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Siranoush Manoukian

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Genes & Molecular Sequences

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Italy

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Laura Ottini; Monica Barile; S Bianchi; Laura Cortesi; Cristina D'Amico; Mario Falchetti; Giuseppe Giannini; V Graziano; Siranoush Manoukian; Giovanna Masala; M Montagna; A S Navazio; Paolo Peterlongo; Paolo Radice; P Rizzolo; A Russo; Calogero Saieva; V Silvestri; S Tommasi; Liliana Varesco; Alessandra Viel; Ines Zanna; Domenico Palli
Association of low-penetrance alleles with male breast cancer risk and clinicopathological characteristics: results from a multicenter study in Italy.
Siranoush Manoukian; Claudia Allemani; John Burn; Mariarosaria Calvello; Patrizia Colapietro; Francesca R Grati; Bernard Peissel; Valeria Pensotti; Sara Pizzamiglio; Paolo Radice; Silvia M Sirchia; Silvia Tabano; Paolo Verderio; Monica Miozzo
X chromosome inactivation pattern in BRCA gene mutation carriers.
Mara Colombo; Giovanna De Vecchi; Filomena Ficarazzi; Claudia Foglia; Siranoush Manoukian; Bernard Peissel; Monica Barile; Laura Caleca; Carla B Ripamonti; Liliana Varesco; Paolo Radice
Comparative in vitro and in silico analyses of variants in splicing regions of BRCA1 and BRCA2 genes and characterization of novel pathogenic mutations.

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All Publications

2013: Laura Ottini; Monica Barile; S Bianchi; Laura Cortesi; Cristina D'Amico; Mario Falchetti; Giuseppe Giannini; V Graziano; Siranoush Manoukian; Giovanna Masala; M Montagna; A S Navazio; Paolo Peterlongo; Paolo Radice; P Rizzolo; A Russo; Calogero Saieva; V Silvestri; S Tommasi; Liliana Varesco; Alessandra Viel; Ines Zanna; Domenico Palli
Association of low-penetrance alleles with male breast cancer risk and clinicopathological characteristics: results from a multicenter study in Italy.
Breast cancer research and treatment 2013;138(3):861-8.
2013: Siranoush Manoukian; Claudia Allemani; John Burn; Mariarosaria Calvello; Patrizia Colapietro; Francesca R Grati; Bernard Peissel; Valeria Pensotti; Sara Pizzamiglio; Paolo Radice; Silvia M Sirchia; Silvia Tabano; Paolo Verderio; Monica Miozzo
X chromosome inactivation pattern in BRCA gene mutation carriers.
European journal of cancer (Oxford, England : 1990) 2013;49(5):1136-41.
2013: Mara Colombo; Giovanna De Vecchi; Filomena Ficarazzi; Claudia Foglia; Siranoush Manoukian; Bernard Peissel; Monica Barile; Laura Caleca; Carla B Ripamonti; Liliana Varesco; Paolo Radice
Comparative in vitro and in silico analyses of variants in splicing regions of BRCA1 and BRCA2 genes and characterization of novel pathogenic mutations.
PloS one 2013;8(2):e57173.
2013: Francisco Javier Gracia-Aznarez; Florentine S M Hilbers; John Hopper; Conchi Lazaro; Henry T Lynch; Siranoush Manoukian; Sylvie Mazoyer; Leticia Moreno; Fabrice Odefrey; Ana Osorio; Paolo Peterlongo; Guillermo Pita; Paolo Radice; Juan Manuel Rosa-Rosa; Olga M Sinilnikova; Melissa C Southey; Christi J van Asperen; Hans F A Vasen; Trinidad Caldes; Irene Catucci; Miguel de la Hoya; Peter Devilee; Orlando Dominguez; Mercedes Duran; Victoria Fernandez; David Goldgar; Anna Gonzalez-Neira; Javier Benitez
Whole exome sequencing suggests much of non-BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles.
PloS one 2013;8(2):e55681.
2012: Brooke L Brewster; Melissa A Brown; Xiaowei Chen; Mary Daly; Stacey L Edwards; Juliet D French; Andrew K Godwin; John L Hopper; Esther M John; Siranoush Manoukian; Bernard Peissel; Sara Pizzamiglio; Paolo Radice; Francesca Rossiello; Melissa C Southey; Amanda B Spurdle; Paolo Verderio; Sara Volorio; Nic Waddell; Phillip Whiley; Ming Wong; Ania Wronski; Irene Andrulis; Monica Barile; Loris Bernard; Betsy Bove; Paolo Peterlongo
Identification of fifteen novel germline variants in the BRCA1 3'UTR reveals a variant in a breast cancer case that introduces a functional miR-103 target site.
Human mutation 2012;33(12):1665-75.
2012: Florentine S Hilbers; Nicoline Hoogerbrugge; Paul A James; Siranoush Manoukian; Kenneth Offit; Jan C Oosterwijk; Paolo Peterlongo; Paolo Radice; Sohela Shah; Ella R Thompson; Alison H Trainer; Christi J van Asperen; Xianshu Wang; Juul Wijnen; Javier Benitez; Ian G Campbell; Fabio Capra; Margriet J Collee; Fergus J Couch; Irene Feroce; Javier Gracia; Lucia Guidugli; Peter Devilee
Rare variants in XRCC2 as breast cancer susceptibility alleles.
Journal of medical genetics 2012;49(10):618-20.
2012: Laura Ottini; Monica Barile; Simonetta Bianchi; Laura Cortesi; Mario Falchetti; Giuseppe Giannini; Siranoush Manoukian; Giovanna Masala; Marco Montagna; Paolo Peterlongo; Paolo Radice; Piera Rizzolo; Antonio Russo; Calogero Saieva; Valentina Silvestri; Stefania Tommasi; Liliana Varesco; Alessandra Viel; Ines Zanna; Domenico Palli
Clinical and pathologic characteristics of BRCA-positive and BRCA-negative male breast cancer patients: results from a collaborative multicenter study in Italy.
Breast cancer research and treatment 2012;134(1):411-8.
2012: Irene Catucci; Valentina Dall'olio; Laura Galastri; Siranoush Manoukian; Bernard Peissel; Sara Pizzamiglio; Paolo Radice; Fernando Ravagnani; Domenico Sardella; Paolo Verderio; Daniela Zaffaroni; Monica Barile; Loris Bernard; Paolo Peterlongo
The SNP rs895819 in miR-27a is not associated with familial breast cancer risk in Italians.
Breast cancer research and treatment 2012;133(2):805-7.
2012: Irene Catucci; Mara Colombo; Filomena Ficarazzi; Siranoush Manoukian; Frederique Mariette; Bernard Peissel; Monica Barile; Loris Bernard; Elisa Cattaneo; Paolo Radice; Paolo Verderio; Paolo Peterlongo
Sequencing analysis of SLX4/FANCP gene in Italian familial breast cancer cases.
PloS one 2012;7(2):e31038.
2011: Siranoush Manoukian; Bernard Peissel; Paolo Radice; Gaia Roversi; Jiri Bartek; Jirina Bartkova; Simona Frigerio; Daniele Lecis; Domenico Delia
Two new CHEK2 germ-line variants detected in breast cancer/sarcoma families negative for BRCA1, BRCA2, and TP53 gene mutations.
Breast cancer research and treatment 2011;130(1):207-15.
2011: Paolo Peterlongo; Fernando Ravagnani; Gianluca Severi; Christoph Sohn; Melissa C Southey; Maria Rosario Alonso; Laura Baglietto; Monica Barile; Javier Benítez; Loris Bernard; Tiziana Bianchi; Barbara Burwinkel; Laura Caleca; Elisa Cattaneo; Valentina Dall'olio; Fernando Fernández; Filomena Ficarazzi; Laura Galastri; Graham G Giles; Anne Langheinz; Siranoush Manoukian; Frederik Marme; Fabrice A Odefrey; Ana Osorio; Bernard Peissel; Paolo Radice
The rs12975333 variant in the miR-125a and breast cancer risk in Germany, Italy, Australia and Spain.
Journal of medical genetics 2011;48(10):703-4.
2011: Patrizia Pasanisi; Bernard Peissel; Elisabetta Venturelli; Monica Barile; Jacopo Berrino; Bernardo Bonanni; Eleonora Bruno; Clelia de Giacomi; Siranoush Manoukian; Franco Berrino
Serum levels of IGF-I and BRCA penetrance: a case control study in breast cancer families.
Familial cancer 2011;10(3):521-8.
2011: Paolo Peterlongo; Irene Catucci; Graziella Pasquini; Paolo Verderio; Bernard Peissel; Monica Barile; Liliana Varesco; Mirko Riboni; Stefano Fortuzzi; Siranoush Manoukian; Paolo Radice
PALB2 germline mutations in familial breast cancer cases with personal and family history of pancreatic cancer.
Breast cancer research and treatment 2011;126(3):825-8.
2011: Jonathan Beesley; Sharon E Johnatty; Xiaoqing Chen; Amanda B Spurdle; Paolo Peterlongo; Monica Barile; Valeria Pensotti; Siranoush Manoukian; Paolo Radice; Georgia Chenevix-Trench
No evidence for an association between the earwax-associated polymorphism in ABCC11 and breast cancer risk in Caucasian women.
Breast cancer research and treatment 2011;126(1):235-9.
2011: Francesco Sardanelli; Franca Podo; Filippo Santoro; Siranoush Manoukian; Silvana Bergonzi; Giovanna Trecate; Daniele Vergnaghi; Massimo Federico; Laura Cortesi; Stefano Corcione; Sandro Morassut; Cosimo Di Maggio; Anna Cilotti; Laura Martincich; Massimo Calabrese; Chiara Zuiani; Lorenzo Preda; Bernardo Bonanni; Luca A Carbonaro; Alma Contegiacomo; Pietro Panizza; Ernesto Di Cesare; Antonella Savarese; Marcello Crecco; Daniela Turchetti; Maura Tonutti; Paolo Belli; Alessandro Del Maschio
Multicenter surveillance of women at high genetic breast cancer risk using mammography, ultrasonography, and contrast-enhanced magnetic resonance imaging (the high breast cancer risk italian 1 study): final results.
Investigative radiology 2011;46(2):94-105.
2011: Irene Catucci; Paolo Verderio; Sara Pizzamiglio; Siranoush Manoukian; Bernard Peissel; Daniela Zaffaroni; Gaia Roversi; Carla B Ripamonti; Barbara Pasini; Monica Barile; Alessandra Viel; Giuseppe Giannini; Laura Papi; Liliana Varesco; Aline Martayan; Mirko Riboni; Sara Volorio; Paolo Radice; Paolo Peterlongo
The CASP8 rs3834129 polymorphism and breast cancer risk in BRCA1 mutation carriers.
Breast cancer research and treatment 2011;125(3):855-60.
2010: Monica Zuradelli; Bernard Peissel; Siranoush Manoukian; Daniela Zaffaroni; Monica Barile; Valeria Pensotti; Ugo Cavallari; Giovanna Masci; Frederique Mariette; Anne Caroline Benski; Armando Santoro; Paolo Radice
Four new cases of double heterozygosity for BRCA1 and BRCA2 gene mutations: clinical, pathological, and family characteristics.
Breast cancer research and treatment 2010;124(1):251-8.
2010: Milena S Nicoloso; Hao Sun; Riccardo Spizzo; Hyunsoo Kim; Priyankara Wickramasinghe; Masayoshi Shimizu; Sylwia E Wojcik; Jana Ferdin; Tanja Kunej; Lianchun Xiao; Siranoush Manoukian; Giorgio Secreto; Fernando Ravagnani; Xuemei Wang; Paolo Radice; Carlo M Croce; Ramana V Davuluri; George A Calin
Single-nucleotide polymorphisms inside microRNA target sites influence tumor susceptibility.
Cancer research 2010;70(7):2789-98.
2010: Irene Catucci; Rongxi Yang; Paolo Verderio; Sara Pizzamiglio; Ludwig Heesen; Kari Hemminki; Christian Sutter; Barbara Wappenschmidt; Michelle Dick; Norbert Arnold; Peter Bugert; Dieter Niederacher; Alfons Meindl; Rita K Schmutzler; Claus C Bartram; Filomena Ficarazzi; Laura Tizzoni; Daniela Zaffaroni; Siranoush Manoukian; Monica Barile; Marco A Pierotti; Paolo Radice; Barbara Burwinkel; Paolo Peterlongo
Evaluation of SNPs in miR-146a, miR196a2 and miR-499 as low-penetrance alleles in German and Italian familial breast cancer cases.
Human mutation 2010;31(1):E1052-7.
2009: William Bruno; Paola Ghiorzo; Linda Battistuzzi; Paolo A Ascierto; Monica Barile; Sara Gargiulo; Francesca Gensini; Sara Gliori; Michele Guida; Maurizio Lombardo; Siranoush Manoukian; Chiara Menin; Sabina Nasti; Paola Origone; Barbara Pasini; Lorenza Pastorino; Bernard Peissel; Maria Antonietta Pizzichetta; Paola Queirolo; Monica Rodolfo; Antonella Romanini; Maria Chiara Scaini; Alessandro Testori; Maria Grazia Tibiletti; Daniela Turchetti; Sancy A Leachman; Giovanna Bianchi-Scarrà
Clinical genetic testing for familial melanoma in Italy: a cooperative study.
Journal of the American Academy of Dermatology 2009;61(5):775-82.
2009: Maria Daniotti; Andrea Ferrari; Simona Frigerio; Paola Casieri; Francesca Miselli; Elisa Zucca; Paola Collini; Gabriella Della Torre; Siranoush Manoukian; Bernard Peissel; Aldo Bono; mario santinami; Giorgio Parmiani; Licia Rivoltini; Silvana Pilotti; Monica Rodolfo
Cutaneous melanoma in childhood and adolescence shows frequent loss of INK4A and gain of KIT.
The Journal of investigative dermatology 2009;129(7):1759-68.
2009: Irene Catucci; Paolo Verderio; Sara Pizzamiglio; Siranoush Manoukian; Bernard Peissel; Monica Barile; Laura Tizzoni; Loris Bernard; Fernando Ravagnani; Laura Galastri; Marco A Pierotti; Paolo Radice; Paolo Peterlongo
SNPs in ultraconserved elements and familial breast cancer risk.
Carcinogenesis 2009;30(3):544-5; author reply 546.
2009: Giovanna De Vecchi; Paolo Verderio; Sara Pizzamiglio; Siranoush Manoukian; Monica Barile; Stefano Fortuzzi; Fernando Ravagnani; Marco A Pierotti; Paolo Radice; Paolo Peterlongo
Evidences for association of the CASP8 -652 6N del promoter polymorphism with age at diagnosis in familial breast cancer cases.
Breast cancer research and treatment 2009;113(3):607-8.
2009: Marcelo Carvalho; Maria A Pino; Rachel Karchin; Jennifer Beddor; Martha Godinho-Netto; Rafael D Mesquita; Renato S Rodarte; Danielle C Vaz; Viviane A Monteiro; Siranoush Manoukian; Mara Colombo; Carla B Ripamonti; Richard Rosenquist; Graeme Suthers; Ake Borg; Paolo Radice; Scott Grist; Alvaro N A Monteiro; Blase Billack
Analysis of a set of missense, frameshift, and in-frame deletion variants of BRCA1.
Mutation research 2009;660(1-2):1-11.
2008: Joanne Kotsopoulos; Clifford L Librach; Jan Lubinski; Jacek Gronwald; Charmaine Kim-Sing; Parviz Ghadirian; Henry T Lynch; Pal Moller; William D Foulkes; Susan Randall; Siranoush Manoukian; Barbara Pasini; Nadine Tung; Peter Ainsworth; Shelly Cummings; Ping Sun; Steven A Narod
Infertility, treatment of infertility, and the risk of breast cancer among women with BRCA1 and BRCA2 mutations: a case-control study.
Cancer causes & control : CCC 2008;19(10):1111-9.
2008: Andrea Eisen; Jan Lubinski; Jacek Gronwald; Pal Moller; Henry T Lynch; Jan Klijn; Charmaine Kim-Sing; Susan L Neuhausen; Lucy Gilbert; Parviz Ghadirian; Siranoush Manoukian; Gad Rennert; Eitan Friedman; Claudine Isaacs; Eliot Rosen; Barry Rosen; Mary Daly; Ping Sun; Steven A Narod
Hormone therapy and the risk of breast cancer in BRCA1 mutation carriers.
Journal of the National Cancer Institute 2008;100(19):1361-7.
2008: Mara Colombo; Monica Giarola; Luigi Mariani; Carla B Ripamonti; Virna De Benedetti; Michele Sardella; Marco Losa; Siranoush Manoukian; Bernard Peissel; Marco A Pierotti; Silvana Pilotti; Paolo Radice
Cyclin D1 expression analysis in familial breast cancers may discriminate BRCAX from BRCA2-linked cases.
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2008;21(10):1262-70.
2008: Lara Lusa; Bernard Peissel; Siranoush Manoukian; Edoardo Marchesi; Paolo Radice; Marco A Pierotti; manuela gariboldi
Re: Molecular basis for estrogen receptor alpha deficiency in BRCA1-linked breast cancer.
Journal of the National Cancer Institute 2008;100(10):752-3; author reply 753-4.
2008: Kelly A Metcalfe; Daphna Birenbaum-Carmeli; Jan Lubinski; Jacek Gronwald; Henry Lynch; Pal Moller; Parviz Ghadirian; William D Foulkes; Jan Klijn; Eitan Friedman; Charmaine Kim-Sing; Peter Ainsworth; Barry Rosen; Susan M Domchek; Teresa Wagner; Nadine Tung; Siranoush Manoukian; Fergus J. Couch; Ping Sun; Steven A Narod
International variation in rates of uptake of preventive options in BRCA1 and BRCA2 mutation carriers.
International journal of cancer. Journal international du cancer 2008;122(9):2017-22.
2008: Kelly A Metcalfe; Jan Lubinski; Parviz Ghadirian; Henry Lynch; Charmaine Kim-Sing; Eitan Friedman; William D Foulkes; Susan M Domchek; Peter Ainsworth; Claudine Isaacs; Nadine Tung; Jacek Gronwald; Shelly Cummings; Teresa Wagner; Siranoush Manoukian; Pål Møller; Jeffrey N Weitzel; Ping Sun; Steven A Narod
Predictors of contralateral prophylactic mastectomy in women with a BRCA1 or BRCA2 mutation: the Hereditary Breast Cancer Clinical Study Group.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2008;26(7):1093-7.
2008: Giovanna De Vecchi; Paolo Verderio; Sara Pizzamiglio; Siranoush Manoukian; Loris Bernard; Valeria Pensotti; Sara Volorio; Fernando Ravagnani; Paolo Radice; Paolo Peterlongo
The p53 Arg72Pro and Ins16bp polymorphisms and their haplotypes are not associated with breast cancer risk in BRCA-mutation negative familial cases.
Cancer detection and prevention 2008;32(2):140-3.
2008: Sandro Malacrida; Simona Agata; Monia Callegaro; Cinzia Casella; Daniela Barana; Maria Chiara Scaini; Siranoush Manoukian; Cristina Oliani; Paolo Radice; Monica Barile; Chiara Menin; Emma D'Andrea; Marco Montagna
BRCA1 p.Val1688del is a deleterious mutation that recurs in breast and ovarian cancer families from Northeast Italy.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2008;26(1):26-31.
2007: Rebecca Jones; Margarida Ruas; Fiona Gregory; Stephanie Moulin; Domenico Delia; Siranoush Manoukian; Janice Rowe; Sharon Brookes; Gordon Peters
A CDKN2A mutation in familial melanoma that abrogates binding of p16INK4a to CDK4 but not CDK6.
Cancer research 2007;67(19):9134-41.
2007: C Pepe; Lucia Guidugli; Elisa Sensi; Paolo Aretini; Emma D'Andrea; Marco Montagna; Siranoush Manoukian; Laura Ottini; Paolo Radice; Alessandra Viel; Generoso Bevilacqua; Maria Adelaide Caligo
Methyl group metabolism gene polymorphisms as modifier of breast cancer risk in Italian BRCA1/2 carriers.
Breast cancer research and treatment 2007;103(1):29-36.
2007: Francesco Sardanelli; Franca Podo; Giuliano D'Agnolo; Arduino Verdecchia; Mariano Santaquilani; Renato Musumeci; Giovanna Trecate; Siranoush Manoukian; Sandro Morassut; Clelia de Giacomi; Massimo Federico; Laura Cortesi; Stefano Corcione; Stefano Cirillo; Vincenzo Marra; Anna Cilotti; Cosimo Di Maggio; Alfonso Fausto; Lorenzo Preda; Chiara Zuiani; Alma Contegiacomo; Antonio Orlacchio; Massimo Calabrese; Lorenzo Bonomo; Ernesto Di Cesare; Maura Tonutti; Pietro Panizza; Alessandro Del Maschio
Multicenter comparative multimodality surveillance of women at genetic-familial high risk for breast cancer (HIBCRIT study): interim results.
Radiology 2007;242(3):698-715.
2007: Marcelo A Carvalho; Sylvia M Marsillac; Rachel Karchin; Siranoush Manoukian; Scott Grist; Ramona F Swaby; Turan P Urmenyi; Edson Rondinelli; Rosane Silva; Luis Gayol; Lisa Baumbach; Rebecca Sutphen; Jennifer L Pickard-Brzosowicz; Katherine L Nathanson; Andrej Sali; David E Goldgar; Fergus J. Couch; Paolo Radice; Alvaro Monteiro
Determination of cancer risk associated with germ line BRCA1 missense variants by functional analysis.
Cancer research 2007;67(4):1494-501.
2007: Siranoush Manoukian; Bernard Peissel; Valeria Pensotti; Monica Barile; Laura Cortesi; Silvia Stacchiotti; Monica Terenziani; Floriana Barbera; Graziella Pasquini; Simona Frigerio; Marco A Pierotti; Paolo Radice; Gabriella Della Torre
Germline mutations of TP53 and BRCA2 genes in breast cancer/sarcoma families.
European journal of cancer (Oxford, England : 1990) 2007;43(3):601-6.
2006: Giovanna Trecate; Daniele Vergnaghi; Siranoush Manoukian; Silvana Bergonzi; Gianfranco Scaperrotta; Monica Marchesini; Claudio Ferranti; Bernard Peissel; Gianbattista Spatti; Silvia Bohm; Alberto Conti; Claudia Costa; Manila Sporeni; Franca Podo; Renato Musumeci
MRI in the early detection of breast cancer in women with high genetic risk.
Tumori 2006;92(6):517-23.
2006: Maria Luisa Carcangiu; Bernard Peissel; Barbara Pasini; Gianbattista Spatti; Paolo Radice; Siranoush Manoukian
Incidental carcinomas in prophylactic specimens in BRCA1 and BRCA2 germ-line mutation carriers, with emphasis on fallopian tube lesions: report of 6 cases and review of the literature.
The American journal of surgical pathology 2006;30(10):1222-30.
2006: Katia Sampieri; Theodora Hadjistilianou; Francesca Mari; Caterina Speciale; Maria Antonietta Mencarelli; Francesco Cetta; Siranoush Manoukian; Bernard Peissel; Daniela Giachino; Barbara Pasini; Antonio Acquaviva; Aldo Caporossi; Renato Frezzotti; Alessandra Renieri; Mirella Bruttini
Mutational screening of the RB1 gene in Italian patients with retinoblastoma reveals 11 novel mutations.
Journal of human genetics 2006;51(3):209-16.
2005: Jeffrey N Weitzel; Mark Robson; Barbara Pasini; Siranoush Manoukian; Dominique Stoppa-Lyonnet; Henry T Lynch; Jane McLennan; William D Foulkes; Teresa Wagner; Nadine Tung; Parviz Ghadirian; Olufunmilayo I Olopade; Claudine Isaacs; Charmaine Kim-Sing; Pal Møller; Susan L Neuhausen; Kelly A Metcalfe; Ping Sun; Steven A Narod
A comparison of bilateral breast cancers in BRCA carriers.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2005;14(6):1534-8.
2005: Siranoush Manoukian; John A Crolla; Palma M A Mammoliti; Maria Adele Testi; Rinaldo Zanini; Maria Luisa Carpanelli; Elena Piozzi; Gabriella Sozzi; Giovanna De Vecchi; Monica Terenziani; Filippo Spreafico; Paola Collini; Paolo Radice; D Perotti
Bilateral preaxial polydactyly in a WAGR syndrome patient.
American journal of medical genetics. Part A 2005;134(4):426-9.
2005: Catherine M Phelan; Virna Dapic; B Tice; Reyna Favis; Elaine Kwan; Francis Barany; Siranoush Manoukian; Paolo Radice; Rob B van der Luijt; B P M van Nesselrooij; G Chenevix-Trench; Trinidad Caldes; Miguel de la Hoya; S Lindquist; Sean V Tavtigian; David E Goldgar; A Borg; Steven A Narod; Alvaro Monteiro
Classification of BRCA1 missense variants of unknown clinical significance.
Journal of medical genetics 2005;42(2):138-46.
2004: Maria Adelaide Caligo; Simona Agata; Gitana Aceto; Rosella Crucianelli; Siranoush Manoukian; Bernard Peissel; Maria Chiara Scaini; Elisa Sensi; Serena Veschi; Alessandro Cama; Paolo Radice; Alessandra Viel; Emma D'Andrea; Marco Montagna
The CHEK2 c.1100delC mutation plays an irrelevant role in breast cancer predisposition in Italy.
Human mutation 2004;24(1):100-1.
2004: Maria Luisa Carcangiu; Paolo Radice; Siranoush Manoukian; Gianbattista Spatti; Morena Gobbo; Valeria Pensotti; Rosella Crucianelli; Barbara Pasini
Atypical epithelial proliferation in fallopian tubes in prophylactic salpingo-oophorectomy specimens from BRCA1 and BRCA2 germline mutation carriers.
International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists 2004;23(1):35-40.
2003: Giovanna Trecate; Daniele Vergnaghi; Silvana Bergonzi; Tiziana De Simone; Elena Fengoni; Claudia Costa; Gianbattista Spatti; Barbara Pasini; Siranoush Manoukian; Franca Podo; Renato Musumeci
Breast MRI screening in patients with increased familial and/or genetic risk for breast cancer: a preliminary experience.
Tumori 2003;89(2):125-31.
2002: Barbara Pasini; G C Casalis Cavalchini; T Genovese; Siranoush Manoukian
Evaluating breast cancer risk: available models to assess individual breast cancer risk and probability to be a BRCA mutation carrier.
Journal of experimental & clinical cancer research : CR 2002;21(3 Suppl):23-9.
1998: V M De Benedetti; Paolo Radice; Barbara Pasini; L Stagi; Valeria Pensotti; Patrizia Mondini; Siranoush Manoukian; A Conti; Gianbattista Spatti; F Rilke; Marco A Pierotti
Characterization of ten novel and 13 recurring BRCA1 and BRCA2 germline mutations in Italian breast and/or ovarian carcinoma patients. Mutations in brief no. 178. Online.
Human mutation 1998;12(3):215.