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Orazio Palumbo
Orazio Palumbo
Biologo Ricercatore, Laboratorio di Genetica Medica, IRCCS Casa Sollievo della Sofferenza, San Giovanni Rotondo (FG)
Verified email at operapadrepio.it
Title
Cited by
Cited by
Year
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
2362010
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
1832011
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
1802012
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
1612015
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
1432012
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
1242017
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
1042014
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
1022014
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
1012017
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
852018
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
842015
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
792014
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
732012
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
662013
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
632012
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
602017
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
582015
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
552015
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
532013
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
502014
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