IRIS
RICCIO, Andrea
 Distribuzione geografica
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Continente #
EU - Europa 7.682
NA - Nord America 3.984
AS - Asia 3.044
SA - Sud America 505
Continente sconosciuto - Info sul continente non disponibili 304
AF - Africa 48
OC - Oceania 6
Totale 15.573
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Nazione #
RU - Federazione Russa 4.950
US - Stati Uniti d'America 3.863
SG - Singapore 1.105
IE - Irlanda 860
CN - Cina 664
IT - Italia 457
HK - Hong Kong 441
BR - Brasile 421
UA - Ucraina 362
GB - Regno Unito 354
VN - Vietnam 322
DE - Germania 293
KR - Corea 133
FI - Finlandia 95
IN - India 93
JP - Giappone 91
CA - Canada 79
SE - Svezia 66
GR - Grecia 64
FR - Francia 55
BD - Bangladesh 45
TR - Turchia 45
AR - Argentina 31
BE - Belgio 28
MX - Messico 23
NL - Olanda 23
PK - Pakistan 22
IQ - Iraq 18
ZA - Sudafrica 18
AT - Austria 17
PL - Polonia 15
EC - Ecuador 14
ID - Indonesia 12
CZ - Repubblica Ceca 11
MA - Marocco 11
CO - Colombia 10
CL - Cile 9
PY - Paraguay 9
ES - Italia 8
UZ - Uzbekistan 8
CH - Svizzera 7
VE - Venezuela 6
CR - Costa Rica 5
KE - Kenya 5
AE - Emirati Arabi Uniti 4
AZ - Azerbaigian 4
IL - Israele 4
PH - Filippine 4
TN - Tunisia 4
AU - Australia 3
JM - Giamaica 3
JO - Giordania 3
LV - Lettonia 3
TT - Trinidad e Tobago 3
UY - Uruguay 3
BG - Bulgaria 2
CY - Cipro 2
DZ - Algeria 2
EG - Egitto 2
GT - Guatemala 2
HN - Honduras 2
IR - Iran 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
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
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 15.268
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Città #
Moscow 1.778
Dublin 860
Jacksonville 553
Santa Clara 547
Singapore 464
Hong Kong 438
Chandler 418
San Jose 355
Ashburn 154
Seoul 117
Bremen 111
Princeton 110
Council Bluffs 109
Ho Chi Minh City 105
Beijing 103
Medford 98
Dallas 96
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 45
The Dalles 41
Caserta 40
New York 39
Elora 37
Woodbridge 37
Aversa 30
Brussels 27
Des Moines 21
Naples 21
Jinan 20
Amsterdam 18
Tokyo 18
Nuremberg 17
Frankfurt am Main 16
Haiphong 15
Columbus 13
Da Nang 13
Haeundae-gu 13
Toronto 13
Zhengzhou 13
Cambridge 12
Hangzhou 12
Houston 12
Pozzuoli 12
Shanghai 12
Brooklyn 11
Johannesburg 11
London 11
Milan 11
Norwalk 11
Rio de Janeiro 11
Brno 10
Falkenstein 10
Guangzhou 10
Santa Maria Capua Vetere 10
Vienna 10
Düsseldorf 9
Montreal 9
Mountain View 9
San Francisco 9
Auburn Hills 8
Curitiba 8
Delhi 8
Giugliano in Campania 8
Gragnano 8
Hải Dương 8
Mexico City 8
Shenyang 8
Viterbo 8
Boston 7
Brasília 7
Bắc Ninh 7
Campinas 7
Chicago 7
Helsinki 7
Marseille 7
Nanjing 7
Paris 7
Phoenix 7
Redwood City 7
Rome 7
Tashkent 7
Tianjin 7
Warsaw 7
Wroclaw 7
Atlanta 6
Belo Horizonte 6
Changsha 6
Guarulhos 6
Ha Long 6
Hebei 6
Messina 6
Totale 8.024
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Nome #
Distinct methylation changes at the IGF2-H19 locus in congenital growth disorders and cancer 189
ZBTB2 protein is a new partner of the Nucleosome Remodeling andDeacetylase (NuRD) complex 185
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] 180
Genetic and epigenetic mutations affect the DNA binding capability of human ZFP57 in transient neonatal diabetes type 1 180
Activation of fetal promoters of insulinlike growth factor II gene in hepatitis C virus-related chronic hepatitis, cirrhosis, and hepatocellular carcinoma 177
Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith - Wiedemann syndrome and Wilms' tumour 176
DNA Methylation in the Diagnosis of Monogenic Diseases 173
Beckwith-Wiedemann syndrome. Clinical and etiopathogenic aspects of a model genomic imprinting entity 167
Imprinting at the PLAGL1 domain is contained within a 70-kb CTCF/cohesin-mediated non-allelic chromatin loop 166
Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith-Wiedemann syndrome 157
Is ZFP57 binding to H19/IGF2: IG-DMR affected in Silver-Russell syndrome? 156
Disruption of genomic neighbourhood at the imprinted IGF2-H19 locus in Beckwith-Wiedemann syndrome and Silver-Russell syndrome 153
In Embryonic Stem Cells, ZFP57/KAP1 Recognize a Methylated Hexanucleotide to Affect Chromatin and DNA Methylation of Imprinting Control Regions 152
Loss-of-function maternal-effect mutations of PADI6 are associated with familial and sporadic Beckwith-Wiedemann syndrome with multi-locus imprinting disturbance 152
Co-occurrence of Beckwith-Wiedemann syndrome and pseudohypoparathyroidism type 1B: coincidence or common molecular mechanism? 150
Assisted Reproductive Techniques and Risk of Beckwith-Wiedemann Syndrome 149
22q11.2 distal deletion syndrome: Description of a new case with truncus arteriosus type 2 and review 146
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 146
Beckwith-Wiedemann Syndrome 145
The H19 endodermal enhancer is required for Igf2 activation and tumor formation in experimental liver carcinogenesis 144
(Epi)genotype-phenotype correlations in Beckwith-Wiedemann syndrome: A paradigm for genomic medicine 144
Inherited and sporadic epimutations at the IGF2-H19 locus in beckwith-wiedemann syndrome and wilms' tumor 143
The phenotypic variations of multi-locus imprinting disturbances associated with maternal-effect variants of NLRP5 range from overt imprinting disorder to apparently healthy phenotype 143
Co-Occurrence of Beckwith–Wiedemann Syndrome and Early-Onset Colorectal Cancer 142
A novel microdeletion in the IGF2/H19 imprinting centre region defines a recurrent mutation mechanism in familial Beckwith-Wiedemann syndrome 142
A novel large deletion of the ICR1 region including H19 and putative enhancer elements 142
(Epi)genotype-phenotype correlations in Beckwith-Wiedemann syndrome 142
A splicing mutation of the HMGA2 gene is associated with Silver-Russell syndrome phenotype 140
Clinical and molecular characterization of patients affected by Beckwith-Wiedemann spectrum conceived through assisted reproduction techniques 139
Different Mechanisms Cause Hypomethylation of Both H19 and KCNQ1OT1 Imprinted Differentially Methylated Regions in Two Cases of Silver-Russell Syndrome Spectrum 138
The mismatch-repair proteins MSH2 and MSH6 interact with the imprinting control regions through the ZFP57-KAP1 complex 137
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 136
Biallelic variant in cyclin B3 is associated with failure of maternal meiosis II and recurrent digynic triploidy 136
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 135
Silver-Russell Syndrome and Beckwith-Wiedemann Syndrome Phenotypes Associated with 11p Duplication in a Single Family 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 134
Developmentally regulated functions of the H19 differentially methylated domain 134
Both Epimutations and Chromosome Aberrations Affect Multiple Imprinted Loci in Aggressive Wilms Tumors 134
A KHDC3L mutation resulting in recurrent hydatidiform mole causes genome-wide DNA methylation loss in oocytes and persistent imprinting defects post-fertilisation 133
Expression and parental imprinting of the H19 gene in human rhabdomyosarcoma 131
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 131
Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome 130
MONO-ALLLIC AND BI-ALLELIC EXPRESSION OF INSULIN-LIKE GROWTH-FACTOR-II GENE IN HUMAN MUSCLE TUMORS 130
ZFP57 recognizes multiple and closely spaced sequence motif variants to maintain repressive epigenetic marks in mouse embryonic stem cells 130
The KCNQ1OT1 imprinting control region and non-coding RNA: New properties derived from the study of Beckwith-Wiedemann syndrome and Silver-Russell syndrome cases 129
Zfp57 inactivation illustrates the role of ICR methylation in imprinted gene expression during neural differentiation of mouse ESCs 128
A maternal-effectPadi6variant causes nuclear and cytoplasmic abnormalities in oocytes, as well as failure of epigenetic reprogramming and zygotic genome activation in embryos 127
Mechanisms causing imprinting defects in familial Beckwith-Wiedemann syndrome with Wilms' tumour 126
Role of histone acetylation and DNA methylation in the maintenance of the imprinted expression of the H19 and Igf2 genes 126
A case of Beckwith-Wiedemann syndrome caused by a cryptic 11p15 deletion encompassing the centromeric imprinted domain of the BWS locus 126
ZFP57 maintains the parent-of-origin-specific expression of the imprinted genes and differentially affects non-imprinted targets in mouse embryonic stem cells 126
Transcription alterations of KCNQ1 associated with imprinted methylation defects in the Beckwith-Wiedemann locus 126
BamHI RFLP linked to the human urokinase gene 125
Genomic imprinting disorders: lessons on how genome, epigenome and environment interact 124
Tissue-specific and mosaic imprinting defects underlie opposite congenital growth disorders in mice 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 122
Familial posterior helical ear pits 121
Epigenetic Alterations in Inborn Errors of Immunity 120
Mosaic segmental and whole-chromosome upd(11)mat in silver-russell syndrome 119
Beckwith-Wiedemann syndrome and twinning: case report and brief review of literature 117
Looking for CDKN1C enhancers 117
Humanized H19/Igf2 locus reveals diverged imprinting mechanism between mouse and human and reflects Silver-Russell syndrome phenotypes 117
Prevalence of beckwith-wiedemann syndrome in North West of Italy 116
The Arabidopsis SUPERMAN protein is able to specifically bind DNA through its single Cys2-His2 zinc finger motif 115
Clinical and molecular diagnosis, screening and management of Beckwith-Wiedemann syndrome: An international consensus statement 115
Performance Metrics of the Scoring System for the Diagnosis of the Beckwith-Wiedemann Spectrum (BWSp) and Its Correlation with Cancer Development 114
ICF1-Syndrome-Associated DNMT3B Mutations Prevent De Novo Methylation at a Subset of Imprinted Loci during iPSC Reprogramming 113
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 112
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. 112
Tumor necrosis factor-α regulates mRNA for urokinase-type plasminogen activator and type-1 plasminogen activator inhibitor in human neoplastic cell lines 112
A paternally inherited 1.4 kb deletion of the 11p15.5 imprinting center 2 is associated with a mild familial Silver–Russell syndrome phenotype 112
LOSS OF HETEROZYGOSITY OF IMPRINTED GENES IN SV40 T/T ANTIGEN-INDUCED HEPATOCELLULAR CARCINOMAS 111
Perlman syndrome: Clinical report and nine-year follow-up 111
Paternal deletion of the 11p15.5 centromeric-imprinting control region is associated with alteration of imprinted gene expression and recurrent severe intrauterine growth restriction 110
Gain of function in CDKN1C 110
Two maternal duplications involving the CDKN1C gene are associated with contrasting growth phenotypes 110
Causes and Consequences of Multi-Locus Imprinting Disturbances in Humans 109
New insights into oocyte cytoplasmic lattice-associated proteins 108
Variable expressivity of the beckwith-wiedemann syndrome in four pedigrees segregating loss-of-function variants of cdkn1c 108
Clinical utility gene card for: Beckwith-Wiedemann Syndrome 107
Identification of trombospondin-1 as a novel amelogenin interactor by functional proteomics 107
A Maternal Loss‐of‐Function Variant in KHDC3L Gene Causes a Range of Adverse Pregnancy Outcomes: A Case Report 106
Microdeletion and IGF2 loss of imprinting in a cascade causing Beckwith-Wiedemann syndrome with Wilms' tumor - Reply 106
Understanding the Variability of 22q11.2 Deletion Syndrome: The Role of Epigenetic Factors 105
Molecular subtypes and phenotypic expression of Beckwith-Wiedemann syndrome 103
A novel iPSC-based model of ICF syndrome subtype 2 recapitulates the molecular phenotype of ZBTB24 deficiency 103
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 102
Structure of the galactokinase gene of Escherichia coli, the last (?) gene of the gal operon 100
The PEG13-DMR and brain-specific enhancers dictate imprinted expression within the 8q24 intellectual disability risk locus 100
Plasminogen activator inhibitor type 1 biosynthesis and mRNA level are increased by dexamethasone in human fibrosarcoma cells 99
Plasminogen activator inhibitor type-1 protein, mRNA and gene transcription are increased by phorbol esters in human rhabdomyosarcoma cells 99
FORSKOLIN DOWN-REGULATES TYPE-1 PLASMINOGEN-ACTIVATOR INHIBITOR AND TISSUE-TYPE PLASMINOGEN-ACTIVATOR AND THEIR MESSENGER-RNAS 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 97
Nephrological findings and genotype-phenotype correlation in Beckwith-Wiedemann syndrome 97
Plasminogen activator inhibitor type 1 gene is located at region q21.3-q22 of chromosome 7 and genetically linked with cystic fibrosis. 96
Recommendations of the Scientific Committee of the Italian Beckwith-Wiedemann Syndrome Association on the diagnosis, Management and follow-up of the syndrome 96
Insulin Like Growth Factor 2 Expression in the Rat Brain Both in Basal Condition and following Learning Predominantly Derives from the Maternal Allele 96
A novel missense variant in PNLDC1 associated with nonobstructive azoospermia 95
Convergently functional, Rho-independent terminator in Salmonella typhimurium 95
EMQN best practice guidelines for the molecular genetic testing and reporting of chromosome 11p15 imprinting disorders: Silver-Russell and Beckwith-Wiedemann syndrome 95
Totale 12.742
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Categoria #
all - tutte 55.322
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 55.322
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022723 0 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
2025/20268.066 321 376 362 392 796 4.576 361 195 290 197 88 112
2026/2027222 51 171 0 0 0 0 0 0 0 0 0 0
Totale 15.573