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Genetics Adviser: a protocol for a mixed-methods randomised controlled trial evaluating a digital platform for genetics service delivery.
BMJ Open. 2022 Apr 29;12(4):e060899. doi: 10.1136/bmjopen-2022-060899.
BMJ Open. 2022.
PMID: 35487723
Free PMC article.
"Doctors shouldn't have to cheat the system": Clinicians' real-world experiences of the utility of genomic sequencing.
Shickh S, Mighton C, Clausen M, Adi-Wauran E, Hirjikaka D, Kodida R, Krishnapillai S, Reble E, Sam J, Shaw A, Lerner-Ellis J, Baxter NN, Laupacis A, Bombard Y.
Shickh S, et al. Among authors: hirjikaka d.
Genet Med. 2022 Sep;24(9):1888-1898. doi: 10.1016/j.gim.2022.04.024. Epub 2022 May 25.
Genet Med. 2022.
PMID: 35612591
Free article.
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Genetics providers' perspectives on the use of digital tools in clinical practice.
Lee W, Hirjikaka D, Grewal S, Shaw A, Luca S, Clausen M, Bombard Y, Hayeems RZ; Genetics Navigator Study Team.
Lee W, et al. Among authors: hirjikaka d.
Genet Med. 2024 Mar 14;26(6):101122. doi: 10.1016/j.gim.2024.101122. Online ahead of print.
Genet Med. 2024.
PMID: 38493336
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"I don't need any more unknowns hanging over my head": Views of patients with cancer on variants of uncertain significance and low/moderate risk results from genomic sequencing.
Shickh S, Mighton C, Clausen M, Kodida R, Adi-Wauran E, Hirjikaka D, Krishnapillai S, Reble E, Sam J, Baxter NN, Laupacis A, Bombard Y; Incidental Genomics Study Team.
Shickh S, et al. Among authors: hirjikaka d.
Genet Med. 2023 Dec;25(12):100960. doi: 10.1016/j.gim.2023.100960. Epub 2023 Aug 11.
Genet Med. 2023.
PMID: 37577963
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