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Joint effect of the SMN2 and SERF1A genes on childhood-onset types of spinal muscular atrophy in Serbian patients

Journal of human genetics, 2015-11, Vol.60 (11), p.723-728

2015

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Association between genetic variant in hsa-miR-146a gene and prostate cancer progression: evidence from Serbian population

Cancer causes & control, 2014-11, Vol.25 (11), p.1571-1575

2014

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Association between a Genetic Variant in the hsa-miR-146a Gene and Cancer Risk: An Updated Meta-Analysis

Public health genomics, 2015-01, Vol.18 (5), p.283-298

2015

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Genetic Variants within Endothelial Nitric Oxide Synthase Gene and Prostate Cancer: A Meta‐Analysis

Clinical and translational science, 2015-02, Vol.8 (1), p.23-31

2015

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The coexistence of myasthenia gravis and myotonic dystrophy type 2 in a single patient

Journal of Clinical Neurology, 2013, 9(2), , pp.130-132

2013

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Common Variants at 8q24 are Associated with Prostate Cancer Risk in Serbian Population

Pathology oncology research, 2013-07, Vol.19 (3), p.559-569

2013

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Assessment of possible association between rs3787016 and prostate cancer risk in Serbian population

International journal of clinical and experimental medicine, 2013-01, Vol.6 (1), p.57-66

2013

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Assessment of Association between Common Variants at 17q12 and Prostate Cancer Risk—Evidence from Serbian Population and Meta‐Analysis

Clinical and translational science, 2014-08, Vol.7 (4), p.307-313

2014

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Programmed cell death proteins and chronic leukemia

Archives of biological sciences, 2011, Vol.63 (3), p.527-535

2011

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Intrafamilial phenotypic and genetic heterogeneity of dystonia

Journal of the neurological sciences, 2006-12, Vol.250 (1), p.92-96

2006

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Assessment of possible association between rs378854 and prostate cancer risk in the Serbian population

Archives of biological sciences, 2013, Vol.65 (2), p.475-486

2013

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Analysis of PMP22 duplication and deletion using a panel of six dinucleotide tandem repeats

Clinical chemistry and laboratory medicine, 2016-05, Vol.54 (5), p.773

2016

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Molecular Genetics and Genetic Testing in Myotonic Dystrophy Type 1

BioMed research international, 2013-01, Vol.2013 (2013), p.1-13

2013

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Population data on 14 STR loci from population of Serbia and Montenegro (new and renewed data)

Forensic science international, 2005-07, Vol.151 (2), p.315-316

2005

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Joint effect of ADARB1 gene, HTR2C gene and stressful life events on suicide attempt risk in patients with major psychiatric disorders

The world journal of biological psychiatry, 2015-06, Vol.16 (4), p.261-271

2015

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The 60th anniversary of the discovery of DNA secondary structure

Vojnosanitetski pregled, 2013-12, Vol.70 (12), p.1165-1170

2013

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Genetics of Lafora progressive myoclonic epilepsy: current perspectives

Application of clinical genetics, 2016-01, Vol.9 (Issue 1), p.49-53

2016

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Tryptophan Hydroxylase 1 Variant rs1800532 is Associated with Suicide Attempt in Serbian Psychiatric Patients but does not Moderate the Effect of Recent Stressful Life Events

Suicide & life-threatening behavior, 2016-12, Vol.46 (6), p.664-668

2016

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Endothelial nitric oxide synthase gene polymorphisms and prostate cancer risk in S erbian population

International journal of experimental pathology, 2013-12, Vol.94 (6), p.355-361

2013

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Lafora disease: Severe phenotype associated with homozygous deletion of the NHLRC1 gene

Journal of the neurological sciences, 2013-02, Vol.325 (1), p.170-173

2013

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Genetic Variants within Endothelial Nitric Oxide Synthase Gene and Prostate Cancer: A Meta-Analysis: Nos3 Variants and Prostate Cancer: A Meta-Analysis

Clinical and translational science, 2015-02, Vol.8 (1), p.23-31

2015

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Heterozygous PINK1 mutations: A susceptibility factor for Parkinson disease?

Movement disorders, 2006-09, Vol.21 (9), p.1526-1530

2006

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Epidemiology of myotonic dystrophy type 1 in the population of central Serbia

Vojnosanitetski pregled, 2005-05, Vol.62 (5), p.377-382

2005

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TPH2 variant rs7305115 and its interaction with acute stressful life events in etiology of suicide attempt in Serbian psychiatric patients

Acta medica international, 2015-07, Vol.2 (2), p.34

2015

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Bcl-2 and Bax interaction in B-lymphocytes of peripheral blood in patients with chronic lymphocytic leukemia

Vojnosanitetski pregled, 2005, Vol.62 (5), p.357-363

2005

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Joint effect of the SMN2 and SERF1A genes on childhood-onset types of spinal muscular atrophy in Serbian patients

Association between genetic variant in hsa-miR-146a gene and prostate cancer progression: evidence from Serbian population

Association between a Genetic Variant in the hsa-miR-146a Gene and Cancer Risk: An Updated Meta-Analysis

Genetic Variants within Endothelial Nitric Oxide Synthase Gene and Prostate Cancer: A Meta‐Analysis

The coexistence of myasthenia gravis and myotonic dystrophy type 2 in a single patient

Common Variants at 8q24 are Associated with Prostate Cancer Risk in Serbian Population

Assessment of possible association between rs3787016 and prostate cancer risk in Serbian population

Assessment of Association between Common Variants at 17q12 and Prostate Cancer Risk—Evidence from Serbian Population and Meta‐Analysis

Programmed cell death proteins and chronic leukemia

Intrafamilial phenotypic and genetic heterogeneity of dystonia

Assessment of possible association between rs378854 and prostate cancer risk in the Serbian population

Analysis of PMP22 duplication and deletion using a panel of six dinucleotide tandem repeats

Molecular Genetics and Genetic Testing in Myotonic Dystrophy Type 1

Population data on 14 STR loci from population of Serbia and Montenegro (new and renewed data)

Joint effect of ADARB1 gene, HTR2C gene and stressful life events on suicide attempt risk in patients with major psychiatric disorders

The 60th anniversary of the discovery of DNA secondary structure

Genetics of Lafora progressive myoclonic epilepsy: current perspectives

Tryptophan Hydroxylase 1 Variant rs1800532 is Associated with Suicide Attempt in Serbian Psychiatric Patients but does not Moderate the Effect of Recent Stressful Life Events

Endothelial nitric oxide synthase gene polymorphisms and prostate cancer risk in S erbian population

Lafora disease: Severe phenotype associated with homozygous deletion of the NHLRC1 gene

Genetic Variants within Endothelial Nitric Oxide Synthase Gene and Prostate Cancer: A Meta-Analysis: Nos3 Variants and Prostate Cancer: A Meta-Analysis

Heterozygous PINK1 mutations: A susceptibility factor for Parkinson disease?

Epidemiology of myotonic dystrophy type 1 in the population of central Serbia

TPH2 variant rs7305115 and its interaction with acute stressful life events in etiology of suicide attempt in Serbian psychiatric patients

Bcl-2 and Bax interaction in B-lymphocytes of peripheral blood in patients with chronic lymphocytic leukemia

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