|
ANTONIOU A.-KARTSONAKI C.-SINILNIKOVA O.-SOUCY P.-MCGUFFOG L.-
HEALEY S.-LEE A.-PETERLONGO P.-MANOUKIAN S.-PEISSEL B.-ZAFFARONI
D.-CATTANEO E.-BARILE M.-PENSOTTI V.-PASINI B.-DOLCETTI R.-
GIANNINI G.-PUTIGNANO A.-VARESCO L.-RADICE P.-MAI P.-GREENE M.-
ANDRULIS I.-GLENDON G.-OZCELIK H.-THOMASSEN M.-GERDES A.-KRUSE T.-
JENSEN U.-CRUGER D.-CALIGO M.-LAITMAN Y.-MILGROM R.-KAUFMAN B.-
PALUCH SHIMON S.-FRIEDMAN E.-LOMAN N.-HARBST K.-LINDBLOM A.-ARVER B.-
EHRENCRONA H.-MELIN B.-SWE/BRCA-NATHANSON K.-DOMCHEK S.-REBBECK T.-
JAKUBOWSKA A.-LUBINSKI J.-GRONWALD J.-HUZARSKI T.-BYRSKI T.-CYBULSKI C.-
GORSKI B.-OSORIO A.-CAJAL T.-FOSTIRA F.-ANDRES R.-BENITEZ J.-HAMANN U.-
HOGERVORST F.-ROOKUS M.-HOONING M.-NELEN M.-VAN DER LUIJT R.-VAN OS T.-VAN
ASPEREN C.-DEVILEE P.-MEIJERS HEIJBOER H.-GOMEZ GARCIA E.-HEBON-
PEOCK S.-COOK M.-FROST D.-PLATTE R.-LEYLAND J.-EVANS D.-LALLOO F.-
EELES R.-IZATT L.-ADLARD J.-DAVIDSON R.-ECCLES D.-ONG K.-COOK J.-
DOUGLAS F.-PATERSON J.-KENNEDY M.-MIEDZYBRODZKA Z.-EMBRACE-GODWIN
A.-STOPPA LYONNET D.-BUECHER B.-BELOTTI M.-TIRAPO C.-MAZOYER S.-
BARJHOUX L.-LASSET C.-LEROUX D.-FAIVRE L.-BRONNER M.-PRIEUR F.-
NOGUES C.-ROULEAU E.-PUJOL P.-COUPIER I.-FRENAY M.-GEMO Study
Collaborators-HOPPER J.-DALY M.-TERRY M.-JOHN E.-BUYS S.-YASSIN Y.-
MIRON A.-GOLDGAR D.-Breast Cancer Family Registry-SINGER C.-TEA M.-
PFEILER G.-DRESSLER A.-HANSEN T.-JONSON L.-EJLERTSEN B.-
BARKARDOTTIR R.-KIRCHHOFF T.-OFFIT K.-PIEDMONTE M.-RODRIGUEZ G.-
SMALL L.-BOGGESS J.-BLANK S.-BASIL J.-AZODI M.-TOLAND A.-MONTAGNA
M.-TOGNAZZO S.-AGATA S.-IMYANITOV E.-JANAVICIUS R.-LAZARO C.-
BLANCO I.-PHAROAH P.-SUCHESTON L.-KARLAN B.-WALSH C.-OLAH E.-
BOZSIK A.-TEO S.-SELDON J.-BEATTIE M.-VAN RENSBURG E.-SLUITER M.-
DIEZ O.-SCHMUTZLER R.-WAPPENSCHMIDT B.-ENGEL C.-MEINDL A.-RUEHL I.-
VARON MATEEVA R.-KAST K.-DEISSLER H.-NIEDERACHER D.-ARNOLD N.-
GADZICKI D.-SCHONBUCHNER I.-CALDES T.-DE LA HOYA M.-NEVANLINNA H.-
AITTOMAKI K.-DUMONT M.-CHIQUETTE J.-TISCHKOWITZ M.-CHEN X.-BEESLEY
J.-SPURDLE A.-KConFab Investigators-NEUHAUSAEN S.-DING Y.-
FREDERICKSEN Z.-WANG X.-PANKRATZ V.-COUCH F.-SIMARD J.-EASTON D.-
CHENEVIX TRENCH G.-CIMBA
Common alleles at 6q25.1 and 1p11.2 are associated with breast
cancer risk for BRCA1 and BRCA2 mutation carriers.
Hum. Mol. Genet. 20(16):3304/3321, 2011
PubMed Abstract
CATUCCI I.-VERDERIO P.-PIZZAMIGLIO S.-MANOUKIAN S.-PEISSEL B.-
ZAFFARONI D.-ROVERSI G.-RIPAMONTI C.-PASINI B.-BARILE M.-VIEL A.-
GIANNINI G.-PAPI L.-VARESCO L.-MARTAYAN A.-RIBONI M.-VOLORIO S.-
RADICE P.-PETERLONGO P.
The CASP8 rs3834129 polymorphism and breast cancer risk in BRCA1
mutation carriers.
Breast Cancer Res. Treat. 125:855/860, 2011 - Epub Jul 22, 2010
PubMed Abstract
PETERLONGO P.-CATUCCI I.-PASQUINI G.-VERDERIO P.-PEISSEL B.-BARILE
M.-VARESCO L.-RIBONI M.-FORTUZZI S.-MANOUKIAN S.-RADICE P.
PALB2 germline mutations in familial breast cancer cases with
personal and family history of pancreatic cancer.
Breast Cancer Res. Treat. 126:825/828, 2011 - Epub Dec 24, 2010
PubMed Abstract
RAMUS S.J.-KARTSONAKI C.-GAYTHER S.-PHAROAH P.-SINILNIKOVA O.-
BEESLEY J.-CHEN X.-MCGUFFOG L.-HEALEY S.-COUCH F.-WANG X.-
FREDERICKSEN Z.-PETERLONGO P.-MANOUKIAN S.-PEISSEL B.-ZAFFARONI D.-
ROVERSI G.-BARILE M.-VIEL A.-ALLAVENA A.-OTTINI L.-PAPI L.-
GISMONDI V.-CAPRA F.-RADICE P.-GREENE M.-MAI P.-ANDRULIS I.-
GLENDON G.-OZCELIK H.-OCGN-THOMASSEN M.-GERDES A.-KRUSE T.-CRUGER
D.-JENSEN U.-CALIGO M.-OLSSON H.-KRISTOFFERSSON U.-LINDBLOM A.-
ARVER B.-KARLSSON P.-STENMARK ASKMALM M.-BORG A.-NEUHAUSEN S.-DING
Y.-NATHANSON K.-DOMCHEK S.-JAKUBOWSKA A.-LUBINSKI J.-HUZARSKI T.-
BYRSKI T.-GRONWALD J.-GORSKI B.-CYBULSKI C.-DEBNIAK T.-OSORIO A.-
DURAN M.-TEJADA M.-BENITEZ J.-HAMANN U.-ROOKUS M.-VERHOEF S.-
TILANUS LINTHORST M.-VREESWIJK M.-BODMER D.-AUSEMS M.-VAN OS T.-
ASPEREN C.-BLOK M.-MEIJERS HEIJBOER H.-HEBON/EMBRACE-PEOCK S.-COOK
M.-OLIVER C.-FROST D.-DUNNING A.-EVANS D.-EELES R.-PICHERT G.-COLE
T.-HODGSON S.-BREWER C.-MORRISON P.-PORTEOUS M.-KENNEDY M.-ROGERS
M.-SIDE L.-DONALDSON A.-GREGORY H.-GODWIN A.-STOPPA LYONNET D.-
MONCOUTIER V.-CASTERA L.-MAZOYER S.-BARJHOUX L.-BONADONA V.-LEROUX
D.-FAIVRE L.-LIDEREAU R.-NOGUES C.-BIGNON Y.-PRIEUR F.-COLLONGE
RAME M.-VENAT BOUVET L.-FERT FERRER S.-GEMO Study Collaborators-
MIRON A.-BUYS S.-HOPPER J.-DALY M.-JOHN E.-TERRY M.-GOLDGAR D.-
BCFR-HANSEN T.-JONSON L.-EJLERTSEN B.-AGNARSSON B.-OFFIT K.-
KIRCHHOFF T.-VIJAI J.-DUTRA CLARKE A.-PRZYBYLO J.-MONTAGNA M.-
CASELLA Ci.-IMYANITOV E.-JANAVICIUS R.-BLANCO I.-LAZARO C.-MOYSICH
K.-KARLAN B.-GROSS J.-BEATTIE M.-SCHMUTZLER R.-WAPPENSCHMIDT B.-
MEINDL A.-RUEHL I.-FIEBIG B.-SUTTER C.-ARNOLD N.-DEISSLER H.-VARON
MATEEVA R.-KAST K.-NIEDERACHER D.-GADZICKI D.-CALDES T.-DE LA HOYA
M.-NEVANLINNA H.-AITTOMAKI K.-SIMARD J.-SOUCY P.-KConFab
Investigators-SPURDLE A.-HOLLAND H.-CHENEVIX TRENCH G.-EASTON D.-
ANTONIOU A.-Consortium Investigators Modifiers BRCA1/2
Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and
BRCA2 mutation carriers.
J. Natl. Cancer Inst. 103:105/116, 2011 - Epub Dec 17, 2010
PubMed Abstract
PEZZI A.-RONCUCCI L.-BENATTI P.-SASSATELLI R.-VARESCO L.-DI
GREGORIO C.-VENESIO T.-PEDRONI M.-MAFFEI S.-REGGIANI BONETTI L.-
BORSI E.-FERRARI M.-MARTELLA P.-ROSSI G.-PONZ DE LEON M.
Relative role of APC and MUTYH mutations in the pathogenesis of
familial adenomatous polyposis.
Scand. J. Gastroenterol. 44:1092/1100, 2009
PubMed Abstract
TRICARICO R.-BET P.-CIAMBOTTI B.-DI GREGORIO C.-GATTESCHI B.-
GISMONDI V.-TOSCHI B.-TONELLI F.-VARESCO L.-GENUARDI M.
Endometrial cancer and somatic G>T KRAS transversion in patients
with constitutional MUTYH biallelic mutations.
Cancer Lett. 274:266/270, 2009 - Epub Nov 1, 2008
PubMed Abstract
PONTI G.-VENESIO T.-LOSI L.-PELLACANI G.-BERTARIO L.-SALA P.-PEDRONI M.-PETTI C.-MAFFEI S.-VARESCO L.-LERCH E.-BAGGIO A.-
BASSOLI S.-LONGO C.-SEIDENARI S.
BRAF mutations in multiple sebaceous hyperplasias of patients belonging to MYH associated polyposis pedigrees.
J. Invest. Dermatol. 127:1387/1391, 2007
PubMed Abstract
PONZ DE LEON M.-BERTARIO L.-GENUARDI M.-LANZA G.-OLIANI C.-RANZANI
G.-ROSSI G.-VARESCO L.-VENESIO T.-VIEL A.
Identification and classification of hereditary nonpolyposis
colorectal cancer (Lynch syndrome): adapting old concepts to
recent advancements. Report from the Italian Association for the
Study of Hereditary Colorectal Tumors Consensus Group.
Dis. Colon Rectum 50:2126/2134, 2007
PubMed Abstract
BIASCO G.-NOBILI E.-CALABRESE C.-SASSATELLI R.-CAMELLINI L.-PANTALEO M.-BERTONI G.-DE VIVO A.-PONZ DE LEON M.-POGGIOLI G.-BEDOGNI G.-VENESIO T.-VARESCO L.-RISIO M.-DI FEBO G.-BRANDI G.
Impact of surgery on the development of duodenal cancer in patients with familial adenomatous polyposis.
Dis. Colon Rectum 49:1860/1866, 2006
PubMed Abstract
DI GREGORIO C.-FRATTINI M.-MAFFEI S.-PONTI G.-LOSI L.-PEDRONI M.-VENESIO T.-BERTARIO L.-VARESCO L.-RISIO M.-PONZ DE LEON M.
Immunohistochemical expression of MYH protein can be used to identify patients with MYH associated polyposis.
Gastroenterology 131:439/444, 2006
PubMed Abstract
PERFUMO C.-BONELLI L.-MENICHINI P.-INGA A.-GISMONDI V.-CIFERRI E.-PERCIVALE P.L.-BIANCHI G.-NASTI S.-FRONZA G.-VARESCO L.
Increased risk of colorectal adenomas in italian subjects carrying the p53 PIN3 A2/Pro72 haplotype.
Digestion 74:228/235, 2006
PubMed Abstract
PICCIOLI P.-SERRA M.-GISMONDI V.-PEDEMONTE S.-LOIACONO F.-LASTRAIOLI S.-BERTARIO L.-DE ANGIOLETTI M.-VARESCO L.- NOTARO R.
Multiplex tetra primer amplification refractory mutation system PCR to detect 6 common germline mutations of the MUTYH gene
associated with polyposis and colorectal cancer.
Clin. Chem. 52:739/743, 2006
PubMed Abstract
Per le pubblicazioni 2000-2005 del personale della struttura vedere gli
elenchi generali.
|