IRIS
CICCODICOLA, Alfredo
 Distribuzione geografica
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Continente #
NA - Nord America 8.002
EU - Europa 5.028
AS - Asia 2.148
SA - Sud America 354
Continente sconosciuto - Info sul continente non disponibili 37
AF - Africa 8
Totale 15.577
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Nazione #
US - Stati Uniti d'America 7.984
RU - Federazione Russa 2.597
UA - Ucraina 1.454
VN - Vietnam 920
SE - Svezia 603
SG - Singapore 582
CN - Cina 545
BR - Brasile 334
DE - Germania 123
GB - Regno Unito 99
IT - Italia 49
EU - Europa 33
CZ - Repubblica Ceca 31
FR - Francia 29
HK - Hong Kong 21
IQ - Iraq 14
BE - Belgio 13
FI - Finlandia 12
CA - Canada 10
PK - Pakistan 10
TR - Turchia 10
BD - Bangladesh 8
AR - Argentina 6
AT - Austria 6
IN - India 6
IR - Iran 6
UZ - Uzbekistan 5
IE - Irlanda 4
MX - Messico 4
PY - Paraguay 4
EC - Ecuador 3
MA - Marocco 3
TW - Taiwan 3
A2 - ???statistics.table.value.countryCode.A2??? 2
AM - Armenia 2
AZ - Azerbaigian 2
CH - Svizzera 2
CO - Colombia 2
GE - Georgia 2
NL - Olanda 2
PH - Filippine 2
QA - Qatar 2
VE - Venezuela 2
XK - ???statistics.table.value.countryCode.XK??? 2
BO - Bolivia 1
BY - Bielorussia 1
EG - Egitto 1
GA - Gabon 1
HN - Honduras 1
ID - Indonesia 1
JM - Giamaica 1
JO - Giordania 1
KE - Kenya 1
KZ - Kazakistan 1
LB - Libano 1
NI - Nicaragua 1
NP - Nepal 1
OM - Oman 1
PA - Panama 1
PE - Perù 1
PS - Palestinian Territory 1
PT - Portogallo 1
RO - Romania 1
SK - Slovacchia (Repubblica Slovacca) 1
TH - Thailandia 1
TN - Tunisia 1
UY - Uruguay 1
ZA - Sudafrica 1
Totale 15.577
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Città #
Fairfield 1.364
Dong Ket 920
Chandler 781
Woodbridge 625
Houston 601
Ashburn 591
Seattle 573
Wilmington 513
Cambridge 484
Nyköping 473
Moscow 353
Singapore 283
Ann Arbor 282
Boardman 257
Princeton 177
Lawrence 175
Jacksonville 174
Beijing 170
San Diego 144
Shanghai 118
Ogden 113
The Dalles 71
New York 51
Yubileyny 44
London 36
Munich 33
Nanjing 33
Brno 26
Jinan 24
São Paulo 23
Hong Kong 21
Norwalk 19
Santa Clara 19
Bremen 16
Shenyang 15
Kunming 14
Brussels 13
Hefei 13
Monmouth Junction 13
Belo Horizonte 12
Des Moines 12
Guangzhou 12
Hanover 12
Nanchang 12
Rio de Janeiro 12
Hebei 11
Helsinki 10
Napoli 10
New Bedfont 10
Ningbo 10
Tianjin 9
Zhengzhou 9
Dallas 8
Frankfurt am Main 8
Lanzhou 8
Los Angeles 8
Milan 8
Toronto 8
Wandsworth 8
Changsha 7
Chengdu 7
Haikou 7
Hangzhou 7
Redwood City 7
Taiyuan 7
Abbottabad 6
Baotou 6
Brasília 6
Faenza 6
Kilburn 6
Leawood 6
Ardabil 5
Council Bluffs 5
Fortaleza 5
Nuremberg 5
Olomouc 5
Roubaix 5
Tashkent 5
Acton 4
Baghdad 4
Dearborn 4
Goiânia 4
Hounslow 4
Istanbul 4
Lauterbourg 4
Southend 4
Taizhou 4
Campinas 3
Cuiabá 3
Curitiba 3
Dhaka 3
Fuzhou 3
Islington 3
Itajaí 3
Mosul 3
Naples 3
Nova Iguaçu 3
Porto Alegre 3
Ribeirão Preto 3
Ribeirão das Neves 3
Totale 10.040
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Nome #
New somatic mutations and WNK1-B4GALNT3 gene fusion in papillary thyroid carcinoma 332
Identification and expression analysis of novel Jakmip 1 transcripts 172
SFMetaDB: a comprehensive annotation of mouse RNA splicing factor RNA-Seq datasets 166
Heart failure: Pilot transcriptomic analysis of cardiac tissue by RNA-sequencing 161
Mutational hot spot within a new RPGR exon in X-linked retinitis pigmentosa 160
Analysis of SEMA6B gene expression in breast cancer: identification of a new isoform 154
A MUSCLE-SPECIFIC DNASE I-LIKE GENE IN HUMAN XQ28 153
A novel pseudoautosomal gene encoding a putative GTP-binding protein resides in the vicinity of the Xp/Yp telomere 153
CONSERVED SEQUENCE-TAGGED SITES - A PHYLOGENETIC APPROACH TO GENOME MAPPING 144
A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X-linked retinitis pigmentosa (RP3) 132
RBPMetaDB: A comprehensive annotation of mouse RNA-Seq datasets with perturbations of RNA-binding proteins 129
AnaLysis of Expression on human chromosome 21, ALE-HSA21: a pilot integrated web resource 127
Complex events in the evolution of the human pseudoautosomal region 2 (PAR2) 125
The DNA sequence of the human X chromosome 123
A synaptobrevin-like gene in the Xq28 pseudoautosomal region undergoes X inactivation 122
HUMAN GLUCOSE-6-PHOSPHATE-DEHYDROGENASE GENE CARRIED ON A YEAST ARTIFICIAL CHROMOSOME ENCODES ACTIVE ENZYME IN MONKEY CELLS 122
Filamin a is mutated in chronic intestinal pseudoobstruction 121
ANALYSIS OF POLYMORPHISMS OF THE NUCLEAR RECEPTOR PPARG GENE IN OBESE INDIVIDUALS FROM SOUTHERN ITALY 121
SEQUENCE OF HUMAN GLUCOSE-6-PHOSPHATE-DEHYDROGENASE CLONED IN PLASMIDS AND A YEAST ARTIFICIAL CHROMOSOME 118
A dominant negative PPARγ isoform at the crossroad between adipogenesis and obesity 118
Alternative Splicing in Adhesion- and Motility-Related Genes in Breast Cancer 117
A new de novo mutation of the connexin-32 gene in a patient with X-linked Charcot-Marie-Tooth type 1 disease 115
Characterization of MPP4, a gene highly expressed in photoreceptor cells, and mutation analysis in retinitis pigmentosa 113
Glucose impairs tamoxifen responsiveness modulating CTGF (Connective Tissue Growth Factor) in breast cancer cells 113
E2 multimeric scaffold for vaccine formulation: immune response by intranasal delivery and transcriptome profile of E2-pulsed dendritic cells 113
Human PRDM2: Structure, function and pathophysiology 110
Glucose impairs tamoxifen responsiveness modulating connective tissue growth factor in breast cancer cells 109
Filamin A is mutated in X-linked chronic idiopathic intestinal pseudo-obstruction with central nervous system involvement 109
Klinefelter's syndrome as a model of anomalous cerebral laterality: Testing gene dosage in the X chromosome pseudoautosomal region using a DNA microarray 108
Expressed STSs and transcription of human Xq28 108
Genetic and epigenetic alterations of RB2/p130 tumor suppressor gene in human sporadic retinoblastoma: implications for pathogenesis and therapeutic approach 107
Human dbl proto-oncogene in 85 kb of Xq26, and determination of the transcription initiation site 106
Escape from X inactivation of two new genes associated with DXS6974E and DXS7020E 106
THE ANTIOXIDANT PHOSPHOLIPID HYDROPEROXIDE GLUTATHIONE PEROXIDASE (GPX4/PHGPX) IN THE FROG HYPOTHALAMUS OF Pelophylax bergeri AS TOOL FOR ITS BIOCONSERVATION ASSESSMENT 105
Genetic counseling in breast cancerThe national cancer institute of Naples experience 105
A novel pseudoautosomal human gene encodes a putative protein similar to Ac-like transposases 105
Genetica molecolare delle distrofie corneali e dei disordini metabolici 104
Clinical and molecular genetics of Leber's congenital amaurosis: A multicenter study of Italian patients 104
Filamin (FLN1), plexin (SEX), major palmitoylated protein p55 (MPP1), and von-Hippel Lindau binding protein (VBP1) are not involved in incontinentia pigmenti type 2 104
Characterization of a Novel Polymorphism in PPARG Regulatory Region Associated with Type 2 Diabetes and Diabetic Retinopathy in Italy 102
YEAST ARTIFICIAL CHROMOSOME-BASED GENOME MAPPING - SOME LESSONS FROM XQ24-Q28 102
MAPPING HUMAN-CHROMOSOMES BY WALKING WITH SEQUENCE-TAGGED SITES FROM END FRAGMENTS OF YEAST ARTIFICIAL CHROMOSOME INSERTS 101
Hoxa5 undergoes dynamic DNA methylation and transcriptional repression in the adipose tissue of mice exposed to high-fat diet 101
The impact of inflammation on alternative splicing at PPARG locus in hypertrophic obesity 100
Uncovering the Complexity of Transcriptomes with RNA-Seq 100
An approach for testing gene dosage as a mechanism for cognitive dysfunction in Klinefelter's syndrome 99
Anomalie dello sviluppo 99
PPARG: Gene Expression Regulation and Next-Generation Sequencing for Unsolved Issues 98
Autosomal recessive familial exudative vitreoretinopathy: evidence for genetic heterogeneity 98
DDX11L: a novel transcript family emerging from human subtelomeric regions 98
ANALYSIS AND SEQUENCING OF THE GENOMIC DNA REGION SPANNING THE HUMAN DBL PROTOONCOGENE 97
Impairment of circulating endothelial progenitors in Down syndrome 97
ZPLD1 gene is disrupted in a patient with balanced translocation that exhibits cerebral cavernous malformations 96
A novel peroxisome proliferator-activated receptor gamma isoform with dominant negative activity generated by alternative splicing 96
Molecular genetics of autosomal dominant retinitis pigmentosa (ADRP): a comprehensive study of 43 Italian families 96
Antigen delivery by filamentous bacteriophage fd displaying an anti-DEC-205 single-chain variable fragment confers adjuvanticity by triggering a TLR9-mediated immune response 96
Isolation, physical mapping, and northern analysis of the X-linked human gene encoding methyl CpG-binding protein, MECP2 96
Molecular characterization of a gene of the 'EGF family' expressed in undifferentiated human NTERA2 teratocarcinoma cells 96
Functional expression of human glucose-6-phosphate dehydrogenase in Escherichia coli 96
Human and mouse SYBL1 gene structure and expression 96
Molecular and functional effects of methylglyoxal on human microvascular retinal cells 96
Filamin a is mutated in chronic intestinal pseudo-obstruction 95
Human homologue of the murine Bare patches/Striated gene is not mutated in Incontinentia Pigmenti type 2 95
Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal region 95
Complete congenital stationary night blindness maps on Xp11.4 in a Sardinian family 95
A new PPAR gamma truncated isoform induced by a regulatory feedback: Is alternative splicing crucial in adipocyte differentiation and defective neoadipogenesis? 95
Locations and contexts of sequences that hybridize to poly d(G-T) d(C-A) in mammalian ribosomal DNAs and two X-linked genes 95
Characterization of a new gene expressed in an undifferentiated teratocarcinoma cell line 94
CLONING OF THE FRAGILE-X LOCUS IN THE CONTEXT OF YEAST ARTIFICIAL CHROMOSOME-BASED MAPPING OF XQ24-28 94
Approccio Clinico alle distrofie corneali ed ai disordini metabolici 94
PR/SET domain family and cancer: Novel insights from the cancer genome atlas 94
Cloning and gene structure of the rod cGMP phosphodiesterase delta subunit gene (PDED) in man and mouse 93
Detrimental effects of Bartonella henselae are counteracted by L-arginine and nitric oxide in human endothelial progenitor cells 93
RNA-Seq for the identification of novel Mediator transcripts in endothelial progenitor cells 93
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 93
Gene expression regulation in heart failure: from pathobiology to bioinformatics 92
New Evidence for the Correlation of the p.G130V Mutation in the GJB2 Gene and Syndromic Hearing Loss With Palmoplantar Keratoderma 92
SEQUENCE-TAGGED SITES (STSS) FROM YAC INSERT-ENDS AND X-SPECIFIC FLOW-SORTED CHROMOSOMES 92
SSCP DETECTION OF NOVEL MUTATIONS IN PATIENTS WITH EMERY-DREIFUSS MUSCULAR-DYSTROPHY - DEFINITION OF A SMALL C-TERMINAL REGION REQUIRED FOR EMERIN FUNCTION 92
YAC CONTIG ORGANIZATION AND CPG ISLAND ANALYSIS IN XQ28 92
A new gene encodes a putative GTP-binding protein, escapes X-inactivation and has related sequences on Y chromosome 91
Diet-induced obesity alters methylation of HOX transcription factors in mouse visceral adipose tissue 90
Investigation of Gamma-aminobutyric acid (GABA) A receptors genes and migraine susceptibility 90
A novel germline mutation in Peroxisome Proliferator-Activated Receptor gamma gene associated with large intestine polyp formation and dyslipidemia 90
Identification and characterisation of the retinitis pigmentosa 1-like1 gene (RP1L1): a novel candidate for retinal degenerations 89
Differential expression pattern of XqPAR-linked genes SYBL1 and IL9R correlates with the structure and evolution of the region 89
Evidence of Bacteroides fragilis protection from Bartonella henselae-induced damage 89
Clinical features of X linked juvenile retinoschisis associated with new mutations in the XLRS1 gene in Italian families 89
Identification and assignment of the human transient receptor potential channel 6 gene TRPC6 to chromosome 11q21 -> q22 89
IDENTIFICATION OF NEW MUTATIONS IN THE EMERY-DREIFUSS MUSCULAR-DYSTROPHY GENE AND EVIDENCE FOR GENETIC-HETEROGENEITY OF THE DISEASE 89
Identification of novel RP2 mutations in a subset of X-linked Retinitis Pigmentosa families and prediction of new domains 88
PPAR gamma isoforms as Dr Jekyll and Mr Hyde in insulin sensitivity and adipocyte hypertrophy 87
Clinical phenotype of an Italian family with a new mutation in the PRPF8 gene 87
Uncovering the complexity of Transcriptomes with RNA-SEQ 86
Computational Analysis of Single Nucleotide Polymorphisms Associated with Altered Drug Responsiveness in Type 2 Diabetes 86
Association between the T239M missense variation in the FGF23 gene and renal phosphate leak 85
Is PPARG the key gene in diabetic retinopathy? 85
Experimental colitis: decreased Octn2 and Atb0+expression in rat colonocytes induces carnitine depletion that is reversible by carnitine-loaded liposomes 85
Analyzing the Whole Transcriptome by RNA-Seq Data: The Tip of the Iceberg 85
Multiple pathogenic and benign genomic rearrangements occur at a 35 kb duplication involving the NEMO and LAGE2 genes 85
Totale 10.702
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Categoria #
all - tutte 89.254
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 89.254
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020447 0 0 0 0 0 0 0 0 0 0 383 64
2020/20214.605 326 177 672 333 512 210 467 82 166 233 168 1.259
2021/20221.688 115 223 177 498 81 19 79 220 79 26 99 72
2022/20232.061 388 247 181 176 152 319 97 149 238 36 46 32
2023/2024633 47 27 63 29 15 68 13 21 181 13 11 145
2024/20254.313 76 270 10 143 95 393 1.319 1.471 288 182 66 0
Totale 15.915