CNR Institutional Research Information System

CICCODICOLA, ALFREDO
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
AS - Asia 3.784
NA - Nord America 2.184
EU - Europa 794
SA - Sud America 718
Continente sconosciuto - Info sul continente non disponibili 71
AF - Africa 63
OC - Oceania 6
AN - Antartide 1
Totale 7.621
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 2.052
SG - Singapore 1.567
CN - Cina 821
BR - Brasile 565
HK - Hong Kong 432
VN - Vietnam 357
IT - Italia 275
FR - Francia 239
KR - Corea 172
JP - Giappone 95
BD - Bangladesh 87
NL - Olanda 62
DE - Germania 59
IN - India 59
AR - Argentina 52
CA - Canada 52
GB - Regno Unito 42
ID - Indonesia 31
MX - Messico 31
CO - Colombia 28
IL - Israele 26
EC - Ecuador 25
FI - Finlandia 21
TR - Turchia 19
ZA - Sudafrica 19
SA - Arabia Saudita 17
MY - Malesia 16
MA - Marocco 15
CL - Cile 13
RU - Federazione Russa 13
PY - Paraguay 12
VE - Venezuela 12
AT - Austria 11
ES - Italia 11
PL - Polonia 11
UZ - Uzbekistan 11
PH - Filippine 10
IQ - Iraq 9
JM - Giamaica 9
UA - Ucraina 9
PK - Pakistan 8
KE - Kenya 7
PE - Perù 7
AU - Australia 6
EG - Egitto 6
HN - Honduras 6
SE - Svezia 6
TH - Thailandia 6
AZ - Azerbaigian 5
CR - Costa Rica 5
DO - Repubblica Dominicana 5
AE - Emirati Arabi Uniti 4
BH - Bahrain 4
IE - Irlanda 4
LK - Sri Lanka 4
NP - Nepal 4
PA - Panama 4
SV - El Salvador 4
TT - Trinidad e Tobago 4
BE - Belgio 3
BG - Bulgaria 3
GE - Georgia 3
GT - Guatemala 3
JO - Giordania 3
KZ - Kazakistan 3
LT - Lituania 3
MK - Macedonia 3
NI - Nicaragua 3
PR - Porto Rico 3
UY - Uruguay 3
AL - Albania 2
BA - Bosnia-Erzegovina 2
BY - Bielorussia 2
CZ - Repubblica Ceca 2
LB - Libano 2
LY - Libia 2
PS - Palestinian Territory 2
PT - Portogallo 2
RW - Ruanda 2
TJ - Tagikistan 2
TN - Tunisia 2
AM - Armenia 1
AO - Angola 1
AQ - Antartide 1
BB - Barbados 1
BJ - Benin 1
BO - Bolivia 1
BS - Bahamas 1
BW - Botswana 1
CH - Svizzera 1
DZ - Algeria 1
GA - Gabon 1
GR - Grecia 1
HU - Ungheria 1
KW - Kuwait 1
LA - Repubblica Popolare Democratica del Laos 1
LV - Lettonia 1
MM - Myanmar 1
MU - Mauritius 1
NE - Niger 1
Totale 7.540
Salva come PNG Salva come JPEG
Città #
Singapore 905
Hong Kong 419
Hefei 402
Santa Clara 345
San Jose 309
Ashburn 188
Lauterbourg 181
Seoul 167
Ho Chi Minh City 137
Beijing 113
Hanoi 83
Dallas 80
Los Angeles 71
Tokyo 68
São Paulo 48
New York 43
Buffalo 41
Naples 31
Rome 28
Milan 25
Frankfurt am Main 22
Minamishinagawa 22
Council Bluffs 21
Da Nang 21
Helsinki 19
Boardman 18
Brasília 18
Rio de Janeiro 18
Bengaluru 15
Philadelphia 14
Atlanta 13
Houston 13
The Bronx 13
Biên Hòa 12
Brooklyn 12
Phoenix 12
Jeddah 11
Tashkent 11
Bologna 10
Charlotte 10
Chicago 10
Guangzhou 10
Montreal 10
Porto Alegre 10
Warsaw 10
Dhaka 9
Quito 9
Turin 9
Belo Horizonte 8
Campinas 8
Cape Town 8
Guayaquil 8
Istanbul 8
Kuala Lumpur 8
London 8
Novara 8
Nuremberg 8
Thái Bình 8
Bogotá 7
Boston 7
Can Tho 7
Detroit 7
Figino 7
Guarulhos 7
Haiphong 7
Jakarta 7
Memphis 7
Mexico City 7
Miami 7
Munich 7
Nairobi 7
Newark 7
Queens 7
Toronto 7
Vienna 7
Asunción 6
Cleveland 6
Columbia 6
Curitiba 6
Florence 6
Franca 6
Johannesburg 6
Kansas City 6
Kingston 6
Las Vegas 6
Marigliano 6
Orem 6
Salvador 6
Santiago 6
Stockholm 6
Betim 5
Casablanca 5
Catania 5
Chennai 5
City of London 5
Düsseldorf 5
Fortaleza 5
Ha Long 5
Hải Dương 5
Lahore 5
Totale 4.405
Salva come PNG Salva come JPEG
Nome #
In Vitro-Generated Hypertrophic-Like Adipocytes Displaying PPARG Isoforms Unbalance Recapitulate Adipocyte Dysfunctions In Vivo 98
Hepatic Insulin Resistance in Hyperthyroid Rat Liver: Vitamin E Supplementation Highlights a Possible Role of ROS 81
AnaLysis of Expression on human chromosome 21, ALE-HSA21: a pilot integrated web resource 78
Filamin a is mutated in chronic intestinal pseudoobstruction 75
Autosomal recessive familial exudative vitreoretinopathy: evidence for genetic heterogeneity. 75
Targeting metabolism by B-raf inhibitors and diclofenac restrains the viability of BRAF-mutated thyroid carcinomas with Hif-1?-mediated glycolytic phenotype 74
PPARγ and Diabetes: Beyond the Genome and Towards Personalized Medicine 74
Identification of new mutations in the Emery-Dreifuss muscular dystrophy gene and evidence for genetic heterogeneity of the disease. 73
Clinical expression of x-linked retinitis pigmentosa in a family with a novel splice defect in the RPGR gene. 72
GIPR expression is induced by thiazolidinediones in a PPAR?-independent manner and repressed by obesogenic stimuli 71
Mutational analysis of the RPGR Exon ORF 15 in South European patients with X-Linked Retinitis Pigmentosa. 70
Mutational hot spot within a new RPGR exon in X-linked retinitis pigmentosa. 70
TNFα mediates inflammation-induced effects on PPARG splicing in adipose tissue and mesenchymal precursor cells 68
Hoxa5 undergoes dynamic DNA methylation and transcriptional repression in the adipose tissue of mice exposed to high-fat diet 67
The Sex Chromosomes: Sequence, Evolution and Human Diseases. In: The Human Genome: Features, Variations and Genetic Disorders 65
PPAR gamma Delta 5, a Naturally Occurring Dominant-Negative Splice Isoform, Impairs PPAR gamma Function and Adipocyte Differentiation 65
The DNA sequence of the human X chromosome 65
Genetic and epigenetic alterations of RB2/P130 tumor suppressor gene in human sporadic retinoplastoma: implications for pathogenesis and therapeutic approach 64
Select item 10671Mutation in the nerve-specific 5'non-coding region of Cx32 gene and absence of specific mRNA in a CMTX1 Italian family. Mutations in brief no. 195. Online. 62
Investigation on alternative splicing in MCF-7 cells by RNA-Seq: identification and characterization of a new transcript of SEMA3F. 62
Diabetic Retinopathy: Are lncRNAs New Molecular Players and Targets? 62
Integrated Network Pharmacology Approach for Drug Combination Discovery: A Multi-Cancer Case Study 61
Oncogenic Properties of the Antisense lncRNA COMET in BRAF- and RET-Driven Papillary Thyroid Carcinomas 61
Malattie ereditarie del segmento anteriore dell"occhio 58
E2 multimeric scaffold for vaccine formulation: immune response by intranasal delivery and transcriptome profile of E2-pulsed dendritic cells. 58
Molecular and Clinical Characterization of Albinism in a Large Cohort of Italian Patients 57
Isolation and characterisation of RPGR gene by positional sequencing involved in X-linked retinitis pigmentosa (RP3). 57
A muscle-specific DNase I-like gene in human Xq28 56
High-Throughput Analysis of Noncoding RNAs: Implications in Clinical Epigenetics, published in the Book "Epigenetic Biomarkers and Diagnostics", 1st Edition 56
Experimental colitis: decreased Octn2 and Atb0+ expression in rat colonocytes induces carnitine depletion that is reversible by carnitine-loaded liposomes 56
Evidence of Bacteroides fragilis protection from Bartonella henselae-induced damage. 55
Heart failure: Pilot transcriptomic analysis of cardiac tissue by RNA-sequencing 55
An approach for testing gene dosage as a mechanism for cognitive dysfunction in Klinefelter's syndrome 54
Escape from X inactivation of two new genes associated with DXS6974E and DXS7020E 54
Non-coding RNA and pseudogenes in neurodegenerative diseases: "The (un)Usual Suspects". 53
Systematic identification and characterization of eye-expressed transcripts: Novel candidate genes for eye diseases. 52
The "next-generation" knowledge of papillary thyroid carcinoma 52
Antigen delivery by filamentous bacteriophage fd displaying an anti-DEC-205 single-chain variable fragment confers adjuvanticity by triggering a TLR9-mediated immune response. 52
Impairment of circulating endothelial progenitors in Down syndrome 52
Glucose impairs tamoxifen responsiveness modulating connective tissue growth factor in breast cancer cells 51
A new de novo mutation of the connexin-32 gene in a patient with X-linked Charcot-Marie-Tooth type 1 disease 50
Molecular cloning and fine mapping of API5L1, a novel human gene strongly related to an antiapoptotic gene 50
Alternative splicing in adhesion- and motility-related genes in breast cancer 50
A novel pseudoautosomal gene encoding a putative GTP-binding protein resides in the vicinity of the Xp/Yp telomere 50
Human PRDM2: Structure, function and pathophysiology 49
Transcriptional Regulation and Its Misregulation in Human Diseases 48
Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal region 48
Conserved sequence-tagged sites: A phylogenetic approach to genome mapping 47
Expressed STSs and transcription of human Xq28. 47
Transcriptional regulation: Molecules, involved mechanisms, and misregulation 47
DDX11L: a novel transcript family emerging from human subtelomeric regions 47
E2 multimeric scaffold for vaccine formulation: transcriptome analysis of pulsed dendritic cells and immune response by intranasal delivery. 47
PR/SET domain family and cancer: Novel insights from the cancer genome atlas 47
Genetic analysis of two unrelated Italian families with non specific X-mental retardation 46
Antigen delivery by filamentous bacteriophage fd displaying an anti-DEC-205 single-chain variable fragment confers adjuvanticity by triggering a TLR9-mediated immune response. 45
Pan-cancer mutational and transcriptional analysis of the integrator complex 45
The "next-generation" knowledge of papillary thyroid carcinoma 45
Genetic and epigenetic alterations of RB2/p130 tumor suppressor gene in human sporadic retinoblastoma: implications for pathogenesis and therapeutic approach. 44
SEQUENCE-TAGGED SITES (STSS) FROM YAC INSERT-ENDS AND X-SPECIFIC FLOW-SORTED CHROMOSOMES 44
Identification and assignment of the human transient receptor potential channel 6 gene TRPC6 to chromosome 11q21 -> q22 43
YAC contig organization and CpG island analysis in Xq28 43
ZPLD1 gene is disrupted in a patient with balanced translocation that exhibits cerebral cavernous malformations 42
Clinical and molecular genetics of Leber's congenital amaurosis: a multicenter study of Italian patients 42
RBPMetaDB: a comprehensive annotation of mouse RNA-Seq datasets with perturbations of RNA-binding proteins 42
Identificazione e caratterizzazione sistematica di cDNA espressi in retina: nuovi geni candidati per malattie oculari. 41
From sequence analysis to diseases identification in the distal human xq28 41
Transcriptome profiling in human diseases: New advances and perspectives 41
Genomic organization of the long arm of the Human X chromosome. 40
New somatic mutations and WNK1-B4GALNT3 gene fusion in papillary thyroid carcinoma. 40
Yeast artificial chromosome-based genome mapping: some lessons from Xq24-q28 39
Genomic rearrangement in NEMO impairs NF-KAPPAB activation and is a cause of incontinentia pigmenti 39
Complex Events In The Evolution Of The Human Pseudoautosomal Region 2 (PAR2) 39
Assembly of a YAC contig spanning 1.6 Mb of Xq28 DNA around the DXS304 locus 38
PPARG in Human Adipogenesis: Differential Contribution of Canonical Transcripts and Dominant Negative Isoforms 37
Analysis of SEMA6B gene expression in breast cancer: Identification of a new isoform. 37
Molecular and clinical characterization of albinism in a large cohort of Italian patients 36
RNA-Seq for the identification of novel Mediator transcripts in endothelial progenitor cells 36
Identification and expression analysis of novel Jakmip1 transcripts. 36
4. Molecular cloning and fine mapping of API5L1, a novel human gene strongly related to an antiapoptotic gene 36
Sequence-tagged sites (STSs) from YAC insert-ends and X-specific flow-sorted chromosomes 36
A novel pseudoautosomal human gene encodes a putative protein similar to Ac-like transposases 35
Identification and characterization of a novel human brain-specific gene, homologous to S. Scrofa tmp83.5, in the chromosome 10q24 critical region for temporal lobe epilepsy and spastic paraplegia. 35
ANALYSIS OF POLYMORPHISMS OF THE NUCLEAR RECEPTOR PPARG GENE IN OBESE INDIVIDUALS FROM SOUTHERN ITALY 35
Metodi di indagine oftalmologici e genetico-molecolare 34
RNA-Seq and human complex diseases: recent accomplishments and future perspectives. 34
Identification and expression analysis of novel Jakmip1 transcripts. 33
PPARG: Gene Expression Regulation and Next-Generation Sequencing for Unsolved Issues 33
Mutation analysis of the RPGR gene reveals novel mutations in south European patients with X-linked retinitis pigmentosa. 32
Mutation analyisis of RPGR gene in patients with X-linked Retinitis Pigmentosa (RP3) 32
A new gene encodes a putative GTP-binding protein, escapes X-inactivation and has related sequences on Y chromosome 32
Mutations of a cytosine tract in exon 10 of NEMO (IKK-gamma) cause atypical forms of Incontinentia pigmenti. 32
Uncovering the complexity of transcriptomes with RNA-Seq 32
Characterization of MPP4, a gene highly expressed in photoreceptor cells, and mutation analysis in retinitis pigmentosa. 32
Genetic analysis of two unrelated Italian Families with non specific X-mental retardation. 30
Caratterizzazione molecolare del melanoma mediante uno studio combinato di genomica e networks molecolari 30
Mutations of a cytosine tract in exon 10 of NEMO (IKK-gamma) cause atypical forms of Incontinentia pigmenti 30
Klinefelter's syndrome as a model of anomalous cerebral laterality: Testing gene dosage in the X chromosome pseudoautosomal region using a DNA microarray 30
Mapping of MRX81 in Xp11.2-Xq12 suggests the presence of a new gene involved in nonspecific X-linked mental retardation. 30
Identification and characterisation of the retinitis pigmentosa 1-like1 gene (RP1L1): a novel candidate for retinal degenerations 30
17th IGB Meeting - The Biology and Development of the Eye in Health and Disease 30
Totale 4.902
Salva come PNG Salva come JPEG
Categoria #
all - tutte 27.796
article - articoli 21.992
book - libri 385
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 578
Totale 50.751
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202467 0 0 0 0 0 0 0 0 7 0 45 15
2024/20252.391 25 15 187 113 306 89 17 85 42 88 744 680
2025/20264.155 215 409 459 656 684 113 659 225 214 223 130 168
2026/20271.008 204 305 499 0 0 0 0 0 0 0 0 0
Totale 7.621