@ARTICLE{
author={Volk Marija,Maver Ales,Vidmar Martina Jarc,Trost Nusa,Visnjar Tanja,Fakin Ana,Kovac Lea,Habjan Maja Sustar,Malinar Lucija,Petrovic Pajic Sanja MI,Jerman Urska Dragin,Romih Rok,Hawlina Marko,Peterlin Borut},
year={2026},
title={Discovery of PHB1 as a Novel Candidate Gene in Dominant Optic Atrophy},
journal={CLINICAL GENETICS},
volume={},
number={},
pages={-},
document_type={Article; Early Access},
} 

@ARTICLE{
author={Volk Marija,Trost Nusa,Visnjar Tanja,Maver Ales,Vidmar Martina Jarc,Fakin Ana,Petrovic-Pajic Sanja,Hawlina Marko,Peterlin Borut},
year={2025},
title={Discovery of PHB1 as a novel candidate gene in dominant optic atrophy},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={33},
number={},
pages={93-93},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Vodnjov Nina,Toplisek Janez,Maver Ales,Cuturilo Goran,Jaklic Helena,Teran Natasa,Visnjar Tanja,Skrjanec-Pusenjak Marusa,Hodzic Alenka,Miljanovic Olivera,Peterlin Borut,Writzl Karin},
year={2024},
title={A novel splice-site FHOD3 founder variant is a common cause of hypertrophic cardiomyopathy in the population of the Balkans - a cohort study},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={32},
number={},
pages={1390-1390},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Vodnjov Nina,Toplisek Janez,Maver Ales,Cuturilo Goran,Jaklic Helena,Teran Natasa,Visnjar Tanja,Pusenjak Marusa Skrjanec,Hodzic Alenka,Miljanovic Olivera,Peterlin Borut,Writzl Karin},
year={2024},
title={A novel splice-site FHOD3 founder variant is a common cause of hypertrophic cardiomyopathy in the population of the Balkans - a cohort study},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={32},
number={},
pages={1390-1390},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Vodnjov Nina,Toplisek Janez,Maver Ales,Cuturilo Goran,Jaklic Helena,Teran Natasa,Visnjar Tanja,Skrjanec Pusenjak Marusa,Hodzic Alenka,Miljanovic Olivera,Peterlin Borut,Writzl Karin,Mahdieh Nejat},
year={2023},
title={A novel splice-site <i>FHOD3</i> founder variant is a common cause of hypertrophic cardiomyopathy in the population of the Balkans-A cohort study},
journal={PLOS ONE},
volume={18},
number={12},
pages={-},
document_type={Article},
} 

