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Comment
. 2020 Nov;22(11):1909.
doi: 10.1038/s41436-020-0888-0. Epub 2020 Jun 30.

Economic value of exome sequencing for suspected monogenic disorders

Bart S Ferket  1 , David L Veenstra  2
Affiliations
Free article
Comment

Economic value of exome sequencing for suspected monogenic disorders

Bart S Ferket et al. Genet Med. 2020 Nov.
Free article
No abstract available

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Comment in

  • Response to Ferket et al.
    Schofield D, Rynehart L, Shresthra R, White SM, Stark Z. Schofield D, et al. Genet Med. 2020 Nov;22(11):1910. doi: 10.1038/s41436-020-0889-z. Epub 2020 Jul 1. Genet Med. 2020. PMID: 32606441 No abstract available.

Comment on

References

    1. Schofield D, Rynehart L, Shresthra R, et al. Long-term economic impacts of exome sequencing for suspected monogenic disorders: diagnosis, management, and reproductive outcomes. Genet Med. 2019;21:2586–2593. - PubMed
    1. Stark Z, Schofield D, Alam K, et al. Prospective comparison of the cost-effectiveness of clinical whole-exome sequencing with that of usual care overwhelmingly supports early use and reimbursement. Genet Med. 2017;19:867–874. - PubMed
    1. Sanders GD, Neumann PJ, Basu A, et al. Recommendations for conduct, methodological practices, and reporting of cost-effectiveness analyses: second panel on cost-effectiveness in health and medicine. JAMA. 2016;316:1093–1103. - PubMed - PMC
    1. Lipstein EA, Brinkman WB, Fiks AG, et al. An emerging field of research: challenges in pediatric decision making. Med Decis Making. 2015;35:403–408. - PubMed - PMC
    1. Lingen M, Albers L, Borchers M, et al. Obtaining a genetic diagnosis in a child with disability: impact on parental quality of life. Clin Genet. 2016;89:258–266. - PubMed - PMC

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