IRIS
CICCODICOLA, Alfredo
 Distribuzione geografica
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Continente #
NA - Nord America 9.307
EU - Europa 5.108
AS - Asia 2.721
SA - Sud America 1.059
AF - Africa 45
Continente sconosciuto - Info sul continente non disponibili 37
Totale 18.277
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Nazione #
US - Stati Uniti d'America 9.232
RU - Federazione Russa 2.608
UA - Ucraina 1.462
VN - Vietnam 1.199
BR - Brasile 894
CN - Cina 676
SE - Svezia 607
SG - Singapore 593
DE - Germania 131
GB - Regno Unito 118
AR - Argentina 71
IT - Italia 50
HK - Hong Kong 42
EU - Europa 33
IN - India 33
CZ - Repubblica Ceca 32
FR - Francia 31
BD - Bangladesh 29
EC - Ecuador 28
IQ - Iraq 28
CA - Canada 27
MX - Messico 25
ID - Indonesia 23
CO - Colombia 17
ZA - Sudafrica 16
PK - Pakistan 15
TR - Turchia 15
BE - Belgio 14
FI - Finlandia 14
PY - Paraguay 13
MA - Marocco 11
VE - Venezuela 10
AT - Austria 9
UZ - Uzbekistan 9
CL - Cile 8
PE - Perù 8
UY - Uruguay 8
DO - Repubblica Dominicana 7
KE - Kenya 7
IE - Irlanda 6
IR - Iran 6
AE - Emirati Arabi Uniti 5
JP - Giappone 5
AZ - Azerbaigian 4
HN - Honduras 4
JM - Giamaica 4
JO - Giordania 4
KZ - Kazakistan 4
NL - Olanda 4
PL - Polonia 4
DZ - Algeria 3
GE - Georgia 3
NP - Nepal 3
TN - Tunisia 3
TT - Trinidad e Tobago 3
TW - Taiwan 3
A2 - ???statistics.table.value.countryCode.A2??? 2
AM - Armenia 2
BO - Bolivia 2
BY - Bielorussia 2
CH - Svizzera 2
ES - Italia 2
IL - Israele 2
KR - Corea 2
KW - Kuwait 2
LB - Libano 2
LV - Lettonia 2
PA - Panama 2
PH - Filippine 2
QA - Qatar 2
RS - Serbia 2
SA - Arabia Saudita 2
XK - ???statistics.table.value.countryCode.XK??? 2
AL - Albania 1
BA - Bosnia-Erzegovina 1
BS - Bahamas 1
CI - Costa d'Avorio 1
EG - Egitto 1
ET - Etiopia 1
GA - Gabon 1
GT - Guatemala 1
HU - Ungheria 1
KG - Kirghizistan 1
KH - Cambogia 1
LT - Lituania 1
NI - Nicaragua 1
NO - Norvegia 1
OM - Oman 1
PS - Palestinian Territory 1
PT - Portogallo 1
RO - Romania 1
SK - Slovacchia (Repubblica Slovacca) 1
SN - Senegal 1
TH - Thailandia 1
TL - Timor Orientale 1
Totale 18.277
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Città #
Fairfield 1.364
Dong Ket 920
Dallas 912
Chandler 781
Woodbridge 625
Ashburn 619
Houston 602
Seattle 574
Wilmington 514
Cambridge 485
Nyköping 473
Moscow 354
Beijing 294
Singapore 292
Ann Arbor 282
Boardman 257
Princeton 177
Lawrence 175
Jacksonville 174
San Diego 144
Shanghai 118
Ho Chi Minh City 115
Ogden 113
São Paulo 74
The Dalles 71
New York 61
Hanoi 50
Los Angeles 45
Yubileyny 44
Hong Kong 39
London 39
Munich 38
Nanjing 34
Chicago 33
Santa Clara 33
Rio de Janeiro 27
Brno 26
Jinan 24
Belo Horizonte 22
Norwalk 19
Brasília 17
Da Nang 17
Bremen 16
Shenyang 15
Brussels 14
Kunming 14
Curitiba 13
Hefei 13
Monmouth Junction 13
Des Moines 12
Guangzhou 12
Hanover 12
Nanchang 12
Campinas 11
Columbus 11
Hebei 11
Porto Alegre 11
Toronto 11
Haiphong 10
Helsinki 10
Napoli 10
New Bedfont 10
Ningbo 10
Ribeirão Preto 10
Salt Lake City 10
Goiânia 9
Johannesburg 9
Milan 9
Montreal 9
Salvador 9
Tashkent 9
Tianjin 9
Zhengzhou 9
Baghdad 8
Brooklyn 8
Dhaka 8
Elk Grove Village 8
Fortaleza 8
Frankfurt am Main 8
Guarulhos 8
Lanzhou 8
Nova Iguaçu 8
Nuremberg 8
San Francisco 8
Wandsworth 8
Changsha 7
Chengdu 7
Cuiabá 7
Haikou 7
Hangzhou 7
Joinville 7
Montevideo 7
Redwood City 7
Ribeirão das Neves 7
São Gonçalo 7
Taiyuan 7
Abbottabad 6
Baotou 6
Can Tho 6
Chennai 6
Totale 11.617
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Nome #
New somatic mutations and WNK1-B4GALNT3 gene fusion in papillary thyroid carcinoma 340
Analysis of SEMA6B gene expression in breast cancer: identification of a new isoform 191
A MUSCLE-SPECIFIC DNASE I-LIKE GENE IN HUMAN XQ28 187
Identification and expression analysis of novel Jakmip 1 transcripts 186
Heart failure: Pilot transcriptomic analysis of cardiac tissue by RNA-sequencing 181
A novel pseudoautosomal gene encoding a putative GTP-binding protein resides in the vicinity of the Xp/Yp telomere 181
Mutational hot spot within a new RPGR exon in X-linked retinitis pigmentosa 174
SFMetaDB: a comprehensive annotation of mouse RNA splicing factor RNA-Seq datasets 172
A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X-linked retinitis pigmentosa (RP3) 170
AnaLysis of Expression on human chromosome 21, ALE-HSA21: a pilot integrated web resource 161
Alternative Splicing in Adhesion- and Motility-Related Genes in Breast Cancer 155
A synaptobrevin-like gene in the Xq28 pseudoautosomal region undergoes X inactivation 155
Complex events in the evolution of the human pseudoautosomal region 2 (PAR2) 151
CONSERVED SEQUENCE-TAGGED SITES - A PHYLOGENETIC APPROACH TO GENOME MAPPING 149
A new de novo mutation of the connexin-32 gene in a patient with X-linked Charcot-Marie-Tooth type 1 disease 148
ANALYSIS OF POLYMORPHISMS OF THE NUCLEAR RECEPTOR PPARG GENE IN OBESE INDIVIDUALS FROM SOUTHERN ITALY 145
A dominant negative PPARγ isoform at the crossroad between adipogenesis and obesity 144
RBPMetaDB: A comprehensive annotation of mouse RNA-Seq datasets with perturbations of RNA-binding proteins 140
A novel pseudoautosomal human gene encodes a putative protein similar to Ac-like transposases 140
The DNA sequence of the human X chromosome 139
A novel peroxisome proliferator-activated receptor gamma isoform with dominant negative activity generated by alternative splicing 135
SEQUENCE OF HUMAN GLUCOSE-6-PHOSPHATE-DEHYDROGENASE CLONED IN PLASMIDS AND A YEAST ARTIFICIAL CHROMOSOME 133
A new PPAR gamma truncated isoform induced by a regulatory feedback: Is alternative splicing crucial in adipocyte differentiation and defective neoadipogenesis? 133
Filamin A is mutated in X-linked chronic idiopathic intestinal pseudo-obstruction with central nervous system involvement 132
Filamin a is mutated in chronic intestinal pseudoobstruction 131
Human PRDM2: Structure, function and pathophysiology 130
ANALYSIS AND SEQUENCING OF THE GENOMIC DNA REGION SPANNING THE HUMAN DBL PROTOONCOGENE 129
THE ANTIOXIDANT PHOSPHOLIPID HYDROPEROXIDE GLUTATHIONE PEROXIDASE (GPX4/PHGPX) IN THE FROG HYPOTHALAMUS OF Pelophylax bergeri AS TOOL FOR ITS BIOCONSERVATION ASSESSMENT 126
Expressed STSs and transcription of human Xq28 126
Genetic and epigenetic alterations of RB2/p130 tumor suppressor gene in human sporadic retinoblastoma: implications for pathogenesis and therapeutic approach 125
Filamin (FLN1), plexin (SEX), major palmitoylated protein p55 (MPP1), and von-Hippel Lindau binding protein (VBP1) are not involved in incontinentia pigmenti type 2 124
Characterization of MPP4, a gene highly expressed in photoreceptor cells, and mutation analysis in retinitis pigmentosa 124
Glucose impairs tamoxifen responsiveness modulating CTGF (Connective Tissue Growth Factor) in breast cancer cells 124
Analyzing the Whole Transcriptome by RNA-Seq Data: The Tip of the Iceberg 124
PR/SET domain family and cancer: Novel insights from the cancer genome atlas 122
HUMAN GLUCOSE-6-PHOSPHATE-DEHYDROGENASE GENE CARRIED ON A YEAST ARTIFICIAL CHROMOSOME ENCODES ACTIVE ENZYME IN MONKEY CELLS 122
An approach for testing gene dosage as a mechanism for cognitive dysfunction in Klinefelter's syndrome 121
Characterization of a Novel Polymorphism in PPARG Regulatory Region Associated with Type 2 Diabetes and Diabetic Retinopathy in Italy 121
Anomalie dello sviluppo 121
Molecular and functional effects of methylglyoxal on human microvascular retinal cells 121
Hoxa5 undergoes dynamic DNA methylation and transcriptional repression in the adipose tissue of mice exposed to high-fat diet 120
Escape from X inactivation of two new genes associated with DXS6974E and DXS7020E 120
Genetica molecolare delle distrofie corneali e dei disordini metabolici 119
Klinefelter's syndrome as a model of anomalous cerebral laterality: Testing gene dosage in the X chromosome pseudoautosomal region using a DNA microarray 119
PPARG: Gene Expression Regulation and Next-Generation Sequencing for Unsolved Issues 119
The impact of inflammation on alternative splicing at PPARG locus in hypertrophic obesity 118
Molecular genetics of autosomal dominant retinitis pigmentosa (ADRP): a comprehensive study of 43 Italian families 118
Clinical and molecular genetics of Leber's congenital amaurosis: A multicenter study of Italian patients 118
A new gene encodes a putative GTP-binding protein, escapes X-inactivation and has related sequences on Y chromosome 117
Human dbl proto-oncogene in 85 kb of Xq26, and determination of the transcription initiation site 117
E2 multimeric scaffold for vaccine formulation: immune response by intranasal delivery and transcriptome profile of E2-pulsed dendritic cells 117
Isolation, physical mapping, and northern analysis of the X-linked human gene encoding methyl CpG-binding protein, MECP2 116
ZPLD1 gene is disrupted in a patient with balanced translocation that exhibits cerebral cavernous malformations 115
Molecular characterization of a gene of the 'EGF family' expressed in undifferentiated human NTERA2 teratocarcinoma cells 115
A novel germline mutation in Peroxisome Proliferator-Activated Receptor gamma gene associated with large intestine polyp formation and dyslipidemia 115
An extensive search for RFLP in the human Glucose 6-phosphate dehydrogenase locus has revealed a silent mutation in the coding sequence 115
YEAST ARTIFICIAL CHROMOSOME-BASED GENOME MAPPING - SOME LESSONS FROM XQ24-Q28 115
Glucose impairs tamoxifen responsiveness modulating connective tissue growth factor in breast cancer cells 114
Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal region 114
Genetic counseling in breast cancerThe national cancer institute of Naples experience 113
Antigen delivery by filamentous bacteriophage fd displaying an anti-DEC-205 single-chain variable fragment confers adjuvanticity by triggering a TLR9-mediated immune response 112
Impairment of circulating endothelial progenitors in Down syndrome 112
Human and mouse SYBL1 gene structure and expression 112
Locations and contexts of sequences that hybridize to poly d(G-T) d(C-A) in mammalian ribosomal DNAs and two X-linked genes 112
Identification and characterisation of the retinitis pigmentosa 1-like1 gene (RP1L1): a novel candidate for retinal degenerations 111
SEQUENCE-TAGGED SITES (STSS) FROM YAC INSERT-ENDS AND X-SPECIFIC FLOW-SORTED CHROMOSOMES 111
SSCP DETECTION OF NOVEL MUTATIONS IN PATIENTS WITH EMERY-DREIFUSS MUSCULAR-DYSTROPHY - DEFINITION OF A SMALL C-TERMINAL REGION REQUIRED FOR EMERIN FUNCTION 111
Human homologue of the murine Bare patches/Striated gene is not mutated in Incontinentia Pigmenti type 2 111
Autosomal recessive familial exudative vitreoretinopathy: evidence for genetic heterogeneity 110
MAPPING HUMAN-CHROMOSOMES BY WALKING WITH SEQUENCE-TAGGED SITES FROM END FRAGMENTS OF YEAST ARTIFICIAL CHROMOSOME INSERTS 109
RNA-Seq for the identification of novel Mediator transcripts in endothelial progenitor cells 109
Uncovering the Complexity of Transcriptomes with RNA-Seq 109
Filamin a is mutated in chronic intestinal pseudo-obstruction 108
Differential expression pattern of XqPAR-linked genes SYBL1 and IL9R correlates with the structure and evolution of the region 108
Investigation of Gamma-aminobutyric acid (GABA) A receptors genes and migraine susceptibility 108
Evidence of Bacteroides fragilis protection from Bartonella henselae-induced damage 108
Detrimental effects of Bartonella henselae are counteracted by L-arginine and nitric oxide in human endothelial progenitor cells 108
Clinical phenotype of an Italian family with a new mutation in the PRPF8 gene 108
Clinical features of X linked juvenile retinoschisis associated with new mutations in the XLRS1 gene in Italian families 106
Complete congenital stationary night blindness maps on Xp11.4 in a Sardinian family 106
IDENTIFICATION OF NEW MUTATIONS IN THE EMERY-DREIFUSS MUSCULAR-DYSTROPHY GENE AND EVIDENCE FOR GENETIC-HETEROGENEITY OF THE DISEASE 106
PPAR gamma isoforms as Dr Jekyll and Mr Hyde in insulin sensitivity and adipocyte hypertrophy 106
Transcriptional and post-transcriptional impact of methylglyoxal in human retinal endothelial cells: New players in diabetic retinopathy? 106
TNFA mediates inflammation-induced effects on PPARG splicing in adipose tissue and mesenchymal precursor cells 106
Approccio Clinico alle distrofie corneali ed ai disordini metabolici 105
Is PPARG the key gene in diabetic retinopathy? 105
Identification and assignment of the human transient receptor potential channel 6 gene TRPC6 to chromosome 11q21 -> q22 104
Cloning and gene structure of the rod cGMP phosphodiesterase delta subunit gene (PDED) in man and mouse 103
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 103
DDX11L: a novel transcript family emerging from human subtelomeric regions 103
Characterization of a new gene expressed in an undifferentiated teratocarcinoma cell line 102
Identification of novel RP2 mutations in a subset of X-linked Retinitis Pigmentosa families and prediction of new domains 101
Molecular and Clinical Characterization of Albinism in a Large Cohort of Italian Patients 101
Molecular cloning and fine mapping of API5L1, a novel human gene strongly related to an antiapoptotic gene 101
Multiple pathogenic and benign genomic rearrangements occur at a 35 kb duplication involving the NEMO and LAGE2 genes 101
Differential expression pattern of XqPAR-linked genes SYBL1 and IL9R correlates with the structure and evolution of the region 100
Computational Analysis of Single Nucleotide Polymorphisms Associated with Altered Drug Responsiveness in Type 2 Diabetes 100
Gene expression regulation in heart failure: from pathobiology to bioinformatics 99
Sequence-based exon prediction around the synaptophysin locus reveals a gene-rich area containing novel genes in human proximal Xp 99
YAC CONTIG ORGANIZATION AND CPG ISLAND ANALYSIS IN XQ28 99
Totale 12.506
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Categoria #
all - tutte 102.767
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 102.767
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20213.430 0 0 0 333 512 210 467 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
2024/20254.545 76 270 10 143 95 393 1.319 1.471 288 182 167 131
2025/20262.468 310 724 1.058 376 0 0 0 0 0 0 0 0
Totale 18.615