Kecmanović, Miljana
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Full Name
Kecmanović, Miljana
Main Affiliation
Email
miljana@bio.bg.ac.rs
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Results 26-50 of 76 (Search time: 0.009 seconds).
| Issue Date | Title | Author(s) | Rank | |
|---|---|---|---|---|
| 26 | 2019 | Carrier rates of 7 founder mutations associated with single – gene disorders in Serbian Romani population – a pilot study | Tanasić, V.; Mihajlović, M.; Keckarević, Dušan ; Mladenović, J.; Kecmanović, Miljana ; Keckarević-Marković, Milica | M64 |
| 27 | Nov-2018 | Comparison of different methods of DNA recovery and PCR amplification in STR profiling of casings—a retrospective study | Radojicic, Verica; Keckarević Marković, Milica ; Puac, Feđa; Kecmanović, Miljana ; Keckarević, Dušan | M21 |
| 28 | 19-May-2018 | A familial search – need for haploid markers confirmation | Keckarević-Marković, Milica ; Mihajlović, M.; Tanasić, V.; Kecmanović, Miljana ; Keckarević, Dušan | M34 |
| 29 | 17-May-2018 | Diversity of Y-STR haplotypes in Serbs from old Hercegovina | Pašaljić, Đ.; Keckarević-Marković, Milica ; Kecmanović, Miljana ; Keckarević, Dušan | M34 |
| 30 | Oct-2017 | Differentiation of Cannabis subspecies by THCA synthase gene analysis using RFLP | Cirovic, Natasa; Kecmanović, Miljana ; Keckarević, Dušan ; Keckarević Marković, Milica | |
| 31 | 20-Sep-2017 | Analysis of mitochondrial dna control region in the domestic dog | Tanasić, V.; Gagić, M.; Keckarević-Marković, Milica ; Keckarević, Dušan ; Kecmanović, Miljana | M64 |
| 32 | 20-Sep-2017 | Predictive DNA analysis: assesment of Irisplex SNPs for eye color prediction in Serbian population | Mihajlović, M.; Radojičić, V.; Keckarević-Marković, Milica ; Kecmanović, Miljana ; Keckarević, Dušan | M64 |
| 33 | 20-Sep-2017 | Assessment of mutation rates for PPY23 STR loci in Serbian father-son pairs | Petrović, V.; Živković, J.; Keckarević-Marković, Milica ; Kecmanović, Miljana ; Keckarević, Dušan | M64 |
| 34 | 20-Sep-2017 | Morphological and micromorphological identification of Cannabis pollen and confirmation of marijuana in forensic traces by THCA synthase gene analysis | Nikolin, B; Gagić, M; Kecmanović, Miljana ; Keckarević, Dušan ; Janaćković, Peđa ; Gavrilović, Milan ; Rajčević, Nemanja ; Keckarević Marković, Milica | M64 |
| 35 | 28-Aug-2017 | Success in obtaining interpretable DNA profile from cartridge casings using different methods of extraction and DNA amplification kits – comparative study | Radojičić, V.; Keckarević-Marković, Milica ; Kecmanović, Miljana ; Puač, F.; Keckarević, Dušan | M34 |
| 36 | 28-Aug-2017 | Mutational analysis of 27 Y-chromosomal STRs performed on 85 males from one deep-rooted Serbian pedigree | Kecmanović, Miljana ; Čokić, V.; Keckarević-Marković, Milica ; Živković, J.; Jakovski, Z.; Zgonjanin, D.; Keckarević, Dušan | M34 |
| 37 | 18-May-2017 | SOD1, TDP-43, FUS/TLS and C9orf72 genes in Serbian ALS patients: long term survey | Keckarević, Dušan ; Janković, M.; Gagić, M.; Keckarević-Marković, Milica ; Kecmanović, Miljana ; Marjanović, A.; Marjanović, I.; Novaković, I.; Stević, Z. | M34 |
| 38 | 2017 | Updates to the Lafora Epilepsy Cure Initiative (LECI) Clinical Center: Development of a data collection tool for measurement of Lafora Epilepsy Disease Progression | Nguyen, V-H.; Serratosa, JM.; Gonzales, B.; Genton, P.; Michelucci, R.; Sinha, S.; Chandra, S.; Beydoun, A.; Arabi, M.; Kecmanović, Miljana ; Whitehouse, W.; Martinez-Juarez, IM.; Guilhoto, L.; Salas-Puig, J.; Ben- Menachem, E.; Goldsmith, D.; Duron, RM.; Medina, MT.; Bailey, JN.; Gentry, M.; Minassian, B.; Delgado- Escueta, AV. | M34 |
| 39 | 2017 | Clinical Center for the Lafora Epilepsy Cure Initiative (LECI): Clinical trial readiness for a global curative drug trial (P2.245) | Nguyen, V-H.; Duron, RM.; Serratosa, JM.; Minassian, B.; Michelucci, R.; Genton, P.; Sinha, S.; Arabi, M.; Beydoun, A.; Ben-Menachem, E.; Kecmanović, Miljana ; Guilhoto, L.; Whitehouse, W.; Salas-Puig, J.; Martinez- Juarez, I.; Gentry, M.; Bailey, J.; Delgado-Escueta, AV. | M34 |
| 40 | 20-May-2016 | Application of rapidly/fast mutated Y- STR loci analzsis in Serbia: haplotype and mutation analysis with nine generation family tree reconstruction | Kecmanović, Miljana ; Čokić, V.; Keckarević-Marković, Milica ; Keckarević, Dušan | M34 |
| 41 | 2-May-2016 | Genetics of lafora progressive myoclonic epilepsy: Current perspectives | Kecmanović, Miljana ; Keckarević Marković, Milica ; Keckarević, Dušan ; Stevanović, Galina; Jović, Nebojša; Romac, Stanka | |
| 42 | May-2016 | Analysis of PMP22 duplication and deletion using a panel of six dinucleotide tandem repeats | Gagic, Milica; Keckarević Marković, Milica ; Kecmanović, Miljana ; Keckarević, Dušan ; Mladenovic, Jelena; Dackovic, Jelena; Milic-Rasic, Vedrana; Romac, Stanka | |
| 43 | Jan-2016 | Clinical and genetic data on Lafora disease patients of Serbian/Montenegrin origin | Kecmanović, Miljana ; Jović, N.; Keckarević Marković, Milica ; Keckarević, Dušan ; Stevanović, G.; Ignjatović, P.; Romac, S. | |
| 44 | Nov-2015 | GSTA1, GSTM1, GSTP1 and GSTT1 polymorphisms in progressive myoclonus epilepsy: A Serbian case-control study | Ercegovac, Marko; Jovic, Nebojsa; Sokic, Dragoslav; Savic-Radojevic, Ana; Coric, Vesna; Radic, Tanja; Nikolic, Dimitrije; Kecmanović, Miljana ; Matic, Marija; Simic, Tatjana; Pljesa-Ercegovac, Marija | |
| 45 | Feb-2014 | A shared haplotype indicates a founder event in unverricht-lundborg disease patients from Serbia | Kecmanović, Miljana ; Ristić, Aleksandar J.; Ercegovac, Marko; Keckarević Marković, Milica ; Keckarević, Dušan ; Sokić, Dragoslav; Romac, Stanka | |
| 46 | 2014 | Microsatellite analysis in CMT1A genetic testing | Gagić, M.; Keckarević-Marković, Milica ; Keckarević, Dušan ; Kecmanović, Miljana ; Mladenović, J.; Milić Rašić, V.; Romac, S. | M64 |
| 47 | 2014 | PALM-LCM in sexual assault cases | Živković, J.; Ostojić, L.; Kecmanović, Miljana ; Keckarević-Marković, Milica ; Keckarević, Dušan | M64 |
| 48 | 2014 | Analysis of hexanucleotide GGGGCC repeats in the first intron of the C9orf72 gene | Labus, O.; Keckarević, Dušan ; Keckarević-Marković, Milica ; Kecmanović, Miljana ; Romac, S. | M64 |
| 49 | 2014 | Deletion of NHLRC1 gene is founder mutation in Lafora disease patients of Serbian/Montenegrim origin | Kecmanović, Miljana ; Jović, N.; Keckarević-Marković, Milica ; Keckarević, Dušan ; Stevanović, G.; Romac, S. | M64 |
| 50 | 25-Jun-2013 | Mutations in PMP22, MPZ0 and GJB1 in Serbian CMT patients: phenotypes and mechanisms of pathogenicity | Keckarević-Marković, Milica ; Kecmanović, Miljana ; Keckarević, Dušan ; Dacković, J.; Mladenović, J.; Milić-Rasić, V.; Romac, S. | M34 |