Sfoglia per Autore
Constitutional de novo deletion of the FBXW7 gene in a patient with focal segmental glomerulosclerosis and multiple primitive tumors
2015 Roversi, G; Picinelli, C; Bestetti, I; Crippa, M; Perotti, D; Ciceri, S; Saccheri, F; Collini, P; Poliani, P; Catania, S; Peissel, B; Pagni, F; Russo, S; Peterlongo, P; Manoukian, S; Finelli, P
Novel physiological RECQL4 alternative transcript disclosed by molecular characterisation of Rothmund–Thomson Syndrome sibs with mild phenotype
2014 Colombo, E; Fontana, L; Roversi, G; Negri, G; Castiglia, D; Paradisi, M; Zambruno, G; Larizza, L
Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers
2014 Kuchenbaecker, K; Neuhausen, S; Robson, M; Barrowdale, D; Mcguffog, L; Mulligan, A; Andrulis, I; Spurdle, A; Schmidt, M; Schmutzler, R; Engel, C; Wappenschmidt, B; Nevanlinna, H; Thomassen, M; Southey, M; Radice, P; Ramus, S; Domchek, S; Nathanson, K; Lee, A; Healey, S; Nussbaum, R; Rebbeck, T; Arun, B; James, P; Karlan, B; Lester, J; Cass, I; Breast Cancer Family, R; Terry, M; Daly, M; Goldgar, D; Buys, S; Janavicius, R; Tihomirova, L; Tung, N; Dorfling, C; van Rensburg, E; Steele, L; v. O. Hansen, T; Ejlertsen, B; Gerdes, A; Nielsen, F; Dennis, J; Cunningham, J; Hart, S; Slager, S; Osorio, A; Benitez, J; Duran, M; Weitzel, J; Tafur, I; Hander, M; Peterlongo, P; Manoukian, S; Peissel, B; Roversi, G; Scuvera, G; Bonanni, B; Mariani, P; Volorio, S; Dolcetti, R; Varesco, L; Papi, L; Tibiletti, M; Giannini, G; Fostira, F; Konstantopoulou, I; Garber, J; Hamann, U; Donaldson, A; Brewer, C; Foo, C; Evans, D; Frost, D; Eccles, D; Embrace, S; Douglas, F; Brady, A; Cook, J; Tischkowitz, M; Adlard, J; Barwell, J; Ong, K; Walker, L; Izatt, L; Side, L; Kennedy, M; Rogers, M; Porteous, M; Morrison, P; Platte, R; Eeles, R; Davidson, R; Hodgson, S; Ellis, S; Godwin, A; Rhiem, K; Meindl, A; Ditsch, N; Arnold, N; Plendl, H; Niederacher, D; Sutter, C; Steinemann, D; Bogdanova Markov, N; Kast, K; Varon Mateeva, R; Wang Gohrke, S; Gehrig, A; Markiefka, B; Buecher, B; Lefol, C; Stoppa Lyonnet, D; Rouleau, E; Prieur, F; Damiola, F; GEMO Study, C; Barjhoux, L; Faivre, L; Longy, M; Sevenet, N; Sinilnikova, O; Mazoyer, S; Bonadona, V; Caux Moncoutier, V; Isaacs, C; Van Maerken, T; Claes, K; Piedmonte, M; Andrews, L; Hays, J; Rodriguez, G; Caldes, T; de la Hoya, M; Khan, S; Hogervorst, F; Aalfs, C; de Lange, J; Meijers Heijboer, H; van der Hout, A; Wijnen, J; van Roozendaal, K; Mensenkamp, A; van den Ouweland, A; van Deurzen, C; van der Luijt, R; Hebon, ; Olah, E; Diez, O; Lazaro, C; Blanco, I; Teulé, A; Menendez, M; Jakubowska, A; Lubinski, J; Cybulski, C; Gronwald, J; Jaworska Bieniek, K; Durda, K; Arason, A; Maugard, C; Soucy, P; Montagna, M; Agata, S; Teixeira, M; Kconfab, I; Olswold, C; Lindor, N; Pankratz, V; Hallberg, E; Wang, X; Szabo, C; Vijai, J; Jacobs, L; Corines, M; Lincoln, A; Berger, A; Fink Retter, A; Singer, C; Rappaport, C; Kaulich, D; Pfeiler, G; Tea, M; Phelan, C; Mai, P; Greene, M; Rennert, G; Imyanitov, E; Glendon, G; Toland, A; Bojesen, A; Pedersen, I; Jensen, U; Caligo, M; Friedman, E; Berger, R; Laitman, Y; Rantala, J; Arver, B; Loman, N; Borg, A; Ehrencrona, H; Olopade, O; Simard, J; Easton, D; Chenevix Trench, G; Offit, K; Couch, F; Antoniou, A; Cimba,
Clinical utility gene card for: Rothmund-Thomson syndrome
2013 Larizza, L; Roversi, G; Verloes, A
An Alternative Approach in Endocrine Pathology Research: MALDI-IMS in Papillary Thyroid Carcinoma
2013 Mainini, V; Pagni, F; Garancini, M; Giardini, V; DE SIO, G; Cusi, C; Arosio, C; Roversi, G; Chinello, C; Caria, P; Vanni, R; Magni, F
Sindrome di Rothmund-Thomson: caratterizzazione clinico-molecolare di tre nuovi pazienti
2012 Colombo, E; Fontana, L; Roversi, G; Negri, G; Paradisi, M; Castiglia, D; Locatelli, A; Zambruno, G; Larizza, L
Two new CHEK2 germ-line variants detected in breast cancer/sarcoma families negative for BRCA1, BRCA2, and TP53 gene mutations
2011 Manoukian, S; Peissel, B; Frigerio, S; Lecis, D; Bartkova, J; Roversi, G; Radice, P; Bartek, J; Delia, D
Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers
2011 Ramus, S; 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; 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; Lubiński, J; Huzarski, T; Byrski, T; Gronwald, J; Górski, B; Cybulski, C; Dębniak, T; Osorio, A; Durán, M; Tejada, M; Benítez, 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; 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; Miron, A; Buys, S; Hopper, J; Daly, M; John, E; Terry, M; Goldgar, D; Hansen, T; Jønson, L; Ejlertsen, B; Agnarsson, B; Offit, K; Kirchhoff, T; Vijai, J; Dutra Clarke, A; Przybylo, J; Montagna, M; Casella, C; Imyanitov, E; Janavicius, R; Blanco, I; Lázaro, 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; Aittomäki, K; Simard, J; Soucy, P; Spurdle, A; Holland, H; Chenevix Trench, G; Easton, D; Antoniou, A
Exploring the link between MORF4L1 and risk of breast cancer
2011 Martrat, G; Maxwell, C; Tominaga, E; Porta de la Riva, M; Bonifaci, N; Gómez Baldó, L; Bogliolo, M; Lázaro, C; Blanco, I; Brunet, J; Aguilar, H; Fernández Rodríguez, J; Seal, S; Renwick, A; Rahman, N; Kühl, J; Neveling, K; Schindler, D; Ramírez, M; Castellà, M; Hernández, G; Embrace, ; Easton, D; Peock, S; Cook, M; Oliver, C; Frost, D; Platte, R; Evans, D; Lalloo, F; Eeles, R; Izatt, L; Chu, C; Davidson, R; Ong, K; Cook, J; Douglas, F; Hodgson, S; Brewer, C; Morrison, P; Porteous, M; Peterlongo, P; Manoukian, S; Peissel, B; Zaffaroni, D; Roversi, G; Barile, M; Viel, A; Pasini, B; Ottini, L; Putignano, A; Savarese, A; Bernard, L; Radice, P; Healey, S; Spurdle, A; Chen, X; Beesley, J; Rookus, M; Verhoef, S; Tilanus Linthorst, M; Vreeswijk, M; Asperen, C; Bodmer, D; Ausems, M; van Os, T; Blok, M; Meijers Heijboer, H; Hogervorst, F; Goldgar, D; Buys, S; John, E; Miron, A; Southey, M; Daly, M; Harbst, K; Borg, A; Rantala, J; Barbany Bustinza, G; Ehrencrona, H; Stenmark Askmalm, M; Kaufman, B; Laitman, Y; Milgrom, R; Friedman, E; Domchek, S; Nathanson, K; Rebbeck, T; Johannsson, O; Couch, F; Wang, X; Fredericksen, Z; Cuadras, D; Moreno, V; Pientka, F; Depping, R; Caldés, T; Osorio, A; Benítez, J; Bueren, J; Heikkinen, T; Nevanlinna, H; Hamann, U; Torres, D; Caligo, M; Godwin, A; Imyanitov, E; Janavicius, R; Sinilnikova, O; Stoppa Lyonnet, D; Mazoyer, S; Verny Pierre, C; Castera, L; de Pauw, A; Bignon, Y; Uhrhammer, N; Peyrat, J; Vennin, P; Ferrer, S; Collonge Rame, M; Mortemousque, I; Mcguffog, L; Chenevix Trench, G; Pereira Smith, O; Antoniou, A; Cerón, J; Tominaga, K; Surrallés, J; Pujana, M
Evidence for a link between TNFRSF11A and risk of breast cancer
2011 Bonifaci, N; Palafox, M; Pellegrini, P; Osorio, A; Benítez, J; Peterlongo, P; Manoukian, S; Peissel, B; Zaffaroni, D; Roversi, G; Barile, M; Viel, A; Mariette, F; Bernard, L; Radice, P; Kaufman, B; Laitman, Y; Milgrom, R; Friedman, E; Sáez, M; Climent, F; Soler, M; Diez, O; Balmaña, J; Lasa, A; Ramón y. Cajal, T; Miramar, M; De la Hoya, M; Pérez Segura, P; Caldés, T; Moreno, V; Urruticoechea, A; Brunet, J; Lázaro, C; Blanco, I; Pujana, M; González Suárez, E
The CASP8 rs3834129 polymorphism and breast cancer risk in BRCA1 mutation carriers
2011 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
Differential cytogenomics and miRNA signature of the Acute Myeloid Leukaemia Kasumi-1 cell line CD34+38- compartment
2010 Pedranzini, L; Mottadelli, F; Ronzoni, S; Rossella, F; Ferracin, M; Magnani, I; Roversi, G; Colapietro, P; Negrini, M; Pelicci, P; Larizza, L
Targeted next-generation sequencing appoints c16orf57 as clericuzio-type poikiloderma with neutropenia gene
2010 Volpi, L; Roversi, G; Colombo, E; Leijsten, N; Concolino, D; Calabria, A; Mencarelli, M; Fimiani, M; Macciardi, F; Pfundt, R; Schoenmakers, E; Larizza, L
Rothmund-Thomson syndrome
2010 Larizza, L; Roversi, G; Volpi, L
Clericuzio-type poikiloderma with neutropenia syndrome in three sibs with mutations in the C16orf57 gene: delineation of the phenotype
2010 Concolino, D; Roversi, G; Muzzi, G; Sestito, S; Colombo, E; Volpi, L; Larizza, L; Strisciuglio, P
Multiple localization of endogenous MARK4L protein in human glioma
2009 Magnani, I; Novielli, C; Bellini, M; Roversi, G; Bello, L; Larizza, L
Search for genomic imbalances in a cohort of 24 Cornelia de Lange patients negative for mutations in the NIPBL and SMC1L1 genes
2008 Gervasini, C; Pfundt, R; Castronovo, P; Russo, S; Roversi, G; Masciadri, M; Milani, D; Zampino, G; Selicorni, A; Schoenmakers, E; Larizza, L
Atypical Rothmund-Thomson syndrome in a patient with compound Heterozygous Mutations in RECQL4 Gene and phenotypic features in RECQL4 syndromes
2008 Sznajer, Y; Siitonen, H; Roversi, G; Dangoisse, C; Scaillon, M; Ziereisen, F; Tenoutasse, S; Kestilä, M; Larizza, L
Piebald trait: implication of kit mutation on in vitro melanocyte survival and on the clinical application of cultured epidermal autografts
2007 Bondanza, S; Bellini, M; Roversi, G; Raskovic, D; Maurelli, R; Paionni, E; Paterna, P; Dellambra, E; Larizza, L; Guerra, L
Identification of novel genomic markers related to progression to glioblastoma through genomic profiling of 25 primary glioma cell lines
2006 Roversi, G; Pfundt, R; Moroni, R; Magnani, I; van Reijmersdal, S; Pollo, B; Straatman, H; Larizza, L; Schoenmakers, E
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