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Future Role of Health Technology Assessment for Genomic Medicine in Oncology: A Canadian Laboratory Perspective.

• Authors : Husereau D; School of Epidemiology and Public Health, University of Ottawa, Ottawa, ON K1G 5Z3, Canada.; Bombard Y

Subjects: Genomic Medicine* ; Technology Assessment, Biomedical*; Humans

• Source: Current oncology (Toronto, Ont.) [Curr Oncol] 2023 Oct 31; Vol. 30 (11), pp. 9660-9669. Date of Electronic Publication: 2023 Oct 31.Publisher: MDPI Country of Publication: Switzerland NLM ID: 9502503 Publication Model: Electronic Cited Medium: Internet ISSN: 1718-7729

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Barriers and Unequal Access to Timely Molecular Testing Results: Addressing the Inequities in Cancer Care Delays across Canada.

• Authors : Snow, Stephanie¹ (AUTHOR); Brezden-Masley, Christine² (AUTHOR); Carter, Michael D.³ (AUTHOR)

• Source: Current Oncology. Mar2024, Vol. 31 Issue 3, p1359-1375. 17p.

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Progress toward Health System Readiness for Genome-Based Testing in Canada.

• Authors : Husereau, Don¹ (AUTHOR) ; Villalba, Eva² (AUTHOR) ; Muthu, Vivek³ (AUTHOR)

• Source: Current Oncology. Jun2023, Vol. 30 Issue 6, p5379-5394. 16p. 2 Charts, 1 Graph.

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Clinical reporting for personalized cancer genomics requires extensive access to subscription-only literature.

• Authors : D'Souza, Schnell¹; Downs, Gregory¹ ; Hendrikx, Shawn²

• Source: Journal of the Medical Library Association. Jan-Apr2023, Vol. 111 Issue 1/2, p579-590. 12p.

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Precision Oncology in Canada: Converting Vision to Reality with Lessons from International Programs.

• Authors : Liu, Geoffrey^1,2 ; Cheung, Winson Y.^3,4; Feilotter, Harriet^5,6

• Source: Current Oncology. Oct2022, Vol. 29 Issue 10, p7257-7271. 15p. 2 Charts, 4 Maps.

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Far and wide: Exploring provider utilization of remote service provision for genome‐wide sequencing in Canada.

• Authors : Enns, Emily A.¹ (AUTHOR); Wainstein, Tasha² (AUTHOR); Dragojlovic, Nick³ (AUTHOR)

• Source: Molecular Genetics & Genomic Medicine. Oct2021, Vol. 9 Issue 10, p1-9. 9p.

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Clinical and genetic analysis of ATP13A2 in hereditary spastic paraplegia expands the phenotype.

• Authors : Estiar, Mehrdad A.^1,2 (AUTHOR); Leveille, Etienne³ (AUTHOR); Spiegelman, Dan^2,4 (AUTHOR)

• Source: Molecular Genetics & Genomic Medicine. Mar2020, Vol. 8 Issue 3, p1-7. 7p.

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FANCC Dutch founder mutation in a Mennonite family from Tamaulipas, México.

• Authors : García‐de Teresa, Benilde¹ (AUTHOR); Frias, Sara^1,2 (AUTHOR); Molina, Bertha¹ (AUTHOR)

• Source: Molecular Genetics & Genomic Medicine. Jun2019, Vol. 7 Issue 6, pN.PAG-N.PAG. 1p.

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Canadian genetic healthcare professionals' attitudes towards discussing private pay options with patients.

• Authors : Di Gioacchino, Vanessa¹ (AUTHOR); Langlois, Sylvie^1,2,3 (AUTHOR); Elliott, Alison M.^1,2,3 (AUTHOR)

• Source: Molecular Genetics & Genomic Medicine. Apr2019, Vol. 7 Issue 4, pN.PAG-N.PAG. 1p.

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The dynamic changes and sex differences of 147 immune-related proteins during acute COVID-19 in 580 individuals.

• Authors : Butler-Laporte, Guillaume^1,2 (AUTHOR); Gonzalez-Kozlova, Edgar³ (AUTHOR); Su, Chen-Yang^1,4 (AUTHOR)

• Source: Clinical Proteomics. 9/28/2022, Vol. 19 Issue 1, p1-11. 11p.

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