IRIS
CICCODICOLA, Alfredo
 Distribuzione geografica
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Continente #
NA - Nord America 9.347
EU - Europa 5.158
AS - Asia 3.351
SA - Sud America 1.452
AF - Africa 68
Continente sconosciuto - Info sul continente non disponibili 37
Totale 19.413
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Nazione #
US - Stati Uniti d'America 9.258
RU - Federazione Russa 2.616
UA - Ucraina 1.464
VN - Vietnam 1.360
BR - Brasile 1.211
SG - Singapore 973
CN - Cina 713
SE - Svezia 608
DE - Germania 134
GB - Regno Unito 119
AR - Argentina 102
IT - Italia 62
HK - Hong Kong 46
EC - Ecuador 41
ID - Indonesia 40
MX - Messico 38
IN - India 36
IQ - Iraq 36
BD - Bangladesh 34
EU - Europa 33
FR - Francia 33
CZ - Repubblica Ceca 32
CA - Canada 27
CO - Colombia 24
ZA - Sudafrica 22
PY - Paraguay 21
LV - Lettonia 18
PK - Pakistan 16
VE - Venezuela 16
CL - Cile 15
MA - Marocco 15
TR - Turchia 15
BE - Belgio 14
FI - Finlandia 14
UZ - Uzbekistan 13
AT - Austria 11
KE - Kenya 11
UY - Uruguay 11
PE - Perù 9
DO - Repubblica Dominicana 8
JP - Giappone 7
IE - Irlanda 6
IR - Iran 6
TN - Tunisia 6
AE - Emirati Arabi Uniti 5
AZ - Azerbaigian 5
BY - Bielorussia 4
DZ - Algeria 4
HN - Honduras 4
JM - Giamaica 4
JO - Giordania 4
KW - Kuwait 4
KZ - Kazakistan 4
NL - Olanda 4
NP - Nepal 4
PL - Polonia 4
GE - Georgia 3
IL - Israele 3
TT - Trinidad e Tobago 3
TW - Taiwan 3
A2 - ???statistics.table.value.countryCode.A2??? 2
AM - Armenia 2
BO - Bolivia 2
CH - Svizzera 2
ES - Italia 2
GA - Gabon 2
KG - Kirghizistan 2
KR - Corea 2
LB - Libano 2
PA - Panama 2
PH - Filippine 2
QA - Qatar 2
RO - Romania 2
RS - Serbia 2
SA - Arabia Saudita 2
SN - Senegal 2
XK - ???statistics.table.value.countryCode.XK??? 2
AL - Albania 1
BA - Bosnia-Erzegovina 1
BS - Bahamas 1
BW - Botswana 1
CI - Costa d'Avorio 1
EG - Egitto 1
ET - Etiopia 1
GT - Guatemala 1
HU - Ungheria 1
KH - Cambogia 1
LT - Lituania 1
ML - Mali 1
MN - Mongolia 1
MY - Malesia 1
NG - Nigeria 1
NI - Nicaragua 1
NO - Norvegia 1
OM - Oman 1
PS - Palestinian Territory 1
PT - Portogallo 1
SK - Slovacchia (Repubblica Slovacca) 1
TH - Thailandia 1
TL - Timor Orientale 1
Totale 19.413
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Città #
Fairfield 1.364
Dong Ket 920
Dallas 912
Chandler 781
Ashburn 635
Woodbridge 625
Houston 602
Seattle 574
Wilmington 514
Cambridge 485
Nyköping 473
Moscow 354
Singapore 306
Beijing 296
Ann Arbor 282
Boardman 257
Princeton 177
Lawrence 175
Jacksonville 174
Ho Chi Minh City 172
San Diego 144
Shanghai 118
Ogden 113
São Paulo 101
Hanoi 72
The Dalles 71
New York 61
Los Angeles 45
Yubileyny 44
Hong Kong 43
London 40
Munich 38
Rio de Janeiro 36
Nanjing 34
Chicago 33
Santa Clara 33
Belo Horizonte 28
Brno 26
Jinan 25
Da Nang 22
Brasília 21
Haiphong 19
Norwalk 19
Porto Alegre 18
Riga 18
Bremen 16
Salvador 16
Shenyang 15
Brussels 14
Campinas 14
Kunming 14
Thái Bình 14
Curitiba 13
Hefei 13
Monmouth Junction 13
Des Moines 12
Goiânia 12
Guangzhou 12
Hanover 12
Nanchang 12
Tashkent 12
Can Tho 11
Columbus 11
Fortaleza 11
Hebei 11
Jakarta 11
Johannesburg 11
Quito 11
Ribeirão Preto 11
Toronto 11
Baghdad 10
Helsinki 10
Nairobi 10
Napoli 10
New Bedfont 10
Ningbo 10
Nuremberg 10
Pelotas 10
Salt Lake City 10
Frankfurt am Main 9
Joinville 9
Milan 9
Montevideo 9
Montreal 9
Ninh Bình 9
Nova Iguaçu 9
Tianjin 9
Zhengzhou 9
Asunción 8
Biên Hòa 8
Brooklyn 8
Dhaka 8
Elk Grove Village 8
Guarulhos 8
Lanzhou 8
Recife 8
San Francisco 8
Taubaté 8
Wandsworth 8
Bắc Giang 7
Totale 11.879
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Nome #
New somatic mutations and WNK1-B4GALNT3 gene fusion in papillary thyroid carcinoma 342
Analysis of SEMA6B gene expression in breast cancer: identification of a new isoform 199
A MUSCLE-SPECIFIC DNASE I-LIKE GENE IN HUMAN XQ28 195
Heart failure: Pilot transcriptomic analysis of cardiac tissue by RNA-sequencing 193
Identification and expression analysis of novel Jakmip 1 transcripts 190
A novel pseudoautosomal gene encoding a putative GTP-binding protein resides in the vicinity of the Xp/Yp telomere 186
A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X-linked retinitis pigmentosa (RP3) 185
Mutational hot spot within a new RPGR exon in X-linked retinitis pigmentosa 175
SFMetaDB: a comprehensive annotation of mouse RNA splicing factor RNA-Seq datasets 174
AnaLysis of Expression on human chromosome 21, ALE-HSA21: a pilot integrated web resource 169
Alternative Splicing in Adhesion- and Motility-Related Genes in Breast Cancer 164
A synaptobrevin-like gene in the Xq28 pseudoautosomal region undergoes X inactivation 163
Complex events in the evolution of the human pseudoautosomal region 2 (PAR2) 159
A new de novo mutation of the connexin-32 gene in a patient with X-linked Charcot-Marie-Tooth type 1 disease 159
CONSERVED SEQUENCE-TAGGED SITES - A PHYLOGENETIC APPROACH TO GENOME MAPPING 152
ANALYSIS OF POLYMORPHISMS OF THE NUCLEAR RECEPTOR PPARG GENE IN OBESE INDIVIDUALS FROM SOUTHERN ITALY 149
A dominant negative PPARγ isoform at the crossroad between adipogenesis and obesity 148
RBPMetaDB: A comprehensive annotation of mouse RNA-Seq datasets with perturbations of RNA-binding proteins 147
A novel pseudoautosomal human gene encodes a putative protein similar to Ac-like transposases 147
A novel peroxisome proliferator-activated receptor gamma isoform with dominant negative activity generated by alternative splicing 144
The DNA sequence of the human X chromosome 143
A new PPAR gamma truncated isoform induced by a regulatory feedback: Is alternative splicing crucial in adipocyte differentiation and defective neoadipogenesis? 141
THE ANTIOXIDANT PHOSPHOLIPID HYDROPEROXIDE GLUTATHIONE PEROXIDASE (GPX4/PHGPX) IN THE FROG HYPOTHALAMUS OF Pelophylax bergeri AS TOOL FOR ITS BIOCONSERVATION ASSESSMENT 139
Filamin A is mutated in X-linked chronic idiopathic intestinal pseudo-obstruction with central nervous system involvement 138
Human PRDM2: Structure, function and pathophysiology 138
Analyzing the Whole Transcriptome by RNA-Seq Data: The Tip of the Iceberg 138
SEQUENCE OF HUMAN GLUCOSE-6-PHOSPHATE-DEHYDROGENASE CLONED IN PLASMIDS AND A YEAST ARTIFICIAL CHROMOSOME 135
PR/SET domain family and cancer: Novel insights from the cancer genome atlas 134
ANALYSIS AND SEQUENCING OF THE GENOMIC DNA REGION SPANNING THE HUMAN DBL PROTOONCOGENE 133
Filamin a is mutated in chronic intestinal pseudoobstruction 132
Hoxa5 undergoes dynamic DNA methylation and transcriptional repression in the adipose tissue of mice exposed to high-fat diet 132
Genetic and epigenetic alterations of RB2/p130 tumor suppressor gene in human sporadic retinoblastoma: implications for pathogenesis and therapeutic approach 131
Filamin (FLN1), plexin (SEX), major palmitoylated protein p55 (MPP1), and von-Hippel Lindau binding protein (VBP1) are not involved in incontinentia pigmenti type 2 130
Escape from X inactivation of two new genes associated with DXS6974E and DXS7020E 130
PPARG: Gene Expression Regulation and Next-Generation Sequencing for Unsolved Issues 129
Clinical and molecular genetics of Leber's congenital amaurosis: A multicenter study of Italian patients 128
Characterization of MPP4, a gene highly expressed in photoreceptor cells, and mutation analysis in retinitis pigmentosa 128
Glucose impairs tamoxifen responsiveness modulating CTGF (Connective Tissue Growth Factor) in breast cancer cells 128
Molecular genetics of autosomal dominant retinitis pigmentosa (ADRP): a comprehensive study of 43 Italian families 127
Characterization of a Novel Polymorphism in PPARG Regulatory Region Associated with Type 2 Diabetes and Diabetic Retinopathy in Italy 127
Expressed STSs and transcription of human Xq28 127
An approach for testing gene dosage as a mechanism for cognitive dysfunction in Klinefelter's syndrome 126
SEQUENCE-TAGGED SITES (STSS) FROM YAC INSERT-ENDS AND X-SPECIFIC FLOW-SORTED CHROMOSOMES 126
The impact of inflammation on alternative splicing at PPARG locus in hypertrophic obesity 125
A novel germline mutation in Peroxisome Proliferator-Activated Receptor gamma gene associated with large intestine polyp formation and dyslipidemia 125
Molecular and functional effects of methylglyoxal on human microvascular retinal cells 125
HUMAN GLUCOSE-6-PHOSPHATE-DEHYDROGENASE GENE CARRIED ON A YEAST ARTIFICIAL CHROMOSOME ENCODES ACTIVE ENZYME IN MONKEY CELLS 125
Genetica molecolare delle distrofie corneali e dei disordini metabolici 124
Isolation, physical mapping, and northern analysis of the X-linked human gene encoding methyl CpG-binding protein, MECP2 124
An extensive search for RFLP in the human Glucose 6-phosphate dehydrogenase locus has revealed a silent mutation in the coding sequence 123
Anomalie dello sviluppo 123
Klinefelter's syndrome as a model of anomalous cerebral laterality: Testing gene dosage in the X chromosome pseudoautosomal region using a DNA microarray 122
Molecular characterization of a gene of the 'EGF family' expressed in undifferentiated human NTERA2 teratocarcinoma cells 122
E2 multimeric scaffold for vaccine formulation: immune response by intranasal delivery and transcriptome profile of E2-pulsed dendritic cells 122
Genetic counseling in breast cancerThe national cancer institute of Naples experience 121
Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal region 121
Impairment of circulating endothelial progenitors in Down syndrome 121
Autosomal recessive familial exudative vitreoretinopathy: evidence for genetic heterogeneity 121
Locations and contexts of sequences that hybridize to poly d(G-T) d(C-A) in mammalian ribosomal DNAs and two X-linked genes 120
A new gene encodes a putative GTP-binding protein, escapes X-inactivation and has related sequences on Y chromosome 119
Glucose impairs tamoxifen responsiveness modulating connective tissue growth factor in breast cancer cells 119
Human dbl proto-oncogene in 85 kb of Xq26, and determination of the transcription initiation site 119
Human homologue of the murine Bare patches/Striated gene is not mutated in Incontinentia Pigmenti type 2 119
Clinical phenotype of an Italian family with a new mutation in the PRPF8 gene 119
Investigation of Gamma-aminobutyric acid (GABA) A receptors genes and migraine susceptibility 118
Antigen delivery by filamentous bacteriophage fd displaying an anti-DEC-205 single-chain variable fragment confers adjuvanticity by triggering a TLR9-mediated immune response 118
Evidence of Bacteroides fragilis protection from Bartonella henselae-induced damage 118
Detrimental effects of Bartonella henselae are counteracted by L-arginine and nitric oxide in human endothelial progenitor cells 118
Differential expression pattern of XqPAR-linked genes SYBL1 and IL9R correlates with the structure and evolution of the region 117
Identification and characterisation of the retinitis pigmentosa 1-like1 gene (RP1L1): a novel candidate for retinal degenerations 117
ZPLD1 gene is disrupted in a patient with balanced translocation that exhibits cerebral cavernous malformations 117
YEAST ARTIFICIAL CHROMOSOME-BASED GENOME MAPPING - SOME LESSONS FROM XQ24-Q28 117
SSCP DETECTION OF NOVEL MUTATIONS IN PATIENTS WITH EMERY-DREIFUSS MUSCULAR-DYSTROPHY - DEFINITION OF A SMALL C-TERMINAL REGION REQUIRED FOR EMERIN FUNCTION 116
Clinical features of X linked juvenile retinoschisis associated with new mutations in the XLRS1 gene in Italian families 116
TNFA mediates inflammation-induced effects on PPARG splicing in adipose tissue and mesenchymal precursor cells 116
Cloning and gene structure of the rod cGMP phosphodiesterase delta subunit gene (PDED) in man and mouse 115
IDENTIFICATION OF NEW MUTATIONS IN THE EMERY-DREIFUSS MUSCULAR-DYSTROPHY GENE AND EVIDENCE FOR GENETIC-HETEROGENEITY OF THE DISEASE 115
Human and mouse SYBL1 gene structure and expression 114
MAPPING HUMAN-CHROMOSOMES BY WALKING WITH SEQUENCE-TAGGED SITES FROM END FRAGMENTS OF YEAST ARTIFICIAL CHROMOSOME INSERTS 112
Is PPARG the key gene in diabetic retinopathy? 112
Uncovering the Complexity of Transcriptomes with RNA-Seq 112
Multiple pathogenic and benign genomic rearrangements occur at a 35 kb duplication involving the NEMO and LAGE2 genes 112
Filamin a is mutated in chronic intestinal pseudo-obstruction 111
Identification of novel RP2 mutations in a subset of X-linked Retinitis Pigmentosa families and prediction of new domains 111
RNA-Seq for the identification of novel Mediator transcripts in endothelial progenitor cells 111
Transcriptional and post-transcriptional impact of methylglyoxal in human retinal endothelial cells: New players in diabetic retinopathy? 111
Characterization of a new gene expressed in an undifferentiated teratocarcinoma cell line 110
Differential expression pattern of XqPAR-linked genes SYBL1 and IL9R correlates with the structure and evolution of the region 110
Approccio Clinico alle distrofie corneali ed ai disordini metabolici 109
Identification and assignment of the human transient receptor potential channel 6 gene TRPC6 to chromosome 11q21 -> q22 109
Computational Analysis of Single Nucleotide Polymorphisms Associated with Altered Drug Responsiveness in Type 2 Diabetes 108
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 108
PPAR gamma isoforms as Dr Jekyll and Mr Hyde in insulin sensitivity and adipocyte hypertrophy 108
Massive-Scale RNA-Seq Analysis of Non Ribosomal Transcriptome in Human Trisomy 21 108
Molecular and Clinical Characterization of Albinism in a Large Cohort of Italian Patients 107
Complete congenital stationary night blindness maps on Xp11.4 in a Sardinian family 107
Molecular cloning and fine mapping of API5L1, a novel human gene strongly related to an antiapoptotic gene 107
Mutation analysis of the RPGR gene reveals novel mutations in south European patients with X-linked retinitis pigmentosa 106
HUMAN PROTEIN-KINASE-C LOTA GENE (PRKCI) IS CLOSELY LINKED TO THE BTK GENE IN XQ21.3 105
DDX11L: a novel transcript family emerging from human subtelomeric regions 105
Totale 13.170
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Categoria #
all - tutte 108.038
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 108.038
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20212.585 0 0 0 0 0 210 467 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
2025/20263.604 310 724 1.058 1.234 210 68 0 0 0 0 0 0
Totale 19.751