D'ANDREA, EMMA
D'ANDREA, EMMA
CDKN2A Unclassified Variants in Familial Malignant Melanoma: Combining Functional and Computational Approaches for Their Assessment.
2014 Scaini, Mc; Minervini, G; Elefanti, L; Ghiorzo, P; Pastorino, L; Tognazzo, S; Agata, S; Quaggio, M; Zullato, D; Bianchi Scarrà, G; Montagna, Marco; D'Andrea, Emma; Menin, Chiara; Tosatto, Silvio
Identification of a BRCA2-specific modifier locus at 6p24 related to breast cancer risk.
2013 Gaudet, Mm; Kuchenbaecker, Kb; Vijai, J; Klein, Rj; Kirchhoff, T; Mcguffog, L; Barrowdale, D; Dunning, Am; Lee, A; Dennis, J; Healey, S; Dicks, E; Soucy, P; Sinilnikova, Om; Pankratz, Vs; Wang, X; Eldridge, Rc; Tessier, Dc; Vincent, D; Bacot, F; Hogervorst, Fb; Peock, S; Stoppa Lyonnet, D; Peterlongo, P; Schmutzler, Rk; Nathanson, Kl; Piedmonte, M; Singer, Cf; Thomassen, M; Hansen, Tv; Neuhausen, Sl; Blanco, I; Greene, Mh; Garber, J; Weitzel, Jn; Andrulis, Il; Goldgar, De; D'Andrea, Emma; Caldes, T; Nevanlinna, H; Osorio, A; van Rensburg, Ej; Arason, A; Rennert, G; van den Ouweland, Am; van der Hout, Ah; Kets, Cm; Aalfs, Cm; Wijnen, Jt; Ausems, Mg; Frost, D; Ellis, S; Fineberg, E; Platte, R; Evans, Dg; Jacobs, C; Adlard, J; Tischkowitz, M; Porteous, Me; Damiola, F; Golmard, L; Barjhoux, L; Longy, M; Belotti, M; Ferrer, Sf; Mazoyer, S; Spurdle, Ab; Manoukian, S; Barile, M; Genuardi, M; Arnold, N; Meindl, A; Sutter, C; Wappenschmidt, B; Domchek, Sm; Pfeiler, G; Friedman, E; Jensen, Ub; Robson, M; Shah, S; Lazaro, C; Mai, Pl; Benitez, J; Southey, Mc; Schmidt, Mk; Fasching, Pa; Peto, J; Humphreys, Mk; Wang, Q; Michailidou, K; Sawyer, Ej; Burwinkel, B; Guénel, P; Bojesen, Se; Milne, Rl; Brenner, H; Lochmann, M; Aittomäki, K; Dörk, T; Margolin, S; Mannermaa, A; Lambrechts, D; Chang Claude, J; Radice, P; Giles, Gg; Haiman, Ca; Winqvist, R; Devillee, P; García Closas, M; Schoof, N; Hooning, Mj; Cox, A; Pharoah, Pd; Jakubowska, A; Orr, N; González Neira, A; Pita, G; Alonso, Mr; Hall, P; Couch, Fj; Simard, J; Altshuler, D; Easton, Df; Chenevix Trench, G; Antoniou, Ac; Offit, K; Kconfab, Investigators; Ontario Cancer Genetics, Network; Hebon, Embrace; GEMO Study, Collaborators; Genica, Network
Association between BRCA1 and BRCA2 mutations and survival in women with invasive epithelial ovarian cancer.
2012 Bolton, Kl; Chenevix Trench, G; Goh, C; Sadetzki, S; Ramus, Sj; Karlan, By; Lambrechts, D; Despierre, E; Barrowdale, D; Mcguffog, L; Healey, S; Easton, Df; Sinilnikova, O; Benítez, J; García, Mj; Neuhausen, S; Gail, Mh; Hartge, P; Peock, S; Frost, D; Evans, Dg; Eeles, R; Godwin, Ak; Daly, Mb; Kwong, A; Ma, Es; Lázaro, C; Blanco, I; Montagna, M; D'Andrea, Emma; Nicoletto, Mo; Johnatty, Se; Kjær, Sk; Jensen, A; Høgdall, E; Goode, El; Fridley, Bl; Loud, Jt; Greene, Mh; Mai, Pl; Chetrit, A; Lubin, F; Hirsh Yechezkel, G; Glendon, G; Andrulis, Il; Toland, Ae; Senter, L; Gore, Me; Gourley, C; Michie, Co; Song, H; Tyrer, J; Whittemore, As; Mcguire, V; Sieh, W; Kristoffersson, U; Olsson, H; Borg, Å; Levine, Da; Steele, L; Beattie, Ms; Chan, S; Nussbaum, Rl; Moysich, Kb; Gross, J; Cass, I; Walsh, C; Li, Aj; Leuchter, R; Gordon, O; Garcia Closas, M; Gayther, Sa; Chanock, Sj; Antoniou, Ac; Pharoah, Pd; Embrace, ; Kconfab, Investigators; Cancer Genome Atlas Research, Network
Pathology of breast and ovarian cancers among BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA).
2012 Mavaddat, N; Barrowdale, D; Andrulis, Il; Domchek, Sm; Eccles, D; Nevanlinna, H; Ramus, Sj; Spurdle, A; Robson, M; Sherman, M; Mulligan, Am; Couch, Fj; Engel, C; Mcguffog, L; Healey, S; Sinilnikova, Om; Southey, Mc; Terry, Mb; Goldgar, D; O'Malley, F; John, Em; Janavicius, R; Tihomirova, L; Hansen, Tv; Nielsen, Fc; Osorio, A; Stavropoulou, A; Benítez, J; Manoukian, S; Peissel, B; Barile, M; Volorio, S; Pasini, B; Dolcetti, R; Putignano, Al; Ottini, L; Radice, P; Hamann, U; Rashid, Mu; Hogervorst, Fb; Kriege, M; van der Luijt, Rb; Peock, S; Frost, D; Evans, Dg; Brewer, C; Walker, L; Rogers, Mt; Side, Le; Houghton, C; Weaver, J; Godwin, Ak; Schmutzler, Rk; Wappenschmidt, B; Meindl, A; Kast, K; Arnold, N; Niederacher, D; Sutter, C; Deissler, H; Gadzicki, D; Preisler Adams, S; Varon Mateeva, R; Schönbuchner, I; Gevensleben, H; Stoppa Lyonnet, D; Belotti, M; Barjhoux, L; Isaacs, C; Peshkin, Bn; Caldes, T; de la Hoya, M; Cañadas, C; Heikkinen, T; Heikkilä, P; Aittomäki, K; Blanco, I; Lazaro, C; Brunet, J; Agnarsson, Ba; Arason, A; Barkardottir, Rb; Dumont, M; Simard, J; Montagna, M; Agata, S; D'Andrea, Emma; Yan, M; Fox, S; Rebbeck, Tr; Rubinstein, W; Tung, N; Garber, Je; Wang, X; Fredericksen, Z; Pankratz, Vs; Lindor, Nm; Szabo, C; Offit, K; Sakr, R; Gaudet, Mm; Singer, Cf; Tea, Mk; Rappaport, C; Mai, Pl; Greene, Mh; Sokolenko, A; Imyanitov, E; Toland, Ae; Senter, L; Sweet, K; Thomassen, M; Gerdes, Am; Kruse, T; Caligo, M; Aretini, P; Rantala, J; von Wachenfeld, A; Henriksson, K; Steele, L; Neuhausen, Sl; Nussbaum, R; Beattie, M; Odunsi, K; Sucheston, L; Gayther, Sa; Nathanson, K; Gross, J; Walsh, C; Karlan, B; Chenevix Trench, G; Easton, Df; Antoniou, Ac; Hebon, Embrace; GEMO Study, Collaborators; Kconfab, Investigators; SWE BRCA, Collaborators; Consortium of Investigators of Modifiers of, Brca1/2
Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2
2011 Anna, Mulligan; Fergus J., Couch; Daniel, Barrowdale; Susan M., Domchek; Diana, Eccles; Heli, Nevanlinna; Susan J., Ramus; Mark, Robson; Mark, Sherman; Amanda B., Spurdle; Barbara, Wappenschmidt; Andrew, Lee; Lesley, Mcguffog; Sue, Healey; Olga M., Sinilnikova; Ramunas, Janavicius; Thomas vO, Hansen; Finn C., Nielsen; Bent, Ejlertsen; Ana, Osorio; Iván Muñoz, Repeto; Mercedes, Durán; Javier, Godino; Maroulio, Pertesi; Javier, Benítez; Paolo, Peterlongo; Siranoush, Manoukian; Bernard, Peissel; Daniela, Zaffaroni; Elisa, Cattaneo; Bernardo, Bonanni; Alessandra, Viel; Barbara, Pasini; Laura, Papi; Laura, Ottini; Antonella, Savarese; Loris, Bernard; Paolo, Radice; Ute, Hamann; Martijn, Verheus; Hanne EJ Meijers, Heijboer; Juul, Wijnen; Encarna B., Gómez García; Marcel R., Nelen; C., Marleen Kets; Caroline, Seynaeve; Madeleine MA Tilanus, Linthorst; Rob B., van der Luijt; Theo, Os; Matti, Rookus; Debra, Frost; J., Louise Jones; D., Gareth Evans; Fiona, Lalloo; Ros, Eeles; Louise, Izatt; Julian, Adlard; Rosemarie, Davidson; Jackie, Cook; Alan, Donaldson; Huw, Dorkins; Helen, Gregory; Jacqueline, Eason; Catherine, Houghton; Julian, Barwell; Lucy E., Side; Emma, Mccann; Alex, Murray; Susan, Peock; Andrew K., Godwin; Rita K., Schmutzler; Kerstin, Rhiem; Christoph, Engel; Alfons, Meindl; Ina, Ruehl; Norbert, Arnold; Dieter, Niederacher; Christian, Sutter; Helmut, Deissler; Dorothea, Gadzicki; Karin, Kast; Sabine Preisler, Adams; Raymonda Varon, Mateeva; Ines, Schoenbuchner; Britta, Fiebig; Wolfram, Heinritz; Dieter, Schäfer; Heidrun, Gevensleben; Virginie Caux, Moncoutier; Marion Fassy, Colcombet; François, Cornelis; Sylvie, Mazoyer; Mélanie, Léoné; Nadia Boutry, Kryza; Agnès, Hardouin; Pascaline, Berthet; Danièle, Muller; Jean Pierre, Fricker; Isabelle, Mortemousque; Pascal, Pujol; Isabelle, Coupier; Marine, Lebrun; Caroline, Kientz; Michel, Longy; Nicolas, Sevenet; Dominique Stoppa, Lyonnet; Claudine, Isaacs; Trinidad, Caldes; Miguel de la, Hoya; Tuomas, Heikkinen; Kristiina, Aittomäki; Ignacio, Blanco; Conxi, Lazaro; Rosa B., Barkardottir; Penny, Soucy; Martine, Dumont; Jacques, Simard; Marco, Montagna; Silvia, Tognazzo; D'Andrea, Emma; Stephen, Fox; Max, Yan; Tim, Rebbeck; Olufunmilayo I., Olopade; Jeffrey N., Weitzel; Henry T., Lynch; Patricia A., Ganz; Gail E., Tomlinson; Xianshu, Wang; Zachary, Fredericksen; Vernon S., Pankratz; Noralane M., Lindor; Csilla, Szabo; Kenneth, Offit; Rita, Sakr; Mia, Gaudet; Jasmine, Bhatia; Noah, Kauff; Christian F., Singer; Muy Kheng, Tea; Daphne Gschwantler, Kaulich; Anneliese Fink, Retter; Phuong L., Mai; Mark H., Greene; Evgeny, Imyanitov; Frances P., O'Malley; Hilmi, Ozcelik; Gordon, Glendon; Amanda E., Toland; Anne Marie, Gerdes; Mads, Thomassen; Torben A., Kruse; Uffe, Jensen; Anne Bine, Skytte; Maria A., Caligo; Maria, Soller; Karin, Henriksson; von Anna, Wachenfeldt; Brita, Arver; Marie Stenmark, Askmalm; Per, Karlsson; Yuan, Ding; Susan L., Neuhausen; Mary, Beattie; Paul DP, Pharoah; Kirsten B., Moysich; Katherine L., Nathanson; Beth Y., Karlan; Jenny, Gross; Esther M., John; Mary B., Daly; Saundra M., Buys; Melissa C., Southey; John L., Hopper; Mary, Terry; Wendy, Chung; Alexander F., Miron; David, Goldgar; Georgia Chenevix, Trench; Douglas F., Easton; Irene L., Andrulis; Antonis C., Antoniou
Contribution of susceptibility gene variants to melanoma risk in families from the Veneto region of Italy
2011 Menin, C; Vecchiato, A; Scaini, Mc; Elefanti, L; Funari, G; De Salvo, Gl; Quaggio, Monica; Tognazzo, S; Agata, S; Santa, Sd; Montagna, M; Alaibac, MAURO SALVATORE ALESSANDRO; Chiarion Sileni, V; D'Andrea, Emma
Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers
2011 Im, Km; Kirchhoff, T; Wang, Xs; Green, T; Chow, Cy; Vijai, J; Korn, J; Gaudet, Mm; Fredericksen, Z; Pankratz, Vs; Guiducci, C; Crenshaw, A; Mcguffog, L; Kartsonaki, C; Morrison, J; Healey, S; Sinilnikova, Om; Mai, Pl; Greene, Mh; Piedmonte, M; Rubinstein, Ws; Hogervorst, Fb; Rookus, Ma; Collee, Jm; Hoogerbrugge, N; VAN ASPEREN, Cj; MEIJERS HEIJBOER, Hej; VAN ROOZENDAAL, Ce; Caldes, T; PEREZ SEGURA, P; Jakubowska, A; Lubinski, J; Huzarski, T; Blecharz, P; Nevanlinna, H; Aittomaki, K; Lazaro, C; Blanco, I; Barkardottir, Rb; Montagna, M; D'Andrea, Emma; Devilee, P; Olopade, Oi; Neuhausen, Sl; Peissel, B; Bonanni, B; Peterlongo, P; Singer, Cf; Rennert, G; Lejbkowicz, F; Andrulis, Il; Glendon, G; Ozcelik, H; Toland, Ae; Caligo, Ma; Beattie, Ms; Chan, S; Domchek, Sm; Nathanson, Kl; Rebbeck, Tr; Phelan, C; Narod, S; John, Em; Hopper, Jl; Buys, Ss; Daly, Mb; Southey, Mc; Terry, Mb; Tung, N; Hansen, Tvo; Osorio, A; Benitez, J; Duran, M; Weitzel, Jn; Garber, J; Hamann, U; Peock, S; Cook, M; Oliver, Ct; Frost, D; Platte, R; Evans, Dg; Eeles, R; Izatt, L; Paterson, J; Brewer, C; Hodgson, S; Morrison, Pj; Porteous, M; Walker, L; Rogers, Mt; Side, Le; Godwin, Ak; Schmutzler, Rk; Wappenschmidt, B; Laitman, Y; Meindl, A; Deissler, H; VARON MATEEVA, R; PREISLER ADAMS, S; Kast, K; VENAT BOUVET, L; STOPPA LYONNET, D; CHENEVIX TRENCH, G; Easton, Df; Klein, Rj; Daly, Mj; Friedman, E; Dean, M; Clark, Ag; Altshuler, Dm; Antoniou, Ac; Couch, Fj; Offit, K; Gold, B.
Common Genetic Variants and Modification of Penetrance of BRCA2-Associated Breast Cancer
2010 Gaudet, Mm; Kirchhoff, T; Green, T; Vijai, J; Korn, Jm; Guiducci, C; Segre, Av; Mcgee, K; Mcguffog, L; Kartsonaki, C; Morrison, J; Healey, S; Sinilnikova, Om; STOPPA LYONNET, D; Mazoyer, S; GAUTHIER VILLARS, M; Sobol, H; Longy, M; Frenay, M; Hogervorst, Fbl; Rookus, Ma; Collee, Jm; Hoogerbrugge, N; VAN ROOZENDAAL, Kep; Piedmonte, M; Rubinstein, W; Nerenstone, S; VAN LE, L; Blank, Sv; Caldes, T; DE LA HOYA, M; Nevanlinna, H; Aittomaki, K; Lazaro, C; Blanco, I; Arason, A; Johannsson, Ot; Barkardottir, Rb; Devilee, P; Olopade, Oi; Neuhausen, Sl; Wang, Xs; Fredericksen, Zs; Peterlongo, P; Manoukian, S; Barile, M; Viel, A; Radice, P; Phelan, Cm; Narod, S; Rennert, G; Lejbkowicz, F; Flugelman, A; Andrulis, Il; Glendon, G; Ozcelik, H; Toland, Ae; Montagna, M; D'Andrea, Emma; Friedman, E; Laitman, Y; Borg, A; Beattie, M; Ramus, Sj; Domchek, Sm; Nathanson, Kl; Rebbeck, T; Spurdle, Ab; Chen, Xq; Holland, H; John, Em; Hopper, Jl; Buys, Ss; Daly, Mb; Southey, Mc; Terry, Mb; Tung, N; Hansen, Tvo; Nielsen, Fc; Greene, Mi; Mai, Pl; Osorio, A; Duran, M; Andres, R; Benitez, J; Weitzel, Jn; Garber, J; Hamann, U; Peock, S; Cook, M; Oliver, C; Frost, D; Platte, R; Evans, Dg; Lalloo, F; Eeles, R; Izatt, L; Walker, L; Eason, J; Barwell, J; Godwin, Ak; Schmutzler, Rk; Wappenschmidt, B; Engert, S; Arnold, N; Gadzicki, D; Dean, M; Gold, B; Klein, Rj; Couch, Fj; CHENEVIX TRENCH, G; Easton, Df; Daly, Mj; Antoniou, Ac; Altshuler, Dm; Offit, K.
Ovarian cancer at the BRCA era: Tube or ovary?Results of tubal sampling protocol applied to all routine cases. III Seminario CientificoCancer: Actualidad, Perspectiva y continuidadCHEMSA Clinica Hospital de Especialidades Medicas Panama (Panama)
2010 Chiarelli, Silvia; Padoan, Ilaria; D'Andrea, Emma
Functional impairment of p16(INK4A) due to CDKN2A p.Gly23Asp missense mutation.
2009 Scaini, Mc; Rossi, E; DE SIQUEIRA TORRES, Pl; Zullato, D; Callegaro, M; Casella, C.; Quaggio, M; Agata, S; Malacrida, S; CHIARION SILENI, V; Vecchiato, A; Alaibac, MAURO SALVATORE ALESSANDRO; Montagna, M; Mann, Gj; Menin, C; D'Andrea, Emma
Pathologic findings in 200 consecutive fallopian tube specimens
2009 Chiarelli, Silvia; Padoan, I; Parenti, A; Ninfo, V; D'Andrea, Emma
Rediscovering the Fallopian tube at the time of BRCAmut. Three years experience on tubal sampling protocol applied to all routine cases.
2009 Chiarelli, Silvia; Padoan, Ilaria; D'Andrea, Emma
BRCA1 p.Val1688del is a deleterious mutation that recurs in breast and ovarian cancer families from northeast Italy
2008 Malacrida, S; Agata, S; Callegaro, M; Casella, C; Barana, D; Scaini, Mariachiara; Manoukian, S; Oliani, C; Radice, P; Barile, M; Menin, C; D'Andrea, Emma; Montagna, M.
Genomic rearrangements of the CDKN2A locus are infrequent in Italian malignant melanoma families without evidence of CDKN2A/CDK4 point mutations
2008 Vignoli, M; Scaini, Mariachiara; Ghiorzo, P; Sestini, R; Bruno, W; Menin, C; Gensini, F; Piazzini, M; Testori, A; Manoukian, S; Orlando, C; D'Andrea, Emma; BIANCHI SCARRA, G; Genuardi, M.
Reconstructing the genealogy of a BRCA1 founder mutation by phylogenetic analysis
2008 Marroni, F; Cipollini, G; Peissel, B; D'Andrea, Emma; Pensabene, M; Radice, P; Caligo, Ma; Presciuttini, S; Bevilacqua, G.
Methyl group metabolism gene polymorphisms as modifier of breast cancer risk in Italian BRCA1/2 carriers
2007 Pepe, C; Guidugli, L; Sensi, E; Aretini, P; D'Andrea, Emma; Montagna, M; Manoukian, S; Ottini, L; Radice, P; Viel, A; Bevilacqua, G; Caligo, Ma
TUMORI DELLA SALPINGE: NON SONO POI COSI' RARI. PROTOCOLLO DI PRELIEVI NELLA ROUTINE
2007 Padoan, Ilaria; Chiarelli, Silvia; Parenti, ANNA ROSITA; D'Andrea, Emma; Ninfo, Vito
Association between MDM2-SNP309 and age at colorectal cancer diagnosis according to p53 mutation status
2006 Menin, C; Scaini, Mc; DE SALVO, Gl; Biscuola, M; Quaggio, A; Nitti, Donato; Belluco, C; Montagna, M; Agata, S; D'Andrea, Emma; Nitti, D; Amadori, Alberto; Bertorelle, R.
Establishment and characterization of xenografts and cancer cell cultures derived from BRCA1 -/- epithelial ovarian cancers
2006 Indraccolo, S; Tisato, V; Agata, S; Moserle, Lidia; Ferrari, S; Callegaro, M; Persano, L; DALLA PALMA, M; Scaini, Mariachiara; Esposito, G; Fassina, Ambrogio; Nicoletto, O; Plebani, Mario; CHIECO BIANCHI, L; Amadori, Alberto; D'Andrea, Emma; Montagna, M.
Prevalence of BRCA1 genomic rearrangements in a large cohort of Italian breast and breast/ovarian cancer families without detectable BRCA1 and BRCA2 point mutations
2006 Agata, S; Viel, A; DELLA PUPPA, L; Cortesi, L; Fersini, G; Callegaro, M; Palma, Md; Dolcetti, R; Federico, M; Venuta, S; Miolo, G; D'Andrea, Emma; Montagna, M.