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



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Rank :  M34

Results 1-25 of 29 (Search time: 0.013 seconds).

Issue DateTitleAuthor(s)Rank
1May-2023Estimation of mutation rates and relative differentiation rate for 30 rapidly mutating Y-STRs in Serbian father-son pairsVuković, M.; Keckarević-Marković, Milica ; Kecmanović, Miljana ; Keckarević, Dušan M34
2May-2023Y-chromosomal landscape in Serbian population groups originating from the Balkan PeninsulaMihajlović, M.; Tanasić, V.; Keckarević-Marković, Milica ; Kecmanović, Miljana ; Keckarević, Dušan M34
32023Аnalysis of paternal and maternal lineages in Serbian Roma populationTanasić, V.; Mihajlović, M.; Kecmanović, Miljana ; Keckarević-Marković, Milica ; Keckarević, Dušan M34
4Sep-2022Differentiation of Cannabis subspecies by THCA synthase gene analysis – an overview and updateKeckarević-Marković, Milica ; Ćirović, Natasa; Kecmanović, Miljana ; Keckarević, Dušan M34
52022Genetic analysis of 12 X-short tandem repeats loci in Serbian populationKecmanović, Miljana ; Keckarević-Marković, Milica ; Keckarević, Dušan M34
69-Sep-2019Comparative analysis of different DNA recovery methods from touch DNA deposited on plastic bags and aluminium foilRadanović, A.; Kecmanović, Miljana ; Tanasić, V.; Mihajlović, M.; Radojičić, V.; Puac, F.; Keckarević-Marković, Milica ; Keckarević, Dušan M34
79-Sep-2019Comparison of Globalfiler TM PCR amplification kit and Precision ID Globalfiler TM NGS STR panel – implications on forensic caseworkKeckarević-Marković, Milica ; Tanasić, V.; Mihajlović, M.; Radojičić, V.; Puac, F.; Kecmanović, Miljana ; Keckarević, Dušan M34
819-May-2018A familial search – need for haploid markers confirmationKeckarević-Marković, Milica ; Mihajlović, M.; Tanasić, V.; Kecmanović, Miljana ; Keckarević, Dušan M34
917-May-2018Diversity of Y-STR haplotypes in Serbs from old HercegovinaPašaljić, Đ.; Keckarević-Marković, Milica ; Kecmanović, Miljana ; Keckarević, Dušan M34
1028-Aug-2017Success in obtaining interpretable DNA profile from cartridge casings using different methods of extraction and DNA amplification kits – comparative studyRadojičić, V.; Keckarević-Marković, Milica ; Kecmanović, Miljana ; Puač, F.; Keckarević, Dušan M34
1128-Aug-2017Mutational analysis of 27 Y-chromosomal STRs performed on 85 males from one deep-rooted Serbian pedigreeKecmanović, Miljana ; Čokić, V.; Keckarević-Marković, Milica ; Živković, J.; Jakovski, Z.; Zgonjanin, D.; Keckarević, Dušan M34
1218-May-2017SOD1, TDP-43, FUS/TLS and C9orf72 genes in Serbian ALS patients: long term surveyKeckarević, Dušan ; Janković, M.; Gagić, M.; Keckarević-Marković, Milica ; Kecmanović, Miljana ; Marjanović, A.; Marjanović, I.; Novaković, I.; Stević, Z.M34
132017Clinical 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
142017Updates to the Lafora Epilepsy Cure Initiative (LECI) Clinical Center: Development of a data collection tool for measurement of Lafora Epilepsy Disease ProgressionNguyen, 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
1520-May-2016Application of rapidly/fast mutated Y- STR loci analzsis in Serbia: haplotype and mutation analysis with nine generation family tree reconstructionKecmanović, Miljana ; Čokić, V.; Keckarević-Marković, Milica ; Keckarević, Dušan M34
1625-Jun-2013Mutations in PMP22, MPZ0 and GJB1 in Serbian CMT patients: phenotypes and mechanisms of pathogenicityKeckarević-Marković, Milica ; Kecmanović, Miljana ; Keckarević, Dušan ; Dacković, J.; Mladenović, J.; Milić-Rasić, V.; Romac, S.M34
178-Sep-2012Founder c.1048-1049delGA mutation in NHLRC1 gene in Lafora’s disease patients from SerbiaKecmanović, Miljana ; Jović, N.; Keckarević-Marković, Milica ; Keckarević, Dušan ; Stevanović, G.; Romac, S.M34
188-Sep-2012Founder R32G mutation in GJB1 gene of Serbian CMT patientsKeckarević-Marković, Milica ; Kecmanović, Miljana ; Keckarević, Dušan ; Mladenović, J.; Milić-Rasić, V.; Romac, S.M34
198-Sep-2012Over- representation of the L144F SOD1mutation in Serbian ALS patients due tofounder effectKeckarević, Dušan ; Stević, Z.; Keckarević-Marković, Milica ; Kecmanović, Miljana ; Romac, S.M34
209-Jul-2012The advancement of molecular diagnostics of CMT in SerbiaKeckarević-Marković, Milica ; Milić-Rašić, V.; Mladenović, J.; Dačković, J.; Kecmanović, Miljana ; Keckarević, Dušan ; Romac, S.M34
2120-Jun-2009Congenital cataracts facial dysmorphism neuropathy in Serbian Romani patientsKeckarević-Marković, Milica ; Milić-Rašić, V.; Kecmanović, Miljana ; Keckarević, Dušan ; Romac, S.M34
227-Jun-2008A novel 9-bp duplication in the connexin 32 gene causing X-linked Charcot-Marie-Tooth diseaseKeckarević-Marković, Milica ; Milić-Rašić, V.; Kecmanović, Miljana ; Keckarević, D.; Todorović, S.; Romac, S.M34
237-Jun-2008Mutations in NHLRC1 gene are predominant cause of Lafora disease in Serbian populationKecmanović, Miljana ; Jović, N.; Keckarević-Marković, Milica ; Dobričić, V.; Keckarević, Dušan ; Ignjatović, P.; Romac, S.M34
2431-May-2008Coexistence of Unvericht-Lundborg disease and congenital deafness in one Serbian familyKecmanović, Miljana ; Ristić, A.; Sokić, D.; Keckarević-Marković, Milica ; Keckarević, Dušan ; Romac, S.M34
2531-May-2008A three generation Serbian family with C263T mutation in MPZ geneKeckarević-Marković, Milica ; Dačković, J.; Mladenović, J.; Kecmanović, Miljana ; Keckarević, Dušan ; Milić-Rašić, V.; Romac, S.M34