RICCIO, Andrea
 Distribuzione geografica
Continente #
EU - Europa 24
NA - Nord America 2
Totale 26
Nazione #
IT - Italia 23
US - Stati Uniti d'America 2
MK - Macedonia 1
Totale 26
Città #
Caserta 14
Naples 3
Santa Maria Capua Vetere 3
Council Bluffs 1
Kumanovo 1
Napoli 1
Wrentham 1
Totale 24
Nome #
The KCNQ1OT1 imprinting control region and non-coding RNA: New properties derived from the study of Beckwith-Wiedemann syndrome and Silver-Russell syndrome cases, file dfd1c04a-5e3e-0799-e053-6605fe0a8ddb 8
Clinical and molecular characterization of patients affected by Beckwith-Wiedemann spectrum conceived through assisted reproduction techniques, file 397f0bc9-3a57-4461-9a10-5080a77ec82e 4
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], file dfd1c04a-6d0a-0799-e053-6605fe0a8ddb 3
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, file cad4abe9-b583-485c-b8ff-811273d520b0 2
Microdeletion and IGF2 loss of imprinting in a cascade causing Beckwith-Wiedemann syndrome with Wilms' tumor - Reply, file dfd1c04a-7a16-0799-e053-6605fe0a8ddb 2
Beckwith-Wiedemann syndrome and twinning: case report and brief review of literature, file 34e1bca7-b9a7-4342-bfc7-68d8a121ddac 1
Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith - Wiedemann syndrome and Wilms' tumour, file dfd1c04a-23a5-0799-e053-6605fe0a8ddb 1
The two-domain hypothesis in Beckwith-Wiedemann syndrome: autonomous imprinting of the telomeric domain of the distal chromosome 7 cluster, file dfd1c04a-2610-0799-e053-6605fe0a8ddb 1
Inherited and sporadic epimutations at the IGF2-H19 locus in beckwith-wiedemann syndrome and wilms' tumor, file dfd1c04a-60ca-0799-e053-6605fe0a8ddb 1
Distinct methylation changes at the IGF2-H19 locus in congenital growth disorders and cancer, file dfd1c04a-680f-0799-e053-6605fe0a8ddb 1
ZFP57 recognizes multiple and closely spaced sequence motif variants to maintain repressive epigenetic marks in mouse embryonic stem cells, file dfd1c04a-8152-0799-e053-6605fe0a8ddb 1
Beckwith-Wiedemann syndrome. Clinical and etiopathogenic aspects of a model genomic imprinting entity, file dfd1c04c-60d1-0799-e053-6605fe0a8ddb 1
A KHDC3L mutation resulting in recurrent hydatidiform mole causes genome-wide DNA methylation loss in oocytes and persistent imprinting defects post-fertilisation, file dfd1c04c-d6ea-0799-e053-6605fe0a8ddb 1
The phenotypic variations of multi-locus imprinting disturbances associated with maternal-effect variants of NLRP5 range from overt imprinting disorder to apparently healthy phenotype, file dfd1c04c-e1d3-0799-e053-6605fe0a8ddb 1
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, file f832ea89-5b45-45cc-825a-1e77a414de5d 1
Totale 29
Categoria #
all - tutte 98
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 98


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20203 0 0 0 0 0 0 2 1 0 0 0 0
2020/20211 0 0 0 0 0 0 0 0 1 0 0 0
2022/20239 0 0 0 3 1 0 3 1 0 1 0 0
2023/20241 0 0 0 0 0 0 1 0 0 0 0 0
Totale 29