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List of works by Dusanka Savic-Pavicevic

A novel recessive TTN founder variant is a common cause of distal myopathy in the Serbian population.

scientific article published on 15 March 2017

Assessment of association between common variants at 17q12 and prostate cancer risk-evidence from Serbian population and meta--analysis

scientific article published on 14 January 2014

Assessment of association between genetic variants in microRNA genes hsa-miR-499, hsa-miR-196a2 and hsa-miR-27a and prostate cancer risk in Serbian population

scientific article

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

scientific article published on 3 September 2015

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

scientific article published on 02 August 2014

Brain sonography insight into the midbrain in myotonic dystrophy type 2.

scientific article published in October 2015

Clusters of cognitive impairment among different phenotypes of myotonic dystrophy type 1 and type 2.

scientific article published on 28 November 2016

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

scientific article published on 28 March 2013

Comparison of temporal and stride characteristics in myotonic dystrophies type 1 and 2 during dual-task walking.

scientific article published on 20 December 2015

Effect of childhood general traumas on suicide attempt depends on TPH2 and ADARB1 variants in psychiatric patients.

scientific article published on 13 January 2017

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

scientific article published on 02 September 2013

Epidemiology of Rett syndrome in Serbia: prevalence, incidence and survival.

scientific article published on 7 January 2015

Frequency of the hemochromatosis gene mutations in the population of Serbia and Montenegro

scientific article published on 01 August 2006

Frontostriatal dysexecutive syndrome: a core cognitive feature of myotonic dystrophy type 2.

scientific article published on 28 October 2014

Genetic testing of individuals with pre-senile cataract identifies patients with myotonic dystrophy type 2.

scientific article

Genetic variants in RNA-induced silencing complex genes and prostate cancer

scientific article published on 6 August 2016

Human Y-specific STR haplotypes in population of Serbia and Montenegro.

scientific article

Intellectual ability in the duchenne muscular dystrophy and dystrophin gene mutation location.

scientific article published on December 2014

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

scientific article

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

scientific article published on 27 August 2015

Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia

Magnetic resonance imaging of leg muscles in patients with myotonic dystrophies

scientific article published on 29 July 2017

Molecular genetic and clinical characterization of myotonic dystrophy type 1 patients carrying variant repeats within DMPK expansions.

scientific article

Molecular genetics and genetic testing in myotonic dystrophy type 1.

scientific article

Multidimensional aspects of pain in myotonic dystrophies

scientific article published on December 2015

Mutational analysis of GJB1, MPZ, PMP22, EGR2, and LITAF/SIMPLE in Serbian Charcot-Marie-Tooth patients

scientific article published on 01 June 2009

Myotonic Dystrophy Type 2 - Data from the Serbian Registry

scientific article published on 01 January 2018

NOS3 gene variants and male infertility: Association of 4a/4b with oligoasthenozoospermia.

scientific article published on 3 May 2017

Neuromyelitis Optica in a Patient from Family with both Myotonic Dystrophy Type 1 and 2.

scientific article published in January 2017

Personality traits in patients with myotonic dystrophy type 2.

scientific article

Polymorphisms of the prion protein gene (PRNP) in a Serbian population.

scientific article published in July 2010

Quality of life in patients with myotonic dystrophy type 2.

scientific article

Retinoic acid induced 1 gene and clinical subtypes of schizophrenia: an association study

scientific article published on 17 December 2010

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

scientific article published on 2 April 2016

WDR45 mutations may cause a MECP2 mutation-negative Rett syndrome phenotype.

scientific article published on 27 March 2018