@ARTICLE{
author={Ugrin Milena M,Komazec Jovana,Klaassen Kristel M,Skakic Anita G,Andjelkovic Marina Z,Spasovski Vesna M,Stevanovic Nina,Parezanovic Marina V,Stankovic Sara S,Jocic Nikola,Pavlovic Sonja T,Stojiljkovic Maja M},
year={2025},
title={Thalassemia syndromes in Serbia:the importance of genetic (re)analysis},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={33},
number={},
pages={393-393},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Stankovic Sara S,Lazic Andrijana,Parezanovic Marina V,Andjelkovic Marina Z,Ugrin Milena M,Stevanovic Milena J,Pavlovic Sonja T,Stojiljkovic Maja M,Klaassen Kristel M},
year={2025},
title={Unravelling phenylalanine-induced neuronal dysfunction: transcriptome analysis of NT2-derived neurons highlights neurite impairment and synaptic connectivity},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={33},
number={},
pages={715-715},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Parezanovic Marina V,Stevanovic Nina,Andjelkovic Marina Z,Ugrin Milena M,Pavlovic Sonja T,Stojiljkovic Maja M,Skakic Anita G},
year={2025},
title={Phenylbutyric Acid Modulates Apoptosis and ER Stress-Related Gene Expression in Glycogen Storage Disease Type Ib In Vitro Model},
journal={MOLECULAR GENETICS & GENOMIC MEDICINE},
volume={13},
number={1},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Stankovic Sara S,Lazic Andrijana,Parezanovic Marina V,Stevanovic Milena J,Pavlovic Sonja T,Stojiljkovic Maja M,Klaassen Kristel M},
year={2024},
title={Transcriptome Profiling of Phenylalanine-Treated Human Neuronal Model: Spotlight on Neurite Impairment and Synaptic Connectivity},
journal={INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES},
volume={25},
number={18},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Klaassen Kristel M,Djordjevic Maja S,Skakic Anita G,Kecman Bozica,Parezanovic Marina V,Andjelkovic Marina Z,Stevanovic Nina,Spasovski Vesna M,Ugrin Milena M,Drmanac Radoje,Pavlovic Sonja T,Stojiljkovic Maja M},
year={2023},
title={Untreated PKU patients without intellectual disability: SHANK gene family as a candidate modifier},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={31},
number={},
pages={433-433},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Parezanovic Marina V,Stojiljkovic Maja M,Andjelkovic Marina Z,Stevanovic Nina,Spasovski Vesna M,Ugrin Milena M,Komazec Jovana,Tosic Natasa M,Pavlovic Sonja T,Celic Dejan,Vucenovic Jelica,Skakic Anita G},
year={2023},
title={Molecular diagnosis of Fabry disease in patients with chronic renal failure of unknown etiology},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={31},
number={},
pages={432-433},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Stevanovic Nina,Andjelkovic Marina Z,Skakic Anita G,Spasovski Vesna M,Stojiljkovic Maja M,Parezanovic Marina V,Ugrin Milena M,Pavlovic Sonja T},
year={2023},
title={Unique pipeline for the assessment of novel genetic variants leads to confirmation of PCD diagnosis},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={31},
number={},
pages={383-383},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Spasovski Vesna M,Andjelkovic Marina Z,Parezanovic Marina V,Komazec Jovana,Ugrin Milena M,Klaassen Kristel M,Stojiljkovic Maja M},
year={2023},
title={The Role of Autophagy and Apoptosis in Affected Skin and Lungs in Patients with Systemic Sclerosis},
journal={INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES},
volume={24},
number={13},
pages={-},
document_type={Review},
}