- Identification, by homozygosity mapping, of a novel locus for autosomal recessive congenital ichthyosis on chromosome 17p, and evidence for further genetic heterogeneity2001 | Ústřední knihovna
- PNPLA1 defects in patients with autosomal recessive congenital ichthyosis and KO mice sustain PNPLA1 irreplaceable function in epidermal omega-O-acylceramide synthesis and skin permeability barrier2017 | Farmaceutická fakulta v Hradci Králové
- Inherited ichthyoses: molecular causes of the disease in Czech patients2019 | Publikace bez příslušnosti k fakultě