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Bernard Peissel

Research Profile

Physiology

Disorders

Genes & Molecular Sequences

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Italy

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DNA Mutational Analysis

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Publications

TOP 3
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.
Carla B Ripamonti; Manoukian Siranoush; Loris Bernard; Mara Colombo; Patrizia Mondini; Bernard Peissel; Paolo Radice; Maria Luisa Carcangiu
First description of an acinic cell carcinoma of the breast in a BRCA1 mutation carrier: a case report.

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All Publications

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: Carla B Ripamonti; Manoukian Siranoush; Loris Bernard; Mara Colombo; Patrizia Mondini; Bernard Peissel; Paolo Radice; Maria Luisa Carcangiu
First description of an acinic cell carcinoma of the breast in a BRCA1 mutation carrier: a case report.
BMC cancer 2013;13():46.
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: 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: Maria Grazia Borrello; Veronica Catalano; Paola Collini; Debora Degl'Innocenti; Morena Gobbo; Angela Greco; Piera Mondellini; Bernard Peissel; Marco A Pierotti; Maria Grazia Rizzetti; Antonella Aiello; Italia Bongarzone; Ettore Seregni
Functional characterization of the MTC-associated germline RET-K666E mutation: evidence of oncogenic potential enhanced by the G691S polymorphism.
Endocrine-related cancer 2011;18(4):519-27.
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: 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: Anna Paola Scioletti; Francesco Brancati; Valentina Gatta; Ivana Antonucci; Bernard Peissel; Antonio Pizzuti; Carmen Mortellaro; Stefano Tetè; Enrico Gherlone; Giandomenico Palka; Liborio Stuppia
Two novel mutations affecting splicing in the IRF6 gene associated with van der Woude syndrome.
The Journal of craniofacial surgery 2010;21(5):1654-6.
2010: Giovanna Trecate; Siranuosh Manoukian; Laura Suman; Daniele Vergnaghi; Monica Marchesini; Roberto Agresti; Cristina Ferraris; Bernard Peissel; Davide Scaramuzza; Silvana Bergonzi
Is there a specific magnetic resonance phenotype characteristic of hereditary breast cancer?
Tumori 2010;96(3):363-84.
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: M Colombo; C B Ripamonti; Valeria Pensotti; C Foglia; Bernard Peissel; Marco A Pierotti; S Manoukian; Paolo Radice
An unusual BRCA2 allele carrying two splice site mutations.
Annals of oncology : official journal of the European Society for Medical Oncology / ESMO 2009;20(6):1143-4.
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.
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.
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.
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: Anna Saran; Monica Spinola; Simonetta Pazzaglia; Bernard Peissel; Cecilia Tiveron; Laura Tatangelo; Mariateresa Mancuso; Vincenzo Covelli; Lisa Giovannelli; Vanessa Pitozzi; Carmen Pignatiello; Silvano Milani; Piero Dolara; Tommaso A Dragani
Loss of tyrosinase activity confers increased skin tumor susceptibility in mice.
Oncogene 2004;23(23):4130-5.
2003: Roberto Benelli; Bernard Peissel; Giacomo Manenti; manuela gariboldi; Christian Vanzetto; Adriana Albini; Tommaso A Dragani
Allele-specific patterns of the mouse parathyroid hormone-related protein: influences on cell adhesion and migration.
Oncogene 2003;22(49):7711-5.
2003: manuela gariboldi; Bernard Peissel; Alessandra Fabbri; Anna Saran; Daniela Zaffaroni; F Stefania Falvella; Monica Spinola; Jun-ichi Tanuma; Simonetta Pazzaglia; Mariateresa Mancuso; Andrea Maurichi; Cesare Bartoli; Sule Cataltepe; Gary A Silverman; Silvana Pilotti; Yoshihide Hayashizaki; Yasushi Okazaki; Tommaso A Dragani
SCCA2-like serpins mediate genetic predisposition to skin tumors.
Cancer research 2003;63(8):1871-5.
2002: Anna Saran; Daniela Zaffaroni; Simonetta Pazzaglia; Bernard Peissel; Federica Galbiati; Monica Spinola; Giacomo Manenti; nicola zanesi; Simonetta Rebessi; Mariateresa Mancuso; Vincenzo Covelli; Tommaso A Dragani
Inhibition of both skin and lung tumorigenesis by Car-R mouse-derived cancer modifier loci.
International journal of cancer. Journal international du cancer 2002;97(5):580-3.
2001: Bernard Peissel; Daniela Zaffaroni; Simonetta Pazzaglia; Giacomo Manenti; nicola zanesi; I Zedda; Simonetta Rebessi; Vincenzo Covelli; Tommaso A Dragani; Anna Saran
Use of intercross outbred mice and single nucleotide polymorphisms to map skin cancer modifier loci.
Mammalian genome : official journal of the International Mammalian Genome Society 2001;12(4):291-4.
2000: Giacomo Manenti; Bernard Peissel; manuela gariboldi; F Stefania Falvella; Daniela Zaffaroni; B Allaria; Simonetta Pazzaglia; Simonetta Rebessi; Vincenzo Covelli; Anna Saran; Tommaso A Dragani
A cancer modifier role for parathyroid hormone-related protein.
Oncogene 2000;19(47):5324-8.
2000: Tommaso A Dragani; Bernard Peissel; nicola zanesi; A Aloisi; Y Dai; M Kato; H Suzuki; I Nakashima
Mapping of melanoma modifier loci in RET transgenic mice.
Japanese journal of cancer research : Gann 2000;91(11):1142-7.
2000: Bernard Peissel; Daniela Zaffaroni; nicola zanesi; I Zedda; Giacomo Manenti; Simonetta Rebessi; Simonetta Pazzaglia; Gino Doria; Vincenzo Covelli; Tommaso A Dragani; Anna Saran
Linkage disequilibrium and haplotype mapping of a skin cancer susceptibility locus in outbred mice.
Mammalian genome : official journal of the International Mammalian Genome Society 2000;11(11):979-81.
1999: Yoav Segal; Bernard Peissel; Alessandra Renieri; Mario De Marchi; A Ballabio; Y Pei; Jing Zhou
LINE-1 elements at the sites of molecular rearrangements in Alport syndrome-diffuse leiomyomatosis.
American journal of human genetics 1999;64(1):62-9.