Sfoglia per Rivista FRONTIERS IN GENETICS
Association of Genetic Variants Affecting microRNAs and Pancreatic Cancer Risk
2021-01-01 Lu, Ye; Corradi, Chiara; Gentiluomo, Manuel; López de Maturana, Evangelina; Theodoropoulos, George E; Roth, Susanne; Maiello, Evaristo; Morelli, Luca; Archibugi, Livia; Izbicki, Jakob R; Sarlós, Patricia; Kiudelis, Vytautas; Oliverius, Martin; Aoki, Mateus Nóbrega; Vashist, Yogesh; van Eijck, Casper H J; Gazouli, Maria; Talar-Wojnarowska, Renata; Mambrini, Andrea; Pezzilli, Raffaele; Bueno-de-Mesquita, Bas; Hegyi, Péter; Souček, Pavel; Neoptolemos, John P; Di Franco, Gregorio; Sperti, Cosimo; Kauffmann, Emanuele F; Hlaváč, Viktor; Uzunoğlu, Faik G; Ermini, Stefano; Małecka-Panas, Ewa; Lucchesi, Maurizio; Vanella, Giuseppe; Dijk, Frederike; Mohelníková-Duchoňová, Beatrice; Bambi, Franco; Petrone, Maria Chiara; Jamroziak, Krzysztof; Guo, Feng; Kolarova, Katerina; Capretti, Giovanni; Milanetto, Anna Caterina; Ginocchi, Laura; Loveček, Martin; Puzzono, Marta; van Laarhoven, Hanneke W M; Carrara, Silvia; Ivanauskas, Audrius; Papiris, Konstantinos; Basso, Daniela; Arcidiacono, Paolo G; Izbéki, Ferenc; Chammas, Roger; Vodicka, Pavel; Hackert, Thilo; Pasquali, Claudio; Piredda, Maria L; Costello-Goldring, Eithne; Cavestro, Giulia Martina; Szentesi, Andrea; Tavano, Francesca; Włodarczyk, Barbara; Brenner, Hermann; Kreivenaite, Edita; Gao, Xin; Bunduc, Stefania; Vermeulen, Roel C H; Schneider, Martin A; Latiano, Anna; Gioffreda, Domenica; Testoni, Sabrina G G; Kupcinskas, Juozas; Lawlor, Rita T; Capurso, Gabriele; Malats, Núria; Campa, Daniele; Canzian, Federico
Case Report: A Novel ARMC5 Germline Mutation in a Patient with Primary Bilateral Macronodular Adrenal Hyperplasia and Hypogammaglobulinemia
2022-01-01 Vena, Walter; Morelli, Valentina; Carrabba, Maria; Elli, Francesca; Fabio, Giovanna; Muller, Ilaria; Lucca, Camilla; Maffini, Maria Antonia; Lania, Andrea Gerardo; Mantovani, Giovanna; Arosio, Maura
Disruption of c-MYC Binding and Chromosomal Looping Involving Genetic Variants Associated With Ankylosing Spondylitis Upstream of the RUNX3 Promoter
2022-01-01 Cohen, Carla J; Davidson, Connor; Selmi, Carlo; Bowness, Paul; Knight, Julian C; Wordsworth, B Paul; Vecellio, Matteo
Editorial: RNA Splicing and Backsplicing: Disease and Therapy
2020-01-01 Asselta, Rosanna; Duga, Stefano; Velasco, Eladio Andrés; Buratti, Emanuele
First Replication of the Involvement of OTUD6B in Intellectual Disability Syndrome With Seizures and Dysmorphic Features
2018-01-01 Straniero, L; Rimoldi, V; Solda, G; Bellini, M; Biasucci, G; Asselta, R; Duga, S
Genomic Analysis Revealed New Oncogenic Signatures in TP53-Mutant Hepatocellular Carcinoma
2018-01-01 Kancherla, Venkatesh; Abdullazade, Samir; Matter Matthias, S.; Lanzafame, Manuela; Quagliata, Luca; Roma, Guglielmo; Hoshida, Yujin; Terracciano Luigi, M.; Ng, KIU YAN CHARLOTTE; Piscuoglio, Salvatore
Interpreting Non-coding Genetic Variation in Multiple Sclerosis Genome-Wide Associated Regions.
2018-01-01 Paraboschi, E; Cardamone, G; Solda', G; Duga, S; Asselta, R.
Network Diffusion Promotes the Integrative Analysis of Multiple Omics
2020-01-01 Noemi Di, Nanni; Bersanelli, Matteo; Luciano, Milanesi; Ettore, Mosca
Network Diffusion-Based Prioritization of Autism Risk Genes Identifies Significantly Connected Gene Modules
2017-01-01 Mosca, Ettore; Bersanelli, Matteo; Gnocchi, Matteo; Moscatelli, Marco; Castellani, Gastone; Milanesi, Luciano; Mezzelani, Alessandra
SLC22A4 Gene in Hereditary Non-syndromic Hearing Loss: Recurrence and Incomplete Penetrance of the p.C113Y Mutation in Northwest Africa
2021-01-01 Chiereghin, Chiara; Robusto, Michela; Mauri, Lucia; Primignani, Paola; Castorina, Pierangela; Ambrosetti, Umberto; Duga, Stefano; Asselta, Rosanna; Soldà, Giulia
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Association of Genetic Variants Affecting microRNAs and Pancreatic Cancer Risk | 1-gen-2021 | Lu, Ye; Corradi, Chiara; Gentiluomo, Manuel; López de Maturana, Evangelina; Theodoropoulos, George E; Roth, Susanne; Maiello, Evaristo; Morelli, Luca; Archibugi, Livia; Izbicki, Jakob R; Sarlós, Patricia; Kiudelis, Vytautas; Oliverius, Martin; Aoki, Mateus Nóbrega; Vashist, Yogesh; van Eijck, Casper H J; Gazouli, Maria; Talar-Wojnarowska, Renata; Mambrini, Andrea; Pezzilli, Raffaele; Bueno-de-Mesquita, Bas; Hegyi, Péter; Souček, Pavel; Neoptolemos, John P; Di Franco, Gregorio; Sperti, Cosimo; Kauffmann, Emanuele F; Hlaváč, Viktor; Uzunoğlu, Faik G; Ermini, Stefano; Małecka-Panas, Ewa; Lucchesi, Maurizio; Vanella, Giuseppe; Dijk, Frederike; Mohelníková-Duchoňová, Beatrice; Bambi, Franco; Petrone, Maria Chiara; Jamroziak, Krzysztof; Guo, Feng; Kolarova, Katerina; Capretti, Giovanni; Milanetto, Anna Caterina; Ginocchi, Laura; Loveček, Martin; Puzzono, Marta; van Laarhoven, Hanneke W M; Carrara, Silvia; Ivanauskas, Audrius; Papiris, Konstantinos; Basso, Daniela; Arcidiacono, Paolo G; Izbéki, Ferenc; Chammas, Roger; Vodicka, Pavel; Hackert, Thilo; Pasquali, Claudio; Piredda, Maria L; Costello-Goldring, Eithne; Cavestro, Giulia Martina; Szentesi, Andrea; Tavano, Francesca; Włodarczyk, Barbara; Brenner, Hermann; Kreivenaite, Edita; Gao, Xin; Bunduc, Stefania; Vermeulen, Roel C H; Schneider, Martin A; Latiano, Anna; Gioffreda, Domenica; Testoni, Sabrina G G; Kupcinskas, Juozas; Lawlor, Rita T; Capurso, Gabriele; Malats, Núria; Campa, Daniele; Canzian, Federico | |
| Case Report: A Novel ARMC5 Germline Mutation in a Patient with Primary Bilateral Macronodular Adrenal Hyperplasia and Hypogammaglobulinemia | 1-gen-2022 | Vena, Walter; Morelli, Valentina; Carrabba, Maria; Elli, Francesca; Fabio, Giovanna; Muller, Ilaria; Lucca, Camilla; Maffini, Maria Antonia; Lania, Andrea Gerardo; Mantovani, Giovanna; Arosio, Maura | |
| Disruption of c-MYC Binding and Chromosomal Looping Involving Genetic Variants Associated With Ankylosing Spondylitis Upstream of the RUNX3 Promoter | 1-gen-2022 | Cohen, Carla J; Davidson, Connor; Selmi, Carlo; Bowness, Paul; Knight, Julian C; Wordsworth, B Paul; Vecellio, Matteo | |
| Editorial: RNA Splicing and Backsplicing: Disease and Therapy | 1-gen-2020 | Asselta, Rosanna; Duga, Stefano; Velasco, Eladio Andrés; Buratti, Emanuele | |
| First Replication of the Involvement of OTUD6B in Intellectual Disability Syndrome With Seizures and Dysmorphic Features | 1-gen-2018 | Straniero, L; Rimoldi, V; Solda, G; Bellini, M; Biasucci, G; Asselta, R; Duga, S | |
| Genomic Analysis Revealed New Oncogenic Signatures in TP53-Mutant Hepatocellular Carcinoma | 1-gen-2018 | Kancherla, Venkatesh; Abdullazade, Samir; Matter Matthias, S.; Lanzafame, Manuela; Quagliata, Luca; Roma, Guglielmo; Hoshida, Yujin; Terracciano Luigi, M.; Ng, KIU YAN CHARLOTTE; Piscuoglio, Salvatore | |
| Interpreting Non-coding Genetic Variation in Multiple Sclerosis Genome-Wide Associated Regions. | 1-gen-2018 | Paraboschi, E; Cardamone, G; Solda', G; Duga, S; Asselta, R. | |
| Network Diffusion Promotes the Integrative Analysis of Multiple Omics | 1-gen-2020 | Noemi Di, Nanni; Bersanelli, Matteo; Luciano, Milanesi; Ettore, Mosca | |
| Network Diffusion-Based Prioritization of Autism Risk Genes Identifies Significantly Connected Gene Modules | 1-gen-2017 | Mosca, Ettore; Bersanelli, Matteo; Gnocchi, Matteo; Moscatelli, Marco; Castellani, Gastone; Milanesi, Luciano; Mezzelani, Alessandra | |
| SLC22A4 Gene in Hereditary Non-syndromic Hearing Loss: Recurrence and Incomplete Penetrance of the p.C113Y Mutation in Northwest Africa | 1-gen-2021 | Chiereghin, Chiara; Robusto, Michela; Mauri, Lucia; Primignani, Paola; Castorina, Pierangela; Ambrosetti, Umberto; Duga, Stefano; Asselta, Rosanna; Soldà, Giulia |
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