IRIS
RICCIO, Andrea
 Distribuzione geografica
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Continente #
EU - Europa 7.483
NA - Nord America 3.185
AS - Asia 2.579
SA - Sud America 480
AF - Africa 38
OC - Oceania 6
Totale 13.771
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Nazione #
RU - Federazione Russa 4.839
US - Stati Uniti d'America 3.103
SG - Singapore 954
IE - Irlanda 860
CN - Cina 599
HK - Hong Kong 416
BR - Brasile 406
IT - Italia 396
UA - Ucraina 361
GB - Regno Unito 349
DE - Germania 287
VN - Vietnam 168
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 16
BD - Bangladesh 15
ZA - Sudafrica 15
EC - Ecuador 14
PL - Polonia 14
IQ - Iraq 12
CZ - Repubblica Ceca 11
ID - Indonesia 10
MA - Marocco 10
PY - Paraguay 9
CO - Colombia 8
CL - Cile 6
UZ - Uzbekistan 6
ES - Italia 5
VE - Venezuela 5
AE - Emirati Arabi Uniti 4
AZ - Azerbaigian 4
CH - Svizzera 4
CR - Costa Rica 4
IL - Israele 4
KE - Kenya 4
AU - Australia 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
SY - Repubblica araba siriana 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
MN - Mongolia 1
MY - Malesia 1
NC - Nuova Caledonia 1
OM - Oman 1
PE - Perù 1
PT - Portogallo 1
RO - Romania 1
SA - Arabia Saudita 1
SN - Senegal 1
TH - Thailandia 1
TJ - Tagikistan 1
TT - Trinidad e Tobago 1
TW - Taiwan 1
Totale 13.771
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Città #
Moscow 1.712
Dublin 860
Jacksonville 552
Santa Clara 517
Chandler 418
Hong Kong 414
Singapore 362
Seoul 116
Bremen 111
Princeton 110
Medford 98
Dallas 91
Hefei 91
Ann Arbor 87
Beijing 85
Roxbury 72
Ashburn 71
Boardman 63
Bengaluru 61
San Mateo 58
Ho Chi Minh City 55
Napoli 52
Wilmington 51
Los Angeles 47
São Paulo 42
The Dalles 41
Caserta 40
Elora 37
Woodbridge 36
Hanoi 34
New York 31
Aversa 30
Brussels 27
Des Moines 20
Jinan 20
Naples 18
Amsterdam 17
Nuremberg 17
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
Rio de Janeiro 11
Brno 10
Falkenstein 10
Guangzhou 10
Johannesburg 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
Haiphong 6
Hebei 6
Messina 6
Munich 6
Palermo 6
Tashkent 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
Totale 7.056
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Nome #
Distinct methylation changes at the IGF2-H19 locus in congenital growth disorders and cancer 171
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] 168
Genetic and epigenetic mutations affect the DNA binding capability of human ZFP57 in transient neonatal diabetes type 1 166
ZBTB2 protein is a new partner of the Nucleosome Remodeling andDeacetylase (NuRD) complex 165
DNA Methylation in the Diagnosis of Monogenic Diseases 162
Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith - Wiedemann syndrome and Wilms' tumour 158
Activation of fetal promoters of insulinlike growth factor II gene in hepatitis C virus-related chronic hepatitis, cirrhosis, and hepatocellular carcinoma 156
Beckwith-Wiedemann syndrome. Clinical and etiopathogenic aspects of a model genomic imprinting entity 155
Is ZFP57 binding to H19/IGF2: IG-DMR affected in Silver-Russell syndrome? 148
In Embryonic Stem Cells, ZFP57/KAP1 Recognize a Methylated Hexanucleotide to Affect Chromatin and DNA Methylation of Imprinting Control Regions 145
Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith-Wiedemann syndrome 143
Imprinting at the PLAGL1 domain is contained within a 70-kb CTCF/cohesin-mediated non-allelic chromatin loop 143
22q11.2 distal deletion syndrome: Description of a new case with truncus arteriosus type 2 and review 140
Loss-of-function maternal-effect mutations of PADI6 are associated with familial and sporadic Beckwith-Wiedemann syndrome with multi-locus imprinting disturbance 140
Assisted Reproductive Techniques and Risk of Beckwith-Wiedemann Syndrome 138
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 137
Disruption of genomic neighbourhood at the imprinted IGF2-H19 locus in Beckwith-Wiedemann syndrome and Silver-Russell syndrome 137
The H19 endodermal enhancer is required for Igf2 activation and tumor formation in experimental liver carcinogenesis 136
Beckwith-Wiedemann Syndrome 135
A novel microdeletion in the IGF2/H19 imprinting centre region defines a recurrent mutation mechanism in familial Beckwith-Wiedemann syndrome 134
(Epi)genotype-phenotype correlations in Beckwith-Wiedemann syndrome: A paradigm for genomic medicine 133
A novel large deletion of the ICR1 region including H19 and putative enhancer elements 133
Co-occurrence of Beckwith-Wiedemann syndrome and pseudohypoparathyroidism type 1B: coincidence or common molecular mechanism? 132
The phenotypic variations of multi-locus imprinting disturbances associated with maternal-effect variants of NLRP5 range from overt imprinting disorder to apparently healthy phenotype 132
Developmentally regulated functions of the H19 differentially methylated domain 130
Inherited and sporadic epimutations at the IGF2-H19 locus in beckwith-wiedemann syndrome and wilms' tumor 130
Different Mechanisms Cause Hypomethylation of Both H19 and KCNQ1OT1 Imprinted Differentially Methylated Regions in Two Cases of Silver-Russell Syndrome Spectrum 129
(Epi)genotype-phenotype correlations in Beckwith-Wiedemann syndrome 128
Co-Occurrence of Beckwith–Wiedemann Syndrome and Early-Onset Colorectal Cancer 127
Clinical and molecular characterization of patients affected by Beckwith-Wiedemann spectrum conceived through assisted reproduction techniques 127
A splicing mutation of the HMGA2 gene is associated with Silver-Russell syndrome phenotype 127
The mismatch-repair proteins MSH2 and MSH6 interact with the imprinting control regions through the ZFP57-KAP1 complex 126
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 126
Biallelic variant in cyclin B3 is associated with failure of maternal meiosis II and recurrent digynic triploidy 126
A KHDC3L mutation resulting in recurrent hydatidiform mole causes genome-wide DNA methylation loss in oocytes and persistent imprinting defects post-fertilisation 123
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 123
Both Epimutations and Chromosome Aberrations Affect Multiple Imprinted Loci in Aggressive Wilms Tumors 122
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 121
Silver-Russell Syndrome and Beckwith-Wiedemann Syndrome Phenotypes Associated with 11p Duplication in a Single Family 121
Expression and parental imprinting of the H19 gene in human rhabdomyosarcoma 121
A case of Beckwith-Wiedemann syndrome caused by a cryptic 11p15 deletion encompassing the centromeric imprinted domain of the BWS locus 121
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 121
ZFP57 recognizes multiple and closely spaced sequence motif variants to maintain repressive epigenetic marks in mouse embryonic stem cells 119
Genomic imprinting disorders: lessons on how genome, epigenome and environment interact 119
Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome 118
ZFP57 maintains the parent-of-origin-specific expression of the imprinted genes and differentially affects non-imprinted targets in mouse embryonic stem cells 118
The KCNQ1OT1 imprinting control region and non-coding RNA: New properties derived from the study of Beckwith-Wiedemann syndrome and Silver-Russell syndrome cases 117
Mechanisms causing imprinting defects in familial Beckwith-Wiedemann syndrome with Wilms' tumour 116
A maternal-effectPadi6variant causes nuclear and cytoplasmic abnormalities in oocytes, as well as failure of epigenetic reprogramming and zygotic genome activation in embryos 115
Transcription alterations of KCNQ1 associated with imprinted methylation defects in the Beckwith-Wiedemann locus 115
Role of histone acetylation and DNA methylation in the maintenance of the imprinted expression of the H19 and Igf2 genes 114
Familial posterior helical ear pits 114
BamHI RFLP linked to the human urokinase gene 114
Zfp57 inactivation illustrates the role of ICR methylation in imprinted gene expression during neural differentiation of mouse ESCs 114
Tissue-specific and mosaic imprinting defects underlie opposite congenital growth disorders in mice 108
Mosaic segmental and whole-chromosome upd(11)mat in silver-russell syndrome 108
Looking for CDKN1C enhancers 107
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 107
Epigenetic Alterations in Inborn Errors of Immunity 105
LOSS OF HETEROZYGOSITY OF IMPRINTED GENES IN SV40 T/T ANTIGEN-INDUCED HEPATOCELLULAR CARCINOMAS 105
Humanized H19/Igf2 locus reveals diverged imprinting mechanism between mouse and human and reflects Silver-Russell syndrome phenotypes 105
A paternally inherited 1.4 kb deletion of the 11p15.5 imprinting center 2 is associated with a mild familial Silver–Russell syndrome phenotype 105
Performance Metrics of the Scoring System for the Diagnosis of the Beckwith-Wiedemann Spectrum (BWSp) and Its Correlation with Cancer Development 104
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. 104
Clinical utility gene card for: Beckwith-Wiedemann Syndrome 102
Prevalence of beckwith-wiedemann syndrome in North West of Italy 102
Paternal deletion of the 11p15.5 centromeric-imprinting control region is associated with alteration of imprinted gene expression and recurrent severe intrauterine growth restriction 102
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 101
Identification of trombospondin-1 as a novel amelogenin interactor by functional proteomics 101
MONO-ALLLIC AND BI-ALLELIC EXPRESSION OF INSULIN-LIKE GROWTH-FACTOR-II GENE IN HUMAN MUSCLE TUMORS 100
Perlman syndrome: Clinical report and nine-year follow-up 100
Gain of function in CDKN1C 100
Two maternal duplications involving the CDKN1C gene are associated with contrasting growth phenotypes 100
Tumor necrosis factor-α regulates mRNA for urokinase-type plasminogen activator and type-1 plasminogen activator inhibitor in human neoplastic cell lines 99
Beckwith-Wiedemann syndrome and twinning: case report and brief review of literature 98
Causes and Consequences of Multi-Locus Imprinting Disturbances in Humans 98
Variable expressivity of the beckwith-wiedemann syndrome in four pedigrees segregating loss-of-function variants of cdkn1c 98
Microdeletion and IGF2 loss of imprinting in a cascade causing Beckwith-Wiedemann syndrome with Wilms' tumor - Reply 97
The Arabidopsis SUPERMAN protein is able to specifically bind DNA through its single Cys2-His2 zinc finger motif 97
Plasminogen activator inhibitor type-1 protein, mRNA and gene transcription are increased by phorbol esters in human rhabdomyosarcoma cells 95
ICF1-Syndrome-Associated DNMT3B Mutations Prevent De Novo Methylation at a Subset of Imprinted Loci during iPSC Reprogramming 93
Understanding the Variability of 22q11.2 Deletion Syndrome: The Role of Epigenetic Factors 93
New insights into oocyte cytoplasmic lattice-associated proteins 93
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 93
Structure of the galactokinase gene of Escherichia coli, the last (?) gene of the gal operon 92
A novel iPSC-based model of ICF syndrome subtype 2 recapitulates the molecular phenotype of ZBTB24 deficiency 92
Plasminogen activator inhibitor type 1 gene is located at region q21.3-q22 of chromosome 7 and genetically linked with cystic fibrosis. 91
Molecular subtypes and phenotypic expression of Beckwith-Wiedemann syndrome 91
A Maternal Loss‐of‐Function Variant in KHDC3L Gene Causes a Range of Adverse Pregnancy Outcomes: A Case Report 90
Plasminogen activator inhibitor type 1 biosynthesis and mRNA level are increased by dexamethasone in human fibrosarcoma cells 90
Convergently functional, Rho-independent terminator in Salmonella typhimurium 90
Nephrological findings and genotype-phenotype correlation in Beckwith-Wiedemann syndrome 90
Congenital imprinting disorders: Eucid.net -a network to decipher their aetiology and to improve the diagnostic and clinical care 90
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 89
PARENTAL IMPRINTING OF RAT INSULIN-LIKE GROWTH-FACTOR-II GENE PROMOTERS IS COORDINATELY REGULATED 89
Insulin Like Growth Factor 2 Expression in the Rat Brain Both in Basal Condition and following Learning Predominantly Derives from the Maternal Allele 89
The PEG13-DMR and brain-specific enhancers dictate imprinted expression within the 8q24 intellectual disability risk locus 88
Clinical and molecular diagnosis, screening and management of Beckwith-Wiedemann syndrome: An international consensus statement 87
Recommendations of the Scientific Committee of the Italian Beckwith-Wiedemann Syndrome Association on the diagnosis, Management and follow-up of the syndrome 86
EMQN best practice guidelines for the molecular genetic testing and reporting of chromosome 11p15 imprinting disorders: Silver-Russell and Beckwith-Wiedemann syndrome 86
Totale 11.599
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Categoria #
all - tutte 47.826
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 47.826
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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
2025/20266.786 321 376 362 392 796 4.539 0 0 0 0 0 0
Totale 14.071