Publications
- Genetic and biochemical study of dual hereditary jaundice: Dubin-Johnson and Gilbert's syndromes. Haplotyping and founder effect of deletion in ABCC22016 | First Faculty of Medicine
- Homozygous Dubin-Johnson Syndrome. A Novel Mutation in MRP2 Gene in a Large Family from SlovakiaPublication without faculty affiliation
- Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies2021 | First Faculty of Medicine
- Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa2019 | First Faculty of Medicine, Central Library of Charles University
- A Novel Mutation in the FECH Gene in a Czech Family with Erythropoietic Protoporphyria and a Population Study of IVS3-48C Variant Contributing to the Disease2015 | First Faculty of Medicine
- A genome-wide association study of anorexia nervosa2014 | First Faculty of Medicine
- Stress Perception and (GT)n Repeat Polymorphism in Haem Oxygenase 1 Promoter Are Both Risk Factors in Development of Eating Disorders2013 | First Faculty of Medicine, Faculty of Education
- Anorexia nervosa - genetic determinants and influence of environment (Polymorphism of serotonin receptor and transporter )2009 | First Faculty of Medicine
- Polymorphisms in Serotonin-Related Genes in Anorexia Nervosa. The First Study in Czech Population and Meta-analyses with Previously Performed Studies2009 | First Faculty of Medicine
- Genetic determinants of anorexia nervosa and polymorfism of gen HSP702009 | First Faculty of Medicine
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