• 689 Citations
  • 12 h-Index
20062019
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Fingerprint Dive into the research topics where Irene Feroce is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 9 Similar Profiles
Breast Neoplasms Medicine & Life Sciences
Fenretinide Medicine & Life Sciences
Ovarian Neoplasms Medicine & Life Sciences
Genetic Counseling Medicine & Life Sciences
Mutation Medicine & Life Sciences
Germ-Line Mutation Medicine & Life Sciences
Cadherins Medicine & Life Sciences
Tamoxifen Medicine & Life Sciences

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Research Output 2006 2019

  • 689 Citations
  • 12 h-Index
  • 25 Article
  • 2 Review article
  • 1 Comment/debate
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
Germ-Line Mutation
Missense Mutation
Ovarian Neoplasms
Mutation
BRCA2 Gene

BRCA1 homozygous unclassified variant in a patient with non-Fanconi anemia: A case report

Bondavalli, D., Francesca, M., Valeria, P., Feroce, I. & Bonanni, B., Mar 1 2018, In : Oncology Letters. 15, 3, p. 3329-3332 4 p.

Research output: Contribution to journalArticle

Fanconi Anemia
Anemia
Hereditary Breast and Ovarian Cancer Syndrome
Phenotype
Mutation
6 Citations (Scopus)

Hereditary lobular breast cancer with an emphasis on E-cadherin genetic defect

Corso, G., Figueiredo, J., La Vecchia, C., Veronesi, P., Pravettoni, G., Macis, D., Karam, R., Lo Gullo, R., Provenzano, E., Toesca, A., Mazzocco, K., Carneiro, F., Seruca, R., Melo, S., Schmitt, F., Roviello, F., De Scalzi, A. M., Intra, M., Feroce, I., De Camilli, E. & 5 others, Villardita, M. G., Trentin, C., De Lorenzi, F., Bonanni, B. & Galimberti, V., Jul 1 2018, In : Journal of Medical Genetics. 55, 7, p. 431-441 11 p.

Research output: Contribution to journalReview article

Cadherins
Breast Neoplasms
Breast
Genetic Testing
Age of Onset