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Comparison of the ABC and ACMG systems for variant classification.
Houge G, Bratland E, Aukrust I, Tveten K, Žukauskaitė G, Sansovic I, Brea-Fernández AJ, Mayer K, Paakkola T, McKenna C, Wright W, Markovic MK, Lildballe DL, Konecny M, Smol T, Alhopuro P, Gouttenoire EA, Obeid K, Todorova A, Jankovic M, Lubieniecka JM, Stojiljkovic M, Buisine MP, Haukanes BI, Lorans M, Roomere H, Petit FM, Haanpää MK, Beneteau C, Pérez B, Plaseska-Karanfilska D, Rath M, Fuhrmann N, Ferreira BI, Stephanou C, Sjursen W, Maver A, Rouzier C, Chirita-Emandi A, Gonçalves J, Kuek WCD, Broly M, Haer-Wigman L, Thong MK, Tae SK, Hyblova M, den Dunnen JT, Laner A. Houge G, et al. Among authors: jankovic m. Eur J Hum Genet. 2024 Jul;32(7):858-863. doi: 10.1038/s41431-024-01617-8. Epub 2024 May 22. Eur J Hum Genet. 2024. PMID: 38778080 Free PMC article.
Secondary findings in 443 exome sequencing data.
Branković M, Han H, Janković M, Marjanović A, Andrejic N, Gunjić I, Virić V, Palibrk A, Lee H, Peric S. Branković M, et al. Among authors: jankovic m. Ann Hum Genet. 2024 Nov 15. doi: 10.1111/ahg.12586. Online ahead of print. Ann Hum Genet. 2024. PMID: 39545406
A multicenter study of genetic testing for Parkinson's disease in the clinical setting.
Kovanda A, Rački V, Bergant G, Georgiev D, Flisar D, Papić E, Brankovic M, Jankovic M, Svetel M, Teran N, Maver A, Kostic VS, Novakovic I, Pirtošek Z, Rakuša M, Vuletić V, Peterlin B. Kovanda A, et al. Among authors: jankovic m. NPJ Parkinsons Dis. 2022 Nov 4;8(1):149. doi: 10.1038/s41531-022-00408-6. NPJ Parkinsons Dis. 2022. PMID: 36333361 Free PMC article.
Reply to: "Differences in Sex-Specific Frequency of Glucocerebrosidase Variant Carriers and Familial Parkinsonism".
Kresojević N, Marković V, Dobričić V, Stanković I, Stojković T, Tomić A, Lukić MJ, Janković M, Marjanović A, Branković M, Novaković I, Petrović I, Dragašević N, Svetel M, Kostić V. Kresojević N, et al. Among authors: jankovic m. Mov Disord. 2023 Apr;38(4):712-713. doi: 10.1002/mds.29351. Mov Disord. 2023. PMID: 37061878 No abstract available.
Clinical and Genetic Features of Huntington's Disease Patients From Republic of Serbia: A Single-Center Experience.
Kresojević N, Perović I, Stanković I, Tomić A, Lukic MJ, Marković V, Stojković T, Mandić G, Janković M, Marjanović A, Branković M, Novaković I, Petrović I, Dragašević N, Stefanova E, Svetel M, Kostić V. Kresojević N, et al. Among authors: jankovic m. J Mov Disord. 2023 Sep;16(3):333-335. doi: 10.14802/jmd.23028. Epub 2023 Jun 9. J Mov Disord. 2023. PMID: 37749975 Free PMC article. No abstract available.
Novel GATOR1 variants in focal epilepsy.
Kovačević M, Janković M, Branković M, Milićević O, Novaković I, Sokić D, Ristić A, Shamsani J, Vojvodić N. Kovačević M, et al. Among authors: jankovic m. Epilepsy Behav. 2023 Apr;141:109139. doi: 10.1016/j.yebeh.2023.109139. Epub 2023 Feb 26. Epilepsy Behav. 2023. PMID: 36848747
Novel variants in established epilepsy genes in focal epilepsy.
Kovačević M, Milićević O, Branković M, Janković M, Novaković I, Sokić D, Ristić A, Shamsani J, Vojvodić N. Kovačević M, et al. Among authors: jankovic m. Seizure. 2023 Aug;110:146-152. doi: 10.1016/j.seizure.2023.06.005. Epub 2023 Jun 7. Seizure. 2023. PMID: 37390664 Free article.
493 results