@ARTICLE{
author={Tanasic Vanja,Vukovic Marija,Mihajlovic-Srejic Milica,Kecmanovic Miljana,Keckarevic-Markovic Milica,Keckarevic Dusan P},
year={2025},
title={Genetic Variability of Roma Population in Serbia: The Perspective From Uniparentally Inherited Markers},
journal={AMERICAN JOURNAL OF HUMAN BIOLOGY},
volume={37},
number={10},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Mihajlovic-Srejic Milica,Tanasic Vanja,Keckarevic-Markovic Milica,Kecmanovic Miljana,Keckarevic Dusan P},
year={2025},
title={Phylogeography of Y-chromosome haplogroup I-P37.2 in Serbian population groups originating from distinct parts of the Balkan Peninsula},
journal={FORENSIC SCIENCE INTERNATIONAL-GENETICS},
volume={74},
number={},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Tanasic Vanja,Vukovic Marija,Mihajlovic-Srejic Milica,Kecmanovic Miljana,Keckarevic-Markovic Milica,Keckarevic Dusan P},
year={2024},
title={Genetic variability of Roma population in Serbia: The perspective from autosomal STR markers},
journal={JOURNAL OF ANTHROPOLOGICAL SCIENCES},
volume={102},
number={},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Mihajlovic Milica Lj,Tanasic Vanja,Keckarevic-Markovic Milica,Kecmanovic Miljana,Keckarevic Dusan P},
year={2022},
title={Distribution of Y-chromosome haplogroups in Serbian population groups originating from historically and geographically significant distinct parts of the Balkan Peninsula},
journal={FORENSIC SCIENCE INTERNATIONAL-GENETICS},
volume={61},
number={},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Stevanovic Galina B,Jovic Nebojsa J,Kecmanovic Miljana},
year={2020},
title={Is adjunctive perampanel beneficial for Lafora disease?},
journal={VOJNOSANITETSKI PREGLED},
volume={77},
number={5},
pages={539-544},
document_type={Article},
} 

@ARTICLE{
author={Cokic Vladan P,Kecmanovic Miljana,Zgonjanin-Bosic Dragana M,Jakovski Zlatko,Veljkovic Aleksandar N,Katic Srdjan D,Keckarevic-Markovic Milica,Keckarevic Dusan P},
year={2019},
title={A comprehensive mutation study in wide deep-rooted R1 b Serbian pedigree: mutation rates and male relative differentiation capacity of 36 Y-STR markers},
journal={FORENSIC SCIENCE INTERNATIONAL-GENETICS},
volume={41},
number={},
pages={137-144},
document_type={Article},
} 

@ARTICLE{
author={Andrejevic Marko,Keckarevic-Markovic Milica,Bursac Biljana N,Mihajlovic Milica Lj,Tanasic Vanja,Kecmanovic Miljana,Keckarevic Dusan P},
year={2019},
title={Identification of a broad spectrum of mammalian and avian species using the short fragment of the mitochondrially encoded cytochrome b gene},
journal={FORENSIC SCIENCE MEDICINE AND PATHOLOGY},
volume={15},
number={2},
pages={169-177},
document_type={Article},
} 

@ARTICLE{
author={Petrovic Vule,Kecmanovic Miljana,Keckarevic-Markovic Milica,Keckarevic Dusan P},
year={2019},
title={Assessment of mutation rates for PPY23 Y chromosome STR loci in Serbian father-son pairs},
journal={FORENSIC SCIENCE INTERNATIONAL-GENETICS},
volume={39},
number={},
pages={E5-E9},
document_type={Letter},
} 

@ARTICLE{
author={Radojicic Verica,Keckarevic-Markovic Milica,Puac Feda,Kecmanovic Miljana,Keckarevic Dusan P},
year={2018},
title={Comparison of different methods of DNA recovery and PCR amplification in STR profiling of casingsa retrospective study},
journal={INTERNATIONAL JOURNAL OF LEGAL MEDICINE},
volume={132},
number={6},
pages={1575-1580},
document_type={Article},
} 

@ARTICLE{
author={Nguyen V-H,...,Kecmanovic Miljana,...,(broj koautora 22)},
year={2017},
title={Updates to the Lafora Epilepsy Cure Initiative (LECI) Clinical Center: Development of a Data Collection Tool for Measurement of Lafora Epilepsy Disease Progression},
journal={EPILEPSIA},
volume={58},
number={},
pages={S194-S195},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Cirovic Natasa,Kecmanovic Miljana,Keckarevic Dusan P,Keckarevic-Markovic Milica},
year={2017},
title={Differentiation of Cannabis subspecies by THCA synthase gene analysis using RFLP},
journal={JOURNAL OF FORENSIC AND LEGAL MEDICINE},
volume={51},
number={},
pages={81-84},
document_type={Article},
} 

@ARTICLE{
author={Ercegovac Marko D,Jovic Nebojsa J,Sokic Dragoslav V,Simic Tatjana P,Savic-Radojevic Ana R,Coric Vesna M,Smiljic Jelena,Nikolic Dimitrije M,Kecmanovic Miljana,Pljesa-Ercegovac Marija S},
year={2016},
title={Single Nucleotide Polymorphisms of Antioxidant Enzymes in Progressive Myoclonus Epilepsy},
journal={EPILEPSIA},
volume={57},
number={},
pages={123-123},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Gagic Milica,Keckarevic-Markovic Milica,Kecmanovic Miljana,Keckarevic Dusan P,Mladenovic Jelena M,Dackovic Jelena,Milic-Rasic Vedrana M,Romac Stanka P},
year={2016},
title={Analysis of PMP22 duplication and deletion using a panel of six dinucleotide tandem repeats},
journal={CLINICAL CHEMISTRY AND LABORATORY MEDICINE},
volume={54},
number={5},
pages={773-780},
document_type={Article},
} 

@ARTICLE{
author={Kecmanovic Miljana,Jovic ND,Keckarevic-Markovic Milica,Keckarevic Dusan P,Stevanovic Galina B,Ignjatovic PM,Romac Stanka P},
year={2016},
title={Clinical and genetic data on Lafora disease patients of Serbian/Montenegrin origin},
journal={CLINICAL GENETICS},
volume={89},
number={1},
pages={104-108},
document_type={Article},
} 

@ARTICLE{
author={Genton Pierre,Jovic Nebojsa J,Lesca G,Kecmanovic Miljana},
year={2015},
title={Is Adjunctive Perampanel An Option for Intractable Seizures in Lafora Disease?},
journal={EPILEPSIA},
volume={56},
number={},
pages={57-58},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Ercegovac Marko D,Jovic Nebojsa J,Sokic Dragoslav V,Savic-Radojevic Ana R,Coric Vesna M,Radic Tanja M,Nikolic Dimitrije M,Kecmanovic Miljana,Matic Marija G,Simic Tatjana P,Pljesa-Ercegovac Marija S},
year={2015},
title={GSTA1, GSTM1, GSTP1 and GSTT1 polymorphisms in progressive myoclonus epilepsy: A Serbian case-control study},
journal={SEIZURE-EUROPEAN JOURNAL OF EPILEPSY},
volume={32},
number={},
pages={30-36},
document_type={Article},
} 

@ARTICLE{
author={Kecmanovic Miljana,Ristic Aleksandar J,Ercegovac Marko D,Keckarevic-Markovic Milica,Keckarevic Dusan P,Sokic Dragoslav V,Romac Stanka P},
year={2014},
title={A Shared Haplotype Indicates a Founder Event in Unverricht-Lundborg Disease Patients from Serbia},
journal={INTERNATIONAL JOURNAL OF NEUROSCIENCE},
volume={124},
number={2},
pages={102-109},
document_type={Article},
} 

@ARTICLE{
author={Kecmanovic Miljana,Jovic Nebojsa J,Cukic Mirjana,Keckarevic-Markovic Milica,Keckarevic Dusan P,Stevanovic Galina B,Romac Stanka P},
year={2013},
title={Lafora disease: Severe phenotype associated with homozygous deletion of the NHLRC1 gene},
journal={JOURNAL OF THE NEUROLOGICAL SCIENCES},
volume={325},
number={1-2},
pages={170-173},
document_type={Article},
} 

@ARTICLE{
author={Keckarevic-Markovic Milica,Dackovic Jelena,Mladenovic Jelena M,Milic-Rasic Vedrana M,Kecmanovic Miljana,Keckarevic Dusan P,Romac Stanka P},
year={2013},
title={An Algorithm for Genetic Testing of Serbian Patients with Demyelinating Charcot-Marie-Tooth},
journal={GENETIC TESTING AND MOLECULAR BIOMARKERS},
volume={17},
number={1},
pages={85-87},
document_type={Article},
} 

@ARTICLE{
author={Keckarevic-Markovic Milica,Kecmanovic Miljana,Keckarevic Dusan P,Mladenovic Jelena M,Milic-Rasic Vedrana M,Romac Stanka P},
year={2012},
title={A founder R32G mutation in GJB1 gene of Serbian CMT patients},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={19},
number={},
pages={783-783},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Keckarevic Dusan P,Stevic Zorica D,Keckarevic-Markovic Milica,Kecmanovic Miljana,Romac Stanka P},
year={2012},
title={Over-representation of the L144F SOD1 mutation in Serbian ALS patients due to founder effect},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={19},
number={},
pages={272-272},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Kecmanovic Miljana,Jovic ND,Keckarevic-Markovic Milica,Keckarevic Dusan P,Stevanovic Galina B,Romac Stanka P},
year={2012},
title={Founder c. 1048-1049delGA mutation in NHLRC1 gene in Lafora's disease patients from Serbia},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={19},
number={},
pages={236-236},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Ercegovac Marko D,Coric Vesna M,Simic Tatjana P,Jovic Nebojsa J,Sokic Dragoslav V,Jakovljevic Jovana,Kecmanovic Miljana,Nikolic Dimitrije M,Jankovic Snezana D,Savic-Radojevic Ana R,Pljesa-Ercegovac Marija S},
year={2012},
title={Glutathione Transferase Polymorphisms in Patients with Progressive Myoclonic Epilepsy},
journal={EPILEPSIA},
volume={53},
number={},
pages={21-21},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Keckarevic Dusan P,Stevic Zorica D,Keckarevic-Markovic Milica,Kecmanovic Miljana,Romac Stanka P},
year={2012},
title={A novel P66S mutation in exon 3 of the SOD1 gene with early onset and rapid progression},
journal={AMYOTROPHIC LATERAL SCLEROSIS},
volume={13},
number={2},
pages={237-240},
document_type={Article},
} 

@ARTICLE{
author={Kecmanovic Miljana,Dobricic Valerija S,Dimitrijevic Rajna D,Keckarevic Dusan P,Savic-Pavicevic Dusanka Lj,Keckarevic-Markovic Milica,Ivkovic Maja,Romac Stanka P},
year={2010},
title={Schizophrenia and Apolipoprotein E Gene Polymorphism in Serbian Population},
journal={INTERNATIONAL JOURNAL OF NEUROSCIENCE},
volume={120},
number={7},
pages={502-506},
document_type={Article},
} 

@ARTICLE{
author={Dimitrijevic Rajna D,Cadez Ivana,Keckarevic-Markovic Milica,Keckarevic Dusan P,Kecmanovic Miljana,Dobricic Valerija S,Savic-Pavicevic Dusanka Lj,Brajuskovic Goran N,Romac Stanka P},
year={2010},
title={Polymorphisms of the Prion Protein Gene (PRNP) in a Serbian Population},
journal={INTERNATIONAL JOURNAL OF NEUROSCIENCE},
volume={120},
number={7},
pages={496-501},
document_type={Article},
} 

@ARTICLE{
author={Keckarevic-Markovic Milica,Milic-Rasic Vedrana M,Mladenovic Jelena M,Dackovic Jelena,Kecmanovic Miljana,Keckarevic Dusan P,Savic-Pavicevic Dusanka Lj,Romac Stanka P},
year={2009},
title={Mutational analysis of GJB1, MPZ, PMP22, EGR2, and LITAF/SIMPLE in Serbian Charcot-Marie-Tooth patients},
journal={JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM},
volume={14},
number={2},
pages={125-136},
document_type={Article},
} 

@ARTICLE{
author={Keckarevic-Markovic Milica,Milic-Rasic Vedrana M,Kecmanovic Miljana,Keckarevic Dusan P,Romac Stanka P},
year={2009},
title={Congenital cataracts facial dysmorphism neuropathy in Serbian Romani patients},
journal={JOURNAL OF NEUROLOGY},
volume={256},
number={},
pages={S182-S182},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Kecmanovic Miljana,Ristic Aleksandar J,Sokic Dragoslav V,Keckarevic-Markovic Milica,Vojvodic Nikola M,Ercegovac Marko D,Jankovic Slavko M,Keckarevic Dusan P,Savic-Pavicevic Dusanka Lj,Romac Stanka P},
year={2009},
title={Coexistence of Unverricht-Lundborg disease and congenital deafness: Molecular resolution of a complex comorbidity},
journal={EPILEPSIA},
volume={50},
number={6},
pages={1612-1615},
document_type={Article},
} 

@ARTICLE{
author={Jovic Nebojsa J,Kecmanovic Miljana},
year={2009},
title={Clinical course of lafora disease associated with epm2b gene mutations in patients of serbian/montenegrin origin},
journal={EPILEPSIA},
volume={50},
number={},
pages={207-207},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Kecmanovic Miljana,Jovic ND,Keckarevic-Markovic Milica,Dobricic Valerija S,Keckarevic Dusan P,Ignjatovic PM,Romac Stanka P},
year={2008},
title={Mutations in NHLRC1 gene are predominant cause of Lafora disease in Serbian population},
journal={JOURNAL OF NEUROLOGY},
volume={255},
number={},
pages={102-103},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Keckarevic-Markovic Milica,Milic-Rasic Vedrana M,Kecmanovic Miljana,Keckarevic Dusan P,Todorovic Slobodanka,Romac Stanka P},
year={2008},
title={A novel 9-bp duplication in the connexin 32 gene causing X-linked Charcot-Marie-Tooth disease},
journal={JOURNAL OF NEUROLOGY},
volume={255},
number={},
pages={76-77},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Jankovic N,Kecmanovic Miljana,Dimitrijevic Rajna D,Keckarevic-Markovic Milica,Dobricic Valerija S,Savic-Pavicevic Dusanka Lj,Romac Stanka P},
year={2008},
title={HD phenocopies - Possible role of saitohin gene},
journal={INTERNATIONAL JOURNAL OF NEUROSCIENCE},
volume={118},
number={3},
pages={391-397},
document_type={Article},
} 

@ARTICLE{
author={Djarmati Ana,Dobricic Valerija S,Kecmanovic Miljana,Marsh P,Jancic-Stefanovic Jasna B,Klein Christine,Djuric Milena Lj,Romac Stanka P},
year={2007},
title={MECP2 mutations in Serbian Rett syndrome patients},
journal={ACTA NEUROLOGICA SCANDINAVICA},
volume={116},
number={6},
pages={413-419},
document_type={Editorial Material},
} 

@ARTICLE{
author={Kecmanovic Miljana,Ercegovac Marko D,Dimitrijevic Rajko N,Dobricic Valerija S,Keckarevic-Markovic Milica,Savic-Pavicevic Dusanka Lj,Keckarevic Dusan P,Saric M,Beslac-Bumbasirevic Ljiljana,Romac Stanka P},
year={2007},
title={Unverricht-Lundborg disease: the first report of genetically confirmed case in Serbia},
journal={JOURNAL OF NEUROLOGY},
volume={254},
number={},
pages={125-125},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Keckarevic-Markovic Milica,Milic-Rasic Vedrana M,Dobricic Valerija S,Kecmanovic Miljana,Dimitrijevic Rajko N,Saric M,Savic-Pavicevic Dusanka Lj,Keckarevic Dusan P,Todorovic Slobodanka,Romac Stanka P},
year={2007},
title={Hereditary motor and sensory neuropathy type Lom in Serbian Romany family},
journal={JOURNAL OF NEUROLOGY},
volume={254},
number={},
pages={109-109},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Saric M,Zamurovic Ljubica,Keckarevic-Markovic Milica,Keckarevic Dusan P,Kecmanovic Miljana,Savic-Pavicevic Dusanka Lj,Jovic Jasna Z,Romac Stanka P},
year={2007},
title={Frequency of the hemochromatosis gene mutations in patients with hereditary hemochromatosis and in control subjects from serbia and montenegro},
journal={AMERICAN JOURNAL OF HEMATOLOGY},
volume={82},
number={6},
pages={554-554},
document_type={Meeting Abstract},
}