| Gene amplification as double minutes or homogeneously staining regions in solid tumors: origin and structure CT Storlazzi, A Lonoce, MC Guastadisegni, D Trombetta, P D'Addabbo, ... Genome research 20 (9), 1198-1206, 2010 | 238 | 2010 |
| Clock gene expression levels and relationship with clinical and pathological features in colorectal cancer patients G Mazzoccoli, A Panza, MR Valvano, O Palumbo, M Carella, V Pazienza, ... Chronobiology international 28 (10), 841-851, 2011 | 183 | 2011 |
| Mirna expression profiles identify drivers in colorectal and pancreatic cancers A Piepoli, F Tavano, M Copetti, T Mazza, O Palumbo, A Panza, FF Di Mola, ... PloS one 7 (3), e33663, 2012 | 180 | 2012 |
| 7q11. 23 dosage-dependent dysregulation in human pluripotent stem cells affects transcriptional programs in disease-relevant lineages A Adamo, S Atashpaz, PL Germain, M Zanella, G D'Agostino, V Albertin, ... Nature genetics 47 (2), 132-141, 2015 | 161 | 2015 |
| The KCNQ1OT1 imprinting control region and non-coding RNA: new properties derived from the study of Beckwith–Wiedemann syndrome and Silver–Russell … N Chiesa, A De Crescenzo, K Mishra, L Perone, M Carella, O Palumbo, ... Human molecular genetics 21 (1), 10-25, 2012 | 143 | 2012 |
| Assisted reproductive techniques and risk of Beckwith-Wiedemann syndrome A Mussa, C Molinatto, F Cerrato, O Palumbo, M Carella, G Baldassarre, ... Pediatrics 140 (1), 2017 | 124 | 2017 |
| Genomic organization and evolution of double minutes/homogeneously staining regions with MYC amplification in human cancer A L'Abbate, G Macchia, P D'Addabbo, A Lonoce, D Tolomeo, D Trombetta, ... Nucleic acids research 42 (14), 9131-9145, 2014 | 105 | 2014 |
| Wnt5a drives an invasive phenotype in human glioblastoma stem-like cells E Binda, A Visioli, F Giani, N Trivieri, O Palumbo, S Restelli, F Dezi, ... Cancer research 77 (4), 996-1007, 2017 | 102 | 2017 |
| Smaller and larger deletions of the Williams Beuren syndrome region implicate genes involved in mild facial phenotype, epilepsy and autistic traits C Fusco, L Micale, B Augello, M Teresa Pellico, D Menghini, P Alfieri, ... European Journal of Human Genetics 22 (1), 64-70, 2014 | 102 | 2014 |
| MYC-containing amplicons in acute myeloid leukemia: genomic structures, evolution, and transcriptional consequences A L′ Abbate, D Tolomeo, I Cifola, M Severgnini, A Turchiano, B Augello, ... Leukemia 32 (10), 2152-2166, 2018 | 86 | 2018 |
| Testis development in the absence of SRY: chromosomal rearrangements at SOX9 and SOX3 A Vetro, MR Dehghani, L Kraoua, R Giorda, S Beri, L Cardarelli, M Merico, ... European Journal of Human Genetics 23 (8), 1025-1032, 2015 | 85 | 2015 |
| A miRNA signature for defining aggressive phenotype and prognosis in gliomas R Barbano, O Palumbo, B Pasculli, M Galasso, S Volinia, V D'Angelo, ... PloS one 9 (10), e108950, 2014 | 79 | 2014 |
| Altered expression of the clock gene machinery in kidney cancer patients G Mazzoccoli, A Piepoli, M Carella, A Panza, V Pazienza, G Benegiamo, ... Biomedicine & Pharmacotherapy 66 (3), 175-179, 2012 | 73 | 2012 |
| Differences in gene expression and cytokine release profiles highlight the heterogeneity of distinct subsets of adipose tissue-derived stem cells in the subcutaneous and … S Perrini, R Ficarella, E Picardi, A Cignarelli, M Barbaro, P Nigro, ... PloS one 8 (3), e57892, 2013 | 66 | 2013 |
| A novel microdeletion syndrome at 3q13. 31 characterised by developmental delay, postnatal overgrowth, hypoplastic male genitals, and characteristic facial features AM Molin, J Andrieux, DA Koolen, V Malan, M Carella, L Colleaux, ... Journal of medical genetics 49 (2), 104-109, 2012 | 64 | 2012 |
| Decreased free d-aspartate levels are linked to enhanced d-aspartate oxidase activity in the dorsolateral prefrontal cortex of schizophrenia patients T Nuzzo, S Sacchi, F Errico, S Keller, O Palumbo, E Florio, D Punzo, ... npj Schizophrenia 3 (1), 16, 2017 | 61 | 2017 |
| Systematic analysis of circadian genes using genome-wide cDNA microarrays in the inflammatory bowel disease transcriptome O Palmieri, G Mazzoccoli, F Bossa, R Maglietta, O Palumbo, N Ancona, ... Chronobiology international 32 (7), 903-916, 2015 | 58 | 2015 |
| MiR-578 and miR-573 as potential players in BRCA-related breast cancer angiogenesis K Danza, S De Summa, R Pinto, B Pilato, O Palumbo, G Merla, G Simone, ... Oncotarget 6 (1), 471, 2015 | 55 | 2015 |
| 3p14. 1 de novo microdeletion involving the FOXP1 gene in an adult patient with autism, severe speech delay and deficit of motor coordination O Palumbo, L D'Agruma, AF Minenna, P Palumbo, R Stallone, T Palladino, ... Gene 516 (1), 107-113, 2013 | 53 | 2013 |
| TBR1 is the candidate gene for intellectual disability in patients with a 2q24.2 interstitial deletion O Palumbo, M Fichera, P Palumbo, R Rizzo, E Mazzolla, DM Cocuzza, ... American Journal of Medical Genetics Part A 164 (3), 828-833, 2014 | 50 | 2014 |
