CNR Institutional Research Information System

CICCODICOLA, ALFREDO
 Distribuzione geografica
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Continente #
AS - Asia 3.712
NA - Nord America 1.570
EU - Europa 660
SA - Sud America 656
AF - Africa 62
OC - Oceania 6
AN - Antartide 1
Continente sconosciuto - Info sul continente non disponibili 1
Totale 6.668
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Nazione #
SG - Singapore 1.563
US - Stati Uniti d'America 1.483
CN - Cina 819
BR - Brasile 541
HK - Hong Kong 425
VN - Vietnam 347
FR - Francia 237
KR - Corea 172
IT - Italia 158
JP - Giappone 95
BD - Bangladesh 68
NL - Olanda 61
DE - Germania 58
IN - India 58
AR - Argentina 48
GB - Regno Unito 35
CA - Canada 34
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
CL - Cile 13
RU - Federazione Russa 13
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
JM - Giamaica 6
MY - Malesia 6
SE - Svezia 6
AZ - Azerbaigian 5
DO - Repubblica Dominicana 5
TH - Thailandia 5
BH - Bahrain 4
IE - Irlanda 4
LK - Sri Lanka 4
SV - El Salvador 4
AE - Emirati Arabi Uniti 3
BE - Belgio 3
CR - Costa Rica 3
GE - Georgia 3
GT - Guatemala 3
JO - Giordania 3
LT - Lituania 3
NP - Nepal 3
AL - Albania 2
BG - Bulgaria 2
BY - Bielorussia 2
CZ - Repubblica Ceca 2
KZ - Kazakistan 2
LY - Libia 2
MK - Macedonia 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
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 6.661
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Città #
Singapore 901
Hong Kong 419
Hefei 402
Santa Clara 335
San Jose 214
Lauterbourg 181
Seoul 167
Ashburn 164
Ho Chi Minh City 135
Beijing 113
Hanoi 80
Dallas 78
Tokyo 68
Los Angeles 67
São Paulo 48
Buffalo 38
New York 34
Naples 23
Frankfurt am Main 22
Minamishinagawa 22
Da Nang 19
Helsinki 19
Boardman 18
Rio de Janeiro 16
Bengaluru 15
Rome 14
Milan 13
Biên Hòa 12
Tashkent 11
Brasília 10
Guangzhou 10
Jeddah 10
Montreal 10
Porto Alegre 10
Warsaw 10
Bologna 9
Brooklyn 9
Quito 9
Atlanta 8
Belo Horizonte 8
Cape Town 8
Nuremberg 8
Thái Bình 8
Boston 7
Campinas 7
Guarulhos 7
Haiphong 7
Jakarta 7
London 7
Munich 7
Nairobi 7
Novara 7
Phoenix 7
Vienna 7
Asunción 6
Can Tho 6
Council Bluffs 6
Dhaka 6
Franca 6
Houston 6
Istanbul 6
Johannesburg 6
Marigliano 6
Orem 6
Salvador 6
Santiago 6
Stockholm 6
The Bronx 6
Turin 6
Betim 5
Casablanca 5
Chennai 5
Chicago 5
City of London 5
Curitiba 5
Düsseldorf 5
Ha Long 5
Hải Dương 5
Kansas City 5
Lahore 5
Las Vegas 5
New Orleans 5
Queens 5
Sorocaba 5
Toronto 5
Amsterdam 4
Aracaju 4
Buenos Aires 4
Cairo 4
Camaçari 4
Fortaleza 4
Guayaquil 4
Juiz de Fora 4
Kingston 4
Kuala Lumpur 4
Memphis 4
Mexico City 4
Miami 4
Mumbai 4
New Delhi 4
Totale 4.082
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Nome #
In Vitro-Generated Hypertrophic-Like Adipocytes Displaying PPARG Isoforms Unbalance Recapitulate Adipocyte Dysfunctions In Vivo 95
Autosomal recessive familial exudative vitreoretinopathy: evidence for genetic heterogeneity. 72
Filamin a is mutated in chronic intestinal pseudoobstruction 71
Identification of new mutations in the Emery-Dreifuss muscular dystrophy gene and evidence for genetic heterogeneity of the disease. 69
PPARγ and Diabetes: Beyond the Genome and Towards Personalized Medicine 69
Clinical expression of x-linked retinitis pigmentosa in a family with a novel splice defect in the RPGR gene. 68
Targeting metabolism by B-raf inhibitors and diclofenac restrains the viability of BRAF-mutated thyroid carcinomas with Hif-1?-mediated glycolytic phenotype 68
Mutational analysis of the RPGR Exon ORF 15 in South European patients with X-Linked Retinitis Pigmentosa. 67
TNFα mediates inflammation-induced effects on PPARG splicing in adipose tissue and mesenchymal precursor cells 65
GIPR expression is induced by thiazolidinediones in a PPAR?-independent manner and repressed by obesogenic stimuli 64
PPAR gamma Delta 5, a Naturally Occurring Dominant-Negative Splice Isoform, Impairs PPAR gamma Function and Adipocyte Differentiation 63
The Sex Chromosomes: Sequence, Evolution and Human Diseases. In: The Human Genome: Features, Variations and Genetic Disorders 62
Hoxa5 undergoes dynamic DNA methylation and transcriptional repression in the adipose tissue of mice exposed to high-fat diet 62
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
Genetic and epigenetic alterations of RB2/P130 tumor suppressor gene in human sporadic retinoplastoma: implications for pathogenesis and therapeutic approach 60
Mutational hot spot within a new RPGR exon in X-linked retinitis pigmentosa. 60
Diabetic Retinopathy: Are lncRNAs New Molecular Players and Targets? 58
Investigation on alternative splicing in MCF-7 cells by RNA-Seq: identification and characterization of a new transcript of SEMA3F. 57
Molecular and Clinical Characterization of Albinism in a Large Cohort of Italian Patients 56
The DNA sequence of the human X chromosome 56
Malattie ereditarie del segmento anteriore dell"occhio 55
Hepatic Insulin Resistance in Hyperthyroid Rat Liver: Vitamin E Supplementation Highlights a Possible Role of ROS 55
E2 multimeric scaffold for vaccine formulation: immune response by intranasal delivery and transcriptome profile of E2-pulsed dendritic cells. 54
Integrated Network Pharmacology Approach for Drug Combination Discovery: A Multi-Cancer Case Study 54
An approach for testing gene dosage as a mechanism for cognitive dysfunction in Klinefelter's syndrome 53
A muscle-specific DNase I-like gene in human Xq28 52
Isolation and characterisation of RPGR gene by positional sequencing involved in X-linked retinitis pigmentosa (RP3). 51
Oncogenic Properties of the Antisense lncRNA COMET in BRAF- and RET-Driven Papillary Thyroid Carcinomas 51
Systematic identification and characterization of eye-expressed transcripts: Novel candidate genes for eye diseases. 50
High-Throughput Analysis of Noncoding RNAs: Implications in Clinical Epigenetics, published in the Book "Epigenetic Biomarkers and Diagnostics", 1st Edition 50
Heart failure: Pilot transcriptomic analysis of cardiac tissue by RNA-sequencing 50
Non-coding RNA and pseudogenes in neurodegenerative diseases: "The (un)Usual Suspects". 49
Escape from X inactivation of two new genes associated with DXS6974E and DXS7020E 49
Evidence of Bacteroides fragilis protection from Bartonella henselae-induced damage. 49
The "next-generation" knowledge of papillary thyroid carcinoma 48
Alternative splicing in adhesion- and motility-related genes in breast cancer 48
Impairment of circulating endothelial progenitors in Down syndrome 48
A new de novo mutation of the connexin-32 gene in a patient with X-linked Charcot-Marie-Tooth type 1 disease 47
Glucose impairs tamoxifen responsiveness modulating connective tissue growth factor in breast cancer cells 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. 46
Conserved sequence-tagged sites: A phylogenetic approach to genome mapping 45
Molecular cloning and fine mapping of API5L1, a novel human gene strongly related to an antiapoptotic gene 43
Transcriptional Regulation and Its Misregulation in Human Diseases 43
Human PRDM2: Structure, function and pathophysiology 43
DDX11L: a novel transcript family emerging from human subtelomeric regions 43
E2 multimeric scaffold for vaccine formulation: transcriptome analysis of pulsed dendritic cells and immune response by intranasal delivery. 43
Transcriptional regulation: Molecules, involved mechanisms, and misregulation 42
Pan-cancer mutational and transcriptional analysis of the integrator complex 42
Genetic and epigenetic alterations of RB2/p130 tumor suppressor gene in human sporadic retinoblastoma: implications for pathogenesis and therapeutic approach. 42
YAC contig organization and CpG island analysis in Xq28 42
Identification and assignment of the human transient receptor potential channel 6 gene TRPC6 to chromosome 11q21 -> q22 41
Antigen delivery by filamentous bacteriophage fd displaying an anti-DEC-205 single-chain variable fragment confers adjuvanticity by triggering a TLR9-mediated immune response. 41
Genetic analysis of two unrelated Italian families with non specific X-mental retardation 41
PR/SET domain family and cancer: Novel insights from the cancer genome atlas 41
Identificazione e caratterizzazione sistematica di cDNA espressi in retina: nuovi geni candidati per malattie oculari. 40
From sequence analysis to diseases identification in the distal human xq28 39
Experimental colitis: decreased Octn2 and Atb0+ expression in rat colonocytes induces carnitine depletion that is reversible by carnitine-loaded liposomes 39
AnaLysis of Expression on human chromosome 21, ALE-HSA21: a pilot integrated web resource 39
Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal region 39
Expressed STSs and transcription of human Xq28. 38
RBPMetaDB: a comprehensive annotation of mouse RNA-Seq datasets with perturbations of RNA-binding proteins 38
SEQUENCE-TAGGED SITES (STSS) FROM YAC INSERT-ENDS AND X-SPECIFIC FLOW-SORTED CHROMOSOMES 38
Assembly of a YAC contig spanning 1.6 Mb of Xq28 DNA around the DXS304 locus 37
ZPLD1 gene is disrupted in a patient with balanced translocation that exhibits cerebral cavernous malformations 37
Transcriptome profiling in human diseases: New advances and perspectives 37
Genomic organization of the long arm of the Human X chromosome. 36
The "next-generation" knowledge of papillary thyroid carcinoma 36
New somatic mutations and WNK1-B4GALNT3 gene fusion in papillary thyroid carcinoma. 35
A novel pseudoautosomal human gene encodes a putative protein similar to Ac-like transposases 34
Complex Events In The Evolution Of The Human Pseudoautosomal Region 2 (PAR2) 34
Molecular and clinical characterization of albinism in a large cohort of Italian patients 33
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
Analysis of SEMA6B gene expression in breast cancer: Identification of a new isoform. 33
Genomic rearrangement in NEMO impairs NF-KAPPAB activation and is a cause of incontinentia pigmenti 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. 32
Identification and expression analysis of novel Jakmip1 transcripts. 32
4. Molecular cloning and fine mapping of API5L1, a novel human gene strongly related to an antiapoptotic gene 32
Clinical and molecular genetics of Leber's congenital amaurosis: a multicenter study of Italian patients 31
PPARG in Human Adipogenesis: Differential Contribution of Canonical Transcripts and Dominant Negative Isoforms 31
Mutation analysis of the RPGR gene reveals novel mutations in south European patients with X-linked retinitis pigmentosa. 30
PPARG: Gene Expression Regulation and Next-Generation Sequencing for Unsolved Issues 30
RNA-Seq and human complex diseases: recent accomplishments and future perspectives. 30
Identification and expression analysis of novel Jakmip1 transcripts. 29
RNA-Seq for the identification of novel Mediator transcripts in endothelial progenitor cells 29
Isolation, physical mapping, and northern analysis of the X-linked human gene encoding methyl CpG-binding protein, MECP2 29
Yeast artificial chromosome-based genome mapping: some lessons from Xq24-q28 28
Caratterizzazione molecolare del melanoma mediante uno studio combinato di genomica e networks molecolari 28
Investigation of Gamma-aminobutyric acid (GABA) A receptors genes and migraine susceptibility 28
Sequence-tagged sites (STSs) from YAC insert-ends and X-specific flow-sorted chromosomes 28
17th IGB Meeting - The Biology and Development of the Eye in Health and Disease 28
Differential expression pattern of XqPAR-linked genes SYBL1 and IL9R correlates with the structure and evolution of the region 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
Tumori 27
Malattie genetiche dell occhio 27
Klinefelter's syndrome as a model of anomalous cerebral laterality: Testing gene dosage in the X chromosome pseudoautosomal region using a DNA microarray 27
X-linked Retinitis Pigmentosa (RP3): Screening for new mutations and promoter analysis of RPGR gene. 27
Molecular genetics of autosomal dominant retinitis pigmentosa (ADRP): a comprehensive study of 43 Italian families 27
Massive-Scale RNA-Seq Analysis of Non Ribosomal Transcriptome in Human Trisomy 21 26
Totale 4.377
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Categoria #
all - tutte 24.445
article - articoli 19.321
book - libri 340
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 516
Totale 44.622
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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
2025/20264.155 215 409 459 656 684 113 659 225 214 223 130 168
2026/2027125 125 0 0 0 0 0 0 0 0 0 0 0
Totale 6.738