Projekty

2018-2022: APVV 17-0296 HYPOMITGEN – GENETIC CAUSES OF RARE DISEASES WITH EMPHASIS ON METABOLIC DISORDERS ASSOCIATED WITH HYPOGLYCEMIA AND MITOCHONDIOPATHIES (Gašperíková)
2021-2025: APVV 20/0239 SYNDEAF – IDENTIFICATION OF NOVEL GENETIC VARIANTS IN SYNDROMIC HEARING LOSS BY WHOLE EXOME SEQUENCING (Gašperíková)
2019-2022 MZ SR 2019/2020 – LFUK-8 – COMPREHENSIVE INNOVATIVE DIAGNOSTICS AND PERSONALIZED TREATMENT OF DIABETES MELLITUS IN CHILDREN (Gašperíková)
2021-2024: VEGA 2/0131/21 GENETICS OF RARE FORMS OF DIABETES WITH FOCUS ON FUNCTIONAL CHARACTERIZATION OF NEW VARIANTS (Škopková)
2021-2024: VEGA 1/0572/21 IDENTIFICATION OF ETIOLOGY IN SPORADIC FORMS OF HEREDITARY HEARING LOSS BY WHOLE EXOME SEQUENCING (Gašperíková)
2022-2025: VEGA 1/0659/22 RESEARCH ON CLINICAL AND GENETIC ASPECTS OF KETOTIC HYPOGLYCAEMIA IN CHILDREN (Gašperíková)
2020-2023 ŠF EÚ BIOFORD – GENETICS OF RARE FORMS OF DIABETES WITH FOCUS ON FUNCTIONAL CHARACTERIZATION OF NEW VARIANTS (Gašperíková)