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Full Name
Keckarević, Dušan
 
Email
duskec@bio.bg.ac.rs
 
 
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Publications

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Results 1-23 of 23 (Search time: 0.011 seconds).

Issue DateTitleAuthor(s)Rank
1Jul-2019A comprehensive mutation study in wide deep-rooted R1b Serbian pedigree: mutation rates and male relative differentiation capacity of 36 Y-STR markersČokić, Vladan P.; Kecmanović, Miljana ; Zgonjanin Bosić, Dragana; Jakovski, Zlatko; Veljković, Aleksandar; Katić, Srdjan; Keckarević Marković, Milica ; Keckarević, Dušan M21a
2Jun-2019Identification of a broad spectrum of mammalian and avian species using the short fragment of the mitochondrially encoded cytochrome b geneAndrejevic, Marko; Keckarević Marković, Milica ; Bursac, Biljana; Mihajlović, Milica ; Tanasic, Vanja; Kecmanović, Miljana ; Keckarević, Dušan M22
3Mar-2019Assessment of mutation rates for PPY23 Y chromosome STR loci in Serbian father-son pairsPetrovic, Vule; Kecmanović, Miljana ; Keckarević Marković, Milica ; Keckarević, Dušan M21a
4Nov-2018Comparison of different methods of DNA recovery and PCR amplification in STR profiling of casings—a retrospective studyRadojicic, Verica; Keckarević Marković, Milica ; Puac, Feđa; Kecmanović, Miljana ; Keckarević, Dušan M21
5Oct-2017Differentiation of Cannabis subspecies by THCA synthase gene analysis using RFLPCirovic, Natasa; Kecmanović, Miljana ; Keckarević, Dušan ; Keckarević Marković, Milica 
62-May-2016Genetics of lafora progressive myoclonic epilepsy: Current perspectivesKecmanović, Miljana ; Keckarević Marković, Milica ; Keckarević, Dušan ; Stevanović, Galina; Jović, Nebojša; Romac, Stanka
7May-2016Analysis of PMP22 duplication and deletion using a panel of six dinucleotide tandem repeatsGagic, Milica; Keckarević Marković, Milica ; Kecmanović, Miljana ; Keckarević, Dušan ; Mladenovic, Jelena; Dackovic, Jelena; Milic-Rasic, Vedrana; Romac, Stanka
8Jan-2016Clinical and genetic data on Lafora disease patients of Serbian/Montenegrin originKecmanović, Miljana ; Jović, N.; Keckarević Marković, Milica ; Keckarević, Dušan ; Stevanović, G.; Ignjatović, P.; Romac, S.
9Feb-2014A shared haplotype indicates a founder event in unverricht-lundborg disease patients from SerbiaKecmanović, Miljana ; Ristić, Aleksandar J.; Ercegovac, Marko; Keckarević Marković, Milica ; Keckarević, Dušan ; Sokić, Dragoslav; Romac, Stanka
1015-Feb-2013Lafora disease: Severe phenotype associated with homozygous deletion of the NHLRC1 geneKecmanović, Miljana ; Jović, Nebojša; Čukić, Mirjana; Keckarević Marković, Milica ; Keckarević, Dušan ; Stevanović, Galina; Romac, Stanka
11Jan-2013An algorithm for genetic testing of serbian patients with demyelinating charcot-marie-toothKeckarević Marković, Milica P. ; Dackovic, Jelena; Mladenovic, Jelena; Milic-Rasic, Vedrana; Kecmanović, Miljana ; Keckarević, Dušan ; Romac, Stanka
12Feb-2012A novel P66S mutation in exon 3 of the SOD1 gene with early onset and rapid progressionKeckarević, Dušan ; Stević, Zorica; Keckarević Marković, Milica ; Kecmanović, Miljana ; Romac, Stanka
13Jul-2010Polymorphisms of the prion protein gene (PRNP) in a Serbian populationDimitrijević, Rajna; Čadež, Ivana; Keckarević Marković, Milica ; Keckarević, Dušan ; Kecmanović, Miljana ; Dobričić, Valerija; Savić Pavićević, Dušanka ; Brajušković, Goran ; Romac, Stanka
14Jul-2010Schizophrenia and apolipoprotein e gene polymorphism in Serbian populationKecmanović, Miljana ; Dobričić, Valerija; Dimitrijević, Rajna; Keckarević, Dušan ; Savić Pavićević, Dušanka ; Keckarević Marković, Milica ; Ivkovic, Maja; Romac, Stanka
15Jun-2009Mutational analysis of GJB1, MPZ, PMP22, EGR2, and LITAF/SIMPLE in Serbian Charcot-Marie-Tooth patientsKeckarević Marković, Milica ; Milic-Rasic, Vedrana; Mladenovic, Jelena; Dackovic, Jelena; Kecmanović, Miljana ; Keckarević, Dušan ; Savić Pavićević, Dušanka ; Romac, Stanka
16Jun-2009Coexistence of Unverricht-Lundborg disease and congenital deafness: Molecular resolution of a complex comorbidityKecmanović, Miljana ; Ristić, Aleksandar J.; Sokić, Dragoslav; Keckarević Marković, Milica ; Vojvodić, Nikola; Ercegovac, Marko; Janković, Slavko; Keckarević, Dušan ; Savić Pavićević, Dušanka ; Romac, Stanka
17Mar-2008HD phenocopies - Possible role of saitohin geneJanković, N.; Kecmanović, M. ; Dimitrijević, R.; Keckarević Marković, M. ; Dobričić, V.; Keckarević, D. ; Savić Pavićević, D. ; Romac, S.
1813-Sep-2007Human Y-specific STR haplotypes in population of Serbia and MontenegroStevanović, Miljana ; Dobričić, Valerija; Keckarević, Dušan ; Perović, Aleksandar; Savić Pavićević, Dušanka ; Keckarević Marković, Milica ; Jovanović, Aleksandar; Romac, Stanka
19Aug-2006Frequency of the hemochromatosis gene mutations in the population of Serbia and Montenegro [2]Šarić, M.; Zamurović, Lj; Keckarević Marković, M. ; Keckarević, D. ; Stevanović, M. ; Savić Pavićević, D. ; Jović, J.; Romac, Stanka
2016-Jul-2005Population data on 14 STR loci from population of Serbia and Montenegro (new and renewed data)Keckarević, Dušan ; Savić, Dušanka ; Keckarević, Milica ; Stevanović, Miljana ; Tarasjev, Aleksej; Čuljković, Biljana; Darmati, Ana; Vukosavić, Slobodanka; Romac, Stanka
21Oct-2002Genetic and clinical analysis of spinocerebellar ataxia type 8 repeat expansion in YugoslaviaTopisirovic, I.; Dragaševic, N.; Savic, D. ; Ristic, A.; Keckarevic, M. ; Keckarevic, D. ; Culjkovic, B.; Petrovic, I.; Romac, S.; Kostic, V. S.
22May-2002Duchenne's and Becker's muscular dystrophy: analysis of phenotype-genotype correlation in 28 patients]Keckarević, Milica ; Savić, Dušanka ; Culjković, Biljana; Zamurović, Natasa; Major, Tamara; Keckarević, Dušan ; Todorović, Slobodanka; Romac, Stanka
231-Dec-2001Is the 31 CAG repeat allele of the spinocerebellar ataxia 1 (SCA1) gene locus non-specifically associated with trinucleotide expansion diseases?Savić, Dušanka ; Topisirović, Ivan; Keckarević, Milica ; Keckarević, Dušan ; Major, Tamara; Čuljković, Biljana; Stojković, Oliver; Rakočević-Stojanović, Vidosava; Mladenović, Jelena; Todorović, Slobodanka; Apostolski, Slobodan; Romac, Stanka