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Association between hsa-mir-146a genotype and tumor age-of-onset in BRCA1/BRCA2-negative familial breast and ovarian cancer patients
Carcinogenesis (New York), 2010-12, Vol.31 (12), p.2124-2126
2010
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Trabectedin may be a valuable treatment option for elderly patients with metastatic soft tissue sarcomas
Frontiers in oncology, 2024-07, Vol.14, p.1437732
2024
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Null Mismatch Repair Proteins Expression Reveals the Temporal Molecular Events in Lynch Syndrome-Related Cancers
Diagnostics (Basel), 2024-05, Vol.14 (9), p.888
2024
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Metabolic Clues to Bile Acid Patterns and Prolonged Survival in Patients with Metastatic Soft-Tissue Sarcoma Treated with Trabectedin
Metabolites, 2023-09, Vol.13 (10), p.1035
2023
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Tracking of the origin of recurrent mutations of the BRCA1 and BRCA2 genes in the North-East of Italy and improved mutation analysis strategy
BMC medical genetics, 2016-02, Vol.17 (1), p.11-11, Article 11
2016
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Integrated analysis of unclassified variants in mismatch repair genes
Genetics in medicine, 2011-02, Vol.13 (2), p.115-124
2011
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Prevalence of BRCA1 genomic rearrangements in a large cohort of Italian breast and breast/ovarian cancer families without detectable BRCA1 and BRCA2 point mutations
Genes chromosomes & cancer, 2006-09, Vol.45 (9), p.791-797
2006
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Selecting for BRCA1 testing using a combination of homogeneous selection criteria and immunohistochemical characteristics of breast cancers
BMC cancer, 2009-10, Vol.9 (1), p.360-360, Article 360
2009
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Phenotypic features and genetic characterization of male breast cancer families: identification of two recurrent BRCA2 mutations in north-east of Italy
BMC cancer, 2006-06, Vol.6 (1), p.156-156, Article 156
2006
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BRCA1 and BRCA2 genes: Role in hereditary breast and ovarian cancer in Italy
International journal of cancer, 1999-09, Vol.83 (1), p.5-9
1999
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Different expressivity of BRCA1 and BRCA2: analysis of 179 Italian pedigrees with identified mutation
Breast cancer research and treatment, 2003-09, Vol.81 (1), p.71-79
2003
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Association of the germline BRCA2 missense variation Glu2663Lys with high sensitivity to trabectedin-based treatment in soft tissue sarcoma
Cancer biology & therapy, 2016-10, Vol.17 (10), p.1017-1021
2016
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Amsterdam criteria II and endometrial cancer index cases for an accurate selection of HNPCC families
Tumori, 2002-01, Vol.88 (1), p.18-20
2002
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FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor
Human molecular genetics, 2015, Vol.24 (18), p.5345
2015
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Prevalence ofBRCA1 genomic rearrangements in a large cohort of Italian breast and breast/ovarian cancer families without detectableBRCA1 andBRCA2 point mutations
Genes chromosomes & cancer, 2006-09, Vol.45 (9), p.791-797
2006
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Phenotypic features and genetic characterization of male breast cancer families: identification of two recurrent BRCA2 mutations in northeast of Italy
BMC cancer, 2006-01, Vol.6 (1)
2006
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Different molecular mechanisms underlie genomic deletions in theMLH1 Gene
Human mutation, 2002-11, Vol.20 (5), p.368-374
2002
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Lack of PMS2 gene-truncating mutations in patients with hereditary colorectal cancer
International journal of oncology, 1998-09, Vol.13 (3), p.565
1998
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BRCA1 andBRCA2 genes: Role in hereditary breast and ovarian cancer in Italy
International journal of cancer, 1999-09, Vol.83 (1), p.5-9
1999
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Microsatellite instability and MLH1 and MSH2 germline defects are related to clinicopathological features in sporadic colorectal cancer
Oncology reports, 2000-01, Vol.7 (1), p.39
2000
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Association of the germline BRCA2 missense variation Glu2663Lys with high sensitivity to trabectedin-based treatment in soft tissue sarcoma
Cancer Biology & Therapy, 2016, Vol.17 (10), p.1017-1021
2016
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