Associated Papers
Understanding and predicting the functional consequences of missense mutations in BRCA1 and BRCA2.
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Scientific Reports, 2022
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Supplement: 41598_2022_13508_MOESM2_ESM.xlsx › Sheet1
Identification of pathogenic variants in cancer genes using base editing screens with editing efficiency correction.
Huang C et al.
Genome Biology, 2021
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Supplement: 13059_2021_2305_MOESM7_ESM.xlsx › Table_S6
Prevalence and Spectrum of Germline BRCA1 and BRCA2 Variants of Uncertain Significance in Breast/Ovarian Cancer: Mysterious Signals From the Genome.
Fanale D et al.
Frontiers in Oncology, 2021
Hereditary Breast and Ovarian Cancer in Families from Southern Italy (Sicily)-Prevalence and Geographic Distribution of Pathogenic Variants in BRCA1/2 Genes.
Incorvaia L et al.
Cancers, 2020
32380732 (PubMed )
Supplement: cancers-12-01158-s001.pdf
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