Tanasic Vanja,Vukovic Marija,Mihajlovic-Srejic Milica,Kecmanovic Miljana,Keckarevic-Markovic Milica,Keckarevic Dusan P (2025) Genetic Variability of Roma Population in Serbia: The Perspective From Uniparentally Inherited Markers, AMERICAN JOURNAL OF HUMAN BIOLOGY, vol. 37, br. 10, str. - (Article) 

Mihajlovic-Srejic Milica,Tanasic Vanja,Keckarevic-Markovic Milica,Kecmanovic Miljana,Keckarevic Dusan P (2025) Phylogeography of Y-chromosome haplogroup I-P37.2 in Serbian population groups originating from distinct parts of the Balkan Peninsula, FORENSIC SCIENCE INTERNATIONAL-GENETICS, vol. 74, br. , str. - (Article) 

Tanasic Vanja,Vukovic Marija,Mihajlovic-Srejic Milica,Kecmanovic Miljana,Keckarevic-Markovic Milica,Keckarevic Dusan P (2024) Genetic variability of Roma population in Serbia: The perspective from autosomal STR markers, JOURNAL OF ANTHROPOLOGICAL SCIENCES, vol. 102, br. , str. - (Article) 

Mihajlovic Milica Lj,Tanasic Vanja,Keckarevic-Markovic Milica,Kecmanovic Miljana,Keckarevic Dusan P (2022) Distribution of Y-chromosome haplogroups in Serbian population groups originating from historically and geographically significant distinct parts of the Balkan Peninsula, FORENSIC SCIENCE INTERNATIONAL-GENETICS, vol. 61, br. , str. - (Article) 

Stevanovic Galina B,Jovic Nebojsa J,Kecmanovic Miljana (2020) Is adjunctive perampanel beneficial for Lafora disease?, VOJNOSANITETSKI PREGLED, vol. 77, br. 5, str. 539-544 (Article) 

Cokic Vladan P,Kecmanovic Miljana,Zgonjanin-Bosic Dragana M,Jakovski Zlatko,Veljkovic Aleksandar N,Katic Srdjan D,Keckarevic-Markovic Milica,Keckarevic Dusan P (2019) A comprehensive mutation study in wide deep-rooted R1 b Serbian pedigree: mutation rates and male relative differentiation capacity of 36 Y-STR markers, FORENSIC SCIENCE INTERNATIONAL-GENETICS, vol. 41, br. , str. 137-144 (Article) 

Andrejevic Marko,Keckarevic-Markovic Milica,Bursac Biljana N,Mihajlovic Milica Lj,Tanasic Vanja,Kecmanovic Miljana,Keckarevic Dusan P (2019) Identification of a broad spectrum of mammalian and avian species using the short fragment of the mitochondrially encoded cytochrome b gene, FORENSIC SCIENCE MEDICINE AND PATHOLOGY, vol. 15, br. 2, str. 169-177 (Article) 

Petrovic Vule,Kecmanovic Miljana,Keckarevic-Markovic Milica,Keckarevic Dusan P (2019) Assessment of mutation rates for PPY23 Y chromosome STR loci in Serbian father-son pairs, FORENSIC SCIENCE INTERNATIONAL-GENETICS, vol. 39, br. , str. E5-E9 (Letter) 

Radojicic Verica,Keckarevic-Markovic Milica,Puac Feda,Kecmanovic Miljana,Keckarevic Dusan P (2018) Comparison of different methods of DNA recovery and PCR amplification in STR profiling of casingsa retrospective study, INTERNATIONAL JOURNAL OF LEGAL MEDICINE, vol. 132, br. 6, str. 1575-1580 (Article) 

Nguyen V-H,...,Kecmanovic Miljana,...,(broj koautora 22) (2017) Updates to the Lafora Epilepsy Cure Initiative (LECI) Clinical Center: Development of a Data Collection Tool for Measurement of Lafora Epilepsy Disease Progression, EPILEPSIA, vol. 58, br. , str. S194-S195 (Meeting Abstract) 

Cirovic Natasa,Kecmanovic Miljana,Keckarevic Dusan P,Keckarevic-Markovic Milica (2017) Differentiation of Cannabis subspecies by THCA synthase gene analysis using RFLP, JOURNAL OF FORENSIC AND LEGAL MEDICINE, vol. 51, br. , str. 81-84 (Article) 

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 (2016) Single Nucleotide Polymorphisms of Antioxidant Enzymes in Progressive Myoclonus Epilepsy, EPILEPSIA, vol. 57, br. , str. 123-123 (Meeting Abstract) 

Gagic Milica,Keckarevic-Markovic Milica,Kecmanovic Miljana,Keckarevic Dusan P,Mladenovic Jelena M,Dackovic Jelena,Milic-Rasic Vedrana M,Romac Stanka P (2016) Analysis of PMP22 duplication and deletion using a panel of six dinucleotide tandem repeats, CLINICAL CHEMISTRY AND LABORATORY MEDICINE, vol. 54, br. 5, str. 773-780 (Article) 

Kecmanovic Miljana,Jovic ND,Keckarevic-Markovic Milica,Keckarevic Dusan P,Stevanovic Galina B,Ignjatovic PM,Romac Stanka P (2016) Clinical and genetic data on Lafora disease patients of Serbian/Montenegrin origin, CLINICAL GENETICS, vol. 89, br. 1, str. 104-108 (Article) 

Genton Pierre,Jovic Nebojsa J,Lesca G,Kecmanovic Miljana (2015) Is Adjunctive Perampanel An Option for Intractable Seizures in Lafora Disease?, EPILEPSIA, vol. 56, br. , str. 57-58 (Meeting Abstract) 

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 (2015) GSTA1, GSTM1, GSTP1 and GSTT1 polymorphisms in progressive myoclonus epilepsy: A Serbian case-control study, SEIZURE-EUROPEAN JOURNAL OF EPILEPSY, vol. 32, br. , str. 30-36 (Article) 

Kecmanovic Miljana,Ristic Aleksandar J,Ercegovac Marko D,Keckarevic-Markovic Milica,Keckarevic Dusan P,Sokic Dragoslav V,Romac Stanka P (2014) A Shared Haplotype Indicates a Founder Event in Unverricht-Lundborg Disease Patients from Serbia, INTERNATIONAL JOURNAL OF NEUROSCIENCE, vol. 124, br. 2, str. 102-109 (Article) 

Kecmanovic Miljana,Jovic Nebojsa J,Cukic Mirjana,Keckarevic-Markovic Milica,Keckarevic Dusan P,Stevanovic Galina B,Romac Stanka P (2013) Lafora disease: Severe phenotype associated with homozygous deletion of the NHLRC1 gene, JOURNAL OF THE NEUROLOGICAL SCIENCES, vol. 325, br. 1-2, str. 170-173 (Article) 

Keckarevic-Markovic Milica,Dackovic Jelena,Mladenovic Jelena M,Milic-Rasic Vedrana M,Kecmanovic Miljana,Keckarevic Dusan P,Romac Stanka P (2013) An Algorithm for Genetic Testing of Serbian Patients with Demyelinating Charcot-Marie-Tooth, GENETIC TESTING AND MOLECULAR BIOMARKERS, vol. 17, br. 1, str. 85-87 (Article) 

Keckarevic-Markovic Milica,Kecmanovic Miljana,Keckarevic Dusan P,Mladenovic Jelena M,Milic-Rasic Vedrana M,Romac Stanka P (2012) A founder R32G mutation in GJB1 gene of Serbian CMT patients, EUROPEAN JOURNAL OF NEUROLOGY, vol. 19, br. , str. 783-783 (Meeting Abstract) 

Keckarevic Dusan P,Stevic Zorica D,Keckarevic-Markovic Milica,Kecmanovic Miljana,Romac Stanka P (2012) Over-representation of the L144F SOD1 mutation in Serbian ALS patients due to founder effect, EUROPEAN JOURNAL OF NEUROLOGY, vol. 19, br. , str. 272-272 (Meeting Abstract) 

Kecmanovic Miljana,Jovic ND,Keckarevic-Markovic Milica,Keckarevic Dusan P,Stevanovic Galina B,Romac Stanka P (2012) Founder c. 1048-1049delGA mutation in NHLRC1 gene in Lafora's disease patients from Serbia, EUROPEAN JOURNAL OF NEUROLOGY, vol. 19, br. , str. 236-236 (Meeting Abstract) 

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 (2012) Glutathione Transferase Polymorphisms in Patients with Progressive Myoclonic Epilepsy, EPILEPSIA, vol. 53, br. , str. 21-21 (Meeting Abstract) 

Keckarevic Dusan P,Stevic Zorica D,Keckarevic-Markovic Milica,Kecmanovic Miljana,Romac Stanka P (2012) A novel P66S mutation in exon 3 of the SOD1 gene with early onset and rapid progression, AMYOTROPHIC LATERAL SCLEROSIS, vol. 13, br. 2, str. 237-240 (Article) 

Kecmanovic Miljana,Dobricic Valerija S,Dimitrijevic Rajna D,Keckarevic Dusan P,Savic-Pavicevic Dusanka Lj,Keckarevic-Markovic Milica,Ivkovic Maja,Romac Stanka P (2010) Schizophrenia and Apolipoprotein E Gene Polymorphism in Serbian Population, INTERNATIONAL JOURNAL OF NEUROSCIENCE, vol. 120, br. 7, str. 502-506 (Article) 

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 (2010) Polymorphisms of the Prion Protein Gene (PRNP) in a Serbian Population, INTERNATIONAL JOURNAL OF NEUROSCIENCE, vol. 120, br. 7, str. 496-501 (Article) 

Keckarevic-Markovic Milica,Milic-Rasic Vedrana M,Mladenovic Jelena M,Dackovic Jelena,Kecmanovic Miljana,Keckarevic Dusan P,Savic-Pavicevic Dusanka Lj,Romac Stanka P (2009) Mutational analysis of GJB1, MPZ, PMP22, EGR2, and LITAF/SIMPLE in Serbian Charcot-Marie-Tooth patients, JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, vol. 14, br. 2, str. 125-136 (Article) 

Keckarevic-Markovic Milica,Milic-Rasic Vedrana M,Kecmanovic Miljana,Keckarevic Dusan P,Romac Stanka P (2009) Congenital cataracts facial dysmorphism neuropathy in Serbian Romani patients, JOURNAL OF NEUROLOGY, vol. 256, br. , str. S182-S182 (Meeting Abstract) 

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 (2009) Coexistence of Unverricht-Lundborg disease and congenital deafness: Molecular resolution of a complex comorbidity, EPILEPSIA, vol. 50, br. 6, str. 1612-1615 (Article) 

Jovic Nebojsa J,Kecmanovic Miljana (2009) Clinical course of lafora disease associated with epm2b gene mutations in patients of serbian/montenegrin origin, EPILEPSIA, vol. 50, br. , str. 207-207 (Meeting Abstract) 

Kecmanovic Miljana,Jovic ND,Keckarevic-Markovic Milica,Dobricic Valerija S,Keckarevic Dusan P,Ignjatovic PM,Romac Stanka P (2008) Mutations in NHLRC1 gene are predominant cause of Lafora disease in Serbian population, JOURNAL OF NEUROLOGY, vol. 255, br. , str. 102-103 (Meeting Abstract) 

Keckarevic-Markovic Milica,Milic-Rasic Vedrana M,Kecmanovic Miljana,Keckarevic Dusan P,Todorovic Slobodanka,Romac Stanka P (2008) A novel 9-bp duplication in the connexin 32 gene causing X-linked Charcot-Marie-Tooth disease, JOURNAL OF NEUROLOGY, vol. 255, br. , str. 76-77 (Meeting Abstract) 

Jankovic N,Kecmanovic Miljana,Dimitrijevic Rajna D,Keckarevic-Markovic Milica,Dobricic Valerija S,Savic-Pavicevic Dusanka Lj,Romac Stanka P (2008) HD phenocopies - Possible role of saitohin gene, INTERNATIONAL JOURNAL OF NEUROSCIENCE, vol. 118, br. 3, str. 391-397 (Article) 

Djarmati Ana,Dobricic Valerija S,Kecmanovic Miljana,Marsh P,Jancic-Stefanovic Jasna B,Klein Christine,Djuric Milena Lj,Romac Stanka P (2007) MECP2 mutations in Serbian Rett syndrome patients, ACTA NEUROLOGICA SCANDINAVICA, vol. 116, br. 6, str. 413-419 (Editorial Material) 

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 (2007) Unverricht-Lundborg disease: the first report of genetically confirmed case in Serbia, JOURNAL OF NEUROLOGY, vol. 254, br. , str. 125-125 (Meeting Abstract) 

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 (2007) Hereditary motor and sensory neuropathy type Lom in Serbian Romany family, JOURNAL OF NEUROLOGY, vol. 254, br. , str. 109-109 (Meeting Abstract) 

Saric M,Zamurovic Ljubica,Keckarevic-Markovic Milica,Keckarevic Dusan P,Kecmanovic Miljana,Savic-Pavicevic Dusanka Lj,Jovic Jasna Z,Romac Stanka P (2007) Frequency of the hemochromatosis gene mutations in patients with hereditary hemochromatosis and in control subjects from serbia and montenegro, AMERICAN JOURNAL OF HEMATOLOGY, vol. 82, br. 6, str. 554-554 (Meeting Abstract)