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Cancer Genomics & Proteomics|April 24, 2021
Clinical Utility of Functional RNA Analysis for the Reclassification of Splicing Gene Variants in Hereditary CancerKonstantinos Agiannitopoulos, Georgia Pepe, Eirini Papadopoulou, et al.
Anticancer Research|December 1, 2022
Genetic Predisposition to Male Breast Cancer: A Case SeriesAngela Apessos, Konstantinos Agiannitopoulos, Georgia Pepe, et al.
Cancer Genomics & Proteomics|December 24, 2021
Revisiting the Implications of Positive Germline Testing Results Using Multi-gene Panels in Breast Cancer PatientsGeorgios N Tsaousis, Eirini Papadopoulou, Konstantinos Agiannitopoulos, et al.
BMC Cancer|June 5, 2019
Analysis of hereditary cancer syndromes by using a panel of genes: novel and multiple pathogenic mutationsGeorgios N Tsaousis, Eirini Papadopoulou, Angela Apessos, et al.
Cancers|November 14, 2023
Only 32.3% of Breast Cancer Families with Pathogenic Variants in Cancer Genes Utilized Cascade Genetic TestingKonstantinos Agiannitopoulos, Kevisa Potska, Anastasia Katseli, et al.
Cancer Genomics & Proteomics|August 27, 2024
The Clinical and Genetic Landscape of Hereditary Cancer: Experience from a Single Clinical Diagnostic LaboratoryNikolaos Tsoulos, Konstantinos Agiannitopoulos, Kevisa Potska, et al.
Cancer Genomics & Proteomics|August 29, 2023
Copy Number Variations (CNVs) Account for 10.8% of Pathogenic Variants in Patients Referred for Hereditary Cancer TestingKonstantinos Agiannitopoulos, Georgia Pepe, Georgios N Tsaousis, et al.
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