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Year | Number of Results |
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2021 | 1 |
2022 | 1 |
2024 | 2 |
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Quantifying prediction of pathogenicity for within-codon concordance (PM5) using 7541 functional classifications of BRCA1 and MSH2 missense variants.
Genet Med. 2022 Mar;24(3):552-563. doi: 10.1016/j.gim.2021.11.011. Epub 2021 Nov 18.
Genet Med. 2022.
PMID: 34906453
Free PMC article.
The PS4-likelihood ratio calculator: flexible allocation of evidence weighting for case-control data in variant classification.
Rowlands CF, Garrett A, Allen S, Durkie M, Burghel GJ, Robinson R, Callaway A, Field J, Frugtniet B, Palmer-Smith S, Grant J, Pagan J, McDevitt T, McVeigh TP, Hanson H, Whiffin N, Jones M, Turnbull C; CanVIG-UK.
Rowlands CF, et al.
J Med Genet. 2024 Sep 3:jmg-2024-110034. doi: 10.1136/jmg-2024-110034. Online ahead of print.
J Med Genet. 2024.
PMID: 39227160
Free article.
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Economic evaluation of extended panel analysis in cancer patients with historical NHS diagnostic germline genetic testing - A modeling study based on real-world data.
Xi Q, Patel R, Linton-Willoughby T, Short J, Tischkowitz M, Snape K, Morris S.
Xi Q, et al. Among authors: linton willoughby t.
Eur J Med Genet. 2024 Sep 12;72:104969. doi: 10.1016/j.ejmg.2024.104969. Online ahead of print.
Eur J Med Genet. 2024.
PMID: 39260602
Free article.
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