Maver Ales,...,Jankovic Milena,...,Novakovic Ivana V,...,(broj koautora 32) (2026) Consensus recommendations for next-generation sequencing-based genetic testing in Rare Neurological diseases, EUROPEAN JOURNAL OF HUMAN GENETICS, vol. , br. , str. - (Article; Early Access) 

Damnjanovic Tatjana M,Maksimovic Nela S,Djuranovic-Uklein Ana S,Bosankic Brankica,Jekic Biljana B,Grk Milka B,Dusanovic Pjevic Marija G,Rasic Milica,Stojanovski Natasa,Pesic Milica,Novakovic Ivana V,Cuturilo Goran,Perovic Dijana (2026) Analysis of Copy Number and Sequence Variants Linked to Cardiac Development in Children with Syndromic Congenital Heart Defects, CARDIOGENETICS, vol. 16, br. 2, str. - (Article) 

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 (2026) Toward clinical application of whole-exome sequencing in the diagnosis of men with severely impaired spermatogenesis, FERTILITY AND STERILITY, vol. 125, br. 6, str. 1136-1141 (Letter) 

Bergant Gaber,...,Brankovic Marija,Jankovic Milena Z,Svetel Marina V,...,Dragasevic-Miskovic Natasa T,Petrovic Igor N,...,Novakovic Ivana V,...,(broj koautora 19) (2026) Enrichment of Rare Variants in Nuclear-Encoded Mitochondrial Metabolism Genes in Patients with Early-Onset or Familial Parkinson's Disease, GENES, vol. 17, br. 4, str. - (Article) 

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 (2025) Increased burden of rare variants in GWAS associated genes in familial multiple sclerosis, EUROPEAN JOURNAL OF HUMAN GENETICS, vol. 33, br. , str. 1046-1046 (Meeting Abstract) 

Kovanda Anja,Susmelj Lara,Lukezic Tadeja,Maver Ales,Racki Valentino,Vuletic Vladimira,Svetel Marina V,Novakovic Ivana V,Peterlin Borut (2025) Biallelic RFC1 expansions as a rare cause of familial and early onset Parkinson's disease in the Slavic population, EUROPEAN JOURNAL OF HUMAN GENETICS, vol. 33, br. , str. 797-798 (Meeting Abstract) 

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 (2025) Clinical application of whole exome sequencing in the diagnosis of men with severely impaired spermatogenesis, EUROPEAN JOURNAL OF HUMAN GENETICS, vol. 33, br. , str. 570-570 (Meeting Abstract) 

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 (2025) A Specific Haplotype of the MMP2 Gene Promoter May Increase the Risk of Developing Cerebral Palsy, DIAGNOSTICS, vol. 15, br. 24, str. - (Article) 

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 (2025) Multi-Center National Study of Genotype-Phenotype Correlation and Clinical Characteristics in Children and Young Adults with Friedreich's Ataxia from Serbia, BIOMEDICINES, vol. 13, br. 11, str. - (Article) 

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 (2025) The role of DNA mismatch repair mutS/mutL homolog genes in spermatogenesis and male infertility: a systematic review and cohort study, REPRODUCTIVE BIOLOGY AND ENDOCRINOLOGY, vol. 23, br. 1, str. - (Review) 

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 (2025) Association of NOS Gene Polymorphisms with Sepsis-Related Complications in Secondary Peritonitis, INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, vol. 26, br. 21, str. - (Article) 

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 (2025) Genetic Testing for Monogenic Forms of Male Infertility Contributes to the Clinical Diagnosis of Men with Severe Idiopathic Male Infertility, WORLD JOURNAL OF MENS HEALTH, vol. 43, br. 4, str. 908-917 (Article) 

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 (2025) Biallelic RFC1 Expansions Are a Rare Cause of Early-Onset and Familial Parkinson's Disease, CLINICAL GENETICS, vol. , br. , str. - (Editorial Material; Early Access) 

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 (2025) ACE gene and male infertility: a South Slavic case-control study and multi-omics data integration, SYSTEMS BIOLOGY IN REPRODUCTIVE MEDICINE, vol. 71, br. 1, str. 524-537 (Article) 

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 (2025) Is GBA1 mutation status a game-changer for impulse control behaviour in Parkinson's disease?, NEUROLOGICAL SCIENCES, vol. , br. , str. - (Article; Early Access) 

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 (2025) Genetic Susceptibility to Glomerulonephritis in Children: Analysis of Structural Kidney Genes and Immune System Genes, JOURNAL OF CLINICAL MEDICINE, vol. 14, br. 14, str. - (Article) 

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 (2025) Increased burden of rare variants in GWAS associated genes in familial multiple sclerosis, SCIENTIFIC REPORTS, vol. 15, br. 1, str. - (Article) 

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 (2025) New evidence supporting female protective effect in patients with congenital anomalies and neurodevelopmental disorders, EARLY HUMAN DEVELOPMENT, vol. 205, br. , str. - (Article) 

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 (2025) Genetic Testing for Monogenic Forms of Male Infertility Contributes to the Clinical Diagnosis of Men with Severe Idiopathic Male Infertility, WORLD JOURNAL OF MENS HEALTH, vol. , br. , str. - (Article; Early Access) 

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 (2025) HIF-1A Gene Polymorphisms are Associated With Clinical and Biochemical Parameters in COVID-19 Patients in Serbian Population, CLINICAL NURSING RESEARCH, vol. , br. , str. - (Article; Early Access) 

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 (2024) Chromosomal Microarray in Children Born Small for Gestational Age - Single Center Experience, BALKAN JOURNAL OF MEDICAL GENETICS, vol. 27, br. 2, str. 13-21 (Article) 

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 (2024) Sleep problems in female carriers of premutation in the FMR1 gene, EUROPEAN JOURNAL OF HUMAN GENETICS, vol. 32, br. , str. 1088-1088 (Meeting Abstract) 

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 (2024) Sleep problems in female carriers of premutation in the <i>FMR1</i> gene, EUROPEAN JOURNAL OF HUMAN GENETICS, vol. 32, br. , str. 1088-1088 (Meeting Abstract) 

Jovicic-Pavlovic Svetlana M,Simic-Ogrizovic Sanja P,Pavlovic Natalija,Bukumiric Zoran M,Novakovic Ivana V (2024) Influence of polymorphisms in genes for interleukin-6 and interleukin-10 on dialysis patients survival, NEPHROLOGY DIALYSIS TRANSPLANTATION, vol. 39, br. , str. - (Meeting Abstract) 

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 (2024) Association of AQP-4 polymorphisms with the clinical and paraclinical characteristics of patients with NMOSD, MULTIPLE SCLEROSIS JOURNAL, vol. 30, br. 3, str. 993-993 (Meeting Abstract) 

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 (2024) Rare and Uncommon Gene Variants Associated with Familial Multiple Sclerosis: A Case-Control Study, MULTIPLE SCLEROSIS JOURNAL, vol. 30, br. 3, str. 866-867 (Meeting Abstract) 

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 (2024) Wilson's disease, SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO, vol. 152, br. 5-6, str. 310-317 (Review) 

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 (2024) Genetic polymorphisms and Methotrexate response in patients with rheumatoid arthritis, JOURNAL OF RESEARCH IN PHARMACY, vol. 28, br. 4, str. 1285-1292 (Article) 

Jovicic-Pavlovic Svetlana M,Simic-Ogrizovic Sanja P,Pavlovic Natalija,Bukumiric Zoran M,Novakovic Ivana V (2024) Influence of polymorphisms in genes for interleukin-6 and interleukin-10 on dialysis patients survival, NEPHROLOGY DIALYSIS TRANSPLANTATION, vol. 39, br. , str. I2520-I2521 (Meeting Abstract) 

Stefanova Elka D,Marjanovic Ana,Dobricic Valerija S,Mandic-Stojmenovic Gorana B,Stojkovic Tanja,Brankovic Marija,Sarcevic Maksim,Novakovic Ivana V,Kostic Vladimir S (2024) Frequency of C9orf72, GRN, and MAPT pathogenic variants in patients recruited at the Belgrade Memory Center, NEUROGENETICS, vol. , br. , str. - (Article; Early Access) 

Stratakis Konstantinos,Terzic-Supic Zorica J,Todorovic Jovana S,Nesic Dejan M,Novakovic Ivana V (2024) Physical Activity and Mental Health of Medical Students, CENTRAL EUROPEAN JOURNAL OF PUBLIC HEALTH, vol. 32, br. 1, str. 39-44 (Article) 

Vidovic Vanja,Novakovic Ivana V,Damnjanovic Tatjana M,Radic-Savic Zana,Vidovic Stojko,Krbic Ranko,Maksimovic Nela S (2024) Galectin 3 Rs4644 Gene Polymorphism Is Associated with Metabolic Traits in Serbian Adolescent Population, JOURNAL OF MEDICAL BIOCHEMISTRY, vol. 43, br. 3, str. 445-450 (Article) 

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 (2024) Earlier age of symptom onset in younger generation of familial cases of multiple sclerosis, NEUROLOGICAL SCIENCES, vol. , br. , str. - (Article; Early Access) 

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 (2024) Whole exome sequencing in Serbian patients with hereditary spastic paraplegia, NEUROGENETICS, vol. , br. , str. - (Article; Early Access) 

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 (2024) <i>ANO10</i>-Related Spinocerebellar Ataxia: MDSGene Systematic Literature Review and a Romani Case Series, MOVEMENT DISORDERS, vol. 39, br. 5, str. 887-892 (Article) 

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 (2024) Exclusive breastfeeding may be a protective factor in individuals with familial multiple sclerosis. A population registry-based case-control study, MULTIPLE SCLEROSIS AND RELATED DISORDERS, vol. 82, br. , str. - (Article) 

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 (2024) Genetic testing for monogenic forms of male infertility contributes to the clinical diagnosis of men with idiopathic severe male infertility, EUROPEAN JOURNAL OF HUMAN GENETICS, vol. 32, br. , str. 356-357 (Meeting Abstract) 

Kovacevic Masa,Jankovic M,Brankovic Marija,Milicevic Ognjen S,Novakovic Ivana V,Sokic Dragoslav V,Ristic Aleksandar J,Berisavac I,Vojvodic Nikola M (2023) Yield of GATOR1 gene sequencing in a Serbian focal epilepsy cohort, EPILEPSIA, vol. 64, br. , str. 386-386 (Meeting Abstract) 

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 (2023) Clinical and Genetic Features of Huntington's Disease Patients From Republic of Serbia: A Single-Center Experience, JOURNAL OF MOVEMENT DISORDERS, vol. 16, br. 3, str. 333-335 (Letter) 

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 (2023) Whole exome sequencing in Serbian patients with hereditary spastic paraplegia, EUROPEAN JOURNAL OF NEUROLOGY, vol. 30, br. , str. 260-260 (Meeting Abstract) 

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 (2023) Motor neuron involvement in facial muscles as characteristic of ANO10 mutation, EUROPEAN JOURNAL OF NEUROLOGY, vol. 30, br. , str. 234-234 (Meeting Abstract) 

Maksic Jasmina,Maksimovic Nela S,Rasulic Lukas G,Milankov Olgica,Marjanovic Ana,Cvetkovic Dragana D,Rakocevic-Stojanovic Vidosava M,Novakovic Ivana V (2023) The importance of direct genetic testing for determining female carriers of the mutation in dystrophinopathies, VOJNOSANITETSKI PREGLED, vol. 80, br. 3, str. 201-207 (Article) 

Kovacevic Masa,Milicevic Ognjen S,Brankovic Marija,Jankovic Milena Z,Novakovic Ivana V,Sokic Dragoslav V,Ristic Aleksandar J,Shamsani Jannah,Vojvodic Nikola M (2023) Novel variants in established epilepsy genes in focal epilepsy, SEIZURE-EUROPEAN JOURNAL OF EPILEPSY, vol. 110, br. , str. 146-152 (Article) 

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 (2023) Reply to: "Differences in Sex-Specific Frequency of Glucocerebrosidase Variant Carriers and Familial Parkinsonism", MOVEMENT DISORDERS, vol. 38, br. 4, str. 712-713 (Letter) 

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 (2023) Association of PRDM16 rs12409277 and CtBP2 rs1561589 gene polymorphisms with lipid profile of adolescents, ARCHIVES OF MEDICAL SCIENCE, vol. 19, br. 3, str. 593-599 (Article) 

Pal Gian,...,Novakovic Ivana V,...,(broj koautora 27) (2023) Genetic Testing in Parkinson's Disease, MOVEMENT DISORDERS, vol. 38, br. 8, str. 1384-1396 (Review) 

Saunders-Pullman Rachel,...,Novakovic Ivana V,...,(broj koautora 29) (2023) International Genetic Testing and Counseling Practices for Parkinson's Disease, MOVEMENT DISORDERS, vol. 38, br. 8, str. 1527-1535 (Article) 

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 (2023) C9orf72 Genetic Screening in Amyotrophic Lateral Sclerosis Patients from Serbia, GENETIKA-BELGRADE, vol. 55, br. 1, str. 1-18 (Article) 

Minic Snezana B,Cerovac Natasa M,Novakovic Ivana V,Gazikalovic Slobodan,Popadic Svetlana P,Trpinac Dusan P (2023) The Impact of the IKBKG Gene on the Appearance of the Corpus Callosum Abnormalities in Incontinentia Pigmenti, DIAGNOSTICS, vol. 13, br. 7, str. - (Article) 

Jankovic Milena Z,Nikolic Dejan P,Novakovic Ivana V,Petrovic Bojana,Lackovic Milan,Santric-Milicevic Milena M (2023) miRNAs as a Potential Biomarker in the COVID-19 Infection and Complications Course, Severity, and Outcome, DIAGNOSTICS, vol. 13, br. 6, str. - (Review) 

Kovacevic Masa,Jankovic Milena Z,Brankovic Marija,Milicevic Ognjen S,Novakovic Ivana V,Sokic Dragoslav V,Ristic Aleksandar J,Shamsani Jannah,Vojvodic Nikola M (2023) Novel GATOR1 variants in focal epilepsy, EPILEPSY & BEHAVIOR, vol. 141, br. , str. - (Article) 

Vidovic Vanja,Maksimovic Nela S,Vidovic Stojko,Damnjanovic Tatjana M,Milovac Irina,Novakovic Ivana V (2022) PPARGC1A Gene Polymorphism and Its Association with Obesity- Related Metabolic Traits in Serbian Adolescent Population, GENETIKA-BELGRADE, vol. 54, br. 3, str. 1375-1384 (Article) 

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 (2022) Analysis of "Clinical Exome" Panel in Serbian Patients with Cognitive Disorders, GENETIKA-BELGRADE, vol. 54, br. 3, str. 1351-1364 (Article) 

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 (2022) C9ORF72 Repeat Expansion Is Not Associated with Atypical Parkinsonism in the Serbian Population, GENETIKA-BELGRADE, vol. 54, br. 3, str. 1313-1330 (Article) 

Kovanda Anja,...,Brankovic Marija,Jankovic Milena Z,Svetel Marina V,...,Kostic Vladimir S,Novakovic Ivana V,...,(broj koautora 17) (2022) A multicenter study of genetic testing for Parkinson's disease in the clinical setting, NPJ PARKINSONS DISEASE, vol. 8, br. 1, str. - (Article) 

Jovicic-Pavlovic Svetlana M,Simic-Ogrizovic Sanja P,Bukumiric Zoran M,Eric Milena,Pavlovic Natalija,Kotlica Boba,Novakovic Ivana V (2022) Impact of the Fetuin Gene Polymorphisms in Coronary Artery Calcification and Mortality of Patients with Chronic Kidney Disease and Renal Transplant, GENETIKA-BELGRADE, vol. 54, br. 1, str. 457-472 (Article) 

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 (2022) Clinical Exome Sequencing in Serbian Patients with Movement Disorders - Single Centre Experience, GENETIKA-BELGRADE, vol. 54, br. 1, str. 395-409 (Article) 

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) (2022) Phenotypic and Genetic Heterogeneity of Adult Patients with Hereditary Spastic Paraplegia from Serbia, CELLS, vol. 11, br. 18, str. - (Article) 

Minic Snezana B,Trpinac Dusan P,Novakovic Ivana V,Cerovac Natasa M,Dobrosavljevic-Vukojevic Danijela,Rosain Jeremie (2022) Challenges in Rare Diseases Diagnostics: Incontinentia Pigmenti with Heterozygous GBA Mutation, DIAGNOSTICS, vol. 12, br. 7, str. - (Article) 

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 (2022) Chromosomal microarray in postnatal diagnosis of congenital anomalies and neurodevelopmental disorders in Serbian patients, JOURNAL OF CLINICAL LABORATORY ANALYSIS, vol. 36, br. 6, str. - (Article) 

Dimitrijevic Sanja S,Jekic Biljana B,Cvjeticanin Suzana,Tucovic Aleksandra,Filipovic Tamara N,Novakovic Ivana V,Ivic Bojana S,Nikolic Dimitrije M (2022) KCC2 rs2297201 Gene Polymorphism Might be a Predictive Genetic Marker of Febrile Seizures, ASN NEURO, vol. 14, br. , str. - (Article) 

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 (2022) Diagnostic yield of whole exome sequencing in early-onset and familial Parkinson's disease in the Balkans, EUROPEAN JOURNAL OF HUMAN GENETICS, vol. 30, br. SUPPL 1, str. 292-292 (Meeting Abstract) 

Jankovic Milena Z,Petrovic Bojana,Novakovic Ivana V,Brankovic Slavko,Radosavljevic Natasa R,Nikolic Dejan P (2022) The Genetic Basis of Strokes in Pediatric Populations and Insight into New Therapeutic Options, INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, vol. 23, br. 3, str. - (Article) 

Pereza Nina,Terzic Rifet,Plaseska-Karanfilska Dijana,Miljanovic Olivera,Novakovic Ivana V,Poslon Zeljka,Ostojic Sasa,Peterlin Borut (2022) Current State of Compulsory Basic and Clinical Courses in Genetics for Medical Students at Medical Faculties in Balkan Countries With Slavic Languages, FRONTIERS IN GENETICS, vol. 12, br. , str. - (Article) 

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 (2022) Genetic and phenotypic variability in adult patients with Niemann Pick type C from Serbia: single-center experience, JOURNAL OF NEUROLOGY, vol. 269, br. 6, str. 3167-3174 (Article) 

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 (2022) Correlation between leukocyte-platelet aggregates and thrombosis in myeloproliferative neoplasms, INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY, vol. 44, br. 2, str. 302-312 (Article) 

Svetel Marina V,Dragasevic Natasa T,Petrovic Igor N,Novakovic Ivana V,Tomic Aleksandra D,Kresojevic Nikola D,Stankovic Iva D,Kostic Vladimir K (2021) NBIA Syndromes: A Step Forward from the Previous Knowledge, NEUROLOGY INDIA, vol. 69, br. 5, str. 1380-1388 (Review) 

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 (2021) Mutational Analysis and mtDNA Haplogroup Characterization in Three Serbian Cases of Mitochondrial Encephalomyopathies and Literature Review, DIAGNOSTICS, vol. 11, br. 11, str. - (Review) 

Jankovic Milena Z,Novakovic Ivana V,Dawod Phepy GA,Dawod Ayman Gamil Anwar,Drinic Aleksandra,Motaleb Abdel F,Ducic Sinisa,Nikolic Dejan P (2021) Current Concepts on Genetic Aspects of Mitochondrial Dysfunction in Amyotrophic Lateral Sclerosis, INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, vol. 22, br. 18, str. - (Review) 

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 (2021) The FKBP5 genotype and childhood trauma effects on FKBP5 DNA methylation in patients with psychosis, their unaffected siblings, and healthy controls, PSYCHONEUROENDOCRINOLOGY, vol. 128, br. , str. - (Article) 

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 (2021) Genetic and Epigenomic Modifiers of Diabetic Neuropathy, INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, vol. 22, br. 9, str. - (Review) 

Djuric Olivera S,Andjelkovic Marina Z,Vreca Misa,Skakic Anita G,Pavlovic Sonja T,Novakovic Ivana V,Jovanovic Bojan Z,Skodric-Trifunovic Vesna D,Markovic-Denic Ljiljana N (2021) Genetic variants in TNFA, LTA, TLR2 and TLR4 genes and risk of sepsis in patients with severe trauma: nested case-control study in a level-1 trauma centre in SERBIA, INJURY-INTERNATIONAL JOURNAL OF THE CARE OF THE INJURED, vol. 52, br. 3, str. 419-425 (Article) 

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 (2021) Premutations in the FMR1 gene in Serbian patients with undetermined tremor, ataxia and parkinsonism, NEUROLOGICAL RESEARCH, vol. 43, br. 4, str. 321-326 (Article) 

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 (2021) Oxidative Stress Profile in Genetically Confirmed Cases of Leber's Hereditary Optic Neuropathy, JOURNAL OF MOLECULAR NEUROSCIENCE, vol. 71, br. 5, str. 1070-1081 (Article) 

Rovcanin Branislav R,Jancic Jasna B,Samardzic Janko M,Rovcanin Marija G,Nikolic Blazo,Ivancevic Nikola,Novakovic Ivana V,Kostic Vladimir K (2020) In silico model of mtDNA mutations effect on secondary and 3D structure of mitochondrial rRNA and tRNA in Leber's hereditary optic neuropathy, EXPERIMENTAL EYE RESEARCH, vol. 201, br. , str. - (Article) 

Gulic Milica,Maksimovic Nela S,Doklestic Krstina S,Grk Milka B,Svircev M,Dusanovic Pjevic Marija G,Kulic M,Novakovic Ivana V (2020) Influence of eNOS gene haplotypes and iNOS rs2297518 gene variant on severe complications and mortality in surgical patients with secondary peritonitis, EUROPEAN JOURNAL OF HUMAN GENETICS, vol. 28, br. SUPPL 1, str. 982-983 (Meeting Abstract) 

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 (2020) Polymorphisms in genes for proinflammatory cytokines IL-6, IL-1 ss, andTNF-alpha in relation with Parkinson's disease progression, EUROPEAN JOURNAL OF HUMAN GENETICS, vol. 28, br. SUPPL 1, str. 888-888 (Meeting Abstract) 

Komnenic-Radovanovic Milica,Novakovic Ivana V,Cuturilo Goran,Ruml-Stojanovic Jelena,Petrovic Bojana,Kontic-Vucinic Olivera (2020) Recurrent congenital microcephaly: a case report, EUROPEAN JOURNAL OF HUMAN GENETICS, vol. 28, br. SUPPL 1, str. 801-802 (Meeting Abstract) 

Nikolic Dejan P,Jankovic Milena Z,Petrovic Bojana,Novakovic Ivana V (2020) Genetic Aspects of Inflammation and Immune Response in Stroke, INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, vol. 21, br. 19, str. - (Review) 

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 (2020) Whole Mitochondrial Genome Analysis in Serbian Cases of Leber's Hereditary Optic Neuropathy, GENES, vol. 11, br. 9, str. - (Article) 

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 (2020) Association of the Brain-Derived Neurotrophic Factor Val66met Polymorphism with Body Mass Index, Fasting Glucose Levels and Lipid Status in Adolescents, BALKAN JOURNAL OF MEDICAL GENETICS, vol. 23, br. 1, str. 77-82 (Article) 

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 (2020) Yield of thePMP22deletion analysis in patients with compression neuropathies, JOURNAL OF NEUROLOGY, vol. 267, br. 12, str. 3617-3623 (Article) 

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 (2020) Analysis of association of ADORA(2)A and ADORA(3) polymorphisms genotypes/haplotypes with efficacy and toxicity of methotrexate in patients with Rheumatoid arthritis, PHARMACOGENOMICS JOURNAL, vol. 20, br. 6, str. 784-791 (Article) 

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 (2020) Quality of life in hereditary neuropathy with liability to pressure palsies is as impaired as in Charcot-Marie-Tooth disease type 1A, EUROPEAN JOURNAL OF NEUROLOGY, vol. 27, br. , str. 400-400 (Meeting Abstract) 

Maksic Jasmina,Dobricic Valerija S,Rasulic Lukas G,Maksimovic Nela S,Brankovic Marija,Milic-Rasic Vedrana M,Rakocevic-Stojanovic Vidosava M,Novakovic Ivana V (2020) Analysis of duplications versus deletions in the dystrophin gene in Serbian cohort with dystrophinopathies, VOJNOSANITETSKI PREGLED, vol. 77, br. 4, str. 387-394 (Article) 

Svetel Marina V,Novakovic Ivana V,Tomic Svetlana,Kresojevic Nikola D,Kostic Vladimir K (2020) Novel PANK2 mutation identified in a patient with pantothenate kinase-associated neurodegeneration, SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO, vol. 148, br. 3-4, str. 203-206 (Article) 

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 (2020) Neuropathic pain in patients with Charcot-Marie-Tooth type 1A, NEUROLOGICAL SCIENCES, vol. 41, br. 3, str. 625-630 (Article) 

Jancic Jasna B,Rovcanin Branislav R,Djuric Vesna,Pepic Ana,Samardzic Janko S,Nikolic Blazo,Novakovic Ivana V,Kostic Vladimir S (2020) Analysis of secondary mtDNA mutations in families with Leber's hereditary optic neuropathy: Four novel variants and their association with clinical presentation, MITOCHONDRION, vol. 50, br. , str. 132-138 (Article) 

Varljen Tatjana J,Sekulovic Gordana,Rakic Olgica,Maksimovic Nela S,Jekic Biljana B,Novakovic Ivana V,Damnjanovic Tatjana M (2020) Genetic variant rs16944 in IL1B gene is a risk factor for early-onset sepsis susceptibility and outcome in preterm infants, INFLAMMATION RESEARCH, vol. 69, br. 2, str. 155-157 (Article) 

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 (2019) phenotypic and genetic heterogeneity of adult patients with hereditary spastic paraplegia from Serbia, JOURNAL OF THE NEUROLOGICAL SCIENCES, vol. 405, br. , str. - (Meeting Abstract) 

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 (2019) Significance of KIT and PDGFRA mutations in gastric gastrointestinal stromal tumor imatinib-naive surgically treated patients, VOJNOSANITETSKI PREGLED, vol. 76, br. 12, str. 1268-1273 (Article) 

Ivancevic Nikola,Cerovac Natasa M,Nikolic Blazo,Cuturilo Goran,Marjanovic Ana,Marjanovic Ana,Novakovic Ivana V (2019) GLUT1 deficiency syndrome: a case report with a novel SLC2A1 mutation, VOJNOSANITETSKI PREGLED, vol. 76, br. 5, str. 543-546 (Article) 

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 (2019) Clinical course of patients with pantothenate kinase-associated neurodegeneration (PKAN) before and after DBS surgery, JOURNAL OF NEUROLOGY, vol. 266, br. 12, str. 2962-2969 (Article) 

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 (2019) Whole mitochondrial genome analysis in carriers of mt3460 mutation with Leber's hereditary optic neuropathy, EUROPEAN JOURNAL OF HUMAN GENETICS, vol. 27, br. , str. 1836-1837 (Meeting Abstract) 

Maksimovic Nela S,Varljen Tatjana J,Sekulovic Gordana,Damnjanovic Tatjana M,Novakovic Ivana V (2019) Genetic variant rs16944 in IL1B gene is a risk factor for early onset sepsis susceptibility and outcome in preterm infants, EUROPEAN JOURNAL OF HUMAN GENETICS, vol. 27, br. , str. 1364-1365 (Meeting Abstract) 

Damnjanovic Tatjana M,Varljen Tatjana J,Rakic Olgica,Jekic Biljana B,Liston J,Novakovic Ivana V (2019) Study of TNF, IL1B, and IL6 genes polymorphisms and susceptibility to bronchopulmonary dysplasia in premature neonates, EUROPEAN JOURNAL OF HUMAN GENETICS, vol. 27, br. , str. 1360-1360 (Meeting Abstract) 

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 (2019) Analysis of ATXN1 and ATXN2 repeat length in C9ORF72 expansion carriers, EUROPEAN JOURNAL OF HUMAN GENETICS, vol. 27, br. , str. 961-961 (Meeting Abstract) 

Maksimovic Nela S,Vidovic Vanja,Damnjanovic Tatjana M,Jekic Biljana B,Perovic Dijana,Vidovic Stojko,Milovac Irina,Novakovic Ivana V (2019) Association of PRDM16 and CtBP2 genes polymorphisms with lipid profile of adolescents, EUROPEAN JOURNAL OF HUMAN GENETICS, vol. 27, br. , str. 658-658 (Meeting Abstract) 

Damnjanovic Tatjana M,Grk Milka B,Varljen Tatjana J,Pantelic Jelica R,Maksimovic Nela S,Jekic Biljana B,Novakovic Ivana V (2019) Association of genetic markers of coagulation and fibrinolysis with prematurity complication, EUROPEAN JOURNAL OF HUMAN GENETICS, vol. 27, br. , str. 641-642 (Meeting Abstract) 

Jankovic Milena Z,Dobricic Valerija S,Marjanovic Ana,Brankovic Marija,Pavlovic Aleksandra M,Dujmovic Irena,Mijajlovic Milija D,Novakovic Ivana V,Kostic Vladimir S (2019) NOTCH3 mutations in Serbian CADASIL patients, EUROPEAN JOURNAL OF HUMAN GENETICS, vol. 27, br. , str. 293-293 (Meeting Abstract) 

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 (2019) Use of clinical exome analysis in rare neurodegenerative disorders in Serbian population: Firs experience, EUROPEAN JOURNAL OF HUMAN GENETICS, vol. 27, br. , str. 292-292 (Meeting Abstract) 

Mitropoulos Konstantinos,...,Dobricic Valerija S,Novakovic Ivana V,Kostic Vladimir S,...,(broj koautora 33) (2019) Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients, EUROPEAN JOURNAL OF HUMAN GENETICS, vol. 27, br. , str. 252-253 (Meeting Abstract) 

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 (2019) Polymorphisms in PPARG gene: association with obesity-related metabolic traits in a Serbian adolescent population, EUROPEAN JOURNAL OF HUMAN GENETICS, vol. 27, br. , str. 190-191 (Meeting Abstract) 

Dawod Phepy GA,Rovcanin Branislav R,Marjanovic Ana,Marjanovic Ana,Jankovic Milena Z,Novakovic Ivana V,Dujmovic Irena,Jancic Jasna B,Kostic Vladimir S (2019) Analysis of mtDNA mutations in Serbian patients with Leber hereditary optic neuropathy, EUROPEAN JOURNAL OF HUMAN GENETICS, vol. 27, br. , str. 181-181 (Meeting Abstract) 

Hodzic Alenka,Maver Ales,Zorn Branko,Plaseska-Karanfilska Dijana,Ristanovic Momcilo,Novakovic Ivana V,Peterlin Borut (2019) De novo mutations in idiopathic male infertility, EUROPEAN JOURNAL OF HUMAN GENETICS, vol. 27, br. , str. 16-17 (Meeting Abstract) 

Peterlin Borut,Vidmar Lovro,Drulovic Jelena S,Sepcic Juraj,Novakovic Ivana V,Ristic Smiljana,Sega-Jazbec Sasa,Maver Ales (2019) Increased burden of ultra-rare genetic variants in the inflammasome regulatory genes in patients with multiple sclerosis, EUROPEAN JOURNAL OF NEUROLOGY, vol. 26, br. , str. 885-885 (Meeting Abstract) 

Mandic-Stojmenovic Gorana B,Stefanova Elka D,Novakovic Ivana V,Dobricic Valerija S,Stojkovic Tanja,Kostic Vladimir K (2019) The pattern of inheritance and genetic status in early onset Alzheimer's disease and frontotemporal dementia, EUROPEAN JOURNAL OF NEUROLOGY, vol. 26, br. , str. 120-120 (Meeting Abstract) 

Vidmar Lovro,Mayer Ales,Drulovic Jelena S,Sepcic Juraj,Novakovic Ivana V,Ristic Smiljana,Sega Sasa,Peterlin Borut (2019) Multiple Sclerosis patients carry an increased burden of exceedingly rare genetic variants in the inflammasome regulatory genes, SCIENTIFIC REPORTS, vol. 9, br. , str. - (Article) 

Svetel Marina V,Hartig Monika B,Cvetkovic Dragana D,Beaubois Cyrielle,Maksic Jasmina,Novakovic Ivana V,Krajinovic Maja,Kostic Vladimir K (2019) Phenotypic expression and founder effect of PANK2 c.1583C > T (p.T528M) mutation in Serbian pantothenate kinase-associated neurodegeneration patients, ARCHIVES OF BIOLOGICAL SCIENCES, vol. 71, br. 2, str. 275-280 (Article) 

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 (2019) Analysis of the Association Between Polymorphisms within PAI-1 and ACE genes and Ischemic Stroke Outcome After rt-PA Therapy, JOURNAL OF PHARMACY AND PHARMACEUTICAL SCIENCES, vol. 22, br. , str. 142-149 (Article) 

Varljen Tatjana J,Rakic Olgica,Sekulovic Gordana,Jekic Biljana B,Maksimovic Nela S,Rankovic-Janevski Milica,Novakovic Ivana V,Damnjanovic Tatjana M (2019) Association between Tumor Necrosis Factor-alpha Promoter-308 G/A Polymorphism and Early Onset Sepsis in Preterm Infants, TOHOKU JOURNAL OF EXPERIMENTAL MEDICINE, vol. 247, br. 4, str. 259-264 (Article) 

Dopsaj Violeta,Topic Aleksandra S,Savkovic Miljan,Milinkovic Neda Lj,Novakovic Ivana V,Cujic Danica,Simic-Ogrizovic Sanja P (2019) Associations of Common Variants in HFE and TMPRSS6 Genes with Hepcidin-25 and Iron Status Parameters in Patients with End-Stage Renal Disease, DISEASE MARKERS, vol. , br. , str. - (Article) 

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 (2019) Association of C35T polymorphism in dihydrofolate reductase gene with toxicity of methotrexate in rheumatoid arthritis patients, EXPERT OPINION ON DRUG METABOLISM & TOXICOLOGY, vol. 15, br. 3, str. 253-257 (Article) 

Novakovic Ivana V,Popovic-Kuzmanovic Dragana,Stojanovic Ljudmila,Trajkovic Vladimir S (2018) Study of the polymorphisms in genes IL-17, IL-23, TGFb, RORgT and FOXP3 in Serbian patients with antiphospholipid syndrome, EUROPEAN JOURNAL OF HUMAN GENETICS, vol. 26, br. , str. 906-906 (Meeting Abstract) 

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 (2018) Identification of mutations in PARK2 gene in Serbian patients with Parkinson's disease, EUROPEAN JOURNAL OF HUMAN GENETICS, vol. 26, br. , str. 410-411 (Meeting Abstract) 

Brankovic Marija,Kresojevic Nikola D,Marjanovic Ana,Novakovic Ivana V,Kostic Vladimir K (2018) NPC1 and NPC2 gene analysis in Serbian patients with Niemann-Pick disease type C, EUROPEAN JOURNAL OF HUMAN GENETICS, vol. 26, br. , str. 406-406 (Meeting Abstract) 

Peterlin AM,Maver Ales,Hodzic A,Sega Sasa,Drulovic Jelena S,Novakovic Ivana V,Pekmezovic Tatjana D,Ristic S,Kapovic Miljenko,Peterlin Borut (2018) The burden of rare genetic variants in genes involved in tumor necrosis factor (TNF) signalling pathway in multiple sclerosis (MS), EUROPEAN JOURNAL OF HUMAN GENETICS, vol. 26, br. , str. 400-400 (Meeting Abstract) 

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 (2018) C9ORF72 genetic screening in Serbian patients with neurodegenerative disorders, EUROPEAN JOURNAL OF HUMAN GENETICS, vol. 26, br. , str. 376-376 (Meeting Abstract) 

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 (2018) Identification of mutations in the PARK2 gene in Serbian patients with Parkinson's disease, JOURNAL OF THE NEUROLOGICAL SCIENCES, vol. 393, br. , str. 27-30 (Article) 

Mitropoulos Konstantinos,...,Dobricic Valerija S,Novakovic Ivana V,Kostic Vladimir S,...,(broj koautora 30) (2018) Genomic Variants in the FTO Gene are Associated with Sporadic Amyotrophic Lateral Sclerosis in Greek Patients, PUBLIC HEALTH GENOMICS, vol. 21, br. , str. 17-17 (Meeting Abstract) 

Hodzic Alenka,Lavtar Polona,Ristanovic Momcilo,Novakovic Ivana V,Dotlic Jelena R,Peterlin Borut (2018) Genetic variation in the CLOCK gene is associated with idiopathic recurrent spontaneous abortion, PLOS ONE, vol. 13, br. 5, str. - (Article) 

Jovicic-Pavlovic Svetlana M,Simic-Ogrizovic Sanja P,Dopsaj Violeta,Novakovic Ivana V,Bukumiric Zoran M,Naumovic Radomir T (2017) Association of Fetuin Gene Polymorphisms with Coronary Artery Calcifications and Mortality in Renal Transplant and Chronic Kidney Disease Patients, NEPHROLOGY DIALYSIS TRANSPLANTATION, vol. 32, br. , str. 733-733 (Meeting Abstract) 

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 (2017) GCH1 mutations are common in Serbian patients with dystonia-parkinsonism: Challenging previously reported prevalence rates of DOPA-responsive dystonia, PARKINSONISM & RELATED DISORDERS, vol. 45, br. , str. 81-84 (Article) 

Mitropoulos Konstantinos,...,Dobricic Valerija S,Novakovic Ivana V,Kostic Vladimir S,...,(broj koautora 33) (2017) Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients, HUMAN GENOMICS, vol. 11, br. , str. - (Article) 

Mihaljevic Marina M,Franic Dusica,Soldatovic Ivan A,Andric Sanja V,Mirjanic Tijana,Novakovic Ivana V,Adzic Miroslav,Maric Nadja P (2017) Fkbp5 Epigenetic Changes in Schizophrenia: Similarity to Stress-Related Conditions, EUROPEAN NEUROPSYCHOPHARMACOLOGY, vol. 27, br. , str. S461-S462 (Meeting Abstract) 

Mihaljevic Marina M,Andric Sanja V,Mirjanic Tijana,Novakovic Ivana V,Maric-Bojovic Nadja P (2017) 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, EUROPEAN NEUROPSYCHOPHARMACOLOGY, vol. 27, br. , str. S258-S259 (Meeting Abstract) 

Jovicic-Pavlovic Svetlana M,Simic-Ogrizovic Sanja P,Dopsaj Violeta,Novakovic Ivana V,Bukumiric Zoran M,Naumovic Radomir T (2017) Influence of Gene Polymorphisms on Serum Fetuin-A Levels and Vascular Calcifications in Renal Transplant and Chronic Kidney Disease Patients, TRANSPLANT INTERNATIONAL, vol. 30, br. , str. 269-270 (Meeting Abstract) 

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 (2017) The emerging role of the FKBP5 gene polymorphisms in vulnerability-stress model of schizophrenia: further evidence from a Serbian population, EUROPEAN ARCHIVES OF PSYCHIATRY AND CLINICAL NEUROSCIENCE, vol. 267, br. 6, str. 527-539 (Article) 

Maver Ales,...,Drulovic Jelena S,Pekmezovic Tatjana D,Novakovic Ivana V,...,(broj koautora 19) (2017) Identification of rare genetic variation of NLRP1 gene in familial multiple sclerosis, SCIENTIFIC REPORTS, vol. 7, br. , str. - (Article) 

Mihaljevic Marina M,Franic Dusica,Soldatovic Ivan A,Andric Sanja V,Mirjanic Tijana,Novakovic Ivana V,Adzic Miroslav,Maric Nadja P (2017) Allele-Specific and Trauma-Related Epigenetic Changes in the FKBP5 Gene: Differences Between Psychotic Patients and Healthy Controls, SCHIZOPHRENIA BULLETIN, vol. 43, br. , str. S195-S195 (Meeting Abstract) 

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 (2017) The Signature of Trauma in Psychosis: a Preliminary Genetic and Epigenetic Analyses of FK506-Binding Protein 5 Regulation, SCHIZOPHRENIA BULLETIN, vol. 43, br. , str. S66-S66 (Meeting Abstract) 

Hodzic Alenka,Ristanovic Momcilo,Zorn Branko,Tulic Cane Dz,Maver Ales,Novakovic Ivana V,Plaseska-Karanfilska Dijana,Peterlin Borut (2017) Genetic variation in leptin and leptin receptor genes as a risk factor for idiopathic male infertility, ANDROLOGY, vol. 5, br. 1, str. 70-74 (Article) 

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 (2017) A pilot study on predictors of brainstem raphe abnormality in patients with major depressive disorder, JOURNAL OF AFFECTIVE DISORDERS, vol. 209, br. , str. 66-70 (Article) 

Svetel Marina V,Tomic Aleksandra D,Mijajlovic Milija D,Dobricic Valerija S,Novakovic Ivana V,Pekmezovic Tatjana D,Brajkovic Lela,Kostic Vladimir S (2017) Transcranial sonography in dopa-responsive dystonia, EUROPEAN JOURNAL OF NEUROLOGY, vol. 24, br. 1, str. 161-166 (Article) 

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 (2016) Clusters of cognitive impairment among different forms of myotonic dystrophies, EUROPEAN JOURNAL OF NEUROLOGY, vol. 23, br. , str. 550-550 (Meeting Abstract) 

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 (2016) Cytomegalovirus induces Interleukin-6 mediated inflammatory response in salivary gland cancer, JOURNAL OF BUON, vol. 21, br. 6, str. 1530-1536 (Article) 

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 (2016) Analysis of T-786c and 4a/b Endothelial Nitric Oxide Synthase Gene Polymorphisms in Retinopathy of Prematurity, GENETIKA-BELGRADE, vol. 48, br. 2, str. 707-716 (Article) 

Peric Stojan Z,Vujnic Milorad,Dobricic Valerija S,Marjanovic Ana,Basta Ivana Z,Novakovic Ivana V,Lavrnic Dragana V,Rakocevic-Stojanovic Vidosava M (2016) Five-year study of quality of life in myotonic dystrophy, ACTA NEUROLOGICA SCANDINAVICA, vol. 134, br. 5, str. 346-351 (Article) 

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 (2016) Association of 63/91 length polymorphism in the DHFR gene major promoter with toxicity of methotrexate in patients with rheumatoid arthritis, PHARMACOGENOMICS, vol. 17, br. 15, str. 1687-1691 (Article) 

Stefanova Elka D,Mandic Gorana B,Dobricic Valerija S,Stojkovic Tanja,Jankovic Milena Z,Novakovic Ivana V,Kostic Vladimir S (2016) Genetic mutations in Frontemporal dementia - report from the memory clinic from Serbia, JOURNAL OF NEUROCHEMISTRY, vol. 138, br. , str. 326-326 (Meeting Abstract) 

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 (2016) The Cumulative Effect of Genetic Polymorphisms on Depression and Brain Structural Integrity, HUMAN BRAIN MAPPING, vol. 37, br. 6, str. 2173-2184 (Article) 

Dobricic Valerija S,Kresojevic Nikola D,Marjanovic Ana,Tomic Aleksandra D,Svetel Marina V,Novakovic Ivana V,Kostic Vladimir S (2016) HPCA-related dystonia: Too rare to be found?, MOVEMENT DISORDERS, vol. 31, br. 7, str. 1071-1071 (Letter) 

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 (2016) Predictive Role of Circulating Leucocyte-Platelet Aggregates for Thromboembolic Complications in Philadelphia-Negative Myeloproliferative Neoplasms: a Prospective Study, HAEMATOLOGICA, vol. 101, br. , str. 266-266 (Meeting Abstract) 

Radunovic Milena,Nikolic Nadja S,Milenkovic Sanja M,Tomanovic Nada R,Boricic Ivan V,Dimitrijevic Milovan V,Novakovic Ivana V,Basta-Jovanovic Gordana M (2016) The MMP-2 and MMP-9 promoter polymorphisms and susceptibility to salivary gland cancer, JOURNAL OF BUON, vol. 21, br. 3, str. 597-602 (Article) 

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 (2016) Analysis of Association Between Polymorphisms of Mthfr, Mthfd and Rfc1 Genes and Efficacy and Toxicity of Methotrexate in Rheumatoid Arthritis Patients, GENETIKA-BELGRADE, vol. 48, br. 1, str. 395-408 (Article) 

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 (2016) Polymorphisms of the eNOS gene are associated with disease activity in rheumatoid arthritis, RHEUMATOLOGY INTERNATIONAL, vol. 36, br. 4, str. 597-602 (Article) 

Dujmovic Irena,Jancic Jasna B,Dobricic Valerija S,Jankovic Slavko M,Novakovic Ivana V,Comabella Manuel,Drulovic Jelena S (2016) Are Leber's mitochondial DNA mutations associated with aquaporin-4 autoimmunity?, MULTIPLE SCLEROSIS JOURNAL, vol. 22, br. 3, str. 393-394 (Letter) 

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 (2016) Clients' Perception of Outcome of Team-Based Prenatal and Reproductive Genetic Counseling in Serbian Service Using the Perceived Personal Control (PPC) Questionnaire, JOURNAL OF GENETIC COUNSELING, vol. 25, br. 1, str. 189-197 (Article) 

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 (2015) Subtelomeric screening in Serbian children with dysmorphic features and unexplained developmental delay/intellectual disabilities, TURKISH JOURNAL OF PEDIATRICS, vol. 57, br. 2, str. 154-160 (Article) 

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 (2015) Effect of accumulation of 5-HTTLPR, BDNF Vall66Met and COMT Val158Met polymorphisms on brain morphology in patients with major depressive disorder, EUROPEAN NEUROPSYCHOPHARMACOLOGY, vol. 25, br. , str. S395-S395 (Meeting Abstract) 

Mihaljevic Marina M,Pekmezovic Tatjana D,Andric Sanja V,Mirjanic Tijana,Novakovic Ivana V,Maric Nadja P (2015) Subclinical psychotic experiences in healthy adults: relationship between genetic variants of FKBP5 gene, neuroticism and childhood trauma, EUROPEAN NEUROPSYCHOPHARMACOLOGY, vol. 25, br. , str. S177-S177 (Meeting Abstract) 

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 (2015) 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, EUROPEAN JOURNAL OF NEUROLOGY, vol. 22, br. , str. 629-629 (Meeting Abstract) 

Mandic-Stojmenovic Gorana B,Stefanova Elka D,Dobricic Valerija S,Novakovic Ivana V,Stojkovic Tanja,Jesic Aleksandar Z,Kostic Vladimir S (2015) Screening for C9orf72 Expansion Mutation in Serbian Patients with Early-Onset Dementia, DEMENTIA AND GERIATRIC COGNITIVE DISORDERS, vol. 40, br. 5-6, str. 358-365 (Article) 

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 (2015) Phenotype of non-c.907_909delGAG mutations in TOR1A: DYT1 dystonia revisited, PARKINSONISM & RELATED DISORDERS, vol. 21, br. 10, str. 1256-1259 (Article) 

Rakocevic-Stojanovic Vidosava M,Peric Stojan Z,Basta Ivana Z,Dobricic Valerija S,Ralic Vesna,Kacar Aleksandra S,Peric Marina,Novakovic Ivana V (2015) Variability of multisystemic features in myotonic dystrophy type 1-lessons from Serbian registry, NEUROLOGICAL RESEARCH, vol. 37, br. 11, str. 939-944 (Article) 

Dzoljic Eleonora D,Novakovic Ivana V,Krajinovic Maja,Grbatinic Ivan I,Kostic Vladimir S (2015) Pharmacogenetics of drug response in Parkinson's disease, INTERNATIONAL JOURNAL OF NEUROSCIENCE, vol. 125, br. 9, str. 635-644 (Review) 

Mihaljevic Marina M,Andric Sanja V,Mirjanic Tijana,Soldatovic Ivan A,Novakovic Ivana V,Maric Nadja P (2015) Further evidence of the impact of the risk variant FKBP5 gene in schizophrenia in a Serbian sample of patients, siblings and controls, EUROPEAN NEUROPSYCHOPHARMACOLOGY, vol. 25, br. , str. S16-S17 (Meeting Abstract) 

Vujnic Milorad,Peric Stojan Z,Popovic Srdjan S,Raseta Nela,Ralic Vesna,Dobricic Valerija S,Novakovic Ivana V,Rakocevic-Stojanovic Vidosava M (2015) Metabolic syndrome in patients with myotonic dystrophy type 1, MUSCLE & NERVE, vol. 52, br. 2, str. 273-277 (Article) 

Pajic Jelena R,Rakic Boban M,Rovcanin Branislav R,Jovicic Dubravka,Novakovic Ivana V,Milovanovic Aleksandar PS,Pajic Vesna S (2015) Inter-individual variability in the response of human peripheral blood lymphocytes to ionizing radiation: comparison of the dicentric and micronucleus assays, RADIATION AND ENVIRONMENTAL BIOPHYSICS, vol. 54, br. 3, str. 317-325 (Article) 

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 (2015) Presenting symptoms of GBA-related Parkinson's disease, PARKINSONISM & RELATED DISORDERS, vol. 21, br. 7, str. 804-807 (Article) 

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 (2015) Presenting symptoms of GBA-related Parkinson's disease, EUROPEAN JOURNAL OF NEUROLOGY, vol. 22, br. , str. 437-437 (Meeting Abstract) 

Svetel Marina V,Tomic Aleksandra D,Dobricic Valerija S,Novakovic Ivana V,Dragasevic-Miskovic Natasa T,Petrovic Igor N,Kostic Vladimir K (2015) Dopa-responsive dystonia in the Serbian population: clinical and genetical characteristics, EUROPEAN JOURNAL OF NEUROLOGY, vol. 22, br. , str. 393-393 (Meeting Abstract) 

Jankovic Milena Z,Kresojevic Nikola D,Dobricic Valerija S,Markovic Vladana V,Petrovic Igor N,Novakovic Ivana V,Kostic Vladimir S (2015) Identification of novel mutations in LRRK2 gene in patients with Parkinson's disease, EUROPEAN JOURNAL OF NEUROLOGY, vol. 22, br. , str. 354-354 (Meeting Abstract) 

Dobricic Valerija S,Kresojevic Nikola D,Zarkovic Milena,Tomic Aleksandra D,Svetel Marina V,Novakovic Ivana V,Kostic Vladimir S (2015) A novel TOR1A mutation in a Serbian patient with cervical dystonia, EUROPEAN JOURNAL OF NEUROLOGY, vol. 22, br. , str. 260-260 (Meeting Abstract) 

Peric Stojan Z,Paunic Teodora,Dobricic Valerija S,Novakovic Ivana V,Basta Ivana Z,Lavrnic Dragana V,Rakocevic-Stojanovic Vidosava M (2015) Echocardiography in patients with myotonic dystrophy type 1, EUROPEAN JOURNAL OF NEUROLOGY, vol. 22, br. , str. 205-205 (Meeting Abstract) 

Jankovic Milena Z,Kresojevic Nikola D,Dobricic Valerija S,Markovic Vladana V,Petrovic Igor N,Novakovic Ivana V,Kostic Vladimir S (2015) Identification of novel variants in LRRK2 gene in patients with Parkinson's disease in Serbian population, JOURNAL OF THE NEUROLOGICAL SCIENCES, vol. 353, br. 1-2, str. 59-62 (Article) 

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 (2015) GSTO1*C/GSTO2*G haplotype is associated with risk of transitional cell carcinoma of urinary bladder, INTERNATIONAL UROLOGY AND NEPHROLOGY, vol. 47, br. 4, str. 625-630 (Article) 

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 (2014) Intellectual Ability in the Duchenne Muscular Dystrophy and Dystrophin Gene Mutation Location, BALKAN JOURNAL OF MEDICAL GENETICS, vol. 17, br. 2, str. 25-35 (Article) 

Svetel Marina V,Dobricic Valerija S,Novakovic Ivana V,Dragasevic Natasa T,Petrovic Igor N,Kostic Vladimir S (2014) Clinical and genetic characteristics of dopa-responsive dystonia in Serbian population, JOURNAL OF NEUROLOGY, vol. 261, br. , str. S433-S433 (Meeting Abstract) 

Vujnic Milorad,Peric Stojan Z,Dobricic Valerija S,Ralic Vesna,Novakovic Ivana V,Rakocevic-Stojanovic Vidosava M (2014) Metabolic syndrome in patients with myotonic dystrophy type 1, JOURNAL OF NEUROLOGY, vol. 261, br. , str. S347-S347 (Meeting Abstract) 

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 (2014) 657del5 Mutation of the Nbs1 Gene in Myelodysplastic Syndrome, ARCHIVES OF BIOLOGICAL SCIENCES, vol. 66, br. 3, str. 1055-1059 (Article) 

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 (2014) Possible Influence of MTHFR C677T Polymorphism on Serum Lipid Levels in Serbian School Children, ARCHIVES OF BIOLOGICAL SCIENCES, vol. 66, br. 2, str. 729-734 (Article) 

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 (2014) De Novo Mutation in the GNAL Gene Causing Seemingly Sporadic Dystonia in a Serbian Patient, MOVEMENT DISORDERS, vol. 29, br. 9, str. 1190-1193 (Article) 

Cetkovic Aleksandar,Kastratovic Biljana,Novakovic Ivana V (2014) Prospective study of perinatal outcome in pregnancies with primary antiphospholipid syndrome, VOJNOSANITETSKI PREGLED, vol. 71, br. 8, str. 742-745 (Article) 

Svetel Marina V,Dobricic Valerija S,Novakovic Ivana V,Dragasevic Natasa T,Petrovic Igor N,Kostic Vladimir S (2014) Clinical and genetic characteristics of dopa-responsive dystonia in a Serbian population, EUROPEAN JOURNAL OF NEUROLOGY, vol. 21, br. , str. 668-668 (Meeting Abstract) 

Vujnic Milorad,Peric Stojan Z,Dobricic Valerija S,Ralic Vesna,Novakovic Ivana V,Rakocevic-Stojanovic Vidosava M (2014) Metabolic syndrome in patients with myotonic dystrophy type 1, EUROPEAN JOURNAL OF NEUROLOGY, vol. 21, br. , str. 528-528 (Meeting Abstract) 

Veselinovic Nikola D,Pavlovic Aleksandra M,Petrovic Boris,Ristic Aleksandar J,Novakovic Ivana V,Svabic-Medjedovic Tamara S,Pavlovic Dragan,Sternic Nadezda M (2014) Altered Basal Ganglia Echogenicity Early in Sporadic Creutzfeldt-Jakob Disease, COGNITIVE AND BEHAVIORAL NEUROLOGY, vol. 27, br. 1, str. 48-50 (Article) 

Novakovic Ivana V,Maksimovic Nela S,Pavlovic Aleksandra,Zarkovic Milena,Rovcanin Branislav R,Mirkovic Dusko S,Pekmezovic Tatjana D,Cvetkovic Dragana D (2014) Introduction to Molecular Genetic Diagnostics, JOURNAL OF MEDICAL BIOCHEMISTRY, vol. 33, br. 1, str. 3-7 (Review) 

Maksimovic Nela S,Novakovic Ivana V,Ralic Vesna,Stefanova Elka D (2013) Distribution of Apolipoprotein E Gene Polymorphism in Students and in High-Educated Elderly from Serbia, GENETIKA-BELGRADE, vol. 45, br. 3, str. 865-872 (Article) 

Svetel Marina V,Pekmezovic Tatjana D,Markovic Vladana V,Novakovic Ivana V,Dobricic Valerija S,Djuric Gordana M,Stefanova Elka D,Kostic Vladimir S (2013) No Association between Brain-Derived Neurotrophic Factor G196A Polymorphism and Clinical Features of Parkinson's Disease, EUROPEAN NEUROLOGY, vol. 70, br. 5-6, str. 257-262 (Article) 

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 (2013) Transcranial brain parenchyma sonography in Parkinson's disease with glucocerebrosidase mutations, CEREBROVASCULAR DISEASES, vol. 35, br. , str. 59-59 (Meeting Abstract) 

Pavlovic Aleksandra M,Dobricic Valerija S,Semnic Robert R,Lackovic Vesna B,Novakovic Ivana V,Bajcetic Milos I,Sternic Nadezda M (2013) A novel Notch3 Gly89Cys mutation in a Serbian CADASIL family, ACTA NEUROLOGICA BELGICA, vol. 113, br. 3, str. 299-302 (Article) 

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 (2013) A common polymorphism in the brain-derived neurotrophic factor gene in patients with adult-onset primary focal and segmental dystonia, ACTA NEUROLOGICA BELGICA, vol. 113, br. 3, str. 243-245 (Article) 

Tomic Aleksandra D,Dobricic Valerija S,Novakovic Ivana V,Svetel Marina V,Pekmezovic Tatjana D,Kresojevic Nikola D,Potrebic Aleksandra,Kostic Vladimir S (2013) Mutational analysis of ATP7B gene and the genotype-phenotype correlation in patients with Wilson's disease in Serbia, VOJNOSANITETSKI PREGLED, vol. 70, br. 5, str. 457-462 (Article) 

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 (2013) Transcranial sonography in patients with Parkinson's disease with glucocerebrosidase mutations, PARKINSONISM & RELATED DISORDERS, vol. 19, br. 4, str. 431-435 (Article) 

Dobricic Valerija S,Kresojevic Nikola D,Svetel Marina V,Jankovic Milena Z,Petrovic Igor N,Tomic Aleksandra D,Novakovic Ivana V,Kostic Vladimir S (2013) Mutation screening of the DYT6/THAP1 gene in Serbian patients with primary dystonia, JOURNAL OF NEUROLOGY, vol. 260, br. 4, str. 1037-1042 (Article) 

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 (2013) 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, EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, vol. 69, br. 3, str. 377-383 (Article) 

Papassotiropoulos A,Stefanova Elka D,...,Novakovic Ivana V,...,Scheffler K,(broj koautora 19) (2013) A genome-wide survey and functional brain imaging study identify CTNNBL1 as a memory-related gene, MOLECULAR PSYCHIATRY, vol. 18, br. 2, str. 255-263 (Article) 

Hodzic Alenka,Ristanovic Momcilo,Zorn Branko,Tulic Cane Dz,Maver Ales,Novakovic Ivana V,Peterlin Borut (2013) Genetic Variation in Circadian Rhythm Genes CLOCK and ARNTL as Risk Factor for Male Infertility, PLOS ONE, vol. 8, br. 3, str. - (Article) 

Popovic-Kuzmanovic Dragana,Novakovic Ivana V,Stojanovic Ljudmila,Aksentijevich Ivona,Zogovic Nevena S,Tovilovic Gordana I,Trajkovic Vladimir S (2013) Increased activity of interleukin-23/interleukin-17 cytokine axis in primary antiphospholipid syndrome, IMMUNOBIOLOGY, vol. 218, br. 2, str. 186-191 (Article) 

Hsu Sandy Chan,...,Dobricic Valerija S,...,Jankovic Milena Z,...,Kostic Vladimir S,...,Novakovic Ivana V,...,(broj koautora 52) (2013) Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification, NEUROGENETICS, vol. 14, br. 1, str. 11-22 (Article) 

Radojevic-Skodric Sanja M,Brasanac Dimitrije C,Novakovic Ivana V,Bogdanovic Ljiljana M,Krstic Z,Basta-Jovanovic Gordana M (2012) Amplification of cyclin A gene in Wilms tumor, VIRCHOWS ARCHIV, vol. 461, br. , str. S220-S220 (Meeting Abstract) 

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 (2012) Skin and Sural Nerve Biopsies: Ultrastructural Findings in the First Genetically Confirmed Cases of CADASIL in Serbia, ULTRASTRUCTURAL PATHOLOGY, vol. 36, br. 5, str. 325-335 (Article) 

Dobricic Valerija S,Stefanova Elka D,Jankovic Milena Z,Gurunlian Nicole,Novakovic Ivana V,Hardy John,Kostic Vladimir S,Guerreiro Rita (2012) Genetic testing in familial and young-onset Alzheimer's disease: mutation spectrum in a Serbian cohort, NEUROBIOLOGY OF AGING, vol. 33, br. 7, str. - (Article) 

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 (2012) Quantitative Analysis of the Dystrophin Gene by Real-Time Pcr, ARCHIVES OF BIOLOGICAL SCIENCES, vol. 64, br. 2, str. 787-792 (Article) 

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 (2012) Association of dihydrofolate reductase (DHFR)-317AA genotype with poor response to methotrexate in patients with rheumatoid arthritis, CLINICAL AND EXPERIMENTAL RHEUMATOLOGY, vol. 30, br. 2, str. 178-183 (Article) 

Mitic Vesna,Cuturilo Goran,Novakovic Ivana V,Dimitrijevic Nikola,Damnjanovic Tatjana M,Dimitrijevic Aleksandar N,Dobricic Valerija S,Kostic Vladimir S,Radlovic Nedeljko P (2011) Epilepsy in a Child with Wolf-Hirschhorn Syndrome, SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO, vol. 139, br. 11-12, str. 795-799 (Article) 

Pavlovic Aleksandra M,Pekmezovic Tatjana D,Obrenovic Radmila R,Novakovic Ivana V,Tomic Gordana G,Mijajlovic Milija D,Sternic Nadezda M (2011) Increased total homocysteine level is associated with clinical status and severity of white matter changes in symptomatic patients with subcortical small vessel disease, CLINICAL NEUROLOGY AND NEUROSURGERY, vol. 113, br. 9, str. 711-715 (Article) 

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 (2011) Mutation and Founder Effect Studies in Pkan Patients with Serbian Origin: Report of Five Cases, EUROPEAN JOURNAL OF NEUROLOGY, vol. 18, br. , str. 516-516 (Meeting Abstract) 

Tomic Aleksandra D,Svetel Marina V,Novakovic Ivana V,Dobricic Valerija S,Kresojevic Nikola D,Kostic Vladimir S (2011) Mutational Analysis of ATP7B Gene and Genotype-Phenotype Correlation in Patients with Wilson's Disease From Serbia, EUROPEAN JOURNAL OF NEUROLOGY, vol. 18, br. , str. 488-488 (Meeting Abstract) 

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 (2011) Anthropometric and Lipid Parameters Trends in School Children: One Decade of YUSAD Study, SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO, vol. 139, br. 7-8, str. 465-469 (Article) 

Kostic Vladimir S,Jecmenica-Lukic Milica V,Novakovic Ivana V,Dobricic Valerija S,Brajkovic Lela,Krajinovic Maja,Klein Christine,Pavlovic Aleksandra M (2011) Exclusion of linkage to chromosomes 14q, 2q37 and 8p21.1-q11.23 in a Serbian family with idiopathic basal ganglia calcification, JOURNAL OF NEUROLOGY, vol. 258, br. 9, str. 1637-1642 (Article) 

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 (2011) Npm1 Gene Mutations in Children with Myelodysplastic Syndromes, ARCHIVES OF BIOLOGICAL SCIENCES, vol. 63, br. 3, str. 649-653 (Article) 

Milincic Zeljka D,Nikolic Dejan P,Simeunovic Slavko D,Novakovic Ivana V,Petronic Ivana,Risimic Dijana S,Simeunovic Dejan S (2011) School children systolic and diastolic blood pressure values: YUSAD study, CENTRAL EUROPEAN JOURNAL OF MEDICINE, vol. 6, br. 5, str. 634-639 (Article) 

Nikolic Dejan P,Petronic Ivana,Milincic Zeljka D,Simeunovic Slavko D,Novakovic Ivana V,Nedeljkovic Srecko I,Cirovic Dragana,Janic Nenad (2011) Evaluation of recreational physical activity correlation and influence on lipid fractions in school children: YUSAD study, MEDICINA DELLO SPORT, vol. 64, br. 1, str. 55-62 (Article) 

Puzovic Dragana Z,Dunjic Dusan J,Popovic Branka M,Stojkovic Oliver V,Novakovic Ivana V,Milasin Jelena M (2011) STR LOCI D19S216, D20S502 and D20S842 Analysis in the Serbian Population Using Dentin Dna, ARCHIVES OF BIOLOGICAL SCIENCES, vol. 63, br. 1, str. 55-58 (Article) 

Kresojevic Nikola D,Svetel Marina V,Dobricic Valerija S,Novakovic Ivana V,Stojkovic Tanja,Kostic Vladimir S (2011) Clinical evaluation of DYT6 dystonia in Serbia, JOURNAL OF NEUROLOGY, vol. 258, br. , str. 83-84 (Meeting Abstract) 

Stojkovic Tanja,Svetel Marina V,Dobricic Valerija S,Novakovic Ivana V,Kostic Vladimir S (2011) Cerebellar ataxia and epilepsy caused by hereditary folate malabsorption, JOURNAL OF NEUROLOGY, vol. 258, br. , str. 82-83 (Meeting Abstract) 

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 (2011) A genome-wide survey of human short-term memory, MOLECULAR PSYCHIATRY, vol. 16, br. 2, str. 184-192 (Article) 

Jecmenica-Lukic Milica V,Petrovic Igor N,Dobricic Valerija S,Novakovic Ivana V,Kostic Vladimir S (2010) Exclusion of linkage to chromosome 14q in Serbian family with idiopathic basal ganglia calcification, EUROPEAN JOURNAL OF NEUROLOGY, vol. 17, br. , str. 381-381 (Meeting Abstract) 

Krcunovic Zorica,Novakovic Ivana V,Maksimovic Nela S,Bukvic Danica,Simic-Ogrizovic Sanja P,Jankovic Slavenka M,Djukanovic Ljubica D,Cvetkovic Dragana D (2010) Genetic Clues to the Etiology of Balkan Endemic Nephropathy: Investigating the Role of Ace and AT1R Polymorphisms, ARCHIVES OF BIOLOGICAL SCIENCES, vol. 62, br. 4, str. 957-965 (Article) 

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 (2010) Physical activity evaluation in Yugoslav Study of the Precursors of Atherosclerosis in School Children - YUSAD study, ARCHIVES OF MEDICAL SCIENCE, vol. 6, br. 6, str. 874-878 (Article) 

Popovic Branka M,Jekic Biljana B,Novakovic Ivana V,Lukovic Ljiljana F,Konstantinovic Vitomir S,Babic Marko,Milasin Jelena M (2010) Cancer genes alterations and HPV infection in oral squamous cell carcinoma, INTERNATIONAL JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY, vol. 39, br. 9, str. 909-915 (Article) 

Novakovic Ivana V,Maksimovic Nela S,Cvetkovic Slobodan D,Cvetkovic Dragana D (2010) Gene Polymorphisms as Markers of Disease Susceptibility, JOURNAL OF MEDICAL BIOCHEMISTRY, vol. 29, br. 3, str. 135-138 (Article) 

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 (2010) Association Between the Methylenetetrahydrofolate Reductase Polymorphisms and Risk of Acute Lymphoblastic Leukemia in Serbian Children, JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, vol. 32, br. 4, str. E148-E150 (Article) 

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 (2010) Investigation of Balkan Endemic Nephropathy in Serbia: How to Proceed?, SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO, vol. 138, br. 3-4, str. 256-261 (Article) 

Simeunovic Slavko D,Milincic Zeljka D,Novakovic Ivana V,Nedeljkovic Srecko I,Vukotic Milija,Simeunovic Dejan S,Nikolic Dejan P (2009) Epidemiology of Precursors of Atherosclerosis in Children - Yusad Study, ATHEROSCLEROSIS SUPPLEMENTS, vol. 10, br. 2, str. - (Meeting Abstract) 

Gurinovic Mirjana A,Glibetic Marija D,Vukotic Milija,Novakovic Ivana V,Ristic-Medic Danijela K,Radicev-Radanov Milena (2009) Obesity And Overweight In Schoolchildren And Adults In Serbia, ANNALS OF NUTRITION AND METABOLISM, vol. 55, br. , str. 271-271 (Meeting Abstract) 

Cuturilo Goran,Stefanovic Igor D,Jovanovic Ida V,Miletic-Grkovic Slobodanka,Novakovic Ivana V (2009) Mowat-Wilson Syndrome - A Case Report, SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO, vol. 137, br. 7-8, str. 426-429 (Article) 

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 (2009) Plasma homocysteine levels and cognitive status in patients with ischemic cerebrovascular disease, JOURNAL OF THE NEUROLOGICAL SCIENCES, vol. 283, br. 1-2, str. 248-248 (Meeting Abstract) 

Pastor Tibor J,Popovic Branka M,Gvozdenovic Ana,Boro Aleksandar,Petrovic Bojana,Novakovic Ivana V,Puzovic Dragana Z,Lukovic Ljiljana F,Milasin Jelena M (2009) Alterations of c-Myc and c-erbB-2 Genes in Ovarian Tumours, SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO, vol. 137, br. 1-2, str. 47-51 (Article) 

Puzovic Dragana Z,Popovic Branka M,Novakovic Ivana V,Milasin Jelena M (2009) Analysis of Microsatellite Markers D18S70 and D20S116 in DNA Isolated from Dentin: Use in Forensic Medicine, SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO, vol. 137, br. 1-2, str. 43-46 (Article) 

Milincic Zeljka D,Nikolic Dejan P,Simeunovic Slavko D,Novakovic Ivana V,Vukotic Milija (2008) Glycemia Trends in School Children in Serbia, ATHEROSCLEROSIS SUPPLEMENTS, vol. 9, br. 1, str. 95-96 (Meeting Abstract) 

Nikolic Dejan P,Milincic Zeljka D,Simeunovic Slavko D,Petronic Ivana,Novakovic Ivana V,Damnjanovic Tatjana M (2008) Systolic Blood Pressure Trends in School Children - Yusad Study, ATHEROSCLEROSIS SUPPLEMENTS, vol. 9, br. 1, str. 94-94 (Meeting Abstract) 

Ristanovic Momcilo,Bunjevacki Vera I,Tulic Cane Dz,Novakovic Ivana V,Ille Tatjana M,Radojkovic Dragica P,Nikolic Aleksandra M (2008) Y chromosome microdeletions in infertile male candidates for microfertilization, SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO, vol. 136, br. 3-4, str. 126-130 (Article) 

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 (2008) APOE genotype and cognitive functioning of college-age adults, EUROPEAN JOURNAL OF NEUROLOGY, vol. 15, br. , str. 189-189 (Meeting Abstract) 

Ristanovic Momcilo,Bunjevacki Vera I,Tulic Cane Dz,Novakovic Ivana V,Perovic Vladimir R,Lukovic Ljiljana F,Milasin Jelena M (2007) Prevalence of Y chromosome microdeletions in infertile men with severe oligozoospermia in Serbia, GENETIC COUNSELING, vol. 18, br. 3, str. 337-342 (Article) 

Damnjanovic Tatjana M,Novakovic Ivana V,Milasin Jelena M,Bunjevacki Vera I,Jekic Biljana B,Cvjeticanin Suzana,Lukovic Ljiljana F (2007) LeX chromosome imprinting in turner syndrome, KOREAN JOURNAL OF GENETICS, vol. 29, br. 3, str. 291-295 (Article) 

Simeunovic Slavko D,Milincic Zeljka D,Nikolic Dejan P,Simeunovic Dejan S,Novakovic Ivana V,Nedeljkovic Srecko I,Vukotic Milija (2007) Evaluation of anthropometric parameters as risk factors for atherosclerosis in children, ATHEROSCLEROSIS SUPPLEMENTS, vol. 8, br. 1, str. 176-177 (Meeting Abstract) 

Nikolic Dejan P,Damnjanovic Tatjana M,Milincic Zeljka D,Simeunovic Slavko D,Novakovic Ivana V,Risimic Dijana S,Vukotic Milija,Nedeljkovic Srecko I (2007) Association of homocysteine enzyme genetic markers and lipid levels in children, ATHEROSCLEROSIS SUPPLEMENTS, vol. 8, br. 1, str. 47-47 (Meeting Abstract) 

Ristanovic Momcilo,Bunjevacki Vera I,Tulic Cane Dz,Novakovic Ivana V,Nikolic Aleksandra M (2007) Molecular analysis of Y chromosome microdeletions in idiopathic cases of male infertility in Serbia, RUSSIAN JOURNAL OF GENETICS, vol. 43, br. 6, str. 705-708 (Article) 

Popovic Branka M,Jekic Biljana B,Novakovic Ivana V,Lukovic Ljiljana F,Tepavcevic Zvezdana,Jurisic Vladimir B,Vukadinovic Miroslav,Milasin Jelena M (2007) Bcl-2 expression in oral squamous cell carcinoma, SIGNAL TRANSDUCTION PATHWAYS, PT C, vol. 1095, br. , str. 19-25 (Article) 

Dzoljic Eleonora D,Novakovic Ivana V,Mirkovic Dusko D,Todorovic Zoran M,Prostran Milica S,Kostic Vladimir S (2006) Parkinson's disease, homocysteine serum levels and MTHFR C667T genotype, JOURNAL OF THE NEUROLOGICAL SCIENCES, vol. 248, br. 1-2, str. 322-322 (Meeting Abstract) 

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 (2006) Homocysteine serum levels and MTHFR C677T genotype in patients with Parkinson's disease, with and without levodopa therapy, JOURNAL OF THE NEUROLOGICAL SCIENCES, vol. 248, br. 1-2, str. 56-61 (Article) 

Jovicic Snezana Z,Simic-Ogrizovic Sanja P,Novakovic Ivana V,Radivojevic Dragana M,Blagojevic Radmila N (2006) Effects of MTHFR 677C > T and 1298A > C on serum homocysteine levels, carotid atherosclerosis and graft failure in renal transplant patients, KIDNEY & BLOOD PRESSURE RESEARCH, vol. 29, br. 3, str. 195-195 (Meeting Abstract) 

Simic-Ogrizovic Sanja P,Stosovic Milan D,Novakovic Ivana V,Pejanovic Svetlana D,Jemcov Tamara K,Radovic Milan M,Djukanovic Ljubica D (2006) Fuzzy role of hyperhomocysteinemia in hemodialysis patients' mortality, BIOMEDICINE & PHARMACOTHERAPY, vol. 60, br. 4, str. 200-207 (Article) 

Puzovic Dragana Z,Dunjic Dusan J,Popovic Branka M,Stojkovic Oliver V,Novakovic Ivana V,Milasin Jelena M (2006) Population data on HLA-DQA1, LDLR, GYPA, HBGG, D7S8, and GC PCR-based loci in Serbia, JOURNAL OF FORENSIC SCIENCES, vol. 51, br. 3, str. 699-699 (Editorial Material) 

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 (2006) Lack of TP53 and FMS gene mutations in children with myelodysplastic syndrome, CANCER GENETICS AND CYTOGENETICS, vol. 166, br. 2, str. 163-165 (Article) 

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 (2006) Genotypic and phenotypic spectrum of PANK2 mutations in patients with neurodegeneration with brain iron accumulation, ANNALS OF NEUROLOGY, vol. 59, br. 2, str. 248-256 (Article) 

Novakovic Ivana V,Bojic Daniela Z,Todorovic Slobodanka,Apostolski Slobodan A,Lukovic Ljiljana F,Stefanovic D,Milasin Jelena M (2005) Proximal dystrophin gene deletions and protein alterations in Becker muscular dystrophy, BIOPHYSICS FROM MOLECULES TO BRAIN: IN MEMORY OF RADOSLAV K. ANDJUS, vol. 1048, br. , str. 406-410 (Article) 

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 (2004) Low frequency of NRAS and KRAS2 gene mutations in childhood myelodysplastic syndromes, CANCER GENETICS AND CYTOGENETICS, vol. 154, br. 2, str. 180-182 (Article) 

Svetel Marina V,Novakovic Ivana V,Petrovic Igor N,Dragasevic Natasa T,Kostic Vladimir S (2004) Clinical presentation of Hallervorden-Spatz disease: Report of four cases, EUROPEAN JOURNAL OF NEUROLOGY, vol. 11, br. , str. 119-119 (Meeting Abstract) 

Novakovic Ivana V,Apostolski Slobodan A,Todorovic Slobodanka,Lukovic Ljiljana F,Bunjevacki Vera I,Bojic Daniela Z,Mestroni L,Milasin Jelena M (2002) Cardiac disorders in BMD patients with distal gene deletions, EUROPEAN JOURNAL OF HUMAN GENETICS, vol. 10, br. , str. 257-257 (Meeting Abstract) 

Popovic Branka M,Milasin Jelena M,Jekic Biljana B,Novakovic Ivana V (2002) The role of H-Ras gene in tumorigenesis of oral squamous cell carcinoma, EUROPEAN JOURNAL OF HUMAN GENETICS, vol. 10, br. , str. 99-99 (Meeting Abstract) 

Jekic Biljana B,Bunjevacki Vera I,Kuzmanovic Milos B,Novakovic Ivana V,Lukovic Ljiljana F (2002) Mutations of N- and K-Ras, p53 and FMS genes in myelodysplastic syndromes in children, EUROPEAN JOURNAL OF HUMAN GENETICS, vol. 10, br. , str. 88-88 (Meeting Abstract)