I. Novaković

M. Pešić, J. Tričković, M. Savic, 2019, Journal of pharmacy & pharmaceutical sciences : a publication of the Canadian Society for Pharmaceutical Sciences, Societe canadienne des sciences pharmaceutiques.

Identification of rare genetic variation of NLRP1 gene in familial multiple sclerosis

G. Zamolo, B. Peterlin, A. Maver, 2017, Scientific Reports.

QUANTITATIVE ANALYSIS OF THE DYSTROPHIN GENE BY REAL-TIME PCR

V. Rakocevic-Stojanovic, V. Milic-Rasic, N. Maksimovic, 2012 .

Clinical exome sequencing in Serbian patients with movement disorders: Single centre experience

V. Kostic, B. Peterlin, A. Maver, 2022, Genetika.

Analysis of secondary mtDNA mutations in families with Leber's hereditary optic neuropathy: four novel variants and their association with clinical presentation.

V. Kostic, J. Jančić, Vesna Djuric, 2019, Mitochondrion.

Current Concepts on Genetic Aspects of Mitochondrial Dysfunction in Amyotrophic Lateral Sclerosis

S. Dučić, I. Novaković, D. Nikolić, 2021, International journal of molecular sciences.

GCH1 mutations are common in Serbian patients with dystonia-parkinsonism: Challenging previously reported prevalence rates of DOPA-responsive dystonia.

V. Kostic, C. Klein, V. Dobričić, 2017, Parkinsonism & related disorders.

Pharmacogenetics of drug response in Parkinson's disease

M. Krajinovic, V. Kostic, I. Novaković, 2015, The International journal of neuroscience.

Identification of novel variants in LRRK2 gene in patients with Parkinson's disease in Serbian population

V. Kostic, V. Dobričić, N. Kresojević, 2015, Journal of the Neurological Sciences.

Yield of the PMP22 deletion analysis in patients with compression neuropathies

S. Peric, V. Rakocevic-Stojanovic, A. Kačar, 2020, Journal of Neurology.

Anthropometric and lipid parameters trends in school children: one decade of YUSAD Study.

S. Nedeljković, Vladimir Radlović, S. Simeunović, 2011, Srpski arhiv za celokupno lekarstvo.

Association of PPARG rs3856806 C>T polymorphism with body mass index, glycaemia and lipid parameters in Serbian adolescents

S. Vidović, N. Maksimovic, I. Novaković, 2021 .

Bcl‐2 Expression in Oral Squamous Cell Carcinoma

V. Jurišić, J. Milašin, I. Novaković, 2007, Annals of the New York Academy of Sciences.

Analysis of association of ADORA2A and ADORA3 polymorphisms genotypes/haplotypes with efficacy and toxicity of methotrexate in patients with Rheumatoid arthritis

M. Pešić, V. Milic, V. Dolžan, 2020, The Pharmacogenomics Journal.

C-5 Hydroxyethyl and Hydroxypropyl Acyclonucleosides as Substrates for Thymidine Kinase of Herpes Simplex Virus Type 1 (HSV-1 TK): Syntheses and Biological Evaluation

S. Ametamey, L. Scapozza, U. Müller, 2013, Molecules.

Association of 63/91 length polymorphism in the DHFR gene major promoter with toxicity of methotrexate in patients with rheumatoid arthritis.

M. Krajinovic, V. Milic, N. Damjanov, 2016, Pharmacogenomics.

In silico model of mtDNA mutations effect on secondary structure of mitochondrial rRNA and tRNA in Leber's hereditary optical neuropathy.

V. Kostic, J. Jančić, J. Samardžić, 2020, Experimental eye research.

NPM1 GENE MUTATIONS IN CHILDREN WITH MYELODYSPLASTIC SYNDROMES

V. Perovic, V. Dobričić, J. Milašin, 2011 .

Low frequency of NRAS and KRAS2 gene mutations in childhood myelodysplastic syndromes.

I. Pastar, J. Milašin, I. Novaković, 2004, Cancer genetics and cytogenetics.

Correlation between leukocyte‐platelet aggregates and thrombosis in myeloproliferative neoplasms

J. Marinković, D. Marković, V. Čokić, 2021, International journal of laboratory hematology.

Analysis of duplications versus deletions in the dystrophin gene in Serbian cohort with dystrophinopathies

V. Rakocevic-Stojanovic, V. Dobričić, V. Milic-Rasic, 2020, Vojnosanitetski pregled.

Comparison of Ras/Raf/MAPK signaling pathway in primary tumour and lymph node metastases – A report on an experimental study of two colorectal cancer cell lines (SW480 and SW620) and tissue samples

I. Novaković, M.N. Calvo, Y. Karliichuk, 2017 .

Analiza antiapoptotskog proteina bcl-2 u skvamocelularnom karcinomu usne regije Analysis of the anti-apoptotic protein bcl-2 in oral squamous cell carcinoma

I. Novaković, 2007 .

Phenotypic and Genetic Heterogeneity of Adult Patients with Hereditary Spastic Paraplegia from Serbia

A. Jordanova, D. Sokić, J. Drulovic, 2019, Journal of the Neurological Sciences.

Phenotypic expression and founder effect of PANK2 c.1583C>T (p.T528M) mutation in Serbian pantothenate kinase-associated neurodegeneration patients

M. Krajinovic, V. Kostic, C. Beaubois, 2019, Archives of Biological Sciences.

Novel PANK2 mutation identified in patient with pantothenate kinase-associated neurodegeneration

V. Kostic, M. Svetel, N. Kresojević, 2020 .

Genomic loci susceptible to replication errors in cancer cells.

D. Labuda, M. Krajinovic, D. Sinnett, 1998, British Journal of Cancer.

[Analysis of loss of heterozygosity of the tumor suppressor genes p53 and BRCA1 in ovarial carcinomas].

I. Novaković, B. Popović, J. Atanacković, 2006, Vojnosanitetski pregled.

Introduction to Molecular Genetic Diagnostics / UVOD U MOLEKULARNU GENETIČU DIJAGNOSTIKU

A. Pavlovic, T. Pekmezović, N. Maksimovic, 2013 .

Analysis of rs34637584 polymorphism in the LRRK2 gene in patients with Parkinson's disease

I. Novaković, M. Ristanović, Boba Kotlica, 2022, Medicinski podmladak.

Chromosomal microarray in postnatal diagnosis of congenital anomalies and neurodevelopmental disorders in Serbian patients

N. Maksimovic, I. Novaković, T. Damnjanovic, 2022, Journal of clinical laboratory analysis.

A multicenter study of genetic testing for Parkinson’s disease in the clinical setting

D. Georgiev, V. Kostic, B. Peterlin, 2022, npj Parkinson's Disease.

Oxidative Stress Profile in Genetically Confirmed Cases of Leber’s Hereditary Optic Neuropathy

V. Kostic, J. Jančić, Vesna Djuric, 2020, Journal of Molecular Neuroscience.

V. Kostic, V. Dobričić, A. Tomić, 2016, Movement disorders : official journal of the Movement Disorder Society.

Challenges in Rare Diseases Diagnostics: Incontinentia Pigmenti with Heterozygous GBA Mutation

J. Rosain, I. Novaković, Natasa Cerovac, 2022, Diagnostics.

KCC2 rs2297201 Gene Polymorphism Might be a Predictive Genetic Marker of Febrile Seizures

I. Novaković, S. Cvjetićanin, B. Jekic, 2022, ASN neuro.

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.

S. Pavlovic, V. Škodrić-Trifunović, L. Marković-Denić, 2021, Injury.

Association of the Brain-derived Neurotrophic Factor Val66Met Polymorphism with Body Mass Index, Fasting Glucose Levels and Lipid Status in Adolescents

S. Vidović, N. Maksimovic, I. Novaković, 2020, Balkan journal of medical genetics : BJMG.

Polymorphisms of the eNOS gene are associated with disease activity in rheumatoid arthritis

V. Milic, N. Damjanov, N. Maksimovic, 2016, Rheumatology International.

The commercial genetic testing landscape for Parkinson's disease.

I. König, C. Blauwendraat, M. Farrer, 2021, Parkinsonism & related disorders.

[Investigation of Balkan endemic nephropathy in Serbia: how to proceed?].

V. Stefanović, S. Janković, I. Marić, 2010, Srpski arhiv za celokupno lekarstvo.

Lack of TP53 and FMS gene mutations in children with myelodysplastic syndrome.

J. Milašin, I. Novaković, B. Popović, 2006, Cancer genetics and cytogenetics.

GSTO1*C/GSTO2*G haplotype is associated with risk of transitional cell carcinoma of urinary bladder

T. Simić, T. Pekmezović, M. Matic, 2015, International Urology and Nephrology.

STR loci D19S216, D20S502 and D20S842 analysis in the Serbian population using dentin DNA

J. Milašin, O. Stojković, I. Novaković, 2011 .

A new N-methyl thymine derivative comprising a dihydroxyisobutenyl unit as ligand for thymidine kinase of herpes simplex virus type 1 (HSV-1 TK).

S. Ametamey, L. Scapozza, P. Lučin, 2011, Bioorganic & medicinal chemistry letters.

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

M. Krajinovic, V. Milic, N. Damjanov, 2013, European Journal of Clinical Pharmacology.

Association of dihydrofolate reductase (DHFR) -317AA genotype with poor response to methotrexate in patients with rheumatoid arthritis.

M. Krajinovic, V. Milic, N. Pejnović, 2012, Clinical and experimental rheumatology.

Genetic and Epigenomic Modifiers of Diabetic Neuropathy

D. Bogićević, S. Dučić, I. Novaković, 2021, International journal of molecular sciences.

Molecular analysis of Y chromosome microdeletions in idiopathic cases of male infertility in Serbia

C. Tulić, A. Nikolic, I. Novaković, 2007, Russian Journal of Genetics.

[Y chromosome microdeletions in infertile male candidates for microfertilization].

C. Tulić, D. Radojkovic, A. Nikolić, 2008, Srpski arhiv za celokupno lekarstvo.

Genetic variation in leptin and leptin receptor genes as a risk factor for idiopathic male infertility

B. Peterlin, D. Plaseska-Karanfilska, A. Maver, 2017, Andrology.

Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice

D. Geschwind, P. Svenningsson, A. Aguzzi, 2013, Nature Genetics.

Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification

D. Geschwind, P. Mazzoni, P. Svenningsson, 2013, neurogenetics.

Homocysteine serum levels and MTHFR C677T genotype in patients with Parkinson's disease, with and without levodopa therapy

M. Krajinovic, V. Kostic, Z. Todorović, 2006, Journal of the Neurological Sciences.

Analysis of “clinical exome” panel in Serbian patients with cognitive disorders

V. Kostic, B. Peterlin, A. Maver, 2022, Genetika.

Identification of mutations in the PARK2 gene in Serbian patients with Parkinson's disease

V. Kostic, T. Pekmezović, V. Dobričić, 2018, Journal of the Neurological Sciences.

De novo mutation in the GNAL gene causing seemingly sporadic dystonia in a Serbian patient

K. Lohmann, V. Kostic, C. Klein, 2014, Movement disorders : official journal of the Movement Disorder Society.

Genetic testing in familial and young-onset Alzheimer's disease: mutation spectrum in a Serbian cohort

John Hardy, Rita Guerreiro, J. Hardy, 2012, Neurobiology of Aging.

Year : 2011 A genome-wide survey of human short-term memory

K. Henke, F. Jessen, W. Maier, 2010 .

The Genetic Basis of Strokes in Pediatric Populations and Insight into New Therapeutic Options

I. Novaković, D. Nikolić, M. Janković, 2022, International journal of molecular sciences.

Epilepsy in a child with Wolf-Hirschhorn syndrome.

V. Kostic, N. Dimitrijević, V. Dobričić, 2011, Srpski arhiv za celokupno lekarstvo.

Genetic Aspects of Inflammation and Immune Response in Stroke

I. Novaković, D. Nikolić, M. Janković, 2020, International journal of molecular sciences.

Subtelomeric screening in Serbian children with dysmorphic features and unexplained developmental delay/intellectual disabilities.

V. Kostic, N. Dimitrijević, V. Dobričić, 2015, The Turkish journal of pediatrics.

Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients

B. Peters, R. Drmanac, D. Cooper, 2017, Human Genomics.

Mutation screening of the DYT6/THAP1 gene in Serbian patients with primary dystonia

V. Kostic, V. Dobričić, A. Tomić, 2013, Journal of Neurology.

[Mowat-Wilson syndrome--a case report].

G. Cuturilo, I. Novaković, I. Jovanović, 2009, Srpski arhiv za celokupno lekarstvo.

NBIA Syndromes: A Step Forward from the Previous Knowledge

V. Kostic, I. Stankovic, N. Dragasevic, 2021, Neurology India.

Increased activity of interleukin-23/interleukin-17 cytokine axis in primary antiphospholipid syndrome.

V. Trajković, Nevena Zogović, I. Aksentijevich, 2013, Immunobiology.

[Analysis of microsatellite markers D18S70 and D20S116 in DNA isolated from dentin: use in forensic medicine].

J. Milašin, I. Novaković, B. Popović, 2009, Srpski arhiv za celokupno lekarstvo.

Association Between the Methylenetetrahydrofolate Reductase Polymorphisms and Risk of Acute Lymphoblastic Leukemia in Serbian Children

T. Novkovic, J. Milašin, I. Novaković, 2010, Journal of pediatric hematology/oncology.

miRNAs as a Potential Biomarker in the COVID-19 Infection and Complications Course, Severity, and Outcome

M. Šantrić-Milićević, I. Novaković, D. Nikolić, 2023, Diagnostics.

Proximal Dystrophin Gene Deletions and Protein Alterations in Becker Muscular Dystrophy

Dejan Stefanović, Jelena Milasin, Ivana Novaković, 2005, Annals of the New York Academy of Sciences.

Genotypic and phenotypic spectrum of PANK2 mutations in patients with neurodegeneration with brain iron accumulation

T. Meitinger, A. Weindl, H. Prokisch, 2006, Annals of neurology.

The cumulative effect of genetic polymorphisms on depression and brain structural integrity

Massimo Filippi, Federica Agosta, Elisa Canu, 2016, Human brain mapping.

Intellectual Ability in the Duchenne Muscular Dystrophy and Dystrophin Gene Mutation Location

D. Vojinović, V. Lukic, S. Romac, 2014, Balkan journal of medical genetics : BJMG.

Cancer genes alterations and HPV infection in oral squamous cell carcinoma.

J. Milašin, V. Konstantinovic, I. Novaković, 2010, International journal of oral and maxillofacial surgery.

Multiple Sclerosis patients carry an increased burden of exceedingly rare genetic variants in the inflammasome regulatory genes

B. Peterlin, A. Maver, J. Drulovic, 2019, Scientific Reports.

Increased total homocysteine level is associated with clinical status and severity of white matter changes in symptomatic patients with subcortical small vessel disease

A. Pavlovic, T. Pekmezović, M. Mijajlovic, 2011, Clinical Neurology and Neurosurgery.

Prospective study of perinatal outcome in pregnancies with primary antiphospholipid syndrome.

I. Novaković, A. Ćetković, B. Kastratović, 2014, Vojnosanitetski pregled.

POSSIBLE INFLUENCE OF MTHFR C677T POLYMORPHISM ON SERUM LIPID LEVELS IN SERBIAN SCHOOL CHILDREN

N. Majkić-Singh, N. Maksimovic, I. Novaković, 2014 .

Transcranial sonography in patients with Parkinson's disease with glucocerebrosidase mutations.

Christine Klein, Marina Svetel, Aleksandra Pavlović, 2013, Parkinsonism & related disorders.

Pharmacogenetics and the Treatment of Thrombophilia

N. Maksimovic, I. Novaković, D. Cvetkovic, 2013 .

School children systolic and diastolic blood pressure values: YUSAD study

S. Simeunović, I. Novaković, I. Petronić, 2011 .

Neuropathic pain in patients with Charcot-Marie-Tooth type 1A

A. Kačar, I. Bozovic, I. Basta, 2019, Neurological Sciences.

Fuzzy role of hyperhomocysteinemia in hemodialysis patients' mortality.

S. Simić-Ogrizović, L. Djukanovic, S. Pejanović, 2006, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.

Genetic Variation in Circadian Rhythm Genes CLOCK and ARNTL as Risk Factor for Male Infertility

B. Peterlin, A. Maver, C. Tulić, 2013, PloS one.

C9ORF72 repeat expansion is not associated with atypical parkinsonism in the Serbian population

V. Kostic, I. Stankovic, E. Stefanova, 2022, Genetika.

The Impact of the IKBKG Gene on the Appearance of the Corpus Callosum Abnormalities in Incontinentia Pigmenti

I. Novaković, S. Popadic, Natasa Cerovac, 2023, Diagnostics.

Novel GATOR1 variants in focal epilepsy

A. Ristić, D. Sokić, N. Vojvodić, 2023, Epilepsy & Behavior.

Premutations in the FMR1 gene in Serbian patients with undetermined tremor, ataxia and parkinsonism

V. Kostic, I. Stankovic, M. Pešić, 2021, Neurological research.

[Radiotherapeutical chromosomal aberrations in laryngeal cancer patients].

D. Kastratović, M. Pavlovic, I. Novaković, 2009, Medicinski pregled.

Mutational Analysis and mtDNA Haplogroup Characterization in Three Serbian Cases of Mitochondrial Encephalomyopathies and Literature Review

V. Kostic, Vladimir Radlović, J. Jančić, 2021, Diagnostics.

Identification of rare genetic variation of NLRP1 gene in familial multiple sclerosis

G. Zamolo, B. Peterlin, A. Maver, 2017, Scientific Reports.

Whole Mitochondrial Genome Analysis in Serbian Cases of Leber’s Hereditary Optic Neuropathy

V. Kostic, S. Mesaros, J. Jančić, 2020, Genes.

Inherited Thrombophilia and the Risk of Vascular Events

N. Maksimovic, I. Novaković, D. Cvetkovic, 2011 .

A pilot study on predictors of brainstem raphe abnormality in patients with major depressive disorder.

M. Kostic, A. Munjiza, V. Dobričić, 2017, Journal of affective disorders.

The emerging role of the FKBP5 gene polymorphisms in vulnerability-stress model of schizophrenia: further evidence from a Serbian population Author list

A. Richards, A. Richards, K. Mantripragada, 2016 .

Screening for C9orf72 Expansion Mutation in Serbian Patients with Early-Onset Dementia

V. Kostic, G. Mandić-Stojmenović, T. Stojkovic, 2015, Dementia and Geriatric Cognitive Disorders.

Association of C35T polymorphism in dihydrofolate reductase gene with toxicity of methotrexate in rheumatoid arthritis patients

M. Krajinovic, V. Milic, N. Damjanov, 2019, Expert opinion on drug metabolism & toxicology.

Exclusion of linkage to chromosomes 14q, 2q37 and 8p21.1-q11.23 in a Serbian family with idiopathic basal ganglia calcification

A. Pavlovic, M. Krajinovic, V. Kostic, 2011, Journal of Neurology.

Variability of multisystemic features in myotonic dystrophy type 1 – lessons from Serbian registry

V. Rakocevic-Stojanovic, A. Kačar, V. Dobričić, 2015, Neurological research.

Mutational analysis of ATP7B gene and the genotype-phenotype correlation in patients with Wilson's disease in Serbia.

V. Kostic, T. Pekmezović, V. Dobričić, 2013, Vojnosanitetski pregled.

Multidimensional aspects of pain in myotonic dystrophies

V. Rakocevic-Stojanovic, D. Lavrnić, V. Dobričić, 2015, Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology.

Inter-individual variability in the response of human peripheral blood lymphocytes to ionizing radiation: comparison of the dicentric and micronucleus assays

Vesna Pajic, Jelena Pajic, Boban Rakic, 2015, Radiation and environmental biophysics.

Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients

B. Peters, R. Drmanac, D. Cooper, 2017, Human Genomics.

Presenting symptoms of GBA-related Parkinson's disease.

V. Kostic, C. Klein, T. Pekmezović, 2015, Parkinsonism & related disorders.

The FKBP5 genotype and childhood trauma effects on FKBP5 DNA methylation in patients with psychosis, their unaffected siblings, and healthy controls

V. Gasic, B. Zukic, S. Pavlovic, 2021, Psychoneuroendocrinology.

A common polymorphism in the brain-derived neurotrophic factor gene in patients with adult-onset primary focal and segmental dystonia

V. Kostic, T. Pekmezović, E. Stefanova, 2013, Acta Neurologica Belgica.

Clients’ Perception of Outcome of Team-Based Prenatal and Reproductive Genetic Counseling in Serbian Service Using the Perceived Personal Control (PPC) Questionnaire

A. Ljubić, S. Ignjatović, G. Cuturilo, 2016, Journal of Genetic Counseling.