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Frontiers in Oncology|April 25, 2022
Management of BRCA Tumour Testing in an Integrated Molecular Tumour Board Multidisciplinary ModelJacopo Azzollini, Andrea Vingiani, Luca Agnelli, et al.
Breast Cancer Research and Treatment|September 15, 2016
Haplotype analyses of the c.1027C>T and c.2167_2168delAT recurrent truncating mutations in the breast cancer-predisposing gene PALB2Irene Catucci, Silvia Casadei, Yuan Chun Ding, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|June 9, 2005
A comparison of bilateral breast cancers in BRCA carriersJeffrey N Weitzel, Mark Robson, Barbara Pasini, et al.
Tumori|August 9, 2025
The e-BRAVE study: A prospective web-based cohort and biobank of women carriers of BRCA mutationsAndreina Oliverio, Carlotta Meli, Eleonora Bruno, et al.
Breast (Edinburgh, Scotland)|December 30, 2017
A possible role of FANCM mutations in male breast cancer susceptibility: Results from a multicenter study in ItalyValentina Silvestri, Piera Rizzolo, Veronica Zelli, et al.
International Journal of Cancer|January 16, 2008
International variation in rates of uptake of preventive options in BRCA1 and BRCA2 mutation carriersKelly A Metcalfe, Daphna Birenbaum-Carmeli, Jan Lubinski, et al.
Endocrine Connections|July 24, 2019
Evaluation of CYP17A1 and CYP1B1 polymorphisms in male breast cancer riskPiera Rizzolo, Valentina Silvestri, Virginia Valentini, et al.
Cancers|March 6, 2019
Usefulness and Limitations of Comprehensive Characterization of mRNA Splicing Profiles in the Definition of the Clinical Relevance of BRCA1/2 Variants of Uncertain SignificanceElisa Gelli, Mara Colombo, Anna Maria Pinto, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 22, 2014
PALB2 sequencing in Italian familial breast cancer cases reveals a high-risk mutation recurrent in the province of BergamoIrene Catucci, Paolo Peterlongo, Sara Ciceri, et al.
Cancer Research|February 20, 2007
Determination of cancer risk associated with germ line BRCA1 missense variants by functional analysisMarcelo A Carvalho, Sylvia M Marsillac, Rachel Karchin, et al.
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