IRIS
CICCODICOLA, Alfredo
 Distribuzione geografica
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Continente #
NA - Nord America 9.992
EU - Europa 5.278
AS - Asia 4.557
SA - Sud America 1.571
AF - Africa 100
Continente sconosciuto - Info sul continente non disponibili 38
OC - Oceania 2
Totale 21.538
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Nazione #
US - Stati Uniti d'America 9.877
RU - Federazione Russa 2.622
VN - Vietnam 1.576
UA - Ucraina 1.467
CN - Cina 1.349
BR - Brasile 1.257
SG - Singapore 1.117
SE - Svezia 609
DE - Germania 145
GB - Regno Unito 134
AR - Argentina 119
HK - Hong Kong 82
IT - Italia 73
IN - India 68
FR - Francia 61
BD - Bangladesh 58
IQ - Iraq 53
EC - Ecuador 49
ID - Indonesia 48
MX - Messico 47
CO - Colombia 42
FI - Finlandia 36
CA - Canada 34
EU - Europa 33
CZ - Repubblica Ceca 32
TR - Turchia 27
PK - Pakistan 26
VE - Venezuela 26
ZA - Sudafrica 26
CL - Cile 24
PY - Paraguay 24
LV - Lettonia 23
MA - Marocco 23
PH - Filippine 19
UZ - Uzbekistan 19
SA - Arabia Saudita 16
BE - Belgio 14
JP - Giappone 13
KE - Kenya 13
PE - Perù 13
UY - Uruguay 13
AT - Austria 11
MY - Malesia 10
NP - Nepal 10
TN - Tunisia 9
AZ - Azerbaigian 8
DO - Repubblica Dominicana 8
DZ - Algeria 8
JM - Giamaica 8
PL - Polonia 8
ES - Italia 7
AE - Emirati Arabi Uniti 6
HN - Honduras 6
IE - Irlanda 6
IR - Iran 6
JO - Giordania 6
KZ - Kazakistan 6
NL - Olanda 6
BY - Bielorussia 4
EG - Egitto 4
GA - Gabon 4
GE - Georgia 4
IL - Israele 4
KW - Kuwait 4
TT - Trinidad e Tobago 4
BO - Bolivia 3
CH - Svizzera 3
ET - Etiopia 3
KG - Kirghizistan 3
PA - Panama 3
SN - Senegal 3
TW - Taiwan 3
XK - ???statistics.table.value.countryCode.XK??? 3
A2 - ???statistics.table.value.countryCode.A2??? 2
AL - Albania 2
AM - Armenia 2
AU - Australia 2
HU - Ungheria 2
KR - Corea 2
LB - Libano 2
NG - Nigeria 2
NI - Nicaragua 2
QA - Qatar 2
RO - Romania 2
RS - Serbia 2
SI - Slovenia 2
SK - Slovacchia (Repubblica Slovacca) 2
TH - Thailandia 2
AD - Andorra 1
BA - Bosnia-Erzegovina 1
BS - Bahamas 1
BW - Botswana 1
CI - Costa d'Avorio 1
CR - Costa Rica 1
GT - Guatemala 1
KH - Cambogia 1
LT - Lituania 1
LY - Libia 1
ML - Mali 1
MN - Mongolia 1
Totale 21.530
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Città #
Fairfield 1.364
Dong Ket 920
Dallas 916
Chandler 781
Ashburn 742
Woodbridge 625
Houston 602
Seattle 574
Wilmington 515
Cambridge 485
Nyköping 473
Singapore 433
San Jose 428
Moscow 354
Beijing 308
Ann Arbor 282
Boardman 257
Ho Chi Minh City 245
Princeton 177
Lawrence 175
Jacksonville 174
San Diego 144
Hanoi 123
Shanghai 118
Ogden 113
São Paulo 102
Hong Kong 76
The Dalles 72
New York 63
Los Angeles 46
Yubileyny 44
London 42
Rio de Janeiro 41
Santa Clara 41
Munich 38
Chicago 34
Nanjing 34
Helsinki 32
Haiphong 31
Belo Horizonte 29
Da Nang 29
Brno 26
Jinan 25
Riga 23
Brasília 21
Porto Alegre 20
Norwalk 19
Frankfurt am Main 18
Tashkent 18
Baghdad 17
Curitiba 17
Salvador 17
Thái Bình 17
Bremen 16
Biên Hòa 15
Des Moines 15
Shenyang 15
Brussels 14
Campinas 14
Can Tho 14
Kunming 14
Chennai 13
Goiânia 13
Hefei 13
Jakarta 13
Monmouth Junction 13
Quito 13
Fortaleza 12
Guangzhou 12
Hanover 12
Hải Dương 12
Johannesburg 12
Nairobi 12
Nanchang 12
Toronto 12
Columbus 11
Hebei 11
Milan 11
Montevideo 11
Ninh Bình 11
Ribeirão Preto 11
Salt Lake City 11
Tokyo 11
Dhaka 10
Hillsboro 10
Joinville 10
Montreal 10
Napoli 10
New Bedfont 10
Ningbo 10
Nuremberg 10
Pelotas 10
San Francisco 10
Asunción 9
Bắc Giang 9
Guayaquil 9
Nova Iguaçu 9
Santiago 9
Tianjin 9
Zhengzhou 9
Totale 12.862
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Nome #
New somatic mutations and WNK1-B4GALNT3 gene fusion in papillary thyroid carcinoma 359
Analysis of SEMA6B gene expression in breast cancer: identification of a new isoform 212
Identification and expression analysis of novel Jakmip 1 transcripts 207
A MUSCLE-SPECIFIC DNASE I-LIKE GENE IN HUMAN XQ28 206
A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X-linked retinitis pigmentosa (RP3) 204
Heart failure: Pilot transcriptomic analysis of cardiac tissue by RNA-sequencing 201
A novel pseudoautosomal gene encoding a putative GTP-binding protein resides in the vicinity of the Xp/Yp telomere 201
Mutational hot spot within a new RPGR exon in X-linked retinitis pigmentosa 196
SFMetaDB: a comprehensive annotation of mouse RNA splicing factor RNA-Seq datasets 188
AnaLysis of Expression on human chromosome 21, ALE-HSA21: a pilot integrated web resource 184
Alternative Splicing in Adhesion- and Motility-Related Genes in Breast Cancer 179
A synaptobrevin-like gene in the Xq28 pseudoautosomal region undergoes X inactivation 177
A new de novo mutation of the connexin-32 gene in a patient with X-linked Charcot-Marie-Tooth type 1 disease 172
A dominant negative PPARγ isoform at the crossroad between adipogenesis and obesity 167
A new PPAR gamma truncated isoform induced by a regulatory feedback: Is alternative splicing crucial in adipocyte differentiation and defective neoadipogenesis? 167
Complex events in the evolution of the human pseudoautosomal region 2 (PAR2) 167
CONSERVED SEQUENCE-TAGGED SITES - A PHYLOGENETIC APPROACH TO GENOME MAPPING 163
The DNA sequence of the human X chromosome 161
A novel pseudoautosomal human gene encodes a putative protein similar to Ac-like transposases 161
ANALYSIS OF POLYMORPHISMS OF THE NUCLEAR RECEPTOR PPARG GENE IN OBESE INDIVIDUALS FROM SOUTHERN ITALY 160
A novel peroxisome proliferator-activated receptor gamma isoform with dominant negative activity generated by alternative splicing 158
RBPMetaDB: A comprehensive annotation of mouse RNA-Seq datasets with perturbations of RNA-binding proteins 157
SEQUENCE OF HUMAN GLUCOSE-6-PHOSPHATE-DEHYDROGENASE CLONED IN PLASMIDS AND A YEAST ARTIFICIAL CHROMOSOME 151
THE ANTIOXIDANT PHOSPHOLIPID HYDROPEROXIDE GLUTATHIONE PEROXIDASE (GPX4/PHGPX) IN THE FROG HYPOTHALAMUS OF Pelophylax bergeri AS TOOL FOR ITS BIOCONSERVATION ASSESSMENT 150
Filamin (FLN1), plexin (SEX), major palmitoylated protein p55 (MPP1), and von-Hippel Lindau binding protein (VBP1) are not involved in incontinentia pigmenti type 2 150
Filamin A is mutated in X-linked chronic idiopathic intestinal pseudo-obstruction with central nervous system involvement 148
Human PRDM2: Structure, function and pathophysiology 148
Analyzing the Whole Transcriptome by RNA-Seq Data: The Tip of the Iceberg 148
Genetic and epigenetic alterations of RB2/p130 tumor suppressor gene in human sporadic retinoblastoma: implications for pathogenesis and therapeutic approach 146
Glucose impairs tamoxifen responsiveness modulating CTGF (Connective Tissue Growth Factor) in breast cancer cells 146
ANALYSIS AND SEQUENCING OF THE GENOMIC DNA REGION SPANNING THE HUMAN DBL PROTOONCOGENE 145
Filamin a is mutated in chronic intestinal pseudoobstruction 144
PR/SET domain family and cancer: Novel insights from the cancer genome atlas 144
Molecular and functional effects of methylglyoxal on human microvascular retinal cells 144
Escape from X inactivation of two new genes associated with DXS6974E and DXS7020E 144
Molecular genetics of autosomal dominant retinitis pigmentosa (ADRP): a comprehensive study of 43 Italian families 143
An approach for testing gene dosage as a mechanism for cognitive dysfunction in Klinefelter's syndrome 142
Hoxa5 undergoes dynamic DNA methylation and transcriptional repression in the adipose tissue of mice exposed to high-fat diet 142
The impact of inflammation on alternative splicing at PPARG locus in hypertrophic obesity 139
Human dbl proto-oncogene in 85 kb of Xq26, and determination of the transcription initiation site 138
TNFA mediates inflammation-induced effects on PPARG splicing in adipose tissue and mesenchymal precursor cells 138
PPARG: Gene Expression Regulation and Next-Generation Sequencing for Unsolved Issues 137
An extensive search for RFLP in the human Glucose 6-phosphate dehydrogenase locus has revealed a silent mutation in the coding sequence 137
Genetica molecolare delle distrofie corneali e dei disordini metabolici 136
Clinical and molecular genetics of Leber's congenital amaurosis: A multicenter study of Italian patients 136
Isolation, physical mapping, and northern analysis of the X-linked human gene encoding methyl CpG-binding protein, MECP2 136
Expressed STSs and transcription of human Xq28 136
Characterization of MPP4, a gene highly expressed in photoreceptor cells, and mutation analysis in retinitis pigmentosa 136
Klinefelter's syndrome as a model of anomalous cerebral laterality: Testing gene dosage in the X chromosome pseudoautosomal region using a DNA microarray 135
Characterization of a Novel Polymorphism in PPARG Regulatory Region Associated with Type 2 Diabetes and Diabetic Retinopathy in Italy 135
A novel germline mutation in Peroxisome Proliferator-Activated Receptor gamma gene associated with large intestine polyp formation and dyslipidemia 135
Clinical phenotype of an Italian family with a new mutation in the PRPF8 gene 135
Transcriptional and post-transcriptional impact of methylglyoxal in human retinal endothelial cells: New players in diabetic retinopathy? 135
E2 multimeric scaffold for vaccine formulation: immune response by intranasal delivery and transcriptome profile of E2-pulsed dendritic cells 135
A new gene encodes a putative GTP-binding protein, escapes X-inactivation and has related sequences on Y chromosome 134
Molecular characterization of a gene of the 'EGF family' expressed in undifferentiated human NTERA2 teratocarcinoma cells 134
Autosomal recessive familial exudative vitreoretinopathy: evidence for genetic heterogeneity 134
Glucose impairs tamoxifen responsiveness modulating connective tissue growth factor in breast cancer cells 133
Anomalie dello sviluppo 133
IDENTIFICATION OF NEW MUTATIONS IN THE EMERY-DREIFUSS MUSCULAR-DYSTROPHY GENE AND EVIDENCE FOR GENETIC-HETEROGENEITY OF THE DISEASE 132
HUMAN GLUCOSE-6-PHOSPHATE-DEHYDROGENASE GENE CARRIED ON A YEAST ARTIFICIAL CHROMOSOME ENCODES ACTIVE ENZYME IN MONKEY CELLS 132
Locations and contexts of sequences that hybridize to poly d(G-T) d(C-A) in mammalian ribosomal DNAs and two X-linked genes 132
Cloning and gene structure of the rod cGMP phosphodiesterase delta subunit gene (PDED) in man and mouse 131
ZPLD1 gene is disrupted in a patient with balanced translocation that exhibits cerebral cavernous malformations 131
SEQUENCE-TAGGED SITES (STSS) FROM YAC INSERT-ENDS AND X-SPECIFIC FLOW-SORTED CHROMOSOMES 131
YEAST ARTIFICIAL CHROMOSOME-BASED GENOME MAPPING - SOME LESSONS FROM XQ24-Q28 131
Genetic counseling in breast cancerThe national cancer institute of Naples experience 130
Impairment of circulating endothelial progenitors in Down syndrome 130
Human homologue of the murine Bare patches/Striated gene is not mutated in Incontinentia Pigmenti type 2 129
Evidence of Bacteroides fragilis protection from Bartonella henselae-induced damage 129
Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal region 129
RNA-Seq for the identification of novel Mediator transcripts in endothelial progenitor cells 129
Characterization of a new gene expressed in an undifferentiated teratocarcinoma cell line 128
SSCP DETECTION OF NOVEL MUTATIONS IN PATIENTS WITH EMERY-DREIFUSS MUSCULAR-DYSTROPHY - DEFINITION OF A SMALL C-TERMINAL REGION REQUIRED FOR EMERIN FUNCTION 128
Investigation of Gamma-aminobutyric acid (GABA) A receptors genes and migraine susceptibility 127
Identification and characterisation of the retinitis pigmentosa 1-like1 gene (RP1L1): a novel candidate for retinal degenerations 127
Antigen delivery by filamentous bacteriophage fd displaying an anti-DEC-205 single-chain variable fragment confers adjuvanticity by triggering a TLR9-mediated immune response 127
Human and mouse SYBL1 gene structure and expression 127
Detrimental effects of Bartonella henselae are counteracted by L-arginine and nitric oxide in human endothelial progenitor cells 126
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 126
Multiple pathogenic and benign genomic rearrangements occur at a 35 kb duplication involving the NEMO and LAGE2 genes 126
Differential expression pattern of XqPAR-linked genes SYBL1 and IL9R correlates with the structure and evolution of the region 125
Clinical features of X linked juvenile retinoschisis associated with new mutations in the XLRS1 gene in Italian families 125
Is PPARG the key gene in diabetic retinopathy? 125
PPAR gamma isoforms as Dr Jekyll and Mr Hyde in insulin sensitivity and adipocyte hypertrophy 123
Differential expression pattern of XqPAR-linked genes SYBL1 and IL9R correlates with the structure and evolution of the region 122
Molecular and Clinical Characterization of Albinism in a Large Cohort of Italian Patients 122
Massive-Scale RNA-Seq Analysis of Non Ribosomal Transcriptome in Human Trisomy 21 122
MAPPING HUMAN-CHROMOSOMES BY WALKING WITH SEQUENCE-TAGGED SITES FROM END FRAGMENTS OF YEAST ARTIFICIAL CHROMOSOME INSERTS 121
Identification of novel RP2 mutations in a subset of X-linked Retinitis Pigmentosa families and prediction of new domains 121
Diet-induced obesity alters methylation of HOX transcription factors in mouse visceral adipose tissue 120
Filamin a is mutated in chronic intestinal pseudo-obstruction 119
YAC CONTIG ORGANIZATION AND CPG ISLAND ANALYSIS IN XQ28 119
RNA-Seq and human complex diseases: recent accomplishments and future perspectives 118
Identification and assignment of the human transient receptor potential channel 6 gene TRPC6 to chromosome 11q21 -> q22 118
Uncovering the Complexity of Transcriptomes with RNA-Seq 118
Experimental colitis: decreased Octn2 and Atb0+expression in rat colonocytes induces carnitine depletion that is reversible by carnitine-loaded liposomes 116
Complete congenital stationary night blindness maps on Xp11.4 in a Sardinian family 116
HUMAN PROTEIN-KINASE-C LOTA GENE (PRKCI) IS CLOSELY LINKED TO THE BTK GENE IN XQ21.3 116
New insights in adipose tissue dysfunctions in diabetic obese patients: a new PPAR gamma truncated isoform mimicking PPARG dominant negative mutations 116
Totale 14.449
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Categoria #
all - tutte 112.104
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 112.104
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20211.660 0 0 0 0 0 0 0 0 0 233 168 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
2025/20265.729 310 724 1.058 1.234 210 102 416 440 741 494 0 0
Totale 21.876