| 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 | 72 | 2017 |
| 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 | 68 | 2017 |
| The SPID-GBA study: sex distribution, penetrance, incidence, and dementia in GBA-PD L Straniero, R Asselta, S Bonvegna, V Rimoldi, G Melistaccio, G Soldą, ... Neurology: Genetics 6 (6), e523, 2020 | 44 | 2020 |
| The LRRK2 variant E193K prevents mitochondrial fission upon MPP+ treatment by altering LRRK2 binding to DRP1 M Perez Carrion, F Pischedda, A Biosa, I Russo, L Straniero, L Civiero, ... Frontiers in molecular neuroscience 11, 64, 2018 | 42 | 2018 |
| A lysosome–plasma membrane–sphingolipid axis linking lysosomal storage to cell growth arrest M Samarani, N Loberto, G Soldą, L Straniero, R Asselta, S Duga, ... The FASEB Journal 32 (10), 5685, 2018 | 35 | 2018 |
| Genome-wide association and meta-analysis of age at onset in Parkinson disease: evidence from the COURAGE-PD consortium S Grover, AA Kumar Sreelatha, L Pihlstrom, C Domenighetti, C Schulte, ... Neurology 99 (7), e698-e710, 2022 | 33 | 2022 |
| Mendelian randomisation study of smoking, alcohol, and coffee drinking in relation to Parkinson’s disease C Domenighetti, PE Sugier, AAK Sreelatha, C Schulte, S Grover, ... Journal of Parkinson's disease 12 (1), 267-282, 2022 | 28 | 2022 |
| Neurofascin (NFASC) gene mutation causes autosomal recessive ataxia with demyelinating neuropathy E Monfrini, L Straniero, S Bonato, GM Compagnoni, A Bordoni, R Dilena, ... Parkinsonism & Related Disorders 63, 66-72, 2019 | 24 | 2019 |
| 2, 6‐Difluorobenzamide Inhibitors of Bacterial Cell Division Protein FtsZ: Design, Synthesis, and Structure–Activity Relationships V Straniero, C Zanotto, L Straniero, A Casiraghi, S Duga, A Radaelli, ... ChemMedChem 12 (16), 1303-1318, 2017 | 24 | 2017 |
| Functional characterization of two novel splicing mutations in the OCA2 gene associated with oculocutaneous albinism type II V Rimoldi, L Straniero, R Asselta, L Mauri, E Manfredini, S Penco, ... Gene 537 (1), 79-84, 2014 | 21 | 2014 |
| Role of Lysosomal Gene Variants in Modulating GBA‐Associated Parkinson's Disease Risk L Straniero, V Rimoldi, E Monfrini, S Bonvegna, G Melistaccio, J Lake, ... Movement Disorders 37 (6), 1202-1210, 2022 | 20 | 2022 |
| First replication of the involvement of OTUD6B in intellectual disability syndrome with seizures and dysmorphic features L Straniero, V Rimoldi, G Soldą, M Bellini, G Biasucci, R Asselta, S Duga Frontiers in genetics 9, 417923, 2018 | 18 | 2018 |
| Dairy intake and Parkinson's disease: a Mendelian randomization study C Domenighetti, PE Sugier, A Ashok Kumar Sreelatha, C Schulte, ... Movement Disorders 37 (4), 857-864, 2022 | 17 | 2022 |
| SLC25A46 mutations in patients with Parkinson's Disease and optic atrophy G Bitetto, MC Malaguti, R Ceravolo, E Monfrini, L Straniero, A Morini, ... Parkinsonism & related disorders 74, 1-5, 2020 | 17 | 2020 |
| A Novel Homozygous VPS11 Variant May Cause Generalized Dystonia E Monfrini, F Cogiamanian, S Salani, L Straniero, G Fagiolari, ... Annals of Neurology 89 (4), 834-839, 2021 | 16 | 2021 |
| Chromosome transplantation: a possible approach to treat human X-linked disorders M Paulis, L Susani, A Castelli, T Suzuki, T Hara, L Straniero, S Duga, ... Molecular Therapy-Methods & Clinical Development 17, 369-377, 2020 | 13 | 2020 |
| Whole-gene CFTR sequencing combined with digital RT-PCR improves genetic diagnosis of cystic fibrosis L Straniero, G Soldą, L Costantino, M Seia, P Melotti, C Colombo, ... Journal of human genetics 61 (12), 977-984, 2016 | 13 | 2016 |
| β-Glucocerebrosidase deficiency activates an aberrant lysosome-plasma membrane axis responsible for the onset of neurodegeneration G Lunghi, EV Carsana, N Loberto, L Cioccarelli, S Prioni, L Mauri, R Bassi, ... Cells 11 (15), 2343, 2022 | 10 | 2022 |
| The Interaction between HLA‐DRB1 and Smoking in Parkinson's Disease Revisited C Domenighetti, V Douillard, PE Sugier, AAK Sreelatha, C Schulte, ... Movement Disorders 37 (9), 1929-1937, 2022 | 9 | 2022 |
| A rapid and low-cost test for screening the most common Parkinson's disease-related GBA variants L Straniero, V Rimoldi, G Melistaccio, A Di Fonzo, G Pezzoli, S Duga, ... Parkinsonism & Related Disorders 80, 138-141, 2020 | 8 | 2020 |
