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A genetic model for determining MSH2 and MLH1 carrier probabilities based on family history and tumor microsatellite instability
2006 Marroni, F; Pastrello, C; Benatti, P; Torrini, M; Barana, D; Cordisco, E; Viel, A; Mareni, C; Oliani, C; Genuardi, Maurizio; Bailey-Wilson, J; de Leon, M; Presciuttini, S
Genetic susceptibility in pharmacodynamic and pharmacokinetic pathways underlying drug-induced arrhythmia and sudden unexplained deaths
2019 Martinez-Matilla, M.; Blanco-Verea, A.; Santori, M.; Ansede-Bermejo, J.; Ramos-Luis, E.; Gil, R.; Bermejo, A. M.; Lotufo-Neto, F.; Hirata, M. H.; Brisighelli, Francesca; Paramo, M.; Carracedo, A.; Brion, M.
Genetic testing among high-risk individuals in families with hereditary nonpolyposis colorectal cancer
2004 de Leon, M; Benatti, P; Di Gregorio, C; Pedroni, M; Losi, L; Genuardi, M; Viel, A; Fornasarig, M; Lucci-Cordisco, E; Anti, M; Ponti, G; Borghi, F; Lamberti, I; Roncucci, L
Genetic testing of cancer predisposition
2000 Genuardi, M; Caluseriu, O; Cordisco, E; Rovella, V; Neri, G
A genetically unique Chinese cattle population shows evidence of common ancestry with wild species when analysed with a reduced ascertainment bias SNP panel
2020 Barbato, Mario; Reichel, M. P.; Passamonti, Matilde Maria; Low, W. Y.; Colli, Licia; Tearle, R.; Williams, John Lewis; Ajmone Marsan, Paolo
A genome-wide association study implicates the BMP7 locus as a risk factor for nonsyndromic metopic craniosynostosis
2020 Justice, Cm; Cuellar, A; Bala, K; Sabourin, Ja; Cunningham, Ml; Crawford, K; Phipps, Jm; Zhou, Y; Cilliers, D; Byren, Jc; Johnson, D; Wall, Sa; Morton, Jev; Noons, P; Sweeney, E; Weber, Bertram; Rees, Kem; Wilson, Lc; Simeonov, E; Kaneva, R; Yaneva, N; Georgiev, K; Bussarsky, A; Senders, C; Zwienenberg, M; Boggan, J; Roscioli, T; Tamburrini, Gianpiero; Barba, Marta; Conway, K; Sheffield, Vc; Brody, L; Mills, Jl; Kay, D; Sicko, Rj; Langlois, Ph; Tittle, Rk; Botto, Ld; Jenkins, Mm; Lasalle, Jm; Lattanzi, Wanda; Wilkie, Aom; Wilson, Af; Romitti, Pa; Boyadjiev, Sa
Genome-wide association study of sporadic brain arteriovenous malformations
2016 Weinsheimer, Shantel; Bendjilali, Nasrine; Nelson, Jeffrey; Guo, Diana E; Zaroff, Jonathan G; Sidney, Stephen; Mcculloch, Charles E; Al Shahi Salman, Rustam; Berg, Jonathan N; Koeleman, Bobby P. C; Simon, Matthias; Bostroem, Azize; Fontanella, Marco; Sturiale, Carmelo Lucio; Pola, Roberto; Puca, Alfredo; Lawton, Michael T; Young, William L; Pawlikowska, Ludmila; Klijn, Catharina J. M; Kim, Helen
Genome-wide methylation analysis demonstrates that 5-aza-2-deoxycytidine treatment does not cause random DNA demethylation in fragile X syndrome cells
2016 Tabolacci, Elisabetta; Mancano, Giorgia; Lanni, Stella; Palumbo, Federica; Goracci, Martina; Ferrè, Fabrizio; Helmer Citterich, Manuela; Neri, Giovanni
Genomic instability and target gene mutations in colon cancers with different degrees of allelic shifts
2000 Percesepe, A; Pedroni, M; Sala, E; Menigatti, M; Borghi, F; Losi, L; Viel, A; Genuardi, Maurizio; Benatti, P; Roncucci, L; Peltomaki, P; de Leon, M
Genomic rearrangements of the CDKN2A locus are infrequent in Italian malignant melanoma families without evidence of CDKN2A/CDK4 point mutations
2008 Vignoli, M; Scaini, M; Ghiorzo, P; Sestini, R; Bruno, W; Menin, C; Gensini, F; Piazzini, M; Testori, A; Manoukian, S; Orlando, C; D'Andrea, E; Bianchi-Scarra, G; Genuardi, Maurizio
Genomic signatures of adaptive introgression from European mouflon into domestic sheep
2017 Barbato, Mario; Hailer, Frank; Orozco-Terwengel, Pablo; Kijas, James; Mereu, Paolo; Cabras, Pierangela; Mazza, Raffaele; Pirastru, Monica; Bruford, Michael W.
Genotype-phenotype associations in a large PTEN Hamartoma Tumor Syndrome (PHTS) patient cohort
2022 Hendricks, Laj; Hoogerbrugge, N; Venselaar, H; Aretz, S; Spier, I; Legius, E; Brems, H; de Putter, R; Claes, Kbm; Evans, Dg; Woodward, Er; Genuardi, Maurizio; Brugnoletti, F; van Ierland, Y; Dijke, K; Tham, E; Tesi, B; Schuurs-Hoeijmakers, Jhm; Branchaud, M; Salvador, H; Jahn, A; Schnaiter, S; Anastasiadou, Vc; Brunet, J; Oliveira, C; Roht, L; Blatnik, A; Irmejs, A; Mensenkamp, Ar; Vos, Jr
Germinal mosaicism for a deletion of the FMR1 gene leading to fragile X syndrome
2016 Jiraanont, P.; Hagerman, R. J.; Neri, Giovanni; Zollino, Marcella; Murdolo, Marina; Tassone, Francesco
A girl with a 14.7 Mb 3q26.32-q28 duplication: A new report of 3q duplication syndrome and a literature review
2016 Pavone, Piero; Praticò, Andrea D.; Falsaperla, Raffaele; Ruggieri, Martino; Neri, Giovanni; Pavone, Vito; Zollino, Marcella
Glioblastoma cusa fluid protein profiling: A comparative investigation of the core and peripheral tumor zones
2021 La Rocca, Giuseppe; Simboli, G. A.; Vincenzoni, F.; Rossetti, Diana Valeria; Urbani, Andrea; Ius, T.; Della Pepa, Giuseppe Maria; Olivi, Alessandro; Sabatino, Giovanni; Desiderio, Claudia
Gut microbiota composition and frailty in elderly patients with Chronic Kidney Disease
2020 Margiotta, Elisabetta; Miragoli, Francesco; Callegari, Maria Luisa; Vettoretti, Simone; Caldiroli, Lara; Meneghini, Maria; Zanoni, Francesca; Messa, Piergiorgio
Gut microbiota in monozygotic twins discordant for Parkinson's disease
2022 Bolliri, Carlotta; Fontana, Alessandra; Cereda, Emanuele; Barichella, Michela; Cilia, Roberto; Ferri, Valentina; Caronni, Serena; Calandrella, Daniela; Morelli, Lorenzo; Pezzoli, Gianni
Hereditary colorectal cancer in the general population: from cancer registration to molecular diagnosis
1999 de Leon, M; Pedroni, M; Benatti, P; Percesepe, A; Di Gregorio, Cristina; Foroni, M; Rossi, G; Genuardi, Maurizio; Neri, G; Leonardi, F; Viel, A; Capozzi, E; Boiocchi, M; Roncucci, L
Hereditary nonpolyposis colorectal cancer: Review of clinical, molecular genetics, and counseling aspects
1996 Bellacosa, A; Genuardi, Maurizio; Anti, M; Viel, A; Deleon, M
Hereditary spastic paraplegia: Novel mutations and expansion of the phenotype variability in SPG56
2016 Masciullo, Marcella; Tessa, A.; Perazza, S.; Santorelli, F. M.; Perna, Alessia; Silvestri, Gabriella
| Data di pubblicazione | Titolo | Autore(i) | File |
|---|---|---|---|
| 1-gen-2006 | A genetic model for determining MSH2 and MLH1 carrier probabilities based on family history and tumor microsatellite instability | Marroni, F; Pastrello, C; Benatti, P; Torrini, M; Barana, D; Cordisco, E; Viel, A; Mareni, C; Oliani, C; Genuardi, Maurizio; Bailey-Wilson, J; de Leon, M; Presciuttini, S | |
| 1-gen-2019 | Genetic susceptibility in pharmacodynamic and pharmacokinetic pathways underlying drug-induced arrhythmia and sudden unexplained deaths | Martinez-Matilla, M.; Blanco-Verea, A.; Santori, M.; Ansede-Bermejo, J.; Ramos-Luis, E.; Gil, R.; Bermejo, A. M.; Lotufo-Neto, F.; Hirata, M. H.; Brisighelli, Francesca; Paramo, M.; Carracedo, A.; Brion, M. | |
| 1-gen-2004 | Genetic testing among high-risk individuals in families with hereditary nonpolyposis colorectal cancer | de Leon, M; Benatti, P; Di Gregorio, C; Pedroni, M; Losi, L; Genuardi, M; Viel, A; Fornasarig, M; Lucci-Cordisco, E; Anti, M; Ponti, G; Borghi, F; Lamberti, I; Roncucci, L | |
| 1-gen-2000 | Genetic testing of cancer predisposition | Genuardi, M; Caluseriu, O; Cordisco, E; Rovella, V; Neri, G | |
| 1-gen-2020 | A genetically unique Chinese cattle population shows evidence of common ancestry with wild species when analysed with a reduced ascertainment bias SNP panel | Barbato, Mario; Reichel, M. P.; Passamonti, Matilde Maria; Low, W. Y.; Colli, Licia; Tearle, R.; Williams, John Lewis; Ajmone Marsan, Paolo | |
| 1-gen-2020 | A genome-wide association study implicates the BMP7 locus as a risk factor for nonsyndromic metopic craniosynostosis | Justice, Cm; Cuellar, A; Bala, K; Sabourin, Ja; Cunningham, Ml; Crawford, K; Phipps, Jm; Zhou, Y; Cilliers, D; Byren, Jc; Johnson, D; Wall, Sa; Morton, Jev; Noons, P; Sweeney, E; Weber, Bertram; Rees, Kem; Wilson, Lc; Simeonov, E; Kaneva, R; Yaneva, N; Georgiev, K; Bussarsky, A; Senders, C; Zwienenberg, M; Boggan, J; Roscioli, T; Tamburrini, Gianpiero; Barba, Marta; Conway, K; Sheffield, Vc; Brody, L; Mills, Jl; Kay, D; Sicko, Rj; Langlois, Ph; Tittle, Rk; Botto, Ld; Jenkins, Mm; Lasalle, Jm; Lattanzi, Wanda; Wilkie, Aom; Wilson, Af; Romitti, Pa; Boyadjiev, Sa | |
| 1-gen-2016 | Genome-wide association study of sporadic brain arteriovenous malformations | Weinsheimer, Shantel; Bendjilali, Nasrine; Nelson, Jeffrey; Guo, Diana E; Zaroff, Jonathan G; Sidney, Stephen; Mcculloch, Charles E; Al Shahi Salman, Rustam; Berg, Jonathan N; Koeleman, Bobby P. C; Simon, Matthias; Bostroem, Azize; Fontanella, Marco; Sturiale, Carmelo Lucio; Pola, Roberto; Puca, Alfredo; Lawton, Michael T; Young, William L; Pawlikowska, Ludmila; Klijn, Catharina J. M; Kim, Helen | |
| 1-gen-2016 | Genome-wide methylation analysis demonstrates that 5-aza-2-deoxycytidine treatment does not cause random DNA demethylation in fragile X syndrome cells | Tabolacci, Elisabetta; Mancano, Giorgia; Lanni, Stella; Palumbo, Federica; Goracci, Martina; Ferrè, Fabrizio; Helmer Citterich, Manuela; Neri, Giovanni | |
| 1-gen-2000 | Genomic instability and target gene mutations in colon cancers with different degrees of allelic shifts | Percesepe, A; Pedroni, M; Sala, E; Menigatti, M; Borghi, F; Losi, L; Viel, A; Genuardi, Maurizio; Benatti, P; Roncucci, L; Peltomaki, P; de Leon, M | |
| 1-gen-2008 | Genomic rearrangements of the CDKN2A locus are infrequent in Italian malignant melanoma families without evidence of CDKN2A/CDK4 point mutations | Vignoli, M; Scaini, M; Ghiorzo, P; Sestini, R; Bruno, W; Menin, C; Gensini, F; Piazzini, M; Testori, A; Manoukian, S; Orlando, C; D'Andrea, E; Bianchi-Scarra, G; Genuardi, Maurizio | |
| 1-gen-2017 | Genomic signatures of adaptive introgression from European mouflon into domestic sheep | Barbato, Mario; Hailer, Frank; Orozco-Terwengel, Pablo; Kijas, James; Mereu, Paolo; Cabras, Pierangela; Mazza, Raffaele; Pirastru, Monica; Bruford, Michael W. | |
| 1-gen-2022 | Genotype-phenotype associations in a large PTEN Hamartoma Tumor Syndrome (PHTS) patient cohort | Hendricks, Laj; Hoogerbrugge, N; Venselaar, H; Aretz, S; Spier, I; Legius, E; Brems, H; de Putter, R; Claes, Kbm; Evans, Dg; Woodward, Er; Genuardi, Maurizio; Brugnoletti, F; van Ierland, Y; Dijke, K; Tham, E; Tesi, B; Schuurs-Hoeijmakers, Jhm; Branchaud, M; Salvador, H; Jahn, A; Schnaiter, S; Anastasiadou, Vc; Brunet, J; Oliveira, C; Roht, L; Blatnik, A; Irmejs, A; Mensenkamp, Ar; Vos, Jr | |
| 1-gen-2016 | Germinal mosaicism for a deletion of the FMR1 gene leading to fragile X syndrome | Jiraanont, P.; Hagerman, R. J.; Neri, Giovanni; Zollino, Marcella; Murdolo, Marina; Tassone, Francesco | |
| 1-gen-2016 | A girl with a 14.7 Mb 3q26.32-q28 duplication: A new report of 3q duplication syndrome and a literature review | Pavone, Piero; Praticò, Andrea D.; Falsaperla, Raffaele; Ruggieri, Martino; Neri, Giovanni; Pavone, Vito; Zollino, Marcella | |
| 1-gen-2021 | Glioblastoma cusa fluid protein profiling: A comparative investigation of the core and peripheral tumor zones | La Rocca, Giuseppe; Simboli, G. A.; Vincenzoni, F.; Rossetti, Diana Valeria; Urbani, Andrea; Ius, T.; Della Pepa, Giuseppe Maria; Olivi, Alessandro; Sabatino, Giovanni; Desiderio, Claudia | |
| 1-gen-2020 | Gut microbiota composition and frailty in elderly patients with Chronic Kidney Disease | Margiotta, Elisabetta; Miragoli, Francesco; Callegari, Maria Luisa; Vettoretti, Simone; Caldiroli, Lara; Meneghini, Maria; Zanoni, Francesca; Messa, Piergiorgio | |
| 1-gen-2022 | Gut microbiota in monozygotic twins discordant for Parkinson's disease | Bolliri, Carlotta; Fontana, Alessandra; Cereda, Emanuele; Barichella, Michela; Cilia, Roberto; Ferri, Valentina; Caronni, Serena; Calandrella, Daniela; Morelli, Lorenzo; Pezzoli, Gianni | |
| 1-gen-1999 | Hereditary colorectal cancer in the general population: from cancer registration to molecular diagnosis | de Leon, M; Pedroni, M; Benatti, P; Percesepe, A; Di Gregorio, Cristina; Foroni, M; Rossi, G; Genuardi, Maurizio; Neri, G; Leonardi, F; Viel, A; Capozzi, E; Boiocchi, M; Roncucci, L | |
| 1-gen-1996 | Hereditary nonpolyposis colorectal cancer: Review of clinical, molecular genetics, and counseling aspects | Bellacosa, A; Genuardi, Maurizio; Anti, M; Viel, A; Deleon, M | |
| 1-gen-2016 | Hereditary spastic paraplegia: Novel mutations and expansion of the phenotype variability in SPG56 | Masciullo, Marcella; Tessa, A.; Perazza, S.; Santorelli, F. M.; Perna, Alessia; Silvestri, Gabriella |
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