- Germline CHEK2 Gene Mutations in Hereditary Breast Cancer Predisposition - Mutation Types and their Biological and Clinical Relevance2019 | First Faculty of Medicine
- Alterations of CHEK2 gene in non-Hodgkin lymphoma patientsPublication without faculty affiliation
- Detection of the CHEK2 1100delC mutation in patients with breast cancerPublication without faculty affiliation
- Analysis of CHEK2 FHA domain in Czech patients with sporadic breast cancer revealed distinct rare genetic alterations2008 | First Faculty of Medicine
- CHEK2 gene alterations in the forkhead-associated domain, 1100delC and del5395 do not modify the risk of sporadic pancreatic cancer.2010 | First Faculty of Medicine
- Occurrence of CHEK2 1100delC mutation in breast cancer patients and control cohort in the Czech Republic2005 | First Faculty of Medicine
- Analysis of the c.1100delC mutation of the CHEK2 gene in sporadic colorectal carcinoma and familial adenomatous polyposis patient population2007 | First Faculty of Medicine
- Functional characterization of CHEK2 variants in a Saccharomyces cerevisiae system2019 | First Faculty of Medicine
- Alterations of CHEK2 forkhead-associated domain increase the risk of Hodgkin lymphoma2011 | First Faculty of Medicine, Second Faculty of Medicine, Third Faculty of Medicine
- CHEK2 Germline Variants in Cancer Predisposition: Stalemate Rather than Checkmate2020 | First Faculty of Medicine
- Identification of deleterious germline CHEK2 mutations and their association with breast and ovarian cancer2019 | First Faculty of Medicine
- ENIGMA CHEK2gether Project: A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer Risk2023 | First Faculty of Medicine, Central Library of Charles University
- The CHEK2 gene I157T mutation and other alterations in its proximity increase the risk of sporadic colorectal cancer in the Czech population2009 | First Faculty of Medicine, Third Faculty of Medicine, Central Library of Charles University
- Whole Genome Sequencing Prioritizes CHEK2, EWSR1, and TIAM1 as Possible Predisposition Genes for Familial Non-Medullary Thyroid Cancer2021 | Faculty of Medicine in Pilsen
- Hereditary breast cancer - new facts2022 | First Faculty of Medicine
- Association of Germline CHEK2 Gene Variants with Risk and Prognosis of Non-Hodgkin Lymphoma2015 | First Faculty of Medicine
- The CHEK2 c. 1100delC germline mutation rarely contributes to breast cancer development in the Czech Republic2005 | First Faculty of Medicine
- Uncommon CHEK2 mis-sense variant and reduced risk of tobacco-related cancers: case-control study2007 | First Faculty of Medicine
- Uncommon CHEK2 mis-sense variant and reduced risk of tobacco-related cancers: case-control study2007 | Faculty of Physical Education and Sport
- Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer2014 | First Faculty of Medicine
- The CHEK2 gene I157T mutation and other alterations in its proximity increase the risk of sporadic colorectal cancer in the Czech population2009 | Publication without faculty affiliation
- Germline BRCA2 K3326X and CHEK2 I157T Mutations Increase Risk for Sporadic Pancreatic Ductal Adenocarcinoma2019 | First Faculty of Medicine, Faculty of Medicine in Pilsen
- CHEK2*1100delC mutation in the Czech Republic may rarely contribute to breast cancer developmentPublication without faculty affiliation
- Spectrum of mutations in BRCA1, BRCA2, ATM, and CHEK2 in families at high-risk of breast and ovarian cancerPublication without faculty affiliation
- Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer (Reprinted from Nature Genetics vol 46, pg 736, 2014 10.1038/ng.3002)2014 | First Faculty of Medicine
- Low frequency of CHEK2 1100delC mutation in breast cancer patients and hereditary breast cancer families in the Czech RepublicPublication without faculty affiliation
- Higher frequency of non-conservative mutations in fork-head associated (FHA) domain of checkpoint kinase 2 (CHEK2) gene in breast cancer patientsPublication without faculty affiliation
- CHEK2p.I157T Mutation Is Associated with Increased Risk of Adult-Type Ovarian Granulosa Cell Tumors2022 | Faculty of Medicine in Pilsen
- The clinical importance of a genetic analysis of moderate-risk cancer susceptibility genes in breast and other cancer patients from the Czech Republic2012 | First Faculty of Medicine
- The PALB2 Gene Is a Strong Candidate for Clinical Testing in BRCA1- and BRCA2-Negative Hereditary Breast Cancer2013 | First Faculty of Medicine