Kravljanac Ruzica M,Klaassen Kristel M,Oparnica Vladimir,Vucetic-Tadic Biljana,Andjelkovic Marina Z,Skakic Anita G,Stankovic Sara S,Stojiljkovic Maja M (2026) RHOBTB2-Associated Neurological Phenotypes and Underlying Mechanisms: Alternating Hemiplegia of Childhood Beyond ATP1A3, DISEASES, vol. 14, br. 5, str. - (Review) 

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 (2026) The importance of elevated basal 17-hydroxyprogesterone in the diagnosis of children with congenital adrenal hyperplasia, JOURNAL OF MEDICAL BIOCHEMISTRY, vol. 45, br. 3, str. 566-571 (Article) 

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 (2026) First Reported Use of Recombinant Parathyroid Hormone in Kenny-Caffey Syndrome Type 2: A Case Report and Literature Review, DISEASES, vol. 14, br. 3, str. - (Review) 

Djordjevic-Milosevic Maja,Skakic Anita G,Kecman Bozica,Stankovic Sara S,Kovacevic Ivona,Pavlovic Sonja T,Stojiljkovic Maja M (2025) Clinical and Genetic Profile of 35 Patients with Glycogen Storage Disease Type 1b: A Comparative Analysis Before and During SGLT2 Inhibitor Therapy, MOLECULAR DIAGNOSIS & THERAPY, vol. , br. , str. - (Article; Early Access) 

Parezanovic Marina V,Stevanovic Nina,Andjelkovic Marina Z,Ugrin Milena M,Pavlovic Sonja T,Stojiljkovic Maja M,Skakic Anita G (2025) Phenylbutyric Acid Modulates Apoptosis and ER Stress-Related Gene Expression in Glycogen Storage Disease Type Ib In Vitro Model, MOLECULAR GENETICS & GENOMIC MEDICINE, vol. 13, br. 1, str. - (Article) 

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 (2024) Characterization of 13 Novel Genetic Variants in Genes Associated with Epilepsy: Implications for Targeted Therapeutic Strategies, MOLECULAR DIAGNOSIS & THERAPY, vol. , br. , str. - (Article; Early Access) 

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 (2024) Genome sequence diversity of SARS-CoV-2 in Serbia: insights gained from a 3-year pandemic study, FRONTIERS IN MICROBIOLOGY, vol. 15, br. , str. - (Article) 

Andjelkovic Marina Z,Skakic Anita G,Ugrin Milena M,Spasovski Vesna M,Klaassen Kristel M,Pavlovic Sonja T,Stojiljkovic Maja M (2022) Crosstalk between Glycogen-Selective Autophagy, Autophagy and Apoptosis as a Road towards Modifier Gene Discovery and New Therapeutic Strategies for Glycogen Storage Diseases, LIFE-BASEL, vol. 12, br. 9, str. - (Review) 

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 (2022) High risk population screening for Fabry disease in hemodialysis patients in Vojvodina - pilot study, SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO, vol. 150, br. 5-6, str. 281-287 (Article) 

Klaassen Kristel M,Djordjevic Maja S,Skakic Anita G,Kecman Bozica,Drmanac Radoje,Pavlovic Sonja T,Stojiljkovic Maja M (2021) Untreated PKU patients without intellectual disability: SHANK gene family as a candidate modifier, MOLECULAR GENETICS AND METABOLISM REPORTS, vol. 29, br. , str. - (Article) 

Ilic Andjelija Z,Bukvic Branko M,Stojiljkovic Maja M,Skakic Anita G,Pavlovic Sonja T,Jovanovic Sinisa P,Ilic Milan M (2021) Planar printed electrodes for electroporation with high EM field homogeneity, JOURNAL OF PHYSICS D-APPLIED PHYSICS, vol. 54, br. 50, str. - (Article) 

Stevanovic Nina,Skakic Anita G,Minic Predrag B,Sovtic Aleksandar D,Stojiljkovic Maja M,Pavlovic Sonja T,Andjelkovic Marina Z (2021) Identification and Classification of Novel Genetic Variants: En Route to the Diagnosis of Primary Ciliary Dyskinesia, INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, vol. 22, br. 16, str. - (Article) 

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 (2021) Association of Vitamin D, Zinc and Selenium Related Genetic Variants With COVID-19 Disease Severity, FRONTIERS IN NUTRITION, vol. 8, br. , str. - (Article) 

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 (2021) 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, INJURY-INTERNATIONAL JOURNAL OF THE CARE OF THE INJURED, vol. 52, br. 3, str. 419-425 (Article) 

Anastasovska Violeta,Kocova Mirjana,Zdraveska Nikolina,Stojiljkovic Maja M,Skakic Anita G,Klaassen Kristel M,Pavlovic Sonja T (2021) A novel 9 bp deletion (c.1271_1279delGTGCCCGCG) in exon 10 of CYP21A2 gene causing severe congenital adrenal hyperplasia, ENDOCRINE, vol. 73, br. 1, str. 196-202 (Article) 

Sarajlija Adrijan,Djordjevic Maja S,Kecman Bozica,Skakic Anita G,Pavlovic Sonja T,Pasic Srdjan S,Stojiljkovic Maja M (2020) Impact of genotype on neutropenia in a large cohort of Serbian patients with glycogen storage disease type Ib, EUROPEAN JOURNAL OF MEDICAL GENETICS, vol. 63, br. 3, str. - (Article) 

Skakic Anita G,Andjelkovic Marina Z,Tosic Natasa M,Klaassen Kristel M,Djordjevic Maja S,Pavlovic Sonja T,Stojiljkovic Maja M (2019) 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, GENE, vol. 703, br. , str. 17-25 (Article) 

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 (2018) Genomic profiling supports the diagnosis of primary ciliary dyskinesia and reveals novel candidate genes and genetic variants, PLOS ONE, vol. 13, br. 10, str. - (Article) 

Klaassen Kristel M,Djordjevic Maja S,Skakic Anita G,Desviat Lourdes R,Pavlovic Sonja T,Perez Belen,Stojiljkovic Maja M (2018) Functional Characterization of Novel Phenylalanine Hydroxylase p.Gln226Lys Mutation Revealed Its Non-responsiveness to Tetrahydrobiopterin Treatment in Hepatoma Cellular Model, BIOCHEMICAL GENETICS, vol. 56, br. 5, str. 533-541 (Article) 

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 (2018) Genetic characterization of GSD I in Serbian population revealed unexpectedly high incidence of GSD Ib and 3 novel SLC37A4 variants, CLINICAL GENETICS, vol. 93, br. 2, str. 350-355 (Article) 

Ugrin Milena M,Milacic Iva,Skakic Anita G,Klaassen Kristel M,Komazec Jovana,Pavlovic Sonja T,Stojiljkovic Maja M (2017) Molecular Genetic Strategy for Diagnosis of Congenital Adrenal Hyperplasia in Serbia, GENETIKA-BELGRADE, vol. 49, br. 2, str. 457-467 (Article) 

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 (2015) Variants in VDR and NRAMP1 Genes as Susceptibility Factors for Tuberculosis in the Population of Serbia, GENETIKA-BELGRADE, vol. 47, br. 3, str. 1021-1028 (Article) 

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 (2015) Molecular genetic study of congenital adrenal hyperplasia in Serbia: novel p.Leu129Pro and p.Ser165Pro CYP21A2 gene mutations, JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION, vol. 38, br. 11, str. 1199-1210 (Article)