Browsing by Author Keckarević, Dušan


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Issue DateTitleAuthor(s)Rank
2014Deletion of NHLRC1 gene is founder mutation in Lafora disease patients of Serbian/Montenegrim originKecmanović, Miljana ; Jović, N.; Keckarević-Marković, Milica ; Keckarević, Dušan ; Stevanović, G.; Romac, S.M64
Oct-2017Differentiation of Cannabis subspecies by THCA synthase gene analysis using RFLPCirovic, Natasa; Kecmanović, Miljana ; Keckarević, Dušan ; Keckarević Marković, Milica 
Sep-2022Differentiation of Cannabis subspecies by THCA synthase gene analysis – an overview and updateKeckarević-Marković, Milica ; Ćirović, Natasa; Kecmanović, Miljana ; Keckarević, Dušan M34
17-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
17-May-2018Diversity of Y-STR haplotypes in Serbs from old HercegovinaPašaljić, Đ.; Keckarević-Marković, Milica ; Kecmanović, Miljana ; Keckarević, Dušan M34
2023DNA methylation in age prediction: a forensic perspective of epigenetic clockKeckarević-Marković, Milica ; Andrejević, Marko; Kecmanović, Miljana ; Keckarević, Dušan M62
May-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
May-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
1-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
19-May-2018A familial search – need for haploid markers confirmationKeckarević-Marković, Milica ; Mihajlović, M.; Tanasić, V.; Kecmanović, Miljana ; Keckarević, Dušan M34
8-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
8-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
2007Frequency of the hemochromatosis gene mutations in patients with hereditary hemochromatosis and in control subjects from Serbia and MontenegroŠarić, M.; Zamurović, Lj.; Keckarević-Marković, Milica ; Keckarević, Dušan ; Kecmanović, Miljana ; Savić-Pavićević, Dušanka ; Jović, J.; Romac, S.M34
31-May-2008Frequency of the hemochromatosis gene mutations in patients with hereditary hemochromatosis and in control subjects from SerbiaŠarić, M.; Zamurović, L.; Keckarević-Marković, Milica ; Keckarević, Dušan ; Kecmanović, Miljana ; Savić-Pavićević, Dušanka ; Jović, J.; Romac, S.M34
Aug-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
5-Sep-2005Friedreich’s ataxia: analysis of mitotic instabilityDobričić, V.; Keckarević-Marković, Milica ; Stevanović, M.; Šarić, M.; Savić, D.; Keckarević, Dušan ; Romac, S.M34
2022Genetic analysis of 12 X-short tandem repeats loci in Serbian populationKecmanović, Miljana ; Keckarević-Marković, Milica ; Keckarević, Dušan M34
Oct-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.
7-Dec-2023A genetic history of the Balkans from Roman frontier to Slavic migrationsOlalde, Iñigo; Carrión, Pablo; Mikić, Ilija; Rohland, Nadin; Mallick, Swapan; Lazaridis, Iosif; Mah, Matthew; Korać, Miomir; Golubović, Snežana; Petković, Sofija; Miladinović-Radmilović, Nataša; Vulović, Dragana; Alihodžić, Timka; Ash, Abigail; Baeta, Miriam; Bartík, Juraj; Bedić, Željka; Bilić, Maja; Bonsall, Clive; Bunčić, Maja; Bužanić, Domagoj; Carić, Mario; Čataj, Lea; Cvetko, Mirna; Drnić, Ivan; Dugonjić, Anita; Đukić, Ana; Đukić, Ksenija; Farkaš, Zdeněk; Jelínek, Pavol; Jovanovic, Marija; Kaić, Iva; Kalafatić, Hrvoje; Krmpotić, Marijana; Krznar, Siniša; Leleković, Tino; M de Pancorbo, Marian; Matijević, Vinka; Milošević Zakić, Branka; Osterholtz, Anna J; Paige, Julianne M; Tresić Pavičić, Dinko; Premužić, Zrinka; Rajić Šikanjić, Petra; Rapan Papeša, Anita; Paraman, Lujana; Sanader, Mirjana; Radovanović, Ivana; Roksandic, Mirjana; Šefčáková, Alena; Stefanović, Sofia; Teschler-Nicola, Maria; Tončinić, Domagoj; Zagorc, Brina; Callan, Kim; Candilio, Francesca; Cheronet, Olivia; Fernandes, Daniel; Kearns, Aisling; Lawson, Ann Marie; Mandl, Kirsten; Wagner, Anna; Zalzala, Fatma; Zettl, Anna; Tomanović, Željko ; Keckarević, Dušan ; Novak, Mario; Harper, Kyle; McCormick, Michael; Pinhasi, Ron; Grbić, Miodrag; Lalueza-Fox, Carles; Reich, DavidM21a
2-May-2016Genetics of lafora progressive myoclonic epilepsy: Current perspectivesKecmanović, Miljana ; Keckarević Marković, Milica ; Keckarević, Dušan ; Stevanović, Galina; Jović, Nebojša; Romac, Stanka