Sfoglia per Rivista FRONTIERS IN GENETICS
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 |
|---|---|---|---|
| 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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