1992 …2020

Research output per year

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Research Output

2020

Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility

AMFS Investigators, MelaNostrum Consortium, GenoMEL Consortium, Q-MEGA and QTWIN Investigators, ATHENS Melanoma Study Group, 23andMe, The SDH Study Group, IBD Investigators & Essen-Heidelberg Investigators, Jan 1 2020, (Accepted/In press) In : Nature Genetics.

Research output: Contribution to journalArticle

2019

Combining common genetic variants and non-genetic risk factors to predict risk of cutaneous melanoma

Gu, F., Chen, T-H., Pfeiffer, R. M., Fargnoli, M. C., Calista, D., Ghiorzo, P., Peris, K., Puig, S., Menin, C., De Nicolo, A., Rodolfo, M., Pellegrini, C., Pastorino, L., Evangelou, E., Zhang, T., Hua, X., DellaValle, C. T., Timothy Bishop, D., MacGregor, S., Iles, M. I. & 10 others, Law, M. H., Cust, A., Brown, K. M., Stratigos, A. J., Nagore, E., Chanock, S., Shi, J., Consortium, MM-A., Consortium, M. & Landi, M. T., Feb 1 2019, In : Human Molecular Genetics. 27, 3, p. 4145-4156 12 p.

Research output: Contribution to journalArticle

Contribution of Common Genetic Variants to Familial Aggregation of Disease and Implications for Sequencing Studies

Schlafly, A., Pfeiffer, R. M., Nagore, E., Puig, S., Calista, D., Ghiorzo, P., Menin, C., Fargnoli, M. C., Peris, K., Song, L., Zhang, T., Shi, J., Landi, M. T. & Sampson, J. N., Nov 1 2019, In : PLoS Genetics. 15, 11, p. e1008490

Research output: Contribution to journalArticle

Open Access

Contribution of Common Genetic Variants to Familial Aggregation of Disease and Implications for Sequencing Studies

Schlafly, A., Pfeiffer, R. M., Nagore, E., Puig, S., Calista, D., Ghiorzo, P., Menin, C., Fargnoli, M. C., Peris, K., Song, L., Zhang, T., Shi, J., Landi, M. T. & Sampson, J. N., Nov 1 2019, In : PLoS Genetics. 15, 11, p. 1-15 15 p., e1008490.

Research output: Contribution to journalArticle

Loss of BAP1 in Pheochromocytomas and Paragangliomas Seems Unrelated to Genetic Mutations

Maffeis, V., Cappellesso, R., Nicolè, L., Guzzardo, V., Menin, C., Elefanti, L., Schiavi, F., Guido, M. & Fassina, A., Dec 2019, In : Endocrine Pathology. 30, 4, p. 276-284 9 p.

Research output: Contribution to journalArticle

MC1R variants in childhood and adolescent melanoma: a retrospective pooled analysis of a multicentre cohort

IMI Study Group, GEM Study Group & M-SKIP Study Group, May 1 2019, In : The Lancet Child and Adolescent Health. 3, 5, p. 332-342 11 p.

Research output: Contribution to journalArticle

MC1R variants in childhood and adolescent melanoma: a retrospective pooled analysis of a multicentre cohort: The Lancet Child and Adolescent Health

IMI Study Group, the GEM Study Group, and the M-SKIP Study Group, 2019, In : Lancet Child Adolesc. Health. 3, 5, p. 332-342 11 p.

Research output: Contribution to journalArticle

Combining common genetic variants and non-genetic risk factors to predict risk of cutaneous melanoma

Gu, F., Chen, T-H., Pfeiffer, R. M., Fargnoli, M. C., Calista, D., Ghiorzo, P., Peris, K., Puig, S., Menin, C., De Nicolo, A., Rodolfo, M., Pellegrini, C., Pastorino, L., Evangelou, E., Zhang, T., Hua, X., DellaValle, C. T., Timothy Bishop, D., MacGregor, S., Iles, M. I. & 10 others, Law, M. H., Cust, A., Brown, K. M., Stratigos, A. J., Nagore, E., Chanock, S., Shi, J., Consortium, MM-A., Consortium, M. & Landi, M. T., 2018, In : Human Molecular Genetics. 27, 3, p. 4145-4156 12 p.

Research output: Contribution to journalArticle

Combining common genetic variants and non-genetic risk factors to predict risk of cutaneous melanoma

Gu, F., Chen, T. H., Pfeiffer, R. M., Fargnoli, M. C., Calista, D., Ghiorzo, P., Peris, K., Puig, S., Menin, C., De Nicolo, A., Rodolfo, M., Pellegrini, C., Pastorino, L., Evangelou, E., Zhang, T., Hua, X., DellaValle, C. T., Timothy Bishop, D., MacGregor, S., Iles, M. I. & 10 others, Law, M. H., Cust, A., Brown, K. M., Stratigos, A. J., Nagore, E., Chanock, S., Shi, J., Consortium, M. M. A., Consortium, M. N. & Landi, M. T., Dec 1 2018, In : Human Molecular Genetics. 27, 23, p. 4145-4156 12 p.

Research output: Contribution to journalArticle

Germline variation of circadian pathway genes and prognosis of gastric cancer patients

Rajendran, S., Benna, C., Monticelli, H., Spiro, G., Menin, C. & Mocellin, S., Apr 4 2018, In : Gut. 67, 4, p. 779-780 2 p.

Research output: Contribution to journalArticle

MC1R variants as melanoma risk factors independent of at-risk phenotypic characteristics: A pooled analysis from the M-SKIP project

M-SKIP Study Group, May 14 2018, In : Cancer Management and Research. 10, p. 1143-1154 12 p.

Research output: Contribution to journalArticle

MC1R variants as melanoma risk factors independent of at-risk phenotypic characteristics: a pooled analysis from the M-SKIP project

Tagliabue, E., Gandini, S., Bellocco, R., Maisonneuve, P., Newton-Bishop, J., Polsky, D., Lazovich, D., Kanetsky, P. A., Ghiorzo, P., Gruis, N. A., Landi, M. T., Menin, C., Fargnoli, M. C., García-Borrón, J. C., Han, J., Little, J., Sera, F. & Raimondi, S., 2018, In : Cancer Management and Research. 10, p. 1143-1154 12 p.

Research output: Contribution to journalArticle

MC1R variants as melanoma risk factors independent of at-risk phenotypic characteristics: A pooled analysis from the M-SKIP project

Tagliabue, E., Gandini, S., Bellocco, R., Maisonneuve, P., Newton-Bishop, J., Polsky, D., Lazovich, D., Kanetsky, P. A., Ghiorzo, P., Gruis, N. A., Landi, M. T., Menin, C., Fargnoli, M. C., García-Borrón, J. C., Han, J., Little, J., Sera, F., Raimondi, S. & Group, M-SKIP. S., 2018, In : Cancer Management and Research. 10, p. 1143-1154 12 p.

Research output: Contribution to journalArticle

MelaNostrum: a consensus questionnaire of standardized epidemiologic and clinical variables for melanoma risk assessment by the melanostrum consortium

Stratigos, A. J., Fargnoli, M. C., De Nicolo, A., Peris, K., Puig, S., Soura, E., Menin, C., Calista, D., Ghiorzo, P., Mandala, M., Massi, D., Rodolfo, M., Del Regno, L., Stefanaki, I., Gogas, H., Bataille, V., Tucker, M. A., Whiteman, D., Nagore, E. & Landi, M. T., 2018, In : Journal of the European Academy of Dermatology and Venereology. 32, 12, p. 2134-2141 8 p.

Research output: Contribution to journalArticle

MelaNostrum: a consensus questionnaire of standardized epidemiologic and clinical variables for melanoma risk assessment by the melanostrum consortium

Stratigos, A. J., Fargnoli, M. C., De Nicolo, A., Peris, K., Puig, S., Soura, E., Menin, C., Calista, D., Ghiorzo, P., Mandala, M., Massi, D., Rodolfo, M., Del Regno, L., Stefanaki, I., Gogas, H., Bataille, V., Tucker, M. A., Whiteman, D., Nagore, E. & Landi, M. T., Dec 2018, In : Journal of the European Academy of Dermatology and Venereology. 32, 12, p. 2134-2141 8 p.

Research output: Contribution to journalArticle

MelaNostrum: a consensus questionnaire of standardized epidemiologic and clinical variables for melanoma risk assessment by the melanostrum consortium

Stratigos, A. J., Fargnoli, M. C., De Nicolo, A., Peris, K., Puig, S., Soura, E., Menin, C., Calista, D., Ghiorzo, P., Mandala, M., Massi, D., Rodolfo, M., Del Regno, L., Stefanaki, I., Gogas, H., Bataille, V., Tucker, M. A., Whiteman, D., Nagore, E. & Landi, M. T., 2018, In : Journal of the European Academy of Dermatology and Venereology. 32, 12, p. 2134-2141 8 p.

Research output: Contribution to journalArticle

2017

Performance of in silico tools for the evaluation of p16INK4a (CDKN2A) variants in CAGI

Carraro, M., Minervini, G., Giollo, M., Bromberg, Y., Capriotti, E., Casadio, R., Dunbrack, R., Elefanti, L., Fariselli, P., Ferrari, C., Gough, J., Katsonis, P., Leonardi, E., Lichtarge, O., Menin, C., Martelli, P. L., Niroula, A., Pal, L. R., Repo, S., Scaini, M. C. & 11 others, Vihinen, M., Wei, Q., Xu, Q., Yang, Y., Yin, Y., Zaucha, J., Zhao, H., Zhou, Y., Brenner, S. E., Moult, J. & Tosatto, S. C. E., Sep 1 2017, In : Human Mutation. 38, 9, p. 1042-1050 9 p.

Research output: Contribution to journalArticle

2016

Association of Melanocortin-1 Receptor Variants with Pigmentary Traits in Humans: A Pooled Analysis from the M-Skip Project

Tagliabue, E., Gandini, S., Maisonneuve, P., Raimondi, S., García-Borrón, J. C., Newton-Bishop, J., Polsky, D., Lazovich, D. A., Kumar, R., Ghiorzo, P., Ghiorzo, P., Ferrucci, L., Gruis, N. A., Puig, S., Kanetsky, P. A., Motokawa, T., Ribas, G., Landi, M. T., Fargnoli, M. C., Wong, T. H. & 76 others, Stratigos, A., Helsing, P., Guida, G., Autier, P., Han, J., Little, J., Sera, F., Raimondi, S., Autier, P., Fargnoli, M. C., García-Borrón, J. C., Han, J., Kanetsky, P. A., Landi, M. T., Little, J., Newton-Bishop, J., Sera, F., Caini, S., Gandini, S., Maisonneuve, P., Hofman, A., Kayser, M., Liu, F., Nijsten, T., Uitterlinden, A. G., Kumar, R., Scherer, D., Bishop, T., Newton-Bishop, J., Elliott, F., Nagore, E., Lazovich, D. A., Polsky, D., Hansson, J., Hoiom, V., Ghiorzo, P., Pastorino, L., Gruis, N. A., Bouwes Bavinck, J. N., Aguilera, P., Badenas, C., Carrera, C., Gimenez-Xavier, P., Malvehy, J., Potrony, M., Puig, S., Puig-Butille, J. A., Tell-Marti, G., Dwyer, T., Blizzard, L., Cochrane, J., Fernandez-de-Misa, R., Branicki, W., Debniak, T., Morling, N., Johansen, P., Mayne, S., Bale, A., Cartmel, B., Ferrucci, L., Pfeiffer, R., Palmieri, G., Ribas, G., Menin, C., Stratigos, A., Kypreou, K., Bowcock, A., Cornelius, L., Council, M. L., Motokawa, T., Anno, S., Helsing, P., Andresen, P. A., Guida, G., Guida, S. & Wong, T. H., Sep 1 2016, In : Journal of Investigative Dermatology. 136, 9, p. 1914-1917 4 p.

Research output: Contribution to journalArticle

Association of Melanocortin-1 Receptor Variants with Pigmentary Traits in Humans: A Pooled Analysis from the M-Skip Project

Tagliabue, E., Gandini, S., Maisonneuve, P., Raimondi, S., García-Borrón, J. C., Newton Bishop, JA. A., Polsky, D., Lazovich, D. A., Kumar, R., Ghiorzo, P., Ghiorzo, P., Ferrucci, L., Gruis, N. A., Puig, S., Kanetsky, P. A., Motokawa, T., Ribas, G., Landi, M. T., Fargnoli, M. C., Wong, T. H. & 76 others, Stratigos, A., Helsing, P., Guida, G., Autier, P., Han, J., Little, J., Sera, F., Raimondi, S., Autier, P., Fargnoli, M. C., García-Borrón, J. C., Han, J., Kanetsky, P. P., Landi, M. T., Little, J., Newton-Bishop, J., Sera, F., Caini, S., Gandini, S., Maisonneuve, P., Hofman, A., Kayser, M., Liu, F., Nijsten, T., Uitterlinden, A. G., Kumar, R., Scherer, D., Bishop, T., Newton-Bishop, J., Elliott, F., Nagore, E., Lazovich, D. A., Polsky, D., Hansson, J., Höiom, V., Ghiorzo, P., Pastorino, L., Gruis, N. A., Bouwes Bavinck, J. N., Aguilera, P., Badenas, C., Carrera, C., Gimenez-Xavier, P., Malvehy, J., Potrony, M., Puig, S., Puig-Butille, J. A., Tell-Marti, G., Dwyer, T., Blizzard, L., Cochrane, J., Fernandez-De-Misa, R., Branicki, W., Dębniak, T., Morling, N., Johansen, P., Mayne, S., Bale, A., Cartmel, B., Ferrucci, L., Pfeiffer, R., Palmieri, G., Ribas, G., Menin, C., Stratigos, A. J., Kypreou, K. P., Bowcock, A., Cornelius, L., Council, M. L., Motokawa, T., Anno, S., Helsing, P., Andresen, P. A., Guida, G., Guida, S. & Wong, T. H., Sep 1 2016, In : Journal of Investigative Dermatology. 136, 9, p. 1914-1917 4 p.

Research output: Contribution to journalArticle

Differences in telomere length between sporadic and familial cutaneous melanoma

Menin, C., Bojnik, E., Del Bianco, P., Elefanti, L., Gianesin, K., Keppel, S., Stagni, C., Mocellin, S., Vecchiato, A. & De Rossi, A., Oct 28 2016, In : British Journal of Dermatology. 175, p. 865-66 2 p.

Research output: Contribution to journalArticle

Human IgGs induce synthesis and secretion of IgGs and neonatal Fc receptor in human umbilical vein endothelial cells

Frigo, G., Tramentozzi, E., Orso, G., Ceolotto, G., Pagetta, A., Stagni, C., Menin, C., Rosato, A. & Finotti, P., 2016, In : Immunobiology. 221, 12, p. 1329-1342

Research output: Contribution to journalArticle

Human IgGs induce synthesis and secretion of IgGs and neonatal Fc receptor in human umbilical vein endothelial cells

Frigo, G., Tramentozzi, E., Orso, G., Ceolotto, G., Pagetta, A., Stagni, C., Menin, C., Rosato, A. & Finotti, P., Dec 2016, In : Immunobiology. 221, 12, p. 1329-1342 14 p.

Research output: Contribution to journalArticle

Multiple primary melanomas (MPMs) and criteria for genetic assessment: MultiMEL, a multicenter study of the Italian Melanoma Intergroup

Bruno, W., Pastorino, L., Ghiorzo, P., Andreotti, V., Martinuzzi, C., Menin, C., Elefanti, L., Stagni, C., Vecchiato, A., Rodolfo, M., Maurichi, A., Manoukian, S., De Giorgi, V., Savarese, I., Gensini, F., Borgognoni, L., Testori, A., Spadola, G., Mandalà, M., Imberti, G. L. & 16 others, Savoia, P., Astrua, C., Ronco, A. M. A., Farnetti, A., Tibiletti, M. G., Lombardo, M., Palmieri, G., Ayala, F., Ascierto, P. A., Ghigliotti, G., Muggianu, M., Spagnolo, F., Picasso, V., Tanda, E. T. E., Queirolo, P. & Bianchi Scarrà, G., Feb 1 2016, In : Journal of the American Academy of Dermatology. 74, 2, p. 325-332 8 p.

Research output: Contribution to journalArticle

Multiple primary melanomas (MPMs) and criteria for genetic assessment: MultiMEL, a multicenter study of the Italian Melanoma Intergroup

Bruno, W., Pastorino, L., Ghiorzo, P., Andreotti, V., Martinuzzi, C., Menin, C., Elefanti, L., Stagni, C., Vecchiato, A., Rodolfo, M., Maurichi, A., Manoukian, S., De Giorgi, V., Savarese, I., Gensini, F., Borgognoni, L., Testori, A., Spadola, G., Mandalà, M., Imberti, G. L. & 16 others, Savoia, P., Astrua, C., Ronco, A. M. A., Farnetti, A., Tibiletti, M. G., Lombardo, M., Palmieri, G., Ayala, F., Ascierto, P. A., Ghigliotti, G., Muggianu, M., Spagnolo, F., Picasso, V., Tanda, E. T. E., Queirolo, P. & Bianchi Scarrà, G., Feb 1 2016, In : Journal of the American Academy of Dermatology. 74, 2, p. 325-332 8 p.

Research output: Contribution to journalArticle

Multiple primary melanomas (MPMs) and criteria for genetic assessment: MultiMEL, a multicenter study of the Italian Melanoma Intergroup

Bruno, W., Pastorino, L., Ghiorzo, P., Andreotti, V., Martinuzzi, C., Menin, C., Elefanti, L., Stagni, C., Vecchiato, A., Rodolfo, M., Maurichi, A., Manoukian, S., De Giorgi, V., Savarese, I., Gensini, F., Borgognoni, L., Testori, A., Spadola, G., Mandalà, M., Imberti, G. L. & 16 others, Savoia, P., Astrua, C., Ronco, A. M. A., Farnetti, A., Tibiletti, M. G., Lombardo, M., Palmieri, G., Ayala, F., Ascierto, P. A., Ghigliotti, G., Muggianu, M., Spagnolo, F., Picasso, V., Tanda, E. T. E., Queirolo, P. & Bianchi Scarrà, G., Feb 1 2016, In : Journal of the American Academy of Dermatology. 74, 2, p. 325-332 8 p.

Research output: Contribution to journalArticle

Multiple primary melanomas (MPMs) and criteria for genetic assessment: MultiMEL, a multicenter study of the Italian Melanoma Intergroup

Bruno, W., Pastorino, L., Ghiorzo, P., Andreotti, V., Martinuzzi, C., Menin, C., Elefanti, L., Stagni, C., Vecchiato, A., Rodolfo, M., Maurichi, A., Manoukian, S., De Giorgi, V., Savarese, I., Gensini, F., Borgognoni, L., Testori, A., Spadola, G., Mandalà, M., Imberti, G. & 16 others, Savoia, P., Astrua, C., Ronco, A. M. A., Farnetti, A., Tibiletti, M. G. R., Lombardo, M., Palmieri, G., Ayala, F., Ascierto, P., Ghigliotti, G., Muggianu, M., Spagnolo, F., Picasso, V., Tanda, E. T. E., Queirolo, P. & Bianchi-Scarrà, G., Feb 1 2016, In : Journal of the American Academy of Dermatology. 74, 2, p. 325-332 8 p.

Research output: Contribution to journalArticle

The CDKN2A/p16INK4a 5'UTR sequence and translational regulation: Impact of novel variants predisposing to melanoma

Andreotti, V., Bisio, A., Bressac-de Paillerets, B., Harland, M., Cabaret, O., Newton-Bishop, J., Pastorino, L., Bruno, W., Bertorelli, R., De Sanctis, V., Provenzani, A., Menin, C., Fronza, G., Queirolo, P., Spitale, R. C., Bianchi-Scarrà, G., Inga, A. & Ghiorzo, P., Mar 1 2016, In : Pigment Cell and Melanoma Research. 29, 2, p. 210-221 12 p.

Research output: Contribution to journalArticle

The CDKN2A/p16INK4a 5'UTR sequence and translational regulation: Impact of novel variants predisposing to melanoma

Andreotti, V., Bisio, A., Bressac-de Paillerets, B., Harland, M., Cabaret, O., Newton-Bishop, J., Pastorino, L., Bruno, W., Bertorelli, R., De Sanctis, V., Provenzani, A., Menin, C., Fronza, G., Queirolo, P., Spitale, R. C., Bianchi Scarrà, G., Inga, A. & Ghiorzo, P., Mar 1 2016, In : Pigment Cell and Melanoma Research. 29, 2, p. 210-221 12 p.

Research output: Contribution to journalArticle

TLR7 Gln11Leu single nucleotide polymorphism and susceptibility to cutaneous melanoma

Elefanti, L., Sacco, G., Stagni, C., Rastrelli, M., Menin, C., Russo, I. & Alaibac, M., Jul 1 2016, In : Oncology Letters. 12, 1, p. 275-280 6 p.

Research output: Contribution to journalArticle

2015

Association of CDK4 germline and BRAF somatic mutations in a patient with multiple primary melanomas and BRAF inhibitor resistance

Governa, M., Caprarella, E., Dalla Pozza, E., Vigato, E., Maritan, M., Caputo, G. G., Zannoni, M., Rosina, P., Elefanti, L., Stagni, C. & Menin, C., Sep 18 2015, In : Melanoma Research. 25, 5, p. 443-446 4 p.

Research output: Contribution to journalArticle

Human IgGs induce synthesis and secretion of IgGs and neonatal Fc receptor in human umbilical vein endothelial cells

Frigo, G., Tramentozzi, E., Orso, G., Ceolotto, G., Pagetta, A., Stagni, C., Menin, C., Rosato, A. & Finotti, P., Dec 17 2015, (Accepted/In press) In : Immunobiology.

Research output: Contribution to journalArticle

2014

CDKN2A Unclassified Variants in Familial Malignant Melanoma: Combining Functional and Computational Approaches for Their Assessment

Scaini, M. C., Minervini, G., Elefanti, L., Ghiorzo, P., Pastorino, L., Tognazzo, S., Agata, S., Quaggio, M., Zullato, D., Bianchi-Scarrà, G., Montagna, M., D'Andrea, E., Menin, C. & Tosatto, S. C. E., 2014, In : Human Mutation. 35, 7, p. 828-840 13 p.

Research output: Contribution to journalArticle

2013

Dried blood spot sampling for detection of monoclonal immunoglobulin gene rearrangement

Petrara, M. R., Elefanti, L., Quaggio, M., Zanchetta, M., Scaini, M. C., Masalu, N., De Rossi, A. & Menin, C., Oct 2013, In : Leukemia Research. 37, 10, p. 1265-1270 6 p.

Research output: Contribution to journalArticle

Survivin expression impacts prognostically on NSCLC but not SCLC

Rosato, A., Menin, C., Boldrin, D., Santa, S. D., Bonaldi, L., Scaini, M. C., Del Bianco, P., Zardo, D., Fassan, M., Cappellesso, R. & Fassina, A., Feb 2013, In : Lung Cancer. 79, 2, p. 180-186 7 p.

Research output: Contribution to journalArticle

2012

The p53 codon 72 Pro/Pro genotype identifies poor-prognosis neuroblastoma patients: Correlation with reduced apoptosis and enhanced senescence by the p53-72P isoform

Cattelani, S., Ferrari-Amorotti, G., Galavotti, S., Defferrari, R., Tanno, B., Cialfi, S., Vergalli, J., Fragliasso, V., Guerzoni, C., Manzotti, G., Soliera, A. R., Menin, C., Bertorelle, R., McDowell, H. P., Inserra, A., Belli, M. L., Varesio, L., Tweddle, D., Tonini, G. P., Altavista, P. & 3 others, Dominici, C., Raschellà, G. & Calabretta, B., Jul 2012, In : Neoplasia (United States). 14, 7, p. 634-643 10 p.

Research output: Contribution to journalArticle

2011

Contribution of susceptibility gene variants to melanoma risk in families from the Veneto region of Italy

Menin, C., Vecchiato, A., Scaini, M. C., Elefanti, L., Funari, G., De Salvo, G. L., Quaggio, M., Tognazzo, S., Agata, S., Santa, S. D., Montagna, M., Alaibac, M., Chiarion-Sileni, V. & D'Andrea, E., Aug 2011, In : Pigment Cell and Melanoma Research. 24, 4, p. 728-730 3 p.

Research output: Contribution to journalArticle

2009

Altered tumor formation and evolutionary selection of genetic variants in the human MDM4 oncogene

Atwal, G. S., Kirchhoff, T., Bond, E. E., Monagna, M., Menin, C., Bertorelle, R., Scaini, M. C., Bartel, F., Böhnke, A., Pempe, C., Gradhand, E., Hauptmann, S., Offit, K., Levine, A. J. & Bond, G. L., Jun 23 2009, In : Proceedings of the National Academy of Sciences of the United States of America. 106, 25, p. 10236-10241 6 p.

Research output: Contribution to journalArticle

Altered tumor formation and evolutionary selection of genetic variants in the human MDM4 oncogene (Proceedings of the National Academy of Sciences of the United States of America (2009) 106, 25 (10236-10241) DOI: 10.1073/pnas. 0901298106)

Atwal, G. S., Kirchhoff, T., Bond, E. E., Monagna, M., Menin, C., Bertorelle, R., Scaini, M. C., Bartel, F., Böhnke, A., Pempe, C., Gradhand, E., Hauptmann, S., Offit, K., Levine, A. J. & Bond, G. L., Jul 21 2009, In : Proceedings of the National Academy of Sciences of the United States of America. 106, 29, p. 12208 1 p.

Research output: Contribution to journalArticle

Clinical genetic testing for familial melanoma in Italy: A cooperative study

Bruno, W., Ghiorzo, P., Battistuzzi, L., Ascierto, P. A., Barile, M., Gargiulo, S., Gensini, F., Gliori, S., Guida, M., Lombardo, M., Manoukian, S., Menin, C., Nasti, S., Origone, P., Pasini, B., Pastorino, L., Peissel, B., Pizzichetta, M. A., Queirolo, P., Rodolfo, M. & 7 others, Romanini, A., Scaini, M. C., Testori, A., Tibiletti, M. G., Turchetti, D., Leachman, S. A. & Bianchi Scarrà, G., Nov 2009, In : Journal of the American Academy of Dermatology. 61, 5, p. 775-782 8 p.

Research output: Contribution to journalArticle

Functional impairment of p16INK4A due to CDKN2A p.Gly23Asp missense mutation

Scaini, M. C., Rossi, E., de Siqueira Torres, P. L. A., Zullato, D., Callegaro, M., Casella, C., Quaggio, M., Agata, S., Malacrida, S., Chiarion-Sileni, V., Vecchiato, A., Alaibac, M., Montagna, M., Mann, G. J., Menin, C. & D'Andrea, E., Dec 1 2009, In : Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis. 671, 1-2, p. 26-32 7 p.

Research output: Contribution to journalArticle

2008

BRCA1 p.Val1688del is a deleterious mutation that recurs in breast and ovarian cancer families from Northeast Italy

Malacrida, S., Agata, S., Callegaro, M., Casella, C., Barana, D., Scaini, M. C., Manoukian, S., Oliani, C., Radice, P., Barile, M., Menin, C., D'Andrea, E. & Montagna, M., Jan 1 2008, In : Journal of Clinical Oncology. 26, 1, p. 26-31 6 p.

Research output: Contribution to journalArticle

Genomic rearrangements of the CDKN2A locus are infrequent in Italian malignant melanoma families without evidence of CDKN2A/CDK4 point mutations

Vignoli, M., Scaini, M. C., Ghiorzo, P., Sestini, R., Bruno, W., Menin, C., Gensini, F., Piazzini, M., Testori, A., Manoukian, S., Orlando, C., D'Andrea, E., Bianchi-Scarrà, G. & Genuardi, M., Dec 2008, In : Melanoma Research. 18, 6, p. 431-437 7 p.

Research output: Contribution to journalArticle

Impact of a single nucleotide polymorphism in the MDM2 gene on neuroblastoma development and aggressiveness: Results of a pilot study on 239 patients

Cattelani, S., Defferrari, R., Marsilio, S., Bussolari, R., Candini, O., Corradini, F., Ferrari-Amorotti, G., Guerzoni, C., Pecorari, L., Menin, C., Bertorelle, R., Altavista, P., McDowell, H. P., Boldrini, R., Dominici, C., Paolotonini, G., Raschellà, G. & Calabretta, B., Jun 1 2008, In : Clinical Cancer Research. 14, 11, p. 3248-3253 6 p.

Research output: Contribution to journalArticle

Isolation and functional assessment of common, polymorphic variants of the B-MYB proto-oncogene associated with a reduced cancer risk

Schwab, R., Bussolari, R., Corvetta, D., Chayka, O., Santilli, G., Kwok, J. M. M., Amorotti, G. F., Tonini, G. P., Iacoviello, L., Bertorelle, R., Menin, C., Hubank, M., Calabretta, B. & Sala, A., May 1 2008, In : Oncogene. 27, 20, p. 2929-2933 5 p.

Research output: Contribution to journalArticle

Isolation and functional assessment of common, polymorphic variants of the B-MYB proto-oncogene associated with a reduced cancer risk (Oncogene (2008) 27, (2929-2933) DOI: 10.1038/sj.onc.1210947)

Schwab, R., Bussolari, R., Corvetta, D., Chayka, O., Santilli, G., Kwok, J. M. M., Ferrari-Amorotti, G., Tonini, G. P., Iacoviello, L., Bertorelle, R., Menin, C., Hubank, M., Calabretta, B. & Sala, A., May 22 2008, In : Oncogene. 27, 23, p. 3360 1 p.

Research output: Contribution to journalArticle

No evidence for linkage with melanoma in Italian melanoma-prone families

Kerstann, K. F., Bradford, P. T., Steighner, R., Calista, D., Fargnoli, M. C., Peris, K., Scaini, M. C., Menin, C., Ghiorzo, P., Bianchi-Scarra', G., Goldstein, A. M. & Landi, M. T., Jul 2008, In : Cancer Epidemiology Biomarkers and Prevention. 17, 7, p. 1838-1840 3 p.

Research output: Contribution to journalArticle

Sequential development of large B cell lymphoma in a patient with peripheral T-cell lymphoma

Furlan, A., Pietrogrande, F., Marino, F., Menin, C., Polato, G. & Vianello, F., Jan 2008, In : Haematologica. 93, 1

Research output: Contribution to journalArticle

2006

Association between MDM2-SNP309 and age at colorectal cancer diagnosis according to p53 mutation status

Menin, C., Scaini, M. C., De Salvo, G. L., Biscuola, M., Quaggio, M., Esposito, G., Belluco, C., Montagna, M., Agata, S., D'Andrea, E., Nitti, D., Amadori, A. & Bertorelle, R., Feb 15 2006, In : Journal of the National Cancer Institute. 98, 4, p. 285-288 4 p.

Research output: Contribution to journalArticle