Two novel sequence variants in MSH2 gene in a patient who underwent cancer genetic counseling for a very early-onset epithelial ovarian cancer Matilde Pensabene et al, 2016, Hereditary Cancer in Clinical Practice CrossRef
Genetics, diagnosis and treatment of Lynch syndrome: Old lessons and current challenges (Review) Francesca Duraturo et al, 2019, Oncology Letters CrossRef
Promising Colorectal Cancer Biomarkers for Precision Prevention and Therapy Mimmo Turano et al, 2019, Cancers CrossRef
Implications of Splicing Alterations in the Onset and Phenotypic Variability of a Family with Subclinical Manifestation of Peutz–Jeghers Syndrome: Bioinformatic and Molecular Evidence Andrea Cerasuolo et al, 2020, International Journal of Molecular Sciences CrossRef
Novel Implications in Molecular Diagnosis of Lynch Syndrome Raffaella Liccardo et al, 2017, Gastroenterology Research and Practice CrossRef
Same MSH2 Gene Mutation But Variable Phenotypes in 2 Families With Lynch Syndrome: Two Case Reports and Review of Genotype-Phenotype Correlation Raffaella Liccardo et al, 2018, Clinical Medicine Insights: Case Reports CrossRef
Characterisation of mesenchymal colon tumour-derived cells in tumourspheres as a model for colorectal cancer progression Mimmo Turano et al, 2018, International Journal of Oncology CrossRef
Cáncer de colon en Colombia, fenotipo molecular: tamizaje para síndromes con agregación familiar Mabel Elena Bohórquez L et al, 2019, Revista de la Asociación Colombiana de Ciencias Biológicas CrossRef
Novel MSH2 splice-site mutation in a young patient with Lynch syndrome Raffaella Liccardo et al, 2018, Molecular Medicine Reports CrossRef
Manipulation of the Immune System for Cancer Defeat: A Focus on the T Cell Inhibitory Checkpoint Molecules Paolo D’Arrigo et al, 2020, Current Medicinal Chemistry CrossRef
Incomplete Segregation of MSH6 Frameshift Variants with Phenotype of Lynch Syndrome Raffaella Liccardo et al, 2017, International Journal of Molecular Sciences CrossRef
A Hereditable Mutation of MSH2 Gene Associated with Lynch Syndrome in a Five Generation Chinese Family
Wei-Hua Shao et al, 2020, Cancer Management and Research CrossRef
MSH2 Overexpression Due to an Unclassified Variant in 3’-Untranslated Region in a Patient with Colon Cancer Raffaella Liccardo et al, 2020, Biomedicines CrossRef
Coexistence of MLH3 germline variants in colon cancer patients belonging to families with Lynch syndrome-associated brain tumors Francesca Duraturo et al, 2016, Journal of Neuro-Oncology CrossRef
Prevalence of DNA Mismatch Repair Deficiency in Endometrial Cancer Using Immunohistochemistry Behnoush Mehdizadeh et al, 2022, International Journal of Cancer Management CrossRef
Characterization of novel, large duplications in the MSH2 gene of three unrelated Lynch syndrome patients Raffaella Liccardo et al, 2018, Cancer Genetics CrossRef
MiR-137 Targets the 3′ Untranslated Region of MSH2: Potential Implications in Lynch Syndrome-Related Colorectal Cancer Raffaella Liccardo et al, 2021, Cancers CrossRef