- Intronic microduplications of RBFOX1 gene and their phenotypic consequencesPublication without faculty affiliation
- Microdeletion Syndromes2006 | Publication without faculty affiliation
- Microdeletion Syndromes2006 | First Faculty of Medicine, Faculty of Physical Education and Sport
- Microdeletion Syndromes2006 | Second Faculty of Medicine
- Application of SNP array method in pranatal diagnosis2011 | First Faculty of Medicine
- New advancements in biological psychiatry2012 | First Faculty of Medicine, Faculty of Medicine in Hradec Králové
- Endophenotypes In Genetic Studies Of Schizophrenia2012 | Faculty of Medicine in Hradec Králové
- A unique coincidence of a 17q12 deletion and duplication in a Czech family led to a refined genotype–phenotype correlation2023 | Second Faculty of Medicine
- Role of cryptic rearrangements of human chromosomes in the aetiology of schizophrenia2023 | Faculty of Science
- Genetics of schizophrenia: A consensus paper of the WFSBP Task Force on Genetics2017 | Faculty of Medicine in Hradec Králové
- Both 17q12 duplication and deletion detected in the patient with normal phenotype and their segregation in family with variably affected members2020 | Second Faculty of Medicine
- Overgrowth in children and in adults: novel clinical view, novel genes, novel phenotypes2017 | Second Faculty of Medicine
- Clinically relevant copy-number variants in exome sequencing data of patients with dystonia2021 | First Faculty of Medicine