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Kecmanović, Miljana

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Full Name
Kecmanović, Miljana
Main Affiliation
 
Email
miljana@bio.bg.ac.rs
 
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Publications

Results 1-25 of 28 (Search time: 0.015 seconds).

Issue DateTitleAuthor(s)Rank
11-Jan-2023EVALUATION OF THE IRISPLEX SYSTEM FOR EYE COLOUR PREDICTION IN THE SERBIAN POPULATIONVukovic, Marija; Srejic, Milica Mihajlovic; Sapic, Katarina; Tanasic, Vanja; Radojicic, Verica; Keckarević-Marković, Milica ; Kecmanović, Miljana ; Keckarević, Dušan M23
217-Aug-2022Distribution of Y-chromosome haplogroups in Serbian population groups originating from historically and geographically significant distinct parts of the Balkan PeninsulaMihajlović, Milica ; Tanasic, Vanja; Keckarević-Marković, Milica ; Kecmanović, Miljana ; Keckarević, Dušan M21a
32022Marker porekla kao adut u forenzičkim analizama DNK u kompleksnim slučajevima iz perspektive Y hromozomaKecmanović, Miljana ; Keckarević-Marković, Milica ; Keckarević, Dušan М45
42022Novi uvid u genetiku naslednih perifernih neuropatijaKeckarević-Marković, Milica ; Kecmanović, Miljana ; Keckarević, Dušan М45
5Sep-2021Nova paradigma u dijagnostici retkih bolestiKeckarević-Marković, Milica ; Kecmanović, Miljana ; Keckarević, Dušan М45
62020Is adjunctive perampanel beneficial for lafora disease?Stevanovic, Galina; Jovic, Nebojsa; Kecmanović, Miljana M23
7Jul-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
8Jun-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
9Mar-2019Assessment of mutation rates for PPY23 Y chromosome STR loci in Serbian father-son pairsPetrovic, Vule; Kecmanović, Miljana ; Keckarević Marković, Milica ; Keckarević, Dušan M21a
10Nov-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
11Oct-2017Differentiation of Cannabis subspecies by THCA synthase gene analysis using RFLPCirovic, Natasa; Kecmanović, Miljana ; Keckarević, Dušan ; Keckarević Marković, Milica 
122-May-2016Genetics of lafora progressive myoclonic epilepsy: Current perspectivesKecmanović, Miljana ; Keckarević Marković, Milica ; Keckarević, Dušan ; Stevanović, Galina; Jović, Nebojša; Romac, Stanka
13May-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
14Jan-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.
15Nov-2015GSTA1, GSTM1, GSTP1 and GSTT1 polymorphisms in progressive myoclonus epilepsy: A Serbian case-control studyErcegovac, Marko; Jovic, Nebojsa; Sokic, Dragoslav; Savic-Radojevic, Ana; Coric, Vesna; Radic, Tanja; Nikolic, Dimitrije; Kecmanović, Miljana ; Matic, Marija; Simic, Tatjana; Pljesa-Ercegovac, Marija
16Feb-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
1715-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
18Jan-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
19Feb-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
20Jul-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
21Jul-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
22Jun-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
23Jun-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
24Mar-2008HD phenocopies - Possible role of saitohin geneJanković, N.; Kecmanović, M. ; Dimitrijević, R.; Keckarević Marković, M. ; Dobričić, V.; Keckarević, D. ; Savić Pavićević, D. ; Romac, S.
25Dec-2007MECP2 mutations in Serbian Rett syndrome patientsDjarmati, A.; Dobričić, V.; Kecmanović, M. ; Marsh, P.; Jančić-Stefanović, J.; Klein, C.; Djurić, M.; Romac, S.