IRIS
RICCIO, Andrea
 Distribuzione geografica
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Continente #
EU - Europa 4.288
NA - Nord America 3.174
AS - Asia 2.537
SA - Sud America 473
AF - Africa 37
OC - Oceania 6
Totale 10.515
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Nazione #
US - Stati Uniti d'America 3.093
RU - Federazione Russa 1.645
SG - Singapore 948
IE - Irlanda 860
CN - Cina 598
HK - Hong Kong 416
BR - Brasile 399
IT - Italia 396
UA - Ucraina 361
GB - Regno Unito 349
DE - Germania 286
VN - Vietnam 141
KR - Corea 131
FI - Finlandia 95
IN - India 89
JP - Giappone 87
SE - Svezia 66
GR - Grecia 64
CA - Canada 56
FR - Francia 54
TR - Turchia 43
BE - Belgio 28
AR - Argentina 27
NL - Olanda 20
AT - Austria 16
MX - Messico 16
PK - Pakistan 15
ZA - Sudafrica 15
BD - Bangladesh 14
EC - Ecuador 14
PL - Polonia 14
CZ - Repubblica Ceca 11
IQ - Iraq 11
ID - Indonesia 10
MA - Marocco 9
PY - Paraguay 9
CO - Colombia 8
CL - Cile 6
ES - Italia 5
UZ - Uzbekistan 5
VE - Venezuela 5
AE - Emirati Arabi Uniti 4
CH - Svizzera 4
IL - Israele 4
KE - Kenya 4
AU - Australia 3
AZ - Azerbaigian 3
CR - Costa Rica 3
JO - Giordania 3
LV - Lettonia 3
TN - Tunisia 3
UY - Uruguay 3
BG - Bulgaria 2
EG - Egitto 2
HN - Honduras 2
IR - Iran 2
LT - Lituania 2
NO - Norvegia 2
NZ - Nuova Zelanda 2
PH - Filippine 2
AG - Antigua e Barbuda 1
AM - Armenia 1
BN - Brunei Darussalam 1
BO - Bolivia 1
CI - Costa d'Avorio 1
DM - Dominica 1
DO - Repubblica Dominicana 1
DZ - Algeria 1
EE - Estonia 1
HR - Croazia 1
IS - Islanda 1
KG - Kirghizistan 1
KZ - Kazakistan 1
LA - Repubblica Popolare Democratica del Laos 1
ML - Mali 1
NC - Nuova Caledonia 1
OM - Oman 1
PE - Perù 1
PT - Portogallo 1
RO - Romania 1
SA - Arabia Saudita 1
SN - Senegal 1
SY - Repubblica araba siriana 1
TH - Thailandia 1
TJ - Tagikistan 1
TT - Trinidad e Tobago 1
TW - Taiwan 1
Totale 10.515
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Città #
Dublin 860
Moscow 553
Jacksonville 552
Santa Clara 517
Chandler 418
Hong Kong 414
Singapore 356
Seoul 116
Bremen 111
Princeton 110
Medford 98
Dallas 91
Hefei 91
Ann Arbor 87
Beijing 85
Roxbury 72
Ashburn 64
Boardman 63
Bengaluru 61
San Mateo 58
Napoli 52
Wilmington 51
Los Angeles 47
Ho Chi Minh City 46
São Paulo 41
The Dalles 41
Caserta 40
Elora 37
Woodbridge 36
New York 31
Aversa 30
Hanoi 30
Brussels 27
Des Moines 20
Jinan 20
Naples 18
Amsterdam 17
Nuremberg 16
Tokyo 15
Haeundae-gu 13
Zhengzhou 13
Cambridge 12
Frankfurt am Main 12
Hangzhou 12
Pozzuoli 12
Brooklyn 11
Columbus 11
London 11
Norwalk 11
Brno 10
Falkenstein 10
Guangzhou 10
Johannesburg 10
Rio de Janeiro 10
Santa Maria Capua Vetere 10
Vienna 10
Düsseldorf 9
Houston 9
Mountain View 9
Shanghai 9
Auburn Hills 8
Delhi 8
Gragnano 8
Shenyang 8
Viterbo 8
Boston 7
Brasília 7
Bắc Ninh 7
Curitiba 7
Helsinki 7
Marseille 7
Montreal 7
Nanjing 7
Paris 7
Redwood City 7
San Francisco 7
Tianjin 7
Wroclaw 7
Belo Horizonte 6
Campinas 6
Changsha 6
Guarulhos 6
Hebei 6
Messina 6
Munich 6
Palermo 6
Warsaw 6
Acerra 5
Asunción 5
Athens 5
Brindisi 5
Chicago 5
Contagem 5
Dhaka 5
Fortaleza 5
Fuzhou 5
Goiânia 5
Lanzhou 5
Newark 5
Porto Alegre 5
Totale 5.866
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Nome #
ZBTB2 protein is a new partner of the Nucleosome Remodeling andDeacetylase (NuRD) complex 139
Distinct methylation changes at the IGF2-H19 locus in congenital growth disorders and cancer 135
Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith - Wiedemann syndrome and Wilms' tumour 134
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] 133
DNA Methylation in the Diagnosis of Monogenic Diseases 129
In Embryonic Stem Cells, ZFP57/KAP1 Recognize a Methylated Hexanucleotide to Affect Chromatin and DNA Methylation of Imprinting Control Regions 128
Beckwith-Wiedemann syndrome. Clinical and etiopathogenic aspects of a model genomic imprinting entity 125
Activation of fetal promoters of insulinlike growth factor II gene in hepatitis C virus-related chronic hepatitis, cirrhosis, and hepatocellular carcinoma 123
Genetic and epigenetic mutations affect the DNA binding capability of human ZFP57 in transient neonatal diabetes type 1 123
Is ZFP57 binding to H19/IGF2: IG-DMR affected in Silver-Russell syndrome? 119
Imprinting at the PLAGL1 domain is contained within a 70-kb CTCF/cohesin-mediated non-allelic chromatin loop 118
Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith-Wiedemann syndrome 115
The H19 endodermal enhancer is required for Igf2 activation and tumor formation in experimental liver carcinogenesis 114
Assisted Reproductive Techniques and Risk of Beckwith-Wiedemann Syndrome 109
22q11.2 distal deletion syndrome: Description of a new case with truncus arteriosus type 2 and review 108
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 107
Loss-of-function maternal-effect mutations of PADI6 are associated with familial and sporadic Beckwith-Wiedemann syndrome with multi-locus imprinting disturbance 106
Developmentally regulated functions of the H19 differentially methylated domain 105
Disruption of genomic neighbourhood at the imprinted IGF2-H19 locus in Beckwith-Wiedemann syndrome and Silver-Russell syndrome 104
Silver-Russell Syndrome and Beckwith-Wiedemann Syndrome Phenotypes Associated with 11p Duplication in a Single Family 102
Beckwith-Wiedemann Syndrome 102
The phenotypic variations of multi-locus imprinting disturbances associated with maternal-effect variants of NLRP5 range from overt imprinting disorder to apparently healthy phenotype 101
Expression and parental imprinting of the H19 gene in human rhabdomyosarcoma 100
Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome 99
Mechanisms causing imprinting defects in familial Beckwith-Wiedemann syndrome with Wilms' tumour 99
A novel microdeletion in the IGF2/H19 imprinting centre region defines a recurrent mutation mechanism in familial Beckwith-Wiedemann syndrome 99
ZFP57 recognizes multiple and closely spaced sequence motif variants to maintain repressive epigenetic marks in mouse embryonic stem cells 99
Inherited and sporadic epimutations at the IGF2-H19 locus in beckwith-wiedemann syndrome and wilms' tumor 98
(Epi)genotype-phenotype correlations in Beckwith-Wiedemann syndrome: A paradigm for genomic medicine 98
A novel large deletion of the ICR1 region including H19 and putative enhancer elements 98
The KCNQ1OT1 imprinting control region and non-coding RNA: New properties derived from the study of Beckwith-Wiedemann syndrome and Silver-Russell syndrome cases 97
(Epi)genotype-phenotype correlations in Beckwith-Wiedemann syndrome 95
Genomic imprinting disorders: lessons on how genome, epigenome and environment interact 95
Role of histone acetylation and DNA methylation in the maintenance of the imprinted expression of the H19 and Igf2 genes 94
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 94
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 94
A KHDC3L mutation resulting in recurrent hydatidiform mole causes genome-wide DNA methylation loss in oocytes and persistent imprinting defects post-fertilisation 94
Co-occurrence of Beckwith-Wiedemann syndrome and pseudohypoparathyroidism type 1B: coincidence or common molecular mechanism? 93
Different Mechanisms Cause Hypomethylation of Both H19 and KCNQ1OT1 Imprinted Differentially Methylated Regions in Two Cases of Silver-Russell Syndrome Spectrum 93
A splicing mutation of the HMGA2 gene is associated with Silver-Russell syndrome phenotype 93
Both Epimutations and Chromosome Aberrations Affect Multiple Imprinted Loci in Aggressive Wilms Tumors 93
Co-Occurrence of Beckwith–Wiedemann Syndrome and Early-Onset Colorectal Cancer 92
ZFP57 maintains the parent-of-origin-specific expression of the imprinted genes and differentially affects non-imprinted targets in mouse embryonic stem cells 92
Clinical and molecular characterization of patients affected by Beckwith-Wiedemann spectrum conceived through assisted reproduction techniques 91
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 91
Biallelic variant in cyclin B3 is associated with failure of maternal meiosis II and recurrent digynic triploidy 90
The number of the CTCF binding sites of the H19/IGF2:IG-DMR correlates with DNA methylation and expression imprinting in a humanized mouse model 90
A case of Beckwith-Wiedemann syndrome caused by a cryptic 11p15 deletion encompassing the centromeric imprinted domain of the BWS locus 89
Transcription alterations of KCNQ1 associated with imprinted methylation defects in the Beckwith-Wiedemann locus 88
Looking for CDKN1C enhancers 87
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 86
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. 85
Novel genetic variants of KHDC3L and other members of the subcortical maternal complex associated with Beckwith-Wiedemann syndrome or Pseudohypoparathyroidism 1B and multi-locus imprinting disturbances 84
The mismatch-repair proteins MSH2 and MSH6 interact with the imprinting control regions through the ZFP57-KAP1 complex 84
LOSS OF HETEROZYGOSITY OF IMPRINTED GENES IN SV40 T/T ANTIGEN-INDUCED HEPATOCELLULAR CARCINOMAS 84
Familial posterior helical ear pits 84
Paternal deletion of the 11p15.5 centromeric-imprinting control region is associated with alteration of imprinted gene expression and recurrent severe intrauterine growth restriction 83
BamHI RFLP linked to the human urokinase gene 83
MONO-ALLLIC AND BI-ALLELIC EXPRESSION OF INSULIN-LIKE GROWTH-FACTOR-II GENE IN HUMAN MUSCLE TUMORS 82
Perlman syndrome: Clinical report and nine-year follow-up 82
Tissue-specific and mosaic imprinting defects underlie opposite congenital growth disorders in mice 82
Humanized H19/Igf2 locus reveals diverged imprinting mechanism between mouse and human and reflects Silver-Russell syndrome phenotypes 81
Zfp57 inactivation illustrates the role of ICR methylation in imprinted gene expression during neural differentiation of mouse ESCs 81
Microdeletion and IGF2 loss of imprinting in a cascade causing Beckwith-Wiedemann syndrome with Wilms' tumor - Reply 80
Clinical utility gene card for: Beckwith-Wiedemann Syndrome 80
Prevalence of beckwith-wiedemann syndrome in North West of Italy 80
Two maternal duplications involving the CDKN1C gene are associated with contrasting growth phenotypes 79
Performance Metrics of the Scoring System for the Diagnosis of the Beckwith-Wiedemann Spectrum (BWSp) and Its Correlation with Cancer Development 78
Gain of function in CDKN1C 78
Causes and Consequences of Multi-Locus Imprinting Disturbances in Humans 78
Mosaic segmental and whole-chromosome upd(11)mat in silver-russell syndrome 78
Epigenetic Alterations in Inborn Errors of Immunity 77
Plasminogen activator inhibitor type-1 protein, mRNA and gene transcription are increased by phorbol esters in human rhabdomyosarcoma cells 77
Identification of trombospondin-1 as a novel amelogenin interactor by functional proteomics 77
Tumor necrosis factor-α regulates mRNA for urokinase-type plasminogen activator and type-1 plasminogen activator inhibitor in human neoplastic cell lines 76
Variable expressivity of the beckwith-wiedemann syndrome in four pedigrees segregating loss-of-function variants of cdkn1c 76
A maternal-effectPadi6variant causes nuclear and cytoplasmic abnormalities in oocytes, as well as failure of epigenetic reprogramming and zygotic genome activation in embryos 75
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 75
The Arabidopsis SUPERMAN protein is able to specifically bind DNA through its single Cys2-His2 zinc finger motif 74
Nephrological findings and genotype-phenotype correlation in Beckwith-Wiedemann syndrome 73
Congenital imprinting disorders: Eucid.net -a network to decipher their aetiology and to improve the diagnostic and clinical care 73
A paternally inherited 1.4 kb deletion of the 11p15.5 imprinting center 2 is associated with a mild familial Silver–Russell syndrome phenotype 73
Molecular subtypes and phenotypic expression of Beckwith-Wiedemann syndrome 72
Convergently functional, Rho-independent terminator in Salmonella typhimurium 72
Structure of the galactokinase gene of Escherichia coli, the last (?) gene of the gal operon 72
Plasminogen activator inhibitor type 1 gene is located at region q21.3-q22 of chromosome 7 and genetically linked with cystic fibrosis. 71
Plasminogen activator inhibitor type 1 biosynthesis and mRNA level are increased by dexamethasone in human fibrosarcoma cells 70
Insulin Like Growth Factor 2 Expression in the Rat Brain Both in Basal Condition and following Learning Predominantly Derives from the Maternal Allele 70
EMQN best practice guidelines for the molecular genetic testing and reporting of chromosome 11p15 imprinting disorders: Silver-Russell and Beckwith-Wiedemann syndrome 70
Clinical and molecular diagnosis, screening and management of Beckwith-Wiedemann syndrome: An international consensus statement 70
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 69
PARENTAL IMPRINTING OF RAT INSULIN-LIKE GROWTH-FACTOR-II GENE PROMOTERS IS COORDINATELY REGULATED 69
Recommendations of the Scientific Committee of the Italian Beckwith-Wiedemann Syndrome Association on the diagnosis, Management and follow-up of the syndrome 68
The PEG13-DMR and brain-specific enhancers dictate imprinted expression within the 8q24 intellectual disability risk locus 68
Paternal imprints can be established on the maternal Igf2-H19 locus without altering replication timing of DNA 66
Cancer Risk in Beckwith-Wiedemann Syndrome: A Systematic Review and Meta-Analysis Outlining a Novel (Epi)Genotype Specific Histotype Targeted Screening Protocol 66
The H19 locus acts in vivo as a tumor suppressor 65
Silver-Russell syndrome due to paternal H19/IGF2 hypomethylation in a twin girl born after in vitro fertilization 65
Wnt/beta-catenin signaling pathway safeguards epigenetic stability and homeostasis of mouse embryonic stem cells 65
Plasminogen activator inhibitor type 1 biosynthesis and mRNA level are increased by dexamethasone in human fibrosarcoma cells 64
Totale 8.984
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Categoria #
all - tutte 43.423
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 43.423
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021434 0 0 0 0 0 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
2024/20252.047 14 63 12 74 339 319 256 173 321 199 123 154
2025/20263.530 321 376 362 392 796 1.283 0 0 0 0 0 0
Totale 10.815