Connection

MARY MAJUMDER to Humans

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

0.620
  1. The BRAIN Initiative data-sharing ecosystem: Characteristics, challenges, benefits, and opportunities. Elife. 2024 Nov 27; 13.
    View in: PubMed
    Score: 0.026
  2. 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: 0.026
  3. An Ethical Framework for Disclosing the Training Status and Roles of Resident-Level Surgeons to Patients. J Surg Educ. 2024 Oct; 81(10):1446-1451.
    View in: PubMed
    Score: 0.026
  4. Translational Research and Health Equity: Gene Therapies for Sickle Cell Disease as a Case Study. Ethics Hum Res. 2024 May-Jun; 46(3):34-39.
    View in: PubMed
    Score: 0.025
  5. Building Effective Mentoring Relationships During Clinical Ethics Fellowships: Pedagogy, Programs, and People. HEC Forum. 2024 Mar; 36(1):1-29.
    View in: PubMed
    Score: 0.022
  6. Direct-to-Consumer Genetic Testing: Value and Risk. Annu Rev Med. 2021 01 27; 72:151-166.
    View in: PubMed
    Score: 0.019
  7. Disability and Contingency Care. Am J Bioeth. 2020 07; 20(7):190-192.
    View in: PubMed
    Score: 0.019
  8. Hashtag who's missing? Lessons for genomic databases. Disabil Health J. 2021 01; 14(1):100945.
    View in: PubMed
    Score: 0.019
  9. 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: 0.019
  10. Laws About Transparent School Vaccination Reporting: Public Health Context and Ethics. Am J Public Health. 2019 12; 109(12):1687-1690.
    View in: PubMed
    Score: 0.018
  11. Genomic Data-Sharing Practices. J Law Med Ethics. 2019 03; 47(1):31-40.
    View in: PubMed
    Score: 0.018
  12. Characterizing the Biomedical Data-Sharing Landscape. J Law Med Ethics. 2019 03; 47(1):21-30.
    View in: PubMed
    Score: 0.018
  13. The Role of Participants in a Medical Information Commons. J Law Med Ethics. 2019 03; 47(1):51-61.
    View in: PubMed
    Score: 0.018
  14. Off-Target Effects of a Defense of Denial. Am J Bioeth. 2018 09; 18(9):22-24.
    View in: PubMed
    Score: 0.017
  15. United States: law and policy concerning transfer of genomic data to third countries. Hum Genet. 2018 Aug; 137(8):647-655.
    View in: PubMed
    Score: 0.017
  16. Serum Homocysteine and its Association with Glycemic Control in Type 2 Diabetic Patients. Mymensingh Med J. 2017 Oct; 26(4):921-926.
    View in: PubMed
    Score: 0.016
  17. Sharing data under the 21st Century Cures Act. Genet Med. 2017 12; 19(12):1289-1294.
    View in: PubMed
    Score: 0.016
  18. Myriad take two: Can genomic databases remain secret? Science. 2017 05 12; 356(6338):586-587.
    View in: PubMed
    Score: 0.016
  19. Beyond Our Borders? Public Resistance to Global Genomic Data Sharing. PLoS Biol. 2016 Nov; 14(11):e2000206.
    View in: PubMed
    Score: 0.015
  20. Federal Privacy Protections: Ethical Foundations, Sources of Confusion in Clinical Medicine, and Controversies in Biomedical Research. AMA J Ethics. 2016 Mar 01; 18(3):288-98.
    View in: PubMed
    Score: 0.014
  21. 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: 0.014
  22. Case study. Bad words. Commentary. Hastings Cent Rep. 2014 Mar-Apr; 44(2):14.
    View in: PubMed
    Score: 0.012
  23. The "Permanent" Patient Problem. J Law Med Ethics. 2014; 42(1):88-92.
    View in: PubMed
    Score: 0.012
  24. Ethical dilemmas surrounding the use of ventricular assist devices in supporting patients with end-stage organ dysfunction. Methodist Debakey Cardiovasc J. 2013 Jan-Mar; 9(1):11-4.
    View in: PubMed
    Score: 0.012
  25. More mud, less crystal? Ambivalence, disability, and PGD. Am J Bioeth. 2012; 12(4):26-8.
    View in: PubMed
    Score: 0.011
  26. Research ethics. The NIH draft guidelines on human stem cell research. Science. 2009 Jun 26; 324(5935):1648-9.
    View in: PubMed
    Score: 0.009
  27. Future directions for oversight of stem cell research in the United States: an update. Kennedy Inst Ethics J. 2009 Jun; 19(2):195-200.
    View in: PubMed
    Score: 0.009
  28. Future directions for oversight of stem cell research in the United States. Kennedy Inst Ethics J. 2009 Mar; 19(1):79-100.
    View in: PubMed
    Score: 0.009
  29. Cyberbanks and other virtual research repositories. J Law Med Ethics. 2005; 33(1):31-9.
    View in: PubMed
    Score: 0.007
  30. The roles of ethicists in managed care litigation. J Law Med Ethics. 2005; 33(2):264-73.
    View in: PubMed
    Score: 0.007
  31. The politics of embryo transfer. Med Ethics (Burlingt Mass). 2005; 12(3):10-1.
    View in: PubMed
    Score: 0.007
  32. Uncharitable care? Hastings Cent Rep. 2004 Jul-Aug; 34(4):7.
    View in: PubMed
    Score: 0.006
  33. 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: 0.006
  34. Data stewardship in FTLD research: Investigator and research participant views. Alzheimers Dement. 2024 04; 20(4):2886-2893.
    View in: PubMed
    Score: 0.006
  35. 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: 0.006
  36. Supplementing the fairness framework: system-level and implementation concerns. Am J Bioeth. 2004; 4(3):112-4; discussion W40-2.
    View in: PubMed
    Score: 0.006
  37. 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: 0.006
  38. 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: 0.006
  39. Prevalence and Risk Factors of Secondary Hyperparathyroidism among CKD Patients and Correlation with Different Laboratory Parameters. Mymensingh Med J. 2022 Oct; 31(4):1084-1092.
    View in: PubMed
    Score: 0.006
  40. Development of an Open Database of Genes Included in Hereditary Cancer Genetic Testing Panels Available From Major Sources in the US. JAMA Oncol. 2022 04 01; 8(4):1-3.
    View in: PubMed
    Score: 0.005
  41. 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: 0.005
  42. 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: 0.005
  43. 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: 0.005
  44. Learning Health System - Moving from Ethical Frameworks to Practical Implementation. J Law Med Ethics. 2019 09; 47(3):454-458.
    View in: PubMed
    Score: 0.005
  45. Introduction: Sharing Data in a Medical Information Commons. J Law Med Ethics. 2019 03; 47(1):7-11.
    View in: PubMed
    Score: 0.004
  46. What is a Medical Information Commons? J Law Med Ethics. 2019 03; 47(1):41-50.
    View in: PubMed
    Score: 0.004
  47. 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: 0.004
  48. 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: 0.004
  49. 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: 0.004
  50. 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: 0.004
  51. Do privacy and security regulations need a status update? Perspectives from an intergenerational survey. PLoS One. 2017; 12(9):e0184525.
    View in: PubMed
    Score: 0.004
  52. 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: 0.004
  53. Ethical and Legal Challenges Associated with Public Molecular Autopsies. J Law Med Ethics. 2016 06; 44(2):309-18.
    View in: PubMed
    Score: 0.004
  54. Persistent confusion and controversy surrounding gene patents. Nat Biotechnol. 2016 Feb; 34(2):145-7.
    View in: PubMed
    Score: 0.004
  55. Cultivating Administrative Support for a Clinical Ethics Consultation Service. J Clin Ethics. 2016; 27(4):341-351.
    View in: PubMed
    Score: 0.004
  56. "Systematizing" ethics consultation services. HEC Forum. 2015 Mar; 27(1):35-45.
    View in: PubMed
    Score: 0.003
  57. Same goal, different path. Am J Bioeth. 2014; 14(1):23-4.
    View in: PubMed
    Score: 0.003
  58. Patient-to-patient encounters: benefits and challenges. J Heart Lung Transplant. 2013 Jun; 32(6):658-9.
    View in: PubMed
    Score: 0.003
  59. The ethics of lawyer-ethicists. J Law Med Ethics. 2005; 33(3):603-7.
    View in: PubMed
    Score: 0.002
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.