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Fingerprint Dive into the research topics where Valentina Zampiga is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 5 Similar Profiles
Mutation Medicine & Life Sciences
Breast Neoplasms Medicine & Life Sciences
Ovarian Neoplasms Medicine & Life Sciences
Germ-Line Mutation Medicine & Life Sciences
Neoplasms Medicine & Life Sciences
Sequence Analysis Medicine & Life Sciences
BRCA1 Gene Medicine & Life Sciences
BRCA2 Gene Medicine & Life Sciences

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Research Output 2008 2019

  • 43 Citations
  • 4 h-Index
  • 9 Article
1 Citation (Scopus)

Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification

Parsons, M. T., Tudini, E., Li, H., Hahnen, E., Wappenschmidt, B., Feliubadaló, L., Aalfs, C. M., Agata, S., Aittomäki, K., Alducci, E., Alonso-Cerezo, M. C., Arnold, N., Auber, B., Austin, R., Azzollini, J., Balmaña, J., Barbieri, E., Bartram, C. R., Blanco, A., Blümcke, B. & 201 others, Bonache, S., Bonanni, B., Borg, Å., Bortesi, B., Brunet, J., Bruzzone, C., Bucksch, K., Cagnoli, G., Caldés, T., Caliebe, A., Caligo, M. A., Calvello, M., Capone, G. L., Caputo, S. M., Carnevali, I., Carrasco, E., Caux-Moncoutier, V., Cavalli, P., Cini, G., Clarke, E. M., Concolino, P., Cops, E. J., Cortesi, L., Couch, F. J., Darder, E., de la Hoya, M., Dean, M., Debatin, I., Del Valle, J., Delnatte, C., Derive, N., Diez, O., Ditsch, N., Domchek, S. M., Dutrannoy, V., Eccles, D. M., Ehrencrona, H., Enders, U., Evans, D. G., Farra, C., Faust, U., Felbor, U., Feroce, I., Fine, M., Foulkes, W. D., Galvao, H. C. R., Gambino, G., Gehrig, A., Gensini, F., Gerdes, A. M., Germani, A., Giesecke, J., Gismondi, V., Gómez, C., Gómez Garcia, E. B., González, S., Grau, E., Grill, S., Gross, E., Guerrieri-Gonzaga, A., Guillaud-Bataille, M., Gutiérrez-Enríquez, S., Haaf, T., Hackmann, K., Hansen, T. V. O., Harris, M., Hauke, J., Heinrich, T., Hellebrand, H., Herold, K. N., Honisch, E., Horvath, J., Houdayer, C., Hübbel, V., Iglesias, S., Izquierdo, A., James, P. A., Janssen, L. A. M., Jeschke, U., Kaulfuß, S., Keupp, K., Kiechle, M., Kölbl, A., Krieger, S., Kruse, T. A., Kvist, A., Lalloo, F., Larsen, M., Lattimore, V. L., Lautrup, C., Ledig, S., Leinert, E., Lewis, A. L., Lim, J., Loeffler, M., López-Fernández, A., Lucci-Cordisco, E., Maass, N., Manoukian, S., Marabelli, M., Matricardi, L., Meindl, A., Michelli, R. D., Moghadasi, S., Moles-Fernández, A., Montagna, M., Montalban, G., Monteiro, A. N., Montes, E., Mori, L., Moserle, L., Müller, C. R., Mundhenke, C., Naldi, N., Nathanson, K. L., Navarro, M., Nevanlinna, H., Nichols, C. B., Niederacher, D., Nielsen, H. R., Ong, K. R., Pachter, N., Palmero, E. I., Papi, L., Pedersen, I. S., Peissel, B., Perez-Segura, P., Pfeifer, K., Pineda, M., Pohl-Rescigno, E., Poplawski, N. K., Porfirio, B., Quante, A. S., Ramser, J., Reis, R. M., Revillion, F., Rhiem, K., Riboli, B., Ritter, J., Rivera, D., Rofes, P., Rump, A., Salinas, M., Sánchez de Abajo, A. M., Schmidt, G., Schoenwiese, U., Seggewiß, J., Solanes, A., Steinemann, D., Stiller, M., Stoppa-Lyonnet, D., Sullivan, K. J., Susman, R., Sutter, C., Tavtigian, S. V., Teo, S. H., Teulé, A., Thomassen, M., Tibiletti, M. G., Tischkowitz, M., Tognazzo, S., Toland, A. E., Tornero, E., Törngren, T., Torres-Esquius, S., Toss, A., Trainer, A. H., Tucker, K. M., van Asperen, C. J., van Mackelenbergh, M. T., Varesco, L., Vargas-Parra, G., Varon, R., Vega, A., Velasco, Á., Vesper, A. S., Viel, A., Vreeswijk, M. P. G., Wagner, S. A., Waha, A., Walker, L. C., Walters, R. J., Wang-Gohrke, S., Weber, B. H. F., Weichert, W., Wieland, K., Wiesmüller, L., Witzel, I., Wöckel, A., Woodward, E. R., Zachariae, S., Zampiga, V., Zeder-Göß, C., Investigators, KC. F., Lázaro, C., De Nicolo, A., Radice, P., Engel, C., Schmutzler, R. K., Goldgar, D. E. & Spurdle, A. B., Sep 1 2019, In : Human Mutation. 40, 9, p. 1557-1578 22 p.

Research output: Contribution to journalArticle

Open Access
Virulence
Neoplasm Genes
Adenosine Monophosphate
Computational Biology
Calibration
4 Citations (Scopus)

BRCA1 p.His1673del is a pathogenic mutation associated with a predominant ovarian cancer phenotype

Zuntini, R., Cortesi, L., Calistri, D., Pippucci, T., Martelli, P. L., Casadio, R., Capizzi, E., Santini, D., Miccoli, S., Medici, V., Danesi, R., Marchi, I., Zampiga, V., Fiorentino, M., Ferrari, S. & Turchetti, D., Jan 1 2017, In : Oncotarget. 8, 14, p. 22640-22648 9 p.

Research output: Contribution to journalArticle

Ovarian Neoplasms
Alleles
Phenotype
Mutation
BRCA1 Protein
19 Citations (Scopus)

Multiple-gene panel analysis in a case series of 255 women with hereditary breast and ovarian cancer

Tedaldi, G., Tebaldi, M., Zampiga, V., Danesi, R., Arcangeli, V., Ravegnani, M., Cangini, I., Pirini, F., Petracci, E., Rocca, A., Falcini, F., Amadori, D. & Calistri, D., Jan 1 2017, In : Oncotarget. 8, 29, p. 47064-47075 12 p.

Research output: Contribution to journalArticle

Ovarian Neoplasms
Breast Neoplasms
Genes
Mutation
BRCA1 Gene

Multiple primary tumors in a family with Li-Fraumeni syndrome with a TP53 germline mutation identified by next-generation sequencing

Zampiga, V., Danesi, R., Tedaldi, G., Tebaldi, M., Cangini, I., Pirini, F., Pittureri, C., Amaducci, E., Guidi, L., Faedi, M., Amadori, D., Falcini, F. & Calistri, D., Dec 23 2016, In : International Journal of Biological Markers. 31, 4, p. e461-e465

Research output: Contribution to journalArticle

Li-Fraumeni Syndrome
Germ-Line Mutation
Tumors
DNA
Mutation
5 Citations (Scopus)

First evidence of a large CHEK2 duplication involved in cancer predisposition in an Italian family with hereditary breast cancer

Tedaldi, G., Danesi, R., Zampiga, V., Tebaldi, M., Bedei, L., Zoli, W., Amadori, D., Falcini, F. & Calistri, D., Jul 1 2014, In : BMC Cancer. 14, 1, 478.

Research output: Contribution to journalArticle

Breast Neoplasms
Mutation
Neoplasms
Germ-Line Mutation
Neoplasm Genes