IRIS
RICCIO, Andrea
 Distribuzione geografica
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Continente #
EU - Europa 2.359
NA - Nord America 2.181
AS - Asia 498
SA - Sud America 8
OC - Oceania 2
Totale 5.048
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Nazione #
US - Stati Uniti d'America 2.142
IE - Irlanda 857
UA - Ucraina 353
GB - Regno Unito 316
IT - Italia 303
DE - Germania 241
CN - Cina 183
SG - Singapore 127
FI - Finlandia 88
KR - Corea 67
GR - Grecia 64
SE - Svezia 64
JP - Giappone 52
CA - Canada 38
TR - Turchia 33
BE - Belgio 24
FR - Francia 16
IN - India 13
PK - Pakistan 13
CZ - Repubblica Ceca 11
NL - Olanda 7
BR - Brasile 4
RU - Federazione Russa 4
AT - Austria 3
CH - Svizzera 3
HK - Hong Kong 3
CO - Colombia 2
ES - Italia 2
VN - Vietnam 2
AU - Australia 1
BD - Bangladesh 1
CL - Cile 1
EC - Ecuador 1
EE - Estonia 1
IR - Iran 1
MX - Messico 1
NZ - Nuova Zelanda 1
PH - Filippine 1
PL - Polonia 1
RO - Romania 1
TW - Taiwan 1
UZ - Uzbekistan 1
Totale 5.048
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Città #
Dublin 857
Jacksonville 551
Chandler 418
Bremen 111
Princeton 110
Medford 98
Ann Arbor 87
Singapore 76
Roxbury 72
Boardman 62
San Mateo 58
Seoul 53
Napoli 52
Beijing 51
Wilmington 50
Caserta 40
Elora 37
Woodbridge 36
Brussels 23
New York 23
Des Moines 20
Jinan 19
Haeundae-gu 13
Cambridge 12
Norwalk 11
Pozzuoli 11
Zhengzhou 11
Brno 10
Santa Maria Capua Vetere 10
Düsseldorf 9
Hangzhou 9
Houston 9
Los Angeles 9
Mountain View 9
Auburn Hills 8
Gragnano 8
Shenyang 8
Delhi 7
Guangzhou 7
Marseille 7
Naples 7
Redwood City 7
Shanghai 7
Amsterdam 6
Aversa 6
Hebei 6
Nanjing 6
Acerra 5
Ashburn 5
Athens 5
Brindisi 5
Changsha 5
Lanzhou 5
Falls Church 4
Fuzhou 4
Moscow 4
Palatine 4
Redmond 4
Afragola 3
Cinisello Balsamo 3
Dadu 3
Mumbai 3
Nanchang 3
San Francisco 3
Terzigno 3
Torino 3
Angri 2
Benevento 2
Boydton 2
Capua 2
Desio 2
Diyarbakır 2
Fairfield 2
Frankfurt am Main 2
Fremont 2
Genova 2
Greenwich 2
Hong Kong 2
Kunming 2
Lappeenranta 2
Medellín 2
Milan 2
Ningbo 2
Pievepelago 2
Pomigliano D'arco 2
Porto Alegre 2
Stella Cilento 2
Thorigny 2
Vienna 2
Évry 2
Angra dos Reis 1
Ansan-si 1
Arad 1
Auckland 1
Avellino 1
Barano d'Ischia 1
Basel 1
Belo Horizonte 1
Bergamo 1
Berlin 1
Totale 3.249
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Nome #
In Embryonic Stem Cells, ZFP57/KAP1 Recognize a Methylated Hexanucleotide to Affect Chromatin and DNA Methylation of Imprinting Control Regions 86
ZBTB2 protein is a new partner of the Nucleosome Remodeling andDeacetylase (NuRD) complex 86
Distinct methylation changes at the IGF2-H19 locus in congenital growth disorders and cancer 81
DNA Methylation in the Diagnosis of Monogenic Diseases 78
Beckwith-Wiedemann syndrome. Clinical and etiopathogenic aspects of a model genomic imprinting entity 77
Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith - Wiedemann syndrome and Wilms' tumour 76
The H19 endodermal enhancer is required for Igf2 activation and tumor formation in experimental liver carcinogenesis 76
Silver-Russell Syndrome and Beckwith-Wiedemann Syndrome Phenotypes Associated with 11p Duplication in a Single Family 71
Genetic and epigenetic mutations affect the DNA binding capability of human ZFP57 in transient neonatal diabetes type 1 [*Esposito S, *Baglivo I, co-first authors] 70
Is ZFP57 binding to H19/IGF2: IG-DMR affected in Silver-Russell syndrome? 69
Activation of fetal promoters of insulinlike growth factor II gene in hepatitis C virus-related chronic hepatitis, cirrhosis, and hepatocellular carcinoma 66
The KCNQ1OT1 imprinting control region and non-coding RNA: New properties derived from the study of Beckwith-Wiedemann syndrome and Silver-Russell syndrome cases 66
Imprinting at the PLAGL1 domain is contained within a 70-kb CTCF/cohesin-mediated non-allelic chromatin loop 66
Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith-Wiedemann syndrome 65
Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome 63
The phenotypic variations of multi-locus imprinting disturbances associated with maternal-effect variants of NLRP5 range from overt imprinting disorder to apparently healthy phenotype 63
Genetic and epigenetic mutations affect the DNA binding capability of human ZFP57 in transient neonatal diabetes type 1 61
22q11.2 distal deletion syndrome: Description of a new case with truncus arteriosus type 2 and review 60
ZFP57 recognizes multiple and closely spaced sequence motif variants to maintain repressive epigenetic marks in mouse embryonic stem cells 60
Mechanisms causing imprinting defects in familial Beckwith-Wiedemann syndrome with Wilms' tumour 58
Looking for CDKN1C enhancers 57
ZFP57 maintains the parent-of-origin-specific expression of the imprinted genes and differentially affects non-imprinted targets in mouse embryonic stem cells 56
Disruption of genomic neighbourhood at the imprinted IGF2-H19 locus in Beckwith-Wiedemann syndrome and Silver-Russell syndrome 55
Microdeletion and IGF2 loss of imprinting in a cascade causing Beckwith-Wiedemann syndrome with Wilms' tumor - Reply 54
Relaxation of insulin-like growth factor 2 imprinting and discordant methylation at KvDMR1 in two first cousins affected by Beckwith-Wiedemann and Klippel-Trenaunay-Weber syndromes 54
Role of histone acetylation and DNA methylation in the maintenance of the imprinted expression of the H19 and Igf2 genes 54
Developmentally regulated functions of the H19 differentially methylated domain 54
Genomic imprinting disorders: lessons on how genome, epigenome and environment interact 54
Transforming growth factor-beta is a strong and fast acting positive regulator of the level of type-1 plasminogen activator inhibitor mRNA in WI-38 human lung fibroblasts. 53
LOSS OF HETEROZYGOSITY OF IMPRINTED GENES IN SV40 T/T ANTIGEN-INDUCED HEPATOCELLULAR CARCINOMAS 52
Plasminogen activator inhibitor type-1 protein, mRNA and gene transcription are increased by phorbol esters in human rhabdomyosarcoma cells 52
High frequency of loss of heterozygosity at 11p15 and IGF2 overexpression are not related to clinical outcome in childhood adrenocortical tumors positive for the R337H TP53 mutation 51
A common response element mediates differential effects of phorbol esters and forskolin on type‐1 plasminogen activator inhibitor gene expression in human breast carcinoma cells 51
MONO-ALLLIC AND BI-ALLELIC EXPRESSION OF INSULIN-LIKE GROWTH-FACTOR-II GENE IN HUMAN MUSCLE TUMORS 50
Expression and parental imprinting of the H19 gene in human rhabdomyosarcoma 50
Paternal deletion of the 11p15.5 centromeric-imprinting control region is associated with alteration of imprinted gene expression and recurrent severe intrauterine growth restriction 49
A new case of de novo 6q24.2-q25.2 deletion on paternal chromosome 6 with growth hormone deficiency: A twelve-year follow-up and literature review 49
A novel large deletion of the ICR1 region including H19 and putative enhancer elements 49
Assisted Reproductive Techniques and Risk of Beckwith-Wiedemann Syndrome 49
Perlman syndrome: Clinical report and nine-year follow-up 48
A novel microdeletion in the IGF2/H19 imprinting centre region defines a recurrent mutation mechanism in familial Beckwith-Wiedemann syndrome 48
Beckwith-Wiedemann Syndrome 48
Plasminogen activator inhibitor type 1 gene is located at region q21.3-q22 of chromosome 7 and genetically linked with cystic fibrosis. 47
Prevalence of beckwith-wiedemann syndrome in North West of Italy 47
Convergently functional, Rho-independent terminator in Salmonella typhimurium 47
MS-MLPA is a specific and sensitive technique for detecting all chromosome 11p15.5 imprinting defects of BWS and SRS in a single-tube experiment 47
Causes and Consequences of Multi-Locus Imprinting Disturbances in Humans 47
Humanized H19/Igf2 locus reveals diverged imprinting mechanism between mouse and human and reflects Silver-Russell syndrome phenotypes 47
A KHDC3L mutation resulting in recurrent hydatidiform mole causes genome-wide DNA methylation loss in oocytes and persistent imprinting defects post-fertilisation 47
The molecular function and clinical phenotype of partial deletions of the IGF2/H19 imprinting control region depends on the spatial arrangement of the remaining CTCF-binding sites 46
Molecular subtypes and phenotypic expression of Beckwith-Wiedemann syndrome 46
Identification of trombospondin-1 as a novel amelogenin interactor by functional proteomics 46
Clinical utility gene card for: Beckwith-Wiedemann Syndrome 45
Familial posterior helical ear pits 45
Inherited and sporadic epimutations at the IGF2-H19 locus in beckwith-wiedemann syndrome and wilms' tumor 45
(Epi)genotype-phenotype correlations in Beckwith-Wiedemann syndrome: A paradigm for genomic medicine 45
A splicing mutation of the HMGA2 gene is associated with Silver-Russell syndrome phenotype 45
The Arabidopsis SUPERMAN protein is able to specifically bind DNA through its single Cys2-His2 zinc finger motif 44
Loss-of-function maternal-effect mutations of PADI6 are associated with familial and sporadic Beckwith-Wiedemann syndrome with multi-locus imprinting disturbance 44
A case of Beckwith-Wiedemann syndrome caused by a cryptic 11p15 deletion encompassing the centromeric imprinted domain of the BWS locus 43
BamHI RFLP linked to the human urokinase gene 43
(Epi)genotype-phenotype correlations in Beckwith-Wiedemann syndrome 43
Transcription alterations of KCNQ1 associated with imprinted methylation defects in the Beckwith-Wiedemann locus 43
Plasminogen activator inhibitor type 1 biosynthesis and mRNA level are increased by dexamethasone in human fibrosarcoma cells 42
Structure of the galactokinase gene of Escherichia coli, the last (?) gene of the gal operon 42
Tissue-specific and mosaic imprinting defects underlie opposite congenital growth disorders in mice 42
Wnt/beta-catenin signaling pathway safeguards epigenetic stability and homeostasis of mouse embryonic stem cells 42
Both Epimutations and Chromosome Aberrations Affect Multiple Imprinted Loci in Aggressive Wilms Tumors 42
The H19 locus acts in vivo as a tumor suppressor 41
Congenital imprinting disorders: Eucid.net -a network to decipher their aetiology and to improve the diagnostic and clinical care 41
Insulin Like Growth Factor 2 Expression in the Rat Brain Both in Basal Condition and following Learning Predominantly Derives from the Maternal Allele 41
Clinical and molecular diagnosis, screening and management of Beckwith-Wiedemann syndrome: An international consensus statement 41
EMQN best practice guidelines for the molecular genetic testing and reporting of chromosome 11p15 imprinting disorders: Silver-Russell and Beckwith-Wiedemann syndrome 39
Cancer Risk in Beckwith-Wiedemann Syndrome: A Systematic Review and Meta-Analysis Outlining a Novel (Epi)Genotype Specific Histotype Targeted Screening Protocol 39
Two maternal duplications involving the CDKN1C gene are associated with contrasting growth phenotypes 38
Molecular Etiology Disclosed by Array CGH in Patients With Silver–Russell Syndrome or Similar Phenotypes 38
Gain of function in CDKN1C 37
Recommendations of the Scientific Committee of the Italian Beckwith-Wiedemann Syndrome Association on the diagnosis, Management and follow-up of the syndrome 36
Biallelic variant in cyclin B3 is associated with failure of maternal meiosis II and recurrent digynic triploidy 36
Plasminogen activator inhibitor type 1 biosynthesis and mRNA level are increased by dexamethasone in human fibrosarcoma cells 35
The 5′ end of the KCNQ10T1 gene is hypomethylated in the Beckwith-Wiedemann syndrome 35
PLASMINOGEN-ACTIVATOR INHIBITORS - HORMONALLY REGULATED SERPINS 35
Nephrological findings and genotype-phenotype correlation in Beckwith-Wiedemann syndrome 34
The two-domain hypothesis in Beckwith-Wiedemann syndrome: autonomous imprinting of the telomeric domain of the distal chromosome 7 cluster 34
Wilms tumor and constitutional epigenetic defects 34
Recent Advances in Imprinting Disorders 34
Variable expressivity of the beckwith-wiedemann syndrome in four pedigrees segregating loss-of-function variants of cdkn1c 34
Paternal imprints can be established on the maternal Igf2-H19 locus without altering replication timing of DNA 33
Zfp57 inactivation illustrates the role of ICR methylation in imprinted gene expression during neural differentiation of mouse ESCs 33
Mosaic segmental and whole-chromosome upd(11)mat in silver-russell syndrome 33
TRANSFORMING GROWTH FACTOR-BETA-1-RESPONSIVE ELEMENT - CLOSELY ASSOCIATED BINDING-SITES FOR USF AND CCAAT-BINDING TRANSCRIPTION FACTOR-NUCLEAR FACTOR-I IN THE TYPE-1 PLASMINOGEN-ACTIVATOR INHIBITOR GENE 32
PARENTAL IMPRINTING OF RAT INSULIN-LIKE GROWTH-FACTOR-II GENE PROMOTERS IS COORDINATELY REGULATED 32
FORSKOLIN DOWN-REGULATES TYPE-1 PLASMINOGEN-ACTIVATOR INHIBITOR AND TISSUE-TYPE PLASMINOGEN-ACTIVATOR AND THEIR MESSENGER-RNAS IN HUMAN FIBROSARCOMA CELLS 32
Multiple levels of control of insulin-like growth factor gene expression 32
Structure and function of the internal promoter (hisBp) of the Escherichia coli K-12 histidine operon 32
Tumor necrosis factor-α regulates mRNA for urokinase-type plasminogen activator and type-1 plasminogen activator inhibitor in human neoplastic cell lines 32
Imprinting disorders: a group of congenital disorders with overlapping patterns of molecular changes affecting imprinted loci 32
The PEG13-DMR and brain-specific enhancers dictate imprinted expression within the 8q24 intellectual disability risk locus 32
Different Mechanisms Cause Hypomethylation of Both H19 and KCNQ1OT1 Imprinted Differentially Methylated Regions in Two Cases of Silver-Russell Syndrome Spectrum 31
Silver-Russell syndrome due to paternal H19/IGF2 hypomethylation in a twin girl born after in vitro fertilization 31
Totale 4.816
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Categoria #
all - tutte 24.274
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 24.274
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020351 0 0 0 4 95 8 111 21 56 27 23 6
2020/2021805 74 22 96 31 148 11 115 91 16 109 75 17
2021/2022787 64 5 29 13 245 7 16 23 25 125 52 183
2022/20231.791 188 6 7 183 208 153 8 109 830 19 33 47
2023/2024678 62 29 23 58 262 49 20 10 4 3 43 115
2024/202592 14 63 12 3 0 0 0 0 0 0 0 0
Totale 5.330