Anastasia Katseli
Athens, ESYE31, Greece
Last Updated: 09/26/2026
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Found 10 publications
The Clinical and Genetic Landscape of Hereditary Cancer: Experience from a Single Clinical Diagnostic Laboratory.
Journal: Cancer genomics & proteomics
Published: June 26, 2024
Microsatellite Instability Is Insufficiently Used as a Biomarker for Lynch Syndrome Testing in Clinical Practice.
Journal: JCO precision oncology
Published: January 25, 2024
Germline Co-deletion of CDKN2A and CDKN2B Genes in Pleomorphic Xanthoastrocytoma: Case Report.
Journal: In vivo (Athens, Greece)
Published: January 19, 2024
Copy Number Variations (CNVs) Account for 10.8% of Pathogenic Variants in Patients Referred for Hereditary Cancer Testing.
Journal: Cancer genomics & proteomics
Published: May 29, 2023
Autoimmune pancreatitis associated with retroperitoneal fibrosis mimicking cholangiocarcinoma.
Journal: Oxford medical case reports
Published: January 31, 2018
Uveal Melanoma: GNAQ and GNA11 Mutations in a Greek Population.
Journal: Anticancer research
Published: July 12, 2017
Tumor heterogeneity revealed by KRAS, BRAF, and PIK3CA pyrosequencing: KRAS and PIK3CA intratumor mutation profile differences and their therapeutic implications.
Journal: Human mutation
Published: May 30, 2013
Multiplex PCR-based detection of circulating tumor cells in lung cancer patients using CK19, PTHrP, and LUNX specific primers.
Journal: Clinical lung cancer
Published: February 19, 2013
Laparoscopic adrenalectomy in patients with subclinical Cushing syndrome.
Journal: Surgical endoscopy
Published: July 18, 2012
Showing 1-10 of 10
Last Updated: 09/26/2026