CDKN2A and BAP1 germline mutations predispose to melanoma and mesothelioma
Betti, M, Aspesi, A, Biasi, A, Casalone, E, Ferrante, D, Ogliara, P, Gironi, L.C, Giorgione, R, Farinelli, P, Grosso, F, Libener, R, Rosato, S, Turchetti, D, Maffè, A, Casadio, C, Ascoli, V, Dianzani, C, Colombo, E, Piccolini, E, Pavesi, M, Miccoli, S, Mirabelli, D, Bracco, C, Righi, L, Boldorini, R, Papotti, M, Matullo, G, Magnani, C, Pasini, B, Dianzani, I
Published in Cancer letters (10.08.2016)
Published in Cancer letters (10.08.2016)
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A novel likely pathogenetic variant p.(Cys235Arg) of the MEN1 gene in multiple endocrine neoplasia type 1 with multifocal glucagonomas
Smirne, C., Giacomini, G. M., Berton, A. M., Pasini, B., Mercalli, F., Prodam, F., Caputo, M., Brosens, L. A. A., Mollero, E. L. M., Pitino, R., Pirisi, M., Aimaretti, G., Ghigo, E.
Published in Journal of endocrinological investigation (2024)
Published in Journal of endocrinological investigation (2024)
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Lynch syndrome-associated endometrial cancer patient with a rare novel germline likely pathogenic variant of MSH2 gene: A case report
Zumstein, L., Tuninetti, V., Vaira, M., Siatis, D., Palermo, F., Petracchini, M., Scotto, G., Turinetto, M., Piva, R., Pasini, B., Valabrega, G.
Published in Gynecologic oncology reports (01.08.2023)
Published in Gynecologic oncology reports (01.08.2023)
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Hypersensitivity to platinum salts according to BRCA status in ovarian cancer: A retrospective analysis of clinical outcomes and systematic review of literature
Giannone, G., Scotto, G., Katsaros, D., De Giorgi, U., Farolfi, A., Borella, F., Cosma, S., Ferrero, A., Mangiacotti, S., Villa, M., Tuninetti, V., Ghisoni, E., Turinetto, M., Mittica, G., Gemmiti, S., Zavallone, L., Aglietta, M., Pasini, B., Di Maio, M., Valabrega, G.
Published in Gynecologic oncology (01.07.2021)
Published in Gynecologic oncology (01.07.2021)
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Average Risks of Breast and Ovarian Cancer Associated with BRCA1 or BRCA2 Mutations Detected in Case Series Unselected for Family History: A Combined Analysis of 22 Studies
Antoniou, A., Pharoah, P.D.P., Narod, S., Risch, H.A., Eyfjord, J.E., Hopper, J.L., Loman, N., Olsson, H., Johannsson, O., Borg, Å., Pasini, B., Radice, P., Manoukian, S., Eccles, D.M., Tang, N., Olah, E., Anton-Culver, H., Warner, E., Lubinski, J., Gronwald, J., Gorski, B., Tulinius, H., Thorlacius, S., Eerola, H., Nevanlinna, H., Syrjäkoski, K., Kallioniemi, O.-P., Thompson, D., Evans, C., Peto, J., Lalloo, F., Evans, D.G., Easton, D.F.
Published in American journal of human genetics (01.05.2003)
Published in American journal of human genetics (01.05.2003)
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Copy number variants analysis in a cohort of isolated and syndromic developmental delay/intellectual disability reveals novel genomic disorders, position effects and candidate disease genes
Di Gregorio, E., Riberi, E., Belligni, E.F., Biamino, E., Spielmann, M., Ala, U., Calcia, A., Bagnasco, I., Carli, D., Gai, G., Giordano, M., Guala, A., Keller, R., Mandrile, G., Arduino, C., Maffè, A., Naretto, V.G., Sirchia, F., Sorasio, L., Ungari, S., Zonta, A., Zacchetti, G., Talarico, F., Pappi, P., Cavalieri, S., Giorgio, E., Mancini, C., Ferrero, M., Brussino, A., Savin, E., Gandione, M., Pelle, A., Giachino, D.F., De Marchi, M., Restagno, G., Provero, P., Cirillo Silengo, M., Grosso, E., Buxbaum, J.D., Pasini, B., De Rubeis, S., Brusco, A., Ferrero, G.B.
Published in Clinical genetics (01.10.2017)
Published in Clinical genetics (01.10.2017)
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Breast and ovarian cancer risks to carriers of the BRCA1 5382insC and 185delAG and BRCA2 6174delT mutations: a combined analysis of 22 population based studies
Antoniou, A C, Pharoah, P D P, Narod, S, Risch, H A, Eyfjord, J E, Hopper, J L, Olsson, H, Johannsson, O, Borg, Å, Pasini, B, Radice, P, Manoukian, S, Eccles, D M, Tang, N, Olah, E, Anton-Culver, H, Warner, E, Lubinski, J, Gronwald, J, Gorski, B, Tulinius, H, Thorlacius, S, Eerola, H, Nevanlinna, H, Syrjäkoski, K, Kallioniemi, O-P, Thompson, D, Evans, C, Peto, J, Lalloo, F, Evans, D G, Easton, D F
Published in Journal of medical genetics (01.07.2005)
Published in Journal of medical genetics (01.07.2005)
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Correlation between genotype and hormonal levels in heterozygous mutation carriers and non-carriers of 21-hydroxylase deficiency
Napolitano, E., Manieri, C., Restivo, F., Composto, E., Lanfranco, F., Repici, M., Pasini, B., Einaudi, S., Menegatti, E.
Published in Journal of endocrinological investigation (01.07.2011)
Published in Journal of endocrinological investigation (01.07.2011)
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Laparoscopic unilateral adrenalectomy in children for isolated primary pigmented nodular adrenocortical disease (PPNAD): case report and literature review
Guanà, R, Gesmundo, R, Morino, M, Matarazzo, P, Pucci, A, Pasini, B, Lala, R, Fiore, L, Repici, M, Canavese, F
Published in European journal of pediatric surgery (01.07.2010)
Published in European journal of pediatric surgery (01.07.2010)
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Population density, spatial patterns and sample size of Edessa meditabunda (F., 1794) (Hemiptera: Pentatomidae) on alternative plants during soybean off-season in southern Brazil
Engel, Eduardo, Silveira, Dienefer A., Bortolotto, Rafael P., Pasini, Mauricio P. B., Ribeiro, Ana L. de P., Antes Beskow, Gustavo
Published in Entomological Communications (20.06.2022)
Published in Entomological Communications (20.06.2022)
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The BOADICEA model of genetic susceptibility to breast and ovarian cancers: updates and extensions
Antoniou, A C, Cunningham, A P, Peto, J, Evans, D G, Lalloo, F, Narod, S A, Risch, H A, Eyfjord, J E, Hopper, J L, Southey, M C, Olsson, H, Johannsson, O, Borg, A, Pasini, B, Radice, P, Manoukian, S, Eccles, D M, Tang, N, Olah, E, Anton-culver, H, Warner, E, Lubinski, J, Gronwald, J, Gorski, B, Tryggvadottir, L, Syrjakoski, K, Kallioniemi, O-p, Eerola, H, Nevanlinna, H, Pharoah, P D P, Easton, D F
Published in British journal of cancer (17.06.2008)
Published in British journal of cancer (17.06.2008)
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CDKN2A and CDK4 mutation analysis in Italian melanoma-prone families: functional characterization of a novel CDKN2A germ line mutation
DELLA TORRE, G, PASINI, B, RODOLFO, M, PARMIANI, G, PIEROTTI, M. A, FRIGERIO, S, DONGHI, R, ROVINI, D, DELIA, D, PETERS, G, HUOT, T. J. G, BIANCHI-SCARRA, G, LANTIERI, F
Published in British journal of cancer (14.09.2001)
Published in British journal of cancer (14.09.2001)
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Association of a new cationic trypsinogen gene mutation (V39A) with chronic pancreatitis in an Italian family
Arduino, C, Salacone, P, Pasini, B, Brusco, A, Salmin, P, Bacillo, E, Robecchi, A, Cestino, L, Cirillo, S, Regge, D, Cappello, N, Gaia, E
Published in Gut (01.11.2005)
Published in Gut (01.11.2005)
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