IRIS
CICCODICOLA, Alfredo
 Distribuzione geografica
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Continente #
NA - Nord America 7.922
EU - Europa 4.990
AS - Asia 2.122
SA - Sud America 270
Continente sconosciuto - Info sul continente non disponibili 35
AF - Africa 6
Totale 15.345
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Nazione #
US - Stati Uniti d'America 7.904
RU - Federazione Russa 2.597
UA - Ucraina 1.454
VN - Vietnam 920
SE - Svezia 602
SG - Singapore 576
CN - Cina 545
BR - Brasile 254
DE - Germania 110
GB - Regno Unito 97
IT - Italia 49
EU - Europa 33
CZ - Repubblica Ceca 31
BE - Belgio 13
IQ - Iraq 12
FR - Francia 11
CA - Canada 10
FI - Finlandia 10
PK - Pakistan 10
TR - Turchia 10
HK - Hong Kong 8
BD - Bangladesh 6
IN - India 6
IR - Iran 6
AR - Argentina 5
UZ - Uzbekistan 5
AT - Austria 4
IE - Irlanda 4
MX - Messico 4
MA - Marocco 3
PY - Paraguay 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
BO - Bolivia 1
BY - Bielorussia 1
EC - Ecuador 1
EG - Egitto 1
HN - Honduras 1
ID - Indonesia 1
JM - Giamaica 1
JO - Giordania 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 15.345
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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
Ann Arbor 282
Singapore 277
Boardman 257
Princeton 177
Lawrence 175
Jacksonville 174
Beijing 170
San Diego 144
Shanghai 118
Ogden 113
New York 50
Yubileyny 44
London 35
Nanjing 33
Munich 29
Brno 26
Jinan 24
Norwalk 19
Santa Clara 18
Bremen 16
São Paulo 16
Shenyang 15
Kunming 14
Brussels 13
Hefei 13
Monmouth Junction 13
Des Moines 12
Guangzhou 12
Hanover 12
Nanchang 12
Hebei 11
Rio de Janeiro 11
Belo Horizonte 10
Helsinki 10
Napoli 10
New Bedfont 10
Ningbo 10
Tianjin 9
Zhengzhou 9
Dallas 8
Hong Kong 8
Lanzhou 8
Milan 8
Toronto 8
Wandsworth 8
Changsha 7
Chengdu 7
Haikou 7
Hangzhou 7
Los Angeles 7
Redwood City 7
Taiyuan 7
Abbottabad 6
Baotou 6
Faenza 6
Kilburn 6
Leawood 6
Ardabil 5
Council Bluffs 5
Olomouc 5
Tashkent 5
The Dalles 5
Acton 4
Dearborn 4
Hounslow 4
Istanbul 4
Lauterbourg 4
Nuremberg 4
Southend 4
Taizhou 4
Baghdad 3
Brasília 3
Cuiabá 3
Dhaka 3
Fuzhou 3
Goiânia 3
Islington 3
Mosul 3
Naples 3
Porto Alegre 3
Ribeirão Preto 3
Ribeirão das Neves 3
San Mateo 3
São José dos Campos 3
São João de Meriti 3
Wuhan 3
Barano D'ischia 2
Bern 2
Cachoeirinha 2
Totale 9.919
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Nome #
New somatic mutations and WNK1-B4GALNT3 gene fusion in papillary thyroid carcinoma 328
Identification and expression analysis of novel Jakmip 1 transcripts 172
SFMetaDB: a comprehensive annotation of mouse RNA splicing factor RNA-Seq datasets 165
Heart failure: Pilot transcriptomic analysis of cardiac tissue by RNA-sequencing 160
Mutational hot spot within a new RPGR exon in X-linked retinitis pigmentosa 159
Analysis of SEMA6B gene expression in breast cancer: identification of a new isoform 150
A MUSCLE-SPECIFIC DNASE I-LIKE GENE IN HUMAN XQ28 150
A novel pseudoautosomal gene encoding a putative GTP-binding protein resides in the vicinity of the Xp/Yp telomere 147
CONSERVED SEQUENCE-TAGGED SITES - A PHYLOGENETIC APPROACH TO GENOME MAPPING 143
RBPMetaDB: A comprehensive annotation of mouse RNA-Seq datasets with perturbations of RNA-binding proteins 129
A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X-linked retinitis pigmentosa (RP3) 127
Complex events in the evolution of the human pseudoautosomal region 2 (PAR2) 125
The DNA sequence of the human X chromosome 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 120
AnaLysis of Expression on human chromosome 21, ALE-HSA21: a pilot integrated web resource 120
A synaptobrevin-like gene in the Xq28 pseudoautosomal region undergoes X inactivation 115
SEQUENCE OF HUMAN GLUCOSE-6-PHOSPHATE-DEHYDROGENASE CLONED IN PLASMIDS AND A YEAST ARTIFICIAL CHROMOSOME 115
ANALYSIS OF POLYMORPHISMS OF THE NUCLEAR RECEPTOR PPARG GENE IN OBESE INDIVIDUALS FROM SOUTHERN ITALY 114
A dominant negative PPARγ isoform at the crossroad between adipogenesis and obesity 114
Characterization of MPP4, a gene highly expressed in photoreceptor cells, and mutation analysis in retinitis pigmentosa 112
E2 multimeric scaffold for vaccine formulation: immune response by intranasal delivery and transcriptome profile of E2-pulsed dendritic cells 112
Alternative Splicing in Adhesion- and Motility-Related Genes in Breast Cancer 111
Glucose impairs tamoxifen responsiveness modulating CTGF (Connective Tissue Growth Factor) in breast cancer cells 111
Human PRDM2: Structure, function and pathophysiology 110
A new de novo mutation of the connexin-32 gene in a patient with X-linked Charcot-Marie-Tooth type 1 disease 110
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
Glucose impairs tamoxifen responsiveness modulating connective tissue growth factor in breast cancer cells 107
Genetic and epigenetic alterations of RB2/p130 tumor suppressor gene in human sporadic retinoblastoma: implications for pathogenesis and therapeutic approach 107
Expressed STSs and transcription of human Xq28 107
Human dbl proto-oncogene in 85 kb of Xq26, and determination of the transcription initiation site 106
THE ANTIOXIDANT PHOSPHOLIPID HYDROPEROXIDE GLUTATHIONE PEROXIDASE (GPX4/PHGPX) IN THE FROG HYPOTHALAMUS OF Pelophylax bergeri AS TOOL FOR ITS BIOCONSERVATION ASSESSMENT 105
Escape from X inactivation of two new genes associated with DXS6974E and DXS7020E 105
Genetic counseling in breast cancerThe national cancer institute of Naples experience 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
Clinical and molecular genetics of Leber's congenital amaurosis: A multicenter study of Italian patients 102
A novel pseudoautosomal human gene encodes a putative protein similar to Ac-like transposases 102
YEAST ARTIFICIAL CHROMOSOME-BASED GENOME MAPPING - SOME LESSONS FROM XQ24-Q28 101
MAPPING HUMAN-CHROMOSOMES BY WALKING WITH SEQUENCE-TAGGED SITES FROM END FRAGMENTS OF YEAST ARTIFICIAL CHROMOSOME INSERTS 100
Uncovering the Complexity of Transcriptomes with RNA-Seq 100
Hoxa5 undergoes dynamic DNA methylation and transcriptional repression in the adipose tissue of mice exposed to high-fat diet 99
The impact of inflammation on alternative splicing at PPARG locus in hypertrophic obesity 98
Autosomal recessive familial exudative vitreoretinopathy: evidence for genetic heterogeneity 98
DDX11L: a novel transcript family emerging from human subtelomeric regions 98
Genetica molecolare delle distrofie corneali e dei disordini metabolici 97
PPARG: Gene Expression Regulation and Next-Generation Sequencing for Unsolved Issues 97
Molecular genetics of autosomal dominant retinitis pigmentosa (ADRP): a comprehensive study of 43 Italian families 96
Molecular characterization of a gene of the 'EGF family' expressed in undifferentiated human NTERA2 teratocarcinoma cells 96
Filamin a is mutated in chronic intestinal pseudo-obstruction 95
Antigen delivery by filamentous bacteriophage fd displaying an anti-DEC-205 single-chain variable fragment confers adjuvanticity by triggering a TLR9-mediated immune response 95
Human homologue of the murine Bare patches/Striated gene is not mutated in Incontinentia Pigmenti type 2 95
Isolation, physical mapping, and northern analysis of the X-linked human gene encoding methyl CpG-binding protein, MECP2 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
Functional expression of human glucose-6-phosphate dehydrogenase in Escherichia coli 95
Human and mouse SYBL1 gene structure and expression 95
Anomalie dello sviluppo 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
Impairment of circulating endothelial progenitors in Down syndrome 94
An approach for testing gene dosage as a mechanism for cognitive dysfunction in Klinefelter's syndrome 93
Approccio Clinico alle distrofie corneali ed ai disordini metabolici 93
Detrimental effects of Bartonella henselae are counteracted by L-arginine and nitric oxide in human endothelial progenitor cells 93
PR/SET domain family and cancer: Novel insights from the cancer genome atlas 93
Molecular and functional effects of methylglyoxal on human microvascular retinal cells 93
ANALYSIS AND SEQUENCING OF THE GENOMIC DNA REGION SPANNING THE HUMAN DBL PROTOONCOGENE 92
A novel peroxisome proliferator-activated receptor gamma isoform with dominant negative activity generated by alternative splicing 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
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 92
New Evidence for the Correlation of the p.G130V Mutation in the GJB2 Gene and Syndromic Hearing Loss With Palmoplantar Keratoderma 91
Cloning and gene structure of the rod cGMP phosphodiesterase delta subunit gene (PDED) in man and mouse 91
ZPLD1 gene is disrupted in a patient with balanced translocation that exhibits cerebral cavernous malformations 91
SEQUENCE-TAGGED SITES (STSS) FROM YAC INSERT-ENDS AND X-SPECIFIC FLOW-SORTED CHROMOSOMES 91
A new PPAR gamma truncated isoform induced by a regulatory feedback: Is alternative splicing crucial in adipocyte differentiation and defective neoadipogenesis? 91
RNA-Seq for the identification of novel Mediator transcripts in endothelial progenitor cells 90
Diet-induced obesity alters methylation of HOX transcription factors in mouse visceral adipose tissue 89
Investigation of Gamma-aminobutyric acid (GABA) A receptors genes and migraine susceptibility 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
A new gene encodes a putative GTP-binding protein, escapes X-inactivation and has related sequences on Y chromosome 88
Gene expression regulation in heart failure: from pathobiology to bioinformatics 88
Identification and characterisation of the retinitis pigmentosa 1-like1 gene (RP1L1): a novel candidate for retinal degenerations 88
Clinical features of X linked juvenile retinoschisis associated with new mutations in the XLRS1 gene in Italian families 88
Identification and assignment of the human transient receptor potential channel 6 gene TRPC6 to chromosome 11q21 -> q22 88
IDENTIFICATION OF NEW MUTATIONS IN THE EMERY-DREIFUSS MUSCULAR-DYSTROPHY GENE AND EVIDENCE FOR GENETIC-HETEROGENEITY OF THE DISEASE 88
PPAR gamma isoforms as Dr Jekyll and Mr Hyde in insulin sensitivity and adipocyte hypertrophy 87
Identification of novel RP2 mutations in a subset of X-linked Retinitis Pigmentosa families and prediction of new domains 86
Computational Analysis of Single Nucleotide Polymorphisms Associated with Altered Drug Responsiveness in Type 2 Diabetes 86
Clinical phenotype of an Italian family with a new mutation in the PRPF8 gene 86
Uncovering the complexity of Transcriptomes with RNA-SEQ 85
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
Differential expression pattern of XqPAR-linked genes SYBL1 and IL9R correlates with the structure and evolution of the region 84
A novel germline mutation in Peroxisome Proliferator-Activated Receptor gamma gene associated with large intestine polyp formation and dyslipidemia 83
Sequence-based exon prediction around the synaptophysin locus reveals a gene-rich area containing novel genes in human proximal Xp 82
Totale 10.531
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Categoria #
all - tutte 86.669
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 86.669
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020656 0 0 0 0 0 0 0 0 0 209 383 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
2024/20254.081 76 270 10 143 95 393 1.319 1.471 288 16 0 0
Totale 15.683