CNR Institutional Research Information System

RICCIO, ANDREA
 Distribuzione geografica
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Continente #
AS - Asia 2.050
NA - Nord America 1.124
EU - Europa 498
SA - Sud America 369
Continente sconosciuto - Info sul continente non disponibili 65
AF - Africa 43
OC - Oceania 3
Totale 4.152
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Nazione #
US - Stati Uniti d'America 1.050
SG - Singapore 831
CN - Cina 473
BR - Brasile 305
VN - Vietnam 218
HK - Hong Kong 211
IT - Italia 170
FR - Francia 106
KR - Corea 89
BD - Bangladesh 68
NL - Olanda 51
DE - Germania 43
IN - India 39
JP - Giappone 39
GB - Regno Unito 35
CA - Canada 25
MX - Messico 25
AR - Argentina 20
FI - Finlandia 20
AT - Austria 14
EC - Ecuador 13
ZA - Sudafrica 11
IL - Israele 10
IQ - Iraq 10
TR - Turchia 10
RU - Federazione Russa 9
UA - Ucraina 9
CL - Cile 7
ES - Italia 7
ID - Indonesia 7
PK - Pakistan 7
TN - Tunisia 7
CO - Colombia 6
JM - Giamaica 6
MA - Marocco 6
IE - Irlanda 5
MY - Malesia 5
SA - Arabia Saudita 5
VE - Venezuela 5
AZ - Azerbaigian 4
BG - Bulgaria 4
HN - Honduras 4
PE - Perù 4
PH - Filippine 4
PL - Polonia 4
SE - Svezia 4
UY - Uruguay 4
AU - Australia 3
DZ - Algeria 3
EG - Egitto 3
JO - Giordania 3
KE - Kenya 3
PY - Paraguay 3
UZ - Uzbekistan 3
BB - Barbados 2
BO - Bolivia 2
CH - Svizzera 2
CZ - Repubblica Ceca 2
DO - Repubblica Dominicana 2
GT - Guatemala 2
KZ - Kazakistan 2
LB - Libano 2
NG - Nigeria 2
RO - Romania 2
TT - Trinidad e Tobago 2
TW - Taiwan 2
AO - Angola 1
BE - Belgio 1
BH - Bahrain 1
BS - Bahamas 1
BW - Botswana 1
BY - Bielorussia 1
BZ - Belize 1
CG - Congo 1
CR - Costa Rica 1
CY - Cipro 1
GA - Gabon 1
GE - Georgia 1
HR - Croazia 1
HU - Ungheria 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
PR - Porto Rico 1
PT - Portogallo 1
RE - Reunion 1
SC - Seychelles 1
SK - Slovacchia (Repubblica Slovacca) 1
SV - El Salvador 1
TH - Thailandia 1
UG - Uganda 1
XK - ???statistics.table.value.countryCode.XK??? 1
ZM - Zambia 1
Totale 4.088
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Città #
Singapore 481
Santa Clara 315
Hong Kong 206
Hefei 184
San Jose 113
Beijing 111
Ashburn 110
Lauterbourg 92
Seoul 87
Ho Chi Minh City 76
Hanoi 65
Dallas 47
Los Angeles 44
New York 27
Naples 25
Tokyo 24
São Paulo 20
Rome 18
Frankfurt am Main 17
Orem 15
Buffalo 14
Avellino 12
Marigliano 12
Minamishinagawa 12
Lappeenranta 11
Milan 11
Nuremberg 11
Council Bluffs 10
Hyderabad 9
Rio de Janeiro 9
Helsinki 8
Quận Bình Thạnh 8
Atlanta 7
Chicago 7
Amsterdam 6
Da Nang 6
Goiânia 6
London 6
Porto Alegre 6
Vienna 6
Baghdad 5
Brasília 5
Chennai 5
Curitiba 5
Dublin 5
Düsseldorf 5
Haiphong 5
Houston 5
Johannesburg 5
Kingston 5
Kyiv 5
Mumbai 5
Newark 5
Philadelphia 5
Quito 5
Baku 4
Bengaluru 4
Bologna 4
Buenos Aires 4
Bắc Ninh 4
Guangzhou 4
Maceió 4
Mexico City 4
Montevideo 4
Norwalk 4
Omaha 4
Paris 4
Portsmouth 4
Salvador 4
Toronto 4
Amman 3
Anaheim 3
Aracaju 3
Aversa 3
Bauru 3
Bắc Giang 3
Cabo Frio 3
Campos dos Goytacazes 3
Cape Town 3
Columbus 3
Denver 3
Elk Grove Village 3
Falkenstein 3
Fortaleza 3
Giugliano in Campania 3
Hortolândia 3
Irvine 3
Istanbul 3
Itajaí 3
Juneau 3
Kuala Lumpur 3
Manchester 3
Montes Claros 3
Nairobi 3
Phoenix 3
Poplar 3
Porterville 3
Qingdao 3
Ribeirão Preto 3
Riverside 3
Totale 2.479
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Nome #
A novel iPSC-based model of ICF syndrome subtype 2 recapitulates the molecular phenotype of ZBTB24 deficiency 124
Zfp57 inactivation illustrates the role of ICR methylation in imprinted gene expression during neural differentiation of mouse ESCs 104
ZFP57 maintains the parent-of-origin-specific expression of the imprinted genes and differentially affects non-imprinted targets in mouse embryonic stem cells 99
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 91
Co-Occurrence of Beckwith-Wiedemann Syndrome and Early-Onset Colorectal Cancer 86
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 81
Beckwith-Wiedemann syndrome and twinning: case report and brief review of literature 80
The mismatch-repair proteins MSH2 and MSH6 interact with the imprinting control regions through the ZFP57-KAP1 complex. 73
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 71
Genome-wide analysis of Zfp57-mediated epigenetic control at imprinted and non imprinted loci in mouse embryonic stem cells 66
ICF1 Syndrome Associated DNMT3B Mutations Prevent de novo Methylation at a subset of Imprinted Loci During iPSC Reprogramming 65
ZFP57/KAP1 Genomic Association and Targeted Epigenetic Regulation at Imprinted and Not Imprinted Loci 64
Trans-acting genetic variants causing multilocus imprinting disturbance (MLID): common mechanisms and consequences 62
Understanding the Variability of 22q11.2 Deletion Syndrome: The Role of Epigenetic Factors 60
ZBTB2 protein is a new partner of the Nucleosome Remodeling and Deacetylase (NuRD) complex 58
New insights into oocyte cytoplasmic lattice-associated proteins 57
Wnt/?-catenin signaling pathway safeguards epigenetic stability and homeostasis of mouse embryonic stem cells 56
Genetic and epigenetic mutations affect the DNA binding capability of human ZFP57 in transient neonatal diabetes type 1. 55
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 53
Glutamine Utilization by Rhizobium etli 51
Epigenomic analysis of the imprinting factor ZFP57, KRAB-ZFPs corepressor KAP1 and associated chromatin modifiers by ChIP seq in mouse embrional stem cells 51
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
Different Mechanisms Cause Hypomethylation of Both H19 and KCNQ1OT1 Imprinted Differentially Methylated Regions in Two Cases of Silver-Russell Syndrome Spectrum. 50
Genomic imprinting disorders: lessons on how genome, epigenome and environment interact 49
Imprinting disorders 47
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. 46
Cancer Risk in Beckwith-Wiedemann Syndrome: A Systematic Review and Meta-Analysis Outlining a Novel (Epi)Genotype Specific Histotype Targeted Screening Protocol 46
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 44
ZFP57 recognizes multiple and closely spaced sequence motif variants to maintain repressive epigenetic marks in mouse embryonic stem cells. 44
Co-occurrence of Beckwith-Wiedemann syndrome and pseudohypoparathyroidism type 1B: coincidence or common molecular mechanism? 43
A novel large deletion of the ICR1 region including H19 and putative enhancer elements 41
Variable expressivity of the beckwith-wiedemann syndrome in four pedigrees segregating loss-of-function variants of cdkn1c 41
Performance Metrics of the Scoring System for the Diagnosis of the Beckwith-Wiedemann Spectrum (BWSp) and Its Correlation with Cancer Development 40
Clinical and molecular characterization of patients affected by Beckwith-Wiedemann spectrum conceived through assisted reproduction techniques. 40
ZFP57 recognizes multiple and closely spaced sequence motif variants to maintain repressive epigenetic marks in mouse embryonic stem cells. 40
Epigenetic Alterations in Inborn Errors of Immunity. 40
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 39
In Embryonic Stem Cells, ZFP57/KAP1 Recognize a Methylated Hexanucleotide to Affect Chromatin and DNA Methylation of Imprinting Control Regions 38
Insulin-like growth factor II (IGF-II) e H19 : imprinting parentale e ruolo nella trasformazione neoplastica. 37
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
Assisted Reproductive Techniques and Risk of Beckwith-Wiedemann Syndrome. 37
The ZFP57 imprinting factor and epigenetic control: further clues stemming from expression profiling, ChIP seq and in vitro-induced differentiation 37
EMQN best practice guidelines for the molecular genetic testing and reporting of chromosome 11p15 imprinting disorders: Silver-Russell and Beckwith-Wiedemann syndrome 37
Dynamics of the ZFP57/KAP1 and associated factors network at DNA methylated targets in murine pluripotent ES cells 36
Congenital imprinting disorders: Eucid.net -a network to decipher their aetiology and to improve the diagnostic and clinical care 35
First step towards a consensus strategy for multi-locus diagnostic testing of imprinting disorders. 35
Expert consensus document: Clinical and molecular diagnosis, screening and management of Beckwith-Wiedemann syndrome: an international consensus statement. 35
Disruption of genomic neighbourhood at the imprinted IGF2-H19 locus in Beckwith-Wiedemann syndrome and Silver-Russell syndrome 35
Mono- and bi-allelic expression of insulin-like growth factor II gene in human muscle tumors. 34
Is ZFP57 binding to H19/IGF2: IG-DMR affected in Silver-Russell syndrome? 33
Looking for CDKN1C enhancers 33
DNA methylation in the diagnosis of monogenic diseases 33
The PEG13-DMR and brain-specific enhancers dictate imprinted expression within the 8q24 intellectual disability risk locus 33
Role of cis-acting elements and trans-acting factors in genomic imprinting defects 32
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
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 32
Causes and Consequences of Multi-Locus Imprinting Disturbances in Humans 31
Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith-Wiedemann syndrome 31
Regulation of the insulin-like growth factor II gene expression in rat liver cells 30
Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumour 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
Identification of genetic and non-genetic modifiers of genomic imprinting through screening of imprinted DMR methylation in humans 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. 29
A KHDC3L mutation resulting in recurrent hydatidiform mole causes genome-wide DNA methylation loss in oocytes and persistent imprinting defects post-fertilisation 29
Regolazione differenziale degli alleli paterno e materno del gene per il fattore insulino-simile tipo II (IGF-II) 28
Clinical utility gene card for: Beckwith-Wiedemann syndrome. 27
A case of Beckwith-Wiedemann syndrome caused by a cryptic 11p15 deletion encompassing the centromeric imprinted domain of the BWS locus 27
Biallelic variant in cyclin B3 is associated with failure of maternal meiosis II and recurrent digynic triploidy 27
Highly variable genomic methylation in the Beckwith-Wiedemann syndrome associated with multi-locus imprinting disturbances 27
Transcription alterations of KCNQ1 associated with imprinted methylation defects in the Beckwith-Wiedemann locus 27
Genetic and epigenetic mutations affect the DNA binding capability of human ZFP57 in transient neonatal diabetes type 1 27
Wilms tumor and constitutional epigenetic defects 27
Meg3 Non-coding RNA Expression Controls Imprinting by Preventing Transcriptional Upregulation in cis 27
Tissue-specific and mosaic imprinting defects underlie opposite congenital growth disorders in mice 27
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 26
Recent Advances in Imprinting Disorders. 26
Loss-of-function maternal-effect mutations of PADI6 are associated with familial and sporadic Beckwith-Wiedemann syndrome with multi-locus imprinting disturbance 26
The H19 locus acts in vivo as a tumor suppressor 26
The human urokinase-plasminogen activator gene and its promoter 26
Both epimutations and chromosome aberrations affect multiple imprinted loci in aggressive wilms tumors 26
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. 25
Imprinting at the PLAGL1 domain is contained within a 70-kb CTCF/cohesin-mediated non-allelic chromatin loop 24
Imprinting at the PLAGL1 domain is contained within a 70-kb CTCF/cohesin-mediated non-allelic chromatin loop. 24
Insulin Like Growth Factor 2 Expression in the Rat Brain Both in Basal Condition and following Learning Predominantly Derives from the Maternal Allele 24
A splicing mutation of the HMGA2 gene is associated with Silver-Russell syndrome phenotype 24
Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome 23
Humanized H19/Igf2 locus reveals diverged imprinting mechanism between mouse and human and reflects Silver-Russell syndrome phenotypes 23
A novel microdeletion in the IGF2/H19 imprinting centre region defines a recurrent mutation mechanism in familial Beckwith-Wiedemann syndrome. 23
Imprinting disorders: A group of congenital disorders with overlapping patterns of molecular changes affecting imprinted loci 23
Inherited and Sporadic Epimutations at the IGF2-H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumor. 23
A novel microdeletion in the IGF2/H19 imprinting centre region defines a recurrent mutation mechanism in familial Beckwith-Wiedemann syndrome 23
Distinct methylation changes at the IGF2-H19 locus in congenital growth disorders and cancer 23
Two maternal duplications involving the CDKN1C gene are associated with contrasting growth phenotypes 23
(Epi)genotype-phenotype correlations in Beckwith-Wiedemann syndrome 22
Recommendations of the Scientific Committee of the Italian Beckwith-Wiedemann Syndrome Association on the diagnosis, management and follow-up of the syndrome 22
BamHI RFLP linked to the human urokinase gene 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
(Epi)genotype-phenotype correlations in Beckwith-Wiedemann syndrome: A paradigm for genomic medicine 22
Giant breast tumors in a patient with Beckwith-Wiedemann syndrome 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
Totale 3.991
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Categoria #
all - tutte 15.533
article - articoli 13.089
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 28.622
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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
2025/20262.473 120 261 213 362 424 94 351 141 130 175 90 112
2026/2027222 167 55 0 0 0 0 0 0 0 0 0 0
Totale 4.152