| Long noncoding RNAs in mouse embryonic stem cell pluripotency and differentiation ME Dinger, PP Amaral, TR Mercer, KC Pang, SJ Bruce, BB Gardiner, ... Genome research 18 (9), 1433-1445, 2008 | 910 | 2008 |
| Survival and dementia in GBA‐associated Parkinson's disease: The mutation matters R Cilia, S Tunesi, G Marotta, E Cereda, C Siri, S Tesei, AL Zecchinelli, ... Annals of neurology 80 (5), 662-673, 2016 | 391 | 2016 |
| A transcriptional sketch of a primary human breast cancer by 454 deep sequencing A Guffanti, M Iacono, P Pelucchi, N Kim, G Soldà, LJ Croft, RJ Taft, E Rizzi, ... BMC genomics 10, 1-17, 2009 | 288 | 2009 |
| Expression of distinct RNAs from 3′ untranslated regions TR Mercer, D Wilhelm, ME Dinger, G Solda, DJ Korbie, EA Glazov, ... Nucleic acids research 39 (6), 2393-2403, 2011 | 248 | 2011 |
| A novel mutation within the MIR96 gene causes non-syndromic inherited hearing loss in an Italian family by altering pre-miRNA processing G Solda, M Robusto, P Primignani, P Castorina, E Benzoni, A Cesarani, ... Human molecular genetics 21 (3), 577-585, 2012 | 126 | 2012 |
| Genetic association and altered gene expression of mir-155 in multiple sclerosis patients EM Paraboschi, G Soldà, D Gemmati, E Orioli, G Zeri, MD Benedetti, ... International journal of molecular sciences 12 (12), 8695-8712, 2011 | 124 | 2011 |
| Tumor-derived prostaglandin E2 promotes p50 NF-κB-dependent differentiation of monocytic MDSCs C Porta, FM Consonni, S Morlacchi, S Sangaletti, A Bleve, MG Totaro, ... Cancer research 80 (13), 2874-2888, 2020 | 109 | 2020 |
| The Characterization of GSDMB Splicing and Backsplicing Profiles Identifies Novel Isoforms and a Circular RNA That Are Dysregulated in Multiple Sclerosis G Cardamone, EM Paraboschi, V Rimoldi, S Duga, G Soldà, R Asselta International journal of molecular sciences 18 (3), 576, 2017 | 100 | 2017 |
| Glucocerebrosidase mutations in primary parkinsonism R Asselta, V Rimoldi, C Siri, R Cilia, I Guella, S Tesei, G Solda, G Pezzoli, ... Parkinsonism & related disorders 20 (11), 1215-1220, 2014 | 85 | 2014 |
| The GBAP1 pseudogene acts as a ceRNA for the glucocerebrosidase gene GBA by sponging miR-22-3p L Straniero, V Rimoldi, M Samarani, S Goldwurm, A Di Fonzo, R Krüger, ... Scientific reports 7 (1), 12702, 2017 | 81 | 2017 |
| Radiomics and gene expression profile to characterise the disease and predict outcome in patients with lung cancer M Kirienko, M Sollini, M Corbetta, E Voulaz, N Gozzi, M Interlenghi, ... European journal of nuclear medicine and molecular imaging 48, 3643-3655, 2021 | 75 | 2021 |
| DNAJC12 and dopa‐responsive nonprogressive parkinsonism L Straniero, I Guella, R Cilia, L Parkkinen, V Rimoldi, A Young, R Asselta, ... Annals of neurology 82 (4), 640-646, 2017 | 72 | 2017 |
| TUBA4A gene analysis in sporadic amyotrophic lateral sclerosis: identification of novel mutations V Pensato, C Tiloca, L Corrado, C Bertolin, V Sardone, R Del Bo, D Calini, ... Journal of neurology 262, 1376-1378, 2015 | 68 | 2015 |
| Not only cancer: the long non-coding RNA MALAT1 affects the repertoire of alternatively spliced transcripts and circular RNAs in multiple sclerosis G Cardamone, EM Paraboschi, G Soldà, C Cantoni, D Supino, L Piccio, ... Human molecular genetics 28 (9), 1414-1428, 2019 | 67 | 2019 |
| SNCA and MAPT genes: Independent and joint effects in Parkinson disease in the Italian population L Trotta, I Guella, G Soldà, F Sironi, S Tesei, M Canesi, G Pezzoli, ... Parkinsonism & related disorders 18 (3), 257-262, 2012 | 67 | 2012 |
| The SPID-GBA study: sex distribution, penetrance, incidence, and dementia in GBA-PD L Straniero, R Asselta, S Bonvegna, V Rimoldi, G Melistaccio, G Soldà, ... Neurology: Genetics 6 (6), e523, 2020 | 55 | 2020 |
| LINE1 are spliced in non-canonical transcript variants to regulate T cell quiescence and exhaustion F Marasca, S Sinha, R Vadalà, B Polimeni, V Ranzani, EM Paraboschi, ... Nature genetics 54 (2), 180-193, 2022 | 53 | 2022 |
| First independent replication of the involvement of LARS2 in Perrault syndrome by whole-exome sequencing of an Italian family G Soldà, S Caccia, M Robusto, C Chiereghin, P Castorina, U Ambrosetti, ... Journal of human genetics 61 (4), 295-300, 2016 | 43 | 2016 |
| Clinical and molecular characterisation of 21 patients affected by quantitative fibrinogen deficiency R Asselta, M Platè, M Robusto, M Borhany, I Guella, G Soldà, A Afrasiabi, ... Thrombosis and Haemostasis 113 (03), 567-576, 2015 | 42 | 2015 |
| Characterization of the genomic structure of the human neuronal nicotinic acetylcholine receptor CHRNA5/A3/B4 gene cluster and identification of novel intragenic polymorphisms S Duga, G Soldà, R Asselta, MT Bonati, L Dalprà, M Malcovati, ... Journal of human genetics 46 (11), 640-648, 2001 | 39 | 2001 |
