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Keywords

medical genetics, neurogenetics

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Employment (3)

University Clinical Centre of Serbia: Belgrade, RS

2017-07-01 to present | Head of Laboratory for Molecular Genetic Diagnostic of Neurological Diseases (Neurology Clinic)
Employment
Source: Self-asserted source
Milena Jankovic

Univerzitetski klinički centar Srbije: Beograd, Beograd, RS

2013-10-21 to 2017-07-01 | MSc in Biology in Laboratory for Molecular Genetic Diagnostic of Neurological Diseases (Neurology Clinic)
Employment
Source: Self-asserted source
Milena Jankovic

University of Belgrade: Belgrade, RS

2010-06-01 to 2014-03-02 | Research Trainee (School of Medicine)
Employment
Source: Self-asserted source
Milena Jankovic

Education and qualifications (2)

University of Belgrade: Belgrade, RS

2019-09-16 | Biology Specialist - Medical Genetic (School of Biology)
Education
Source: Self-asserted source
Milena Jankovic

University of Belgrade: Belgrade, RS

2009-10-01 to 2015-07-10 | PhD in Biology (Genetics) (School of Biology)
Education
Source: Self-asserted source
Milena Jankovic

Works (34)

Basophilic peripheral nerve inclusions in a patient with L144F SOD1 amyotrophic lateral sclerosis

Vojnosanitetski pregled
2023 | Journal article
DOI: 10.2298/VSP210717097A
Contributors: Dejan Aleksic; Stojan Peric; Sanja Milenkovic; Milena Jankovic; Vidosava Rakocevic-Stojanovic; Zorica Stevic
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Clinical and Genetic Features of Huntington’s Disease Patients From Republic of Serbia: A Single-Center Experience

Journal of Movement Disorders
2023-09-30 | Journal article
DOI: 10.14802/jmd.23028
Contributors: Nikola Kresojević; Ivana Perović; Iva Stanković; Aleksandra Tomić; Milica Jecˇmenica Lukic´; Vladana Marković; Tanja Stojković; Gorana Mandić; Milena Janković; Ana Marjanović et al.
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Stroke vs. Preeclampsia: Dangerous Liaisons of Hypertension and Pregnancy

Medicina
2023-09-24 | Journal article
DOI: 10.3390/medicina59101707
Contributors: Milan Lackovic; Dejan Nikolic; Milena Jankovic; Marija Rovcanin; Sladjana Mihajlovic
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miRNAs as a Potential Biomarker in the COVID-19 Infection and Complications Course, Severity, and Outcome

Diagnostics
2023-03-14 | Journal article
DOI: 10.3390/diagnostics13061091
Contributors: Milena Jankovic; Dejan Nikolic; Ivana Novakovic; Bojana Petrovic; Milan Lackovic; Milena Santric-Milicevic
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Analysis of “clinical exome” panel in Serbian patients with cognitive disorders

Genetika
2022 | Journal article
DOI: 10.2298/GENSR2203351B
Contributors: Marija Brankovic; Elka Stefanova; Gorana Mandic; Ana Marjanovic; Valerija Dobricic; Ales Maver; Gaber Bergant; Zorica Stevic; Milena Jankovic; Ivana Novakovic et al.
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C9ORF72 repeat expansion is not associated with atypical parkinsonism in the Serbian population

Genetika
2022 | Journal article
DOI: 10.2298/GENSR2203313M
Contributors: Ana Marjanovic; Valerija Dobricic; Milica Jecmenica-Lukic; Iva Stankovic; Ognjen Milicevic; Natasa Dragasevic-Miskovic; Marija Brankovic; Milena Jankovic; Ivana Novakovic; Marina Svetel et al.
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Clinical exome sequencing in Serbian patients with movement disorders: Single centre experience

Genetika
2022 | Journal article
DOI: 10.2298/GENSR2201395B
Contributors: Marija Brankovic; Natasa Dragasevic; Valerija Dobricic; Ales Maver; Gaber Bergant; Igor Petrovic; Stojan Peric; Ana Marjanovic; Milena Jankovic; Jasna Jancic et al.
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A multicenter study of genetic testing for Parkinson’s disease in the clinical setting

npj Parkinson's Disease
2022-11-04 | Journal article
DOI: 10.1038/s41531-022-00408-6
Contributors: Anja Kovanda; Valentino Rački; Gaber Bergant; Dejan Georgiev; Dušan Flisar; Eliša Papić; Marija Brankovic; Milena Jankovic; Marina Svetel; Nataša Teran et al.
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Genetic and phenotypic variability in adult patients with Niemann Pick type C from Serbia: single-center experience

Journal of Neurology
2022-06 | Journal article
DOI: 10.1007/s00415-021-10918-7
Contributors: Nikola Kresojević; Valerija Dobričić; Milica Ječmenica Lukić; Aleksandra Tomić; Igor Petrović; Nataša Dragašević; Ivana Perović; Ana Marjanović; Marija Branković; Milena Janković et al.
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The Genetic Basis of Strokes in Pediatric Populations and Insight into New Therapeutic Options

International Journal of Molecular Sciences
2022-01-29 | Journal article
DOI: 10.3390/ijms23031601
Contributors: Milena Jankovic; Bojana Petrovic; Ivana Novakovic; Slavko Brankovic; Natasa Radosavljevic; Dejan Nikolic
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Genetic and epigenomic modifiers of diabetic neuropathy

International Journal of Molecular Sciences
2021 | Journal article
DOI: 10.3390/ijms22094887
EID:

2-s2.0-85105152581

Part of ISSN: 14220067 16616596
Contributors: Jankovic, M.; Novakovic, I.; Nikolic, D.; Maksic, J.M.; Brankovic, S.; Petronic, I.; Cirovic, D.; Ducic, S.; Grajic, M.; Bogicevic, D.
Source: Self-asserted source
Milena Jankovic via Scopus - Elsevier

Novel TEAD1 gene variant in a Serbian family with Sveinsson's chorioretinal atrophy

Experimental Eye Research
2021 | Journal article
DOI: 10.1016/j.exer.2021.108575
EID:

2-s2.0-85104591805

Part of ISSN: 10960007 00144835
Contributors: Grubisa, I.; Jankovic, M.; Nikolic, N.; Jaksic, V.; Risimic, D.; Mavija, M.; Stamenkovic, M.; Zlatovic, M.; Milasin, J.
Source: Self-asserted source
Milena Jankovic via Scopus - Elsevier

Mutational Analysis and mtDNA Haplogroup Characterization in Three Serbian Cases of Mitochondrial Encephalomyopathies and Literature Review

Diagnostics
2021-10-23 | Journal article
DOI: 10.3390/diagnostics11111969
Contributors: Phepy G. A. Dawod; Jasna Jancic; Ana Marjanovic; Marija Brankovic; Milena Jankovic; Janko Samardzic; Ayman Gamil Anwar Dawod; Ivana Novakovic; Fayda I. Abdel Motaleb; Vladimir Radlovic et al.
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Current Concepts on Genetic Aspects of Mitochondrial Dysfunction in Amyotrophic Lateral Sclerosis

International Journal of Molecular Sciences
2021-09-11 | Journal article
DOI: 10.3390/ijms22189832
Contributors: Milena Jankovic; Ivana Novakovic; Phepy Gamil Anwar Dawod; Ayman Gamil Anwar Dawod; Aleksandra Drinic; Fayda I. Abdel Motaleb; Sinisa Ducic; Dejan Nikolic
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Genetic aspects of inflammation and immune response in stroke

International Journal of Molecular Sciences
2020 | Journal article
DOI: 10.3390/ijms21197409
EID:

2-s2.0-85092775376

Part of ISSN: 14220067 16616596
Contributors: Nikolic, D.; Jankovic, M.; Petrovic, B.; Novakovic, I.
Source: Self-asserted source
Milena Jankovic via Scopus - Elsevier

Neuropathic pain in patients with Charcot-Marie-Tooth type 1A

Neurological Sciences
2020 | Journal article
DOI: 10.1007/s10072-019-04142-5
EID:

2-s2.0-85075182565

Part of ISSN: 15903478 15901874
Contributors: Bjelica, B.; Peric, S.; Basta, I.; Bozovic, I.; Kacar, A.; Marjanovic, A.; Ivanovic, V.; Brankovic, M.; Jankovic, M.; Novakovic, I. et al.
Source: Self-asserted source
Milena Jankovic via Scopus - Elsevier

Quality of life in hereditary neuropathy with liability to pressure palsies is as impaired as in Charcot–Marie–Tooth disease type 1A

Acta Neurologica Belgica
2020 | Journal article
DOI: 10.1007/s13760-020-01355-w
EID:

2-s2.0-85084128226

Part of ISSN: 22402993 03009009
Contributors: Bjelica, B.; Peric, S.; Bozovic, I.; Jankovic, M.; Brankovic, M.; Palibrk, A.; Rakocevic Stojanovic, V.
Source: Self-asserted source
Milena Jankovic via Scopus - Elsevier

Whole mitochondrial genome analysis in serbian cases of leber’s hereditary optic neuropathy

Genes
2020 | Journal article
DOI: 10.3390/genes11091037
EID:

2-s2.0-85090506804

Part of ISSN: 20734425
Contributors: Dawod, P.G.A.; Jancic, J.; Marjanovic, A.; Brankovic, M.; Jankovic, M.; Samardzic, J.; Potkonjak, D.; Djuric, V.; Mesaros, S.; Novakovic, I. et al.
Source: Self-asserted source
Milena Jankovic via Scopus - Elsevier

Yield of the PMP22 deletion analysis in patients with compression neuropathies

Journal of Neurology
2020 | Journal article
DOI: 10.1007/s00415-020-10052-w
EID:

2-s2.0-85087704149

Part of ISSN: 14321459 03405354
Contributors: Ivanovic, V.; Brankovic, M.; Bjelica, B.; Kacar, A.; Tubic, R.; Jankovic, M.; Marjanovic, A.; Novakovic, I.; Rakocevic-Stojanovic, V.; Peric, S.
Source: Self-asserted source
Milena Jankovic via Scopus - Elsevier

Body composition analysis in patients with myotonic dystrophy types 1 and 2

Neurological Sciences
2019 | Journal article
DOI: 10.1007/s10072-019-03763-0
EID:

2-s2.0-85064817044

Part of ISSN: 15903478 15901874
Contributors: Peric, S.; Bozovic, I.; Nisic, T.; Banovic, M.; Vujnic, M.; Svabic, T.; Pesovic, J.; Brankovic, M.; Basta, I.; Jankovic, M. et al.
Source: Self-asserted source
Milena Jankovic via Scopus - Elsevier

Phenotypic and genetic spectrum of patients with limb-girdle muscular dystrophy type 2A from Serbia

Acta Myologica
2019 | Journal article
EID:

2-s2.0-85075953814

Part of ISSN: 25321900 11282460
Contributors: Peric, S.; Stevanovic, J.; Johnson, K.; Kosac, A.; Peric, M.; Brankovic, M.; Marjanovic, A.; Jankovic, M.; Banko, B.; Milenkovic, S. et al.
Source: Self-asserted source
Milena Jankovic via Scopus - Elsevier

Identification of mutations in the PARK2 gene in Serbian patients with Parkinson's disease

Journal of the Neurological Sciences
2018 | Journal article
DOI: 10.1016/j.jns.2018.07.020
EID:

2-s2.0-85051109770

Part of ISSN: 18785883 0022510X
Contributors: Jankovic, M.Z.; Dobricic, V.; Kresojevic, N.; Markovic, V.; Petrovic, I.; Svetel, M.; Pekmezovic, T.; Novakovic, I.; Kostic, V.
Source: Self-asserted source
Milena Jankovic via Scopus - Elsevier

Unraveling ALS due to SOD1 mutation through the combination of brain and cervical cord MRI

Neurology
2018 | Journal article
DOI: 10.1212/WNL.0000000000005002
EID:

2-s2.0-85045927835

Part of ISSN: 1526632X
Contributors: Agosta, F.; Spinelli, E.G.; Marjanovic, I.V.; Stevic, Z.; Pagani, E.; Valsasina, P.; Salak-Djokic, B.; Jankovic, M.; Lavrnic, D.; Kostic, V.S. et al.
Source: Self-asserted source
Milena Jankovic via Scopus - Elsevier

Comparison of the clinical and cognitive features of genetically positive ALS patients from the largest tertiary center in Serbia

Journal of Neurology
2017 | Journal article
DOI: 10.1007/s00415-017-8495-y
EID:

2-s2.0-85018663426

Part of ISSN: 14321459 03405354
Contributors: Marjanović, I.V.; Selak-Djokić, B.; Perić, S.; Janković, M.; Arsenijević, V.; Basta, I.; Lavrnić, D.; Stefanova, E.; Stević, Z.
Source: Self-asserted source
Milena Jankovic via Scopus - Elsevier

GCH1 mutations are common in Serbian patients with dystonia-parkinsonism: Challenging previously reported prevalence rates of DOPA-responsive dystonia

Parkinsonism and Related Disorders
2017 | Journal article
DOI: 10.1016/j.parkreldis.2017.09.017
EID:

2-s2.0-85029796649

Part of ISSN: 18735126 13538020
Contributors: Dobričić, V.; Tomić, A.; Branković, V.; Kresojević, N.; Janković, M.; Westenberger, A.; Rašić, V.M.; Klein, C.; Novaković, I.; Svetel, M. et al.
Source: Self-asserted source
Milena Jankovic via Scopus - Elsevier

Are Leber's mitochondial DNA mutations associated with aquaporin-4 autoimmunity?

Multiple Sclerosis
2016 | Journal article
DOI: 10.1177/1352458515590649
EID:

2-s2.0-84986575767

Part of ISSN: 14770970 13524585
Contributors: Dujmovic, I.; Jancic, J.; Dobricic, V.; Jankovic, M.; Novakovic, I.; Comabella, M.; Drulovic, J.
Source: Self-asserted source
Milena Jankovic via Scopus - Elsevier

Identification of novel variants in LRRK2 gene in patients with Parkinson's disease in Serbian population

Journal of the Neurological Sciences
2015 | Journal article
DOI: 10.1016/j.jns.2015.04.002
EID:

2-s2.0-84929513525

Part of ISSN: 18785883 0022510X
Contributors: Janković, M.Z.; Kresojević, N.D.; Dobričić, V.S.; Marković, V.V.; Petrović, I.N.; Novaković, I.V.; Kostić, V.S.
Source: Self-asserted source
Milena Jankovic via Scopus - Elsevier

Presenting symptoms of GBA-related Parkinson's disease

Parkinsonism and Related Disorders
2015 | Journal article
DOI: 10.1016/j.parkreldis.2015.04.028
EID:

2-s2.0-84930933311

Part of ISSN: 18735126 13538020
Contributors: Kresojević, N.; Janković, M.; Petrović, I.; Kumar, K.R.; Dragašević, N.; Dobričić, V.; Novaković, I.; Svetel, M.; Klein, C.; Pekmezović, T. et al.
Source: Self-asserted source
Milena Jankovic via Scopus - Elsevier

A common polymorphism in the brain-derived neurotrophic factor gene in patients with adult-onset primary focal and segmental dystonia

Acta Neurologica Belgica
2013 | Journal article
DOI: 10.1007/s13760-013-0183-9
EID:

2-s2.0-84880792465

Part of ISSN: 22402993 03009009
Contributors: Svetel, M.V.; Djuric, G.; Novakovic, I.; Dobricic, V.; Stefanova, E.; Kresojevic, N.; Tomic, A.; Jankovic, M.; Petrovic, I.; Pekmezovic, T. et al.
Source: Self-asserted source
Milena Jankovic via Scopus - Elsevier

Mutation screening of the DYT6/THAP1 gene in Serbian patients with primary dystonia

Journal of Neurology
2013 | Journal article
DOI: 10.1007/s00415-012-6753-6
EID:

2-s2.0-84876481227

Part of ISSN: 03405354 14321459
Contributors: Dobričić, V.S.; Kresojević, N.D.; Svetel, M.V.; Janković, M.Z.; Petrović, I.N.; Tomić, A.D.; Novaković, I.V.; Kostić, V.S.
Source: Self-asserted source
Milena Jankovic via Scopus - Elsevier

Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification

Neurogenetics
2013 | Journal article
DOI: 10.1007/s10048-012-0349-2
EID:

2-s2.0-84873738898

Part of ISSN: 13646745 13646753
Contributors: Hsu, S.C.; Sears, R.L.; Lemos, R.R.; Quintáns, B.; Huang, A.; Spiteri, E.; Nevarez, L.; Mamah, C.; Zatz, M.; Pierce, K.D. et al.
Source: Self-asserted source
Milena Jankovic via Scopus - Elsevier

Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice

Nature Genetics
2013 | Journal article
DOI: 10.1038/ng.2723
EID:

2-s2.0-84883463387

Part of ISSN: 10614036 15461718
Contributors: Keller, A.; Westenberger, A.; Sobrido, M.J.; García-Murias, M.; Domingo, A.; Sears, R.L.; Lemos, R.R.; Ordoñez-Ugalde, A.; Nicolas, G.; Da Cunha, J.E.G. et al.
Source: Self-asserted source
Milena Jankovic via Scopus - Elsevier

Transcranial sonography in patients with Parkinson's disease with glucocerebrosidase mutations

Parkinsonism and Related Disorders
2013 | Journal article
DOI: 10.1016/j.parkreldis.2012.12.006
EID:

2-s2.0-84875240657

Part of ISSN: 13538020 18735126
Contributors: Kresojević, N.; Mijajlović, M.; Perić, S.; Pavlović, A.; Svetel, M.; Janković, M.; Dobričić, V.; Novaković, I.; Lakočević, M.B.; Klein, C. et al.
Source: Self-asserted source
Milena Jankovic via Scopus - Elsevier

Genetic testing in familial and young-onset Alzheimer's disease: Mutation spectrum in a Serbian cohort

Neurobiology of Aging
2012 | Journal article
DOI: 10.1016/j.neurobiolaging.2011.12.007
EID:

2-s2.0-84861185819

Part of ISSN: 15581497 01974580
Contributors: Dobricic, V.; Stefanova, E.; Jankovic, M.; Gurunlian, N.; Novakovic, I.; Hardy, J.; Kostic, V.; Guerreiro, R.
Source: Self-asserted source
Milena Jankovic via Scopus - Elsevier

Peer review (2 reviews for 2 publications/grants)

Review activity for Cells. (1)
Review activity for NPJ Parkinson's disease. (1)
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