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Year | Number of Results |
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2023 | 3 |
2024 | 2 |
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Page 1
Occurrence of variants of unknown clinical significance in genetic testing for hereditary breast and ovarian cancer syndrome and Lynch syndrome: a literature review and analytical observational retrospective cohort study.
BMC Med Genomics. 2023 Jan 16;16(1):7. doi: 10.1186/s12920-023-01437-7.
BMC Med Genomics. 2023.
PMID: 36647026
Free PMC article.
Review.
ACCESS: an empirically-based framework developed by the International Nursing CASCADE Consortium to address genomic disparities through the nursing workforce.
Katapodi MC, Pedrazzani C, Barnoy S, Dagan E, Fluri M, Jones T, Kim S, Underhill-Blazey ML, Uveges MK, Dwyer AA.
Katapodi MC, et al. Among authors: fluri m.
Front Genet. 2024 Jan 8;14:1337366. doi: 10.3389/fgene.2023.1337366. eCollection 2023.
Front Genet. 2024.
PMID: 38264211
Free PMC article.
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Predicting Openness of Communication in Families With Hereditary Breast and Ovarian Cancer Syndrome: Natural Language Processing Analysis.
Baroutsou V, Cerqueira Gonzalez Pena R, Schweighoffer R, Caiata-Zufferey M, Kim S, Hesse-Biber S, Ciorba FM, Lauer G, Katapodi M; CASCADE Consortium.
Baroutsou V, et al.
JMIR Form Res. 2023 Jan 19;7:e38399. doi: 10.2196/38399.
JMIR Form Res. 2023.
PMID: 36656633
Free PMC article.
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Real-World Data on Institutional Implementation of Screening for Mismatch Repair Deficiency and Lynch Syndrome in Endometrial Cancer Patients.
Joder C, Gmür A, Solass W, Christe L, Rabaglio M, Fluri M, Rau TT, Saner FAM, Knabben L, Imboden S, Mueller MD, Siegenthaler F.
Joder C, et al. Among authors: fluri m.
Cancers (Basel). 2024 Feb 4;16(3):671. doi: 10.3390/cancers16030671.
Cancers (Basel). 2024.
PMID: 38339422
Free PMC article.
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