Editorial
doi: 10.4161/cbt.3.5.831.
Epub 2004 May 7.
Methods to classify BRCA1 variants of uncertain clinical significance: the more the merrier
Affiliations
- PMID: 15118412
- DOI: 10.4161/cbt.3.5.831
Item in Clipboard
Editorial
Methods to classify BRCA1 variants of uncertain clinical significance: the more the merrier
Cancer Biol Ther.
2004 May.
Free article
No abstract available
Comment on
-
Functional characterization of BRCA1 sequence variants using a yeast small colony phenotype assay.Cancer Biol Ther. 2004 May;3(5):453-7. doi: 10.4161/cbt.3.5.809. Epub 2004 May 18. Cancer Biol Ther. 2004. PMID: 15004537
Similar articles
-
Functional characterization of BRCA1 sequence variants using a yeast small colony phenotype assay.Cancer Biol Ther. 2004 May;3(5):453-7. doi: 10.4161/cbt.3.5.809. Epub 2004 May 18. Cancer Biol Ther. 2004. PMID: 15004537
-
A yeast recombination assay to characterize human BRCA1 missense variants of unknown pathological significance.Hum Mutat. 2009 Jan;30(1):123-33. doi: 10.1002/humu.20817. Hum Mutat. 2009. PMID: 18680205
-
A high-throughput functional complementation assay for classification of BRCA1 missense variants.Cancer Discov. 2013 Oct;3(10):1142-55. doi: 10.1158/2159-8290.CD-13-0094. Epub 2013 Jul 18. Cancer Discov. 2013. PMID: 23867111
-
DNA repair-related functional assays for the classification of BRCA1 and BRCA2 variants: a critical review and needs assessment.J Med Genet. 2017 Nov;54(11):721-731. doi: 10.1136/jmedgenet-2017-104707. Epub 2017 Sep 2. J Med Genet. 2017. PMID: 28866612 Review.
-
BRCA1 and BRCA2 genetic testing-pitfalls and recommendations for managing variants of uncertain clinical significance.Ann Oncol. 2015 Oct;26(10):2057-65. doi: 10.1093/annonc/mdv278. Epub 2015 Jul 7. Ann Oncol. 2015. PMID: 26153499 Free PMC article. Review.
Cited by
-
Autism-associated missense genetic variants impact locomotion and neurodevelopment in Caenorhabditis elegans.Hum Mol Genet. 2019 Jul 1;28(13):2271-2281. doi: 10.1093/hmg/ddz051. Hum Mol Genet. 2019. PMID: 31220273 Free PMC article.
-
A systematic genetic assessment of 1,433 sequence variants of unknown clinical significance in the BRCA1 and BRCA2 breast cancer-predisposition genes.Am J Hum Genet. 2007 Nov;81(5):873-83. doi: 10.1086/521032. Epub 2007 Sep 6. Am J Hum Genet. 2007. PMID: 17924331 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Miscellaneous
