IRIS
RICCIO, Andrea
 Distribuzione geografica
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Continente #
EU - Europa 7.675
NA - Nord America 3.800
AS - Asia 3.011
SA - Sud America 501
AF - Africa 48
OC - Oceania 6
Totale 15.041
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Nazione #
RU - Federazione Russa 4.950
US - Stati Uniti d'America 3.690
SG - Singapore 1.087
IE - Irlanda 860
CN - Cina 655
IT - Italia 451
HK - Hong Kong 437
BR - Brasile 419
UA - Ucraina 362
GB - Regno Unito 354
VN - Vietnam 322
DE - Germania 293
KR - Corea 133
FI - Finlandia 95
IN - India 93
JP - Giappone 90
CA - Canada 72
SE - Svezia 66
GR - Grecia 64
FR - Francia 55
BD - Bangladesh 45
TR - Turchia 45
AR - Argentina 30
BE - Belgio 28
MX - Messico 23
NL - Olanda 23
PK - Pakistan 22
ZA - Sudafrica 18
AT - Austria 17
IQ - Iraq 17
EC - Ecuador 14
PL - Polonia 14
ID - Indonesia 12
CZ - Repubblica Ceca 11
MA - Marocco 11
CL - Cile 9
CO - Colombia 9
PY - Paraguay 9
ES - Italia 8
UZ - Uzbekistan 8
CH - Svizzera 7
VE - Venezuela 6
KE - Kenya 5
AE - Emirati Arabi Uniti 4
AZ - Azerbaigian 4
CR - Costa Rica 4
IL - Israele 4
PH - Filippine 4
TN - Tunisia 4
AU - Australia 3
JO - Giordania 3
LV - Lettonia 3
UY - Uruguay 3
BG - Bulgaria 2
CY - Cipro 2
DZ - Algeria 2
EG - Egitto 2
HN - Honduras 2
IR - Iran 2
JM - Giamaica 2
KW - Kuwait 2
KZ - Kazakistan 2
LT - Lituania 2
MY - Malesia 2
NO - Norvegia 2
NZ - Nuova Zelanda 2
RO - Romania 2
SA - Arabia Saudita 2
SY - Repubblica araba siriana 2
TH - Thailandia 2
TT - Trinidad e Tobago 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
EE - Estonia 1
GE - Georgia 1
GT - Guatemala 1
HR - Croazia 1
HU - Ungheria 1
IS - Islanda 1
KG - Kirghizistan 1
LA - Repubblica Popolare Democratica del Laos 1
LY - Libia 1
MD - Moldavia 1
ML - Mali 1
MN - Mongolia 1
NC - Nuova Caledonia 1
NG - Nigeria 1
NP - Nepal 1
OM - Oman 1
PE - Perù 1
PT - Portogallo 1
SN - Senegal 1
SO - Somalia 1
SV - El Salvador 1
TJ - Tagikistan 1
Totale 15.040
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Città #
Moscow 1.778
Dublin 860
Jacksonville 553
Santa Clara 532
Singapore 462
Hong Kong 434
Chandler 418
San Jose 355
Ashburn 132
Seoul 117
Bremen 111
Princeton 110
Ho Chi Minh City 105
Medford 98
Beijing 97
Dallas 93
Hefei 92
Ann Arbor 87
Hanoi 77
Roxbury 72
Boardman 63
Bengaluru 61
San Mateo 58
Napoli 52
Wilmington 51
Los Angeles 50
São Paulo 43
The Dalles 41
Caserta 40
New York 39
Elora 37
Woodbridge 36
Aversa 30
Brussels 27
Des Moines 21
Naples 21
Jinan 20
Amsterdam 18
Nuremberg 17
Tokyo 17
Frankfurt am Main 16
Haiphong 15
Columbus 13
Da Nang 13
Haeundae-gu 13
Zhengzhou 13
Cambridge 12
Hangzhou 12
Pozzuoli 12
Shanghai 12
Brooklyn 11
Johannesburg 11
London 11
Milan 11
Norwalk 11
Rio de Janeiro 11
Toronto 11
Brno 10
Falkenstein 10
Guangzhou 10
Houston 10
Santa Maria Capua Vetere 10
Vienna 10
Düsseldorf 9
Montreal 9
Mountain View 9
Auburn Hills 8
Council Bluffs 8
Curitiba 8
Delhi 8
Giugliano in Campania 8
Gragnano 8
Hải Dương 8
Mexico City 8
San Francisco 8
Shenyang 8
Viterbo 8
Boston 7
Brasília 7
Bắc Ninh 7
Campinas 7
Helsinki 7
Marseille 7
Nanjing 7
Paris 7
Redwood City 7
Tashkent 7
Tianjin 7
Wroclaw 7
Atlanta 6
Belo Horizonte 6
Changsha 6
Chicago 6
Guarulhos 6
Ha Long 6
Hebei 6
Messina 6
Munich 6
Ninh Bình 6
Palermo 6
Totale 7.858
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Nome #
Distinct methylation changes at the IGF2-H19 locus in congenital growth disorders and cancer 187
ZBTB2 protein is a new partner of the Nucleosome Remodeling andDeacetylase (NuRD) complex 182
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] 179
Genetic and epigenetic mutations affect the DNA binding capability of human ZFP57 in transient neonatal diabetes type 1 179
Activation of fetal promoters of insulinlike growth factor II gene in hepatitis C virus-related chronic hepatitis, cirrhosis, and hepatocellular carcinoma 176
Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith - Wiedemann syndrome and Wilms' tumour 174
DNA Methylation in the Diagnosis of Monogenic Diseases 171
Beckwith-Wiedemann syndrome. Clinical and etiopathogenic aspects of a model genomic imprinting entity 166
Imprinting at the PLAGL1 domain is contained within a 70-kb CTCF/cohesin-mediated non-allelic chromatin loop 163
Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith-Wiedemann syndrome 155
Is ZFP57 binding to H19/IGF2: IG-DMR affected in Silver-Russell syndrome? 154
Disruption of genomic neighbourhood at the imprinted IGF2-H19 locus in Beckwith-Wiedemann syndrome and Silver-Russell syndrome 152
Loss-of-function maternal-effect mutations of PADI6 are associated with familial and sporadic Beckwith-Wiedemann syndrome with multi-locus imprinting disturbance 151
In Embryonic Stem Cells, ZFP57/KAP1 Recognize a Methylated Hexanucleotide to Affect Chromatin and DNA Methylation of Imprinting Control Regions 150
Co-occurrence of Beckwith-Wiedemann syndrome and pseudohypoparathyroidism type 1B: coincidence or common molecular mechanism? 148
Assisted Reproductive Techniques and Risk of Beckwith-Wiedemann Syndrome 146
22q11.2 distal deletion syndrome: Description of a new case with truncus arteriosus type 2 and review 145
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 145
The H19 endodermal enhancer is required for Igf2 activation and tumor formation in experimental liver carcinogenesis 144
Beckwith-Wiedemann Syndrome 143
Inherited and sporadic epimutations at the IGF2-H19 locus in beckwith-wiedemann syndrome and wilms' tumor 141
(Epi)genotype-phenotype correlations in Beckwith-Wiedemann syndrome: A paradigm for genomic medicine 141
A novel large deletion of the ICR1 region including H19 and putative enhancer elements 141
Co-Occurrence of Beckwith–Wiedemann Syndrome and Early-Onset Colorectal Cancer 140
A novel microdeletion in the IGF2/H19 imprinting centre region defines a recurrent mutation mechanism in familial Beckwith-Wiedemann syndrome 140
The phenotypic variations of multi-locus imprinting disturbances associated with maternal-effect variants of NLRP5 range from overt imprinting disorder to apparently healthy phenotype 139
Clinical and molecular characterization of patients affected by Beckwith-Wiedemann spectrum conceived through assisted reproduction techniques 138
A splicing mutation of the HMGA2 gene is associated with Silver-Russell syndrome phenotype 138
(Epi)genotype-phenotype correlations in Beckwith-Wiedemann syndrome 137
The mismatch-repair proteins MSH2 and MSH6 interact with the imprinting control regions through the ZFP57-KAP1 complex 136
Different Mechanisms Cause Hypomethylation of Both H19 and KCNQ1OT1 Imprinted Differentially Methylated Regions in Two Cases of Silver-Russell Syndrome Spectrum 136
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 135
Developmentally regulated functions of the H19 differentially methylated domain 134
Biallelic variant in cyclin B3 is associated with failure of maternal meiosis II and recurrent digynic triploidy 134
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 134
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 133
Silver-Russell Syndrome and Beckwith-Wiedemann Syndrome Phenotypes Associated with 11p Duplication in a Single Family 132
Both Epimutations and Chromosome Aberrations Affect Multiple Imprinted Loci in Aggressive Wilms Tumors 132
A KHDC3L mutation resulting in recurrent hydatidiform mole causes genome-wide DNA methylation loss in oocytes and persistent imprinting defects post-fertilisation 131
MONO-ALLLIC AND BI-ALLELIC EXPRESSION OF INSULIN-LIKE GROWTH-FACTOR-II GENE IN HUMAN MUSCLE TUMORS 130
Expression and parental imprinting of the H19 gene in human rhabdomyosarcoma 130
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 130
Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome 129
ZFP57 recognizes multiple and closely spaced sequence motif variants to maintain repressive epigenetic marks in mouse embryonic stem cells 129
The KCNQ1OT1 imprinting control region and non-coding RNA: New properties derived from the study of Beckwith-Wiedemann syndrome and Silver-Russell syndrome cases 127
Zfp57 inactivation illustrates the role of ICR methylation in imprinted gene expression during neural differentiation of mouse ESCs 127
A maternal-effectPadi6variant causes nuclear and cytoplasmic abnormalities in oocytes, as well as failure of epigenetic reprogramming and zygotic genome activation in embryos 126
Mechanisms causing imprinting defects in familial Beckwith-Wiedemann syndrome with Wilms' tumour 125
A case of Beckwith-Wiedemann syndrome caused by a cryptic 11p15 deletion encompassing the centromeric imprinted domain of the BWS locus 125
ZFP57 maintains the parent-of-origin-specific expression of the imprinted genes and differentially affects non-imprinted targets in mouse embryonic stem cells 125
Role of histone acetylation and DNA methylation in the maintenance of the imprinted expression of the H19 and Igf2 genes 124
Transcription alterations of KCNQ1 associated with imprinted methylation defects in the Beckwith-Wiedemann locus 124
BamHI RFLP linked to the human urokinase gene 123
Genomic imprinting disorders: lessons on how genome, epigenome and environment interact 123
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 121
Tissue-specific and mosaic imprinting defects underlie opposite congenital growth disorders in mice 121
Familial posterior helical ear pits 120
Mosaic segmental and whole-chromosome upd(11)mat in silver-russell syndrome 118
Epigenetic Alterations in Inborn Errors of Immunity 117
Humanized H19/Igf2 locus reveals diverged imprinting mechanism between mouse and human and reflects Silver-Russell syndrome phenotypes 116
Beckwith-Wiedemann syndrome and twinning: case report and brief review of literature 115
Looking for CDKN1C enhancers 114
Prevalence of beckwith-wiedemann syndrome in North West of Italy 114
The Arabidopsis SUPERMAN protein is able to specifically bind DNA through its single Cys2-His2 zinc finger motif 114
Performance Metrics of the Scoring System for the Diagnosis of the Beckwith-Wiedemann Spectrum (BWSp) and Its Correlation with Cancer Development 113
LOSS OF HETEROZYGOSITY OF IMPRINTED GENES IN SV40 T/T ANTIGEN-INDUCED HEPATOCELLULAR CARCINOMAS 111
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 111
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. 111
A paternally inherited 1.4 kb deletion of the 11p15.5 imprinting center 2 is associated with a mild familial Silver–Russell syndrome phenotype 111
ICF1-Syndrome-Associated DNMT3B Mutations Prevent De Novo Methylation at a Subset of Imprinted Loci during iPSC Reprogramming 110
Perlman syndrome: Clinical report and nine-year follow-up 109
Paternal deletion of the 11p15.5 centromeric-imprinting control region is associated with alteration of imprinted gene expression and recurrent severe intrauterine growth restriction 109
Tumor necrosis factor-α regulates mRNA for urokinase-type plasminogen activator and type-1 plasminogen activator inhibitor in human neoplastic cell lines 109
Two maternal duplications involving the CDKN1C gene are associated with contrasting growth phenotypes 108
Causes and Consequences of Multi-Locus Imprinting Disturbances in Humans 107
Clinical and molecular diagnosis, screening and management of Beckwith-Wiedemann syndrome: An international consensus statement 107
Microdeletion and IGF2 loss of imprinting in a cascade causing Beckwith-Wiedemann syndrome with Wilms' tumor - Reply 106
Gain of function in CDKN1C 106
Identification of trombospondin-1 as a novel amelogenin interactor by functional proteomics 106
Variable expressivity of the beckwith-wiedemann syndrome in four pedigrees segregating loss-of-function variants of cdkn1c 106
Clinical utility gene card for: Beckwith-Wiedemann Syndrome 105
A Maternal Loss‐of‐Function Variant in KHDC3L Gene Causes a Range of Adverse Pregnancy Outcomes: A Case Report 104
New insights into oocyte cytoplasmic lattice-associated proteins 104
Understanding the Variability of 22q11.2 Deletion Syndrome: The Role of Epigenetic Factors 103
Molecular subtypes and phenotypic expression of Beckwith-Wiedemann syndrome 102
A novel iPSC-based model of ICF syndrome subtype 2 recapitulates the molecular phenotype of ZBTB24 deficiency 102
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 101
Structure of the galactokinase gene of Escherichia coli, the last (?) gene of the gal operon 100
Plasminogen activator inhibitor type-1 protein, mRNA and gene transcription are increased by phorbol esters in human rhabdomyosarcoma cells 99
The PEG13-DMR and brain-specific enhancers dictate imprinted expression within the 8q24 intellectual disability risk locus 99
Plasminogen activator inhibitor type 1 biosynthesis and mRNA level are increased by dexamethasone in human fibrosarcoma cells 98
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 96
FORSKOLIN DOWN-REGULATES TYPE-1 PLASMINOGEN-ACTIVATOR INHIBITOR AND TISSUE-TYPE PLASMINOGEN-ACTIVATOR AND THEIR MESSENGER-RNAS IN HUMAN FIBROSARCOMA CELLS 96
Plasminogen activator inhibitor type 1 gene is located at region q21.3-q22 of chromosome 7 and genetically linked with cystic fibrosis. 95
Recommendations of the Scientific Committee of the Italian Beckwith-Wiedemann Syndrome Association on the diagnosis, Management and follow-up of the syndrome 95
Insulin Like Growth Factor 2 Expression in the Rat Brain Both in Basal Condition and following Learning Predominantly Derives from the Maternal Allele 95
A novel missense variant in PNLDC1 associated with nonobstructive azoospermia 94
Convergently functional, Rho-independent terminator in Salmonella typhimurium 94
Nephrological findings and genotype-phenotype correlation in Beckwith-Wiedemann syndrome 94
EMQN best practice guidelines for the molecular genetic testing and reporting of chromosome 11p15 imprinting disorders: Silver-Russell and Beckwith-Wiedemann syndrome 94
Totale 12.579
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Categoria #
all - tutte 53.001
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 53.001
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202117 0 0 0 0 0 0 0 0 0 0 0 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
2025/20268.059 321 376 362 392 796 4.576 361 195 290 197 88 105
Totale 15.344