IRIS
LICCARDO, RAFFAELLA
 Distribuzione geografica
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Continente #
NA - Nord America 447
EU - Europa 243
AS - Asia 103
AF - Africa 8
Continente sconosciuto - Info sul continente non disponibili 1
Totale 802
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Nazione #
US - Stati Uniti d'America 444
IT - Italia 125
CN - Cina 66
FR - Francia 53
IE - Irlanda 27
IN - India 20
VN - Vietnam 16
FI - Finlandia 15
CI - Costa d'Avorio 8
UA - Ucraina 8
SE - Svezia 5
GB - Regno Unito 4
CA - Canada 3
NL - Olanda 3
CZ - Repubblica Ceca 2
DE - Germania 1
EU - Europa 1
SG - Singapore 1
Totale 802
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Città #
Chandler 109
Napoli 34
Millbury 29
Ashburn 23
Princeton 22
Beijing 19
Nanjing 18
Naples 18
Pune 17
Dong Ket 16
Boston 15
Des Moines 15
Wilmington 11
Nanchang 10
Jacksonville 9
Lawrence 8
Redwood City 8
Sarno 7
Shenyang 7
Brescia 6
Norwalk 5
Dublin 4
Seattle 4
Amsterdam 3
Ottawa 3
Pozzuoli 3
Tianjin 3
Verona 3
Changsha 2
Hangzhou 2
Hebei 2
Milan 2
Prague 2
Villaricca 2
Boardman 1
Brindisi 1
Busto Arsizio 1
Castellammare Di Stabia 1
Changchun 1
Chieti 1
Eboli 1
Edinburgh 1
Fairfield 1
Falls Church 1
Indiana 1
Jiaxing 1
Lanzhou 1
Maddaloni 1
Matera 1
Montecatini Terme 1
Nola 1
Perugia 1
Portici 1
Redmond 1
Romano Di Lombardia 1
Serio 1
Woodbridge 1
Totale 464
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Nome #
Characterization of novel, large duplications in the MSH2 gene of three unrelated Lynch syndrome patients. 58
Characterisation of mesenchymal colon tumour-derived cells in tumourspheres as a model for colorectal cancer progression 45
Incomplete segregation of MSH6 mutations with phenotype of Lynch syndrome. 40
Association of low-risk MSH3 and MSH2 variant alleles with Lynch syndrome: probability of synergistic effects. 39
Lithium chloride induces mesenchymal‑to‑epithelial reverting transition in primary colon cancer cell cultures 38
Two novel sequence variants in MSH2 gene in a patient who underwent cancer genetic counseling for a very early-onset epithelial ovarian cancer 38
Clinical and anamnestic evaluation rôle for the diagnosis and treatment of families affected by Lynch syndrome. Case report and review of the literature 35
Differential expression of PTEN gene correlates with phenotypic heterogeneity in three cases of patients showing clinical manifestations of PTEN hamartoma tumour syndrome. 33
MSH2 Overexpression Due to an Unclassified Variant in 3'-Untranslated Region in a Patient with Colon Cancer 32
Incomplete Segregation of MSH6 Frameshift Variants with Phenotype of Lynch Syndrome 31
Lithium chloride induces mesenchymal‑to‑epithelial reverting transition in primary colon cancer cell cultures 31
Mir-137 targets the 3′ untranslated region of msh2: Potential implications in lynch syndrome-related colorectal cancer 31
Multivariate analysis as a method for evaluating the pathogenicity of novel genetic MLH1 variants in patients with colorectal cancer and microsatellite instability 30
Coexistence of MLH3 germline variants in colon cancer patients belonging to families with Lynch syndrome-associated brain tumors 30
Same MSH2 Gene Mutation But Variable Phenotypes in 2 Families With Lynch Syndrome: Two Case Reports and Review of Genotype-Phenotype Correlation. 29
Contribution of Large Genomic Rearrangements in Italian Lynch Syndrome Patients: Characterization of a Novel Alu-Mediated Deletion 27
Novel MSH2 splice-site mutation in a young patient with Lynch syndrome 27
Genetics, diagnosis and treatment of lynch syndrome: Old lessons and current challenges (Review) 26
“Minor” mismatch repair genes involvement in genetic predisposition to lynch syndrome. 26
Association of ‘minor’mismatch repair gene unclassified variants with hereditary non-polyposis colorectal cancer: probability of synergistic effects 26
Hereditary gastrointestinal polyposis: Diagnosis, genetic test and risk assessment 24
Identification and molecular characterization of a novel mutation in MSH2 gene in a Lynch syndrome family 23
Hereditary Colorectal Cancer: State of the Art in Lynch Syndrome. 23
Involvement of large rearrangements in MSH6 and PMS2 genes in southern Italian patients with Lynch syndrome 21
Sporadic pediatric severe familial adenomatous polyposis: A case report 21
‘‘Minor’’ mismatch repair genes involvement in geneticpredisposition to Lynch sindrome 20
Significance of rare variants in genes involved in the pathogenesis of Lynch syndrome. 18
Novel Implications in Molecular Diagnosis of Lynch Syndrome 16
SALT-INDUCIBLE KINASE 1 MESSENGER ALTERATIONS ARE INVOLVED IN COLORECTAL TUMORIGENESIS 15
Synergistic Effects of Low-Risk Variant Alleles in Cancer Predisposition 13
Primary colon cancer cell cultures re-express e-cadherin during mesenchymal to epithelial reverting transition in vitro 12
Novel variants of unknown significance in the PMS2 gene identified in patients with hereditary colon cancer 10
Totale 888
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Categoria #
all - tutte 3.321
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 3.321
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/20198 0 0 0 0 0 0 0 0 0 2 2 4
2019/2020109 51 3 3 13 9 3 2 2 0 3 17 3
2020/202183 2 1 8 6 10 8 2 9 7 1 11 18
2021/2022221 5 0 1 1 1 33 7 11 26 18 50 68
2022/2023242 31 14 5 16 40 29 12 33 43 6 7 6
2023/2024113 10 22 17 5 12 30 2 13 0 2 0 0
Totale 888