IRIS
CICCODICOLA, Alfredo
 Distribuzione geografica
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Continente #
NA - Nord America 11.294
EU - Europa 5.342
AS - Asia 4.753
SA - Sud America 1.585
Continente sconosciuto - Info sul continente non disponibili 376
AF - Africa 100
OC - Oceania 2
Totale 23.452
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Nazione #
US - Stati Uniti d'America 11.083
RU - Federazione Russa 2.622
VN - Vietnam 1.582
UA - Ucraina 1.468
CN - Cina 1.443
BR - Brasile 1.262
SG - Singapore 1.178
SE - Svezia 609
DE - Germania 148
GB - Regno Unito 142
IT - Italia 121
AR - Argentina 120
HK - Hong Kong 94
CA - Canada 82
IN - India 68
BD - Bangladesh 66
FR - Francia 62
IQ - Iraq 53
MX - Messico 51
EC - Ecuador 50
ID - Indonesia 48
CO - Colombia 46
FI - Finlandia 36
EU - Europa 33
CZ - Repubblica Ceca 32
TR - Turchia 28
VE - Venezuela 27
PK - Pakistan 26
ZA - Sudafrica 26
CL - Cile 25
PY - Paraguay 24
LV - Lettonia 23
MA - Marocco 23
PH - Filippine 20
UZ - Uzbekistan 19
SA - Arabia Saudita 17
JP - Giappone 15
BE - Belgio 14
JM - Giamaica 14
NP - Nepal 14
PE - Perù 14
KE - Kenya 13
UY - Uruguay 13
CR - Costa Rica 12
MY - Malesia 12
AT - Austria 11
HN - Honduras 11
TN - Tunisia 9
TT - Trinidad e Tobago 9
AZ - Azerbaigian 8
DO - Repubblica Dominicana 8
DZ - Algeria 8
ES - Italia 8
PL - Polonia 8
AE - Emirati Arabi Uniti 6
IE - Irlanda 6
IL - Israele 6
IR - Iran 6
JO - Giordania 6
KZ - Kazakistan 6
NL - Olanda 6
NI - Nicaragua 5
SV - El Salvador 5
BY - Bielorussia 4
EG - Egitto 4
GA - Gabon 4
GE - Georgia 4
KW - Kuwait 4
PA - Panama 4
PR - Porto Rico 4
TH - Thailandia 4
BO - Bolivia 3
CH - Svizzera 3
ET - Etiopia 3
KG - Kirghizistan 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
BS - Bahamas 2
GT - Guatemala 2
HU - Ungheria 2
KR - Corea 2
LB - Libano 2
LC - Santa Lucia 2
NG - Nigeria 2
PT - Portogallo 2
QA - Qatar 2
RO - Romania 2
RS - Serbia 2
SI - Slovenia 2
SK - Slovacchia (Repubblica Slovacca) 2
AD - Andorra 1
BA - Bosnia-Erzegovina 1
BW - Botswana 1
CI - Costa d'Avorio 1
EE - Estonia 1
Totale 23.102
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Città #
Fairfield 1.365
Dallas 926
Dong Ket 920
Ashburn 789
Chandler 781
San Jose 684
Woodbridge 625
Houston 606
Seattle 576
Wilmington 531
Cambridge 485
Nyköping 473
Singapore 451
Moscow 354
Beijing 326
Ann Arbor 282
Boardman 257
Ho Chi Minh City 245
Council Bluffs 188
Princeton 177
Lawrence 175
Jacksonville 174
San Diego 146
Chesapeake 138
Hanoi 127
Shanghai 119
Ogden 113
São Paulo 102
Hong Kong 88
New York 76
The Dalles 73
Santa Clara 70
Los Angeles 66
Yubileyny 44
Chicago 43
London 42
Rio de Janeiro 41
Munich 38
Phoenix 36
Nanjing 34
Helsinki 32
Haiphong 31
Belo Horizonte 29
Da Nang 29
Brno 26
Toronto 26
Jinan 25
Cleveland 23
Riga 23
Brasília 21
Porto Alegre 20
Frankfurt am Main 19
Norwalk 19
Tashkent 18
Baghdad 17
Curitiba 17
Salvador 17
Thái Bình 17
Bremen 16
Montreal 16
Naples 16
Salt Lake City 16
Biên Hòa 15
Des Moines 15
Shenyang 15
Brussels 14
Campinas 14
Can Tho 14
Dhaka 14
Kunming 14
Milan 14
Chennai 13
Columbus 13
Goiânia 13
Hefei 13
Jakarta 13
Monmouth Junction 13
Quito 13
Brooklyn 12
Fortaleza 12
Guangzhou 12
Hanover 12
Hải Dương 12
Johannesburg 12
Nairobi 12
Nanchang 12
Ribeirão Preto 12
Atlanta 11
Changsha 11
Chengdu 11
Hebei 11
Hillsboro 11
Montevideo 11
Ninh Bình 11
San Francisco 11
San José 11
Tokyo 11
Bogotá 10
Joinville 10
Medellín 10
Totale 13.727
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Nome #
New somatic mutations and WNK1-B4GALNT3 gene fusion in papillary thyroid carcinoma 368
Analysis of SEMA6B gene expression in breast cancer: identification of a new isoform 226
A MUSCLE-SPECIFIC DNASE I-LIKE GENE IN HUMAN XQ28 221
A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X-linked retinitis pigmentosa (RP3) 220
Heart failure: Pilot transcriptomic analysis of cardiac tissue by RNA-sequencing 213
Identification and expression analysis of novel Jakmip 1 transcripts 213
A novel pseudoautosomal gene encoding a putative GTP-binding protein resides in the vicinity of the Xp/Yp telomere 208
Mutational hot spot within a new RPGR exon in X-linked retinitis pigmentosa 198
AnaLysis of Expression on human chromosome 21, ALE-HSA21: a pilot integrated web resource 196
SFMetaDB: a comprehensive annotation of mouse RNA splicing factor RNA-Seq datasets 193
Alternative Splicing in Adhesion- and Motility-Related Genes in Breast Cancer 192
A synaptobrevin-like gene in the Xq28 pseudoautosomal region undergoes X inactivation 189
A dominant negative PPARγ isoform at the crossroad between adipogenesis and obesity 183
Complex events in the evolution of the human pseudoautosomal region 2 (PAR2) 180
A new de novo mutation of the connexin-32 gene in a patient with X-linked Charcot-Marie-Tooth type 1 disease 178
A new PPAR gamma truncated isoform induced by a regulatory feedback: Is alternative splicing crucial in adipocyte differentiation and defective neoadipogenesis? 177
The DNA sequence of the human X chromosome 171
A novel pseudoautosomal human gene encodes a putative protein similar to Ac-like transposases 171
A novel peroxisome proliferator-activated receptor gamma isoform with dominant negative activity generated by alternative splicing 167
CONSERVED SEQUENCE-TAGGED SITES - A PHYLOGENETIC APPROACH TO GENOME MAPPING 167
ANALYSIS OF POLYMORPHISMS OF THE NUCLEAR RECEPTOR PPARG GENE IN OBESE INDIVIDUALS FROM SOUTHERN ITALY 166
SEQUENCE OF HUMAN GLUCOSE-6-PHOSPHATE-DEHYDROGENASE CLONED IN PLASMIDS AND A YEAST ARTIFICIAL CHROMOSOME 166
PPARG: Gene Expression Regulation and Next-Generation Sequencing for Unsolved Issues 165
RBPMetaDB: A comprehensive annotation of mouse RNA-Seq datasets with perturbations of RNA-binding proteins 165
Clinical and molecular genetics of Leber's congenital amaurosis: A multicenter study of Italian patients 158
Analyzing the Whole Transcriptome by RNA-Seq Data: The Tip of the Iceberg 158
Filamin A is mutated in X-linked chronic idiopathic intestinal pseudo-obstruction with central nervous system involvement 157
THE ANTIOXIDANT PHOSPHOLIPID HYDROPEROXIDE GLUTATHIONE PEROXIDASE (GPX4/PHGPX) IN THE FROG HYPOTHALAMUS OF Pelophylax bergeri AS TOOL FOR ITS BIOCONSERVATION ASSESSMENT 156
PR/SET domain family and cancer: Novel insights from the cancer genome atlas 156
Human PRDM2: Structure, function and pathophysiology 156
Molecular and functional effects of methylglyoxal on human microvascular retinal cells 156
The impact of inflammation on alternative splicing at PPARG locus in hypertrophic obesity 155
Filamin (FLN1), plexin (SEX), major palmitoylated protein p55 (MPP1), and von-Hippel Lindau binding protein (VBP1) are not involved in incontinentia pigmenti type 2 155
Molecular genetics of autosomal dominant retinitis pigmentosa (ADRP): a comprehensive study of 43 Italian families 154
A novel germline mutation in Peroxisome Proliferator-Activated Receptor gamma gene associated with large intestine polyp formation and dyslipidemia 154
Glucose impairs tamoxifen responsiveness modulating CTGF (Connective Tissue Growth Factor) in breast cancer cells 154
Transcriptional and post-transcriptional impact of methylglyoxal in human retinal endothelial cells: New players in diabetic retinopathy? 154
TNFA mediates inflammation-induced effects on PPARG splicing in adipose tissue and mesenchymal precursor cells 154
ANALYSIS AND SEQUENCING OF THE GENOMIC DNA REGION SPANNING THE HUMAN DBL PROTOONCOGENE 153
Hoxa5 undergoes dynamic DNA methylation and transcriptional repression in the adipose tissue of mice exposed to high-fat diet 153
An extensive search for RFLP in the human Glucose 6-phosphate dehydrogenase locus has revealed a silent mutation in the coding sequence 153
An approach for testing gene dosage as a mechanism for cognitive dysfunction in Klinefelter's syndrome 152
Filamin a is mutated in chronic intestinal pseudoobstruction 151
Cloning and gene structure of the rod cGMP phosphodiesterase delta subunit gene (PDED) in man and mouse 151
Escape from X inactivation of two new genes associated with DXS6974E and DXS7020E 151
Genetic and epigenetic alterations of RB2/p130 tumor suppressor gene in human sporadic retinoblastoma: implications for pathogenesis and therapeutic approach 150
Genetica molecolare delle distrofie corneali e dei disordini metabolici 149
E2 multimeric scaffold for vaccine formulation: immune response by intranasal delivery and transcriptome profile of E2-pulsed dendritic cells 147
A new gene encodes a putative GTP-binding protein, escapes X-inactivation and has related sequences on Y chromosome 145
Identification and characterisation of the retinitis pigmentosa 1-like1 gene (RP1L1): a novel candidate for retinal degenerations 145
Klinefelter's syndrome as a model of anomalous cerebral laterality: Testing gene dosage in the X chromosome pseudoautosomal region using a DNA microarray 144
Isolation, physical mapping, and northern analysis of the X-linked human gene encoding methyl CpG-binding protein, MECP2 144
Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal region 144
Molecular characterization of a gene of the 'EGF family' expressed in undifferentiated human NTERA2 teratocarcinoma cells 144
Human dbl proto-oncogene in 85 kb of Xq26, and determination of the transcription initiation site 143
Impairment of circulating endothelial progenitors in Down syndrome 143
Characterization of a Novel Polymorphism in PPARG Regulatory Region Associated with Type 2 Diabetes and Diabetic Retinopathy in Italy 142
IDENTIFICATION OF NEW MUTATIONS IN THE EMERY-DREIFUSS MUSCULAR-DYSTROPHY GENE AND EVIDENCE FOR GENETIC-HETEROGENEITY OF THE DISEASE 142
Expressed STSs and transcription of human Xq28 141
Characterization of MPP4, a gene highly expressed in photoreceptor cells, and mutation analysis in retinitis pigmentosa 141
Anomalie dello sviluppo 141
Clinical phenotype of an Italian family with a new mutation in the PRPF8 gene 141
ZPLD1 gene is disrupted in a patient with balanced translocation that exhibits cerebral cavernous malformations 140
RNA-Seq and human complex diseases: recent accomplishments and future perspectives 140
Evidence of Bacteroides fragilis protection from Bartonella henselae-induced damage 140
YEAST ARTIFICIAL CHROMOSOME-BASED GENOME MAPPING - SOME LESSONS FROM XQ24-Q28 140
Differential expression pattern of XqPAR-linked genes SYBL1 and IL9R correlates with the structure and evolution of the region 139
Autosomal recessive familial exudative vitreoretinopathy: evidence for genetic heterogeneity 139
HUMAN GLUCOSE-6-PHOSPHATE-DEHYDROGENASE GENE CARRIED ON A YEAST ARTIFICIAL CHROMOSOME ENCODES ACTIVE ENZYME IN MONKEY CELLS 138
Genetic counseling in breast cancerThe national cancer institute of Naples experience 137
Glucose impairs tamoxifen responsiveness modulating connective tissue growth factor in breast cancer cells 137
SEQUENCE-TAGGED SITES (STSS) FROM YAC INSERT-ENDS AND X-SPECIFIC FLOW-SORTED CHROMOSOMES 137
Antigen delivery by filamentous bacteriophage fd displaying an anti-DEC-205 single-chain variable fragment confers adjuvanticity by triggering a TLR9-mediated immune response 137
Human and mouse SYBL1 gene structure and expression 137
Characterization of a new gene expressed in an undifferentiated teratocarcinoma cell line 136
SSCP DETECTION OF NOVEL MUTATIONS IN PATIENTS WITH EMERY-DREIFUSS MUSCULAR-DYSTROPHY - DEFINITION OF A SMALL C-TERMINAL REGION REQUIRED FOR EMERIN FUNCTION 136
Locations and contexts of sequences that hybridize to poly d(G-T) d(C-A) in mammalian ribosomal DNAs and two X-linked genes 135
Human homologue of the murine Bare patches/Striated gene is not mutated in Incontinentia Pigmenti type 2 134
Is PPARG the key gene in diabetic retinopathy? 134
RNA-Seq for the identification of novel Mediator transcripts in endothelial progenitor cells 134
Detrimental effects of Bartonella henselae are counteracted by L-arginine and nitric oxide in human endothelial progenitor cells 133
PPAR gamma isoforms as Dr Jekyll and Mr Hyde in insulin sensitivity and adipocyte hypertrophy 133
MAPPING HUMAN-CHROMOSOMES BY WALKING WITH SEQUENCE-TAGGED SITES FROM END FRAGMENTS OF YEAST ARTIFICIAL CHROMOSOME INSERTS 132
Clinical features of X linked juvenile retinoschisis associated with new mutations in the XLRS1 gene in Italian families 132
Molecular and Clinical Characterization of Albinism in a Large Cohort of Italian Patients 132
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 132
Investigation of Gamma-aminobutyric acid (GABA) A receptors genes and migraine susceptibility 131
Identification of novel RP2 mutations in a subset of X-linked Retinitis Pigmentosa families and prediction of new domains 131
YAC CONTIG ORGANIZATION AND CPG ISLAND ANALYSIS IN XQ28 131
Multiple pathogenic and benign genomic rearrangements occur at a 35 kb duplication involving the NEMO and LAGE2 genes 130
Nutritional genomics era: opportunities toward a genome-tailored nutritional regimen 130
Diet-induced obesity alters methylation of HOX transcription factors in mouse visceral adipose tissue 129
Approccio Clinico alle distrofie corneali ed ai disordini metabolici 128
Massive-Scale RNA-Seq Analysis of Non Ribosomal Transcriptome in Human Trisomy 21 128
Differential expression pattern of XqPAR-linked genes SYBL1 and IL9R correlates with the structure and evolution of the region 127
Identification and assignment of the human transient receptor potential channel 6 gene TRPC6 to chromosome 11q21 -> q22 126
Experimental colitis: decreased Octn2 and Atb0+expression in rat colonocytes induces carnitine depletion that is reversible by carnitine-loaded liposomes 126
Computational Analysis of Single Nucleotide Polymorphisms Associated with Altered Drug Responsiveness in Type 2 Diabetes 126
Filamin a is mutated in chronic intestinal pseudo-obstruction 124
New insights in adipose tissue dysfunctions in diabetic obese patients: a new PPAR gamma truncated isoform mimicking PPARG dominant negative mutations 124
Totale 15.435
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Categoria #
all - tutte 122.931
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 122.931
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.173 0 0 0 498 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
2025/20266.173 310 724 1.058 1.234 210 102 416 440 741 576 216 146
2026/20271.132 143 77 534 378 0 0 0 0 0 0 0 0
Totale 23.452