Works by Viel, Alessandra

Results: 60
    1
    2

    Small Bowel Carcinoma in Hereditary Nonpolyposis Colorectal Cancer.

    Published in:
    American Journal of Gastroenterology (Springer Nature), 1998, v. 93, n. 11, p. 2219, doi. 10.1111/j.1572-0241.1998.00618.x
    By:
    • Benatti, Piero;
    • Roncucci, Luca;
    • Percesepe, Antonio;
    • Viel, Alessandra;
    • Pedroni, Monica;
    • Tamassia, Maria Grazia;
    • Vaccina, Fabiana;
    • Fante, Rossella;
    • De Pietri, Stefano;
    • De Leon, Maurizio Ponz
    Publication type:
    Article
    3
    4

    MUTYH-associated polyposis (MAP): evidence for the origin of the common European mutations p.Tyr179Cys and p.Gly396Asp by founder events.

    Published in:
    European Journal of Human Genetics, 2014, v. 22, n. 7, p. 923, doi. 10.1038/ejhg.2012.309
    By:
    • Aretz, Stefan;
    • Tricarico, Rossella;
    • Papi, Laura;
    • Spier, Isabel;
    • Pin, Elisa;
    • Horpaopan, Sukanya;
    • Cordisco, Emanuela Lucci;
    • Pedroni, Monica;
    • Stienen, Dietlinde;
    • Gentile, Annamaria;
    • Panza, Anna;
    • Piepoli, Ada;
    • de Leon, Maurizio Ponz;
    • Friedl, Waltraut;
    • Viel, Alessandra;
    • Genuardi, Maurizio
    Publication type:
    Article
    5

    Reply to Jaskowski et al.

    Published in:
    2007
    By:
    • Pastrello, Chiara;
    • Tricarico, Rossella;
    • Tibiletti, Maria Grazia;
    • Papi, Laura;
    • Fornasarig, Mara;
    • Morabito, Alberto;
    • Agostini, Marco;
    • Genuardi, Maurizio;
    • Viel, Alessandra
    Publication type:
    Letter
    6

    Assessing the pathogenicity of MLH1 missense mutations in patients with suspected hereditary nonpolyposis colorectal cancer: correlation with clinical, genetic and functional features.

    Published in:
    European Journal of Human Genetics, 2006, v. 14, n. 7, p. 853, doi. 10.1038/sj.ejhg.5201628
    By:
    • Belvederesi, Laura;
    • Bianchi, Francesca;
    • Loretelli, Cristian;
    • Gagliardini, Daniela;
    • Galizia, Eva;
    • Bracci, Raffaella;
    • Rosati, Saverio;
    • Bearzi, Italo;
    • Viel, Alessandra;
    • Cellerino, Riccardo;
    • Porfiri, Emilio
    Publication type:
    Article
    7
    8

    Penetrances of breast and ovarian cancer in a large series of families tested for BRCA1/2 mutations.

    Published in:
    European Journal of Human Genetics, 2004, v. 12, n. 11, p. 899, doi. 10.1038/sj.ejhg.5201256
    By:
    • Marroni, Fabio;
    • Aretini, Paolo;
    • D'Andrea, Emma;
    • Caligo, Maria Adelaide;
    • Cortesi, Laura;
    • Viel, Alessandra;
    • Ricevuto, Enrico;
    • Montagna, Marco;
    • Cipollini, Giovanna;
    • Federico, Massimo;
    • Santarosa, Manuela;
    • Marchetti, Paolo;
    • Bailey-Wilson, Joan E;
    • Bevilacqua, Generoso;
    • Parmigiani, Giovanni;
    • Presciuttini, Silvano
    Publication type:
    Article
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    11
    12
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    14
    15

    Human MRE11 is inactivated in mismatch repair-deficient cancers.

    Published in:
    2002
    By:
    • Giannini, Giuseppe;
    • Ristori, Elisabetta;
    • Cerignoli, Fabio;
    • Rinaldi, Christian;
    • Zani, Massimo;
    • Viel, Alessandra;
    • Ottini, Laura;
    • Crescenzi, Marco;
    • Martinotti, Stefano;
    • Bignami, Margherita;
    • Frati, Luigi;
    • Screpanti, Isabella;
    • Gulino, Alberto
    Publication type:
    Report
    16

    MLH1 and MSH2 constitutinal mutations in colorectal cancer families not meeting the standard criteria for hereditary nonpolyposis colorectal cancer.

    Published in:
    International Journal of Cancer, 1998, v. 75, n. 6, p. 835, doi. 10.1002/(SICI)1097-0215(19980316)75:6<835::AID-IJC4>3.0.CO;2-W
    By:
    • Genuardi, Maurizio;
    • Anti, Marcello;
    • Capozzi, Eugenia;
    • Leonardi, Francesca;
    • Fornasarig, Mara;
    • Novella, Elisabetta;
    • Bellacosa, Alfonso;
    • Valenti, Agostino;
    • Gasbarrini, Giovanni Battista;
    • Roncucci, Luca;
    • Benatti, Piero;
    • Percesepe, Antonio;
    • de Leòn, Maurizio Ponz;
    • Coco, Claudio;
    • de Paoli, Antonio;
    • Valentini, Maurizio;
    • Boiocchi, Mauro;
    • Neri, Giovanni;
    • Viel, Alessandra
    Publication type:
    Article
    17

    Survival analysis in families affected by hereditary non-polyposis colorectal cancer.

    Published in:
    International Journal of Cancer, 1997, v. 71, n. 3, p. 373, doi. 10.1002/(SICI)1097-0215(19970502)71:3<373::AID-IJC12>3.0.CO;2-H
    By:
    • Percesepe, Antonio;
    • Benatti, Piero;
    • Roncucci, Luca;
    • Sassatelli, Romano;
    • Fante, Rossella;
    • Ganazzi, Dorval;
    • Bellacosa, Alfonso;
    • Genuardi, Maurizio;
    • Neri, Giovanni;
    • Viel, Alessandra;
    • Ponz de Leon, Maurizio
    Publication type:
    Article
    18
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    Clinical and pathologic characteristics of BRCA-positive and BRCA-negative male breast cancer patients: results from a collaborative multicenter study in Italy.

    Published in:
    Breast Cancer Research & Treatment, 2012, v. 134, n. 1, p. 411, doi. 10.1007/s10549-012-2062-0
    By:
    • Ottini, Laura;
    • Silvestri, Valentina;
    • Rizzolo, Piera;
    • Falchetti, Mario;
    • Zanna, Ines;
    • Saieva, Calogero;
    • Masala, Giovanna;
    • Bianchi, Simonetta;
    • Manoukian, Siranoush;
    • Barile, Monica;
    • Peterlongo, Paolo;
    • Varesco, Liliana;
    • Tommasi, Stefania;
    • Russo, Antonio;
    • Giannini, Giuseppe;
    • Cortesi, Laura;
    • Viel, Alessandra;
    • Montagna, Marco;
    • Radice, Paolo;
    • Palli, Domenico
    Publication type:
    Article
    21

    Evidence for a link between TNFRSF11A and risk of breast cancer.

    Published in:
    Breast Cancer Research & Treatment, 2011, v. 129, n. 3, p. 947, doi. 10.1007/s10549-011-1546-7
    By:
    • Bonifaci, Núria;
    • Palafox, Marta;
    • Pellegrini, Pasquale;
    • Osorio, Ana;
    • Benítez, Javier;
    • Peterlongo, Paolo;
    • Manoukian, Siranoush;
    • Peissel, Bernard;
    • Zaffaroni, Daniela;
    • Roversi, Gaia;
    • Barile, Monica;
    • Viel, Alessandra;
    • Mariette, Frederique;
    • Bernard, Loris;
    • Radice, Paolo;
    • Kaufman, Bella;
    • Laitman, Yael;
    • Milgrom, Roni;
    • Friedman, Eitan;
    • Sáez, María
    Publication type:
    Article
    22

    The CASP8 rs3834129 polymorphism and breast cancer risk in BRCA1 mutation carriers.

    Published in:
    Breast Cancer Research & Treatment, 2011, v. 125, n. 3, p. 855, doi. 10.1007/s10549-010-1068-8
    By:
    • Catucci, Irene;
    • Verderio, Paolo;
    • Pizzamiglio, Sara;
    • Manoukian, Siranoush;
    • Peissel, Bernard;
    • Zaffaroni, Daniela;
    • Roversi, Gaia;
    • Ripamonti, Carla;
    • Pasini, Barbara;
    • Barile, Monica;
    • Viel, Alessandra;
    • Giannini, Giuseppe;
    • Papi, Laura;
    • Varesco, Liliana;
    • Martayan, Aline;
    • Riboni, Mirko;
    • Volorio, Sara;
    • Radice, Paolo;
    • Peterlongo, Paolo
    Publication type:
    Article
    23

    APC I1307K mutations and forkhead box gene (FOXO1A): another piece of an interesting correlation.

    Published in:
    International Journal of Biological Markers, 2012, v. 27, n. 1, p. 13, doi. 10.5301/JBM.2011.8908
    By:
    • Agostini, Marco;
    • Bedin, Chiara;
    • Pucciarelli, Salvatore;
    • Enzo, Mariavittoria;
    • Briarava, Marta;
    • Seraglia, Roberta;
    • Ragazzi, Eugenio;
    • Traldi, Pietro;
    • Molin, Laura;
    • Urso, Emanuele Damiano;
    • Mammi, Isabella;
    • Viel, Alessandra;
    • Lise, Mario;
    • Tasciotti, Ennio;
    • Biasiolo, Alessandra;
    • Pontisso, Patrizia;
    • Nitti, Donato
    Publication type:
    Article
    24

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

    Published in:
    International Journal of Cancer, 2004, v. 109, n. 5, p. 680, doi. 10.1002/ijc.20054
    By:
    • Gismondi, Viviana;
    • Meta, Maurizio;
    • Bonelli, Luigina;
    • Radice, Paolo;
    • Sala, Paola;
    • Bertario, Lucio;
    • Viel, Alessandra;
    • Fornasarig, Mara;
    • Arrigoni, Arrigo;
    • Gentile, Mattia;
    • Ponz de Leon, Maurizio;
    • Anselmi, Luca;
    • Mareni, Cristina;
    • Bruzzi, Paolo;
    • Varesco, Liliana
    Publication type:
    Article
    25

    Clinical and biologic heterogeneity of hereditary nonpolyposis colorectal cancer.

    Published in:
    International Journal of Cancer, 2001, v. 95, n. 5, p. 323, doi. 10.1002/1097-0215(20010920)95:5<323::AID-IJC1056>3.0.CO;2-H
    By:
    • Benatti, Piero;
    • Roncucci, Luca;
    • Ganazzi, Dorval;
    • Percesepe, Antonio;
    • Di Gregorio, Carmela;
    • Pedroni, Monica;
    • Borghi, Francesca;
    • Sala, Elisa;
    • Scarselli, Alessandra;
    • Menigatti, Mirco;
    • Rossi, Giuseppina;
    • Genuardi, Maurizio;
    • Viel, Alessandra;
    • Ponz de Leon, Maurizio
    Publication type:
    Article
    26

    BRCA1 and BRCA2 genes: Role in hereditary breast and ovarian cancer in Italy.

    Published in:
    International Journal of Cancer, 1999, v. 83, n. 1, p. 5, doi. 10.1002/(SICI)1097-0215(19990924)83:1<5::AID-IJC2>3.0.CO;2-U
    By:
    • Santarosa, Manuela;
    • Dolcetti, Riccardo;
    • Magri, Maria Donatella;
    • Crivellari, Diana;
    • Tibiletti, Maria Grazia;
    • Gallo, Angelo;
    • Tumolo, Salvatore;
    • Della Puppa, Lara;
    • Furlan, Daniela;
    • Boiocchi, Mauro;
    • Viel, Alessandra
    Publication type:
    Article
    27

    Low incidence of BRCA1 mutations among Italian families with breast and ovarian cancer.

    Published in:
    International Journal of Cancer, 1998, v. 78, n. 5, p. 581, doi. 10.1002/(SICI)1097-0215(19981123)78:5<581::AID-IJC9>3.0.CO;2-G
    By:
    • Santarosa, Manuela;
    • Viel, Alessandra;
    • Dolcetti, Riccardo;
    • Crivellari, Diana;
    • Magri, Maria Donatella;
    • Pizzichetta, Maria Antonietta;
    • Tibiletti, Maria Grazia;
    • Gallo, Angelo;
    • Tumolo, Salvatore;
    • Del Tin, Laura;
    • Boiocchi, Mauro
    Publication type:
    Article
    28

    BRCA1 modulates the expression of hnRNPA2B1 and KHSRP.

    Published in:
    Cell Cycle, 2010, v. 9, n. 23, p. 4666, doi. 10.4161/cc.9.23.14022
    By:
    • Santarosa, Manuela;
    • Del Col, Laura;
    • Viel, Alessandra;
    • Bivi, Nicoletta;
    • D'Ambrosio, Chiara;
    • Scaloni, Andrea;
    • Tell, Gianluca;
    • Maestro, Roberta
    Publication type:
    Article
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    Characterization of MSH2 and MLH1 mutations in Italian families with hereditary nonpolyposis colorectal cancer.

    Published in:
    Genes, Chromosomes & Cancer, 1997, v. 18, n. 1, p. 8, doi. 10.1002/(SICI)1098-2264(199701)18:1<8::AID-GCC2>3.0.CO;2-7
    By:
    • Viel, Alessandra;
    • Genuardi, Maurizio;
    • Capozzi, Eugenia;
    • Leonardi, Francesca;
    • Bellacosa, Alfonso;
    • Paravatou-Petsotas, Maria;
    • Pomponi, Maria Grazia;
    • Fornasarig, Mara;
    • Percesepe, Antonio;
    • Roncucci, Luca;
    • Tamassia, Maria Grazia;
    • Benatti, Piero;
    • de Leon, Maurizio Ponz;
    • Valenti, Agostino;
    • Covino, Marcello;
    • Anti, Marcello;
    • Foletto, Mirto;
    • Boiocchi, Mauro;
    • Neri, Giovanni
    Publication type:
    Article
    33
    34

    Different molecular mechanisms underlie genomic deletions in the MLH1 Gene.

    Published in:
    Human Mutation, 2002, v. 20, n. 5, p. 368, doi. 10.1002/humu.10138
    By:
    • Viel, Alessandra;
    • Petronzelli, Fiorella;
    • Puppa, Lara Della;
    • Lucci-Cordisco, Emanuela;
    • Fornasarig, Mara;
    • Pucciarelli, Salvatore;
    • Rovella, Valentina;
    • Quaia, Michele;
    • de Leon, Maurizio Ponz;
    • Boiocchi, Mauro;
    • Genuardi, Maurizio
    Publication type:
    Article
    35

    Evidence of a founder mutation of BRCA1 in a highly homogeneous population from southern Italy with breast/ovarian cancer.

    Published in:
    Human Mutation, 2001, v. 18, n. 2, p. 163, doi. 10.1002/humu.1167
    By:
    • Baudi, Francesco;
    • Quaresima, Barbara;
    • Grandinetti, Cristina;
    • Cuda, Giovanni;
    • Faniello, Concetta;
    • Tassone, Pierfrancesco;
    • Barbieri, Vito;
    • Bisegna, Roberta;
    • Ricevuto, Enrico;
    • Conforti, Serafino;
    • Viel, Alessandra;
    • Marchetti, Paolo;
    • Ficorella, Corrado;
    • Radice, Paolo;
    • Costanzo, Francesco;
    • Venuta, Salvatore
    Publication type:
    Article
    36
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    Factors affecting the treatment of multiple colorectal adenomas.

    Published in:
    Surgical Endoscopy & Other Interventional Techniques, 2013, v. 27, n. 1, p. 207, doi. 10.1007/s00464-012-2421-2
    By:
    • Urso, Emanuele;
    • Nascimbeni, Riccardo;
    • Pucciarelli, Salvatore;
    • Agostini, Marco;
    • Casella, Claudio;
    • Moneghini, Dario;
    • Lorenzo, Diego;
    • Maretto, Isacco;
    • Sullivan, Maribel;
    • Mammi, Isabella;
    • Viel, Alessandra;
    • Nitti, Donato
    Publication type:
    Article
    38

    Insight into genetic susceptibility to male breast cancer by multigene panel testing: Results from a multicenter study in Italy.

    Published in:
    International Journal of Cancer, 2019, v. 145, n. 2, p. 390, doi. 10.1002/ijc.32106
    By:
    • Rizzolo, Piera;
    • Zelli, Veronica;
    • Silvestri, Valentina;
    • Valentini, Virginia;
    • Zanna, Ines;
    • Bianchi, Simonetta;
    • Masala, Giovanna;
    • Spinelli, Alessandro Mauro;
    • Tibiletti, Maria Grazia;
    • Russo, Antonio;
    • Varesco, Liliana;
    • Giannini, Giuseppe;
    • Capalbo, Carlo;
    • Calistri, Daniele;
    • Cortesi, Laura;
    • Viel, Alessandra;
    • Bonanni, Bernardo;
    • Azzollini, Jacopo;
    • Manoukian, Siranoush;
    • Montagna, Marco
    Publication type:
    Article
    39

    MUTYH c.933+3A>C, associated with a severely impaired gene expression, is the first Italian founder mutation in MUTYH-Associated Polyposis.

    Published in:
    International Journal of Cancer, 2013, v. 132, n. 5, p. 1060, doi. 10.1002/ijc.27761
    By:
    • Pin, Elisa;
    • Pastrello, Chiara;
    • Tricarico, Rossella;
    • Papi, Laura;
    • Quaia, Michele;
    • Fornasarig, Mara;
    • Carnevali, Ileana;
    • Oliani, Cristina;
    • Fornasin, Alessio;
    • Agostini, Marco;
    • Maestro, Roberta;
    • Barana, Daniela;
    • Aretz, Stefan;
    • Genuardi, Maurizio;
    • Viel, Alessandra
    Publication type:
    Article
    40

    An American founder mutation in MLH1.

    Published in:
    International Journal of Cancer, 2012, v. 130, n. 9, p. 2088, doi. 10.1002/ijc.26233
    By:
    • Tomsic, Jerneja;
    • Liyanarachchi, Sandya;
    • Hampel, Heather;
    • Morak, Monika;
    • Thomas, Brittany C.;
    • Raymond, Victoria M.;
    • Chittenden, Anu;
    • Schackert, Hans K.;
    • Gruber, Stephen B.;
    • Syngal, Sapna;
    • Viel, Alessandra;
    • Holinski-Feder, Elke;
    • Thibodeau, Stephen N.;
    • de la Chapelle, Albert
    Publication type:
    Article
    41

    Whole-exome sequencing and targeted gene sequencing provide insights into the role of PALB2 as a male breast cancer susceptibility gene.

    Published in:
    2017
    By:
    • Silvestri, Valentina;
    • Zelli, Veronica;
    • Valentini, Virginia;
    • Rizzolo, Piera;
    • Navazio, Anna Sara;
    • Coppa, Anna;
    • Agata, Simona;
    • Oliani, Cristina;
    • Barana, Daniela;
    • Castrignanò, Tiziana;
    • Viel, Alessandra;
    • Russo, Antonio;
    • Tibiletti, Maria Grazia;
    • Zanna, Ines;
    • Masala, Giovanna;
    • Cortesi, Laura;
    • Manoukian, Siranoush;
    • Azzollini, Jacopo;
    • Peissel, Bernard;
    • Bonanni, Bernardo
    Publication type:
    journal article
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    Comprehensive genetic and epigenetic characterization of Lynch‐like syndrome patients.

    Published in:
    International Journal of Cancer, 2025, v. 157, n. 4, p. 788, doi. 10.1002/ijc.35451
    By:
    • Pirini, Francesca;
    • Calzari, Luciano;
    • Tedaldi, Gianluca;
    • Tebaldi, Michela;
    • Zampiga, Valentina;
    • Cangini, Ilaria;
    • Danesi, Rita;
    • Ravegnani, Mila;
    • Arcangeli, Valentina;
    • Passardi, Alessandro;
    • Petracci, Elisabetta;
    • Bravaccini, Sara;
    • Marisi, Giorgia;
    • Viel, Alessandra;
    • Barana, Daniela;
    • Pedroni, Monica;
    • Roncucci, Luca;
    • Calistri, Daniele;
    • Gentilini, Davide
    Publication type:
    Article
    49
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    Male with an apparently normal phenotype carrying a BRCA1 exon 20 duplication in trans to a BRCA1 frameshift variant.

    Published in:
    Breast Cancer Research, 2024, v. 26, n. 1, p. 1, doi. 10.1186/s13058-023-01755-9
    By:
    • Block, Ines;
    • Mateu-Regué, Àngels;
    • Do, Thi Tuyet Nhu;
    • Miceikaite, Ieva;
    • Sdogati, Daniel;
    • Larsen, Martin J.;
    • Hao, Qin;
    • Nielsen, Henriette Roed;
    • Boonen, Susanne E.;
    • Skytte, Anne-Bine;
    • Jensen, Uffe Birk;
    • Høffding, Louise K.;
    • De Nicolo, Arcangela;
    • Viel, Alessandra;
    • Tudini, Emma;
    • Parsons, Michael T.;
    • Hansen, Thomas V. O.;
    • Rossing, Maria;
    • Kruse, Torben A.;
    • Spurdle, Amanda B.
    Publication type:
    Article