Connection

Co-Authors

This is a "connection" page, showing publications co-authored by AMY MCGUIRE and STACEY PEREIRA.
Connection Strength

5.167
  1. 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: 0.775
  2. 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: 0.581
  3. Open access data sharing in genomic research. Genes (Basel). 2014 Aug 29; 5(3):739-47.
    View in: PubMed
    Score: 0.513
  4. 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: 0.228
  5. 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: 0.227
  6. 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: 0.226
  7. 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: 0.215
  8. 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: 0.211
  9. Pediatric Oncologists' Experiences Returning and Incorporating Genomic Sequencing Results into Cancer Care. J Pers Med. 2021 Jun 18; 11(6).
    View in: PubMed
    Score: 0.205
  10. Responsibility, culpability, and parental views on genomic testing for seriously ill children. Genet Med. 2019 12; 21(12):2791-2797.
    View in: PubMed
    Score: 0.179
  11. 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: 0.173
  12. Do privacy and security regulations need a status update? Perspectives from an intergenerational survey. PLoS One. 2017; 12(9):e0184525.
    View in: PubMed
    Score: 0.158
  13. Should you profit from your genome? Nat Biotechnol. 2017 01 10; 35(1):18-20.
    View in: PubMed
    Score: 0.151
  14. 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: 0.146
  15. Potential Psychosocial Risks of Sequencing Newborns. Pediatrics. 2016 Jan; 137 Suppl 1:S24-9.
    View in: PubMed
    Score: 0.141
  16. Adult genetic risk screening. Annu Rev Med. 2014; 65:1-17.
    View in: PubMed
    Score: 0.121
  17. Research Participants' Perspectives on Precision Diagnostics for Alzheimer's Disease. J Alzheimers Dis. 2024; 97(3):1261-1274.
    View in: PubMed
    Score: 0.061
  18. 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: 0.059
  19. 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: 0.059
  20. Parental Attitudes Toward Standard Newborn Screening and Newborn Genomic Sequencing: Findings From the BabySeq Study. Front Genet. 2022; 13:867371.
    View in: PubMed
    Score: 0.054
  21. Researcher Views on Changes in Personality, Mood, and Behavior in Next-Generation Deep Brain Stimulation. AJOB Neurosci. 2023 Jul-Sep; 14(3):287-299.
    View in: PubMed
    Score: 0.054
  22. Researchers' Ethical Concerns About Using Adaptive Deep Brain Stimulation for Enhancement. Front Hum Neurosci. 2022; 16:813922.
    View in: PubMed
    Score: 0.054
  23. Patient, Caregiver, and Decliner Perspectives on Whether to Enroll in Adaptive Deep Brain Stimulation Research. Front Neurosci. 2021; 15:734182.
    View in: PubMed
    Score: 0.052
  24. 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: 0.052
  25. 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: 0.052
  26. Researcher Perspectives on Data Sharing in Deep Brain Stimulation. Front Hum Neurosci. 2020; 14:578687.
    View in: PubMed
    Score: 0.050
  27. Researcher Perspectives on Ethical Considerations in Adaptive Deep Brain Stimulation Trials. Front Hum Neurosci. 2020; 14:578695.
    View in: PubMed
    Score: 0.049
  28. Neuroethics at 15: Keep the Kant but Add More Bacon. AJOB Neurosci. 2019 Jul-Sep; 10(3):97-100.
    View in: PubMed
    Score: 0.045
  29. 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: 0.044
  30. 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: 0.043
  31. 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: 0.042
  32. The BabySeq project: implementing genomic sequencing in newborns. BMC Pediatr. 2018 07 09; 18(1):225.
    View in: PubMed
    Score: 0.042
  33. Newborn Sequencing in Genomic Medicine and Public Health. Pediatrics. 2017 Feb; 139(2).
    View in: PubMed
    Score: 0.038
  34. An open access pilot freely sharing cancer genomic data from participants in Texas. Sci Data. 2016 Feb 16; 3:160010.
    View in: PubMed
    Score: 0.035
  35. Personalized genomic disease risk of volunteers. Proc Natl Acad Sci U S A. 2013 Oct 15; 110(42):16957-62.
    View in: PubMed
    Score: 0.030
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.