D. Keckarević

发表

Human Y-specific STR haplotypes in population of Serbia and Montenegro.

V. Dobričić, A. Perović, A. Jovanovic, 2007, Forensic science international.

Genetic and clinical analysis of spinocerebellar ataxia type 8 repeat expansion in Yugoslavia

V. Kostic, I. Topisirovic, A. Ristić, 2002, Clinical genetics.

Polymorphisms of the Prion Protein Gene (PRNP) in a Serbian Population

V. Dobričić, S. Romac, R. Dimitrijević, 2010, The International journal of neuroscience.

Analysis of PMP22 duplication and deletion using a panel of six dinucleotide tandem repeats

V. Milic-Rasic, J. Dačković, S. Romac, 2016, Clinical chemistry and laboratory medicine.

Mutational analysis of GJB1, MPZ, PMP22, EGR2, and LITAF/SIMPLE in Serbian Charcot‐Marie‐Tooth patients

V. Milic-Rasic, J. Dačković, S. Romac, 2009, Journal of the peripheral nervous system : JPNS.

Frequency of the hemochromatosis gene mutations in the population of Serbia and Montenegro

M. Šarić, J. Jović, S. Romac, 2006, Clinical genetics.

An algorithm for genetic testing of Serbian patients with demyelinating Charcot-Marie-Tooth.

V. Milic-Rasic, J. Dačković, S. Romac, 2013, Genetic testing and molecular biomarkers.

Coexistence of Unverricht‐Lundborg disease and congenital deafness: Molecular resolution of a complex comorbidity

A. Ristić, D. Sokić, N. Vojvodić, 2009, Epilepsia.

Duchenne's/Becker's muscular dystrophy: Analysis of genotype-feno-type correlation in 28 patients

N. Zamurović, B. Culjković, D. Savic, 2002 .

Distribution of Y-chromosome haplogroups in Serbian population groups originating from historically and geographically significant distinct parts of the Balkan Peninsula.

M. Mihajlovic, D. Keckarević, M. Kecmanović, 2022, Forensic science international. Genetics.

Cosmopolitanism at the Roman Danubian Frontier, Slavic Migrations, and the Genomic Formation of Modern Balkan Peoples

D. Reich, C. Lalueza-Fox, Iosif Lazaridis, 2021, bioRxiv.

Genetics of Lafora progressive myoclonic epilepsy: current perspectives

S. Romac, N. Jović, G. Stevanović, 2016, The application of clinical genetics.

Schizophrenia and Apolipoprotein E Gene Polymorphism in Serbian Population

V. Dobričić, S. Romac, R. Dimitrijević, 2010, The International journal of neuroscience.

CLINICAL CASE REPORT ATYPICAL MYOPATHY IN A YOUNG GIRL WITH 91 CTG REPEATS IN DM1 LOCUS AND A POSITIVE DM1 FAMILY HISTORY

S. Apostolski, D. Savic, S. Romac, 2006, The International journal of neuroscience.

250 CTG repeats in DMPK is a threshold for correlation of expansion size and age at onset of juvenile–adult DM1

B. Culjković, S. Apostolski, D. Savic, 2002, Human mutation.

HD Phenocopies—Possible Role of Saitohin Gene

V. Dobričić, S. Romac, R. Dimitrijević, 2008, The International journal of neuroscience.

Identification of a broad spectrum of mammalian and avian species using the short fragment of the mitochondrially encoded cytochrome b gene

M. Andrejevic, Biljana N Bursać, D. Keckarević, 2019, Forensic Science, Medicine and Pathology.

A novel P66S mutation in exon 3 of the SOD1 gene with early onset and rapid progression

S. Romac, D. Keckarević, M. Keckarević-Marković, 2012, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

Assessment of mutation rates for PPY23 Y chromosome STR loci in Serbian father-son pairs.

D. Keckarević, M. Kecmanović, M. Keckarević Marković, 2019, Forensic science international. Genetics.

A comprehensive mutation study in wide deep-rooted R1b Serbian pedigree: mutation rates and male relative differentiation capacity of 36 Y-STR markers.

V. Čokić, Z. Jakovski, D. Keckarević, 2019, Forensic science international. Genetics.

Differentiation of Cannabis subspecies by THCA synthase gene analysis using RFLP.

D. Keckarević, M. Kecmanović, M. Keckarević Marković, 2017, Journal of Forensic and Legal Medicine.

Population data on 14 STR loci from population of Serbia and Montenegro (new and renewed data).

B. Culjković, A. Tarasjev, D. Savic, 2005, Forensic science international.

Clinical and genetic data on Lafora disease patients of Serbian/Montenegrin origin

S. Romac, N. Jović, G. Stevanović, 2016, Clinical genetics.

Lafora disease: Severe phenotype associated with homozygous deletion of the NHLRC1 gene

S. Romac, N. Jović, G. Stevanović, 2013, Journal of the Neurological Sciences.

A Shared Haplotype Indicates a Founder Event in Unverricht–Lundborg Disease Patients from Serbia

A. Ristić, D. Sokić, S. Romac, 2014, The International journal of neuroscience.