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daniel assaad
(7 results)?
Patient-facing digital tools for delivering genetic services: a systematic review.
J Med Genet. 2023 Jan;60(1):1-10. doi: 10.1136/jmg-2022-108653. Epub 2022 Sep 22.
J Med Genet. 2023.
PMID: 36137613
Review.
Utility of Genetic Testing from the Perspective of Parents/Caregivers: A Scoping Review.
Hayeems RZ, Luca S, Assamad D, Bhatt A, Ungar WJ.
Hayeems RZ, et al. Among authors: assamad d.
Children (Basel). 2021 Mar 27;8(4):259. doi: 10.3390/children8040259.
Children (Basel). 2021.
PMID: 33801725
Free PMC article.
Review.
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Digital Health Tools in Genomics: Advancing Diversity, Equity, and Inclusion.
Assamad D, Majeed S, Aguda V, Grewal S, Butkowsky C, Clausen M, D'Amours G, Bombard Y.
Assamad D, et al.
Public Health Genomics. 2023;26(1):194-200. doi: 10.1159/000534804. Epub 2023 Oct 26.
Public Health Genomics. 2023.
PMID: 37883926
Free article.
No abstract available.
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Evaluation of the diagnostic accuracy of exome sequencing and its impact on diagnostic thinking for patients with rare disease in a publicly funded health care system: A prospective cohort study.
Hartley T, Marshall D, Acker M, Fooks K, Gillespie MK, Price EM, Graham ID, White-Brown A, MacKay L, Macdonald SK, Brady L, Hui AY, Andrews JD, Chowdhury A, Wall E, Soubry É, Ediae GU, Rojas S, Assamad D, Dyment D, Tarnopolsky M, Sawyer SL, Chisholm C, Lemire G, Amburgey K, Lazier J, Mendoza-Londono R, Dowling JJ, Balci TB, Armour CM, Bhola PT, Costain G, Dupuis L, Carter M, Badalato L, Richer J, Boswell-Patterson C, Kannu P, Cordeiro D, Warman-Chardon J, Graham G, Siu VM, Cytrynbaum C, Rusnak A, Aul RB, Yoon G, Gonorazky H, McNiven V, Mercimek-Andrews S, Guerin A, Deshwar AR, Marwaha A, Weksberg R, Karp N, Campbell M, Al-Qattan S, Shuen AY, Inbar-Feigenberg M, Cohn R, Szuto A, Inglese C, Poirier M, Chad L, Potter B, Boycott KM, Hayeems R; Care4Rare Canada Consortium.
Hartley T, et al. Among authors: assamad d.
Genet Med. 2024 Feb;26(2):101012. doi: 10.1016/j.gim.2023.101012. Epub 2023 Nov 1.
Genet Med. 2024.
PMID: 37924259
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