Raffaella Liccardo

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Genetics, diagnosis and treatment of Lynch syndrome: Old lessons and current challenges

P. Izzo, M. De Rosa, Francesca Duraturo, 2019, Oncology letters.

Differential expression of PTEN gene correlates with phenotypic heterogeneity in three cases of patients showing clinical manifestations of PTEN hamartoma tumour syndrome

P. Delrio, L. Paparo, P. Izzo, 2013, Hereditary cancer in clinical practice.

Hereditary gastrointestinal polyposis: Diagnosis, genetic test and risk assessment

P. Izzo, M. Rosa, Francesca Duraturo, 2013 .

Abstract. The molecular characterization of patients with Lynch syndrome (LS) involves germline testing to detect a deleterious mutation in one of the genes of the mismatch repair

P. Izzo, M. De Rosa, M. Lambiase, 2022 .

Association of low‐risk MSH3 and MSH2 variant alleles with Lynch syndrome: Probability of synergistic effects

M. Grosso, P. Izzo, M. Rosa, 2011, International journal of cancer.

Novel variants of unknown significance in the PMS2 gene identified in patients with hereditary colon cancer

P. Izzo, M. De Rosa, N. Mitilini, 2019, Cancer management and research.

Novel MSH2 splice-site mutation in a young patient with Lynch syndrome

P. Izzo, M. De Rosa, Francesca Duraturo, 2018, Molecular medicine reports.

Identification and molecular characterization of a novel mutation in MSH2 gene in a lynch syndrome family

P. Izzo, A. I. Monte, Francesca Duraturo, 2017 .

Hereditary Colorectal Cancer: State of the Art in Lynch Syndrome

P. Izzo, M. De Rosa, Francesca Duraturo, 2022, Cancers.

Novel Implications in Molecular Diagnosis of Lynch Syndrome

P. Izzo, M. De Rosa, Francesca Duraturo, 2017, Gastroenterology research and practice.

Two novel sequence variants in MSH2 gene in a patient who underwent cancer genetic counseling for a very early-onset epithelial ovarian cancer

S. de Placido, M. Pensabene, C. Carlomagno, 2016, Hereditary cancer in clinical practice.

Lithium chloride induces mesenchymal-to-epithelial reverting transition in primary colon cancer cell cultures

P. Delrio, R. Genesio, L. Nitsch, 2015, International journal of oncology.

Characterisation of mesenchymal colon tumour-derived cells in tumourspheres as a model for colorectal cancer progression

P. Delrio, C. Dodaro, P. Izzo, 2018, International journal of oncology.

Contribution of Large Genomic Rearrangements in Italian Lynch Syndrome Patients: Characterization of a Novel Alu-Mediated Deletion

P. Izzo, M. De Rosa, G. Diana, 2012, BioMed research international.

Synergistic Effects of Low-Risk Variant Alleles in Cancer Predisposition

P. Izzo, M. Rosa, Francesca Duraturo, 2013 .

Characterization of novel, large duplications in the MSH2 gene of three unrelated Lynch syndrome patients.

P. Izzo, G. Rossi, M. De Rosa, 2018, Cancer genetics.

Incomplete Segregation of MSH6 Frameshift Variants with Phenotype of Lynch Syndrome

N. Carlomagno, P. Izzo, G. Rossi, 2017, International journal of molecular sciences.

Multivariate analysis as a method for evaluating the pathogenicity of novel genetic MLH1 variants in patients with colorectal cancer and microsatellite instability.

P. Izzo, G. Rossi, M. De Rosa, 2015, International journal of molecular medicine.

MiR-137 Targets the 3′ Untranslated Region of MSH2: Potential Implications in Lynch Syndrome-Related Colorectal Cancer

M. Grosso, R. Sessa, P. Izzo, 2021, Cancers.

Coexistence of MLH3 germline variants in colon cancer patients belonging to families with Lynch syndrome-associated brain tumors

P. Izzo, Francesca Duraturo, Raffaella Liccardo, 2016, Journal of Neuro-Oncology.

Sporadic pediatric severe familial adenomatous polyposis: A case report.

E. Miele, P. Izzo, M. Rosa, 2020, Molecular and clinical oncology.

Abstract. Familial adenomatous polyposis (FAP) is an auto‐ somal dominant hereditary precancerous condition caused by germline pathogenetic variants in the tumor suppressor adeno‐ matous polyposis coli (APC) gene. Patients with FAP develop multiple gastrointestinal adenomatous polyps usually at the

E. Miele, P. Izzo, M. Rosa, 2020 .

Germline Variants in MLH1 and ATM Genes in a Young Patient with MSI-H in a Precancerous Colonic Lesion

P. Izzo, G. Rossi, M. Rosa, 2023, International journal of molecular sciences.

MSH2 Overexpression Due to an Unclassified Variant in 3’-Untranslated Region in a Patient with Colon Cancer

P. Izzo, M. De Rosa, M. Lambiase, 2020, Biomedicines.

Two novel sequence variants in MSH2 gene in a patient who underwent cancer genetic counseling for a very early-onset epithelial ovarian cancer

M. Pensabene, C. Carlomagno, Francesca Duraturo, 2016, Hereditary cancer in clinical practice.

Same MSH2 Gene Mutation But Variable Phenotypes in 2 Families With Lynch Syndrome: Two Case Reports and Review of Genotype-Phenotype Correlation

M. De Rosa, Francesca Duraturo, Raffaella Liccardo, 2018, Clinical medicine insights. Case reports.

Involvement of large rearrangements in MSH6 and PMS2 genes in Southern Italian patients with Lynch syndrome.

P. Izzo, A. I. Monte, Francesca Duraturo, 2018 .

Significance of rare variants in genes involved in the pathogenesis of Lynch syndrome

P. Izzo, M. De Rosa, M. Lambiase, 2022, International journal of molecular medicine.