CNR Institutional Research Information System

RICCIO, ANDREA
 Distribuzione geografica
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Continente #
EU - Europa 15
AS - Asia 4
NA - Nord America 2
Totale 21
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Nazione #
IT - Italia 13
SG - Singapore 4
US - Stati Uniti d'America 2
NL - Olanda 1
SE - Svezia 1
Totale 21
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Città #
Naples 5
Rome 5
Singapore 3
Aversa 2
Forest City 2
Amsterdam 1
Formia 1
Totale 19
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Nome #
Zfp57 inactivation illustrates the role of ICR methylation in imprinted gene expression during neural differentiation of mouse ESCs 4
ICF1-Syndrome-Associated DNMT3B Mutations Prevent De Novo Methylation at a Subset of Imprinted Loci during iPSC Reprogramming 4
Beckwith-Wiedemann syndrome and twinning: case report and brief review of literature 3
Co-Occurrence of Beckwith-Wiedemann Syndrome and Early-Onset Colorectal Cancer 3
ICF1 Syndrome Associated DNMT3B Mutations Prevent de novo Methylation at a subset of Imprinted Loci During iPSC Reprogramming 3
A novel iPSC-based model of ICF syndrome subtype 2 recapitulates the molecular phenotype of ZBTB24 deficiency 2
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 1
Biallelic variant in cyclin B3 is associated with failure of maternal meiosis II and recurrent digynic triploidy 1
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. 1
Giant breast tumors in a patient with Beckwith-Wiedemann syndrome 1
A paternally inherited 1.4 kb deletion of the 11p15.5 Imprinting Center 2 is associated with a mild familial Silver-Russell syndrome phenotype 1
DNA methylation in the diagnosis of monogenic diseases 1
Cancer Risk in Beckwith-Wiedemann Syndrome: A Systematic Review and Meta-Analysis Outlining a Novel (Epi)Genotype Specific Histotype Targeted Screening Protocol 1
Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith-Wiedemann syndrome 1
EMQN best practice guidelines for the molecular genetic testing and reporting of chromosome 11p15 imprinting disorders: Silver-Russell and Beckwith-Wiedemann syndrome 1
Totale 28
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Categoria #
all - tutte 1.155
article - articoli 958
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 2.113
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202414 0 0 0 0 0 0 0 0 4 0 7 3
2024/202514 12 2 0 0 0 0 0 0 0 0 0 0
Totale 28