@ARTICLE{
author={Bergant Gaber,...,Brankovic Marija,Jankovic Milena Z,Svetel Marina V,...,Dragasevic-Miskovic Natasa T,Petrovic Igor N,...,Novakovic Ivana V,...,(broj koautora 19)},
year={2026},
title={Enrichment of Rare Variants in Nuclear-Encoded Mitochondrial Metabolism Genes in Patients with Early-Onset or Familial Parkinson's Disease},
journal={GENES},
volume={17},
number={4},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Brankovic Marija,Stefanova Elka D,Mandic Gorana B,Marjanovic Ana,Dobricic Valerija S,Maver Ales,Bergant Gaber,Stevic Zorica D,Jankovic Milena Z,Novakovic Ivana V,Peterlin Borut,Kostic Vladimir K},
year={2022},
title={Analysis of "Clinical Exome" Panel in Serbian Patients with Cognitive Disorders},
journal={GENETIKA-BELGRADE},
volume={54},
number={3},
pages={1351-1364},
document_type={Article},
} 

@ARTICLE{
author={Brankovic Marija,Dragasevic Natasa T,Dobricic Valerija S,Maver Ales,Bergant Gaber,Petrovic Igor N,Peric Stojan Z,Marjanovic Ana,Jankovic Milena Z,Jancic Jasna B,Novakovic Ivana V,Peterlin Borut,Svetel Marina V,Kostic Vladimir K},
year={2022},
title={Clinical Exome Sequencing in Serbian Patients with Movement Disorders - Single Centre Experience},
journal={GENETIKA-BELGRADE},
volume={54},
number={1},
pages={395-409},
document_type={Article},
} 

@ARTICLE{
author={Maver Ales,Kovanda Anja,Bergant Gaber,Teran Natasa,Vrecar Irena,Brankovic Marija,Jankovic Milena Z,Svetel Marina V,Kostic Vladimir S,Novakovic Ivana V,Racki Valentino,Vuletic Vladimira,Peterlin Borut},
year={2022},
title={Diagnostic yield of whole exome sequencing in early-onset and familial Parkinson's disease in the Balkans},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={30},
number={SUPPL 1},
pages={292-292},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Bergant Gaber,Maver Ales,Lovrecic Luca,Cuturilo Goran,Hodzic Alenka,Peterlin Borut},
year={2018},
title={Comprehensive use of extended exome analysis improves diagnostic yield in rare disease: a retrospective survey in 1,059 cases},
journal={GENETICS IN MEDICINE},
volume={20},
number={3},
pages={303-312},
document_type={Article},
} 

