ROVERSI, GAIA
ROVERSI, GAIA
DIPARTIMENTO DI MEDICINA E CHIRURGIA (SCHOOL OF MEDICINE AND SURGERY)
RNA hyperediting and alternative splicing of hematopoietic cell phosphatase (PTPN6) gene in acute myeloid leukemia
2000 Beghini, A; Ripamonti, C; Peterlongo, P; Roversi, G; Cairoli, R; Morra, E; Larizza, L
Germline mutation in the juxtamembrane domain of the kit gene in a family with gastrointestinal stromal tumors and urticaria pigmentosa
2001 Beghini, A; Tibiletti, M; Roversi, G; Chiaravalli, A; Serio, G; Capella, C; Larizza, L
Identification of two novel RECQL4 exonic SNPs and genomic characterization of the IVS12 minisatellite
2003 Roversi, G; Beghini, A; Zambruno, G; Paradisi, M; Larizza, L
The neural progenitor-restricted isoform of the MARK4 gene in 19q13.2 is upregulated in human gliomas and overexpressed in a subset of glioblastoma cell lines
2003 Beghini, A; Magnani, I; Roversi, G; Piepoli, T; Di Terlizzi, S; Moroni, R; Pollo, B; Conti, A; Cowell, J; Finocchiaro, G; Larizza, L
RNA processing defects of the helicase gene RECQL4 in a compound heterozygous Rothmund-Thomson patient
2003 Beghini, A; Castorina, P; Roversi, G; Modiano, P; Larizza, L
Identification of oligodendroglioma specific chromosomal copy number changes in the glioblastoma MI-4 cell line by array-CGH and FISH analyses
2005 Magnani, I; Moroni, R; Ramona, R; Roversi, G; Beghini, A; Pfundt, R; Schoenmakers, E; Larizza, L
Rothmund-Thomson syndrome and RECQL4 defect: splitting and lumping
2006 Larizza, L; Magnani, I; Roversi, G
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
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
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
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
Multiple localization of endogenous MARK4L protein in human glioma
2009 Magnani, I; Novielli, C; Bellini, M; Roversi, G; Bello, L; Larizza, 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
Rothmund-Thomson syndrome
2010 Larizza, L; Roversi, G; Volpi, 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
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
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
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
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