IRIS
RICCIO, Andrea
 Distribuzione geografica
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Continente #
EU - Europa 2.399
NA - Nord America 2.310
AS - Asia 569
SA - Sud America 8
OC - Oceania 3
Totale 5.289
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Nazione #
US - Stati Uniti d'America 2.271
IE - Irlanda 857
UA - Ucraina 353
IT - Italia 329
GB - Regno Unito 317
DE - Germania 245
CN - Cina 204
SG - Singapore 172
FI - Finlandia 92
KR - Corea 68
GR - Grecia 64
SE - Svezia 64
JP - Giappone 53
CA - Canada 38
TR - Turchia 33
BE - Belgio 24
FR - Francia 19
IN - India 13
PK - Pakistan 13
CZ - Repubblica Ceca 11
NL - Olanda 8
HK - Hong Kong 6
AT - Austria 4
BR - Brasile 4
RU - Federazione Russa 4
CH - Svizzera 3
AU - Australia 2
CO - Colombia 2
ES - Italia 2
VN - Vietnam 2
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 5.289
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Città #
Dublin 857
Jacksonville 551
Chandler 418
Santa Clara 128
Singapore 117
Bremen 111
Princeton 110
Medford 98
Ann Arbor 87
Roxbury 72
Boardman 62
San Mateo 58
Beijing 54
Seoul 53
Napoli 52
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
Naples 9
Auburn Hills 8
Gragnano 8
Shenyang 8
Amsterdam 7
Delhi 7
Guangzhou 7
Marseille 7
Redwood City 7
Shanghai 7
Aversa 6
Hebei 6
Messina 6
Nanjing 6
Palermo 6
Acerra 5
Ashburn 5
Athens 5
Brindisi 5
Changsha 5
Lanzhou 5
Falls Church 4
Fuzhou 4
Helsinki 4
Hong Kong 4
Moscow 4
Palatine 4
Paris 4
Redmond 4
Afragola 3
Cinisello Balsamo 3
Dadu 3
Frankfurt am Main 3
Mumbai 3
Nanchang 3
Ningbo 3
San Francisco 3
Terzigno 3
Torino 3
Angri 2
Benevento 2
Boydton 2
Capua 2
Desio 2
Diyarbakır 2
Fairfield 2
Fremont 2
Genova 2
Greenwich 2
Kunming 2
Lappeenranta 2
London 2
Medellín 2
Melbourne 2
Milan 2
Pievepelago 2
Pomigliano D'arco 2
Porto Alegre 2
Quanzhou 2
Shenzhen 2
Stella Cilento 2
Thorigny 2
Tokyo 2
Vienna 2
Yuncheng 2
Totale 3.448
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Nome #
ZBTB2 protein is a new partner of the Nucleosome Remodeling andDeacetylase (NuRD) complex 88
In Embryonic Stem Cells, ZFP57/KAP1 Recognize a Methylated Hexanucleotide to Affect Chromatin and DNA Methylation of Imprinting Control Regions 87
Distinct methylation changes at the IGF2-H19 locus in congenital growth disorders and cancer 84
DNA Methylation in the Diagnosis of Monogenic Diseases 81
Beckwith-Wiedemann syndrome. Clinical and etiopathogenic aspects of a model genomic imprinting entity 79
Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith - Wiedemann syndrome and Wilms' tumour 78
The H19 endodermal enhancer is required for Igf2 activation and tumor formation in experimental liver carcinogenesis 78
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] 74
Is ZFP57 binding to H19/IGF2: IG-DMR affected in Silver-Russell syndrome? 73
Silver-Russell Syndrome and Beckwith-Wiedemann Syndrome Phenotypes Associated with 11p Duplication in a Single Family 72
Imprinting at the PLAGL1 domain is contained within a 70-kb CTCF/cohesin-mediated non-allelic chromatin loop 70
Activation of fetal promoters of insulinlike growth factor II gene in hepatitis C virus-related chronic hepatitis, cirrhosis, and hepatocellular carcinoma 68
The KCNQ1OT1 imprinting control region and non-coding RNA: New properties derived from the study of Beckwith-Wiedemann syndrome and Silver-Russell syndrome cases 67
Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith-Wiedemann syndrome 66
The phenotypic variations of multi-locus imprinting disturbances associated with maternal-effect variants of NLRP5 range from overt imprinting disorder to apparently healthy phenotype 65
Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome 64
Genetic and epigenetic mutations affect the DNA binding capability of human ZFP57 in transient neonatal diabetes type 1 63
22q11.2 distal deletion syndrome: Description of a new case with truncus arteriosus type 2 and review 62
ZFP57 recognizes multiple and closely spaced sequence motif variants to maintain repressive epigenetic marks in mouse embryonic stem cells 61
Mechanisms causing imprinting defects in familial Beckwith-Wiedemann syndrome with Wilms' tumour 60
Looking for CDKN1C enhancers 58
Developmentally regulated functions of the H19 differentially methylated domain 57
ZFP57 maintains the parent-of-origin-specific expression of the imprinted genes and differentially affects non-imprinted targets in mouse embryonic stem cells 57
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 56
Role of histone acetylation and DNA methylation in the maintenance of the imprinted expression of the H19 and Igf2 genes 56
Disruption of genomic neighbourhood at the imprinted IGF2-H19 locus in Beckwith-Wiedemann syndrome and Silver-Russell syndrome 56
Genomic imprinting disorders: lessons on how genome, epigenome and environment interact 56
Microdeletion and IGF2 loss of imprinting in a cascade causing Beckwith-Wiedemann syndrome with Wilms' tumor - Reply 55
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. 55
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 55
LOSS OF HETEROZYGOSITY OF IMPRINTED GENES IN SV40 T/T ANTIGEN-INDUCED HEPATOCELLULAR CARCINOMAS 54
Beckwith-Wiedemann Syndrome 54
Plasminogen activator inhibitor type-1 protein, mRNA and gene transcription are increased by phorbol esters in human rhabdomyosarcoma cells 53
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 53
MONO-ALLLIC AND BI-ALLELIC EXPRESSION OF INSULIN-LIKE GROWTH-FACTOR-II GENE IN HUMAN MUSCLE TUMORS 52
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 52
A novel large deletion of the ICR1 region including H19 and putative enhancer elements 52
Assisted Reproductive Techniques and Risk of Beckwith-Wiedemann Syndrome 52
Expression and parental imprinting of the H19 gene in human rhabdomyosarcoma 51
Paternal deletion of the 11p15.5 centromeric-imprinting control region is associated with alteration of imprinted gene expression and recurrent severe intrauterine growth restriction 51
A novel microdeletion in the IGF2/H19 imprinting centre region defines a recurrent mutation mechanism in familial Beckwith-Wiedemann syndrome 50
A KHDC3L mutation resulting in recurrent hydatidiform mole causes genome-wide DNA methylation loss in oocytes and persistent imprinting defects post-fertilisation 50
Perlman syndrome: Clinical report and nine-year follow-up 49
Humanized H19/Igf2 locus reveals diverged imprinting mechanism between mouse and human and reflects Silver-Russell syndrome phenotypes 49
Plasminogen activator inhibitor type 1 gene is located at region q21.3-q22 of chromosome 7 and genetically linked with cystic fibrosis. 48
Prevalence of beckwith-wiedemann syndrome in North West of Italy 48
Convergently functional, Rho-independent terminator in Salmonella typhimurium 48
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 48
Causes and Consequences of Multi-Locus Imprinting Disturbances in Humans 48
Both Epimutations and Chromosome Aberrations Affect Multiple Imprinted Loci in Aggressive Wilms Tumors 48
Clinical utility gene card for: Beckwith-Wiedemann Syndrome 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 47
Molecular subtypes and phenotypic expression of Beckwith-Wiedemann syndrome 47
(Epi)genotype-phenotype correlations in Beckwith-Wiedemann syndrome: A paradigm for genomic medicine 47
A splicing mutation of the HMGA2 gene is associated with Silver-Russell syndrome phenotype 47
Identification of trombospondin-1 as a novel amelogenin interactor by functional proteomics 47
The Arabidopsis SUPERMAN protein is able to specifically bind DNA through its single Cys2-His2 zinc finger motif 46
A case of Beckwith-Wiedemann syndrome caused by a cryptic 11p15 deletion encompassing the centromeric imprinted domain of the BWS locus 46
Familial posterior helical ear pits 46
Inherited and sporadic epimutations at the IGF2-H19 locus in beckwith-wiedemann syndrome and wilms' tumor 46
BamHI RFLP linked to the human urokinase gene 45
(Epi)genotype-phenotype correlations in Beckwith-Wiedemann syndrome 45
Transcription alterations of KCNQ1 associated with imprinted methylation defects in the Beckwith-Wiedemann locus 45
Loss-of-function maternal-effect mutations of PADI6 are associated with familial and sporadic Beckwith-Wiedemann syndrome with multi-locus imprinting disturbance 45
Plasminogen activator inhibitor type 1 biosynthesis and mRNA level are increased by dexamethasone in human fibrosarcoma cells 44
Structure of the galactokinase gene of Escherichia coli, the last (?) gene of the gal operon 43
Congenital imprinting disorders: Eucid.net -a network to decipher their aetiology and to improve the diagnostic and clinical care 43
Tissue-specific and mosaic imprinting defects underlie opposite congenital growth disorders in mice 43
Wnt/beta-catenin signaling pathway safeguards epigenetic stability and homeostasis of mouse embryonic stem cells 43
The H19 locus acts in vivo as a tumor suppressor 42
Insulin Like Growth Factor 2 Expression in the Rat Brain Both in Basal Condition and following Learning Predominantly Derives from the Maternal Allele 42
Cancer Risk in Beckwith-Wiedemann Syndrome: A Systematic Review and Meta-Analysis Outlining a Novel (Epi)Genotype Specific Histotype Targeted Screening Protocol 42
Clinical and molecular diagnosis, screening and management of Beckwith-Wiedemann syndrome: An international consensus statement 42
EMQN best practice guidelines for the molecular genetic testing and reporting of chromosome 11p15 imprinting disorders: Silver-Russell and Beckwith-Wiedemann syndrome 40
Two maternal duplications involving the CDKN1C gene are associated with contrasting growth phenotypes 39
Molecular Etiology Disclosed by Array CGH in Patients With Silver–Russell Syndrome or Similar Phenotypes 39
Biallelic variant in cyclin B3 is associated with failure of maternal meiosis II and recurrent digynic triploidy 39
Different Mechanisms Cause Hypomethylation of Both H19 and KCNQ1OT1 Imprinted Differentially Methylated Regions in Two Cases of Silver-Russell Syndrome Spectrum 38
Gain of function in CDKN1C 38
Recommendations of the Scientific Committee of the Italian Beckwith-Wiedemann Syndrome Association on the diagnosis, Management and follow-up of the syndrome 37
Plasminogen activator inhibitor type 1 biosynthesis and mRNA level are increased by dexamethasone in human fibrosarcoma cells 36
The 5′ end of the KCNQ10T1 gene is hypomethylated in the Beckwith-Wiedemann syndrome 36
PLASMINOGEN-ACTIVATOR INHIBITORS - HORMONALLY REGULATED SERPINS 36
Nephrological findings and genotype-phenotype correlation in Beckwith-Wiedemann syndrome 35
The two-domain hypothesis in Beckwith-Wiedemann syndrome: autonomous imprinting of the telomeric domain of the distal chromosome 7 cluster 35
Wilms tumor and constitutional epigenetic defects 35
Recent Advances in Imprinting Disorders 35
Zfp57 inactivation illustrates the role of ICR methylation in imprinted gene expression during neural differentiation of mouse ESCs 35
Mosaic segmental and whole-chromosome upd(11)mat in silver-russell syndrome 35
Variable expressivity of the beckwith-wiedemann syndrome in four pedigrees segregating loss-of-function variants of cdkn1c 35
Paternal imprints can be established on the maternal Igf2-H19 locus without altering replication timing of DNA 34
FORSKOLIN DOWN-REGULATES TYPE-1 PLASMINOGEN-ACTIVATOR INHIBITOR AND TISSUE-TYPE PLASMINOGEN-ACTIVATOR AND THEIR MESSENGER-RNAS IN HUMAN FIBROSARCOMA CELLS 34
The PEG13-DMR and brain-specific enhancers dictate imprinted expression within the 8q24 intellectual disability risk locus 34
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 33
PARENTAL IMPRINTING OF RAT INSULIN-LIKE GROWTH-FACTOR-II GENE PROMOTERS IS COORDINATELY REGULATED 33
Multiple levels of control of insulin-like growth factor gene expression 33
Structure and function of the internal promoter (hisBp) of the Escherichia coli K-12 histidine operon 33
Tumor necrosis factor-α regulates mRNA for urokinase-type plasminogen activator and type-1 plasminogen activator inhibitor in human neoplastic cell lines 33
Imprinting disorders: a group of congenital disorders with overlapping patterns of molecular changes affecting imprinted loci 33
Silver-Russell syndrome due to paternal H19/IGF2 hypomethylation in a twin girl born after in vitro fertilization 32
Totale 4.996
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Categoria #
all - tutte 25.923
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 25.923
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020347 0 0 0 0 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
2024/2025341 14 63 12 74 178 0 0 0 0 0 0 0
Totale 5.579