CNR Institutional Research Information System

RICCIO, ANDREA
 Distribuzione geografica
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Continente #
AS - Asia 1.971
NA - Nord America 917
EU - Europa 446
SA - Sud America 362
AF - Africa 42
OC - Oceania 3
Continente sconosciuto - Info sul continente non disponibili 1
Totale 3.742
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Nazione #
US - Stati Uniti d'America 861
SG - Singapore 827
CN - Cina 470
BR - Brasile 303
VN - Vietnam 210
HK - Hong Kong 208
IT - Italia 126
FR - Francia 102
KR - Corea 89
NL - Olanda 50
DE - Germania 43
JP - Giappone 39
IN - India 36
GB - Regno Unito 35
MX - Messico 22
AR - Argentina 20
FI - Finlandia 20
CA - Canada 19
BD - Bangladesh 15
AT - Austria 14
EC - Ecuador 12
ZA - Sudafrica 11
IL - Israele 10
IQ - Iraq 10
TR - Turchia 10
RU - Federazione Russa 9
UA - Ucraina 9
CL - Cile 7
PK - Pakistan 7
TN - Tunisia 7
ES - Italia 6
MA - Marocco 6
ID - Indonesia 5
IE - Irlanda 5
SA - Arabia Saudita 5
AZ - Azerbaigian 4
BG - Bulgaria 4
MY - Malesia 4
PE - Perù 4
PL - Polonia 4
SE - Svezia 4
UY - Uruguay 4
VE - Venezuela 4
AU - Australia 3
CO - Colombia 3
DZ - Algeria 3
EG - Egitto 3
HN - Honduras 3
JM - Giamaica 3
JO - Giordania 3
KE - Kenya 3
PH - Filippine 3
PY - Paraguay 3
UZ - Uzbekistan 3
BB - Barbados 2
BO - Bolivia 2
CZ - Repubblica Ceca 2
DO - Repubblica Dominicana 2
KZ - Kazakistan 2
NG - Nigeria 2
RO - Romania 2
TT - Trinidad e Tobago 2
TW - Taiwan 2
AO - Angola 1
BE - Belgio 1
BH - Bahrain 1
BW - Botswana 1
BY - Bielorussia 1
BZ - Belize 1
CG - Congo 1
CY - Cipro 1
GA - Gabon 1
GE - Georgia 1
GT - Guatemala 1
HR - Croazia 1
HU - Ungheria 1
LB - Libano 1
LK - Sri Lanka 1
LT - Lituania 1
LV - Lettonia 1
MD - Moldavia 1
ME - Montenegro 1
MN - Mongolia 1
NI - Nicaragua 1
NO - Norvegia 1
NP - Nepal 1
OM - Oman 1
PT - Portogallo 1
RE - Reunion 1
SK - Slovacchia (Repubblica Slovacca) 1
TH - Thailandia 1
UG - Uganda 1
XK - ???statistics.table.value.countryCode.XK??? 1
ZM - Zambia 1
Totale 3.742
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Città #
Singapore 478
Santa Clara 296
Hong Kong 205
Hefei 184
Beijing 111
San Jose 94
Lauterbourg 92
Seoul 87
Ho Chi Minh City 74
Ashburn 72
Hanoi 62
Dallas 45
Los Angeles 44
New York 26
Tokyo 24
São Paulo 20
Frankfurt am Main 17
Naples 16
Orem 15
Rome 13
Avellino 12
Marigliano 12
Minamishinagawa 12
Lappeenranta 11
Nuremberg 11
Council Bluffs 10
Hyderabad 9
Rio de Janeiro 9
Buffalo 8
Helsinki 8
Quận Bình Thạnh 8
Chicago 7
Milan 7
Amsterdam 6
Goiânia 6
London 6
Porto Alegre 6
Vienna 6
Baghdad 5
Chennai 5
Curitiba 5
Da Nang 5
Dublin 5
Düsseldorf 5
Haiphong 5
Johannesburg 5
Kyiv 5
Mumbai 5
Atlanta 4
Baku 4
Bengaluru 4
Brasília 4
Buenos Aires 4
Bắc Ninh 4
Guangzhou 4
Maceió 4
Mexico City 4
Montevideo 4
Portsmouth 4
Quito 4
Salvador 4
Toronto 4
Amman 3
Aracaju 3
Aversa 3
Bauru 3
Bắc Giang 3
Cabo Frio 3
Campos dos Goytacazes 3
Cape Town 3
Denver 3
Elk Grove Village 3
Falkenstein 3
Fortaleza 3
Giugliano in Campania 3
Hortolândia 3
Houston 3
Istanbul 3
Itajaí 3
Juneau 3
Kingston 3
Manchester 3
Montes Claros 3
Nairobi 3
Newark 3
Phoenix 3
Poplar 3
Ribeirão Preto 3
Riyadh 3
Rosario 3
Shanghai 3
Slough 3
Tashkent 3
Teramo 3
Thái Bình 3
Tunis 3
Tây Ninh 3
Uberlândia 3
Warsaw 3
Abuja 2
Totale 2.348
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Nome #
A novel iPSC-based model of ICF syndrome subtype 2 recapitulates the molecular phenotype of ZBTB24 deficiency 107
Zfp57 inactivation illustrates the role of ICR methylation in imprinted gene expression during neural differentiation of mouse ESCs 99
ZFP57 maintains the parent-of-origin-specific expression of the imprinted genes and differentially affects non-imprinted targets in mouse embryonic stem cells 95
Genomic association of the imprinting maintenance factor ZFP57 and associated chromatin regulators in murine embryonal stem cells at imprinted and non imprinted loci and its expression in the developing mouse embryo 87
Beckwith-Wiedemann syndrome and twinning: case report and brief review of literature 78
Co-Occurrence of Beckwith-Wiedemann Syndrome and Early-Onset Colorectal Cancer 77
A maternal-effect Padi6 variant causes nuclear and cytoplasmic abnormalities in oocytes, as well as failure of epigenetic reprogramming and zygotic genome activation in embryos 77
The mismatch-repair proteins MSH2 and MSH6 interact with the imprinting control regions through the ZFP57-KAP1 complex. 66
ICF1 Syndrome Associated DNMT3B Mutations Prevent de novo Methylation at a subset of Imprinted Loci During iPSC Reprogramming 62
Wnt/?-catenin signaling pathway safeguards epigenetic stability and homeostasis of mouse embryonic stem cells 54
Genetic and epigenetic mutations affect the DNA binding capability of human ZFP57 in transient neonatal diabetes type 1. 54
New insights into oocyte cytoplasmic lattice-associated proteins 54
Dynamics of the imprinting maintenance ZFP57/KAP1 and associated factors network at DNA methylated targets in pluripotent ES cells and insights into a potential developmental/differentiation role 54
Understanding the Variability of 22q11.2 Deletion Syndrome: The Role of Epigenetic Factors 53
ZFP57/KAP1 Genomic Association and Targeted Epigenetic Regulation at Imprinted and Not Imprinted Loci 52
The KCNQ1OT1 imprinting control region and non-coding RNA: new properties derived from the study of Beckwith-Wiedemann syndrome and Silver-Russell syndrome cases 50
ZBTB2 protein is a new partner of the Nucleosome Remodeling and Deacetylase (NuRD) complex 48
Genome-wide analysis of Zfp57-mediated epigenetic control at imprinted and non imprinted loci in mouse embryonic stem cells 48
Different Mechanisms Cause Hypomethylation of Both H19 and KCNQ1OT1 Imprinted Differentially Methylated Regions in Two Cases of Silver-Russell Syndrome Spectrum. 48
Glutamine Utilization by Rhizobium etli 47
Trans-acting genetic variants causing multilocus imprinting disturbance (MLID): common mechanisms and consequences 46
Genomic imprinting disorders: lessons on how genome, epigenome and environment interact 44
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. 44
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 44
Genome-wide profiling of the imprinting maintenance factor ZFP57 and associated chromatin regulators in murine embryonal stem cells at imprinted and non-imprinted loci and its role in the neural development of the mouse embryo 41
Epigenomic analysis of the imprinting factor ZFP57, KRAB-ZFPs corepressor KAP1 and associated chromatin modifiers by ChIP seq in mouse embrional stem cells 41
A novel large deletion of the ICR1 region including H19 and putative enhancer elements 40
Performance Metrics of the Scoring System for the Diagnosis of the Beckwith-Wiedemann Spectrum (BWSp) and Its Correlation with Cancer Development 40
Variable expressivity of the beckwith-wiedemann syndrome in four pedigrees segregating loss-of-function variants of cdkn1c 40
ZFP57 recognizes multiple and closely spaced sequence motif variants to maintain repressive epigenetic marks in mouse embryonic stem cells. 40
Imprinting disorders 40
Co-occurrence of Beckwith-Wiedemann syndrome and pseudohypoparathyroidism type 1B: coincidence or common molecular mechanism? 40
Clinical and molecular characterization of patients affected by Beckwith-Wiedemann spectrum conceived through assisted reproduction techniques. 39
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 38
The phenotypic variations of multi-locus imprinting disturbances associated with maternal-effect variants of NLRP5 range from overt imprinting disorder to apparently healthy phenotype 37
ZFP57 recognizes multiple and closely spaced sequence motif variants to maintain repressive epigenetic marks in mouse embryonic stem cells. 37
Dynamics of the ZFP57/KAP1 and associated factors network at DNA methylated targets in murine pluripotent ES cells 36
Epigenetic Alterations in Inborn Errors of Immunity. 36
EMQN best practice guidelines for the molecular genetic testing and reporting of chromosome 11p15 imprinting disorders: Silver-Russell and Beckwith-Wiedemann syndrome 36
Insulin-like growth factor II (IGF-II) e H19 : imprinting parentale e ruolo nella trasformazione neoplastica. 35
First step towards a consensus strategy for multi-locus diagnostic testing of imprinting disorders. 35
Cancer Risk in Beckwith-Wiedemann Syndrome: A Systematic Review and Meta-Analysis Outlining a Novel (Epi)Genotype Specific Histotype Targeted Screening Protocol 35
The ZFP57 imprinting factor and epigenetic control: further clues stemming from expression profiling, ChIP seq and in vitro-induced differentiation 35
Congenital imprinting disorders: Eucid.net -a network to decipher their aetiology and to improve the diagnostic and clinical care 34
Mono- and bi-allelic expression of insulin-like growth factor II gene in human muscle tumors. 34
In Embryonic Stem Cells, ZFP57/KAP1 Recognize a Methylated Hexanucleotide to Affect Chromatin and DNA Methylation of Imprinting Control Regions 33
Looking for CDKN1C enhancers 33
Assisted Reproductive Techniques and Risk of Beckwith-Wiedemann Syndrome. 33
A paternally inherited 1.4 kb deletion of the 11p15.5 Imprinting Center 2 is associated with a mild familial Silver-Russell syndrome phenotype 32
Causes and Consequences of Multi-Locus Imprinting Disturbances in Humans 31
Expert consensus document: Clinical and molecular diagnosis, screening and management of Beckwith-Wiedemann syndrome: an international consensus statement. 30
Role of cis-acting elements and trans-acting factors in genomic imprinting defects 30
DNA methylation in the diagnosis of monogenic diseases 30
DNA methylation status of imprinted and non imprinted loci bound by ZFP57 and associated chromatin modifiers identified by ChIP seq in murine embrional stem cells 30
The PEG13-DMR and brain-specific enhancers dictate imprinted expression within the 8q24 intellectual disability risk locus 29
Deregulation of Insulin Like Growth Factor-2(IGF-2) activity as possible common mechanism in the pathogenesis of different overgrwth disorders: molecular studies on Beckwith-Wiedemann syndrome, Klippel-Trenaunay-Weber syndrome and isolated Hemihypertrophy. 28
Regolazione differenziale degli alleli paterno e materno del gene per il fattore insulino-simile tipo II (IGF-II) 28
Analisi degli elementi di controllo dell'espressione del gene per il fattore di crescita insulino-simile di tipo II (IGF-II) in cellule di fegato di ratto 28
A case of Beckwith-Wiedemann syndrome caused by a cryptic 11p15 deletion encompassing the centromeric imprinted domain of the BWS locus 27
Disruption of genomic neighbourhood at the imprinted IGF2-H19 locus in Beckwith-Wiedemann syndrome and Silver-Russell syndrome 27
Regulation of the insulin-like growth factor II gene expression in rat liver cells 27
Is ZFP57 binding to H19/IGF2: IG-DMR affected in Silver-Russell syndrome? 27
Meg3 Non-coding RNA Expression Controls Imprinting by Preventing Transcriptional Upregulation in cis 27
Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith-Wiedemann syndrome 27
Transcription alterations of KCNQ1 associated with imprinted methylation defects in the Beckwith-Wiedemann locus 26
Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumour 26
Wilms tumor and constitutional epigenetic defects 26
Clinical utility gene card for: Beckwith-Wiedemann syndrome. 25
Identification of genetic and non-genetic modifiers of genomic imprinting through screening of imprinted DMR methylation in humans 25
A KHDC3L mutation resulting in recurrent hydatidiform mole causes genome-wide DNA methylation loss in oocytes and persistent imprinting defects post-fertilisation 25
Loss-of-function maternal-effect mutations of PADI6 are associated with familial and sporadic Beckwith-Wiedemann syndrome with multi-locus imprinting disturbance 25
The human urokinase-plasminogen activator gene and its promoter 25
Tissue-specific and mosaic imprinting defects underlie opposite congenital growth disorders in mice 25
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 24
Biallelic variant in cyclin B3 is associated with failure of maternal meiosis II and recurrent digynic triploidy 24
Highly variable genomic methylation in the Beckwith-Wiedemann syndrome associated with multi-locus imprinting disturbances 24
The H19 locus acts in vivo as a tumor suppressor 24
Both epimutations and chromosome aberrations affect multiple imprinted loci in aggressive wilms tumors 24
Preferential loss of heterozygosity of chromosome 7 loci in simian virus 40 t/T antigen-induced mouse hepatocellular carcinomas does not involve H-ras mutations. 24
Imprinting at the PLAGL1 domain is contained within a 70-kb CTCF/cohesin-mediated non-allelic chromatin loop 23
A novel microdeletion in the IGF2/H19 imprinting centre region defines a recurrent mutation mechanism in familial Beckwith-Wiedemann syndrome. 23
Recent Advances in Imprinting Disorders. 23
Genetic and epigenetic mutations affect the DNA binding capability of human ZFP57 in transient neonatal diabetes type 1 23
Humanized H19/Igf2 locus reveals diverged imprinting mechanism between mouse and human and reflects Silver-Russell syndrome phenotypes 22
Paternal deletion of the 11p15.5 centromeric-imprinting control region is associated with alteration of imprinted gene expression and recurrent severe intrauterine growth restriction. 22
Inherited and Sporadic Epimutations at the IGF2-H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumor. 22
A novel microdeletion in the IGF2/H19 imprinting centre region defines a recurrent mutation mechanism in familial Beckwith-Wiedemann syndrome 22
Two maternal duplications involving the CDKN1C gene are associated with contrasting growth phenotypes 22
(Epi)genotype-phenotype correlations in Beckwith-Wiedemann syndrome 21
Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome 21
Giant breast tumors in a patient with Beckwith-Wiedemann syndrome 21
Imprinting disorders: A group of congenital disorders with overlapping patterns of molecular changes affecting imprinted loci 21
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 21
Imprinting at the PLAGL1 domain is contained within a 70-kb CTCF/cohesin-mediated non-allelic chromatin loop. 21
Insulin Like Growth Factor 2 Expression in the Rat Brain Both in Basal Condition and following Learning Predominantly Derives from the Maternal Allele 21
A splicing mutation of the HMGA2 gene is associated with Silver-Russell syndrome phenotype 21
Recommendations of the Scientific Committee of the Italian Beckwith-Wiedemann Syndrome Association on the diagnosis, management and follow-up of the syndrome 20
BamHI RFLP linked to the human urokinase gene 20
Distinct methylation changes at the IGF2-H19 locus in congenital growth disorders and cancer 20
Prevalence of beckwith-wiedemann syndrome in North West of Italy. 19
Totale 3.655
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Categoria #
all - tutte 13.122
article - articoli 11.093
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 24.215
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202411 0 0 0 0 0 0 0 0 4 0 4 3
2024/20251.446 11 4 108 67 288 41 24 99 33 63 349 359
2025/20262.349 120 261 213 362 424 94 351 141 130 175 78 0
Totale 3.806