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Researcher Profile Statistics: Brkušanin, Miloš

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Region #
NA - North America 512
EU - Europe 196
AS - Asia, other 124
OC - Oceania 11
AF - Africa 2
SA - South America 1
Unknown 37
Total 883
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Country #
US - United States of America 511
RS - Serbia 116
SG - Singapore 87
CN - China 32
IE - Ireland 26
RU - Russian Federation 15
AU - Australia 10
DE - Germany 6
NL - Netherlands 6
FR - France 4
other - Other Country 70
Total 883
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City #
Belgrade 106
Boardman 98
Chandler 54
Singapore 28
Dublin 25
New York 5
Shenyang 5
Tappahannock 5
Brisbane 4
Kragujevac 4
other 549
Total 883
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Most viewed items #
ID: 8622 - evolutionizing Spinal Muscular Atrophy Prevention in Serbia: Implementing a Mandatory Statewide Newborn Screening 60
ID: 6192 - Clinical score for early diagnosis of myotonic dystrophy type 2 59
ID: 7483 - Mutation rates of 22 autosomal STR loci in a European population from central Balkan, Republic of Serbia 51
ID: 7486 - One year of newborn screening for spinal muscular atrophy – results of a Serbian pilot project 47
ID: 7485 - Genetic risk factors in patients with Myasthenia gravis 45
ID: 7023 - Neonatal screening (NBS) for spinal muscular atrophy (SMA) in Serbia – first results 43
ID: 6486 - A treatise about reliability in dating events of evolutionary history of brown trout Salmo cf. trutta (Actinopterygii) at Western Balkans: Impassable barriers, isolation of populations and assistance of geological timeframe 36
ID: 7757 - Neurofilament as a biomarker of response to genetically designed therapies for spinal muscular atrophy 34
ID: 6194 - CpG sites surrounding DMPK expansions are heterogeneously methylated in myotonic dystrophy type 1 patients with variant repeats 32
ID: 6079 - Lokus CTLA4 je asociran sa rizikom za razvoj rane forme miastenije gravis u populaciji Srbije 31
ID: 6218 - Analysis of circulating myomiRs as potential biomarkers of progression of muscular impairment in myotonic dystrophy type 1 patients 31
ID: 6122 -  LTBP4, SPP1, and CD40 Variants: Genetic Modifiers of Duchenne Muscular Dystrophy Analyzed in Serbian Patients 30
ID: 6818 - CpG места у околини DMPK експанзија са варијантним мотивима су хетерогено метилована код болесника са миотоничном дистрофијом тип 1 29
ID: 7769 - A sequencing error or the presence of heteroplasmy? 28
ID: 7768 - Outcome of a Serbian pilot initiative: spinal muscular atrophy newborn screening over a 16-month period 27
ID: 8173 - Chloroplast trnL-trnF region variation in the genus Centaurium Hill as a molecular indicator of natural interspecific hybridization 26
ID: 2356 - SMN1 Copy number as a modifying factor of survival in Serbian patients with sporadic amyotrophic lateral sclerosis 22
ID: 4079 - New records about haplotype diversity of brown trout (Salmo trutta L.) from Adriatic slopes in Montenegro 22
ID: 80 - Effect of childhood general traumas on suicide attempt depends on TPH2 and ADARB1 variants in psychiatric patients 21
ID: 19 - Repeat Interruptions Modify Age at Onset in Myotonic Dystrophy Type 1 by Stabilizing DMPK Expansions in Somatic Cells 20
ID: 82 - Effect of the introgression of Atlantic brown trout, Salmo Trutta, into adriatic trout, Salmo Farioides in a stream at the drainage area of the adriatic sea basin of Montenegro 20
ID: 22 - Molecular genetic and clinical characterization of myotonic dystrophy type 1 patients carrying variant repeats within DMPK expansions 18
ID: 2403 - Trichome-specific and developmentally regulated biosynthesis of nepetalactones in leaves of cultivated Nepeta rtanjensis plants 18
ID: 58 - Myotonic Dystrophy Type 2 - Data from the Serbian Registry 17
ID: 5104 - Gene modifiers of Duchenne muscular dystrophy - Serbian experience 16
ID: 81 - Molecular genetics and genetic testing in myotonic dystrophy type 1 16
ID: 23 - Genetic testing of individuals with pre-senile cataract identifies patients with myotonic dystrophy type 2 14
ID: 7028 - Repeat-primed PCR in diagnostic testing of repeat expansion diseases 14
ID: 53 - Joint effect of the SMN2 and SERF1A genes on childhood-onset types of spinal muscular atrophy in Serbian patients 13
ID: 2401 - A novel recessive TTN founder variant is a common cause of distal myopathy in the Serbian population 9
ID: 4078 - Population genetic characteristics of Eastern-Serbian Salmo trutta L populations 9
ID: 7027 - Interactions of TPH2 variants and childhood abuse as risk factors for suicide attempt in Serbian psychiatric patients 9
ID: 7016 - Effect of childhood general traumas on suicide attempt depends on TPH2 and ADARB1 variants in psychiatric patients 8
ID: 7029 - From genotype to phenotype: in silico modelling of serotonergic system 8
Total 883
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Most type viewed #
ID: all - 0
ID: other - 0
ID: journal - 254
ID: conference - 629
ID: patent - 0
ID: book - 0
ID: dataset - 0
ID: selected - 0
Total 883
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Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec Tot
2023 021 642228 48121822 70102 371
2024 7118 10393200 0000 00 512
Ever 883