IRIS
CERRATO, Flavia
 Distribuzione geografica
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Continente #
EU - Europa 979
NA - Nord America 936
AS - Asia 98
SA - Sud America 3
OC - Oceania 1
Totale 2.017
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Nazione #
US - Stati Uniti d'America 912
IE - Irlanda 358
IT - Italia 183
GB - Regno Unito 126
UA - Ucraina 119
DE - Germania 93
CN - Cina 67
FI - Finlandia 28
GR - Grecia 25
CA - Canada 24
SE - Svezia 19
BE - Belgio 15
TR - Turchia 12
FR - Francia 7
PK - Pakistan 7
IN - India 5
NL - Olanda 4
HK - Hong Kong 2
AT - Austria 1
AU - Australia 1
BR - Brasile 1
CH - Svizzera 1
CL - Cile 1
IR - Iran 1
PE - Perù 1
PH - Filippine 1
SG - Singapore 1
UZ - Uzbekistan 1
VN - Vietnam 1
Totale 2.017
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Città #
Dublin 358
Chandler 200
Jacksonville 186
Ann Arbor 60
Bremen 44
Princeton 41
Medford 33
Caserta 28
Beijing 27
Napoli 25
Elora 24
Boardman 23
Roxbury 23
San Mateo 20
Wilmington 19
Woodbridge 18
Brussels 15
New York 15
Gragnano 11
Pozzuoli 11
Jinan 10
Des Moines 9
Cambridge 8
Aversa 5
Houston 5
Santa Maria Capua Vetere 5
Amsterdam 4
Delhi 4
Fuzhou 4
Nanjing 4
Norwalk 4
Redwood City 4
Afragola 3
Ashburn 3
Auburn Hills 3
Cinisello Balsamo 3
Marseille 3
Mountain View 3
Athens 2
Benevento 2
Brindisi 2
Capua 2
Frankfurt am Main 2
Genova 2
Guangzhou 2
Hebei 2
Hong Kong 2
Lanzhou 2
Los Angeles 2
Ningbo 2
Pievepelago 2
Pomigliano D'arco 2
Redmond 2
Shenyang 2
Stella Cilento 2
Zhengzhou 2
Angra dos Reis 1
Angri 1
Avellino 1
Barano d'Ischia 1
Basel 1
Berlin 1
Birmingham 1
Bologna 1
Carmignano di Brenta 1
Centro 1
Changsha 1
Dadu 1
Düsseldorf 1
Gricignano di Aversa 1
Haikou 1
Hangzhou 1
Hefei 1
Kunming 1
Lahore 1
Marina di Camerota 1
Nanchang 1
Naples 1
Oppido Lucano 1
Oristano 1
Paris 1
Poggiomarino 1
Pune 1
Puxian 1
Saint Louis 1
San Francisco 1
San Remo 1
Sant'Antonio Abate 1
Santiago 1
Shanghai 1
Striano 1
Sydney 1
Taiyuan 1
Taizhou 1
Tappahannock 1
Tashkent 1
Thorigny 1
Torre Del Greco 1
Vienna 1
Totale 1.344
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Nome #
Distinct methylation changes at the IGF2-H19 locus in congenital growth disorders and cancer 79
The H19 endodermal enhancer is required for Igf2 activation and tumor formation in experimental liver carcinogenesis 75
DNA Methylation in the Diagnosis of Monogenic Diseases 75
Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith - Wiedemann syndrome and Wilms' tumour 73
Is ZFP57 binding to H19/IGF2: IG-DMR affected in Silver-Russell syndrome? 66
Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith-Wiedemann syndrome 63
The KCNQ1OT1 imprinting control region and non-coding RNA: New properties derived from the study of Beckwith-Wiedemann syndrome and Silver-Russell syndrome cases 62
Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome 61
EFFECTS OF PROLONGED WAKEFULNESS: THE ROLE OF PERIOD3 GENOTYPES AND PERSONALITY TRAITS 60
The phenotypic variations of multi-locus imprinting disturbances associated with maternal-effect variants of NLRP5 range from overt imprinting disorder to apparently healthy phenotype 59
ZFP57 recognizes multiple and closely spaced sequence motif variants to maintain repressive epigenetic marks in mouse embryonic stem cells 58
Mechanisms causing imprinting defects in familial Beckwith-Wiedemann syndrome with Wilms' tumour 55
Looking for CDKN1C enhancers 54
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 52
Role of histone acetylation and DNA methylation in the maintenance of the imprinted expression of the H19 and Igf2 genes 52
Developmentally regulated functions of the H19 differentially methylated domain 52
Microdeletion and IGF2 loss of imprinting in a cascade causing Beckwith-Wiedemann syndrome with Wilms' tumor - Reply 51
BEHAVIORAL CHANGES FOLLOWING TOTAL SLEEP DEPRIVATION. THE ROLE OF PER3 POLYMORPHISM AND OF PERSONALITY FACTORS 51
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 49
Paternal deletion of the 11p15.5 centromeric-imprinting control region is associated with alteration of imprinted gene expression and recurrent severe intrauterine growth restriction 47
A novel large deletion of the ICR1 region including H19 and putative enhancer elements 47
A novel microdeletion in the IGF2/H19 imprinting centre region defines a recurrent mutation mechanism in familial Beckwith-Wiedemann syndrome 46
Assisted Reproductive Techniques and Risk of Beckwith-Wiedemann Syndrome 46
Humanized H19/Igf2 locus reveals diverged imprinting mechanism between mouse and human and reflects Silver-Russell syndrome phenotypes 45
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 44
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 44
Beckwith-Wiedemann Syndrome 44
Inherited and sporadic epimutations at the IGF2-H19 locus in beckwith-wiedemann syndrome and wilms' tumor 43
A splicing mutation of the HMGA2 gene is associated with Silver-Russell syndrome phenotype 43
Loss-of-function maternal-effect mutations of PADI6 are associated with familial and sporadic Beckwith-Wiedemann syndrome with multi-locus imprinting disturbance 42
Tissue-specific and mosaic imprinting defects underlie opposite congenital growth disorders in mice 40
Transcription alterations of KCNQ1 associated with imprinted methylation defects in the Beckwith-Wiedemann locus 40
Both Epimutations and Chromosome Aberrations Affect Multiple Imprinted Loci in Aggressive Wilms Tumors 39
Origins of DNA methylation defects in Wilms tumors 38
Two maternal duplications involving the CDKN1C gene are associated with contrasting growth phenotypes 36
The two-domain hypothesis in Beckwith-Wiedemann syndrome: autonomous imprinting of the telomeric domain of the distal chromosome 7 cluster 33
The 5′ end of the KCNQ10T1 gene is hypomethylated in the Beckwith-Wiedemann syndrome 33
Paternal imprints can be established on the maternal Igf2-H19 locus without altering replication timing of DNA 31
Mosaic segmental and whole-chromosome upd(11)mat in silver-russell syndrome 31
Zfp57 inactivation illustrates the role of ICR methylation in imprinted gene expression during neural differentiation of mouse ESCs 30
Variable expressivity of the beckwith-wiedemann syndrome in four pedigrees segregating loss-of-function variants of cdkn1c 30
Different Mechanisms Cause Hypomethylation of Both H19 and KCNQ1OT1 Imprinted Differentially Methylated Regions in Two Cases of Silver-Russell Syndrome Spectrum 29
Clinical and molecular characterization of patients affected by Beckwith-Wiedemann spectrum conceived through assisted reproduction techniques 25
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 25
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 20
Co-Occurrence of Beckwith–Wiedemann Syndrome and Early-Onset Colorectal Cancer 17
Co-occurrence of Beckwith-Wiedemann syndrome and pseudohypoparathyroidism type 1B: coincidence or common molecular mechanism? 7
Beckwith-Wiedemann syndrome and twinning: case report and brief review of literature 1
Totale 2.143
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Categoria #
all - tutte 7.798
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 7.798
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201910 0 0 0 0 0 0 0 0 0 2 6 2
2019/2020225 38 33 5 4 34 3 42 16 21 15 11 3
2020/2021298 29 12 37 12 54 2 45 30 4 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
2023/2024191 21 13 14 25 77 20 12 5 3 1 0 0
Totale 2.143