| Mutational analysis of COASY in an Italian patient with NBIA G Annesi, M Gagliardi, G Iannello, A Quattrone Parkinsonism & Related Disorders 28, 150-151, 2016 | 26 | 2016 |
| C19orf12 gene mutations in patients with neurodegeneration with brain iron accumulation M Gagliardi, G Annesi, G Lesca, E Broussolle, G Iannello, V Vaiti, ... Parkinsonism & Related Disorders 21 (7), 813-816, 2015 | 25 | 2015 |
| A new SLC20A2 mutation identified in southern Italy family with primary familial brain calcification M Gagliardi, M Morelli, G Annesi, G Nicoletti, P Perrotta, G Pustorino, ... Gene 568 (1), 109-111, 2015 | 24 | 2015 |
| DNAJC13 mutation screening in patients with Parkinson's disease from South Italy M Gagliardi, G Annesi, R Procopio, M Morelli, G Iannello, G Bonapace, ... Parkinsonism & Related Disorders 55, 134-137, 2018 | 18 | 2018 |
| A new CHCHD2 mutation identified in a southern Italy patient with multiple system atrophy G Nicoletti, M Gagliardi, R Procopio, G Iannello, M Morelli, G Annesi, ... Parkinsonism & Related Disorders 47, 91-93, 2018 | 14 | 2018 |
| Corrigendum to “A new PLA2G6 mutation in a family with infantile neuroaxonal dystrophy”[J. Neurol. Sci. 381C (2017) 209–212] G Iannello, C Graziano, G Cenacchi, DM Cordelli, R Zuntini, V Papa, ... Journal of the Neurological Sciences 385, 238, 2018 | 13* | 2018 |
| Analysis of CHCHD2 gene in familial Parkinson's disease from Calabria M Gagliardi, G Iannello, C Colica, G Annesi, A Quattrone Neurobiology of Aging 50, 169. e5-169. e6, 2017 | 12 | 2017 |
| Simple, Fast, and Efficient Method for Derivation of Dermal Fibroblasts From Skin Biopsies G Iannello, A Patel, D Sirabella, AG Diaz, BN Hoover, H Sarmah, ... Current Protocols 3 (3), e714, 2023 | 10 | 2023 |
| Mutational analysis of TARDBP gene in patients affected by Parkinson's disease from Calabria M Gagliardi, G Arabia, R Nisticò, G Iannello, R Procopio, L Manfredini, ... Journal of the Neurological Sciences 390, 209-211, 2018 | 8 | 2018 |
| Intracellular FMRpolyG-Hsp70 complex in fibroblast cells from a patient affected by fragile X tremor ataxia syndrome G Bonapace, R Gullace, D Concolino, G Iannello, R Procopio, M Gagliardi, ... Heliyon 5 (6), 2019 | 7 | 2019 |
| A SLC20A2 mutation identified in an asymptomatic patient with brain calcification M Gagliardi, M Morelli, G Iannello, C Colica, G Annesi, A Quattrone Journal of the Neurological Sciences 372, 70-72, 2017 | 6 | 2017 |
| Endocrine and behavioural features of Lowe syndrome and their potential molecular mechanisms C Sena, G Iannello, AA Skowronski, K Dannheim, L Cheung, PB Agrawal, ... Journal of medical genetics 59 (12), 1171-1178, 2022 | 4 | 2022 |
| Efficient Cas9‐based Genome Editing Using CRISPR Analysis Webtools in Severe Early‐onset‐obesity Patient‐derived iPSCs A Patel, G Iannello, AG Diaz, D Sirabella, V Thaker, B Corneo Current protocols 2 (8), e519, 2022 | 4 | 2022 |
| Genetic study in a cohort of children with ROHHAD syndrome G Iannello, C Sena, L Pais, E Seaby, R Sathanayagam, N Ebrahim, ... Journal of the Endocrine Society 5 (Supplement_1), A503-A504, 2021 | 3 | 2021 |
| Role of G-protein coupled receptor kinase 5 gene in cognitive impairment in Parkinson's disease G Nicoletti, V De Luca, P Tarantino, M Gagliardi, G Iannello, F Novellino, ... Psychiatry Research 230 (3), 975-977, 2015 | 3 | 2015 |
| Corrigendum to “Generation of the iPSC line CUIMCi003-A derived from a patient with severe early onset obesity” G Iannello, A Patel, D Sirabella, B Corneo, V Thaker Stem cell research 61, 102778, 2022 | 2* | 2022 |
| Derivation and characterization of the induced pluripotent stem cell line CUIMCi004-A from a patient with a novel frameshift variant in exon 18a of OCRL G Iannello, A Patel, D Sirabella, B Corneo, VV Thaker Stem cell research 59, 102635, 2022 | 1 | 2022 |
| CRISPR-Cas9 Mediated Gene Deletion in Human Pluripotent Stem Cells Cultured Under Feeder-Free Conditions MA Sheikh, FH Afandi, G Iannello, B Corneo, BS Emerald, SA Ansari Journal of Visualized Experiments (JoVE), e67296, 2024 | | 2024 |
| Endocrine features of Lowe syndrome and their potential molecular mechanisms C Sena, G Iannello, A Skowronski, L Pais, K Dannheim, L Cheung, ... HORMONE RESEARCH IN PAEDIATRICS 95 (SUPPL 1), 146-147, 2022 | | 2022 |
| Mutations in TMEM230 are not a common cause of Parkinson’s disease in southern Italy G Annesi, M Gagliardi, G Iannello, R Procopio, G Nicoletti, M Morelli, ... NEUROLOGICAL SCIENCES 38, S194-S194, 2017 | | 2017 |
