CNR Institutional Research Information System

CICCODICOLA, ALFREDO
 Distribuzione geografica
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Continente #
AS - Asia 3.671
NA - Nord America 1.345
SA - Sud America 654
EU - Europa 624
AF - Africa 62
OC - Oceania 6
AN - Antartide 1
Continente sconosciuto - Info sul continente non disponibili 1
Totale 6.364
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Nazione #
SG - Singapore 1.563
US - Stati Uniti d'America 1.271
CN - Cina 817
BR - Brasile 540
HK - Hong Kong 425
VN - Vietnam 347
FR - Francia 236
KR - Corea 172
IT - Italia 125
JP - Giappone 95
NL - Olanda 61
DE - Germania 58
IN - India 58
AR - Argentina 48
GB - Regno Unito 35
BD - Bangladesh 30
CA - Canada 27
IL - Israele 26
ID - Indonesia 25
MX - Messico 24
FI - Finlandia 21
ZA - Sudafrica 19
EC - Ecuador 17
TR - Turchia 17
SA - Arabia Saudita 16
MA - Marocco 15
RU - Federazione Russa 13
CL - Cile 12
PY - Paraguay 12
AT - Austria 11
PL - Polonia 11
UZ - Uzbekistan 11
CO - Colombia 9
ES - Italia 9
IQ - Iraq 8
PK - Pakistan 8
UA - Ucraina 8
KE - Kenya 7
PE - Perù 7
PH - Filippine 7
VE - Venezuela 7
AU - Australia 6
EG - Egitto 6
MY - Malesia 6
SE - Svezia 6
AZ - Azerbaigian 5
DO - Repubblica Dominicana 5
TH - Thailandia 5
BH - Bahrain 4
IE - Irlanda 4
JM - Giamaica 4
LK - Sri Lanka 4
AE - Emirati Arabi Uniti 3
GE - Georgia 3
JO - Giordania 3
LT - Lituania 3
SV - El Salvador 3
AL - Albania 2
BE - Belgio 2
BG - Bulgaria 2
BY - Bielorussia 2
CR - Costa Rica 2
GT - Guatemala 2
KZ - Kazakistan 2
LY - Libia 2
MK - Macedonia 2
NP - Nepal 2
PA - Panama 2
PT - Portogallo 2
RW - Ruanda 2
TJ - Tagikistan 2
TN - Tunisia 2
TT - Trinidad e Tobago 2
UY - Uruguay 2
AM - Armenia 1
AO - Angola 1
AQ - Antartide 1
BA - Bosnia-Erzegovina 1
BB - Barbados 1
BJ - Benin 1
BW - Botswana 1
CH - Svizzera 1
CZ - Repubblica Ceca 1
DZ - Algeria 1
GA - Gabon 1
GR - Grecia 1
HN - Honduras 1
HU - Ungheria 1
KW - Kuwait 1
LA - Repubblica Popolare Democratica del Laos 1
LB - Libano 1
LV - Lettonia 1
MM - Myanmar 1
MU - Mauritius 1
NE - Niger 1
NI - Nicaragua 1
NO - Norvegia 1
OM - Oman 1
PS - Palestinian Territory 1
RE - Reunion 1
Totale 6.358
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Città #
Singapore 901
Hong Kong 419
Hefei 402
Santa Clara 334
San Jose 195
Lauterbourg 181
Seoul 167
Ho Chi Minh City 135
Ashburn 113
Beijing 112
Hanoi 80
Dallas 73
Tokyo 68
Los Angeles 64
São Paulo 48
Buffalo 32
New York 31
Frankfurt am Main 22
Minamishinagawa 22
Naples 20
Da Nang 19
Helsinki 19
Rio de Janeiro 16
Bengaluru 15
Boardman 13
Biên Hòa 12
Tashkent 11
Brasília 10
Guangzhou 10
Jeddah 10
Milan 10
Porto Alegre 10
Rome 10
Warsaw 10
Montreal 9
Quito 9
Belo Horizonte 8
Cape Town 8
Nuremberg 8
Thái Bình 8
Campinas 7
Guarulhos 7
Haiphong 7
Jakarta 7
Munich 7
Nairobi 7
Novara 7
Phoenix 7
Vienna 7
Asunción 6
Atlanta 6
Can Tho 6
Dhaka 6
Franca 6
Istanbul 6
Johannesburg 6
London 6
Marigliano 6
Orem 6
Salvador 6
Santiago 6
Stockholm 6
Betim 5
Boston 5
Casablanca 5
Chennai 5
Chicago 5
City of London 5
Curitiba 5
Düsseldorf 5
Ha Long 5
Hải Dương 5
Lahore 5
Las Vegas 5
New Orleans 5
Sorocaba 5
Amsterdam 4
Aracaju 4
Bologna 4
Buenos Aires 4
Cairo 4
Camaçari 4
Council Bluffs 4
Fortaleza 4
Guayaquil 4
Houston 4
Juiz de Fora 4
Kuala Lumpur 4
Mexico City 4
Mumbai 4
New Delhi 4
Ninh Bình 4
Pisa 4
Porto Velho 4
Queens 4
Riyadh 4
Shanghai 4
Shenzhen 4
São Gonçalo 4
Teresina 4
Totale 3.951
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Nome #
In Vitro-Generated Hypertrophic-Like Adipocytes Displaying PPARG Isoforms Unbalance Recapitulate Adipocyte Dysfunctions In Vivo 93
Autosomal recessive familial exudative vitreoretinopathy: evidence for genetic heterogeneity. 71
Filamin a is mutated in chronic intestinal pseudoobstruction 69
Clinical expression of x-linked retinitis pigmentosa in a family with a novel splice defect in the RPGR gene. 67
Targeting metabolism by B-raf inhibitors and diclofenac restrains the viability of BRAF-mutated thyroid carcinomas with Hif-1?-mediated glycolytic phenotype 67
Identification of new mutations in the Emery-Dreifuss muscular dystrophy gene and evidence for genetic heterogeneity of the disease. 66
Mutational analysis of the RPGR Exon ORF 15 in South European patients with X-Linked Retinitis Pigmentosa. 66
PPARγ and Diabetes: Beyond the Genome and Towards Personalized Medicine 64
GIPR expression is induced by thiazolidinediones in a PPAR?-independent manner and repressed by obesogenic stimuli 63
The Sex Chromosomes: Sequence, Evolution and Human Diseases. In: The Human Genome: Features, Variations and Genetic Disorders 62
PPAR gamma Delta 5, a Naturally Occurring Dominant-Negative Splice Isoform, Impairs PPAR gamma Function and Adipocyte Differentiation 61
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. 60
Mutational hot spot within a new RPGR exon in X-linked retinitis pigmentosa. 60
TNFα mediates inflammation-induced effects on PPARG splicing in adipose tissue and mesenchymal precursor cells 60
Hoxa5 undergoes dynamic DNA methylation and transcriptional repression in the adipose tissue of mice exposed to high-fat diet 58
Investigation on alternative splicing in MCF-7 cells by RNA-Seq: identification and characterization of a new transcript of SEMA3F. 57
Genetic and epigenetic alterations of RB2/P130 tumor suppressor gene in human sporadic retinoplastoma: implications for pathogenesis and therapeutic approach 57
Malattie ereditarie del segmento anteriore dell"occhio 55
Molecular and Clinical Characterization of Albinism in a Large Cohort of Italian Patients 55
Diabetic Retinopathy: Are lncRNAs New Molecular Players and Targets? 54
E2 multimeric scaffold for vaccine formulation: immune response by intranasal delivery and transcriptome profile of E2-pulsed dendritic cells. 54
An approach for testing gene dosage as a mechanism for cognitive dysfunction in Klinefelter's syndrome 53
The DNA sequence of the human X chromosome 52
Hepatic Insulin Resistance in Hyperthyroid Rat Liver: Vitamin E Supplementation Highlights a Possible Role of ROS 52
Integrated Network Pharmacology Approach for Drug Combination Discovery: A Multi-Cancer Case Study 52
A muscle-specific DNase I-like gene in human Xq28 51
Systematic identification and characterization of eye-expressed transcripts: Novel candidate genes for eye diseases. 50
Oncogenic Properties of the Antisense lncRNA COMET in BRAF- and RET-Driven Papillary Thyroid Carcinomas 50
Escape from X inactivation of two new genes associated with DXS6974E and DXS7020E 49
High-Throughput Analysis of Noncoding RNAs: Implications in Clinical Epigenetics, published in the Book "Epigenetic Biomarkers and Diagnostics", 1st Edition 49
The "next-generation" knowledge of papillary thyroid carcinoma 48
Isolation and characterisation of RPGR gene by positional sequencing involved in X-linked retinitis pigmentosa (RP3). 47
Alternative splicing in adhesion- and motility-related genes in breast cancer 47
Glucose impairs tamoxifen responsiveness modulating connective tissue growth factor in breast cancer cells 46
Heart failure: Pilot transcriptomic analysis of cardiac tissue by RNA-sequencing 46
A new de novo mutation of the connexin-32 gene in a patient with X-linked Charcot-Marie-Tooth type 1 disease 45
Non-coding RNA and pseudogenes in neurodegenerative diseases: "The (un)Usual Suspects". 45
Conserved sequence-tagged sites: A phylogenetic approach to genome mapping 44
Antigen delivery by filamentous bacteriophage fd displaying an anti-DEC-205 single-chain variable fragment confers adjuvanticity by triggering a TLR9-mediated immune response. 43
Identification and assignment of the human transient receptor potential channel 6 gene TRPC6 to chromosome 11q21 -> q22 41
Transcriptional Regulation and Its Misregulation in Human Diseases 41
Genetic analysis of two unrelated Italian families with non specific X-mental retardation 41
Human PRDM2: Structure, function and pathophysiology 41
E2 multimeric scaffold for vaccine formulation: transcriptome analysis of pulsed dendritic cells and immune response by intranasal delivery. 41
PR/SET domain family and cancer: Novel insights from the cancer genome atlas 41
Molecular cloning and fine mapping of API5L1, a novel human gene strongly related to an antiapoptotic gene 40
Identificazione e caratterizzazione sistematica di cDNA espressi in retina: nuovi geni candidati per malattie oculari. 40
Genetic and epigenetic alterations of RB2/p130 tumor suppressor gene in human sporadic retinoblastoma: implications for pathogenesis and therapeutic approach. 40
YAC contig organization and CpG island analysis in Xq28 40
Antigen delivery by filamentous bacteriophage fd displaying an anti-DEC-205 single-chain variable fragment confers adjuvanticity by triggering a TLR9-mediated immune response. 39
Transcriptional regulation: Molecules, involved mechanisms, and misregulation 39
Pan-cancer mutational and transcriptional analysis of the integrator complex 39
AnaLysis of Expression on human chromosome 21, ALE-HSA21: a pilot integrated web resource 38
Assembly of a YAC contig spanning 1.6 Mb of Xq28 DNA around the DXS304 locus 37
From sequence analysis to diseases identification in the distal human xq28 37
Genomic organization of the long arm of the Human X chromosome. 36
Expressed STSs and transcription of human Xq28. 36
RBPMetaDB: a comprehensive annotation of mouse RNA-Seq datasets with perturbations of RNA-binding proteins 36
SEQUENCE-TAGGED SITES (STSS) FROM YAC INSERT-ENDS AND X-SPECIFIC FLOW-SORTED CHROMOSOMES 36
ZPLD1 gene is disrupted in a patient with balanced translocation that exhibits cerebral cavernous malformations 35
Transcriptome profiling in human diseases: New advances and perspectives 35
The "next-generation" knowledge of papillary thyroid carcinoma 35
Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal region 35
A novel pseudoautosomal human gene encodes a putative protein similar to Ac-like transposases 34
Evidence of Bacteroides fragilis protection from Bartonella henselae-induced damage. 34
A novel pseudoautosomal gene encoding a putative GTP-binding protein resides in the vicinity of the Xp/Yp telomere 33
Metodi di indagine oftalmologici e genetico-molecolare 33
New somatic mutations and WNK1-B4GALNT3 gene fusion in papillary thyroid carcinoma. 33
Molecular and clinical characterization of albinism in a large cohort of Italian patients 32
Complex Events In The Evolution Of The Human Pseudoautosomal Region 2 (PAR2) 32
Analysis of SEMA6B gene expression in breast cancer: Identification of a new isoform. 32
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. 31
Mutation analysis of the RPGR gene reveals novel mutations in south European patients with X-linked retinitis pigmentosa. 30
4. Molecular cloning and fine mapping of API5L1, a novel human gene strongly related to an antiapoptotic gene 30
Experimental colitis: decreased Octn2 and Atb0+ expression in rat colonocytes induces carnitine depletion that is reversible by carnitine-loaded liposomes 30
Yeast artificial chromosome-based genome mapping: some lessons from Xq24-q28 28
Genomic rearrangement in NEMO impairs NF-KAPPAB activation and is a cause of incontinentia pigmenti 28
Caratterizzazione molecolare del melanoma mediante uno studio combinato di genomica e networks molecolari 28
PPARG in Human Adipogenesis: Differential Contribution of Canonical Transcripts and Dominant Negative Isoforms 28
Sequence-tagged sites (STSs) from YAC insert-ends and X-specific flow-sorted chromosomes 28
PPARG: Gene Expression Regulation and Next-Generation Sequencing for Unsolved Issues 28
17th IGB Meeting - The Biology and Development of the Eye in Health and Disease 28
DDX11L: a novel transcript family emerging from human subtelomeric regions 28
RNA-Seq and human complex diseases: recent accomplishments and future perspectives. 28
Mutation analyisis of RPGR gene in patients with X-linked Retinitis Pigmentosa (RP3) 27
A new gene encodes a putative GTP-binding protein, escapes X-inactivation and has related sequences on Y chromosome 27
Identification and expression analysis of novel Jakmip1 transcripts. 27
Investigation of Gamma-aminobutyric acid (GABA) A receptors genes and migraine susceptibility 27
Molecular genetics of autosomal dominant retinitis pigmentosa (ADRP): a comprehensive study of 43 Italian families 27
Isolation, physical mapping, and northern analysis of the X-linked human gene encoding methyl CpG-binding protein, MECP2 27
RNA-Seq for the identification of novel Mediator transcripts in endothelial progenitor cells 26
Massive-Scale RNA-Seq Analysis of Non Ribosomal Transcriptome in Human Trisomy 21 26
Clinical and molecular genetics of Leber's congenital amaurosis: a multicenter study of Italian patients 26
Mutations of a cytosine tract in exon 10 of NEMO (IKK-gamma) cause atypical forms of Incontinentia pigmenti. 26
Malattie genetiche dell occhio 26
Filamin a is mutated in chronic intestinal pseudo-obstruction 26
X-Cromosome STSs: a tool for mapping the human X chromosome. 26
Organization of a 1.2 Mb YAC contig spanning the entire iduronate sulfatase gene 26
Systematic generation of X-chromosome specific sequence-tagged sites (STSs). 26
Identification and characterization of C1orf36, a transcript highly expressed in photoreceptor cells, and mutation analysis in retinitis pigmentosa 26
Totale 4.165
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Categoria #
all - tutte 21.912
article - articoli 17.323
book - libri 306
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 475
Totale 40.016
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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
2025/20263.976 215 409 459 656 684 113 659 225 214 223 119 0
Totale 6.434