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Amelia Buffone · SciRah

Researcher profile · Semantic Scholar

Amelia Buffone

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Amelia Buffone — researcher profile on SciRah

h-index: 10
Works: 17
Citations: 256

Most-cited papers

PRDX1 and PRDX6 are repressed in papillary thyroid carcinomas via BRAF V600E-dependent and -independent mechanisms.
Arianna Nicolussi, S. D’Inzeo, G. Mincione, Amelia Buffone +8 more
2014International Journal of Oncology36 citations Open access
Semantic Scholar
Characterization of medulloblastoma in Fanconi Anemia: a novel mutation in the BRCA2 gene and SHH molecular subgroup
E. Miele, A. Mastronuzzi, A. Pò, A. Carai +15 more
2015Biomarker Research35 citations Open access
Semantic Scholar
Prevalence of BRCA1 and BRCA2 genomic rearrangements in a cohort of consecutive Italian breast and/or ovarian cancer families
Amelia Buffone, C. Capalbo, E. Ricevuto, T. Sidoni +13 more
2007Breast Cancer Research and Treatment30 citations
Semantic Scholar
Validation of the Ion Torrent PGM sequencing for the prospective routine molecular diagnostic of colorectal cancer.
F. Belardinilli, C. Capalbo, Amelia Buffone, Marialaura Petroni +9 more
2015Clinical Biochemistry27 citations
Semantic Scholar
Optimizing the identification of risk‐relevant mutations by multigene panel testing in selected hereditary breast/ovarian cancer families
A. Coppa, Arianna Nicolussi, S. D’Inzeo, C. Capalbo +11 more
2017Cancer Medicine24 citations Open access
Semantic Scholar
Novel BRCA1 and BRCA2 germline mutations and assessment of mutation spectrum and prevalence in Italian breast and/or ovarian cancer families
G. Giannini, C. Capalbo, Elisabetta Ristori, E. Ricevuto +12 more
2006Breast Cancer Research and Treatment24 citations
Semantic Scholar
Vemurafenib and panitumumab combination tailored therapy in BRAF-mutated metastatic colorectal cancer
C. Capalbo, P. Marchetti, A. Coppa, A. Calogero +9 more
2014Cancer Biology & Therapy21 citations Open access
Semantic Scholar
Clinical classification of BRCA1 DNA missense variants: H1686Q is a novel pathogenic mutation occurring in the ontogenetically invariant THV motif of the N-terminal BRCT domain.
G. Giannini, C. Capalbo, L. Ottini, Amelia Buffone +12 more
2008Journal of Clinical Oncology15 citations
Semantic Scholar
Improving the accuracy of BRCA1/2 mutation prediction: validation of the novel country-customized IC software
C. Capalbo, E. Ricevuto, A. Vestri, T. Sidoni +12 more
2006European Journal of Human Genetics13 citations
Semantic Scholar
Novel and recurrent BRCA2 mutations in Italian breast/ovarian cancer families widen the ovarian cancer cluster region boundaries to exons 13 and 14
A. Coppa, Amelia Buffone, C. Capalbo, Arianna Nicolussi +11 more
2014Breast Cancer Research and Treatment11 citations
Semantic Scholar
Detection of ATM germline variants by the p53 mitotic centrosomal localization test in BRCA1/2-negative patients with early-onset breast cancer
A. Prodosmo, Amelia Buffone, M. Mattioni, A. Barnabei +18 more
2016Journal of experimental & clinical cancer research : CR9 citations Open access
Semantic Scholar
Does the search for large genomic rearrangements impact BRCAPRO carrier prediction?
C. Capalbo, Amelia Buffone, A. Vestri, E. Ricevuto +7 more
2007Journal of Clinical Oncology6 citations
Semantic Scholar
PRDX 1 and PRDX 6 are repressed in papillary thyroid carcinomas via BRAF V 600 E-dependent and-independent mechanisms
Arianna Nicolussi, S. D’Inzeo, G. Mincione, Amelia Buffone +8 more
20133 citations
Semantic Scholar
Erratum to: Detection of ATM germline variants by the p53 mitotic centrosomal localization test in BRCA1/2-negative patients with early-onset breast cancer
A. Prodosmo, Amelia Buffone, M. Mattioni, A. Barnabei +18 more
2016Journal of experimental & clinical cancer research : CR1 citations Open access
Semantic Scholar
Novel BRCA 1 and BRCA 2 germline mutations and assessment of mutation spectrum and prevalence in Italian breast and / or ovarian cancer families
G. Giannini, C. Capalbo, Elisabetta Ristori, E. Ricevuto +12 more
1 citations
Semantic Scholar
Characterization of medulloblastoma in Fanconi Anemia: a novel mutation in the BRCA2 gene and SHH molecular subgroup
E. Miele, A. Mastronuzzi, A. Pò, A. Carai +15 more
2015Biomarker Research0 citations Open access
Semantic Scholar
Diagnostic accuracy of small intestine contrast ultrasonography (Sicus) in the assessment of small intestinal lesions in Crohn's disease
Emma Calabrese, N. Pallotta, E. Tomei, A. Viscido +4 more
20030 citations
Semantic Scholar

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P. Marchetti — researcher profile on SciRah