@ARTICLE{
author={Mijovic Marija,Cuturilo Goran,Ruml-Stojanovic Jelena,Brankovic Marija,Miletic A,Bosankic Brankica,Dedovic Maja,Perovic D,Maksimovic N,Damnjanovic Tatjana M},
year={2025},
title={A Novel 4.2 kb deletion of the 3′UTR of RUNX2 Gene Causes Cleidocranial Dysplasia: Further Delineation of the Role of yhe 3′UTR},
journal={BALKAN JOURNAL OF MEDICAL GENETICS},
volume={28},
number={2},
pages={107-112},
document_type={Article},
} 

@ARTICLE{
author={Dusanovic-Pjevic Marija G,Sarenac Lena,Grk Milka B,Jekic Biljana B,Vojvodic Ljubica M,Damnjanovic Tatjana M,Rasic Milica,Perovic Dijana,Maksimovic Nela S},
year={2025},
title={Analysis of the association between MMP-9 gene polymorphisms and the occurrence of hemorrhagic transformations in acute ischemic stroke patients treated with thrombolysis},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={33},
number={},
pages={450-451},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Djuranovic-Uklein Ana S,Cerovac Natasa M,Perovic Dijana,Maksimovic Nela S,Jekic Biljana B,Grk Milka B,Dusanovic-Pjevic Marija G,Rasic Milica,Stojanovski Natasa,Pesic Milica,Novakovic Ivana V,Damnjanovic Tatjana M},
year={2025},
title={A Specific Haplotype of the MMP2 Gene Promoter May Increase the Risk of Developing Cerebral Palsy},
journal={DIAGNOSTICS},
volume={15},
number={24},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Rasic Milica,Maksimovic Nela S,Grk Milka B,Dusanovic-Pjevic Marija G,Rasic Petar,Svircev Milos,Damnjanovic Tatjana M,Perovic Dijana,Djuranovic-Uklein Ana S,Stojanovski Natasa,Pesic Milica,Novakovic Ivana V,Doklestic-Vasiljev Krstina S},
year={2025},
title={Association of NOS Gene Polymorphisms with Sepsis-Related Complications in Secondary Peritonitis},
journal={INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES},
volume={26},
number={21},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Maksimovic Nela S,Damnjanovic Tatjana M,Jekic Biljana B,Novakovic Ivana V,Djuric-Zdravkovic Aleksandra,Dusanovic-Pjevic Marija G,Grk Milka B,Pesic Milica,Djuranovic-Uklein Ana S,Rasic Milica,Stojanovski Natasa,Perovic Dijana},
year={2025},
title={New evidence supporting female protective effect in patients with congenital anomalies and neurodevelopmental disorders},
journal={EARLY HUMAN DEVELOPMENT},
volume={205},
number={},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Joksic Ivana D,Toljic Mina,Maksimovic Nela S,Perovic Dijana,Damnjanovic Tatjana M,Jurisic Aleksandar I},
year={2025},
title={Prenatal diagnosis of chromothripsis causing complex chromosomal rearrangement involving chromosomes 5, 7 and 11 leading to TWIST1 deletion and Saethre-Chotzen syndrome},
journal={TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY},
volume={64},
number={1},
pages={134-137},
document_type={Article},
} 

@ARTICLE{
author={Ljujic Biljana T,Maksimovic Nela S,Damnjanovic Tatjana M,Novakovic Ivana V,Grk Milka B,Gulic Milica,Dusanovic-Pjevic Marija G,Popovska-Jovicic Biljana D,Rakovic Ivana R,Gazdic-Jankovic Marina M,Miletic-Kovacevic Marina,Jekic Biljana B},
year={2025},
title={HIF-1A Gene Polymorphisms are Associated With Clinical and Biochemical Parameters in COVID-19 Patients in Serbian Population},
journal={CLINICAL NURSING RESEARCH},
volume={},
number={},
pages={-},
document_type={Article; Early Access},
} 

@ARTICLE{
author={Perovic Dijana,Barzegar Parsa,Damnjanovic Tatjana M,Jekic Biljana B,Grk Milka B,Dusanovic-Pjevic Marija G,Cvetkovic D,Djuranovic Uklein A,Stojanovski Natasa,Rasic Milica,Novakovic Ivana V,Elhayani B,Maksimovic Nela S},
year={2024},
title={Chromosomal Microarray in Children Born Small for Gestational Age - Single Center Experience},
journal={BALKAN JOURNAL OF MEDICAL GENETICS},
volume={27},
number={2},
pages={13-21},
document_type={Article},
} 

@ARTICLE{
author={Perovic Dijana,Maksimovic Nela S,Damnjanovic Tatjana M,Jekic Biljana B,Dusanovic-Pjevic Marija G,Grk Milka B,Djuranovic Ana S,Stojanovski Natasa},
year={2024},
title={Enrichment of pathogenic copy number variants on 17q chromosome in patients with skeletal findings},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={32},
number={},
pages={1384-1385},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Maksimovic Nela S,Damnjanovic Tatjana M,Jekic Biljana B,Grk Milka B,Dusanovic-Pjevic Marija G,Djuranovic Ana S,Rasic Milica,Barzegar Parsa,El Hayani Badr,Perovic Dijana},
year={2024},
title={Chromosomal microarray analysis in children with syndromic short stature},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={32},
number={},
pages={1115-1115},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Damnjanovic Tatjana M,Perovic Dijana,Maksimovic Nela S,Jekic Biljana B,Dusanovic-Pjevic Marija G,Grk Milka B,Djuranovic Ana S},
year={2024},
title={Diagnostic yield of chromosomal microarray analysis in patients with congenital heart disease},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={32},
number={},
pages={1018-1018},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Maksimovic Nela S,Jekic Biljana B,Grk Milka B,Damnjanovic Tatjana M,Perovic Dijana,Ljujic Biljana T,Dusanovic-Pjevic Marija G,Djonov Valentin G,Rasic Milica,Volarevic Vladislav B},
year={2024},
title={Association of LGALS3 gene polymorphisms with methotrexate treatment efficacy in patients with rheumatoid arthritis},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={32},
number={},
pages={988-988},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Perovic Dijana,Maksimovic Nela S,Damnjanovic Tatjana M,Jekic Biljana B,Dusanovic-Pjevic Marija G,Grk Milka B,Djuranovic Ana S,Stojanovski Natasa},
year={2024},
title={Enrichment of pathogenic copy number variants on 17q chromosome in patients with skeletal findings},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={32},
number={},
pages={1384-1385},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Maksimovic Nela S,Damnjanovic Tatjana M,Jekic Biljana B,Grk Milka B,Dusanovic-Pjevic Marija G,Djuranovic Ana S,Rasic Milica,Barzegar Parsa,El Hayani Badr,Perovic Dijana},
year={2024},
title={Chromosomal microarray analysis in children with syndromic short stature},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={32},
number={},
pages={1115-1115},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Damnjanovic Tatjana M,Perovic Dijana,Maksimovic Nela S,Jekic Biljana B,Dusanovic-Pjevic Marija G,Grk Milka B,Djuranovic Ana S},
year={2024},
title={Diagnostic yield of chromosomal microarray analysis in patients with congenital heart disease},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={32},
number={},
pages={1018-1018},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Maksimovic Nela S,Jekic Biljana B,Grk Milka B,Damnjanovic Tatjana M,Perovic Dijana,Ljujic Biljana T,Dusanovic-Pjevic Marija G,Djonov Valentin G,Rasic Milica,Volarevic Vladislav B},
year={2024},
title={Association of LGALS3 gene polymorphisms with methotrexate treatment efficacy in patients with rheumatoid arthritis},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={32},
number={},
pages={988-988},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Grk Milka B,Jekic Biljana B,Dolzan Vita,Maksimovic Nela S,Damnjanovic Tatjana M,Rasic Milica,Novakovic Ivana V,Perovic Dijana,Carkic Jelena,Dusanovic-Pjevic Marija G},
year={2024},
title={Genetic polymorphisms and Methotrexate response in patients with rheumatoid arthritis},
journal={JOURNAL OF RESEARCH IN PHARMACY},
volume={28},
number={4},
pages={1285-1292},
document_type={Article},
} 

@ARTICLE{
author={Vidovic Vanja,Novakovic Ivana V,Damnjanovic Tatjana M,Radic-Savic Zana,Vidovic Stojko,Krbic Ranko,Maksimovic Nela S},
year={2024},
title={Galectin 3 Rs4644 Gene Polymorphism Is Associated with Metabolic Traits in Serbian Adolescent Population},
journal={JOURNAL OF MEDICAL BIOCHEMISTRY},
volume={43},
number={3},
pages={445-450},
document_type={Article},
} 

@ARTICLE{
author={Dusanovic-Pjevic Marija G,Grk Milka B,Vojvodic Ljubica M,Rasic Milica,Perovic Dijana,Damnjanovic Tatjana M,Pesic Milica,Jekic Biljana B},
year={2024},
title={Analysis of the association between MMP-8 gene polymorphisms and the occurrence of adverse effects after acute ischemic stroke treated with recombinant tissue plasminogen activator},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={32},
number={},
pages={303-303},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Dusanovic-Pjevic Marija G,Vojvodic Ljubica M,Grk Milka B,Todorovic Jovana S,Maksimovic Nela S,Rasic Milica,Perovic Dijana,Damnjanovic Tatjana M,Trickovic Jelena,Kacar Katarina,Jekic Biljana B},
year={2024},
title={Association of <i>IL-6</i> rs1800795, but not <i>TNF-α</i> rs1800629, and <i>IL-1β</i> rs16944 polymorphisms' genotypes with recovery of ischemic stroke patients following thrombolysis},
journal={NEUROLOGICAL RESEARCH},
volume={46},
number={2},
pages={157-164},
document_type={Article},
} 

@ARTICLE{
author={Dusanovic-Pjevic Marija G,Grk Milka B,Vojvodic Ljubica M,Damnjanovic Tatjana M,Rasic Milica,Jekic Biljana B},
year={2023},
title={Analysis of the association between IL-1β and IL-6 gene polymorphisms and acute ischemic stroke patients' recovery after thrombolytic therapy},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={31},
number={},
pages={302-302},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Perovic Dijana,Maksimovic Nela S,Damnjanovic Tatjana M,Djuranovic Ana S,Sarajlija Adrijan,Mijovic Marija},
year={2023},
title={Three case reports of patients with rare copy number variations in the recurrent 2q11.1-q11.2 region},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={31},
number={},
pages={267-268},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Djuranovic Ana S,Cerovac Natasa M,Perovic Dijana,Stojanovski Natasa,Damnjanovic Tatjana M},
year={2023},
title={Study of IL6 and TNF genes polymorphisms as a risk factor for the development of early neurological disorders and subsequent consequences in neonates},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={31},
number={},
pages={171-171},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Maksimovic Nela S,Vidovic Vanja,Damnjanovic Tatjana M,Jekic Biljana B,Majkic-Singh Nada T,Simeunovic Slavko D,Savic-Bozovic Dara,Vidovic Stojko,Novakovic Ivana V},
year={2023},
title={Association of PRDM16 rs12409277 and CtBP2 rs1561589 gene polymorphisms with lipid profile of adolescents},
journal={ARCHIVES OF MEDICAL SCIENCE},
volume={19},
number={3},
pages={593-599},
document_type={Article},
} 

@ARTICLE{
author={Vidovic Vanja,Maksimovic Nela S,Vidovic Stojko,Damnjanovic Tatjana M,Milovac Irina,Novakovic Ivana V},
year={2022},
title={PPARGC1A Gene Polymorphism and Its Association with Obesity- Related Metabolic Traits in Serbian Adolescent Population},
journal={GENETIKA-BELGRADE},
volume={54},
number={3},
pages={1375-1384},
document_type={Article},
} 

@ARTICLE{
author={Perovic Dijana,Damnjanovic Tatjana M,Jekic Biljana B,Dusanovic-Pjevic Marija G,Grk Milka B,Djuranovic Ana S,Rasic Milica,Novakovic Ivana V,Maksimovic Nela S},
year={2022},
title={Chromosomal microarray in postnatal diagnosis of congenital anomalies and neurodevelopmental disorders in Serbian patients},
journal={JOURNAL OF CLINICAL LABORATORY ANALYSIS},
volume={36},
number={6},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Dusanovic-Pjevic Marija G,Jekic Biljana B,Beslac-Bumbasirevic Ljiljana,Vojvodic Ljubica M,Damnjanovic Tatjana M,Grk Milka B,Maksimovic Nela S,Pesic Milica,Gulic Milica,Trickovic Jelena,Kacar Katarina},
year={2021},
title={TT genotype of the MMP-9-1562C/T polymorphism may be a risk factor for thrombolytic therapy-induced hemorrhagic complications after acute ischemic stroke},
journal={PHARMACOTHERAPY},
volume={41},
number={7},
pages={562-571},
document_type={Article},
} 

@ARTICLE{
author={Grk Milka B,Milic Vera D,Dusanovic-Pjevic Marija G,Maksimovic Nela S,Damnjanovic Tatjana M,Pesic Milica,Gulic Milica,Jekic Biljana B},
year={2020},
title={Analysis of association of MMP-2 gene promoter haplotype with efficacy and toxicity of methotrexate in patients with Rheumatoid arthritis},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={28},
number={SUPPL 1},
pages={979-979},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Dusanovic-Pjevic Marija G,Vojvodic Ljubica M,Grk Milka B,Maksimovic Nela S,Damnjanovic Tatjana M,Pesic Milica,Gulic Milica,Kacar Katarina,Jekic Biljana B},
year={2020},
title={Analysis of the association withinMMP-2gene polymorphisms and ischemic stroke outcome after thrombolytic therapy},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={28},
number={SUPPL 1},
pages={978-978},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Djuranovic Ana S,Cerovac Natasa M,Perovic Dijana,Grk Milka B,Pesic Milica,Damnjanovic Tatjana M},
year={2020},
title={Investigation of the MMP2 haplotype as a risk factor for the development of cerebral palsy},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={28},
number={SUPPL 1},
pages={351-351},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Vidovic Vanja,Maksimovic Nela S,Novakovic Ivana V,Damnjanovic Tatjana M,Jekic Biljana B,Vidovic Stojko,Majkic-Singh Nada T,Stamenkovic-Radak Marina M,Nikolic Dejan P,Marisavljevic Dragomir Z},
year={2020},
title={Association of the Brain-Derived Neurotrophic Factor Val66met Polymorphism with Body Mass Index, Fasting Glucose Levels and Lipid Status in Adolescents},
journal={BALKAN JOURNAL OF MEDICAL GENETICS},
volume={23},
number={1},
pages={77-82},
document_type={Article},
} 

@ARTICLE{
author={Grk Milka B,Milic Vera D,Dolzan Vita,Maksimovic Nela S,Damnjanovic Tatjana M,Dusanovic-Pjevic Marija G,Pesic Milica,Novakovic Ivana V,Jekic Biljana B},
year={2020},
title={Analysis of association of ADORA(2)A and ADORA(3) polymorphisms genotypes/haplotypes with efficacy and toxicity of methotrexate in patients with Rheumatoid arthritis},
journal={PHARMACOGENOMICS JOURNAL},
volume={20},
number={6},
pages={784-791},
document_type={Article},
} 

@ARTICLE{
author={Varljen Tatjana J,Sekulovic Gordana,Rakic Olgica,Maksimovic Nela S,Jekic Biljana B,Novakovic Ivana V,Damnjanovic Tatjana M},
year={2020},
title={Genetic variant rs16944 in IL1B gene is a risk factor for early-onset sepsis susceptibility and outcome in preterm infants},
journal={INFLAMMATION RESEARCH},
volume={69},
number={2},
pages={155-157},
document_type={Article},
} 

@ARTICLE{
author={Jekic Biljana B,Maksimovic Nela S,Damnjanovic Tatjana M},
year={2019},
title={Methotrexate pharmacogenetics in the treatment of rheumatoid arthritis},
journal={PHARMACOGENOMICS},
volume={20},
number={17},
pages={1235-1245},
document_type={Review},
} 

@ARTICLE{
author={Maksimovic Nela S,Varljen Tatjana J,Sekulovic Gordana,Damnjanovic Tatjana M,Novakovic Ivana V},
year={2019},
title={Genetic variant rs16944 in IL1B gene is a risk factor for early onset sepsis susceptibility and outcome in preterm infants},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={27},
number={},
pages={1364-1365},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Damnjanovic Tatjana M,Varljen Tatjana J,Rakic Olgica,Jekic Biljana B,Liston J,Novakovic Ivana V},
year={2019},
title={Study of TNF, IL1B, and IL6 genes polymorphisms and susceptibility to bronchopulmonary dysplasia in premature neonates},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={27},
number={},
pages={1360-1360},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Maksimovic Nela S,Vidovic Vanja,Damnjanovic Tatjana M,Jekic Biljana B,Perovic Dijana,Vidovic Stojko,Milovac Irina,Novakovic Ivana V},
year={2019},
title={Association of PRDM16 and CtBP2 genes polymorphisms with lipid profile of adolescents},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={27},
number={},
pages={658-658},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Damnjanovic Tatjana M,Grk Milka B,Varljen Tatjana J,Pantelic Jelica R,Maksimovic Nela S,Jekic Biljana B,Novakovic Ivana V},
year={2019},
title={Association of genetic markers of coagulation and fibrinolysis with prematurity complication},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={27},
number={},
pages={641-642},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Grk Milka B,Jekic Biljana B,Milic Vera D,Dolzan Vita,Maksimovic Nela S,Damnjanovic Tatjana M,Dusanovic-Pjevic Marija G,Pesic Milica},
year={2019},
title={Association of ADORA3 gene polymorphisms with efficacy and toxicity of methotrexate},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={27},
number={},
pages={543-544},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Pesic Milica,Maksimovic Nela S,Vidovic Vanja,Vidovic Stojko,Jekic Biljana B,Damnjanovic Tatjana M,Grk Milka B,Dusanovic-Pjevic Marija G,Novakovic Ivana V},
year={2019},
title={Polymorphisms in PPARG gene: association with obesity-related metabolic traits in a Serbian adolescent population},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={27},
number={},
pages={190-191},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Dusanovic-Pjevic Marija G,Beslac-Bumbasirevic Ljiljana,Vojvodic Ljubica M,Grk Milka B,Maksimovic Nela S,Damnjanovic Tatjana M,Novakovic Ivana V,Kacar Katarina,Pesic Milica,Perovic Dijana,Savic Milan B,Maksic Veljko,Trickovic Jelena,Jekic Biljana B},
year={2019},
title={Analysis of the Association Between Polymorphisms within PAI-1 and ACE genes and Ischemic Stroke Outcome After rt-PA Therapy},
journal={JOURNAL OF PHARMACY AND PHARMACEUTICAL SCIENCES},
volume={22},
number={},
pages={142-149},
document_type={Article},
} 

@ARTICLE{
author={Varljen Tatjana J,Rakic Olgica,Sekulovic Gordana,Jekic Biljana B,Maksimovic Nela S,Rankovic-Janevski Milica,Novakovic Ivana V,Damnjanovic Tatjana M},
year={2019},
title={Association between Tumor Necrosis Factor-alpha Promoter-308 G/A Polymorphism and Early Onset Sepsis in Preterm Infants},
journal={TOHOKU JOURNAL OF EXPERIMENTAL MEDICINE},
volume={247},
number={4},
pages={259-264},
document_type={Article},
} 

@ARTICLE{
author={Vejnovic Dubravka,Milic Vera D,Popovic Branka M,Damnjanovic Tatjana M,Maksimovic Nela S,Bunjevacki Vera I,Krajinovic Maja,Novakovic Ivana V,Damjanov Nemanja S,Jekic Biljana B},
year={2019},
title={Association of C35T polymorphism in dihydrofolate reductase gene with toxicity of methotrexate in rheumatoid arthritis patients},
journal={EXPERT OPINION ON DRUG METABOLISM & TOXICOLOGY},
volume={15},
number={3},
pages={253-257},
document_type={Article},
} 

@ARTICLE{
author={Savin Marina S,Hadzibulic Edvin B,Damnjanovic Tatjana M,Santric Veljko,Stankovic Sanja Dj},
year={2017},
title={Association of I/D angiotensin-converting enzyme genotype with erythropoietin stimulation in kidney failure},
journal={ARCHIVES OF BIOLOGICAL SCIENCES},
volume={69},
number={1},
pages={15-22},
document_type={Article},
} 

@ARTICLE{
author={Pantelic Jelica R,Varljen Tatjana J,Maksimovic Nela S,Jekic Biljana B,Oros Ana J,Nikolic Tatjana V,Stefanovic Ivan B,Novakovic Ivana V,Damnjanovic Tatjana M},
year={2016},
title={Analysis of T-786c and 4a/b Endothelial Nitric Oxide Synthase Gene Polymorphisms in Retinopathy of Prematurity},
journal={GENETIKA-BELGRADE},
volume={48},
number={2},
pages={707-716},
document_type={Article},
} 

@ARTICLE{
author={Jekic Biljana B,Vejnovic Dubravka,Milic Vera D,Maksimovic Nela S,Damnjanovic Tatjana M,Bunjevacki Vera I,Novakovic Ivana V,Lukovic Ljiljana F,Damjanov Nemanja S,Krajinovic Maja},
year={2016},
title={Association of 63/91 length polymorphism in the DHFR gene major promoter with toxicity of methotrexate in patients with rheumatoid arthritis},
journal={PHARMACOGENOMICS},
volume={17},
number={15},
pages={1687-1691},
document_type={Article},
} 

@ARTICLE{
author={Vejnovic Dubravka,Milic Vera D,Damnjanovic Tatjana M,Maksimovic Nela S,Bunjevacki Vera I,Lukovic Ljiljana F,Novakovic Ivana V,Krajinovic Maja,Damjanov Nemanja S,Radunovic Goran L,Pavkovic-Lucic Sofija B,Jekic Biljana B},
year={2016},
title={Analysis of Association Between Polymorphisms of Mthfr, Mthfd and Rfc1 Genes and Efficacy and Toxicity of Methotrexate in Rheumatoid Arthritis Patients},
journal={GENETIKA-BELGRADE},
volume={48},
number={1},
pages={395-408},
document_type={Article},
} 

@ARTICLE{
author={Bunjevacki Vera I,Maksimovic Nela S,Jekic Biljana B,Milic Vera D,Lukovic Ljiljana F,Novakovic Ivana V,Damjanov Nemanja S,Radunovic Goran L,Damnjanovic Tatjana M},
year={2016},
title={Polymorphisms of the eNOS gene are associated with disease activity in rheumatoid arthritis},
journal={RHEUMATOLOGY INTERNATIONAL},
volume={36},
number={4},
pages={597-602},
document_type={Article},
} 

@ARTICLE{
author={Damnjanovic Tatjana M,Cuturilo Goran,Maksimovic Nela S,Dimitrijevic Nikola,Mitic Vesna,Jekic Biljana B,Lukovic Ljiljana F,Bunjevacki Vera I,Varljen Tatjana J,Dobricic Valerija S,Jovanovic Ida V,Kostic Vladimir S,Novakovic Ivana V},
year={2015},
title={Subtelomeric screening in Serbian children with dysmorphic features and unexplained developmental delay/intellectual disabilities},
journal={TURKISH JOURNAL OF PEDIATRICS},
volume={57},
number={2},
pages={154-160},
document_type={Article},
} 

@ARTICLE{
author={Bunjevacki Vera I,Maksimovic Nela S,Damnjanovic Tatjana M,Cvjeticanin Suzana,Novakovic Ivana V,Lukovic Ljiljana F,Ristanovic Momcilo,Bogdanovic Andrija D,Jekic Biljana B},
year={2014},
title={657del5 Mutation of the Nbs1 Gene in Myelodysplastic Syndrome},
journal={ARCHIVES OF BIOLOGICAL SCIENCES},
volume={66},
number={3},
pages={1055-1059},
document_type={Article},
} 

@ARTICLE{
author={Damnjanovic Tatjana M,Lukovic Ljiljana F,Cvetkovic Dragana D,Jekic Biljana B,Bunjevacki Vera I,Maksimovic Nela S,Cvjeticanin Suzana,Majkic-Singh Nada T,Slavko S,Novakovic Ivana V},
year={2014},
title={Possible Influence of MTHFR C677T Polymorphism on Serum Lipid Levels in Serbian School Children},
journal={ARCHIVES OF BIOLOGICAL SCIENCES},
volume={66},
number={2},
pages={729-734},
document_type={Article},
} 

@ARTICLE{
author={Jekic Biljana B,Lukovic Ljiljana F,Bunjevacki Vera I,Milic Vera D,Novakovic Ivana V,Damnjanovic Tatjana M,Milasin Jelena M,Popovic Branka M,Maksimovic Nela S,Damjanov Nemanja S,Radunovic Goran L,Kovacevic Ljiljana V,Krajinovic Maja},
year={2013},
title={Association of the TYMS 3G/3G genotype with poor response and GGH 354GG genotype with the bone marrow toxicity of the methotrexate in RA patients},
journal={EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY},
volume={69},
number={3},
pages={377-383},
document_type={Article},
} 

@ARTICLE{
author={Djordjevic Valentina J,Stankovic Marija M,Brankovic-Sreckovic Vesna,Rakicevic Ljiljana B,Damnjanovic Tatjana M,Antonijevic Nebojsa M,Radojkovic Dragica P},
year={2012},
title={Prothrombotic Genetic Risk Factors in Stroke: A Possible Different Role in Pediatric and Adult Patients},
journal={CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS},
volume={18},
number={6},
pages={658-661},
document_type={Article},
} 

@ARTICLE{
author={Maksimovic Nela S,Andjelkovic Ana,Milic-Rasic Vedrana M,Rakocevic-Stojanovic Vidosava M,Kastratovic-Kotlica Biljana A,Brankovic Slavko,Damnjanovic Tatjana M,Jekic Biljana B,Bunjevacki Vera I,Lukovic Ljiljana F,Perovic Dijana,Cvjeticanin Suzana,Novakovic Ivana V},
year={2012},
title={Quantitative Analysis of the Dystrophin Gene by Real-Time Pcr},
journal={ARCHIVES OF BIOLOGICAL SCIENCES},
volume={64},
number={2},
pages={787-792},
document_type={Article},
} 

@ARTICLE{
author={Milic Vera D,Jekic Biljana B,Lukovic Ljiljana F,Bunjevacki Vera I,Milasin Jelena M,Novakovic Ivana V,Damnjanovic Tatjana M,Popovic Branka M,Maksimovic Nela S,Damjanov Nemanja S,Radunovic Goran L,Pejnovic Nada N,Krajinovic Maja},
year={2012},
title={Association of dihydrofolate reductase (DHFR)-317AA genotype with poor response to methotrexate in patients with rheumatoid arthritis},
journal={CLINICAL AND EXPERIMENTAL RHEUMATOLOGY},
volume={30},
number={2},
pages={178-183},
document_type={Article},
} 

@ARTICLE{
author={Regueiro Maria,Rivera Luis,Damnjanovic Tatjana M,Lukovic Ljiljana F,Milasin Jelena M,Herrera Rene J},
year={2012},
title={High levels of Paleolithic Y-chromosome lineages characterize Serbia},
journal={GENE},
volume={498},
number={1},
pages={59-67},
document_type={Article},
} 

@ARTICLE{
author={Mitic Vesna,Cuturilo Goran,Novakovic Ivana V,Dimitrijevic Nikola,Damnjanovic Tatjana M,Dimitrijevic Aleksandar N,Dobricic Valerija S,Kostic Vladimir S,Radlovic Nedeljko P},
year={2011},
title={Epilepsy in a Child with Wolf-Hirschhorn Syndrome},
journal={SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO},
volume={139},
number={11-12},
pages={795-799},
document_type={Article},
} 

@ARTICLE{
author={Jekic Biljana B,Bunjevacki Vera I,Dobricic Valerija S,Novakovic Ivana V,Milasin Jelena M,Popovic Branka M,Damnjanovic Tatjana M,Maksimovic Nela S,Perovic Vladimir R,Lukovic Ljiljana F},
year={2011},
title={Npm1 Gene Mutations in Children with Myelodysplastic Syndromes},
journal={ARCHIVES OF BIOLOGICAL SCIENCES},
volume={63},
number={3},
pages={649-653},
document_type={Article},
} 

@ARTICLE{
author={Nikolic Dejan P,Cvjeticanin Suzana,Petronic Ivana,Jekic Biljana B,Brdar Radivoj S,Damnjanovic Tatjana M,Bunjevacki Vera I,Maksimovic Nela S},
year={2010},
title={Degree of genetic homozygosity and distribution of AB0 blood types among patients with spina bifida occulta and spina bifida aperta},
journal={ARCHIVES OF MEDICAL SCIENCE},
volume={6},
number={6},
pages={854-859},
document_type={Article},
} 

@ARTICLE{
author={Damnjanovic Tatjana M,Milicevic Radomir,Novkovic Tanja,Jovicic Olivera,Bunjevacki Vera I,Jekic Biljana B,Lukovic Ljiljana F,Novakovic Ivana V,Redzic Danka,Milasin Jelena M},
year={2010},
title={Association Between the Methylenetetrahydrofolate Reductase Polymorphisms and Risk of Acute Lymphoblastic Leukemia in Serbian Children},
journal={JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY},
volume={32},
number={4},
pages={E148-E150},
document_type={Article},
} 

@ARTICLE{
author={Nikolic Dejan P,Milincic Zeljka D,Simeunovic Slavko D,Petronic Ivana,Novakovic Ivana V,Damnjanovic Tatjana M},
year={2008},
title={Systolic Blood Pressure Trends in School Children - Yusad Study},
journal={ATHEROSCLEROSIS SUPPLEMENTS},
volume={9},
number={1},
pages={94-94},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Cvjeticanin Suzana,Nikolic Dejan P,Petronic Ivana,Jekic Biljana B,Damnjanovic Tatjana M,Cirovic Dragana,Radlovic Vladimir N,Knezevic Tatjana},
year={2008},
title={Degree Of Genetic Homozygosity Among Patients With Spinal Dysraphia},
journal={SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO},
volume={136},
number={9-10},
pages={519-523},
document_type={Article},
} 

@ARTICLE{
author={Stefanova Elka D,Novakovic Ivana V,Maksimovic Nela S,Strbacki M,Slavic S,Palibrk V,Bajcetic Milos I,Sternic Nadezda M,Damnjanovic Tatjana M,Kostic Jelena R,Kostic Vladimir S},
year={2008},
title={APOE genotype and cognitive functioning of college-age adults},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={15},
number={},
pages={189-189},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Damnjanovic Tatjana M,Novakovic Ivana V,Milasin Jelena M,Bunjevacki Vera I,Jekic Biljana B,Cvjeticanin Suzana,Lukovic Ljiljana F},
year={2007},
title={LeX chromosome imprinting in turner syndrome},
journal={KOREAN JOURNAL OF GENETICS},
volume={29},
number={3},
pages={291-295},
document_type={Article},
} 

@ARTICLE{
author={Nikolic Dejan P,Damnjanovic Tatjana M,Milincic Zeljka D,Simeunovic Slavko D,Novakovic Ivana V,Risimic Dijana S,Vukotic Milija,Nedeljkovic Srecko I},
year={2007},
title={Association of homocysteine enzyme genetic markers and lipid levels in children},
journal={ATHEROSCLEROSIS SUPPLEMENTS},
volume={8},
number={1},
pages={47-47},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Jekic Biljana B,Novakovic Ivana V,Lukovic Ljiljana F,Kuzmanovic Milos B,Popovic Branka M,Milasin Jelena M,Bunjevacki Gordana,Damnjanovic Tatjana M,Cvjeticanin Suzana,Bunjevacki Vera I},
year={2006},
title={Lack of TP53 and FMS gene mutations in children with myelodysplastic syndrome},
journal={CANCER GENETICS AND CYTOGENETICS},
volume={166},
number={2},
pages={163-165},
document_type={Article},