1. 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
  2. Genetics, diagnosis and treatment of Lynch syndrome: Old lessons and current challenges (Review)
    Francesca Duraturo et al, 2019, Oncology Letters CrossRef
  3. Promising Colorectal Cancer Biomarkers for Precision Prevention and Therapy
    Mimmo Turano et al, 2019, Cancers CrossRef
  4. 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
  5. Novel Implications in Molecular Diagnosis of Lynch Syndrome
    Raffaella Liccardo et al, 2017, Gastroenterology Research and Practice CrossRef
  6. 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
  7. 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
  8. 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
  9. Novel MSH2 splice-site mutation in a young patient with Lynch syndrome
    Raffaella Liccardo et al, 2018, Molecular Medicine Reports CrossRef
  10. 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
  11. Incomplete Segregation of MSH6 Frameshift Variants with Phenotype of Lynch Syndrome
    Raffaella Liccardo et al, 2017, International Journal of Molecular Sciences CrossRef
  12. 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
  13. MSH2 Overexpression Due to an Unclassified Variant in 3’-Untranslated Region in a Patient with Colon Cancer
    Raffaella Liccardo et al, 2020, Biomedicines CrossRef
  14. 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
  15. Prevalence of DNA Mismatch Repair Deficiency in Endometrial Cancer Using Immunohistochemistry
    Behnoush Mehdizadeh et al, 2022, International Journal of Cancer Management CrossRef
  16. Characterization of novel, large duplications in the MSH2 gene of three unrelated Lynch syndrome patients
    Raffaella Liccardo et al, 2018, Cancer Genetics CrossRef
  17. MiR-137 Targets the 3′ Untranslated Region of MSH2: Potential Implications in Lynch Syndrome-Related Colorectal Cancer
    Raffaella Liccardo et al, 2021, Cancers CrossRef