- Identifying Novel Susceptibility Genes for Colorectal Cancer Risk From a Transcriptome-Wide Association Study of 125,478 Subjects2021 | First Faculty of Medicine
- Re: ERCC3, a new ovarian cancer susceptibility gene?2021 | First Faculty of Medicine
- Mapping susceptibility genes for bipolar disorder: a pharmacogenetic approach based on excellent response to lithium2001 | First Faculty of Medicine
- Search for Susceptibility Genes in Bipolar Disorder using a Pharmacogenetic StrategyPublication without faculty affiliation
- 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
- Association of Obesity Susceptibility Gene Variants with Metabolic Syndrome and Related Traits in 1,443 Czech Adolescents2013 | Third Faculty of Medicine, Faculty of Science
- Target sequencing, cell experiments, and a population study establish endothelial nitric oxide synthase (eNOS) gene as hypertension susceptibility gene2013 | Faculty of Medicine in Pilsen
- Mutation Analysis of the RAD51C and RAD51D Genes in High-Risk Ovarian Cancer Patients and Families from the Czech Republic2015 | First Faculty of Medicine
- Contribution of mutations in ATM to breast cancer development in the Czech population2008 | First Faculty of Medicine
- Genetic Testing and Clinical Management Practices for Variants in Non-BRCA1/2 Breast (and Breast/Ovarian) Cancer Susceptibility Genes: An International Survey by the Evidence-Based Network for the Interpretation of Germline Mutant Alleles (ENIGMA) Clinical Working Group2018 | First Faculty of Medicine
- Cancer Risks Associated With Germline PALB2 Pathogenic Variants: An International Study of 524 Families2020 | 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
- CZECANCA: CZEch CAncer paNel for Clinical Application - Design and Optimization of the Targeted Sequencing Panel for the Identification of Cancer Susceptibility in High-risk Individuals from the Czech Republi2016 | First Faculty of Medicine
- Prerequisites for preimplantation genetic diagnosis (PGD in carriers of mutations responsible for hereditary cancers2009 | First Faculty of Medicine, Third Faculty of Medicine
- Novel insights into genetic susceptibility for colorectal cancer from transcriptome-wide association and functional investigation2024 | First Faculty of Medicine, Faculty of Medicine in Pilsen
- Genetics of pheochromocytoma and paraganglioma syndromes: new advances and future treatment options2013 | First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine
- Women at high risk of breast cancer: Molecular characteristics, clinical presentation and management2016 | First Faculty of Medicine
- A solitary skeletal metastasis in the thumb of a silent bilateral clear cell renal cell carcinoma pT1a in a patient with a sporadic uro-oncological triplicity2017 | First Faculty of Medicine
- ImmunoChip Study Implicates Antigen Presentation to T Cells in Narcolepsy2013 | First Faculty of Medicine
- Population-based study of BRCA1/2 mutations: family history based criteria identify minority of mutation carriers.2010 | First Faculty of Medicine
- The phenotypes of bipolar disorder: relevance for genetic investigations2005 | Third Faculty of Medicine
- Genome-wide meta-analysis identifies five new susceptibility loci for pancreatic cancer2018 | Faculty of Medicine in Pilsen, Second Faculty of Medicine
- Comprehensive Molecular Characterization of Pheochromocytoma and Paraganglioma2017 | First Faculty of Medicine
- A systems biology approach uncovers cell-specific gene regulatory effects of genetic associations in multiple sclerosis2019 | First Faculty of Medicine
- Genetics of autoimmune diabetes mellitus2008 | Third Faculty of Medicine
- BRCA1 and BRCA2 5 ' noncoding region variants identified in breast cancer patients alter promoter activity and protein binding2018 | First Faculty of Medicine
- HIF Signaling Pathway in Pheochromocytoma and Other Neuroendocrine Tumors2014 | First Faculty of Medicine
- Identification and Functional Testing of ERCC2 Mutations in a Multi-national Cohort of Patients with Familial Breast- and Ovarian Cancer2016 | First Faculty of Medicine
- A rare CACNA1H variant associated with amyotrophic lateral sclerosis causes complete loss of Ca(v)3.2 T-type channel activity2020 | Central Library of Charles University
- Hereditary truncating mutations of DNA repair and other genes in BRCA1/BRCA2/PALB2-negatively tested breast cancer patients2016 | First Faculty of Medicine