|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
|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
|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
|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, 2011
|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, 2015
|ALS mutations in FUS cause neuronal dysfunction and death in Caenorhabditis elegans by a dominant gain-of-function mechanism|
T Murakami, SP Yang, L Xie, T Kawano, D Fu, A Mukai, C Bohm, F Chen, ...
Human molecular genetics 21 (1), 1-9, 2011
|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, MT Pellico, D Menghini, P Alfieri, MC Digilio, ...
European Journal of Human Genetics 22 (1), 64, 2014
|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
|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
|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, 2015
|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
|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
|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
|Assisted reproductive techniques and risk of Beckwith-Wiedemann syndrome|
A Mussa, C Molinatto, F Cerrato, O Palumbo, M Carella, G Baldassarre, ...
Pediatrics 140 (1), e20164311, 2017
|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
|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
|Large rearrangements detected by MLPA, point mutations, and survey of the frequency of mutations within the SLC3A1 and SLC7A9 genes in a cohort of 172 cystinuric Italian patients|
L Bisceglia, L Fischetti, P De Bonis, O Palumbo, B Augello, P Stanziale, ...
Molecular genetics and metabolism 99 (1), 42-52, 2010
|Incomplete penetrance and phenotypic variability of 6q16 deletions including SIM1|
L El Khattabi, F Guimiot, E Pipiras, J Andrieux, C Baumann, S Bouquillon, ...
European Journal of Human Genetics 23 (8), 1010, 2015
|Variable phenotype in 17q12 microdeletions: clinical and molecular characterization of a new case|
P Palumbo, V Antona, O Palumbo, M Piccione, R Nardello, A Fontana, ...
Gene 538 (2), 373-378, 2014
|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