IRIS
CICCODICOLA, Alfredo
 Distribuzione geografica
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Continente #
NA - Nord America 7.478
EU - Europa 2.255
AS - Asia 1.342
Continente sconosciuto - Info sul continente non disponibili 35
Totale 11.110
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Nazione #
US - Stati Uniti d'America 7.467
UA - Ucraina 1.452
VN - Vietnam 920
SE - Svezia 602
CN - Cina 410
GB - Regno Unito 96
IT - Italia 40
DE - Germania 33
EU - Europa 33
BE - Belgio 13
CA - Canada 10
FR - Francia 6
IR - Iran 6
IN - India 5
IE - Irlanda 4
RU - Federazione Russa 3
A2 - ???statistics.table.value.countryCode.A2??? 2
CH - Svizzera 2
FI - Finlandia 2
MX - Messico 1
NL - Olanda 1
QA - Qatar 1
RO - Romania 1
Totale 11.110
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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
Ann Arbor 282
Princeton 177
Lawrence 175
Jacksonville 174
Beijing 170
San Diego 144
Ogden 113
Boardman 50
New York 50
London 35
Nanjing 33
Jinan 23
Norwalk 19
Bremen 16
Shenyang 15
Kunming 14
Brussels 13
Monmouth Junction 13
Des Moines 12
Guangzhou 12
Hanover 12
Hefei 12
Nanchang 12
Hebei 11
Napoli 10
New Bedfont 10
Ningbo 10
Tianjin 9
Zhengzhou 9
Lanzhou 8
Toronto 8
Wandsworth 8
Chengdu 7
Haikou 7
Hangzhou 7
Redwood City 7
Taiyuan 7
Baotou 6
Changsha 6
Faenza 6
Kilburn 6
Leawood 6
Milan 6
Ardabil 5
Acton 4
Dearborn 4
Hounslow 4
Los Angeles 4
Southend 4
Taizhou 4
Fuzhou 3
Islington 3
Naples 3
San Mateo 3
Wuhan 3
Barano D'ischia 2
Bern 2
Chaoyang 2
Chennai 2
Chiswick 2
Grafing 2
Helsinki 2
Jiaxing 2
Paris 2
Pune 2
Redmond 2
Shanghai 2
Tappahannock 2
Ballybane 1
Belaya Glina 1
Bentonville 1
Camerino 1
Dublin 1
Fushan 1
Hongtong 1
Kolkata 1
Munich 1
Saddle Lake 1
Southwark 1
Tehran 1
Veracruz 1
Washington 1
Wenzhou 1
Yinchuan 1
Totale 8.741
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Nome #
New somatic mutations and WNK1-B4GALNT3 gene fusion in papillary thyroid carcinoma 303
Identification and expression analysis of novel Jakmip 1 transcripts 147
Heart failure: Pilot transcriptomic analysis of cardiac tissue by RNA-sequencing 140
SFMetaDB: a comprehensive annotation of mouse RNA splicing factor RNA-Seq datasets 138
Mutational hot spot within a new RPGR exon in X-linked retinitis pigmentosa 136
A MUSCLE-SPECIFIC DNASE I-LIKE GENE IN HUMAN XQ28 111
Analysis of SEMA6B gene expression in breast cancer: identification of a new isoform 110
RBPMetaDB: A comprehensive annotation of mouse RNA-Seq datasets with perturbations of RNA-binding proteins 106
A novel pseudoautosomal gene encoding a putative GTP-binding protein resides in the vicinity of the Xp/Yp telomere 103
HUMAN GLUCOSE-6-PHOSPHATE-DEHYDROGENASE GENE CARRIED ON A YEAST ARTIFICIAL CHROMOSOME ENCODES ACTIVE ENZYME IN MONKEY CELLS 100
Complex events in the evolution of the human pseudoautosomal region 2 (PAR2) 98
Filamin A is mutated in X-linked chronic idiopathic intestinal pseudo-obstruction with central nervous system involvement 93
The DNA sequence of the human X chromosome 93
Filamin a is mutated in chronic intestinal pseudoobstruction 92
CONSERVED SEQUENCE-TAGGED SITES - A PHYLOGENETIC APPROACH TO GENOME MAPPING 92
Human PRDM2: Structure, function and pathophysiology 92
SEQUENCE OF HUMAN GLUCOSE-6-PHOSPHATE-DEHYDROGENASE CLONED IN PLASMIDS AND A YEAST ARTIFICIAL CHROMOSOME 90
Glucose impairs tamoxifen responsiveness modulating connective tissue growth factor in breast cancer cells 86
Characterization of a Novel Polymorphism in PPARG Regulatory Region Associated with Type 2 Diabetes and Diabetic Retinopathy in Italy 85
Filamin (FLN1), plexin (SEX), major palmitoylated protein p55 (MPP1), and von-Hippel Lindau binding protein (VBP1) are not involved in incontinentia pigmenti type 2 85
E2 multimeric scaffold for vaccine formulation: immune response by intranasal delivery and transcriptome profile of E2-pulsed dendritic cells 85
Clinical and molecular genetics of Leber's congenital amaurosis: A multicenter study of Italian patients 84
THE ANTIOXIDANT PHOSPHOLIPID HYDROPEROXIDE GLUTATHIONE PEROXIDASE (GPX4/PHGPX) IN THE FROG HYPOTHALAMUS OF Pelophylax bergeri AS TOOL FOR ITS BIOCONSERVATION ASSESSMENT 83
Klinefelter's syndrome as a model of anomalous cerebral laterality: Testing gene dosage in the X chromosome pseudoautosomal region using a DNA microarray 83
AnaLysis of Expression on human chromosome 21, ALE-HSA21: a pilot integrated web resource 82
Hoxa5 undergoes dynamic DNA methylation and transcriptional repression in the adipose tissue of mice exposed to high-fat diet 82
A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X-linked retinitis pigmentosa (RP3) 81
Uncovering the Complexity of Transcriptomes with RNA-Seq 81
DDX11L: a novel transcript family emerging from human subtelomeric regions 81
Human homologue of the murine Bare patches/Striated gene is not mutated in Incontinentia Pigmenti type 2 80
Characterization of MPP4, a gene highly expressed in photoreceptor cells, and mutation analysis in retinitis pigmentosa 80
Complete congenital stationary night blindness maps on Xp11.4 in a Sardinian family 79
Genetic counseling in breast cancerThe national cancer institute of Naples experience 78
Human dbl proto-oncogene in 85 kb of Xq26, and determination of the transcription initiation site 78
Molecular characterization of a gene of the 'EGF family' expressed in undifferentiated human NTERA2 teratocarcinoma cells 78
Detrimental effects of Bartonella henselae are counteracted by L-arginine and nitric oxide in human endothelial progenitor cells 78
Autosomal recessive familial exudative vitreoretinopathy: evidence for genetic heterogeneity 78
Genetic and epigenetic alterations of RB2/p130 tumor suppressor gene in human sporadic retinoblastoma: implications for pathogenesis and therapeutic approach 77
PPARG: Gene Expression Regulation and Next-Generation Sequencing for Unsolved Issues 77
Expressed STSs and transcription of human Xq28 77
Filamin a is mutated in chronic intestinal pseudo-obstruction 76
ANALYSIS OF POLYMORPHISMS OF THE NUCLEAR RECEPTOR PPARG GENE IN OBESE INDIVIDUALS FROM SOUTHERN ITALY 76
New Evidence for the Correlation of the p.G130V Mutation in the GJB2 Gene and Syndromic Hearing Loss With Palmoplantar Keratoderma 75
Cloning and gene structure of the rod cGMP phosphodiesterase delta subunit gene (PDED) in man and mouse 75
Antigen delivery by filamentous bacteriophage fd displaying an anti-DEC-205 single-chain variable fragment confers adjuvanticity by triggering a TLR9-mediated immune response 75
Impairment of circulating endothelial progenitors in Down syndrome 75
A dominant negative PPARγ isoform at the crossroad between adipogenesis and obesity 75
Investigation of Gamma-aminobutyric acid (GABA) A receptors genes and migraine susceptibility 74
MAPPING HUMAN-CHROMOSOMES BY WALKING WITH SEQUENCE-TAGGED SITES FROM END FRAGMENTS OF YEAST ARTIFICIAL CHROMOSOME INSERTS 73
SEQUENCE-TAGGED SITES (STSS) FROM YAC INSERT-ENDS AND X-SPECIFIC FLOW-SORTED CHROMOSOMES 73
Molecular genetics of autosomal dominant retinitis pigmentosa (ADRP): a comprehensive study of 43 Italian families 73
Alternative Splicing in Adhesion- and Motility-Related Genes in Breast Cancer 73
Evidence of Bacteroides fragilis protection from Bartonella henselae-induced damage 73
YEAST ARTIFICIAL CHROMOSOME-BASED GENOME MAPPING - SOME LESSONS FROM XQ24-Q28 73
Escape from X inactivation of two new genes associated with DXS6974E and DXS7020E 73
Identification and characterisation of the retinitis pigmentosa 1-like1 gene (RP1L1): a novel candidate for retinal degenerations 72
Isolation, physical mapping, and northern analysis of the X-linked human gene encoding methyl CpG-binding protein, MECP2 72
Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal region 72
Locations and contexts of sequences that hybridize to poly d(G-T) d(C-A) in mammalian ribosomal DNAs and two X-linked genes 72
A synaptobrevin-like gene in the Xq28 pseudoautosomal region undergoes X inactivation 71
Clinical features of X linked juvenile retinoschisis associated with new mutations in the XLRS1 gene in Italian families 71
Characterization of a new gene expressed in an undifferentiated teratocarcinoma cell line 70
SSCP DETECTION OF NOVEL MUTATIONS IN PATIENTS WITH EMERY-DREIFUSS MUSCULAR-DYSTROPHY - DEFINITION OF A SMALL C-TERMINAL REGION REQUIRED FOR EMERIN FUNCTION 70
Identification and assignment of the human transient receptor potential channel 6 gene TRPC6 to chromosome 11q21 -> q22 70
Is PPARG the key gene in diabetic retinopathy? 70
Functional expression of human glucose-6-phosphate dehydrogenase in Escherichia coli 70
PR/SET domain family and cancer: Novel insights from the cancer genome atlas 70
Differential expression pattern of XqPAR-linked genes SYBL1 and IL9R correlates with the structure and evolution of the region 69
IDENTIFICATION OF NEW MUTATIONS IN THE EMERY-DREIFUSS MUSCULAR-DYSTROPHY GENE AND EVIDENCE FOR GENETIC-HETEROGENEITY OF THE DISEASE 69
Human and mouse SYBL1 gene structure and expression 69
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 69
CLONING OF THE FRAGILE-X LOCUS IN THE CONTEXT OF YEAST ARTIFICIAL CHROMOSOME-BASED MAPPING OF XQ24-28 68
Computational Analysis of Single Nucleotide Polymorphisms Associated with Altered Drug Responsiveness in Type 2 Diabetes 68
A new de novo mutation of the connexin-32 gene in a patient with X-linked Charcot-Marie-Tooth type 1 disease 67
Experimental colitis: decreased Octn2 and Atb0+expression in rat colonocytes induces carnitine depletion that is reversible by carnitine-loaded liposomes 66
Molecular and Clinical Characterization of Albinism in a Large Cohort of Italian Patients 66
Massive-Scale RNA-Seq Analysis of Non Ribosomal Transcriptome in Human Trisomy 21 66
Identification of novel RP2 mutations in a subset of X-linked Retinitis Pigmentosa families and prediction of new domains 65
Clinical phenotype of an Italian family with a new mutation in the PRPF8 gene 65
Gene expression regulation in heart failure: from pathobiology to bioinformatics 64
The impact of inflammation on alternative splicing at PPARG locus in hypertrophic obesity 64
Uncovering the complexity of Transcriptomes with RNA-SEQ 63
Mapping of MRX81 in Xp11.2-Xq12 suggests the presence of a new gene involved in nonspecific X-linked mental retardation 63
ZPLD1 gene is disrupted in a patient with balanced translocation that exhibits cerebral cavernous malformations 63
Identification of a novel mutation in the myosin VIIA motor domain in a family with autosomal dominant hearing loss (DFNA11) 63
YAC CONTIG ORGANIZATION AND CPG ISLAND ANALYSIS IN XQ28 63
Molecular cloning and fine mapping of API5L1, a novel human gene strongly related to an antiapoptotic gene 63
Glucose impairs tamoxifen responsiveness modulating CTGF (Connective Tissue Growth Factor) in breast cancer cells 63
High-Throughput Analysis of Noncoding RNAs: Implications in Clinical Epigenetics 63
A novel pseudoautosomal human gene encodes a putative protein similar to Ac-like transposases 62
Differential expression pattern of XqPAR-linked genes SYBL1 and IL9R correlates with the structure and evolution of the region 61
ANALYSIS AND SEQUENCING OF THE GENOMIC DNA REGION SPANNING THE HUMAN DBL PROTOONCOGENE 61
Sequence-based exon prediction around the synaptophysin locus reveals a gene-rich area containing novel genes in human proximal Xp 61
Oncogenic properties of the antisense lncRNA COMET in BRAF- and RET-driven papillary thyroid carcinomas 61
The complete genomic sequence of the human RPGR gene reveals new expressed sequences 60
Genetica molecolare delle distrofie corneali e dei disordini metabolici 60
Pan-Cancer Mutational and Transcriptional Analysis of the Integrator Complex 60
PPAR gamma isoforms as Dr Jekyll and Mr Hyde in insulin sensitivity and adipocyte hypertrophy 60
Multiple pathogenic and benign genomic rearrangements occur at a 35 kb duplication involving the NEMO and LAGE2 genes 60
From sequence analysis to diseases identification in the distal human xq28 59
Totale 7.968
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Categoria #
all - tutte 61.234
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 61.234
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/20199 0 0 0 0 0 0 0 0 0 0 5 4
2019/20202.590 5 2 4 10 4 3 524 636 746 209 383 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
2023/2024479 47 27 63 29 15 68 13 21 181 13 2 0
Totale 11.448