Dragojlovic N - Search Results

1

The cost and diagnostic yield of exome sequencing for children with suspected genetic disorders: a benchmarking study.

Dragojlovic N, Elliott AM, Adam S, van Karnebeek C, Lehman A, Mwenifumbo JC, Nelson TN, du Souich C, Friedman JM, Lynd LD. Dragojlovic N, et al. Genet Med. 2018 Sep;20(9):1013-1021. doi: 10.1038/gim.2017.226. Epub 2018 Jan 4. Genet Med. 2018. PMID: 29300375 Free article. Review.

2

Crowdfunding drug development: the state of play in oncology and rare diseases.

Dragojlovic N, Lynd LD. Dragojlovic N, et al. Drug Discov Today. 2014 Nov;19(11):1775-1780. doi: 10.1016/j.drudis.2014.06.019. Epub 2014 Jun 25. Drug Discov Today. 2014. PMID: 24973645 Review.

3

Challenges in measuring the societal value of orphan drugs: insights from a canadian stated preference survey.

Dragojlovic N, Rizzardo S, Bansback N, Mitton C, Marra CA, Lynd LD. Dragojlovic N, et al. Patient. 2015 Feb;8(1):93-101. doi: 10.1007/s40271-014-0109-5. Patient. 2015. PMID: 25586645

4

What will the crowd fund? Preferences of prospective donors for drug development fundraising campaigns.

Dragojlovic N, Lynd LD. Dragojlovic N, et al. Drug Discov Today. 2016 Dec;21(12):1863-1868. doi: 10.1016/j.drudis.2016.07.002. Epub 2016 Jul 12. Drug Discov Today. 2016. PMID: 27422268

5

Evaluating the use of parental reports to estimate health care resource utilization in children with suspected genetic disorders.

Dragojlovic N, Kim E, Elliott AM; CAUSES Study; Friedman JM, Lynd LD. Dragojlovic N, et al. J Eval Clin Pract. 2018 Apr;24(2):416-422. doi: 10.1111/jep.12876. J Eval Clin Pract. 2018. PMID: 29603523

6

The Genomic Consultation Service: A clinical service designed to improve patient selection for genome-wide sequencing in British Columbia.

Elliott AM, du Souich C, Adam S, Dragojlovic N, van Karnebeek C, Nelson TN, Lehman A; CAUSES Study; Lynd LD, Friedman JM. Elliott AM, et al. Among authors: dragojlovic n. Mol Genet Genomic Med. 2018 May 30;6(4):592-600. doi: 10.1002/mgg3.410. Online ahead of print. Mol Genet Genomic Med. 2018. PMID: 29851296 Free PMC article.

7

Evaluating Canadians' Values for Drug Coverage Decision Making.

Rizzardo S, Bansback N, Dragojlovic N, Douglas C, Li KH, Mitton C, Marra C, Blanis L, Lynd LD. Rizzardo S, et al. Among authors: dragojlovic n. Value Health. 2019 Mar;22(3):362-369. doi: 10.1016/j.jval.2018.08.008. Epub 2018 Nov 27. Value Health. 2019. PMID: 30832975 Free article.

8

Genetic counseling considerations with rapid genome-wide sequencing in a neonatal intensive care unit.

Smith EE, du Souich C, Dragojlovic N; CAUSES Study; RAPIDOMICS Study; Elliott AM. Smith EE, et al. Among authors: dragojlovic n. J Genet Couns. 2019 Apr;28(2):263-272. doi: 10.1002/jgc4.1074. Epub 2018 Dec 31. J Genet Couns. 2019. PMID: 30964583

9

The cost trajectory of the diagnostic care pathway for children with suspected genetic disorders.

Dragojlovic N, van Karnebeek CDM, Ghani A, Genereaux D, Kim E, Birch P; CAUSES Study; Elliott AM, Friedman JM, Lynd LD. Dragojlovic N, et al. Genet Med. 2020 Feb;22(2):292-300. doi: 10.1038/s41436-019-0635-6. Epub 2019 Aug 29. Genet Med. 2020. PMID: 31462755 Free article.

10

SETD1B-associated neurodevelopmental disorder.

Roston A, Evans D, Gill H, McKinnon M, Isidor B, Cogné B, Mwenifumbo J, van Karnebeek C, An J, Jones SJM, Farrer M, Demos M, Connolly M, Gibson WT; CAUSES Study; EPGEN Study. Roston A, et al. J Med Genet. 2021 Mar;58(3):196-204. doi: 10.1136/jmedgenet-2019-106756. Epub 2020 Jun 16. J Med Genet. 2021. PMID: 32546566

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