Orazio Palumbo
Orazio Palumbo
Biologo Ricercatore, Laboratorio di Genetica Medica, IRCCS Casa Sollievo della Sofferenza, San Giovanni Rotondo (FG)
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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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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