Suppl 1:5-8.
    View in: PubMed
    Score: 0.009
  52. Adult genetic risk screening. Annu Rev Med. 2014; 65:1-17.
    View in: PubMed
    Score: 0.009
  53. 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: 0.009
  54. Policy uncertainty, sequencing, and cell lines. G3 (Bethesda). 2013 Aug 07; 3(8):1205-7.
    View in: PubMed
    Score: 0.009
  55. Point-counterpoint. Ethics and genomic incidental findings. Science. 2013 May 31; 340(6136):1047-8.
    View in: PubMed
    Score: 0.009
  56. Investigators' perspectives on translating human microbiome research into clinical practice. Public Health Genomics. 2013; 16(3):127-33.
    View in: PubMed
    Score: 0.009
  57. The indispensable role of professional judgment in genomic medicine. JAMA. 2013 Apr 10; 309(14):1465-6.
    View in: PubMed
    Score: 0.008
  58. Research results: preserving newborn blood samples. Sci Transl Med. 2012 Nov 07; 4(159):159cm12.
    View in: PubMed
    Score: 0.008
  59. "Snake-oil," "quack medicine," and "industrially cultured organisms:" biovalue and the commercialization of human microbiome research. BMC Med Ethics. 2012 Oct 30; 13:28.
    View in: PubMed
    Score: 0.008
  60. Athletes' use of unproven stem cell therapies: adding to inappropriate media hype? Mol Ther. 2012 Sep; 20(9):1656-8.
    View in: PubMed
    Score: 0.008
  61. The legal risks of returning results of genomics research. Genet Med. 2012 Apr; 14(4):473-7.
    View in: PubMed
    Score: 0.008
  62. Currents in contemporary bioethics. Identifying consanguinity through routine genomic analysis: reporting requirements. J Law Med Ethics. 2012; 40(4):1040-6.
    View in: PubMed
    Score: 0.008
  63. 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: 0.008
  64. 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: 0.008
  65. Direct-to-consumer genetic testing: perceptions, problems, and policy responses. Annu Rev Med. 2012; 63:23-33.
    View in: PubMed
    Score: 0.008
  66. 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: 0.007
  67. Health system implications of direct-to-consumer personal genome testing. Public Health Genomics. 2011; 14(1):53-8.
    View in: PubMed
    Score: 0.007
  68. Science and regulation. Regulating direct-to-consumer personal genome testing. Science. 2010 Oct 08; 330(6001):181-2.
    View in: PubMed
    Score: 0.007
  69. 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: 0.007
  70. Personal genome research : what should the participant be told? Trends Genet. 2010 May; 26(5):199-201.
    View in: PubMed
    Score: 0.007
  71. Informed consent in genomics and genetic research. Annu Rev Genomics Hum Genet. 2010; 11:361-81.
    View in: PubMed
    Score: 0.007
  72. The ethical use of existing samples for genome research. Genet Med. 2009 Oct; 11(10):712-5.
    View in: PubMed
    Score: 0.007
  73. Currents in contemporary ethics. Direct-to-consumer genetic testing: is it the practice of medicine? J Law Med Ethics. 2009; 37(2):369-74.
    View in: PubMed
    Score: 0.006
  74. Social networkers' attitudes toward direct-to-consumer personal genome testing. Am J Bioeth. 2009; 9(6-7):3-10.
    View in: PubMed
    Score: 0.006
  75. Please don't call my mom: pediatric consent and confidentiality. Clin Pediatr (Phila). 2009 Apr; 48(3):243-6.
    View in: PubMed
    Score: 0.006
  76. An unwelcome side effect of direct-to-consumer personal genome testing: raiding the medical commons. JAMA. 2008 Dec 10; 300(22):2669-71.
    View in: PubMed
    Score: 0.006
  77. 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: 0.006
  78. Ethical, legal, and social considerations in conducting the Human Microbiome Project. Genome Res. 2008 Dec; 18(12):1861-4.
    View in: PubMed
    Score: 0.006
  79. Identifiability of DNA data: the need for consistent federal policy. Am J Bioeth. 2008 Oct; 8(10):75-6.
    View in: PubMed
    Score: 0.006
  80. Confidentiality, privacy, and security of genetic and genomic test information in electronic health records: points to consider. Genet Med. 2008 Jul; 10(7):495-9.
    View in: PubMed
    Score: 0.006
  81. Beyond shared decision making: an expanded typology of medical decisions. Med Decis Making. 2008 Sep-Oct; 28(5):699-705.
    View in: PubMed
    Score: 0.006
  82. Research ethics and the challenge of whole-genome sequencing. Nat Rev Genet. 2008 02; 9(2):152-6.
    View in: PubMed
    Score: 0.006
  83. Medicine. The future of personal genomics. Science. 2007 Sep 21; 317(5845):1687.
    View in: PubMed
    Score: 0.006
  84. Genetics. No longer de-identified. Science. 2006 Apr 21; 312(5772):370-1.
    View in: PubMed
    Score: 0.005
  85. Meeting the growing demands of genetic research. J Law Med Ethics. 2006; 34(4):809-12.
    View in: PubMed
    Score: 0.005
  86. Missed expectations? Physicians' views of patients' participation in medical decision-making. Med Care. 2005 May; 43(5):466-70.
    View in: PubMed
    Score: 0.005
  87. Respect as an organizing normative category for research ethics. Am J Bioeth. 2005; 5(1):W1-2.
    View in: PubMed
    Score: 0.005
  88. The ethics of lawyer-ethicists. J Law Med Ethics. 2005; 33(3):603-7.
    View in: PubMed
    Score: 0.005
  89. The BRAIN Initiative data-sharing ecosystem: Characteristics, challenges, benefits, and opportunities. Elife. 2024 Nov 27; 13.
    View in: PubMed
    Score: 0.005
  90. "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: 0.005
  91. 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: 0.005
  92. Comparing the Diagnostic Yield of Germline Exome Versus Panel Sequencing in the Diverse Population of the Texas KidsCanSeq Pediatric Cancer Study. JCO Precis Oncol. 2024 Sep; 8:e2400187.
    View in: PubMed
    Score: 0.005
  93. 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: 0.005
  94. "The truth should not be hidden": Experiences and recommendations of individuals making NPE discoveries through genetic genealogy databases. Genet Med. 2024 Oct; 26(10):101210.
    View in: PubMed
    Score: 0.005
  95. What happens when the tasks dry up? Exploring the impact of medical technology on workforce planning. Soc Sci Med. 2024 Jul; 352:117014.
    View in: PubMed
    Score: 0.005
  96. 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: 0.005
  97. 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: 0.005
  98. Public Perspectives on Investigative Genetic Genealogy: Findings from a National Focus Group Study. AJOB Empir Bioeth. 2024 Oct-Dec; 15(4):280-290.
    View in: PubMed
    Score: 0.005
  99. Genetic Researchers' Use of and Interest in Research With Diverse Ancestral Groups. JAMA Netw Open. 2024 04 01; 7(4):e246805.
    View in: PubMed
    Score: 0.005
  100. 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: 0.004
  101. Research Participants' Perspectives on Precision Diagnostics for Alzheimer's Disease. J Alzheimers Dis. 2024; 97(3):1261-1274.
    View in: PubMed
    Score: 0.004
  102. Benefits of sharing neurophysiology data from the BRAIN Initiative Research Opportunities in Humans Consortium. Neuron. 2023 Dec 06; 111(23):3710-3715.
    View in: PubMed
    Score: 0.004
  103. Ethically cleared to launch? Science. 2023 09 29; 381(6665):1408-1411.
    View in: PubMed
    Score: 0.004
  104. Participant perceptions of changes in psychosocial domains following participation in an adaptive deep brain stimulation trial. Brain Stimul. 2023 Jul-Aug; 16(4):990-998.
    View in: PubMed
    Score: 0.004
  105. 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: 0.004
  106. 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: 0.004
  107. Parents' decision-making regarding whether to receive adult-onset only genetic findings for their children: Findings from the BabySeq Project. Genet Med. 2023 03; 25(3):100002.
    View in: PubMed
    Score: 0.004
  108. 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: 0.004
  109. "Extremely slow and capricious": A qualitative exploration of genetic researcher priorities in selecting shared data resources. Genet Med. 2023 01; 25(1):115-124.
    View in: PubMed
    Score: 0.004
  110. Deciding with Others: Interdependent Decision-Making. Hastings Cent Rep. 2022 11; 52(6):23-32.
    View in: PubMed
    Score: 0.004
  111. Patient and Clinician Perceptions of Precision Cardiology Care: Findings From the HeartCare Study. Circ Genom Precis Med. 2022 12; 15(6):e003605.
    View in: PubMed
    Score: 0.004
  112. Toward Meeting the Obligation of Respect for Persons in Pragmatic Clinical Trials. Hastings Cent Rep. 2022 05; 52(3):9-17.
    View in: PubMed
    Score: 0.004
  113. Clearing the mist. Am J Bioeth. 2002; 2(4):W7.
    View in: PubMed
    Score: 0.004
  114. Psychosocial Effect of Newborn Genomic Sequencing on Families in the BabySeq Project: A Randomized Clinical Trial. JAMA Pediatr. 2021 11 01; 175(11):1132-1141.
    View in: PubMed
    Score: 0.004
  115. Conceptualization of utility in translational clinical genomics research. Am J Hum Genet. 2021 11 04; 108(11):2027-2036.
    View in: PubMed
    Score: 0.004
  116. Genetic testing in ambulatory cardiology clinics reveals high rate of findings with clinical management implications. Genet Med. 2021 12; 23(12):2404-2414.
    View in: PubMed
    Score: 0.004
  117. 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: 0.004
  118. Hospital-Based Education for Hospitalized Children: Current Practice and Future Direction. Hosp Pediatr. 2021 05; 11(5):e75-e77.
    View in: PubMed
    Score: 0.004
  119. Family-level impact of genetic testing: integrating health economics and ethical, legal, and social implications. Per Med. 2021 05; 18(3):209-212.
    View in: PubMed
    Score: 0.004
  120. Toward better governance of human genomic data. Nat Genet. 2021 01; 53(1):2-8.
    View in: PubMed
    Score: 0.004
  121. Ventilator Triage Policies During the COVID-19 Pandemic at U.S. Hospitals Associated With Members of the Association of Bioethics Program Directors. Ann Intern Med. 2020 08 04; 173(3):188-194.
    View in: PubMed
    Score: 0.003
  122. 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: 0.003
  123. The case for implementing sustainable routine, population-level genomic reanalysis. Genet Med. 2020 04; 22(4):815-816.
    View in: PubMed
    Score: 0.003
  124. Device Removal Following Brain Implant Research. Neuron. 2019 09 04; 103(5):759-761.
    View in: PubMed
    Score: 0.003
  125. Quantifying Argonaute 2 (Ago2) expression to stratify breast cancer. BMC Cancer. 2019 Jul 19; 19(1):712.
    View in: PubMed
    Score: 0.003
  126. 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: 0.003
  127. 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: 0.003
  128. In support of mitochondrial replacement therapy. Nat Med. 2019 06; 25(6):870-871.
    View in: PubMed
    Score: 0.003
  129. 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: 0.003
  130. Genomic Data-Sharing Practices. J Law Med Ethics. 2019 03; 47(1):31-40.
    View in: PubMed
    Score: 0.003
  131. What is a Medical Information Commons? J Law Med Ethics. 2019 03; 47(1):41-50.
    View in: PubMed
    Score: 0.003
  132. Characterizing the Biomedical Data-Sharing Landscape. J Law Med Ethics. 2019 03; 47(1):21-30.
    View in: PubMed
    Score: 0.003
  133. Predispositional genome sequencing in healthy adults: design, participant characteristics, and early outcomes of the PeopleSeq Consortium. Genome Med. 2019 02 27; 11(1):10.
    View in: PubMed
    Score: 0.003
  134. 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: 0.003
  135. How the tobacco industry continues to keep the home fires burning. Tob Control. 1999; 8(1):67-9.
    View in: PubMed
    Score: 0.003
  136. Perceived Benefits, Risks, and Utility of Newborn Genomic Sequencing in the BabySeq Project. Pediatrics. 2019 01; 143(Suppl 1):S6-S13.
    View in: PubMed
    Score: 0.003
  137. Challenging the Current Recommendations for Carrier Testing in Children. Pediatrics. 2019 01; 143(Suppl 1):S27-S32.
    View in: PubMed
    Score: 0.003
  138. Returning a Genomic Result for an Adult-Onset Condition to the Parents of a Newborn: Insights From the BabySeq Project. Pediatrics. 2019 01; 143(Suppl 1):S37-S43.
    View in: PubMed
    Score: 0.003
  139. Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association. Circulation. 2018 11 20; 138(21):e653-e711.
    View in: PubMed
    Score: 0.003
  140. Exome sequencing disclosures in pediatric cancer care: Patterns of communication among oncologists, genetic counselors, and parents. Patient Educ Couns. 2019 04; 102(4):680-686.
    View in: PubMed
    Score: 0.003
  141. 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: 0.003
  142. Parental interest in genomic sequencing of newborns: enrollment experience from the BabySeq Project. Genet Med. 2019 03; 21(3):622-630.
    View in: PubMed
    Score: 0.003
  143. 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: 0.003
  144. Reconciling newborn screening and a novel splice variant in BTD associated with partial biotinidase deficiency: a BabySeq Project case report. Cold Spring Harb Mol Case Stud. 2018 08; 4(4).
    View in: PubMed
    Score: 0.003
  145. The BabySeq project: implementing genomic sequencing in newborns. BMC Pediatr. 2018 07 09; 18(1):225.
    View in: PubMed
    Score: 0.003
  146. Continued access to investigational brain implants. Nat Rev Neurosci. 2018 06; 19(6):317-318.
    View in: PubMed
    Score: 0.003
  147. The phenotypic spectrum of Xia-Gibbs syndrome. Am J Med Genet A. 2018 06; 176(6):1315-1326.
    View in: PubMed
    Score: 0.003
  148. Short-term costs of integrating whole-genome sequencing into primary care and cardiology settings: a pilot randomized trial. Genet Med. 2018 12; 20(12):1544-1553.
    View in: PubMed
    Score: 0.003
  149. How Primary Care Providers Talk to Patients about Genome Sequencing Results: Risk, Rationale, and Recommendation. J Gen Intern Med. 2018 06; 33(6):877-885.
    View in: PubMed
    Score: 0.003
  150. 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: 0.003
  151. 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: 0.003
  152. Do privacy and security regulations need a status update? Perspectives from an intergenerational survey. PLoS One. 2017; 12(9):e0184525.
    View in: PubMed
    Score: 0.003
  153. 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: 0.003
  154. The Impact of Whole-Genome Sequencing on the Primary Care and Outcomes of Healthy Adult Patients: A Pilot Randomized Trial. Ann Intern Med. 2017 08 01; 167(3):159-169.
    View in: PubMed
    Score: 0.003
  155. Consumer Perspectives on Access to Direct-to-Consumer Genetic Testing: Role of Demographic Factors and the Testing Experience. Milbank Q. 2017 06; 95(2):291-318.
    View in: PubMed
    Score: 0.003
  156. Myriad take two: Can genomic databases remain secret? Science. 2017 05 12; 356(6338):586-587.
    View in: PubMed
    Score: 0.003
  157. Newborn Sequencing in Genomic Medicine and Public Health. Pediatrics. 2017 Feb; 139(2).
    View in: PubMed
    Score: 0.003
  158. A curated gene list for reporting results of newborn genomic sequencing. Genet Med. 2017 07; 19(7):809-818.
    View in: PubMed
    Score: 0.003
  159. A Conceptual Model for the Translation of Bioethics Research and Scholarship. Hastings Cent Rep. 2016 09; 46(5):34-9.
    View in: PubMed
    Score: 0.003
  160. 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: 0.003
  161. Community crystal gazing. Nat Biotechnol. 2016 Mar; 34(3):276-83.
    View in: PubMed
    Score: 0.003
  162. Participants and Study Decliners' Perspectives About the Risks of Participating in a Clinical Trial of Whole Genome Sequencing. J Empir Res Hum Res Ethics. 2016 02; 11(1):21-30.
    View in: PubMed
    Score: 0.003
  163. An open access pilot freely sharing cancer genomic data from participants in Texas. Sci Data. 2016 Feb 16; 3:160010.
    View in: PubMed
    Score: 0.003
  164. Legal Barriers to Adolescent Participation in Research About HIV and Other Sexually Transmitted Infections. Am J Public Health. 2016 Jan; 106(1):40-4.
    View in: PubMed
    Score: 0.003
  165. Is Whole-Exome Sequencing an Ethically Disruptive Technology? Perspectives of Pediatric Oncologists and Parents of Pediatric Patients With Solid Tumors. Pediatr Blood Cancer. 2016 Mar; 63(3):511-5.
    View in: PubMed
    Score: 0.003
  166. Pregnant patients' risk perception of prenatal test results with uncertain fetal clinical significance: ultrasound versus advanced genetic testing. Prenat Diagn. 2015 Dec; 35(12):1213-7.
    View in: PubMed
    Score: 0.003
  167. Are physicians prepared for whole genome sequencing? a qualitative analysis. Clin Genet. 2016 Feb; 89(2):228-34.
    View in: PubMed
    Score: 0.002
  168. A one-page summary report of genome sequencing for the healthy adult. Public Health Genomics. 2015; 18(2):123-9.
    View in: PubMed
    Score: 0.002
  169. 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: 0.002
  170. Why information alone is not enough: behavioral economics and the future of genomic medicine. Ann Intern Med. 2014 Oct 21; 161(8):605-6.
    View in: PubMed
    Score: 0.002
  171. 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: 0.002
  172. Do recent US Supreme Court rulings on patenting of genes and genetic diagnostics affect the practice of genetic screening and diagnosis in prenatal and reproductive care? Prenat Diagn. 2014 Oct; 34(10):921-6.
    View in: PubMed
    Score: 0.002
  173. The MedSeq Project: a randomized trial of integrating whole genome sequencing into clinical medicine. Trials. 2014 Mar 20; 15:85.
    View in: PubMed
    Score: 0.002
  174. 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: 0.002
  175. Pediatric data sharing in genomic research: attitudes and preferences of parents. Pediatrics. 2014 Apr; 133(4):690-7.
    View in: PubMed
    Score: 0.002
  176. 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: 0.002
  177. 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: 0.002
  178. Personalized genomic disease risk of volunteers. Proc Natl Acad Sci U S A. 2013 Oct 15; 110(42):16957-62.
    View in: PubMed
    Score: 0.002
  179. 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: 0.002
  180. Experiences and attitudes of genome investigators regarding return of individual genetic test results. Genet Med. 2013 Nov; 15(11):882-7.
    View in: PubMed
    Score: 0.002
  181. Return of research results from genomic biobanks: a call for data. Genet Med. 2013 Feb; 15(2):159-60.
    View in: PubMed
    Score: 0.002
  182. Identifying personal genomes by surname inference. Science. 2013 Jan 18; 339(6117):321-4.
    View in: PubMed
    Score: 0.002
  183. Return of research results from genomic biobanks: cost matters. Genet Med. 2013 Feb; 15(2):103-5.
    View in: PubMed
    Score: 0.002
  184. The Human Microbiome Project: a community resource for the healthy human microbiome. PLoS Biol. 2012; 10(8):e1001377.
    View in: PubMed
    Score: 0.002
  185. Incidental copy-number variants identified by routine genome testing in a clinical population. Genet Med. 2013 Jan; 15(1):45-54.
    View in: PubMed
    Score: 0.002
  186. Exploring concordance and discordance for return of incidental findings from clinical sequencing. Genet Med. 2012 Apr; 14(4):405-10.
    View in: PubMed
    Score: 0.002
  187. Return of individual research results from genome-wide association studies: experience of the Electronic Medical Records and Genomics (eMERGE) Network. Genet Med. 2012 Apr; 14(4):424-31.
    View in: PubMed
    Score: 0.002
  188. Disclosing pathogenic genetic variants to research participants: quantifying an emerging ethical responsibility. Genome Res. 2012 Mar; 22(3):421-8.
    View in: PubMed
    Score: 0.002
  189. Informed consent in research to improve the number and quality of deceased donor organs. Crit Care Med. 2011 Feb; 39(2):280-3.
    View in: PubMed
    Score: 0.002
  190. Shaping patients' decisions. Chest. 2011 Feb; 139(2):424-429.
    View in: PubMed
    Score: 0.002
  191. Ethical and practical guidelines for reporting genetic research results to study participants: updated guidelines from a National Heart, Lung, and Blood Institute working group. Circ Cardiovasc Genet. 2010 Dec; 3(6):574-80.
    View in: PubMed
    Score: 0.002
  192. 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: 0.002
  193. Beneficent persuasion: techniques and ethical guidelines to improve patients' decisions. Ann Fam Med. 2010 May-Jun; 8(3):260-4.
    View in: PubMed
    Score: 0.002
  194. 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: 0.002
  195. Personalized genomic information: preparing for the future of genetic medicine. Nat Rev Genet. 2010 02; 11(2):161-5.
    View in: PubMed
    Score: 0.002
  196. Developing a tissue resource to characterize the genome of pancreatic cancer. World J Surg. 2009 Apr; 33(4):723-31.
    View in: PubMed
    Score: 0.002
  197. Beyond breaking bad news: the roles of hope and hopefulness. Cancer. 2008 Jul 15; 113(2):442-5.
    View in: PubMed
    Score: 0.002
  198. The complete genome of an individual by massively parallel DNA sequencing. Nature. 2008 Apr 17; 452(7189):872-6.
    View in: PubMed
    Score: 0.002
  199. Principal investigator views of the IRB system. Int J Med Sci. 2008 Apr 02; 5(2):68-72.
    View in: PubMed
    Score: 0.001
  200. Research ethics recommendations for whole-genome research: consensus statement. PLoS Biol. 2008 Mar 25; 6(3):e73.
    View in: PubMed
    Score: 0.001
  201. Consent: informed, simple, implied and presumed. Am J Bioeth. 2007 Dec; 7(12):49-50; discussion W3-4.
    View in: PubMed
    Score: 0.001
  202. A typology of shared decision making, informed consent, and simple consent. Ann Intern Med. 2004 Jan 06; 140(1):54-9.
    View in: PubMed
    Score: 0.001
  203. Cost-effectiveness of different ACE inhibitor treatment scenarios post-myocardial infarction. Eur Heart J. 1997 Sep; 18(9):1411-5.
    View in: PubMed
    Score: 0.001
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.