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2019

Clustered protocadherins methylation alterations in cancer

Vega-Benedetti, A. F., Loi, E., Moi, L., Blois, S., Fadda, A., Antonelli, M., Arcella, A., Badiali, M., Giangaspero, F., Morra, I., Columbano, A., Restivo, A., Zorcolo, L., Gismondi, V., Varesco, L., Bellomo, S. E., Giordano, S., Canale, M., Casadei-Gardini, A., Faloppi, L. & 10 others, Puzzoni, M., Scartozzi, M., Ziranu, P., Cabras, G., Cocco, P., Ennas, M. G., Satta, G., Zucca, M., Canzio, D. & Zavattari, P., 2019, In : Clinical Epigenetics. 11, 1

Research output: Contribution to journalArticle

Clustered protocadherins methylation alterations in cancer

Vega-Benedetti, A. F., Loi, E., Moi, L., Blois, S., Fadda, A., Antonelli, M., Arcella, A., Badiali, M., Giangaspero, F., Morra, I., Columbano, A., Restivo, A., Zorcolo, L., Gismondi, V., Varesco, L., Bellomo, S. E., Giordano, S., Canale, M., Casadei-Gardini, A., Faloppi, L. & 10 others, Puzzoni, M., Scartozzi, M., Ziranu, P., Cabras, G., Cocco, P., Ennas, M. G., Satta, G., Zucca, M., Canzio, D. & Zavattari, P., Jul 9 2019, In : Clinical Epigenetics. 11, 1, 100.

Research output: Contribution to journalArticle

Open Access

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

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

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

ENIGMA Consortium, Sep 2019, In : Human Mutation. 40, 9, p. 1557-1578 22 p.

Research output: Contribution to journalArticle

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

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, K., Lázaro, C., De Nicolo, A., Radice, P., Engel, C., Schmutzler, R. K., Goldgar, D. E. & Spurdle, A. B., 2019, In : Hum. Mutat.. 40, 9, p. 1557-1578 22 p.

Research output: Contribution to journalArticle

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, K., Lázaro, C., De Nicolo, A., Radice, P., Engel, C., Schmutzler, R. K., Goldgar, D. E. & Spurdle, A. B., 2019, In : Human Mutation. 40, 9, p. 1557-1578 22 p.

Research output: Contribution to journalArticle

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

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. & 30 others, Bonache, S., Bonanni, B., Borg, Å., Bortesi, B., Brunet, J., Bruzzone, C., Bucksch, K., Cagnoli, G., Caldés, T., Caliebe, A., Calvello, M., Cini, G., Concolino, P., Cortesi, L., Feroce, I., Gismondi, V., Guerrieri-Gonzaga, A., Manoukian, S., Marabelli, M., Matricardi, L., Montagna, M., Moserle, L., Peissel, B., Rivera, D., Tognazzo, S., Varesco, L., Viel, A., Zampiga, V., De Nicolo, A. & Radice, P., 2019, In : Human Mutation. 40, 9, p. 1557-1578 22 p.

Research output: Contribution to journalArticle

2018

Colorectal cancer early methylation alterations affect the crosstalk between cell and surrounding environment, tracing a biomarker signature specific for this tumor

Fadda, A., Gentilini, D., Moi, L., Barault, L., Leoni, V. P., Sulas, P., Zorcolo, L., Restivo, A., Cabras, F., Fortunato, F., Zavattari, C., Varesco, L., Gismondi, V., De Miglio, M. R., Scanu, A. M., Colombi, F., Lombardi, P., Sarotto, I., Loi, E., Leone, F. & 4 others, Giordano, S., Di Nicolantonio, F., Columbano, A. & Zavattari, P., Aug 15 2018, In : International Journal of Cancer. 143, 4, p. 907-920 14 p.

Research output: Contribution to journalArticle

Colorectal cancer early methylation alterations affect the crosstalk between cell and surrounding environment, tracing a biomarker signature specific for this tumor

Fadda, A., Gentilini, D., Moi, L., Barault, L., Leoni, V. P., Sulas, P., Zorcolo, L., Restivo, A., Cabras, F., Fortunato, F., Zavattari, C., Varesco, L., Gismondi, V., De Miglio, M. R., Scanu, A. M., Colombi, F., Lombardi, P., Sarotto, I., Loi, E., Leone, F. & 4 others, Giordano, S., Di Nicolantonio, F., Columbano, A. & Zavattari, P., Aug 15 2018, In : International Journal of Cancer. 143, 4, p. 907-920 14 p.

Research output: Contribution to journalArticle

Leucocytes telomere length and breast cancer risk/ susceptibility: A case-control study

Pavanello, S., Varesco, L., Gismondi, V., Bruzzi, P. & Bolognesi, C., May 1 2018, In : PLoS One. 13, 5, e0197522.

Research output: Contribution to journalArticle

2017

A novel APC promoter 1B deletion shows a founder effect in Italian patients with classical familial adenomatous polyposis phenotype

Marabelli, M., Gismondi, V., Ricci, M. T., Vetro, A., Abou Khouzam, R., Rea, V., Vitellaro, M., Zuffardi, O., Varesco, L. & Ranzani, G. N., Dec 2017, In : Genes Chromosomes and Cancer. 56, 12, p. 846-854 9 p.

Research output: Contribution to journalArticle

A novel APC promoter 1B deletion shows a founder effect in Italian patients with classical familial adenomatous polyposis phenotype

Marabelli, M., Gismondi, V., Ricci, M. T., Vetro, A., Abou Khouzam, R., Rea, V., Vitellaro, M., Zuffardi, O., Varesco, L. & Ranzani, G. N., Dec 1 2017, In : Genes Chromosomes and Cancer. 56, 12, p. 846-854 9 p.

Research output: Contribution to journalArticle

A novel APC promoter 1B deletion shows a founder effect in Italian patients with classical familial adenomatous polyposis phenotype

Marabelli, M., Gismondi, V., Ricci, M. T., Vetro, A., Khouzam, R. A., Rea, V., Vitellaro, M., Zuffardi, O., Varesco, L. & Ranzani, G. N., Dec 1 2017, In : Genes Chromosomes and Cancer. 56, 12, p. 846-854 9 p.

Research output: Contribution to journalArticle

Type and frequency of MUTYH variants in Italian patients with suspected MAP: A retrospective multicenter study

Ricci, M. T., Miccoli, S., Turchetti, D., Bondavalli, D., Viel, A., Quaia, M., Giacomini, E., Gismondi, V., Sanchez-Mete, L., Stigliano, V., Martayan, A., Mazzei, F., Bignami, M., Bonelli, L. & Varesco, L., 2017, In : Journal of Human Genetics. 62, 2, p. 309-315 7 p.

Research output: Contribution to journalArticle

2016

Type and frequency of MUTYH variants in Italian patients with suspected MAP: A retrospective multicenter study

Ricci, M. T., Miccoli, S., Turchetti, D., Bondavalli, D., Viel, A., Quaia, M., Giacomini, E., Gismondi, V., Sanchez-Mete, L., Stigliano, V., Martayan, A., Mazzei, F., Bignami, M., Bonelli, L. & Varesco, L., Nov 10 2016, In : Journal of Human Genetics. 62, 2

Research output: Contribution to journalArticle

2015

APC rearrangements in familial adenomatous polyposis: heterogeneity of deletion lengths and breakpoint sequences underlies similar phenotypes

Quadri, M., Vetro, A., Gismondi, V., Marabelli, M., Bertario, L., Sala, P., Varesco, L., Zuffardi, O. & Ranzani, G. N., Mar 18 2015, In : Familial Cancer. 14, 1, p. 41-49 9 p.

Research output: Contribution to journalArticle

Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer

Rebbeck, T. R., Mitra, N., Wan, F., Sinilnikova, O. M., Healey, S., McGuffog, L., Chenevix-Trench, G., Easton, D. F., Antoniou, A. C., Nathanson, K. L., Laitman, Y., Kushnir, A., Paluch-Shimon, S., Berger, R., Zidan, J., Friedman, E., Ehrencrona, H., Stenmark-Askmalm, M., Einbeigi, Z., Loman, N. & 234 others, Harbst, K., Rantala, J., Melin, B., Huo, D., Olopade, O. I., Seldon, J., Ganz, P. A., Nussbaum, R. L., Chan, S. B., Odunsi, K., Gayther, S. A., Domchek, S. M., Arun, B. K., Lu, K. H., Mitchell, G., Karlan, B. Y., Walsh, C., Lester, J., Godwin, A. K., Pathak, H., Ross, E., Daly, M. B., Whittemore, A. S., John, E. M., Miron, A., Terry, M. B., Chung, W. K., Goldgar, D. E., Buys, S. S., Janavičius, R., Tihomirova, L., Tung, N., Dorfling, C. M., Van Rensburg, E. J., Steele, L., Neuhausen, S. L., Ding, Y. C., Ejlertsen, B., Gerdes, A. M., Hansen, T. V. O., Ramon Y Cajal, T., Osorio, A., Benitez, J., Godino, J., Tejada, M. I., Duran, M., Weitzel, J. N., Bobolis, K. A., Sand, S. R., Fontaine, A., Savarese, A., Pasini, B., Peissel, B., Bonanni, B., Zaffaroni, D., Vignolo-Lutati, F., Scuvera, G., Giannini, G., Bernard, L., Genuardi, M., Radice, P., Dolcetti, R., Manoukian, S., Pensotti, V., Gismondi, V., Yannoukakos, D., Fostira, F., Garber, J., Torres, D., Rashid, M. U., Hamann, U., Peock, S., Frost, D., Platte, R., Evans, D. G., Eeles, R., Davidson, R., Eccles, D., Cole, T., Cook, J., Brewer, C., Hodgson, S., Morrison, P. J., Walker, L., Porteous, M. E., Kennedy, M. J., Izatt, L., Adlard, J., Donaldson, A., Ellis, S., Sharma, P., Schmutzler, R. K., Wappenschmidt, B., Becker, A., Rhiem, K., Hahnen, E., Engel, C., Meindl, A., Engert, S., Ditsch, N., Arnold, N., Plendl, H. J., Mundhenke, C., Niederacher, D., Fleisch, M., Sutter, C., Bartram, C. R., Dikow, N., Wang-Gohrke, S., Gadzicki, D., Steinemann, D., Kast, K., Beer, M., Varon-Mateeva, R., Gehrig, A., Weber, B. H., Stoppa-Lyonnet, D., Belotti, M., Gauthier-Villars, M., Damiola, F., Boutry-Kryza, N., Lasset, C., Sobol, H., Peyrat, J. P., Muller, D., Fricker, J. P., Collonge-Rame, M. A., Mortemousque, I., Nogues, C., Rouleau, E., Isaacs, C., De Paepe, A., Poppe, B., Claes, K., De Leeneer, K., Piedmonte, M., Rodriguez, G., Wakely, K., Boggess, J., Blank, S. V., Basil, J., Azodi, M., Phillips, K. A., Caldes, T., De La Hoya, M., Romero, A., Nevanlinna, H., Aittomaki, K., Van Der Hout, A. H., Hogervorst, F. B. L., Verhoef, S., Collee, J. M., Seynaeve, C., Oosterwijk, J. C., Gille, J. J. P., Wijnen, J. T., Gomez Garcia, E. B., Kets, C. M., Ausems, M. G. E. M., Aalfs, C. M., Devilee, P., Mensenkamp, A. R., Kwong, A., Olah, E., Papp, J., Diez, O., Lazaro, C., Darder, E., Blanco, I., Salinas, M., Jakubowska, A., Lubinski, J., Gronwald, J., Jaworska-Bieniek, K., Durda, K., Sukiennicki, G., Huzarski, T., Byrski, T., Cybulski, C., Toloczko-Grabarek, A., Złowocka-Perłowska, E., Menkiszak, J., Arason, A., Barkardottir, R. B., Simard, J., Laframboise, R., Montagna, M., Agata, S., Alducci, E., Peixoto, A., Teixeira, M. R., Spurdle, A. B., Lee, M. H., Park, S. K., Kim, S. W., Friebel, T. M., Couch, F. J., Lindor, N. M., Pankratz, V. S., Guidugli, L., Wang, X., Tischkowitz, M., Foretova, L., Vijai, J., Offit, K., Robson, M., Rau-Murthy, R., Kauff, N., Fink-Retter, A., Singer, C. F., Rappaport, C., Gschwantler-Kaulich, D., Pfeiler, G., Tea, M. K., Berger, A., Greene, M. H., Mai, P. L., Imyanitov, E. N., Toland, A. E., Senter, L., Bojesen, A., Pedersen, I. S., Skytte, A. B., Sunde, L., Thomassen, M., Moeller, S. T., Kruse, T. A., Jensen, U. B., Caligo, M. A., Aretini, P., Teo, S. H., Selkirk, C. G., Hulick, P. J. & Andrulis, I., Apr 7 2015, In : Journal of the American Medical Association. 313, 13, p. 1347-1361 15 p.

Research output: Contribution to journalArticle

FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor

Peterlongo, P., Catucci, I., Colombo, M., Caleca, L., Mucaki, E., Bogliolo, M., Marin, M., Damiola, F., Bernard, L., Pensotti, V., Volorio, S., Dall'Olio, V., Meindl, A., Bartram, C., Sutter, C., Surowy, H., Sornin, V., Dondon, M. G., Eon-Marchais, S., Stoppa-Lyonnet, D. & 76 others, Andrieu, N., Sinilnikova, O. M., Mitchell, G., James, P. A., Thompson, E., Marchetti, M., Verzeroli, C., Tartari, C., Capone, G. L., Putignano, A. L., Genuardi, M., Medici, V., Marchi, I., Federico, M., Tognazzo, S., Matricardi, L., Agata, S., Dolcetti, R., Puppa, L. D., Cini, G., Gismondi, V., Viassolo, V., Perfumo, C., Mencarelli, M. A., Baldassarri, M., Peissel, B., Roversi, G., Silvestri, V., Rizzolo, P., Spina, F., Vivanet, C., Tibiletti, M. G., Caligo, M. A., Gambino, G., Tommasi, S., Pilato, B., Tondini, C., Corna, C., Bonanni, B., Barile, M., Osorio, A., Benitez, J., Balestrino, L., Ottini, L., Manoukian, S., Pierotti, M. A., Renieri, A., Varesco, L., Couch, F. J., Wang, X., Devilee, P., Hilbers, F. S., van Asperen, C. J., Viel, A., Montagna, M., Cortesi, L., Diez, O., Balmaña, J., Hauke, J., Schmutzler, R. K., Papi, L., Pujana, M. A., Lázaro, C., Falanga, A., Offit, K., Vijai, J., Campbell, I., Burwinkel, B., Kvist, A., Ehrencrona, H., Mazoyer, S., Pizzamiglio, S., Verderio, P., Surralles, J., Rogan, P. K. & Radice, P., Apr 9 2015, In : Human Molecular Genetics. 24, 18, p. 5345-5355 11 p., ddv251.

Research output: Contribution to journalArticle

Referral of Ovarian Cancer Patients for Genetic Counselling by Oncologists: Need for Improvement

Ricci, M. T., Sciallero, S., Mammoliti, S., Gismondi, V., Franiuk, M., Bruzzi, P. & Varesco, L., Jul 25 2015, In : Public Health Genomics. 18, 4, p. 225-232 8 p.

Research output: Contribution to journalArticle

2014

Clinical application of micronucleus test: A case-control study on the prediction of breast cancer risk/susceptibility

Bolognesi, C., Bruzzi, P., Gismondi, V., Volpi, S., Viassolo, V., Pedemonte, S. & Varesco, L., Nov 21 2014, In : PLoS One. 9, 11, e112354.

Research output: Contribution to journalArticle

Genetic instability in lymphoblastoid cell lines expressing biallelic and monoallelic variants in the human MUTYH gene

Grasso, F., Giacomini, E., Sanchez, M., Degan, P., Gismondi, V., Mazzei, F., Varesco, L., Viel, A. & Bignami, M., 2014, In : Human Molecular Genetics. 23, 14, p. 3843-3852 10 p., ddu097.

Research output: Contribution to journalArticle

The FMR1 CGG repeat test is not a candidate prescreening tool for identifying women with a high probability of being carriers of BRCA mutations

Ricci, M. T., Pennese, L., Gismondi, V., Perfumo, C., Grasso, M., Gennaro, E., Bruzzi, P. & Varesco, L., Feb 2014, In : European Journal of Human Genetics. 22, 2, p. 280-282 3 p.

Research output: Contribution to journalArticle

2013

Performance of BOADICEA and BRCAPRO genetic models and of empirical criteria based on cancer family history for predicting BRCA mutation carrier probabilities: A retrospective study in a sample of Italian cancer genetics clinics

Varesco, L., Viassolo, V., Viel, A., Gismondi, V., Radice, P., Montagna, M., Alducci, E., Della Puppa, L., Oliani, C., Tommasi, S., Caligo, M. A., Vivanet, C., Zuradelli, M., Mandich, P., Tibiletti, M. G., Cavalli, P., Lucci Cordisco, E., Turchetti, D., Boggiani, D., Bracci, R. & 2 others, Bruzzi, P. & Bonelli, L., Dec 2013, In : Breast. 22, 6, p. 1130-1135 6 p.

Research output: Contribution to journalArticle

2011

Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers

Ramus, S. J., Kartsonaki, C., Gayther, S. A., Pharoah, P. D. P., Sinilnikova, O. M., Beesley, J., Chen, X., McGuffog, L., Healey, S., Couch, F. J., Wang, X., Fredericksen, Z., Peterlongo, P., Manoukian, S., Peissel, B., Zaffaroni, D., Roversi, G., Barile, M., Viel, A., Allavena, A. & 133 others, Ottini, L., Papi, L., Gismondi, V., Capra, F., Radice, P., Greene, M. H., Mai, P. L., Andrulis, I. L., Glendon, G., Ozcelik, H., Thomassen, M., Gerdes, A. M., Kruse, T. A., Cruger, D., Jensen, U. B., Caligo, M. A., Olsson, H., Kristoffersson, U., Lindblom, A., Arver, B., Karlsson, P., Stenmark Askmalm, M., Borg, A., Neuhausen, S. L., Ding, Y. C., Nathanson, K. L., Domchek, S. M., Jakubowska, A., Lubiński, J., Huzarski, T., Byrski, T., Gronwald, J., Górski, B., Cybulski, C., Dbniak, T., Osorio, A., Durán, M., Tejada, M. I., Benítez, J., Hamann, U., Rookus, M. A., Verhoef, S., Tilanus-Linthorst, M. A., Vreeswijk, M. P., Bodmer, D., Ausems, M. G. E. M., Van Os, T. A., Asperen, C. J., Blok, M. J., Meijers-Heijboer, H. E. J., Peock, S., Cook, M., Oliver, C., Frost, D., Dunning, A. M., Evans, D. G., Eeles, R., Pichert, G., Cole, T., Hodgson, S., Brewer, C., Morrison, P. J., Porteous, M., Kennedy, M. J., Rogers, M. T., Side, L. E., Donaldson, A., Gregory, H., Godwin, A., Stoppa-Lyonnet, D., Moncoutier, V., Castera, L., Mazoyer, S., Barjhoux, L., Bonadona, V., Leroux, D., Faivre, L., Lidereau, R., Nogues, C., Bignon, Y. J., Prieur, F., Collonge-Rame, M. A., Venat-Bouvet, L., Fert-Ferrer, S., Miron, A., Buys, S. S., Hopper, J. L., Daly, M. B., John, E. M., Terry, M. B., Goldgar, D., Hansen, T. V. O., Jønson, L., Ejlertsen, B., Agnarsson, B. A., Offit, K., Kirchhoff, T., Vijai, J., Dutra-Clarke, A. V. C., Przybylo, J. A., Montagna, M., Casella, C., Imyanitov, E. N., Janavicius, R., Blanco, I., Lázaro, C., Moysich, K. B., Karlan, B. Y., Gross, J., Beattie, M. S., Schmutzler, R., Wappenschmidt, B., Meindl, A., Ruehl, I., Fiebig, B., Sutter, C., Arnold, N., Deissler, H., Varon-Mateeva, R., Kast, K., Niederacher, D., Gadzicki, D., Caldes, T., De La Hoya, M., Nevanlinna, H., Aittomäki, K., Simard, J., Soucy, P., Spurdle, A. B., Holland, H., Chenevix-Trench, G., Easton, D. F. & Antoniou, A. C., Jan 19 2011, In : Journal of the National Cancer Institute. 103, 2, p. 105-116 12 p.

Research output: Contribution to journalArticle

2009

Endometrial cancer and somatic G>T KRAS transversion in patients with constitutional MUTYH biallelic mutations

Tricarico, R., Bet, P., Ciambotti, B., Di Gregorio, C., Gatteschi, B., Gismondi, V., Toschi, B., Tonelli, F., Varesco, L. & Genuardi, M., Feb 18 2009, In : Cancer Letters. 274, 2, p. 266-270 5 p.

Research output: Contribution to journalArticle

2007

Increased risk of colorectal adenomas in Italian subjects carrying the p53 PIN3 A2-Pro72 haplotype

Perfumo, C., Bonelli, L., Menichini, P., Inga, A., Gismondi, V., Ciferri, E., Percivale, P., Bianchi Scarrà, G., Nasti, S., Fronza, G. & Varesco, L., Apr 2007, In : Digestion. 74, 3-4, p. 228-235 8 p.

Research output: Contribution to journalArticle

2006

Multiplex tetra-primer amplification refractory mutation system PCR to detect 6 common germline mutations of the MUTYH gene associated with polyposis and colorectal cancer

Piccioli, P., Serra, M., Gismondi, V., Pedemonte, S., Loiacono, F., Lastraioli, S., Bertario, L., De Angioletti, M., Varesco, L. & Notaro, R., Apr 2006, In : Clinical Chemistry. 52, 4, p. 739-743 5 p.

Research output: Contribution to journalArticle

2005

Attenuated familial adenomatous polyposis and Muir- Torre syndrome linked to compound biallelic constitutional MYH gene mutations

Ponti, G., Ponz de Leon, M., Maffei, S., Pedroni, M., Losi, L., Di Gregorio, C., Gismondi, V., Scarselli, A., Benatti, P., Roncari, B., Seidenari, S., Pellacani, G., Varotti, C., Prete, E., Varesco, L. & Roncucci, L., Nov 2005, In : Clinical Genetics. 68, 5, p. 442-447 6 p.

Research output: Contribution to journalArticle

Cyclooxygenase-2 expression in FAP patients carrying germ line MYH mutations

Frattini, M., Carnevali, I., Signoroni, S., Balestra, D., Moiraghi, M. L., Radice, P., Varesco, L., Gismondi, V., Ballardini, G., Sala, P., Pierotti, M. A., Pilotti, S. & Bertario, L., Aug 2005, In : Cancer Epidemiology Biomarkers and Prevention. 14, 8, p. 2049-2052 4 p.

Research output: Contribution to journalArticle

2004

Prevalence of the Y165C, G382D and 1395delGGA germline mutations of the MYH gene in Italian patients with adenomatous polyposis coli and colorectal adenomas

Gismondi, V., Meta, M., Bonelli, L., Radice, P., Sala, P., Bertario, L., Viel, A., Fornasarig, M., Arrigoni, A., Gentile, M., Ponz De Leon, M., Anselmi, L., Mareni, C., Bruzzi, P. & Varesco, L., May 1 2004, In : International Journal of Cancer. 109, 5, p. 680-684 5 p.

Research output: Contribution to journalArticle

2002

Prevalence of the E1317Q variant of the APC gene in Italian patients with colorectal adenomas

Gismondi, V., Bonelli, L., Sciallero, S., Margiocco, P., Viel, A., Radice, P., Mondini, P., Sala, P., Montera, M. P., Mareni, C., Quaia, M., Fornasarig, M., Gentile, M., Pietro, G., Rossini, P., Arrigoni, A., Meucci, G. M., Bruzzi, P. & Varesco, L., Dec 2002, In : Genetic Testing. 6, 4, p. 313-317 5 p.

Research output: Contribution to journalArticle

2001

A distinct splice form of APC is highly expressed in neurones but not commonly mutated in neuroepithelial tumours [7]

Steigerwald, K., Santoro, I. M., Kordich, J. J., Gismondi, V., Trzepacz, C., Badiali, M., Giangaspero, F., Balko, M. G., Graham, J. S., Ratner, N., Lowy, A. M., Varesco, L. & Groden, J., 2001, In : Journal of Medical Genetics. 38, 4, p. 257-262 6 p.

Research output: Contribution to journalArticle

A silent mutation in exon 14 of the APC gene is associated with exon skipping in a FAP family [5]

Montera, M., Piaggio, F., Marchese, C., Gismondi, V., Stella, A., Resta, N., Varesco, L., Guanti, G. & Mareni, C., 2001, In : Journal of Medical Genetics. 38, 12, p. 863-867 5 p.

Research output: Contribution to journalArticle

Cloning and characterization of a senescence inducing and class II tumor suppressor gene in ovarian carcinoma at chromosome region 6q27

Acquati, F., Morelli, C., Cinquetti, R., Bianchi, M. G., Porrini, D., Varesco, L., Gismondi, V., Rocchetti, R., Talevi, S., Possati, L., Magnanini, C., Tibiletti, M. G., Bernasconi, B., Daidone, M. G., Shridhar, V., Smith, D. I., Negrini, M., Barbanti-Brodano, G. & Taramelli, R., Feb 22 2001, In : Oncogene. 20, 8, p. 980-988 9 p.

Research output: Contribution to journalArticle

Genotype and phenotype factors as determinants of desmoid tumors in patients with familial adenomatous polyposis

Bertario, L., Russo, A., Sala, P., Eboli, M., Giarola, M., D'Amico, F., Gismondi, V., Varesco, L., Pierotti, M. A. & Radice, P., Mar 20 2001, In : International Journal of Cancer. 95, 2, p. 102-107 6 p.

Research output: Contribution to journalArticle

Numerous colonic adenomas in an individual with Bloom's syndrome

Lowy, A. M., Kordich, J. J., Gismondi, V., Varesco, L., Blough, R. I. & Groden, J., 2001, In : Gastroenterology. 121, 2, p. 435-439 5 p.

Research output: Contribution to journalArticle

Phenotype-genotype correlations in an extended family with adenomatosis coli and an unusual APC gene mutation

Ponz de Leon, M., Varesco, L., Benatti, P., Sassatelli, R., Izzo, P., Scarano, M. I., Rossi, G. B., Di Gregorio, C., Gismondi, V., Percesepe, A., De Rosa, M. & Roncucci, L., 2001, In : Diseases of the Colon and Rectum. 44, 11, p. 1597-1604 8 p.

Research output: Contribution to journalArticle

1999

Clinical features and genotype-phenotype correlations in 41 Italian families with adenomatosis coli

De Ponz Leon, M., Benatti, P., Percesepe, A., Cacciatore, A., Sassatelli, R., Bertoni, G., Sabadini, G., Varesco, L., Gismondi, V., Mareni, C., Montera, M., Di Gregorio, C., Landi, P. & Roncucci, L., 1999, In : Italian Journal of Gastroenterology and Hepatology. 31, 9, p. 850-860 11 p.

Research output: Contribution to journalArticle

Different expressivity of two adjacent mutations of the APC gene

Presciuttini, S., Gismondi, V., Scarcello, E., Sala, P., D'Elia, F., Rossetti, C., Caroti-Ghelli, C., Molina, F., Groden, J., Mosca, F., Bertario, L. & Varesco, L., Jan 1999, In : Tumori. 85, 1, p. 28-31 4 p.

Research output: Contribution to journalArticle

1998

310 Basepair APC deletion with duplication of breakpoint (4394ins15del310) in an Italian polyposis patient

Gismondi, V., Bafico, A., Biticchi, R., Pedemonte, S., Di Pietri, S., De Leon, M. P., Groden, J. & Varesco, L., 1998, In : Human Mutation. 11, 1

Research output: Contribution to journalArticle

Chain-terminating mutations in the APC gene lead to alterations in APC RNA and protein concentration

Gismondi, V., Stagnaro, P., Pedemonte, S., Biticchi, R., Presciuttini, S., Grammatico, P., Sala, P., Bertario, L., Groden, J. & Varesco, L., 1998, In : Genes Chromosomes and Cancer. 22, 4, p. 278-286 9 p.

Research output: Contribution to journalArticle

Novel germline APC variants in patients with multiple adenomas

Pedemonte, S., Sciallero, S., Gismondi, V., Stagnaro, P., Biticchi, R., Haeouaine, A., Bonelli, L., Nicolo, G., Groden, J., Bruzzi, P., Aste, H. & Varesco, L., 1998, In : Genes Chromosomes and Cancer. 22, 4, p. 257-267 11 p.

Research output: Contribution to journalArticle

The familial adenomatous polyposis region exhibits many different haplotypes

Stella, A., Resta, N., Polizzi, A., Montera, M., Cariola, F., Susca, F., Gismondi, V., Bertario, L., Marchese, C., Tenconi, R., Tibiletti, M. G., Izzo, P., Gentile, M., Prete, F., Pannarale, O., Di Matteo, G., Sala, P., Varesco, L., Mareni, C. & Guanti, G., 1998, In : Human Genetics. 102, 6, p. 624-628 5 p.

Research output: Contribution to journalArticle

1997

Analysis of K-ras, p53, bcl-2 and Rb expression in non-small cell lung cancer cell lines

Loprevite, M., Varesco, L., Favoni, R., Ferrara, G. B., Moro, F., Ottaggio, L., Fronza, G., Campomenosi, P., Abbondandolo, A., Cutrona, G., Roncella, S., Albini, A., Aluigi, M. G., Pozzi, S., Pera, C., Biticchi, R., Gismondi, V., Grossi, F., Pennucci, M. C. & Ardizzoni, A., 1997, In : International Journal of Oncology. 11, 6, p. 1203-1208 6 p.

Research output: Contribution to journalArticle

Characterization of 19 novel and six recurring APC mutations in Italian adenomatous polyposis patients, using two different mutation detection techniques

Gismondi, V., Bafico, A., Biticchi, R., Pedemonte, S., Molina, F., Heouaine, A., Sala, P., Bertario, L., Presciuttini, S., Strigini, P., Groden, J. & Varesco, L., 1997, In : Human Mutation. 9, 4, p. 370-373 4 p.

Research output: Contribution to journalArticle

1995

Clinical and biologic features of adenomatosis coli in northern Italy

De Pietri, S., Sassatelli, R., Roncucci, L., Bertoni, G., Landi, P., Sabadini, G., Tansini, P., Cavallini, G., Cantoni, E., Mareni, C., Montera, M., Varesco, L., Gismondi, V., Davighi, C. & de Leon, M. P., 1995, In : Scandinavian Journal of Gastroenterology. 30, 8, p. 771-779 9 p.

Research output: Contribution to journalArticle

1994

Age of onset in familial adenomatous polyposis: Heterogeneity within families and among APC mutations

Presciuttini, S., Varesco, L., Sala, P., Gismondi, V., Rossetti, C., Bafico, A., Ferrara, G. B. & Bertario, L., 1994, In : Annals of Human Genetics. 58, 4, p. 331-342 12 p.

Research output: Contribution to journalArticle

Association of APC gene mutations and histological characteristics of colorectal adenomas

De Benedetti, L., Sciallero, S., Gismondi, V., James, R., Bafico, A., Biticchi, R., Masetti, E., Bonelli, L., Heouaine, A., Picasso, M., Groden, J., Robertson, M., Risio, M., Caprilli, R., Bruzzi, P., White, R. L., Aste, H., Santi, L., Varesco, L. & Ferrara, G. B., Jul 1 1994, In : Cancer Research. 54, 13, p. 3553-3556 4 p.

Research output: Contribution to journalArticle

Mutation in a splice-donor site of the APC gene in a family with polyposis and late age of colonic cancer death

Varesco, L., Gismondi, V., Presciuttini, S., Groden, J., Spirio, L., Sala, P., Rossetti, C., De Benedetti, L., Bafico, A., Heouaine, A., Grammatico, P., Del Porto, G., White, R., Bertario, L. & Ferrara, G. B., Mar 1994, In : Human Genetics. 93, 3, p. 281-286 6 p.

Research output: Contribution to journalArticle