M Kecmanović - Publications, H-index & Citations

M Kecmanović

university of belgrade

10H指数

63论文数

206被引数

收录论文 9

发表时间

Genetic Variability of Roma Population in Serbia: The Perspective From Uniparentally Inherited Markers 塞尔维亚罗姆人群的遗传变异：单系遗传标记的视角

AMERICAN JOURNAL OF HUMAN BIOLOGY

IF1.7

2025-09-30

PREAI

Tanasic, Vanja; Vukovic, Marija; Srejic, Milica Mihajlovic; Kecmanovic, Miljana; Markovic, Milica Keckarevic; Keckarevic, Dusan

Phylogeography of Y-chromosome haplogroup I-P37.2 in Serbian population groups originating from distinct parts of the Balkan Peninsula

FORENSIC SCIENCE INTERNATIONAL-GENETICS

IF3.1

2025-01-01

PREAI

Srejic, Milica Mihajlovic; Tanasic, Vanja; Markovic, Milica Keckarevic; Kecmanovic, Miljana; Keckarevic, Dusan

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

IF3.1

2022-11-01

PREAI

Mihajlovic, Milica; Tanasic, Vanja; Markovic, Milica Keckarevic; Kecmanovic, Miljana; Keckarevic, Dusan

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

IF3.1

2019-07-01

PREAI

Cokic, Vladan P.; Kecmanovic, Miljana; Bosic, Dragana Zgonjanin; Jakovski, Zlatko; Veljkovic, Aleksandar; Katic, Srdjan; Markovic, Milica Keckarevic; Keckarevic, Dusan

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

FORENSIC SCIENCE INTERNATIONAL-GENETICS

IF3.1

2019-03-01

PREAI

Petrovic, Vule; Kecmanovic, Miljana; Markovic, Milica Keckarevic; Keckarevic, Dusan

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

CLINICAL CHEMISTRY AND LABORATORY MEDICINE

IF3.7

2016-01-01

PREAI

Gagic, Milica; Markovic, Milica Keckarevic; Kecmanovic, Miljana; Keckarevic, Dusan; Mladenovic, Jelena; Dackovic, Jelena; Milic-Rasic, Vedrana; Romac, Stanka

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

JOURNAL OF THE NEUROLOGICAL SCIENCES

IF3.2

2013-02-01

PREAI

Kecmanovic, Miljana; Jovic, Nebojsa; Cukic, Mirjana; Keckarevic-Markovic, Milica; Keckarevic, Dusan; Stevanovic, Galina; Romac, Stanka

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

JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM

IF3.2

2009-08-06

PREAI

Keckarevic-Markovic, Milica; Milic-Rasic, Vedrana; Mladenovic, Jelena; Dackovic, Jelena; Kecmanovic, Miljana; Keckarevic, Dusan; Savic-Pavicevic, Dusanka; Romac, Stanka

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

EPILEPSIA

IF6.6

2009-06-10

OAAI

Kecmanovic, Miljana; Ristic, Aleksandar J.; Sokic, Dragoslav; Keckarevic-Markovic, Milica; Vojvodic, Nikola; Ercegovac, Marko; Jankovic, Slavko; Keckarevic, Dusan; Savic-Pavicevic, Dusanka; Romac, Stanka

研究方向