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Genetics providers' perspectives on the use of digital tools in clinical practice.
Genet Med. 2024 Mar 14;26(6):101122. doi: 10.1016/j.gim.2024.101122. Online ahead of print.
Genet Med. 2024.
PMID: 38493336
"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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"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 Adviser: a protocol for a mixed-methods randomised controlled trial evaluating a digital platform for genetics service delivery.
Shickh S, Hirjikaka D, Clausen M, Kodida R, Mighton C, Reble E, Sam J, Panchal S, Aronson M, Graham T, Armel SR, Glogowski E, Elser C, Eisen A, Carroll JC, Shuman C, Seto E, Baxter NN, Scheer A, Shastri-Estrada S, Feldman G, Thorpe KE, Schrader KA, Lerner-Ellis J, Kim RH, Faghfoury H, Bombard Y.
Shickh S, et al. Among authors: hirjikaka d.
BMJ Open. 2022 Apr 29;12(4):e060899. doi: 10.1136/bmjopen-2022-060899.
BMJ Open. 2022.
PMID: 35487723
Free PMC article.
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