Lenka Stolarova
Prague, PR, Czech Republic
Last Updated: 09/26/2026
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Found 13 publications
Case-Control Study for 23 Cancer Types With Functional Analysis of CHEK2: Risk Estimation and Clinical Recommendations in East Asia.
Journal: JCO precision oncology
Published: September 02, 2025
A comprehensive study evaluating germline FANCG variants in predisposition to breast and ovarian cancer.
Journal: Cancer medicine
Published: February 15, 2024
ENIGMA CHEK2gether Project: A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer Risk.
Journal: Clinical cancer research : an official journal of the American Association for Cancer Research
Published: January 28, 2023
CHEK2 Germline Variants in Cancer Predisposition: Stalemate Rather than Checkmate.
Journal: Cells
Published: November 15, 2020
Identification of Germline Mutations in Melanoma Patients with Early Onset, Double Primary Tumors, or Family Cancer History by NGS Analysis of 217 Genes.
Journal: Biomedicines
Published: August 31, 2020
Phosphorylation of PLK3 Is Controlled by Protein Phosphatase 6.
Journal: Cells
Published: May 15, 2020
Multigene Panel Germline Testing of 1333 Czech Patients with Ovarian Cancer.
Journal: Cancers
Published: March 15, 2020
Germline CHEK2 Gene Mutations in Hereditary Breast Cancer Predisposition - Mutation Types and their Biological and Clinical Relevance.
Journal: Klinicka onkologie : casopis Ceske a Slovenske onkologicke spolecnosti
Published: August 15, 2019
Contribution of Massive Parallel Sequencing to Diagnosis of Hereditary Ovarian Cancer in the Czech Republic.
Journal: Klinicka onkologie : casopis Ceske a Slovenske onkologicke spolecnosti
Published: August 15, 2019
Identification of deleterious germline CHEK2 mutations and their association with breast and ovarian cancer.
Journal: International journal of cancer
Published: February 06, 2019
BRCA1 and BRCA2 5' noncoding region variants identified in breast cancer patients alter promoter activity and protein binding.
Journal: Human mutation
Published: April 16, 2018
Last Updated: 09/26/2026