| Genomic profiling supports the diagnosis of primary ciliary dyskinesia and reveals novel candidate genes and genetic variants M Andjelkovic, P Minic, M Vreca, M Stojiljkovic, A Skakic, A Sovtic, ... PloS one 13 (10), e0205422, 2018 | 36 | 2018 |
| Association of vitamin D, zinc and selenium related genetic variants with COVID-19 disease severity N Kotur, A Skakic, K Klaassen, V Gasic, B Zukic, V Skodric-Trifunovic, ... Frontiers in Nutrition 8, 689419, 2021 | 33 | 2021 |
| Molecular genetic study of congenital adrenal hyperplasia in Serbia: novel p.Leu129Pro and p.Ser165Pro CYP21A2 gene mutations I Milacic, M Barac, T Milenkovic, M Ugrin, K Klaassen, A Skakic, M Jesic, ... Journal of Endocrinological Investigation 38, 1199-1210, 2015 | 23 | 2015 |
| Genetic characterization of GSD I in Serbian population revealed unexpectedly high incidence of GSD Ib and 3 novel SLC37A4 variants A Skakic, M Djordjevic, A Sarajlija, K Klaassen, N Tosic, B Kecman, ... Clinical genetics 93 (2), 350-355, 2018 | 22 | 2018 |
| Impact of genotype on neutropenia in a large cohort of Serbian patients with glycogen storage disease type Ib A Sarajlija, M Djordjevic, B Kecman, A Skakic, S Pavlovic, S Pasic, ... European Journal of Medical Genetics 63 (3), 103767, 2020 | 13 | 2020 |
| Untreated PKU patients without intellectual disability: SHANK gene family as a candidate modifier K Klaassen, M Djordjevic, A Skakic, B Kecman, R Drmanac, S Pavlovic, ... Molecular Genetics and Metabolism Reports 29, 100822, 2021 | 9 | 2021 |
| Variants in VDR and NRAMP1 Genes as Susceptibility Factors for Tuberculosis in the Population of Serbia PST Skodric-Trifunovic Vesna D, Buha Ivana B, Jovanovic Dragana D, Vucinic ... Genetika 47 (3), 1021-1028, 2015 | 8* | 2015 |
| Genetic variants in TNFA, LTA, TLR2 and TLR4 genes and risk of sepsis in patients with severe trauma: nested case-control study in a level-1 trauma centre in SERBIA O Djuric, M Andjelkovic, M Vreca, A Skakic, S Pavlovic, I Novakovic, ... Injury, 2020 | 7 | 2020 |
| CRISPR/Cas9 genome editing of SLC37A4 gene elucidates the role of molecular markers of endoplasmic reticulum stress and apoptosis in renal involvement in glycogen storage … A Skakic, M Andjelkovic, N Tosic, K Klaassen, M Djordjevic, S Pavlovic, ... Gene 703, 17-25, 2019 | 7 | 2019 |
| Identification and classification of novel genetic variants: en route to the diagnosis of primary ciliary dyskinesia N Stevanovic, A Skakic, P Minic, A Sovtic, M Stojiljkovic, S Pavlovic, ... International journal of molecular sciences 22 (16), 8821, 2021 | 5 | 2021 |
| Functional characterization of novel phenylalanine hydroxylase p. Gln226Lys mutation revealed Its non-responsiveness to tetrahydrobiopterin treatment in hepatoma cellular model K Klaassen, M Djordjevic, A Skakic, LR Desviat, S Pavlovic, B Perez, ... Biochemical genetics 56, 533-541, 2018 | 3 | 2018 |
| Molecular genetic strategy for diagnosis of congenital adrenal hyperplasia in Serbia M Ugrin, I Milacić, A Skakić, T Karan-Đurašević, J Komazec, S Pavlović, ... Genetika-Belgrade 49 (2), 457-467, 2017 | 3 | 2017 |
| Crosstalk between Glycogen-Selective Autophagy, Autophagy and Apoptosis as a Road towards Modifier Gene Discovery and New Therapeutic Strategies for Glycogen Storage Diseases M Andjelkovic, A Skakic, M Ugrin, V Spasovski, K Klaassen, S Pavlovic, ... Life 12 (9), 1396, 2022 | 1 | 2022 |
| Genome sequence diversity of SARS-CoV-2 in Serbia: insights gained from a 3-year pandemic study M Novkovic, B Banovic Djeri, B Ristivojevic, A Knezevic, M Jankovic, ... Frontiers in Microbiology 15, 1332276, 2024 | | 2024 |
| PHENYLBUTYRIC ACID REDUCES MOLECULAR MARKERS OF ER STRESS-INDUCED APOPTOSIS IN GLYCOGEN STORAGE DISEASE TYPE IB IN VITRO MODEL SYSTEM M Parezanović, N Stevanović, M Anđelković, M Ugrin, S Pavlović, ... International Journal of Medical Genetics 26 (Supplement), 54-54, 2023 | | 2023 |
| Unique pipeline for the assessment of novel genetic variants leads to confirmation of PCD diagnosis N Stevanović, M Anđelković, A Skakić, V Spasovski, M Stojiljković, ... European Journal of Human Genetic 31 (Supplement S1), 383-383, 2023 | | 2023 |
| Molecular diagnosis of Fabry disease in patients with chronic renal failure of unknown etiology M Parezanović, M Stojiljković, M Anđelković, N Stevanović, V Spasovski, ... European Journal of Human Genetic 31 (Supplement S1), 432-433, 2023 | | 2023 |
| THE IMPACT OF NEXT-GENERATION SEQUENCING ON DIAGNOSIS AND TREATMENT OF RARE DISEASES M Stojiljković, M Ugrin, K Klaassen, A Skakić, M Anđelković, J Komazec, ... International Journal of Medical Genetics 26 (Supplement), 38-38, 2023 | | 2023 |
| CHARACTERIZATION OF 16 NOVEL GENETIC VARIANTS IN GENES RELATED TO CHILDHOOD EPILEPSIES M Anđelković, K Klaassen, A Skakić, I Marjanović, R Kravljana, ... International Journal of Medical Genetics 26 (Supplement), 114-114, 2023 | | 2023 |
| Application of CRISPR/cas9 technology for in vitro disease modelling in glycogen storage disease type IB M Parezanović, M Anđelković, N Stevanović, K Klaassen, V Spasovski, ... CoMBoS2–the Second Congress of Molecular Biologists of Serbia, Abstract Book …, 2023 | | 2023 |
Sonja PavlovicInstitute of Molecular Genetics and Genetic Engineering University of BelgradeVerified email at sezampro.rs
