@ARTICLE{
author={Kravljanac Ruzica M,Klaassen Kristel M,Oparnica Vladimir,Vucetic-Tadic Biljana,Andjelkovic Marina Z,Skakic Anita G,Stankovic Sara S,Stojiljkovic Maja M},
year={2026},
title={RHOBTB2-Associated Neurological Phenotypes and Underlying Mechanisms: Alternating Hemiplegia of Childhood Beyond ATP1A3},
journal={DISEASES},
volume={14},
number={5},
pages={-},
document_type={Review},
} 

@ARTICLE{
author={Miolski Jelena,Jesic Maja D,Skakic Anita G,Pavlovic Sonja T,Vorgucin Ivana,Bojic Vladislav,Kovacevic Smiljka,Blagojevic Jelena,Didic Nevena,Doknic Mirjana,Zdravkovic Vera M},
year={2026},
title={The importance of elevated basal 17-hydroxyprogesterone in the diagnosis of children with congenital adrenal hyperplasia},
journal={JOURNAL OF MEDICAL BIOCHEMISTRY},
volume={45},
number={3},
pages={566-571},
document_type={Article},
} 

@ARTICLE{
author={Djordjevic-Milosevic Maja,Skakic Anita G,Andjelkovic Marina Z,Delgado-Vega Angelica Maria,Thonberg Hakan,Klaassen Kristel M,Komazec Jovana,Kecman Bozica,Jocic Nikola,Bjorck Erik,Lindstrand Anna,Stojiljkovic Maja M},
year={2026},
title={First Reported Use of Recombinant Parathyroid Hormone in Kenny-Caffey Syndrome Type 2: A Case Report and Literature Review},
journal={DISEASES},
volume={14},
number={3},
pages={-},
document_type={Review},
} 

@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={Domazet Milan,Ugrin Milena M,Andjelkovic Marina Z,Klaassen Kristel M,Skakic Anita G,Komazec Jovana,Spasovski Vesna M,Todorovic Sasa,Stojiljkovic Maja M},
year={2025},
title={Applications of the new tool: VUS Notifier},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={33},
number={},
pages={888-888},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Jovicic-Pavlovic Svetlana M,Nikolic Jelena,Petrovic Kristina,Stojadinovic Milorad M,Skakic Anita G,Pavlovic Sonja T,Radovic Milan M},
year={2025},
title={Genetic testing for kidney disease-single centre experience},
journal={NEPHROLOGY DIALYSIS TRANSPLANTATION},
volume={40},
number={},
pages={-},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Djordjevic-Milosevic Maja,Skakic Anita G,Kecman Bozica,Stankovic Sara S,Kovacevic Ivona,Pavlovic Sonja T,Stojiljkovic Maja M},
year={2025},
title={Clinical and Genetic Profile of 35 Patients with Glycogen Storage Disease Type 1b: A Comparative Analysis Before and During SGLT2 Inhibitor Therapy},
journal={MOLECULAR DIAGNOSIS & THERAPY},
volume={},
number={},
pages={-},
document_type={Article; Early Access},
} 

@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={Andjelkovic Marina Z,Klaassen Kristel M,Skakic Anita G,Marjanovic Irena M,Kravljanac Ruzica M,Djordjevic Maja S,Vucetic-Tadic Biljana,Kecman Bozica,Pavlovic Sonja T,Stojiljkovic Maja M},
year={2024},
title={Characterization of 13 Novel Genetic Variants in Genes Associated with Epilepsy: Implications for Targeted Therapeutic Strategies},
journal={MOLECULAR DIAGNOSIS & THERAPY},
volume={},
number={},
pages={-},
document_type={Article; Early Access},
} 

@ARTICLE{
author={Novkovic Mirjana M,Banovic Djeri Bojana,Ristivojevic Bojan M,Knezevic Aleksandra M,Jankovic Marko,Tanasic Vanja,Radojicic Verica,Keckarevic Dusan P,Vidanovic Dejan S,Tesovic Bojana,Skakic Anita G,Tolinacki Maja S,Moric Ivana R,Djordjevic Valentina J},
year={2024},
title={Genome sequence diversity of SARS-CoV-2 in Serbia: insights gained from a 3-year pandemic study},
journal={FRONTIERS IN MICROBIOLOGY},
volume={15},
number={},
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,Vreca Misa,Andjelkovic Marina Z,Stojiljkovic Maja M,Skakic Anita G,Klaassen Kristel M,Zekovic Ana,Damjanov Nemanja S,Pavlovic Sonja T},
year={2023},
title={Differential expression of TLR7 and miRNA-146a genes in peripheral blood and skin samples of patients with systemic sclerosis},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={31},
number={},
pages={132-132},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Andjelkovic Marina Z,Skakic Anita G,Ugrin Milena M,Spasovski Vesna M,Klaassen Kristel M,Pavlovic Sonja T,Stojiljkovic Maja M},
year={2022},
title={Crosstalk between Glycogen-Selective Autophagy, Autophagy and Apoptosis as a Road towards Modifier Gene Discovery and New Therapeutic Strategies for Glycogen Storage Diseases},
journal={LIFE-BASEL},
volume={12},
number={9},
pages={-},
document_type={Review},
} 

@ARTICLE{
author={Celic Dejan,Pavlovic Sonja T,Skakic Anita G,Vucenovic Jelica,Pilipovic Dragana,Golubovic Sonja B,Stojsic Tatjana,Milicevic Olivera,Vojinovic Goran,Dudic Svetlana,Petrovic Lada V,Mitic Igor M},
year={2022},
title={High risk population screening for Fabry disease in hemodialysis patients in Vojvodina - pilot study},
journal={SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO},
volume={150},
number={5-6},
pages={281-287},
document_type={Article},
} 

@ARTICLE{
author={Klaassen Kristel M,Djordjevic Maja S,Skakic Anita G,Kecman Bozica,Drmanac Radoje,Pavlovic Sonja T,Stojiljkovic Maja M},
year={2021},
title={Untreated PKU patients without intellectual disability: SHANK gene family as a candidate modifier},
journal={MOLECULAR GENETICS AND METABOLISM REPORTS},
volume={29},
number={},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Ilic Andjelija Z,Bukvic Branko M,Stojiljkovic Maja M,Skakic Anita G,Pavlovic Sonja T,Jovanovic Sinisa P,Ilic Milan M},
year={2021},
title={Planar printed electrodes for electroporation with high EM field homogeneity},
journal={JOURNAL OF PHYSICS D-APPLIED PHYSICS},
volume={54},
number={50},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Stevanovic Nina,Skakic Anita G,Minic Predrag B,Sovtic Aleksandar D,Stojiljkovic Maja M,Pavlovic Sonja T,Andjelkovic Marina Z},
year={2021},
title={Identification and Classification of Novel Genetic Variants: En Route to the Diagnosis of Primary Ciliary Dyskinesia},
journal={INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES},
volume={22},
number={16},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Kotur Nikola M,Skakic Anita G,Klaassen Kristel M,Gasic Vladimir V,Zukic Branka,Skodric-Trifunovic Vesna D,Stjepanovic Mihailo I,Zivkovic Zorica M,Ostojic Olivera,Stevanovic Goran D,Lavadinovic Lidija S,Pavlovic Sonja T,Stankovic Biljana B},
year={2021},
title={Association of Vitamin D, Zinc and Selenium Related Genetic Variants With COVID-19 Disease Severity},
journal={FRONTIERS IN NUTRITION},
volume={8},
number={},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Djuric Olivera S,Andjelkovic Marina Z,Vreca Misa,Skakic Anita G,Pavlovic Sonja T,Novakovic Ivana V,Jovanovic Bojan Z,Skodric-Trifunovic Vesna D,Markovic-Denic Ljiljana N},
year={2021},
title={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},
journal={INJURY-INTERNATIONAL JOURNAL OF THE CARE OF THE INJURED},
volume={52},
number={3},
pages={419-425},
document_type={Article},
} 

@ARTICLE{
author={Anastasovska Violeta,Kocova Mirjana,Zdraveska Nikolina,Stojiljkovic Maja M,Skakic Anita G,Klaassen Kristel M,Pavlovic Sonja T},
year={2021},
title={A novel 9 bp deletion (c.1271_1279delGTGCCCGCG) in exon 10 of CYP21A2 gene causing severe congenital adrenal hyperplasia},
journal={ENDOCRINE},
volume={73},
number={1},
pages={196-202},
document_type={Article},
} 

@ARTICLE{
author={Sarajlija Adrijan,Djordjevic Maja S,Kecman Bozica,Skakic Anita G,Pavlovic Sonja T,Pasic Srdjan S,Stojiljkovic Maja M},
year={2020},
title={Impact of genotype on neutropenia in a large cohort of Serbian patients with glycogen storage disease type Ib},
journal={EUROPEAN JOURNAL OF MEDICAL GENETICS},
volume={63},
number={3},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Andjelkovic Marina Z,Minic Predrag B,Vreca Misa,Stojiljkovic Maja M,Skakic Anita G,Sovtic Aleksandar D,Rodic Milan,Skodric-Trifunovic Vesna D,Maric Nina,Visekruna Jelena,Spasovski Vesna M,Pavlovic Sonja T},
year={2019},
title={The importance of comprehensive genomic profiling in differential diagnosis and discovery of novel disease causing genetic variants in patients with pediatric lung diseases},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={27},
number={},
pages={89-90},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Skakic Anita G,Andjelkovic Marina Z,Tosic Natasa M,Klaassen Kristel M,Djordjevic Maja S,Pavlovic Sonja T,Stojiljkovic Maja M},
year={2019},
title={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 disease type Ib},
journal={GENE},
volume={703},
number={},
pages={17-25},
document_type={Article},
} 

@ARTICLE{
author={Andjelkovic Marina Z,Minic Predrag B,Vreca Misa,Stojiljkovic Maja M,Skakic Anita G,Sovtic Aleksandar D,Rodic Milan,Skodric-Trifunovic Vesna D,Maric Nina,Visekruna Jelena,Spasovski Vesna M,Pavlovic Sonja T},
year={2018},
title={Genomic profiling supports the diagnosis of primary ciliary dyskinesia and reveals novel candidate genes and genetic variants},
journal={PLOS ONE},
volume={13},
number={10},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Klaassen Kristel M,Djordjevic Maja S,Skakic Anita G,Desviat Lourdes R,Pavlovic Sonja T,Perez Belen,Stojiljkovic Maja M},
year={2018},
title={Functional Characterization of Novel Phenylalanine Hydroxylase p.Gln226Lys Mutation Revealed Its Non-responsiveness to Tetrahydrobiopterin Treatment in Hepatoma Cellular Model},
journal={BIOCHEMICAL GENETICS},
volume={56},
number={5},
pages={533-541},
document_type={Article},
} 

@ARTICLE{
author={Skakic Anita G,Djordjevic Maja S,Sarajlija Adrijan,Klaassen Kristel M,Tosic Natasa M,Kecman Bozica,Ugrin Milena M,Spasovski Vesna M,Pavlovic Sonja T,Stojiljkovic Maja M},
year={2018},
title={Genetic characterization of GSD I in Serbian population revealed unexpectedly high incidence of GSD Ib and 3 novel SLC37A4 variants},
journal={CLINICAL GENETICS},
volume={93},
number={2},
pages={350-355},
document_type={Article},
} 

@ARTICLE{
author={Ugrin Milena M,Milacic Iva,Skakic Anita G,Klaassen Kristel M,Komazec Jovana,Pavlovic Sonja T,Stojiljkovic Maja M},
year={2017},
title={Molecular Genetic Strategy for Diagnosis of Congenital Adrenal Hyperplasia in Serbia},
journal={GENETIKA-BELGRADE},
volume={49},
number={2},
pages={457-467},
document_type={Article},
} 

@ARTICLE{
author={Skodric-Trifunovic Vesna D,Buha Ivana B,Jovanovic Dragana D,Vucinic Violeta V,Stjepanovic Mihailo I,Spasovski Vesna M,Andjelkovic Marina Z,Vreca Misa,Skakic Anita G,Gasic Vladimir V,Pavlovic Sonja T},
year={2015},
title={Variants in VDR and NRAMP1 Genes as Susceptibility Factors for Tuberculosis in the Population of Serbia},
journal={GENETIKA-BELGRADE},
volume={47},
number={3},
pages={1021-1028},
document_type={Article},
} 

@ARTICLE{
author={Milacic Iva,Barac Marija,Milenkovic Tatjana,Ugrin Milena M,Klaassen Kristel M,Skakic Anita G,Jesic Maja D,Joksic Ivana D,Mitrovic Katarina,Todorovic Sladjana,Vujovic Svetlana Z,Pavlovic Sonja T,Stojiljkovic Maja M},
year={2015},
title={Molecular genetic study of congenital adrenal hyperplasia in Serbia: novel p.Leu129Pro and p.Ser165Pro CYP21A2 gene mutations},
journal={JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION},
volume={38},
number={11},
pages={1199-1210},
document_type={Article},
}