Orazio Palumbo
Orazio Palumbo
Biologo Ricercatore, Laboratorio di Genetica Medica, IRCCS Casa Sollievo della Sofferenza, San Giovanni Rotondo (FG)
Verified email at operapadrepio.it
TitleCited byYear
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
1412012
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
1162011
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
1112010
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
942011
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
852015
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
742011
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
582014
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
562014
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
472012
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
452015
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
422013
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
422012
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
412014
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
362017
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
342014
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
342013
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
302010
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
282015
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
252014
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
242015
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