JMIR Publications

Journal of Medical Internet Research

Citing this Article

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Published on 29.09.10 in Vol 12, No 3 (2010): Jul-Sep

This paper is in the following e-collection/theme issue:

Works citing "Consumers’ Use of Web-Based Information and Their Decisions About Multiplex Genetic Susceptibility Testing"

According to Crossref, the following articles are citing this article (DOI 10.2196/jmir.1587):

(note that this is only a small subset of citations)

  1. Hughes Halbert C, Welch B, Lynch C, Magwood G, Rice L, Jefferson M, Riley J. Social determinants of family health history collection. Journal of Community Genetics 2016;7(1):57
    CrossRef
  2. Carere DA, Kraft P, Kaphingst KA, Roberts JS, Green RC. Consumers report lower confidence in their genetics knowledge following direct-to-consumer personal genomic testing. Genetics in Medicine 2016;18(1):65
    CrossRef
  3. Nelson SC, Crouch JM, Bamshad MJ, Tabor HK, Yu J. Use of metaphors about exome and whole genome sequencing. American Journal of Medical Genetics Part A 2016;170(5):1127
    CrossRef
  4. Covolo L, Rubinelli S, Ceretti E, Gelatti U. Internet-Based Direct-to-Consumer Genetic Testing: A Systematic Review. Journal of Medical Internet Research 2015;17(12):e279
    CrossRef
  5. Birch P. Interactive e-counselling for genetics pre-test decisions: where are we now?. Clinical Genetics 2015;87(3):209
    CrossRef
  6. Bernhardt BA, Roche MI, Perry DL, Scollon SR, Tomlinson AN, Skinner D. Experiences with obtaining informed consent for genomic sequencing. American Journal of Medical Genetics Part A 2015;167(11):2635
    CrossRef
  7. Madeo AC, Tercyak KP, Tarini BA, McBride CM. Effects of Undergoing Multiplex Genetic Susceptibility Testing on Parent Attitudes towards Testing Their Children. Annals of Behavioral Medicine 2014;47(3):388
    CrossRef
  8. Ye XC, Ng I, Seid-Karbasi P, Imam T, Lee CE, Chen SY, Herman A, Sharma B, Johal G, Gu B, Wasserman WW. Portal for Families Overcoming Neurodevelopmental Disorders (PFOND): Implementation of a Software Framework for Facilitated Community Website Creation by Nontechnical Volunteers. JMIR Research Protocols 2013;2(2):e25
    CrossRef
  9. Hurle B, Citrin T, Jenkins JF, Kaphingst KA, Lamb N, Roseman JE, Bonham VL. What does it mean to be genomically literate?: National Human Genome Research Institute Meeting Report. Genetics in Medicine 2013;15(8):658
    CrossRef
  10. Bunnik EM, Janssens ACJW, Schermer MHN. A tiered-layered-staged model for informed consent in personal genome testing. European Journal of Human Genetics 2013;21(6):596
    CrossRef
  11. Rosenfeld L, Shepherd A, Agunwamba AA, McCray AT. Iterative Evaluation of a Web-Based Health Information Resource. Journal of Health Communication 2013;18(8):974
    CrossRef
  12. Wade CH, Shiloh S, Woolford SW, Roberts JS, Alford SH, Marteau TM, Biesecker BB. Modelling decisions to undergo genetic testing for susceptibility to common health conditions: An ancillary study of the Multiplex Initiative. Psychology & Health 2012;27(4):430
    CrossRef
  13. Goldsmith L, Jackson L, O'Connor A, Skirton H. Direct-to-consumer genomic testing: systematic review of the literature on user perspectives. European Journal of Human Genetics 2012;20(8):811
    CrossRef
  14. Wasson K, Hogan NS, Sanders TN, Helzlsouer KJ. Primary Care Patients’ Views, Attitudes, and Decision-Making Factors Regarding Direct-to-Consumer Personal Genome Testing: Results From a Qualitative Study. AJOB Primary Research 2012;3(2):24
    CrossRef
  15. Hawkins AK, Ho A. Genetic Counseling and the Ethical Issues Around Direct to Consumer Genetic Testing. Journal of Genetic Counseling 2012;21(3):367
    CrossRef
  16. Wade C, Shiloh S, Roberts J, Hensley Alford S, Marteau T, Biesecker B. Preferences among Diseases on a Genetic Susceptibility Test for Common Health Conditions: An Ancillary Study of the Multiplex Initiative. Public Health Genomics 2012;15(6):322
    CrossRef
  17. Hall TO, Renz AD, Snapinn KW, Bowen DJ, Edwards KL. Awareness and Uptake of Direct-to-Consumer Genetic Testing Among Cancer Cases, Their Relatives, and Controls: The Northwest Cancer Genetics Network. Genetic Testing and Molecular Biomarkers 2012;16(7):744
    CrossRef
  18. Laedtke AL, O’Neill SM, Rubinstein WS, Vogel KJ. Family Physicians’ Awareness and Knowledge of the Genetic Information Non-Discrimination Act (GINA). Journal of Genetic Counseling 2012;21(2):345
    CrossRef
  19. Kaphingst KA, McBride CM, Wade C, Alford SH, Reid R, Larson E, Baxevanis AD, Brody LC. Patients’ understanding of and responses to multiplex genetic susceptibility test results. Genetics in Medicine 2012;14(7):681
    CrossRef
  20. Bloss CS, Darst BF, Topol EJ, Schork NJ. Direct-to-consumer personalized genomic testing. Human Molecular Genetics 2011;20(R2):R132
    CrossRef
  21. Hesse BW, Suls JM. Informatics-Enabled Behavioral Medicine in Oncology. The Cancer Journal 2011;17(4):222
    CrossRef
  22. Tarini BA, Tercyak KP, Wilfond BS. Commentary: Children and Predictive Genomic Testing: Disease Prevention, Research Protection, and Our Future. Journal of Pediatric Psychology 2011;36(10):1113
    CrossRef