@ARTICLE{
author={Bergant Gaber,...,Brankovic Marija,Jankovic Milena Z,Svetel Marina V,...,Dragasevic-Miskovic Natasa T,Petrovic Igor N,...,Novakovic Ivana V,...,(broj koautora 19)},
year={2026},
title={Enrichment of Rare Variants in Nuclear-Encoded Mitochondrial Metabolism Genes in Patients with Early-Onset or Familial Parkinson's Disease},
journal={GENES},
volume={17},
number={4},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Turk Aleksander,Maver Ales,Juvan Peter,Drulovic Jelena S,Mesaros Sarlota T,Novakovic Ivana V,Cizmarevic Nada S,Ristic Smiljana,Matic Ivana S,Peterlin Borut},
year={2025},
title={Increased burden of rare variants in GWAS associated genes in familial multiple sclerosis},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={33},
number={},
pages={1046-1046},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Kovanda Anja,Susmelj Lara,Lukezic Tadeja,Maver Ales,Racki Valentino,Vuletic Vladimira,Svetel Marina V,Novakovic Ivana V,Peterlin Borut},
year={2025},
title={Biallelic RFC1 expansions as a rare cause of familial and early onset Parkinson's disease in the Slavic population},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={33},
number={},
pages={797-798},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Podgrajsek Rebeka,Hodzic Alenka,Maver Ales,Stimpfel Martin,Andjelic Aleksander,Miljanovic Olivera,Ristanovic Momcilo,Novakovic Ivana V,Plaseska-Karanfilska Dijana,Noveski Predrag,Ostojic Sasa,Buretic-Tomljanovic Alena,Peterlin Borut},
year={2025},
title={Clinical application of whole exome sequencing in the diagnosis of men with severely impaired spermatogenesis},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={33},
number={},
pages={570-570},
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={Kovacevic Gordana S,Todorovic Slobodanka,Novakovic Ivana V,Dobricic Valerija S,Savic-Pavicevic Dusanka Lj,Milic-Rasic Vedrana M,Svetel Marina V,Brkusanin Milos,Vukomanovic Vladislav A,Vucinic Dragana M,Ostojic Slavica B,Putnik Jovana,Kosac Ana P},
year={2025},
title={Multi-Center National Study of Genotype-Phenotype Correlation and Clinical Characteristics in Children and Young Adults with Friedreich's Ataxia from Serbia},
journal={BIOMEDICINES},
volume={13},
number={11},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Podgrajsek Rebeka,Hodzic Alenka,Maver Ales,Stimpfel Martin,Andjelic Aleksander,Miljanovic Olivera,Ristanovic Momcilo,Novakovic Ivana V,Plaseska-Karanfilska Dijana,Noveski Predrag,Ostojic Sasa,Buretic-Tomljanovic Alena,Peterlin Borut},
year={2025},
title={The role of DNA mismatch repair mutS/mutL homolog genes in spermatogenesis and male infertility: a systematic review and cohort study},
journal={REPRODUCTIVE BIOLOGY AND ENDOCRINOLOGY},
volume={23},
number={1},
pages={-},
document_type={Review},
} 

@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={Podgrajsek Rebeka,Hodzic Alenka,Maver Ales,Stimpfel Martin,Andjelic Aleksander,Miljanovic Olivera,Ristanovic Momcilo,Novakovic Ivana V,Plaseska-Karanfilska Dijana,Noveski Predrag,Ostojic Sasa,Grskovic Antun,Buretic-Tomljanovic Alena,Peterlin Borut},
year={2025},
title={Genetic Testing for Monogenic Forms of Male Infertility Contributes to the Clinical Diagnosis of Men with Severe Idiopathic Male Infertility},
journal={WORLD JOURNAL OF MENS HEALTH},
volume={43},
number={4},
pages={908-917},
document_type={Article},
} 

@ARTICLE{
author={Kovanda Anja,Susmelj Lara,Jaklic Helena,Lukezic Tadeja,Maver Ales,Petrovic Igor N,Dragasevic-Miskovic Natasa T,Svetel Marina V,Racki Valentino,Vuletic Vladimira,Novakovic Ivana V,Peterlin Borut},
year={2025},
title={Biallelic RFC1 Expansions Are a Rare Cause of Early-Onset and Familial Parkinson's Disease},
journal={CLINICAL GENETICS},
volume={},
number={},
pages={-},
document_type={Editorial Material; Early Access},
} 

@ARTICLE{
author={Kunej Tanja,Podgrajsek Rebeka,Jaklic Helena,Hodzic Alenka,Stimpfel Martin,Miljanovic Olivera,Ristanovic Momcilo,Novakovic Ivana V,Plaseska-Karanfilska Dijana,Noveski Predrag,Ostojic Sasa,Buretic-Tomljanovic Alena,Grskovic Antun,Peterlin Borut},
year={2025},
title={ACE gene and male infertility: a South Slavic case-control study and multi-omics data integration},
journal={SYSTEMS BIOLOGY IN REPRODUCTIVE MEDICINE},
volume={71},
number={1},
pages={524-537},
document_type={Article},
} 

@ARTICLE{
author={Kresojevic Nikola D,Markovic Vladana V,Geratovic Cveta,Jecmenica-Lukic Milica V,Tomic Aleksandra D,Dobricic Valerija S,Stankovic Iva D,Stojkovic Tanja,Dragasevic Natasa T,Sarcevic Maksim,Jankovic Milena Z,Marjanovic Ana,Novakovic Ivana V,Kostic Vladimir K,Svetel Marina V,Petrovic Igor N},
year={2025},
title={Is GBA1 mutation status a game-changer for impulse control behaviour in Parkinson's disease?},
journal={NEUROLOGICAL SCIENCES},
volume={},
number={},
pages={-},
document_type={Article; Early Access},
} 

@ARTICLE{
author={Peric Marina,Anicin Aleksandra,Brankovic Marija,Stajic Natasa,Putnik Jovana,Paripovic Aleksandra,Jankovic Milena Z,Bozovic Ivo,Perovic Vladimir S,Novakovic Ivana V,Vukomanovic Vladislav A,Milosevic Emina},
year={2025},
title={Genetic Susceptibility to Glomerulonephritis in Children: Analysis of Structural Kidney Genes and Immune System Genes},
journal={JOURNAL OF CLINICAL MEDICINE},
volume={14},
number={14},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Turk Aleksander,Maver Ales,Juvan Peter,Drulovic Jelena S,Mesaros Sarlota T,Novakovic Ivana V,Starcevic-Cizmarevic Nada,Ristic Smiljana,Stankovic-Matic Ivana,Peterlin Borut},
year={2025},
title={Increased burden of rare variants in GWAS associated genes in familial multiple sclerosis},
journal={SCIENTIFIC REPORTS},
volume={15},
number={1},
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={Podgrajsek Rebeka,Hodzic Alenka,Maver Ales,Stimpfel Martin,Andjelic Aleksander,Miljanovic Olivera,Ristanovic Momcilo,Novakovic Ivana V,Plaseska-Karanfilska Dijana,Noveski Predrag,Ostojic Sasa,Grskovic Antun,Buretic-Tomljanovic Alena,Peterlin Borut},
year={2025},
title={Genetic Testing for Monogenic Forms of Male Infertility Contributes to the Clinical Diagnosis of Men with Severe Idiopathic Male Infertility},
journal={WORLD JOURNAL OF MENS HEALTH},
volume={},
number={},
pages={-},
document_type={Article; Early Access},
} 

@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={Pesic Milica,Stevanovic Milena,Andrejic Nikola,Pesovic Jovan,Cirkovic Sanja S,Dimitrijevic Sanja S,Bascarevic Danijela,Dragasevic-Miskovic Natasa T,Novakovic Ivana V,Protic Dragana D},
year={2024},
title={Sleep problems in female carriers of premutation in the FMR1 gene},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={32},
number={},
pages={1088-1088},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Pesic Milica,Stevanovic Milena,Andrejic Nikola,Pesovic Jovan,Cirkovic Sanja S,Dimitrijevic Sanja S,Bascarevic Danijela,Dragasevic-Miskovic Natasa T,Novakovic Ivana V,Protic Dragana D},
year={2024},
title={Sleep problems in female carriers of premutation in the <i>FMR1</i> gene},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={32},
number={},
pages={1088-1088},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Jovicic-Pavlovic Svetlana M,Simic-Ogrizovic Sanja P,Pavlovic Natalija,Bukumiric Zoran M,Novakovic Ivana V},
year={2024},
title={Influence of polymorphisms in genes for interleukin-6 and interleukin-10 on dialysis patients survival},
journal={NEPHROLOGY DIALYSIS TRANSPLANTATION},
volume={39},
number={},
pages={-},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Andabaka Marko M,Novakovic Ivana V,Brankovic Marija,Mesaros Sarlota T,Veselinovic Nikola D,Tamas Olivera S,Budimkic Maja S,Martinovic Vanja N,Momcilovic Nikola,Maric Gorica D,Suknjaja Vesna,Sakalas Lorand,Pekmezovic Tatjana D,Habek Mario,Drulovic Jelena S},
year={2024},
title={Association of AQP-4 polymorphisms with the clinical and paraclinical characteristics of patients with NMOSD},
journal={MULTIPLE SCLEROSIS JOURNAL},
volume={30},
number={3},
pages={993-993},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Jovanovic Aleksa Lj,Turk Aleksander,Novakovic Ivana V,Mesaros Sarlota T,Veselinovic Nikola D,Tamas Olivera S,Maric Gorica D,Andabaka Marko M,Momcilovic Nikola,Pekmezovic Tatjana D,Peterlin Borut,Drulovic Jelena S},
year={2024},
title={Rare and Uncommon Gene Variants Associated with Familial Multiple Sclerosis: A Case-Control Study},
journal={MULTIPLE SCLEROSIS JOURNAL},
volume={30},
number={3},
pages={866-867},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Svetel Marina V,Kresojevic Nikola D,Tomic Aleksandra D,Jecmenica-Lukic Milica V,Markovic Vladana V,Stankovic Iva D,Petrovic Igor N,Pekmezovic Tatjana D,Novakovic Ivana V,Bozic Marija M,Svetel Marko,Vitkovic Jelena,Dragasevic Natasa T},
year={2024},
title={Wilson's disease},
journal={SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO},
volume={152},
number={5-6},
pages={310-317},
document_type={Review},
} 

@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={Jovicic-Pavlovic Svetlana M,Simic-Ogrizovic Sanja P,Pavlovic Natalija,Bukumiric Zoran M,Novakovic Ivana V},
year={2024},
title={Influence of polymorphisms in genes for interleukin-6 and interleukin-10 on dialysis patients survival},
journal={NEPHROLOGY DIALYSIS TRANSPLANTATION},
volume={39},
number={},
pages={I2520-I2521},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Stefanova Elka D,Marjanovic Ana,Dobricic Valerija S,Mandic-Stojmenovic Gorana B,Stojkovic Tanja,Brankovic Marija,Sarcevic Maksim,Novakovic Ivana V,Kostic Vladimir S},
year={2024},
title={Frequency of C9orf72, GRN, and MAPT pathogenic variants in patients recruited at the Belgrade Memory Center},
journal={NEUROGENETICS},
volume={},
number={},
pages={-},
document_type={Article; Early Access},
} 

@ARTICLE{
author={Stratakis Konstantinos,Terzic-Supic Zorica J,Todorovic Jovana S,Nesic Dejan M,Novakovic Ivana V},
year={2024},
title={Physical Activity and Mental Health of Medical Students},
journal={CENTRAL EUROPEAN JOURNAL OF PUBLIC HEALTH},
volume={32},
number={1},
pages={39-44},
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={Jovanovic Aleksa Lj,Pekmezovic Tatjana D,Mesaros Sarlota T,Novakovic Ivana V,Peterlin Borut,Veselinovic Nikola D,Tamas Olivera S,Ivanovic Jovana B,Maric Gorica D,Andabaka Marko M,Momcilovic Nikola,Drulovic Jelena S},
year={2024},
title={Earlier age of symptom onset in younger generation of familial cases of multiple sclerosis},
journal={NEUROLOGICAL SCIENCES},
volume={},
number={},
pages={-},
document_type={Article; Early Access},
} 

@ARTICLE{
author={Brankovic Marija,Ivanovic Vukan,Basta Ivana Z,...,Stevic Zorica D,Ralic Branislav M,Tubic Radoje M,...,Markovic Vladana V,Bozovic Ivo,Svetel Marina V,Marjanovic Ana,Veselinovic Nikola D,Mesaros Sarlota T,Jankovic Milena Z,Savic-Pavicevic Dusanka Lj,Jovin Zita B,Novakovic Ivana V,...,Peric Stojan Z},
year={2024},
title={Whole exome sequencing in Serbian patients with hereditary spastic paraplegia},
journal={NEUROGENETICS},
volume={},
number={},
pages={-},
document_type={Article; Early Access},
} 

@ARTICLE{
author={Milovanovic Andona,...,Stankovic Iva D,Tamas Olivera S,Brankovic Marija,Marjanovic Ana,...,Brankovic Vesna,Novakovic Ivana V,Petrovic Igor N,Svetel Marina V,...,Kostic Vladimir S,Dragasevic-Miskovic Natasa T},
year={2024},
title={<i>ANO10</i>-Related Spinocerebellar Ataxia: MDSGene Systematic Literature Review and a Romani Case Series},
journal={MOVEMENT DISORDERS},
volume={39},
number={5},
pages={887-892},
document_type={Article},
} 

@ARTICLE{
author={Jovanovic Aleksa Lj,Pekmezovic Tatjana D,Mesaros Sarlota T,Novakovic Ivana V,Peterlin Borut,Veselinovic Nikola D,Tamas Olivera S,Ivanovic Jovana B,Maric Gorica D,Andabaka Marko M,Momcilovic Nikola,Drulovic Jelena S},
year={2024},
title={Exclusive breastfeeding may be a protective factor in individuals with familial multiple sclerosis. A population registry-based case-control study},
journal={MULTIPLE SCLEROSIS AND RELATED DISORDERS},
volume={82},
number={},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Podgrajsek Rebeka,Hodzic Alenka,Maver Ales,Stimpfel Martin,Andjelic Aleksander,Miljanovic Olivera,Ristanovic Momcilo,Novakovic Ivana V,Plaseska-Karanfilska Dijana,Noveski Predrag,Ostojic Sasa,Grskovic Antun,Buretic-Tomljanovic Alena,Peterlin Borut},
year={2024},
title={Genetic testing for monogenic forms of male infertility contributes to the clinical diagnosis of men with idiopathic severe male infertility},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={32},
number={},
pages={356-357},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Kovacevic Masa,Jankovic M,Brankovic Marija,Milicevic Ognjen S,Novakovic Ivana V,Sokic Dragoslav V,Ristic Aleksandar J,Berisavac I,Vojvodic Nikola M},
year={2023},
title={Yield of GATOR1 gene sequencing in a Serbian focal epilepsy cohort},
journal={EPILEPSIA},
volume={64},
number={},
pages={386-386},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Kresojevic Nikola D,Perovic Ivana,Stankovic Iva D,Tomic Aleksandra D,Jecmenica-Lukic Milica V,Markovic Vladana V,Stojkovic Tanja,Mandic Gorana B,Jankovic Milena Z,Marjanovic Ana,Brankovic Marija,Novakovic Ivana V,Petrovic Igor N,Dragasevic Natasa T,Stefanova Elka D,Svetel Marina V,Kostic Vladimir K},
year={2023},
title={Clinical and Genetic Features of Huntington's Disease Patients From Republic of Serbia: A Single-Center Experience},
journal={JOURNAL OF MOVEMENT DISORDERS},
volume={16},
number={3},
pages={333-335},
document_type={Letter},
} 

@ARTICLE{
author={Ivanovic Vukan,Brankovic Marija,Bozovic Ivo,Stevic Zorica D,Basta Ivana Z,Markovic Vladana V,Svetel Marina V,Tubic Radoje M,Marjanovic Ana,Veselinovic Nikola D,Mesaros Sarlota T,Jankovic Milena Z,Rakocevic-Stojanovic Vidosava M,Savic-Pavicevic Dusanka Lj,Novakovic Ivana V,Peric Stojan Z},
year={2023},
title={Whole exome sequencing in Serbian patients with hereditary spastic paraplegia},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={30},
number={},
pages={260-260},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Dragasevic-Miskovic Natasa T,Milovanovic Andona,Stankovic I,Marjanovic Ana,Brankovic Marija,Dobricic Valerija S,Petrovic Igor N,Svetel Marina V,Novakovic Ivana V,Kostic V},
year={2023},
title={Motor neuron involvement in facial muscles as characteristic of ANO10 mutation},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={30},
number={},
pages={234-234},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Maksic Jasmina,Maksimovic Nela S,Rasulic Lukas G,Milankov Olgica,Marjanovic Ana,Cvetkovic Dragana D,Rakocevic-Stojanovic Vidosava M,Novakovic Ivana V},
year={2023},
title={The importance of direct genetic testing for determining female carriers of the mutation in dystrophinopathies},
journal={VOJNOSANITETSKI PREGLED},
volume={80},
number={3},
pages={201-207},
document_type={Article},
} 

@ARTICLE{
author={Kovacevic Masa,Milicevic Ognjen S,Brankovic Marija,Jankovic Milena Z,Novakovic Ivana V,Sokic Dragoslav V,Ristic Aleksandar J,Shamsani Jannah,Vojvodic Nikola M},
year={2023},
title={Novel variants in established epilepsy genes in focal epilepsy},
journal={SEIZURE-EUROPEAN JOURNAL OF EPILEPSY},
volume={110},
number={},
pages={146-152},
document_type={Article},
} 

@ARTICLE{
author={Kresojevic Nikola D,Markovic Vladana V,Dobricic Valerija S,Stankovic Iva D,Stojkovic Tanja,Tomic Aleksandra D,Jecmenica-Lukic Milica V,Jankovic Milena Z,Marjanovic Ana,Brankovic Marija,Novakovic Ivana V,Petrovic Igor N,Dragasevic Natasa T,Svetel Marina V,Kostic Vladimir K},
year={2023},
title={Reply to: "Differences in Sex-Specific Frequency of Glucocerebrosidase Variant Carriers and Familial Parkinsonism"},
journal={MOVEMENT DISORDERS},
volume={38},
number={4},
pages={712-713},
document_type={Letter},
} 

@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={Pal Gian,...,Novakovic Ivana V,...,(broj koautora 27)},
year={2023},
title={Genetic Testing in Parkinson's Disease},
journal={MOVEMENT DISORDERS},
volume={38},
number={8},
pages={1384-1396},
document_type={Review},
} 

@ARTICLE{
author={Saunders-Pullman Rachel,...,Novakovic Ivana V,...,(broj koautora 29)},
year={2023},
title={International Genetic Testing and Counseling Practices for Parkinson's Disease},
journal={MOVEMENT DISORDERS},
volume={38},
number={8},
pages={1527-1535},
document_type={Article},
} 

@ARTICLE{
author={Marjanovic Ana,Palibrk Aleksa,Dobricic Valerija S,Milicevic Ognjen S,Brankovic Marija,Viric Vanja,Drinic Aleksandra,Mandic-Stojmenovic Gorana B,Jankovic Milena Z,Basta Ivana Z,Peric Stojan Z,Novakovic Ivana V,Stefanova Elka D,Stevic Zorica D},
year={2023},
title={C9orf72 Genetic Screening in Amyotrophic Lateral Sclerosis Patients from Serbia},
journal={GENETIKA-BELGRADE},
volume={55},
number={1},
pages={1-18},
document_type={Article},
} 

@ARTICLE{
author={Minic Snezana B,Cerovac Natasa M,Novakovic Ivana V,Gazikalovic Slobodan,Popadic Svetlana P,Trpinac Dusan P},
year={2023},
title={The Impact of the IKBKG Gene on the Appearance of the Corpus Callosum Abnormalities in Incontinentia Pigmenti},
journal={DIAGNOSTICS},
volume={13},
number={7},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Jankovic Milena Z,Nikolic Dejan P,Novakovic Ivana V,Petrovic Bojana,Lackovic Milan,Santric-Milicevic Milena M},
year={2023},
title={miRNAs as a Potential Biomarker in the COVID-19 Infection and Complications Course, Severity, and Outcome},
journal={DIAGNOSTICS},
volume={13},
number={6},
pages={-},
document_type={Review},
} 

@ARTICLE{
author={Kovacevic Masa,Jankovic Milena Z,Brankovic Marija,Milicevic Ognjen S,Novakovic Ivana V,Sokic Dragoslav V,Ristic Aleksandar J,Shamsani Jannah,Vojvodic Nikola M},
year={2023},
title={Novel GATOR1 variants in focal epilepsy},
journal={EPILEPSY & BEHAVIOR},
volume={141},
number={},
pages={-},
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={Brankovic Marija,Stefanova Elka D,Mandic Gorana B,Marjanovic Ana,Dobricic Valerija S,Maver Ales,Bergant Gaber,Stevic Zorica D,Jankovic Milena Z,Novakovic Ivana V,Peterlin Borut,Kostic Vladimir K},
year={2022},
title={Analysis of "Clinical Exome" Panel in Serbian Patients with Cognitive Disorders},
journal={GENETIKA-BELGRADE},
volume={54},
number={3},
pages={1351-1364},
document_type={Article},
} 

@ARTICLE{
author={Marjanovic Ana,Dobricic Valerija S,Jecmenica-Lukic Milica V,Stankovic Iva D,Milicevic Ognjen S,Dragasevic-Miskovic Natasa T,Brankovic Marija,Jankovic Milena Z,Novakovic Ivana V,Svetel Marina V,Stefanova Elka D,Kostic Vladimir K},
year={2022},
title={C9ORF72 Repeat Expansion Is Not Associated with Atypical Parkinsonism in the Serbian Population},
journal={GENETIKA-BELGRADE},
volume={54},
number={3},
pages={1313-1330},
document_type={Article},
} 

@ARTICLE{
author={Kovanda Anja,...,Brankovic Marija,Jankovic Milena Z,Svetel Marina V,...,Kostic Vladimir S,Novakovic Ivana V,...,(broj koautora 17)},
year={2022},
title={A multicenter study of genetic testing for Parkinson's disease in the clinical setting},
journal={NPJ PARKINSONS DISEASE},
volume={8},
number={1},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Jovicic-Pavlovic Svetlana M,Simic-Ogrizovic Sanja P,Bukumiric Zoran M,Eric Milena,Pavlovic Natalija,Kotlica Boba,Novakovic Ivana V},
year={2022},
title={Impact of the Fetuin Gene Polymorphisms in Coronary Artery Calcification and Mortality of Patients with Chronic Kidney Disease and Renal Transplant},
journal={GENETIKA-BELGRADE},
volume={54},
number={1},
pages={457-472},
document_type={Article},
} 

@ARTICLE{
author={Brankovic Marija,Dragasevic Natasa T,Dobricic Valerija S,Maver Ales,Bergant Gaber,Petrovic Igor N,Peric Stojan Z,Marjanovic Ana,Jankovic Milena Z,Jancic Jasna B,Novakovic Ivana V,Peterlin Borut,Svetel Marina V,Kostic Vladimir K},
year={2022},
title={Clinical Exome Sequencing in Serbian Patients with Movement Disorders - Single Centre Experience},
journal={GENETIKA-BELGRADE},
volume={54},
number={1},
pages={395-409},
document_type={Article},
} 

@ARTICLE{
author={Peric Stojan Z,Markovic Vladana V,...,Momcilovic Nikola,Savic Andrija,Dragasevic-Miskovic Natasa T,Svetel Marina V,Stevic Zorica D,Bozovic Ivo,Mesaros Sarlota T,Drulovic Jelena S,Basta Ivana Z,Petrovic Igor N,Tamas Olivera S,Mijajlovic Milija D,Novakovic Ivana V,Sokic Dragoslav V,(broj koautora 19)},
year={2022},
title={Phenotypic and Genetic Heterogeneity of Adult Patients with Hereditary Spastic Paraplegia from Serbia},
journal={CELLS},
volume={11},
number={18},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Minic Snezana B,Trpinac Dusan P,Novakovic Ivana V,Cerovac Natasa M,Dobrosavljevic-Vukojevic Danijela,Rosain Jeremie},
year={2022},
title={Challenges in Rare Diseases Diagnostics: Incontinentia Pigmenti with Heterozygous GBA Mutation},
journal={DIAGNOSTICS},
volume={12},
number={7},
pages={-},
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={Dimitrijevic Sanja S,Jekic Biljana B,Cvjeticanin Suzana,Tucovic Aleksandra,Filipovic Tamara N,Novakovic Ivana V,Ivic Bojana S,Nikolic Dimitrije M},
year={2022},
title={KCC2 rs2297201 Gene Polymorphism Might be a Predictive Genetic Marker of Febrile Seizures},
journal={ASN NEURO},
volume={14},
number={},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Maver Ales,Kovanda Anja,Bergant Gaber,Teran Natasa,Vrecar Irena,Brankovic Marija,Jankovic Milena Z,Svetel Marina V,Kostic Vladimir S,Novakovic Ivana V,Racki Valentino,Vuletic Vladimira,Peterlin Borut},
year={2022},
title={Diagnostic yield of whole exome sequencing in early-onset and familial Parkinson's disease in the Balkans},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={30},
number={SUPPL 1},
pages={292-292},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Jankovic Milena Z,Petrovic Bojana,Novakovic Ivana V,Brankovic Slavko,Radosavljevic Natasa R,Nikolic Dejan P},
year={2022},
title={The Genetic Basis of Strokes in Pediatric Populations and Insight into New Therapeutic Options},
journal={INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES},
volume={23},
number={3},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Pereza Nina,Terzic Rifet,Plaseska-Karanfilska Dijana,Miljanovic Olivera,Novakovic Ivana V,Poslon Zeljka,Ostojic Sasa,Peterlin Borut},
year={2022},
title={Current State of Compulsory Basic and Clinical Courses in Genetics for Medical Students at Medical Faculties in Balkan Countries With Slavic Languages},
journal={FRONTIERS IN GENETICS},
volume={12},
number={},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Kresojevic Nikola D,Dobricic Valerija S,Jecmenica-Lukic Milica V,Tomic Aleksandra D,Petrovic Igor N,Dragasevic Natasa T,Perovic Ivana,Marjanovic Ana,Brankovic Marija,Jankovic Milena Z,Novakovic Ivana V,Svetel Marina V,Kostic Vladimir S},
year={2022},
title={Genetic and phenotypic variability in adult patients with Niemann Pick type C from Serbia: single-center experience},
journal={JOURNAL OF NEUROLOGY},
volume={269},
number={6},
pages={3167-3174},
document_type={Article},
} 

@ARTICLE{
author={Sefer Dijana,Miljic Predrag S,Kraguljac-Kurtovic Nada,Bizic-Radulovic Sandra,Bogdanovic Andrija D,Knezevic Vesna,Markovic Dragana C,Beleslin-Cokic Bojana B,Novakovic Ivana V,Marinkovic Jelena M,Lekovic Danijela R,Gotic Mirjana D,Cokic Vladan P},
year={2022},
title={Correlation between leukocyte-platelet aggregates and thrombosis in myeloproliferative neoplasms},
journal={INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY},
volume={44},
number={2},
pages={302-312},
document_type={Article},
} 

@ARTICLE{
author={Svetel Marina V,Dragasevic Natasa T,Petrovic Igor N,Novakovic Ivana V,Tomic Aleksandra D,Kresojevic Nikola D,Stankovic Iva D,Kostic Vladimir K},
year={2021},
title={NBIA Syndromes: A Step Forward from the Previous Knowledge},
journal={NEUROLOGY INDIA},
volume={69},
number={5},
pages={1380-1388},
document_type={Review},
} 

@ARTICLE{
author={Dawod Phepy GA,Jancic Jasna B,Marjanovic Ana,Marjanovic Ana,Jankovic Milena Z,Samardzic Janko M,Dawod Ayman Gamil Anwar,Novakovic Ivana V,Abdel Motaleb Fayda I,Radlovic Vladimir N,Kostic Vladimir S,Nikolic Dejan P},
year={2021},
title={Mutational Analysis and mtDNA Haplogroup Characterization in Three Serbian Cases of Mitochondrial Encephalomyopathies and Literature Review},
journal={DIAGNOSTICS},
volume={11},
number={11},
pages={-},
document_type={Review},
} 

@ARTICLE{
author={Jankovic Milena Z,Novakovic Ivana V,Dawod Phepy GA,Dawod Ayman Gamil Anwar,Drinic Aleksandra,Motaleb Abdel F,Ducic Sinisa,Nikolic Dejan P},
year={2021},
title={Current Concepts on Genetic Aspects of Mitochondrial Dysfunction in Amyotrophic Lateral Sclerosis},
journal={INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES},
volume={22},
number={18},
pages={-},
document_type={Review},
} 

@ARTICLE{
author={Mihaljevic Marina M,Franic Dusanka,Soldatovic Ivan A,Lukic Iva S,Andric-Petrovic Sanja V,Mirjanic Tijana,Stankovic Biljana B,Zukic Branka,Zeljic Katarina,Gasic Vladimir V,Novakovic Ivana V,Pavlovic Sonja T,Adzic Miroslav,Maric Nadja P},
year={2021},
title={The FKBP5 genotype and childhood trauma effects on FKBP5 DNA methylation in patients with psychosis, their unaffected siblings, and healthy controls},
journal={PSYCHONEUROENDOCRINOLOGY},
volume={128},
number={},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Jankovic Milena Z,Novakovic Ivana V,Nikolic Dejan P,Mitrovic-Maksic Jasmina,Brankovic Slavko,Petronic Ivana,Cirovic Dragana,Ducic Sinisa,Grajic Mirko M,Bogicevic Dragana},
year={2021},
title={Genetic and Epigenomic Modifiers of Diabetic Neuropathy},
journal={INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES},
volume={22},
number={9},
pages={-},
document_type={Review},
} 

@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={Pesic Milica,Dragasevic-Miskovic Natasa T,Marjanovic Ana,Dobricic Valerija S,Maksimovic Nela S,Svetel Marina V,Perovic Dijana,Novakovic Ivana V,Cirkovic Sanja,Stankovic Iva D,Kostic Vladimir K},
year={2021},
title={Premutations in the FMR1 gene in Serbian patients with undetermined tremor, ataxia and parkinsonism},
journal={NEUROLOGICAL RESEARCH},
volume={43},
number={4},
pages={321-326},
document_type={Article},
} 

@ARTICLE{
author={Rovcanin Branislav R,Jancic Jasna B,Pajic Jelena R,Rovcanin Marija G,Samardzic Janko M,Djuric Vesna,Nikolic Blazo,Ivancevic Nikola,Novakovic Ivana V,Kostic Vladimir K},
year={2021},
title={Oxidative Stress Profile in Genetically Confirmed Cases of Leber's Hereditary Optic Neuropathy},
journal={JOURNAL OF MOLECULAR NEUROSCIENCE},
volume={71},
number={5},
pages={1070-1081},
document_type={Article},
} 

@ARTICLE{
author={Rovcanin Branislav R,Jancic Jasna B,Samardzic Janko M,Rovcanin Marija G,Nikolic Blazo,Ivancevic Nikola,Novakovic Ivana V,Kostic Vladimir K},
year={2020},
title={In silico model of mtDNA mutations effect on secondary and 3D structure of mitochondrial rRNA and tRNA in Leber's hereditary optic neuropathy},
journal={EXPERIMENTAL EYE RESEARCH},
volume={201},
number={},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Gulic Milica,Maksimovic Nela S,Doklestic Krstina S,Grk Milka B,Svircev M,Dusanovic-Pjevic Marija G,Kulic M,Novakovic Ivana V},
year={2020},
title={Influence of eNOS gene haplotypes and iNOS rs2297518 gene variant on severe complications and mortality in surgical patients with secondary peritonitis},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={28},
number={SUPPL 1},
pages={982-983},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Pesic Milica,Maksimovic Nela S,Aleksic Andjelka,Gulic Milica,Djuranovic Ana S,Grk Milka B,Dusanovic-Pjevic Marija G,Stankovic Iva D,Markovic Vladana V,Marjanovic Ana,Novakovic Ivana V,Dragasevic-Miskovic Natasa T,Kostic Vladimir S},
year={2020},
title={Polymorphisms in genes for proinflammatory cytokines IL-6, IL-1 ss, andTNF-alpha in relation with Parkinson's disease progression},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={28},
number={SUPPL 1},
pages={888-888},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Komnenic-Radovanovic Milica,Novakovic Ivana V,Cuturilo Goran,Ruml-Stojanovic Jelena,Petrovic Bojana,Kontic-Vucinic Olivera},
year={2020},
title={Recurrent congenital microcephaly: a case report},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={28},
number={SUPPL 1},
pages={801-802},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Nikolic Dejan P,Jankovic Milena Z,Petrovic Bojana,Novakovic Ivana V},
year={2020},
title={Genetic Aspects of Inflammation and Immune Response in Stroke},
journal={INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES},
volume={21},
number={19},
pages={-},
document_type={Review},
} 

@ARTICLE{
author={Dawod Phepy GA,Jancic Jasna B,Marjanovic Ana,Marjanovic Ana,Jankovic Milena Z,Samardzic Janko M,Potkonjak Dario,Djuric Vesna,Mesaros Sarlota T,Novakovic Ivana V,Abdel Motaleb Fayda I,Kostic Vladimir S,Nikolic Dejan P},
year={2020},
title={Whole Mitochondrial Genome Analysis in Serbian Cases of Leber's Hereditary Optic Neuropathy},
journal={GENES},
volume={11},
number={9},
pages={-},
document_type={Article},
} 

@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={Ivanovic Vukan,Marjanovic Ana,Bjelica Bogdan,Kacar Aleksandra S,Tubic Radoje M,Jankovic Milena Z,Marjanovic Ana,Novakovic Ivana V,Rakocevic-Stojanovic Vidosava M,Peric Stojan Z},
year={2020},
title={Yield of thePMP22deletion analysis in patients with compression neuropathies},
journal={JOURNAL OF NEUROLOGY},
volume={267},
number={12},
pages={3617-3623},
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={Bjelica Bogdan,Peric Stojan Z,Bozovic Ivo,Basta Ivana Z,Kacar Aleksandra S,Jankovic Milena Z,Brankovic Marija,Palibrk Aleksa,Novakovic Ivana V,Lavrnic Dragana V,Stevic Zorica D,Rakocevic-Stojanovic Vidosava M},
year={2020},
title={Quality of life in hereditary neuropathy with liability to pressure palsies is as impaired as in Charcot-Marie-Tooth disease type 1A},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={27},
number={},
pages={400-400},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Maksic Jasmina,Dobricic Valerija S,Rasulic Lukas G,Maksimovic Nela S,Brankovic Marija,Milic-Rasic Vedrana M,Rakocevic-Stojanovic Vidosava M,Novakovic Ivana V},
year={2020},
title={Analysis of duplications versus deletions in the dystrophin gene in Serbian cohort with dystrophinopathies},
journal={VOJNOSANITETSKI PREGLED},
volume={77},
number={4},
pages={387-394},
document_type={Article},
} 

@ARTICLE{
author={Svetel Marina V,Novakovic Ivana V,Tomic Svetlana,Kresojevic Nikola D,Kostic Vladimir K},
year={2020},
title={Novel PANK2 mutation identified in a patient with pantothenate kinase-associated neurodegeneration},
journal={SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO},
volume={148},
number={3-4},
pages={203-206},
document_type={Article},
} 

@ARTICLE{
author={Bjelica Bogdan,Peric Stojan Z,Basta Ivana Z,Bozovic Ivo,Kacar Aleksandra S,Marjanovic Ana,Ivanovic Vukan,Marjanovic Ana,Jankovic Milena Z,Novakovic Ivana V,Rakocevic-Stojanovic Vidosava M},
year={2020},
title={Neuropathic pain in patients with Charcot-Marie-Tooth type 1A},
journal={NEUROLOGICAL SCIENCES},
volume={41},
number={3},
pages={625-630},
document_type={Article},
} 

@ARTICLE{
author={Jancic Jasna B,Rovcanin Branislav R,Djuric Vesna,Pepic Ana,Samardzic Janko S,Nikolic Blazo,Novakovic Ivana V,Kostic Vladimir S},
year={2020},
title={Analysis of secondary mtDNA mutations in families with Leber's hereditary optic neuropathy: Four novel variants and their association with clinical presentation},
journal={MITOCHONDRION},
volume={50},
number={},
pages={132-138},
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={Peric Stojan Z,Markovic Vladana V,De Vriendt E,Estrada-Cuzcano A,Svetel Marina V,Rakocevic-Stojanovic Vidosava M,Dragasevic-Miskovic Natasa T,Stevic Zorica D,Bozovic Ivo,Mijajlovic Milija D,Mesaros Sarlota T,Drulovic Jelena S,Novakovic Ivana V,Kostic Vladimir S,Jordanova A},
year={2019},
title={phenotypic and genetic heterogeneity of adult patients with hereditary spastic paraplegia from Serbia},
journal={JOURNAL OF THE NEUROLOGICAL SCIENCES},
volume={405},
number={},
pages={-},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Ebrahimi Keramatollah,Sabljak Predrag V,Simic Aleksandar P,Skrobic Ognjan M,Velickovic Dejan,Sljukic Vladimir M,Novakovic Ivana V,Dobricic Valerija S,Micev Marjan T,Pasko Predrag},
year={2019},
title={Significance of KIT and PDGFRA mutations in gastric gastrointestinal stromal tumor imatinib-naive surgically treated patients},
journal={VOJNOSANITETSKI PREGLED},
volume={76},
number={12},
pages={1268-1273},
document_type={Article},
} 

@ARTICLE{
author={Ivancevic Nikola,Cerovac Natasa M,Nikolic Blazo,Cuturilo Goran,Marjanovic Ana,Marjanovic Ana,Novakovic Ivana V},
year={2019},
title={GLUT1 deficiency syndrome: a case report with a novel SLC2A1 mutation},
journal={VOJNOSANITETSKI PREGLED},
volume={76},
number={5},
pages={543-546},
document_type={Article},
} 

@ARTICLE{
author={Svetel Marina V,Tomic Aleksandra D,Dragasevic Natasa T,Petrovic Igor N,Kresojevic Nikola D,Jech Robert,Urgosik Dusan,Banjac Isidora,Vitkovic Jelena,Novakovic Ivana V,Kostic Vladimir S},
year={2019},
title={Clinical course of patients with pantothenate kinase-associated neurodegeneration (PKAN) before and after DBS surgery},
journal={JOURNAL OF NEUROLOGY},
volume={266},
number={12},
pages={2962-2969},
document_type={Article},
} 

@ARTICLE{
author={Dawod Phepy GA,Rovcanin Branislav R,Marjanovic Ana,Marjanovic Ana,Jankovic Milena Z,Novakovic Ivana V,Motaleb Abdel F,Jancic Jasna B,Kostic Vladimir S},
year={2019},
title={Whole mitochondrial genome analysis in carriers of mt3460 mutation with Leber's hereditary optic neuropathy},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={27},
number={},
pages={1836-1837},
document_type={Meeting Abstract},
} 

@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={Marjanovic Ana,Dobricic Valerija S,Brankovic Marija,Jankovic Milena Z,Mandic Gorana B,Stefanova Elka D,Stevic Zorica D,Novakovic Ivana V,Kostic Vladimir S},
year={2019},
title={Analysis of ATXN1 and ATXN2 repeat length in C9ORF72 expansion carriers},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={27},
number={},
pages={961-961},
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={Jankovic Milena Z,Dobricic Valerija S,Marjanovic Ana,Brankovic Marija,Pavlovic Aleksandra M,Dujmovic Irena,Mijajlovic Milija D,Novakovic Ivana V,Kostic Vladimir S},
year={2019},
title={NOTCH3 mutations in Serbian CADASIL patients},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={27},
number={},
pages={293-293},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Brankovic M,Dobricic Valerija S,Svetel Marina V,Peric Stojan Z,Stefanova Elka D,Marjanovic Ana,Petrovic Igor N,Novakovic Ivana V,Kostic Vladimir S},
year={2019},
title={Use of clinical exome analysis in rare neurodegenerative disorders in Serbian population: Firs experience},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={27},
number={},
pages={292-292},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Mitropoulos Konstantinos,...,Dobricic Valerija S,Novakovic Ivana V,Kostic Vladimir S,...,(broj koautora 33)},
year={2019},
title={Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={27},
number={},
pages={252-253},
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={Dawod Phepy GA,Rovcanin Branislav R,Marjanovic Ana,Marjanovic Ana,Jankovic Milena Z,Novakovic Ivana V,Dujmovic Irena,Jancic Jasna B,Kostic Vladimir S},
year={2019},
title={Analysis of mtDNA mutations in Serbian patients with Leber hereditary optic neuropathy},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={27},
number={},
pages={181-181},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Hodzic Alenka,Maver Ales,Zorn Branko,Plaseska-Karanfilska Dijana,Ristanovic Momcilo,Novakovic Ivana V,Peterlin Borut},
year={2019},
title={De novo mutations in idiopathic male infertility},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={27},
number={},
pages={16-17},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Peterlin Borut,Vidmar Lovro,Drulovic Jelena S,Sepcic Juraj,Novakovic Ivana V,Ristic Smiljana,Sega-Jazbec Sasa,Maver Ales},
year={2019},
title={Increased burden of ultra-rare genetic variants in the inflammasome regulatory genes in patients with multiple sclerosis},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={26},
number={},
pages={885-885},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Mandic-Stojmenovic Gorana B,Stefanova Elka D,Novakovic Ivana V,Dobricic Valerija S,Stojkovic Tanja,Kostic Vladimir K},
year={2019},
title={The pattern of inheritance and genetic status in early onset Alzheimer's disease and frontotemporal dementia},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={26},
number={},
pages={120-120},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Vidmar Lovro,Mayer Ales,Drulovic Jelena S,Sepcic Juraj,Novakovic Ivana V,Ristic Smiljana,Sega Sasa,Peterlin Borut},
year={2019},
title={Multiple Sclerosis patients carry an increased burden of exceedingly rare genetic variants in the inflammasome regulatory genes},
journal={SCIENTIFIC REPORTS},
volume={9},
number={},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Svetel Marina V,Hartig Monika B,Cvetkovic Dragana D,Beaubois Cyrielle,Maksic Jasmina,Novakovic Ivana V,Krajinovic Maja,Kostic Vladimir K},
year={2019},
title={Phenotypic expression and founder effect of PANK2 c.1583C > T (p.T528M) mutation in Serbian pantothenate kinase-associated neurodegeneration patients},
journal={ARCHIVES OF BIOLOGICAL SCIENCES},
volume={71},
number={2},
pages={275-280},
document_type={Article},
} 

@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={Dopsaj Violeta,Topic Aleksandra S,Savkovic Miljan,Milinkovic Neda Lj,Novakovic Ivana V,Cujic Danica,Simic-Ogrizovic Sanja P},
year={2019},
title={Associations of Common Variants in HFE and TMPRSS6 Genes with Hepcidin-25 and Iron Status Parameters in Patients with End-Stage Renal Disease},
journal={DISEASE MARKERS},
volume={},
number={},
pages={-},
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={Novakovic Ivana V,Popovic-Kuzmanovic Dragana,Stojanovic Ljudmila,Trajkovic Vladimir S},
year={2018},
title={Study of the polymorphisms in genes IL-17, IL-23, TGFb, RORgT and FOXP3 in Serbian patients with antiphospholipid syndrome},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={26},
number={},
pages={906-906},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Jankovic Milena Z,Dobricic Valerija S,Kresojevic Nikola D,Markovic Vladana V,Petrovic Igor N,Svetel Marina V,Pekmezovic Tatjana D,Novakovic Ivana V,Kostic Vladimir K},
year={2018},
title={Identification of mutations in PARK2 gene in Serbian patients with Parkinson's disease},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={26},
number={},
pages={410-411},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Brankovic Marija,Kresojevic Nikola D,Marjanovic Ana,Novakovic Ivana V,Kostic Vladimir K},
year={2018},
title={NPC1 and NPC2 gene analysis in Serbian patients with Niemann-Pick disease type C},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={26},
number={},
pages={406-406},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Peterlin AM,Maver Ales,Hodzic A,Sega Sasa,Drulovic Jelena S,Novakovic Ivana V,Pekmezovic Tatjana D,Ristic S,Kapovic Miljenko,Peterlin Borut},
year={2018},
title={The burden of rare genetic variants in genes involved in tumor necrosis factor (TNF) signalling pathway in multiple sclerosis (MS)},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={26},
number={},
pages={400-400},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Marjanovic Ana,Dobricic Valerija S,Marjanovic Ivan V,Brankovic Marija,Jankovic Milena Z,Mandic Gorana B,Stevic Zorica D,Novakovic Ivana V,Stefanova Elka D,Kostic Vladimir K},
year={2018},
title={C9ORF72 genetic screening in Serbian patients with neurodegenerative disorders},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={26},
number={},
pages={376-376},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Jankovic Milena Z,Dobricic Valerija S,Kresojevic Nikola D,Markovic Vladana V,Petrovic Igor N,Svetel Marina V,Pekmezovic Tatjana D,Novakovic Ivana V,Kostic Vladimir K},
year={2018},
title={Identification of mutations in the PARK2 gene in Serbian patients with Parkinson's disease},
journal={JOURNAL OF THE NEUROLOGICAL SCIENCES},
volume={393},
number={},
pages={27-30},
document_type={Article},
} 

@ARTICLE{
author={Mitropoulos Konstantinos,...,Dobricic Valerija S,Novakovic Ivana V,Kostic Vladimir S,...,(broj koautora 30)},
year={2018},
title={Genomic Variants in the FTO Gene are Associated with Sporadic Amyotrophic Lateral Sclerosis in Greek Patients},
journal={PUBLIC HEALTH GENOMICS},
volume={21},
number={},
pages={17-17},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Hodzic Alenka,Lavtar Polona,Ristanovic Momcilo,Novakovic Ivana V,Dotlic Jelena R,Peterlin Borut},
year={2018},
title={Genetic variation in the CLOCK gene is associated with idiopathic recurrent spontaneous abortion},
journal={PLOS ONE},
volume={13},
number={5},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Jovicic-Pavlovic Svetlana M,Simic-Ogrizovic Sanja P,Dopsaj Violeta,Novakovic Ivana V,Bukumiric Zoran M,Naumovic Radomir T},
year={2017},
title={Association of Fetuin Gene Polymorphisms with Coronary Artery Calcifications and Mortality in Renal Transplant and Chronic Kidney Disease Patients},
journal={NEPHROLOGY DIALYSIS TRANSPLANTATION},
volume={32},
number={},
pages={733-733},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Dobricic Valerija S,Tomic Aleksandra D,Brankovic Vesna,Kresojevic Nikola D,Jankovic Milena Z,Westenberger Ana,Milic-Rasic Vedrana M,Klein Christine,Novakovic Ivana V,Svetel Marina V,Kostic Vladimir S},
year={2017},
title={GCH1 mutations are common in Serbian patients with dystonia-parkinsonism: Challenging previously reported prevalence rates of DOPA-responsive dystonia},
journal={PARKINSONISM & RELATED DISORDERS},
volume={45},
number={},
pages={81-84},
document_type={Article},
} 

@ARTICLE{
author={Mitropoulos Konstantinos,...,Dobricic Valerija S,Novakovic Ivana V,Kostic Vladimir S,...,(broj koautora 33)},
year={2017},
title={Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients},
journal={HUMAN GENOMICS},
volume={11},
number={},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Mihaljevic Marina M,Franic Dusica,Soldatovic Ivan A,Andric Sanja V,Mirjanic Tijana,Novakovic Ivana V,Adzic Miroslav,Maric Nadja P},
year={2017},
title={Fkbp5 Epigenetic Changes in Schizophrenia: Similarity to Stress-Related Conditions},
journal={EUROPEAN NEUROPSYCHOPHARMACOLOGY},
volume={27},
number={},
pages={S461-S462},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Mihaljevic Marina M,Andric Sanja V,Mirjanic Tijana,Novakovic Ivana V,Maric-Bojovic Nadja P},
year={2017},
title={Single Nucleotide Polymorphism of the FK506-Binding Protein 51 (FKBP5) Gene Is Associated with Increased Risk for Psychosis and Impaired Social Cognition in a Serbian Population},
journal={EUROPEAN NEUROPSYCHOPHARMACOLOGY},
volume={27},
number={},
pages={S258-S259},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Jovicic-Pavlovic Svetlana M,Simic-Ogrizovic Sanja P,Dopsaj Violeta,Novakovic Ivana V,Bukumiric Zoran M,Naumovic Radomir T},
year={2017},
title={Influence of Gene Polymorphisms on Serum Fetuin-A Levels and Vascular Calcifications in Renal Transplant and Chronic Kidney Disease Patients},
journal={TRANSPLANT INTERNATIONAL},
volume={30},
number={},
pages={269-270},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Mihaljevic Marina M,Zeljic Katarina,Soldatovic Ivan A,Andric Sanja V,Mirjanic Tijana,Richards Alexander,Mantripragada Kiran,Pekmezovic Tatjana D,Novakovic Ivana V,Maric Nadja P},
year={2017},
title={The emerging role of the FKBP5 gene polymorphisms in vulnerability-stress model of schizophrenia: further evidence from a Serbian population},
journal={EUROPEAN ARCHIVES OF PSYCHIATRY AND CLINICAL NEUROSCIENCE},
volume={267},
number={6},
pages={527-539},
document_type={Article},
} 

@ARTICLE{
author={Maver Ales,...,Drulovic Jelena S,Pekmezovic Tatjana D,Novakovic Ivana V,...,(broj koautora 19)},
year={2017},
title={Identification of rare genetic variation of NLRP1 gene in familial multiple sclerosis},
journal={SCIENTIFIC REPORTS},
volume={7},
number={},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Mihaljevic Marina M,Franic Dusica,Soldatovic Ivan A,Andric Sanja V,Mirjanic Tijana,Novakovic Ivana V,Adzic Miroslav,Maric Nadja P},
year={2017},
title={Allele-Specific and Trauma-Related Epigenetic Changes in the FKBP5 Gene: Differences Between Psychotic Patients and Healthy Controls},
journal={SCHIZOPHRENIA BULLETIN},
volume={43},
number={},
pages={S195-S195},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Maric Nadja P,Mihaljevic Marina M,Franic Dusanka,Soldatovic Ivan A,Andric Sanja V,Lukic Iva S,Mirjanic Tijana,Stankovic Biljana B,Zukic Branka,Dobricic Valerija S,Novakovic Ivana V,Pavlovic Sonja T,Adzic Miroslav},
year={2017},
title={The Signature of Trauma in Psychosis: a Preliminary Genetic and Epigenetic Analyses of FK506-Binding Protein 5 Regulation},
journal={SCHIZOPHRENIA BULLETIN},
volume={43},
number={},
pages={S66-S66},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Hodzic Alenka,Ristanovic Momcilo,Zorn Branko,Tulic Cane Dz,Maver Ales,Novakovic Ivana V,Plaseska-Karanfilska Dijana,Peterlin Borut},
year={2017},
title={Genetic variation in leptin and leptin receptor genes as a risk factor for idiopathic male infertility},
journal={ANDROLOGY},
volume={5},
number={1},
pages={70-74},
document_type={Article},
} 

@ARTICLE{
author={Kostic Milutin V,Munjiza Ana M,Pesic Danilo R,Peljto Amir N,Novakovic Ivana V,Dobricic Valerija S,Lecic-Tosevski Dusica M,Mijajlovic Milija D},
year={2017},
title={A pilot study on predictors of brainstem raphe abnormality in patients with major depressive disorder},
journal={JOURNAL OF AFFECTIVE DISORDERS},
volume={209},
number={},
pages={66-70},
document_type={Article},
} 

@ARTICLE{
author={Svetel Marina V,Tomic Aleksandra D,Mijajlovic Milija D,Dobricic Valerija S,Novakovic Ivana V,Pekmezovic Tatjana D,Brajkovic Lela,Kostic Vladimir S},
year={2017},
title={Transcranial sonography in dopa-responsive dystonia},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={24},
number={1},
pages={161-166},
document_type={Article},
} 

@ARTICLE{
author={Peric Stojan Z,Mandic-Stojmenovic Gorana B,Ilic Vera,Kovacevic Masa,Parojcic Aleksandra,Dobricic Valerija S,Pesovic Jovan,Novakovic Ivana V,Savic-Pavicevic Dusanka Lj,Rakocevic-Stojanovic Vidosava M},
year={2016},
title={Clusters of cognitive impairment among different forms of myotonic dystrophies},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={23},
number={},
pages={550-550},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Radunovic Milena,Tomanovic Nada R,Novakovic Ivana V,Boricic Ivan V,Milenkovic Sanja M,Dimitrijevic Milovan V,Radojevic-Skodric Sanja M,Bogdanovic Ljiljana M,Basta-Jovanovic Gordana M},
year={2016},
title={Cytomegalovirus induces Interleukin-6 mediated inflammatory response in salivary gland cancer},
journal={JOURNAL OF BUON},
volume={21},
number={6},
pages={1530-1536},
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={Peric Stojan Z,Vujnic Milorad,Dobricic Valerija S,Marjanovic Ana,Basta Ivana Z,Novakovic Ivana V,Lavrnic Dragana V,Rakocevic-Stojanovic Vidosava M},
year={2016},
title={Five-year study of quality of life in myotonic dystrophy},
journal={ACTA NEUROLOGICA SCANDINAVICA},
volume={134},
number={5},
pages={346-351},
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={Stefanova Elka D,Mandic Gorana B,Dobricic Valerija S,Stojkovic Tanja,Jankovic Milena Z,Novakovic Ivana V,Kostic Vladimir S},
year={2016},
title={Genetic mutations in Frontemporal dementia - report from the memory clinic from Serbia},
journal={JOURNAL OF NEUROCHEMISTRY},
volume={138},
number={},
pages={326-326},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Kostic Milutin V,Canu Elisa,Agosta Federica,Munjiza Ana M,Novakovic Ivana V,Dobricic Valerija S,Ferraro Pilar Maria,Miler-Jerkovic Vera M,Pekmezovic Tatjana D,Lecic-Tosevski Dusica M,Filippi Massimo},
year={2016},
title={The Cumulative Effect of Genetic Polymorphisms on Depression and Brain Structural Integrity},
journal={HUMAN BRAIN MAPPING},
volume={37},
number={6},
pages={2173-2184},
document_type={Article},
} 

@ARTICLE{
author={Dobricic Valerija S,Kresojevic Nikola D,Marjanovic Ana,Tomic Aleksandra D,Svetel Marina V,Novakovic Ivana V,Kostic Vladimir S},
year={2016},
title={HPCA-related dystonia: Too rare to be found?},
journal={MOVEMENT DISORDERS},
volume={31},
number={7},
pages={1071-1071},
document_type={Letter},
} 

@ARTICLE{
author={Sefer Dijana,Miljic Predrag S,Kraguljac-Kurtovic Nada,Bizic-Radulovic Sandra,Cokic Vladan P,Markovic Dragana C,Beleslin-Cokic Bojana B,Novakovic Ivana V,Marinkovic-Eric Jelena M,Lekovic Danijela R,Bodrozic Jelena N,Gotic Mirjana D},
year={2016},
title={Predictive Role of Circulating Leucocyte-Platelet Aggregates for Thromboembolic Complications in Philadelphia-Negative Myeloproliferative Neoplasms: a Prospective Study},
journal={HAEMATOLOGICA},
volume={101},
number={},
pages={266-266},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Radunovic Milena,Nikolic Nadja S,Milenkovic Sanja M,Tomanovic Nada R,Boricic Ivan V,Dimitrijevic Milovan V,Novakovic Ivana V,Basta-Jovanovic Gordana M},
year={2016},
title={The MMP-2 and MMP-9 promoter polymorphisms and susceptibility to salivary gland cancer},
journal={JOURNAL OF BUON},
volume={21},
number={3},
pages={597-602},
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={Dujmovic Irena,Jancic Jasna B,Dobricic Valerija S,Jankovic Slavko M,Novakovic Ivana V,Comabella Manuel,Drulovic Jelena S},
year={2016},
title={Are Leber's mitochondial DNA mutations associated with aquaporin-4 autoimmunity?},
journal={MULTIPLE SCLEROSIS JOURNAL},
volume={22},
number={3},
pages={393-394},
document_type={Letter},
} 

@ARTICLE{
author={Cuturilo Goran,Kontic-Vucinic Olivera,Novakovic Ivana V,Ignjatovic Svetlana D,Mijovic Marija,Sulovic Nenad,Vukolic D,Komnenic Milica,Tadic Jasmina,Cetkovic Aleksandar,Belic Aleksandra,Ljubic Aleksandar D},
year={2016},
title={Clients' Perception of Outcome of Team-Based Prenatal and Reproductive Genetic Counseling in Serbian Service Using the Perceived Personal Control (PPC) Questionnaire},
journal={JOURNAL OF GENETIC COUNSELING},
volume={25},
number={1},
pages={189-197},
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={Kostic Milutin V,Canu Elisa,Munjiza Ana M,Agosta Federica,Novakovic Ivana V,Dobricic Valerija S,Jerkovic Vera M,Miler-Jerkovic Vera M,Pekmezovic Tatjana D,Lecic-Tosevski Dusica M,Filippi Massimo},
year={2015},
title={Effect of accumulation of 5-HTTLPR, BDNF Vall66Met and COMT Val158Met polymorphisms on brain morphology in patients with major depressive disorder},
journal={EUROPEAN NEUROPSYCHOPHARMACOLOGY},
volume={25},
number={},
pages={S395-S395},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Mihaljevic Marina M,Pekmezovic Tatjana D,Andric Sanja V,Mirjanic Tijana,Novakovic Ivana V,Maric Nadja P},
year={2015},
title={Subclinical psychotic experiences in healthy adults: relationship between genetic variants of FKBP5 gene, neuroticism and childhood trauma},
journal={EUROPEAN NEUROPSYCHOPHARMACOLOGY},
volume={25},
number={},
pages={S177-S177},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Canu Elisa,Kostic Milutin V,Munjiza Ana M,Agosta Federica,Novakovic Ivana V,Dobricic Valerija S,Miler-Jerkovic Vera M,Pekmezovic Tatjana D,Lecic-Tosevski Dusica M,Filippi Massimo},
year={2015},
title={Three-way interaction of 5-HTTLPR, BDNF Vall66Met and COMT Val158Met polymorphisms and its effect on regional gray matter volume in patients with major depressive disorder},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={22},
number={},
pages={629-629},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Mandic-Stojmenovic Gorana B,Stefanova Elka D,Dobricic Valerija S,Novakovic Ivana V,Stojkovic Tanja,Jesic Aleksandar Z,Kostic Vladimir S},
year={2015},
title={Screening for C9orf72 Expansion Mutation in Serbian Patients with Early-Onset Dementia},
journal={DEMENTIA AND GERIATRIC COGNITIVE DISORDERS},
volume={40},
number={5-6},
pages={358-365},
document_type={Article},
} 

@ARTICLE{
author={Dobricic Valerija S,Kresojevic Nikola D,Zarkovic Milena,Tomic Aleksandra D,Marjanovic Ana,Westenberger Ana,Cvetkovic Dragana D,Svetel Marina V,Novakovic Ivana V,Kostic Vladimir S},
year={2015},
title={Phenotype of non-c.907_909delGAG mutations in TOR1A: DYT1 dystonia revisited},
journal={PARKINSONISM & RELATED DISORDERS},
volume={21},
number={10},
pages={1256-1259},
document_type={Article},
} 

@ARTICLE{
author={Rakocevic-Stojanovic Vidosava M,Peric Stojan Z,Basta Ivana Z,Dobricic Valerija S,Ralic Vesna,Kacar Aleksandra S,Peric Marina,Novakovic Ivana V},
year={2015},
title={Variability of multisystemic features in myotonic dystrophy type 1-lessons from Serbian registry},
journal={NEUROLOGICAL RESEARCH},
volume={37},
number={11},
pages={939-944},
document_type={Article},
} 

@ARTICLE{
author={Dzoljic Eleonora D,Novakovic Ivana V,Krajinovic Maja,Grbatinic Ivan I,Kostic Vladimir S},
year={2015},
title={Pharmacogenetics of drug response in Parkinson's disease},
journal={INTERNATIONAL JOURNAL OF NEUROSCIENCE},
volume={125},
number={9},
pages={635-644},
document_type={Review},
} 

@ARTICLE{
author={Mihaljevic Marina M,Andric Sanja V,Mirjanic Tijana,Soldatovic Ivan A,Novakovic Ivana V,Maric Nadja P},
year={2015},
title={Further evidence of the impact of the risk variant FKBP5 gene in schizophrenia in a Serbian sample of patients, siblings and controls},
journal={EUROPEAN NEUROPSYCHOPHARMACOLOGY},
volume={25},
number={},
pages={S16-S17},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Vujnic Milorad,Peric Stojan Z,Popovic Srdjan S,Raseta Nela,Ralic Vesna,Dobricic Valerija S,Novakovic Ivana V,Rakocevic-Stojanovic Vidosava M},
year={2015},
title={Metabolic syndrome in patients with myotonic dystrophy type 1},
journal={MUSCLE & NERVE},
volume={52},
number={2},
pages={273-277},
document_type={Article},
} 

@ARTICLE{
author={Pajic Jelena R,Rakic Boban M,Rovcanin Branislav R,Jovicic Dubravka,Novakovic Ivana V,Milovanovic Aleksandar PS,Pajic Vesna S},
year={2015},
title={Inter-individual variability in the response of human peripheral blood lymphocytes to ionizing radiation: comparison of the dicentric and micronucleus assays},
journal={RADIATION AND ENVIRONMENTAL BIOPHYSICS},
volume={54},
number={3},
pages={317-325},
document_type={Article},
} 

@ARTICLE{
author={Kresojevic Nikola D,Jankovic Milena Z,Petrovic Igor N,Kumar Kishore R,Dragasevic Natasa T,Dobricic Valerija S,Novakovic Ivana V,Svetel Marina V,Klein Christine,Pekmezovic Tatjana D,Kostic Vladimir S},
year={2015},
title={Presenting symptoms of GBA-related Parkinson's disease},
journal={PARKINSONISM & RELATED DISORDERS},
volume={21},
number={7},
pages={804-807},
document_type={Article},
} 

@ARTICLE{
author={Kresojevic Nikola D,Jankovic Milena Z,Petrovic Igor N,Kumar Kishore R,Dragasevic Natasa T,Dobricic Valerija S,Novakovic Ivana V,Svetel Marina V,Klein Christine,Pekmezovic Tatjana D,Kostic Vladimir K},
year={2015},
title={Presenting symptoms of GBA-related Parkinson's disease},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={22},
number={},
pages={437-437},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Svetel Marina V,Tomic Aleksandra D,Dobricic Valerija S,Novakovic Ivana V,Dragasevic-Miskovic Natasa T,Petrovic Igor N,Kostic Vladimir K},
year={2015},
title={Dopa-responsive dystonia in the Serbian population: clinical and genetical characteristics},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={22},
number={},
pages={393-393},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Jankovic Milena Z,Kresojevic Nikola D,Dobricic Valerija S,Markovic Vladana V,Petrovic Igor N,Novakovic Ivana V,Kostic Vladimir S},
year={2015},
title={Identification of novel mutations in LRRK2 gene in patients with Parkinson's disease},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={22},
number={},
pages={354-354},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Dobricic Valerija S,Kresojevic Nikola D,Zarkovic Milena,Tomic Aleksandra D,Svetel Marina V,Novakovic Ivana V,Kostic Vladimir S},
year={2015},
title={A novel TOR1A mutation in a Serbian patient with cervical dystonia},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={22},
number={},
pages={260-260},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Peric Stojan Z,Paunic Teodora,Dobricic Valerija S,Novakovic Ivana V,Basta Ivana Z,Lavrnic Dragana V,Rakocevic-Stojanovic Vidosava M},
year={2015},
title={Echocardiography in patients with myotonic dystrophy type 1},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={22},
number={},
pages={205-205},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Jankovic Milena Z,Kresojevic Nikola D,Dobricic Valerija S,Markovic Vladana V,Petrovic Igor N,Novakovic Ivana V,Kostic Vladimir S},
year={2015},
title={Identification of novel variants in LRRK2 gene in patients with Parkinson's disease in Serbian population},
journal={JOURNAL OF THE NEUROLOGICAL SCIENCES},
volume={353},
number={1-2},
pages={59-62},
document_type={Article},
} 

@ARTICLE{
author={Djukic Tatjana I,Simic Tatjana P,Radic Tanja M,Matic Marija G,Pljesa-Ercegovac Marija S,Suvakov Sonja R,Coric Vesna M,Pekmezovic Tatjana D,Novakovic Ivana V,Dragicevic Dejan P,Savic-Radojevic Ana R},
year={2015},
title={GSTO1*C/GSTO2*G haplotype is associated with risk of transitional cell carcinoma of urinary bladder},
journal={INTERNATIONAL UROLOGY AND NEPHROLOGY},
volume={47},
number={4},
pages={625-630},
document_type={Article},
} 

@ARTICLE{
author={Milic-Rasic Vedrana M,Vojinovic Dina,Pesovic Jovan,Mijalkovic G,Lukic V,Mladenovic Jelena M,Kosac Ana P,Novakovic Ivana V,Maksimovic Nela S,Romac Stanka P,Todorovic Slobodanka,Pavicevic Savic D},
year={2014},
title={Intellectual Ability in the Duchenne Muscular Dystrophy and Dystrophin Gene Mutation Location},
journal={BALKAN JOURNAL OF MEDICAL GENETICS},
volume={17},
number={2},
pages={25-35},
document_type={Article},
} 

@ARTICLE{
author={Svetel Marina V,Dobricic Valerija S,Novakovic Ivana V,Dragasevic Natasa T,Petrovic Igor N,Kostic Vladimir S},
year={2014},
title={Clinical and genetic characteristics of dopa-responsive dystonia in Serbian population},
journal={JOURNAL OF NEUROLOGY},
volume={261},
number={},
pages={S433-S433},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Vujnic Milorad,Peric Stojan Z,Dobricic Valerija S,Ralic Vesna,Novakovic Ivana V,Rakocevic-Stojanovic Vidosava M},
year={2014},
title={Metabolic syndrome in patients with myotonic dystrophy type 1},
journal={JOURNAL OF NEUROLOGY},
volume={261},
number={},
pages={S347-S347},
document_type={Meeting Abstract},
} 

@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={Dobricic Valerija S,Kresojevic Nikola D,Westenberger Ana,Svetel Marina V,Tomic Aleksandra D,Ralic Vesna,Petrovic Igor N,Jecmenica-Lukic Milica V,Lohmann Katja,Novakovic Ivana V,Klein Christine,Kostic Vladimir S},
year={2014},
title={De Novo Mutation in the GNAL Gene Causing Seemingly Sporadic Dystonia in a Serbian Patient},
journal={MOVEMENT DISORDERS},
volume={29},
number={9},
pages={1190-1193},
document_type={Article},
} 

@ARTICLE{
author={Cetkovic Aleksandar,Kastratovic Biljana,Novakovic Ivana V},
year={2014},
title={Prospective study of perinatal outcome in pregnancies with primary antiphospholipid syndrome},
journal={VOJNOSANITETSKI PREGLED},
volume={71},
number={8},
pages={742-745},
document_type={Article},
} 

@ARTICLE{
author={Svetel Marina V,Dobricic Valerija S,Novakovic Ivana V,Dragasevic Natasa T,Petrovic Igor N,Kostic Vladimir S},
year={2014},
title={Clinical and genetic characteristics of dopa-responsive dystonia in a Serbian population},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={21},
number={},
pages={668-668},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Vujnic Milorad,Peric Stojan Z,Dobricic Valerija S,Ralic Vesna,Novakovic Ivana V,Rakocevic-Stojanovic Vidosava M},
year={2014},
title={Metabolic syndrome in patients with myotonic dystrophy type 1},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={21},
number={},
pages={528-528},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Veselinovic Nikola D,Pavlovic Aleksandra M,Petrovic Boris,Ristic Aleksandar J,Novakovic Ivana V,Svabic-Medjedovic Tamara S,Pavlovic Dragan,Sternic Nadezda M},
year={2014},
title={Altered Basal Ganglia Echogenicity Early in Sporadic Creutzfeldt-Jakob Disease},
journal={COGNITIVE AND BEHAVIORAL NEUROLOGY},
volume={27},
number={1},
pages={48-50},
document_type={Article},
} 

@ARTICLE{
author={Novakovic Ivana V,Maksimovic Nela S,Pavlovic Aleksandra,Zarkovic Milena,Rovcanin Branislav R,Mirkovic Dusko S,Pekmezovic Tatjana D,Cvetkovic Dragana D},
year={2014},
title={Introduction to Molecular Genetic Diagnostics},
journal={JOURNAL OF MEDICAL BIOCHEMISTRY},
volume={33},
number={1},
pages={3-7},
document_type={Review},
} 

@ARTICLE{
author={Maksimovic Nela S,Novakovic Ivana V,Ralic Vesna,Stefanova Elka D},
year={2013},
title={Distribution of Apolipoprotein E Gene Polymorphism in Students and in High-Educated Elderly from Serbia},
journal={GENETIKA-BELGRADE},
volume={45},
number={3},
pages={865-872},
document_type={Article},
} 

@ARTICLE{
author={Svetel Marina V,Pekmezovic Tatjana D,Markovic Vladana V,Novakovic Ivana V,Dobricic Valerija S,Djuric Gordana M,Stefanova Elka D,Kostic Vladimir S},
year={2013},
title={No Association between Brain-Derived Neurotrophic Factor G196A Polymorphism and Clinical Features of Parkinson's Disease},
journal={EUROPEAN NEUROLOGY},
volume={70},
number={5-6},
pages={257-262},
document_type={Article},
} 

@ARTICLE{
author={Mijajlovic Milija D,Kresojevic Nikola D,Peric Stojan Z,Pavlovic Aleksandra M,Svetel Marina V,Jankovic Milena Z,Dobricic Valerija S,Novakovic Ivana V,Lakocevic Milan B,Kostic Vladimir S},
year={2013},
title={Transcranial brain parenchyma sonography in Parkinson's disease with glucocerebrosidase mutations},
journal={CEREBROVASCULAR DISEASES},
volume={35},
number={},
pages={59-59},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Pavlovic Aleksandra M,Dobricic Valerija S,Semnic Robert R,Lackovic Vesna B,Novakovic Ivana V,Bajcetic Milos I,Sternic Nadezda M},
year={2013},
title={A novel Notch3 Gly89Cys mutation in a Serbian CADASIL family},
journal={ACTA NEUROLOGICA BELGICA},
volume={113},
number={3},
pages={299-302},
document_type={Article},
} 

@ARTICLE{
author={Svetel Marina V,Djuric Gordana M,Novakovic Ivana V,Dobricic Valerija S,Stefanova Elka D,Kresojevic Nikola D,Tomic Aleksandra D,Jankovic Milena Z,Petrovic Igor N,Pekmezovic Tatjana D,Kostic Vladimir S},
year={2013},
title={A common polymorphism in the brain-derived neurotrophic factor gene in patients with adult-onset primary focal and segmental dystonia},
journal={ACTA NEUROLOGICA BELGICA},
volume={113},
number={3},
pages={243-245},
document_type={Article},
} 

@ARTICLE{
author={Tomic Aleksandra D,Dobricic Valerija S,Novakovic Ivana V,Svetel Marina V,Pekmezovic Tatjana D,Kresojevic Nikola D,Potrebic Aleksandra,Kostic Vladimir S},
year={2013},
title={Mutational analysis of ATP7B gene and the genotype-phenotype correlation in patients with Wilson's disease in Serbia},
journal={VOJNOSANITETSKI PREGLED},
volume={70},
number={5},
pages={457-462},
document_type={Article},
} 

@ARTICLE{
author={Kresojevic Nikola D,Mijajlovic Milija D,Peric Stojan Z,Pavlovic Aleksandra M,Svetel Marina V,Jankovic Milena Z,Dobricic Valerija S,Novakovic Ivana V,Lakocevic Milan B,Klein Christine,Kostic Vladimir S},
year={2013},
title={Transcranial sonography in patients with Parkinson's disease with glucocerebrosidase mutations},
journal={PARKINSONISM & RELATED DISORDERS},
volume={19},
number={4},
pages={431-435},
document_type={Article},
} 

@ARTICLE{
author={Dobricic Valerija S,Kresojevic Nikola D,Svetel Marina V,Jankovic Milena Z,Petrovic Igor N,Tomic Aleksandra D,Novakovic Ivana V,Kostic Vladimir S},
year={2013},
title={Mutation screening of the DYT6/THAP1 gene in Serbian patients with primary dystonia},
journal={JOURNAL OF NEUROLOGY},
volume={260},
number={4},
pages={1037-1042},
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={Papassotiropoulos A,Stefanova Elka D,...,Novakovic Ivana V,...,Scheffler K,(broj koautora 19)},
year={2013},
title={A genome-wide survey and functional brain imaging study identify CTNNBL1 as a memory-related gene},
journal={MOLECULAR PSYCHIATRY},
volume={18},
number={2},
pages={255-263},
document_type={Article},
} 

@ARTICLE{
author={Hodzic Alenka,Ristanovic Momcilo,Zorn Branko,Tulic Cane Dz,Maver Ales,Novakovic Ivana V,Peterlin Borut},
year={2013},
title={Genetic Variation in Circadian Rhythm Genes CLOCK and ARNTL as Risk Factor for Male Infertility},
journal={PLOS ONE},
volume={8},
number={3},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Popovic-Kuzmanovic Dragana,Novakovic Ivana V,Stojanovic Ljudmila,Aksentijevich Ivona,Zogovic Nevena S,Tovilovic Gordana I,Trajkovic Vladimir S},
year={2013},
title={Increased activity of interleukin-23/interleukin-17 cytokine axis in primary antiphospholipid syndrome},
journal={IMMUNOBIOLOGY},
volume={218},
number={2},
pages={186-191},
document_type={Article},
} 

@ARTICLE{
author={Hsu Sandy Chan,...,Dobricic Valerija S,...,Jankovic Milena Z,...,Kostic Vladimir S,...,Novakovic Ivana V,...,(broj koautora 52)},
year={2013},
title={Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification},
journal={NEUROGENETICS},
volume={14},
number={1},
pages={11-22},
document_type={Article},
} 

@ARTICLE{
author={Radojevic-Skodric Sanja M,Brasanac Dimitrije C,Novakovic Ivana V,Bogdanovic Ljiljana M,Krstic Z,Basta-Jovanovic Gordana M},
year={2012},
title={Amplification of cyclin A gene in Wilms tumor},
journal={VIRCHOWS ARCHIV},
volume={461},
number={},
pages={S220-S220},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Lackovic Vesna B,Bajcetic Milos I,Lackovic Maja M,Novakovic Ivana V,Labudovic-Borovic Milica M,Pavlovic Aleksandra M,Zidverc-Trajkovic Jasna J,Dzoljic Eleonora D,Rovcanin Branislav R,Sternic Nadezda M,Kostic Vladimir S},
year={2012},
title={Skin and Sural Nerve Biopsies: Ultrastructural Findings in the First Genetically Confirmed Cases of CADASIL in Serbia},
journal={ULTRASTRUCTURAL PATHOLOGY},
volume={36},
number={5},
pages={325-335},
document_type={Article},
} 

@ARTICLE{
author={Dobricic Valerija S,Stefanova Elka D,Jankovic Milena Z,Gurunlian Nicole,Novakovic Ivana V,Hardy John,Kostic Vladimir S,Guerreiro Rita},
year={2012},
title={Genetic testing in familial and young-onset Alzheimer's disease: mutation spectrum in a Serbian cohort},
journal={NEUROBIOLOGY OF AGING},
volume={33},
number={7},
pages={-},
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={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={Pavlovic Aleksandra M,Pekmezovic Tatjana D,Obrenovic Radmila R,Novakovic Ivana V,Tomic Gordana G,Mijajlovic Milija D,Sternic Nadezda M},
year={2011},
title={Increased total homocysteine level is associated with clinical status and severity of white matter changes in symptomatic patients with subcortical small vessel disease},
journal={CLINICAL NEUROLOGY AND NEUROSURGERY},
volume={113},
number={9},
pages={711-715},
document_type={Article},
} 

@ARTICLE{
author={Svetel Marina V,Novakovic Ivana V,Hoertnagel K,Hartig Monika B,Kozic Dusko B,Pekmezovic Tatjana D,Dragasevic Natasa T,Petrovic Igor N,Kostic Vladimir S},
year={2011},
title={Mutation and Founder Effect Studies in Pkan Patients with Serbian Origin: Report of Five Cases},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={18},
number={},
pages={516-516},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Tomic Aleksandra D,Svetel Marina V,Novakovic Ivana V,Dobricic Valerija S,Kresojevic Nikola D,Kostic Vladimir S},
year={2011},
title={Mutational Analysis of ATP7B Gene and Genotype-Phenotype Correlation in Patients with Wilson's Disease From Serbia},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={18},
number={},
pages={488-488},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Simeunovic Slavko D,Nedeljkovic Srecko I,Milincic Zeljka D,Vukotic Milija,Novakovic Ivana V,Majkic-Singh Nada T,Nikolic Dejan P,Risimic Dijana S,Simeunovic Dejan S,Petronic Ivana,Radlovic Vladimir N},
year={2011},
title={Anthropometric and Lipid Parameters Trends in School Children: One Decade of YUSAD Study},
journal={SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO},
volume={139},
number={7-8},
pages={465-469},
document_type={Article},
} 

@ARTICLE{
author={Kostic Vladimir S,Jecmenica-Lukic Milica V,Novakovic Ivana V,Dobricic Valerija S,Brajkovic Lela,Krajinovic Maja,Klein Christine,Pavlovic Aleksandra M},
year={2011},
title={Exclusion of linkage to chromosomes 14q, 2q37 and 8p21.1-q11.23 in a Serbian family with idiopathic basal ganglia calcification},
journal={JOURNAL OF NEUROLOGY},
volume={258},
number={9},
pages={1637-1642},
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={Milincic Zeljka D,Nikolic Dejan P,Simeunovic Slavko D,Novakovic Ivana V,Petronic Ivana,Risimic Dijana S,Simeunovic Dejan S},
year={2011},
title={School children systolic and diastolic blood pressure values: YUSAD study},
journal={CENTRAL EUROPEAN JOURNAL OF MEDICINE},
volume={6},
number={5},
pages={634-639},
document_type={Article},
} 

@ARTICLE{
author={Nikolic Dejan P,Petronic Ivana,Milincic Zeljka D,Simeunovic Slavko D,Novakovic Ivana V,Nedeljkovic Srecko I,Cirovic Dragana,Janic Nenad},
year={2011},
title={Evaluation of recreational physical activity correlation and influence on lipid fractions in school children: YUSAD study},
journal={MEDICINA DELLO SPORT},
volume={64},
number={1},
pages={55-62},
document_type={Article},
} 

@ARTICLE{
author={Puzovic Dragana Z,Dunjic Dusan J,Popovic Branka M,Stojkovic Oliver V,Novakovic Ivana V,Milasin Jelena M},
year={2011},
title={STR LOCI D19S216, D20S502 and D20S842 Analysis in the Serbian Population Using Dentin Dna},
journal={ARCHIVES OF BIOLOGICAL SCIENCES},
volume={63},
number={1},
pages={55-58},
document_type={Article},
} 

@ARTICLE{
author={Kresojevic Nikola D,Svetel Marina V,Dobricic Valerija S,Novakovic Ivana V,Stojkovic Tanja,Kostic Vladimir S},
year={2011},
title={Clinical evaluation of DYT6 dystonia in Serbia},
journal={JOURNAL OF NEUROLOGY},
volume={258},
number={},
pages={83-84},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Stojkovic Tanja,Svetel Marina V,Dobricic Valerija S,Novakovic Ivana V,Kostic Vladimir S},
year={2011},
title={Cerebellar ataxia and epilepsy caused by hereditary folate malabsorption},
journal={JOURNAL OF NEUROLOGY},
volume={258},
number={},
pages={82-83},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Papassotiropoulos A,Henke K,Stefanova Elka D,Aerni A,Mueller A,Demougin P,Vogler C,Sigmund JC,Gschwind L,Huynh K-D,Coluccia D,Mondadori CR,Haenggi J,Buchmann A,Kostic Vladimir S,Novakovic Ivana V,van den Bussche H,Kaduszkiewicz H,Weyerer S,Bickel H,Riedel-Heller S,Pentzek M,Wiese B,Dichgans M,Wagner M,Jessen F,Maier W,de Quervain DJ-F},
year={2011},
title={A genome-wide survey of human short-term memory},
journal={MOLECULAR PSYCHIATRY},
volume={16},
number={2},
pages={184-192},
document_type={Article},
} 

@ARTICLE{
author={Jecmenica-Lukic Milica V,Petrovic Igor N,Dobricic Valerija S,Novakovic Ivana V,Kostic Vladimir S},
year={2010},
title={Exclusion of linkage to chromosome 14q in Serbian family with idiopathic basal ganglia calcification},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={17},
number={},
pages={381-381},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Krcunovic Zorica,Novakovic Ivana V,Maksimovic Nela S,Bukvic Danica,Simic-Ogrizovic Sanja P,Jankovic Slavenka M,Djukanovic Ljubica D,Cvetkovic Dragana D},
year={2010},
title={Genetic Clues to the Etiology of Balkan Endemic Nephropathy: Investigating the Role of Ace and AT1R Polymorphisms},
journal={ARCHIVES OF BIOLOGICAL SCIENCES},
volume={62},
number={4},
pages={957-965},
document_type={Article},
} 

@ARTICLE{
author={Simeunovic Slavko D,Milincic Zeljka D,Nikolic Dejan P,Simeunovic Dejan S,Arandjelovic Dragana,Novakovic Ivana V,Petronic Ivana,Risimic Dijana S,Nedeljkovic Srecko I,Vukotic Milija},
year={2010},
title={Physical activity evaluation in Yugoslav Study of the Precursors of Atherosclerosis in School Children - YUSAD study},
journal={ARCHIVES OF MEDICAL SCIENCE},
volume={6},
number={6},
pages={874-878},
document_type={Article},
} 

@ARTICLE{
author={Popovic Branka M,Jekic Biljana B,Novakovic Ivana V,Lukovic Ljiljana F,Konstantinovic Vitomir S,Babic Marko,Milasin Jelena M},
year={2010},
title={Cancer genes alterations and HPV infection in oral squamous cell carcinoma},
journal={INTERNATIONAL JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY},
volume={39},
number={9},
pages={909-915},
document_type={Article},
} 

@ARTICLE{
author={Novakovic Ivana V,Maksimovic Nela S,Cvetkovic Slobodan D,Cvetkovic Dragana D},
year={2010},
title={Gene Polymorphisms as Markers of Disease Susceptibility},
journal={JOURNAL OF MEDICAL BIOCHEMISTRY},
volume={29},
number={3},
pages={135-138},
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={Djukanovic Ljubica D,Stefanovic Vladisav B,Basta-Jovanovic Gordana M,Bukvic Danica,Glogovac Stevan,Dimitrijevic Jovan Z,Djuric Suncica,Jankovic Slavenka M,Lukic Ljiljana Z,Maric Ivko,Nikolic Jovan,Novakovic Ivana V,Pejovic Vesna,Radisavljevic Snezana,Rakic Nenad,Savic Vojin P},
year={2010},
title={Investigation of Balkan Endemic Nephropathy in Serbia: How to Proceed?},
journal={SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO},
volume={138},
number={3-4},
pages={256-261},
document_type={Article},
} 

@ARTICLE{
author={Simeunovic Slavko D,Milincic Zeljka D,Novakovic Ivana V,Nedeljkovic Srecko I,Vukotic Milija,Simeunovic Dejan S,Nikolic Dejan P},
year={2009},
title={Epidemiology of Precursors of Atherosclerosis in Children - Yusad Study},
journal={ATHEROSCLEROSIS SUPPLEMENTS},
volume={10},
number={2},
pages={-},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Gurinovic Mirjana A,Glibetic Marija D,Vukotic Milija,Novakovic Ivana V,Ristic-Medic Danijela K,Radicev-Radanov Milena},
year={2009},
title={Obesity And Overweight In Schoolchildren And Adults In Serbia},
journal={ANNALS OF NUTRITION AND METABOLISM},
volume={55},
number={},
pages={271-271},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Cuturilo Goran,Stefanovic Igor D,Jovanovic Ida V,Miletic-Grkovic Slobodanka,Novakovic Ivana V},
year={2009},
title={Mowat-Wilson Syndrome - A Case Report},
journal={SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO},
volume={137},
number={7-8},
pages={426-429},
document_type={Article},
} 

@ARTICLE{
author={Sternic Nadezda M,Pavlovic Aleksandra M,Pekmezovic Tatjana D,Zidverc-Trajkovic Jasna J,Jovanovic Zagorka B,Mijajlovic Milija D,Radojicic Aleksandra P,Tomic Gordana G,Novakovic Ivana V,Obrenovic Radmila R,Kostic Vladimir S},
year={2009},
title={Plasma homocysteine levels and cognitive status in patients with ischemic cerebrovascular disease},
journal={JOURNAL OF THE NEUROLOGICAL SCIENCES},
volume={283},
number={1-2},
pages={248-248},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Pastor Tibor J,Popovic Branka M,Gvozdenovic Ana,Boro Aleksandar,Petrovic Bojana,Novakovic Ivana V,Puzovic Dragana Z,Lukovic Ljiljana F,Milasin Jelena M},
year={2009},
title={Alterations of c-Myc and c-erbB-2 Genes in Ovarian Tumours},
journal={SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO},
volume={137},
number={1-2},
pages={47-51},
document_type={Article},
} 

@ARTICLE{
author={Puzovic Dragana Z,Popovic Branka M,Novakovic Ivana V,Milasin Jelena M},
year={2009},
title={Analysis of Microsatellite Markers D18S70 and D20S116 in DNA Isolated from Dentin: Use in Forensic Medicine},
journal={SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO},
volume={137},
number={1-2},
pages={43-46},
document_type={Article},
} 

@ARTICLE{
author={Milincic Zeljka D,Nikolic Dejan P,Simeunovic Slavko D,Novakovic Ivana V,Vukotic Milija},
year={2008},
title={Glycemia Trends in School Children in Serbia},
journal={ATHEROSCLEROSIS SUPPLEMENTS},
volume={9},
number={1},
pages={95-96},
document_type={Meeting Abstract},
} 

@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={Ristanovic Momcilo,Bunjevacki Vera I,Tulic Cane Dz,Novakovic Ivana V,Ille Tatjana M,Radojkovic Dragica P,Nikolic Aleksandra M},
year={2008},
title={Y chromosome microdeletions in infertile male candidates for microfertilization},
journal={SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO},
volume={136},
number={3-4},
pages={126-130},
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={Ristanovic Momcilo,Bunjevacki Vera I,Tulic Cane Dz,Novakovic Ivana V,Perovic Vladimir R,Lukovic Ljiljana F,Milasin Jelena M},
year={2007},
title={Prevalence of Y chromosome microdeletions in infertile men with severe oligozoospermia in Serbia},
journal={GENETIC COUNSELING},
volume={18},
number={3},
pages={337-342},
document_type={Article},
} 

@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={Simeunovic Slavko D,Milincic Zeljka D,Nikolic Dejan P,Simeunovic Dejan S,Novakovic Ivana V,Nedeljkovic Srecko I,Vukotic Milija},
year={2007},
title={Evaluation of anthropometric parameters as risk factors for atherosclerosis in children},
journal={ATHEROSCLEROSIS SUPPLEMENTS},
volume={8},
number={1},
pages={176-177},
document_type={Meeting Abstract},
} 

@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={Ristanovic Momcilo,Bunjevacki Vera I,Tulic Cane Dz,Novakovic Ivana V,Nikolic Aleksandra M},
year={2007},
title={Molecular analysis of Y chromosome microdeletions in idiopathic cases of male infertility in Serbia},
journal={RUSSIAN JOURNAL OF GENETICS},
volume={43},
number={6},
pages={705-708},
document_type={Article},
} 

@ARTICLE{
author={Popovic Branka M,Jekic Biljana B,Novakovic Ivana V,Lukovic Ljiljana F,Tepavcevic Zvezdana,Jurisic Vladimir B,Vukadinovic Miroslav,Milasin Jelena M},
year={2007},
title={Bcl-2 expression in oral squamous cell carcinoma},
journal={SIGNAL TRANSDUCTION PATHWAYS, PT C},
volume={1095},
number={},
pages={19-25},
document_type={Article},
} 

@ARTICLE{
author={Dzoljic Eleonora D,Novakovic Ivana V,Mirkovic Dusko D,Todorovic Zoran M,Prostran Milica S,Kostic Vladimir S},
year={2006},
title={Parkinson's disease, homocysteine serum levels and MTHFR C667T genotype},
journal={JOURNAL OF THE NEUROLOGICAL SCIENCES},
volume={248},
number={1-2},
pages={322-322},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Todorovic Zoran M,Dzoljic Eleonora D,Novakovic Ivana V,Mirkovic Dusko D,Stojanovic Radan M,Nesic Zorica I,Krajinovic Maja,Prostran Milica S,Kostic Vladimir S},
year={2006},
title={Homocysteine serum levels and MTHFR C677T genotype in patients with Parkinson's disease, with and without levodopa therapy},
journal={JOURNAL OF THE NEUROLOGICAL SCIENCES},
volume={248},
number={1-2},
pages={56-61},
document_type={Article},
} 

@ARTICLE{
author={Jovicic Snezana Z,Simic-Ogrizovic Sanja P,Novakovic Ivana V,Radivojevic Dragana M,Blagojevic Radmila N},
year={2006},
title={Effects of MTHFR 677C > T and 1298A > C on serum homocysteine levels, carotid atherosclerosis and graft failure in renal transplant patients},
journal={KIDNEY & BLOOD PRESSURE RESEARCH},
volume={29},
number={3},
pages={195-195},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Simic-Ogrizovic Sanja P,Stosovic Milan D,Novakovic Ivana V,Pejanovic Svetlana D,Jemcov Tamara K,Radovic Milan M,Djukanovic Ljubica D},
year={2006},
title={Fuzzy role of hyperhomocysteinemia in hemodialysis patients' mortality},
journal={BIOMEDICINE & PHARMACOTHERAPY},
volume={60},
number={4},
pages={200-207},
document_type={Article},
} 

@ARTICLE{
author={Puzovic Dragana Z,Dunjic Dusan J,Popovic Branka M,Stojkovic Oliver V,Novakovic Ivana V,Milasin Jelena M},
year={2006},
title={Population data on HLA-DQA1, LDLR, GYPA, HBGG, D7S8, and GC PCR-based loci in Serbia},
journal={JOURNAL OF FORENSIC SCIENCES},
volume={51},
number={3},
pages={699-699},
document_type={Editorial Material},
} 

@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},
} 

@ARTICLE{
author={Hartig Monika B,Hortnagel K,Garavaglia B,Zorzi G,Kmiec T,Klopstock T,Rostasy K,Svetel Marina V,Kostic Vladimir S,Schuelke M,Botz E,Weindl A,Novakovic Ivana V,Nardocci N,Prokisch H,Meitinger T},
year={2006},
title={Genotypic and phenotypic spectrum of PANK2 mutations in patients with neurodegeneration with brain iron accumulation},
journal={ANNALS OF NEUROLOGY},
volume={59},
number={2},
pages={248-256},
document_type={Article},
} 

@ARTICLE{
author={Novakovic Ivana V,Bojic Daniela Z,Todorovic Slobodanka,Apostolski Slobodan A,Lukovic Ljiljana F,Stefanovic D,Milasin Jelena M},
year={2005},
title={Proximal dystrophin gene deletions and protein alterations in Becker muscular dystrophy},
journal={BIOPHYSICS FROM MOLECULES TO BRAIN: IN MEMORY OF RADOSLAV K. ANDJUS},
volume={1048},
number={},
pages={406-410},
document_type={Article},
} 

@ARTICLE{
author={Jekic Biljana B,Novakovic Ivana V,Lukovic Ljiljana F,Kuzmanovic Milos B,Popovic Branka M,Pastar Irena,Milasin Jelena M,Bunjevacki Gordana,Bunjevacki Vera I},
year={2004},
title={Low frequency of NRAS and KRAS2 gene mutations in childhood myelodysplastic syndromes},
journal={CANCER GENETICS AND CYTOGENETICS},
volume={154},
number={2},
pages={180-182},
document_type={Article},
} 

@ARTICLE{
author={Svetel Marina V,Novakovic Ivana V,Petrovic Igor N,Dragasevic Natasa T,Kostic Vladimir S},
year={2004},
title={Clinical presentation of Hallervorden-Spatz disease: Report of four cases},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={11},
number={},
pages={119-119},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Novakovic Ivana V,Apostolski Slobodan A,Todorovic Slobodanka,Lukovic Ljiljana F,Bunjevacki Vera I,Bojic Daniela Z,Mestroni L,Milasin Jelena M},
year={2002},
title={Cardiac disorders in BMD patients with distal gene deletions},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={10},
number={},
pages={257-257},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Popovic Branka M,Milasin Jelena M,Jekic Biljana B,Novakovic Ivana V},
year={2002},
title={The role of H-Ras gene in tumorigenesis of oral squamous cell carcinoma},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={10},
number={},
pages={99-99},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Jekic Biljana B,Bunjevacki Vera I,Kuzmanovic Milos B,Novakovic Ivana V,Lukovic Ljiljana F},
year={2002},
title={Mutations of N- and K-Ras, p53 and FMS genes in myelodysplastic syndromes in children},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={10},
number={},
pages={88-88},
document_type={Meeting Abstract},
}