IRIS
CERRATO, Flavia
 Distribuzione geografica
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Continente #
EU - Europa 3.364
NA - Nord America 1.596
AS - Asia 1.265
SA - Sud America 166
AF - Africa 21
OC - Oceania 3
Totale 6.415
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Nazione #
RU - Federazione Russa 2.162
US - Stati Uniti d'America 1.543
SG - Singapore 435
IE - Irlanda 359
IT - Italia 287
CN - Cina 283
HK - Hong Kong 185
VN - Vietnam 156
GB - Regno Unito 145
BR - Brasile 139
UA - Ucraina 121
DE - Germania 118
KR - Corea 76
CA - Canada 37
IN - India 37
FI - Finlandia 30
FR - Francia 30
GR - Grecia 25
TR - Turchia 21
SE - Svezia 19
BE - Belgio 18
JP - Giappone 18
NL - Olanda 15
AR - Argentina 11
PK - Pakistan 11
AT - Austria 9
BD - Bangladesh 9
MX - Messico 9
ZA - Sudafrica 7
EC - Ecuador 6
IQ - Iraq 6
ES - Italia 5
MA - Marocco 5
PL - Polonia 5
CL - Cile 4
PY - Paraguay 4
AZ - Azerbaigian 3
CH - Svizzera 3
CZ - Repubblica Ceca 3
KE - Kenya 3
PH - Filippine 3
UZ - Uzbekistan 3
AU - Australia 2
CR - Costa Rica 2
DZ - Algeria 2
ID - Indonesia 2
IL - Israele 2
IR - Iran 2
KZ - Kazakistan 2
LT - Lituania 2
LV - Lettonia 2
NO - Norvegia 2
SA - Arabia Saudita 2
AE - Emirati Arabi Uniti 1
AG - Antigua e Barbuda 1
BG - Bulgaria 1
DM - Dominica 1
DO - Repubblica Dominicana 1
EG - Egitto 1
HN - Honduras 1
HU - Ungheria 1
IS - Islanda 1
JO - Giordania 1
KW - Kuwait 1
LA - Repubblica Popolare Democratica del Laos 1
MN - Mongolia 1
MY - Malesia 1
NG - Nigeria 1
NP - Nepal 1
NZ - Nuova Zelanda 1
PE - Perù 1
PT - Portogallo 1
SO - Somalia 1
SY - Repubblica araba siriana 1
TH - Thailandia 1
TN - Tunisia 1
TT - Trinidad e Tobago 1
VE - Venezuela 1
Totale 6.415
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Città #
Moscow 795
Dublin 359
Santa Clara 207
Chandler 200
Jacksonville 186
Hong Kong 184
Singapore 179
San Jose 119
Seoul 76
Ann Arbor 60
Dallas 58
Ashburn 57
Ho Chi Minh City 50
Beijing 49
Bremen 44
Princeton 41
Hanoi 39
Hefei 38
Medford 33
Caserta 28
Napoli 25
Elora 24
Bengaluru 23
Boardman 23
Roxbury 23
Aversa 22
São Paulo 21
The Dalles 21
San Mateo 20
New York 19
Wilmington 19
Brussels 18
Los Angeles 18
Woodbridge 18
Da Nang 12
Pozzuoli 12
Amsterdam 11
Frankfurt am Main 11
Gragnano 11
Haiphong 10
Jinan 10
Des Moines 9
Cambridge 8
Naples 8
Nuremberg 8
Tokyo 8
Viterbo 8
Falkenstein 7
Giugliano in Campania 7
Vienna 7
Boston 6
Columbus 6
Houston 6
Johannesburg 6
Messina 6
Palermo 6
Fuzhou 5
London 5
Pagani 5
Santa Maria Capua Vetere 5
Toronto 5
Afragola 4
Asunción 4
Birmingham 4
Brooklyn 4
Bắc Ninh 4
Delhi 4
Guangzhou 4
Guarulhos 4
Hải Dương 4
Montreal 4
Nanjing 4
Norwalk 4
Orem 4
Paris 4
Redwood City 4
Roubaix 4
Tianjin 4
Ankara 3
Auburn Hills 3
Baku 3
Bexley 3
Biên Hòa 3
Brasília 3
Brno 3
Chennai 3
Cinisello Balsamo 3
Clifton 3
Contagem 3
Council Bluffs 3
Curitiba 3
Dhaka 3
Faisalabad 3
Fortaleza 3
Marseille 3
Mexico City 3
Mountain View 3
Nairobi 3
Newark 3
Ningbo 3
Totale 3.438
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Nome #
Distinct methylation changes at the IGF2-H19 locus in congenital growth disorders and cancer 185
DNA Methylation in the Diagnosis of Monogenic Diseases 170
Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith - Wiedemann syndrome and Wilms' tumour 169
BEHAVIORAL CHANGES FOLLOWING TOTAL SLEEP DEPRIVATION. THE ROLE OF PER3 POLYMORPHISM AND OF PERSONALITY FACTORS 155
Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith-Wiedemann syndrome 153
Is ZFP57 binding to H19/IGF2: IG-DMR affected in Silver-Russell syndrome? 153
Assisted Reproductive Techniques and Risk of Beckwith-Wiedemann Syndrome 146
Co-occurrence of Beckwith-Wiedemann syndrome and pseudohypoparathyroidism type 1B: coincidence or common molecular mechanism? 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
EFFECTS OF PROLONGED WAKEFULNESS: THE ROLE OF PERIOD3 GENOTYPES AND PERSONALITY TRAITS 145
Loss-of-function maternal-effect mutations of PADI6 are associated with familial and sporadic Beckwith-Wiedemann syndrome with multi-locus imprinting disturbance 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 140
A novel microdeletion in the IGF2/H19 imprinting centre region defines a recurrent mutation mechanism in familial Beckwith-Wiedemann syndrome 140
A novel large deletion of the ICR1 region including H19 and putative enhancer elements 140
Co-Occurrence of Beckwith–Wiedemann Syndrome and Early-Onset Colorectal Cancer 138
A splicing mutation of the HMGA2 gene is associated with Silver-Russell syndrome phenotype 137
The phenotypic variations of multi-locus imprinting disturbances associated with maternal-effect variants of NLRP5 range from overt imprinting disorder to apparently healthy phenotype 137
Clinical and molecular characterization of patients affected by Beckwith-Wiedemann spectrum conceived through assisted reproduction techniques 136
Different Mechanisms Cause Hypomethylation of Both H19 and KCNQ1OT1 Imprinted Differentially Methylated Regions in Two Cases of Silver-Russell Syndrome Spectrum 134
Developmentally regulated functions of the H19 differentially methylated domain 133
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 132
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 131
Both Epimutations and Chromosome Aberrations Affect Multiple Imprinted Loci in Aggressive Wilms Tumors 130
ZFP57 recognizes multiple and closely spaced sequence motif variants to maintain repressive epigenetic marks in mouse embryonic stem cells 125
A maternal-effectPadi6variant causes nuclear and cytoplasmic abnormalities in oocytes, as well as failure of epigenetic reprogramming and zygotic genome activation in embryos 124
Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome 124
The KCNQ1OT1 imprinting control region and non-coding RNA: New properties derived from the study of Beckwith-Wiedemann syndrome and Silver-Russell syndrome cases 124
Role of histone acetylation and DNA methylation in the maintenance of the imprinted expression of the H19 and Igf2 genes 124
Mechanisms causing imprinting defects in familial Beckwith-Wiedemann syndrome with Wilms' tumour 123
Zfp57 inactivation illustrates the role of ICR methylation in imprinted gene expression during neural differentiation of mouse ESCs 123
Transcription alterations of KCNQ1 associated with imprinted methylation defects in the Beckwith-Wiedemann locus 122
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 120
Tissue-specific and mosaic imprinting defects underlie opposite congenital growth disorders in mice 118
Mosaic segmental and whole-chromosome upd(11)mat in silver-russell syndrome 116
Humanized H19/Igf2 locus reveals diverged imprinting mechanism between mouse and human and reflects Silver-Russell syndrome phenotypes 115
Beckwith-Wiedemann syndrome and twinning: case report and brief review of literature 113
Looking for CDKN1C enhancers 113
Paternal deletion of the 11p15.5 centromeric-imprinting control region is associated with alteration of imprinted gene expression and recurrent severe intrauterine growth restriction 107
Two maternal duplications involving the CDKN1C gene are associated with contrasting growth phenotypes 107
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 106
Variable expressivity of the beckwith-wiedemann syndrome in four pedigrees segregating loss-of-function variants of cdkn1c 105
Microdeletion and IGF2 loss of imprinting in a cascade causing Beckwith-Wiedemann syndrome with Wilms' tumor - Reply 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 99
Origins of DNA methylation defects in Wilms tumors 93
Paternal imprints can be established on the maternal Igf2-H19 locus without altering replication timing of DNA 89
Identification of genetic and non-genetic modifiers of genomic imprinting through screening of imprinted DMR methylation in humans 84
Highly variable genomic methylation in the Beckwith-Wiedemann syndrome associated with multi-locus imprinting disturbances 84
The two-domain hypothesis in Beckwith-Wiedemann syndrome: autonomous imprinting of the telomeric domain of the distal chromosome 7 cluster 83
The 5′ end of the KCNQ10T1 gene is hypomethylated in the Beckwith-Wiedemann syndrome 79
Multi-locus imprinting disturbance (MLID): interim joint statement for clinical and molecular diagnosis 60
Adult‐Onset β‐Thalassemia Major as Acquired Imprinting Disorder 23
Hypomethylation of the MEG8:Int2-DMR in patients with pathogenic PLAG1 variants suggests new role of the chr14q32 imprinting cluster in Silver-Russell syndrome 16
Totale 6.548
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Categoria #
all - tutte 20.930
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 20.930
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202173 0 0 0 0 0 0 0 0 0 41 29 3
2021/2022312 24 2 22 6 88 1 9 11 10 48 27 64
2022/2023835 88 4 5 101 86 72 5 54 360 14 23 23
2023/2024255 21 13 14 25 77 20 12 5 3 1 14 50
2024/2025895 4 53 8 48 129 139 113 87 130 69 59 56
2025/20263.446 143 172 142 149 379 2.000 158 115 116 72 0 0
Totale 6.548