1. BIOREpository

Researcher Profile Statistics: Savić-Pavićević, Dušanka

From:   ever     To:   now     Change date range
Email Alert
RSS Feed
 
Geo Map
Save as a PNG Save as a JPEG
Region #
NA - North America 1303
EU - Europe 385
AS - Asia, other 384
OC - Oceania 45
SA - South America 5
AF - Africa 3
Unknown 94
Total 2219
Save as a PNG Save as a JPEG
Country #
US - United States of America 1300
SG - Singapore 259
RS - Serbia 215
CN - China 101
AU - Australia 44
IE - Ireland 35
DE - Germany 24
FR - France 23
RU - Russian Federation 22
GB - United Kingdom 16
other - Other Country 180
Total 2219
Save as a PNG Save as a JPEG
City #
Boardman 295
Belgrade 177
Chandler 132
Singapore 90
Dublin 34
Brisbane 19
Paris 18
Kragujevac 17
Shihezi 15
Melbourne 14
other 1380
Total 2191
Save as a PNG Save as a JPEG
Most viewed items #
ID: 8623 - Longitudinal analysis of CTG repeat somatic instability in myotonic dystrophy type 1 patients 102
ID: 8622 - evolutionizing Spinal Muscular Atrophy Prevention in Serbia: Implementing a Mandatory Statewide Newborn Screening 63
ID: 6192 - Clinical score for early diagnosis of myotonic dystrophy type 2 61
ID: 7483 - Mutation rates of 22 autosomal STR loci in a European population from central Balkan, Republic of Serbia 54
ID: 7486 - One year of newborn screening for spinal muscular atrophy – results of a Serbian pilot project 48
ID: 7485 - Genetic risk factors in patients with Myasthenia gravis 47
ID: 6221 - Myotonic Dystrophy Type 2 and Autoimmune Diseases 46
ID: 7023 - Neonatal screening (NBS) for spinal muscular atrophy (SMA) in Serbia – first results 46
ID: 7584 - COMPARATIVE TRANSCRIPTOMIC ANALYSIS IMPLIES INNATE IMMUNE RESPONSE AND CELL CYCLE DISREGULATION IN PATIENT-DERIVED DM1 CELL MODELS 45
ID: 7484 - Effect of enriched environment on serotonin and RNA editing of serotonin 2C receptor is specific for brain regions and mouse strains 39
ID: 7755 - Genetic predisposition of suicidal behavior: variants in GRIN2B, GABRG2, and ODC1 genes in suicide attempt and completed suicide in two Balkan populations 37
ID: 7583 - TWO MAIN SKELETAL MUSCLE MOLECULAR PHENOTYPES OF MOUSE DM1 MODELS: A COMPARATIVE TRANSCRIPTOMIC ANALYSIS 36
ID: 7585 - GENERATION OF EXPANDED CTG REPEAT PLASMIDS IN E. COLI FOR MYOTONIC DYSTROPHY TYPE 1 MODEL SYSTEMS 35
ID: 7757 - Neurofilament as a biomarker of response to genetically designed therapies for spinal muscular atrophy 35
ID: 6194 - CpG sites surrounding DMPK expansions are heterogeneously methylated in myotonic dystrophy type 1 patients with variant repeats 34
ID: 7756 - Identification of potentally causal variants for myasthenia gravis: a bioinformatics-driven fine-mapping approach combined with genetic association study 34
ID: 7482 - Association of PRMT6, PEX10 and SOX5 genetic variants with idiopathic male infertility: Evidence from North Macedonian population and an updated meta-analysis 33
ID: 6079 - Lokus CTLA4 je asociran sa rizikom za razvoj rane forme miastenije gravis u populaciji Srbije 32
ID: 6122 -  LTBP4, SPP1, and CD40 Variants: Genetic Modifiers of Duchenne Muscular Dystrophy Analyzed in Serbian Patients 32
ID: 6218 - Analysis of circulating myomiRs as potential biomarkers of progression of muscular impairment in myotonic dystrophy type 1 patients 32
ID: 6080 - Uticaj obogaćene sredine na editovanje serotoninskog receptora 2C 31
ID: 6818 - CpG места у околини DMPK експанзија са варијантним мотивима су хетерогено метилована код болесника са миотоничном дистрофијом тип 1 31
ID: 6076 - Predikcija pokušaja samoubistva pomoću algoritama nadgledanog mašinskog učenja 30
ID: 6219 - Analysis of Phenotypic Characteristics in patients with Myotonic dystrophy type 2 30
ID: 6452 - MiR-375 and miR-21 as Potential Biomarkers of Prostate Cancer: Comparison of Matching Samples of Plasma and Exosomes 30
ID: 4332 - Association study between single-nucleotide variants rs12097821, rs2477686, and rs10842262 and idiopathic male infertility risk in Serbian population with meta-analysis 29
ID: 6825 - Predicting suicide: serotonin presynapse dynamic modelling and machine learning approach 29
ID: 7481 - The effect of epistatic interactions between genetic variants located in MicroRNA and silencing complex genes on prostate cancer progression risk 29
ID: 7768 - Outcome of a Serbian pilot initiative: spinal muscular atrophy newborn screening over a 16-month period 29
ID: 6817 - Кластер анализа фенотипских карактеристика пацијената који болују од миотоничне дистрофије типа 2 28
ID: 6296 - Copy number variants within AZF region of Y chromosome and their association with idiopathic male infertility in Serbian population 27
ID: 6824 - Predicting suicide: serotonin presynapse dynamic modelling and machine learning approach 27
ID: 2407 - Analysis of association of potentially functional genetic variants within genes encoding miR-34b/c, miR-378 and miR-143/145 with prostate cancer in Serbian population 26
ID: 4338 - Association of KLK3, VAMP8 and MDM4 Genetic Variants within microRNA Binding Sites with Prostate Cancer: Evidence from Serbian Population 24
ID: 7015 - Adenosine to inosine editing sites of serotonin receptor 2C transcript in primate brains 24
ID: 6189 - Cognitive assessment in patients with myotonic dystrophy type 2 23
ID: 2356 - SMN1 Copy number as a modifying factor of survival in Serbian patients with sporadic amyotrophic lateral sclerosis 22
ID: 80 - Effect of childhood general traumas on suicide attempt depends on TPH2 and ADARB1 variants in psychiatric patients 22
ID: 4337 - Association between genetic variants in genes encoding Argonaute proteins and cancer risk: A meta-analysis 21
ID: 19 - Repeat Interruptions Modify Age at Onset in Myotonic Dystrophy Type 1 by Stabilizing DMPK Expansions in Somatic Cells 20
ID: 4328 - Association between genetic variants in DICER1 and cancer risk: An updated meta-analysis 19
ID: 6190 - Autoimmune Diseases in Patients With Myotonic Dystrophy Type 2 19
ID: 22 - Molecular genetic and clinical characterization of myotonic dystrophy type 1 patients carrying variant repeats within DMPK expansions 18
ID: 58 - Myotonic Dystrophy Type 2 - Data from the Serbian Registry 17
ID: 3056 - Frequency of the hemochromatosis gene mutations in the population of Serbia and Montenegro [2] 16
ID: 5104 - Gene modifiers of Duchenne muscular dystrophy - Serbian experience 16
ID: 7024 - Association of variants in RNA editing genes, serotonergic system genes and stressful life events with suicide attempt in psychiatric patients 16
ID: 7028 - Repeat-primed PCR in diagnostic testing of repeat expansion diseases 16
ID: 81 - Molecular genetics and genetic testing in myotonic dystrophy type 1 16
ID: 8513 - Unverricht-Lundborg disease: the first report of genetically confirmed case in Serbia 16
ID: 2410 - 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 15
ID: 7021 - Molecular genetics of diseases with unstable expansion of repeats 15
ID: 23 - Genetic testing of individuals with pre-senile cataract identifies patients with myotonic dystrophy type 2 14
ID: 2425 - Polymorphisms of the prion protein gene (PRNP) in a Serbian population 14
ID: 7025 - Joint effects of variants in RNA editing and serotonergic system genes and stressful life events in predisposition for suicide attempt in psychiatric patients 14
ID: 78 - Joint effect of ADARB1 gene, HTR2C gene and stressful life events on suicide attempt risk in patients with major psychiatric disorders 14
ID: 79 - 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 14
ID: 8512 - Hereditary Motor and Sensory Neuropathy type Lom in Serbian Romani family 14
ID: 2412 - NOS3 gene variants and male infertility: Association of 4a/4b with oligoasthenozoospermia 13
ID: 2420 - Assessment of possible association between rs3787016 and prostate cancer risk in Serbian population 13
ID: 2422 - The 60th anniversary of the discovery of DNA secondary structure 13
ID: 3050 - Human Y-specific STR haplotypes in population of Serbia and Montenegro 13
ID: 53 - Joint effect of the SMN2 and SERF1A genes on childhood-onset types of spinal muscular atrophy in Serbian patients 13
ID: 6188 - Molecular and Clinical Implications of Variant Repeats in Myotonic Dystrophy Type 1 13
ID: 6712 - Značaj DNK analiza u utvrđivanju biološkog srodstva 13
ID: 85 - Retinoic acid inducible-1 gene (RAI1) and clinical subtypes of schizophrenia. In: Li-Hong C and Yuto I, eds. Retinoic acid: Structure, Metabolism and Roles in Disease. 13
ID: 2409 - Association between a genetic variant in the hsa-miR-146a gene and cancer risk: An updated meta-analysis 12
ID: 3061 - HD phenocopies - Possible role of saitohin gene 12
ID: 83 - TPH2 variant rs7305115 and its interaction with acute stressful life events in etiology of suicide attempt in Serbian psychiatric patients 12
ID: 3049 - Coexistence of Unverricht-Lundborg disease and congenital deafness: Molecular resolution of a complex comorbidity 11
ID: 3051 - Population data on 14 STR loci from population of Serbia and Montenegro (new and renewed data) 11
ID: 8514 - Frequency of the hemochromatosis gene mutations in patients with hereditary hemochromatosis and in control subjects from Serbia and Montenegro 11
ID: 8528 - Neurofiziološke i kliničke karakteristike neuromiotonije u novoj neuromišićnoj bolesti 11
ID: 2408 - Genetic variants in RNA-induced silencing complex genes and prostate cancer 10
ID: 2415 - Endothelial nitric oxide synthase gene polymorphisms and prostate cancer risk in serbian population 10
ID: 2426 - Variability of the chloroplast dna of sessile oak (Quercus petraea agg. Ehrendorfer, 1967) in Serbia 10
ID: 3344 - Yugoslav HD phenocopies analyzed on the presence of mutations in PrP, ferritin and JP-3 genes 10
ID: 45 - Magnetic resonance imaging of leg muscles in patients with myotonic dystrophies 10
ID: 46 - Comparison of temporal and stride characteristics in myotonic dystrophies type 1 and 2 during dual-task walking 10
ID: 59 - Personality traits in patients with myotonic dystrophy type 2 10
ID: 7017 - Association of HTR2C gene with suicide attempt risk in Serbian patients with major psychiatric disorders 10
ID: 8655 - Exosomal Prostate-Specific Membrane Antigen (PSMA) and Caveolin-1 as Potential Biomarkers of Prostate Cancer-Evidence from Serbian Population 10
ID: 2401 - A novel recessive TTN founder variant is a common cause of distal myopathy in the Serbian population 9
ID: 2411 - Association between genetic variant in hsa-miR-146a gene and prostate cancer progression: evidence from Serbian population 9
ID: 2414 - Assessment of association between common variants at 17q12 and prostate cancer risk-evidence from serbian population and meta-analysis 9
ID: 3342 - Is the 31 CAG repeat allele of the spinocerebellar ataxia 1 (SCA1) gene locus non-specifically associated with trinucleotide expansion diseases? 9
ID: 3346 - Duchenne's and Becker's muscular dystrophy: analysis of phenotype-genotype correlation in 28 patients] 9
ID: 48 - Frontostriatal dysexecutive syndrome: A core cognitive feature of myotonic dystrophy type 2 9
ID: 49 - Body composition analysis in patients with myotonic dystrophy types 1 and 2 9
ID: 56 - Metabolic impairments in patients with myotonic dystrophy type 2 9
ID: 7019 - Association of ADARB1 gene with major psychiatric disorders 9
ID: 7026 - Association of serotonin receptor 1A gene with bipolar disorder in Serbian population - a preliminary result 9
ID: 7027 - Interactions of TPH2 variants and childhood abuse as risk factors for suicide attempt in Serbian psychiatric patients 9
ID: 8488 - Is it easy to recognize HINT1 neuropathy (oral presentation) 9
ID: 2413 - Genetic Variants within Endothelial Nitric Oxide Synthase Gene and Prostate Cancer: A Meta-Analysis 8
ID: 2421 - Assessment of possible association between RS378854 and prostate cancer risk in the Serbian population 8
ID: 3048 - Mutational analysis of GJB1, MPZ, PMP22, EGR2, and LITAF/SIMPLE in Serbian Charcot-Marie-Tooth patients 8
ID: 3059 - Schizophrenia and apolipoprotein e gene polymorphism in Serbian population 8
ID: 3341 - Genetic and clinical analysis of spinocerebellar ataxia type 8 repeat expansion in Yugoslavia 8
ID: 50 - Clusters of cognitive impairment among different phenotypes of myotonic dystrophy type 1 and type 2 8
Total 2136
Save as a PNG Save as a JPEG
Most type viewed #
ID: all - 0
ID: other - 0
ID: journal - 931
ID: conference - 1262
ID: patent - 0
ID: book - 26
ID: dataset - 0
ID: selected - 0
Total 2219
Save as a PNG Save as a JPEG


Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec Tot
2023 021 3682771 118393948 134245 813
2024 17268 3510111137 0000 00 1406
Ever 2219