Regier DA - Search Results

1

"I Just Assumed This Was Already Being Done": Canadian Patient Preferences for Enhanced Data Sharing for Precision Oncology.

Pollard S, Ehman M, Hermansen A, Weymann D, Krebs E, Ho C, Lim HJ, Jones S, Bombard Y, Hanna TP, Hessels C, Longstaff H, Cook-Deegan R, Bubela T, Regier DA. Pollard S, et al. Among authors: regier da. JCO Precis Oncol. 2024 Aug;8:e2400184. doi: 10.1200/PO.24.00184. JCO Precis Oncol. 2024. PMID: 39116357 Free PMC article.

2

Public Perceptions of the Benefits and Risks of Newborn Screening.

Miller FA, Hayeems RZ, Bombard Y, Cressman C, Barg CJ, Carroll JC, Wilson BJ, Little J, Allanson J, Chakraborty P, Giguère Y, Regier DA. Miller FA, et al. Among authors: regier da. Pediatrics. 2015 Aug;136(2):e413-23. doi: 10.1542/peds.2015-0518. Epub 2015 Jul 13. Pediatrics. 2015. PMID: 26169426

3

The cost and cost trajectory of whole-genome analysis guiding treatment of patients with advanced cancers.

Weymann D, Laskin J, Roscoe R, Schrader KA, Chia S, Yip S, Cheung WY, Gelmon KA, Karsan A, Renouf DJ, Marra M, Regier DA. Weymann D, et al. Among authors: regier da. Mol Genet Genomic Med. 2017 Mar 12;5(3):251-260. doi: 10.1002/mgg3.281. eCollection 2017 May. Mol Genet Genomic Med. 2017. PMID: 28546995 Free PMC article.

4

Patient preferences for massively parallel sequencing genetic testing of colorectal cancer risk: a discrete choice experiment.

Weymann D, Veenstra DL, Jarvik GP, Regier DA. Weymann D, et al. Among authors: regier da. Eur J Hum Genet. 2018 Sep;26(9):1257-1265. doi: 10.1038/s41431-018-0161-z. Epub 2018 May 25. Eur J Hum Genet. 2018. PMID: 29802320 Free PMC article. Clinical Trial.

5

Valuation of Health and Nonhealth Outcomes from Next-Generation Sequencing: Approaches, Challenges, and Solutions.

Regier DA, Weymann D, Buchanan J, Marshall DA, Wordsworth S. Regier DA, et al. Value Health. 2018 Sep;21(9):1043-1047. doi: 10.1016/j.jval.2018.06.010. Epub 2018 Aug 18. Value Health. 2018. PMID: 30224107 Free article. Review.

6

Balancing uncertainty with patient autonomy in precision medicine.

Pollard S, Sun S, Regier DA. Pollard S, et al. Among authors: regier da. Nat Rev Genet. 2019 May;20(5):251-252. doi: 10.1038/s41576-019-0111-9. Nat Rev Genet. 2019. PMID: 30872766 No abstract available.

7

Allocating healthcare resources to genomic testing in Canada: latest evidence and current challenges.

Weymann D, Dragojlovic N, Pollard S, Regier DA. Weymann D, et al. Among authors: regier da. J Community Genet. 2022 Oct;13(5):467-476. doi: 10.1007/s12687-019-00428-5. Epub 2019 Jul 5. J Community Genet. 2022. PMID: 31273679 Free PMC article.

8

Validation of a Cyclic Algorithm to Proxy Number of Lines of Systemic Cancer Therapy Using Administrative Data.

Weymann D, Costa S, Regier DA. Weymann D, et al. Among authors: regier da. JCO Clin Cancer Inform. 2019 Aug;3:1-10. doi: 10.1200/CCI.19.00022. JCO Clin Cancer Inform. 2019. PMID: 31365273

9

Raymakers AJN, Regier DA, Peacock SJ. Raymakers AJN, et al. Among authors: regier da. Cancer. 2020 Jan 1;126(1):148-155. doi: 10.1002/cncr.32455. Epub 2019 Sep 23. Cancer. 2020. PMID: 31544234 Free article.

10

Genetic testing for hereditary cancer syndromes: patient recommendations for improved risk communication.

Pollard S, Kalloger S, Weymann D, Sun S, Nuk J, Schrader KA, Regier DA. Pollard S, et al. Among authors: regier da. Health Expect. 2020 Aug;23(4):884-892. doi: 10.1111/hex.13062. Epub 2020 Apr 27. Health Expect. 2020. PMID: 32338425 Free PMC article.

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