Nela Maksimović

479 total citations
39 papers, 345 citations indexed

About

Nela Maksimović is a scholar working on Molecular Biology, Hematology and Rheumatology. According to data from OpenAlex, Nela Maksimović has authored 39 papers receiving a total of 345 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 9 papers in Hematology and 8 papers in Rheumatology. Recurrent topics in Nela Maksimović's work include Rheumatoid Arthritis Research and Therapies (8 papers), Prenatal Screening and Diagnostics (5 papers) and Acute Lymphoblastic Leukemia research (4 papers). Nela Maksimović is often cited by papers focused on Rheumatoid Arthritis Research and Therapies (8 papers), Prenatal Screening and Diagnostics (5 papers) and Acute Lymphoblastic Leukemia research (4 papers). Nela Maksimović collaborates with scholars based in Serbia, Bosnia and Herzegovina and Poland. Nela Maksimović's co-authors include Biljana Jekić, Ivana Novaković, Ljiljana Luković, Nemanja Damjanov, Maja Krajinović, Vera Milić, Goran Radunović, Branka Popović, Heidi Stöhr and Agnes B. Renner and has published in prestigious journals such as SHILAP Revista de lepidopterología, International Journal of Molecular Sciences and The American Journal of Human Genetics.

In The Last Decade

Nela Maksimović

34 papers receiving 336 citations

Peers

Nela Maksimović

RHEUM

PHEOH

GENET

HEMAT

Hilmi Tozkır Türkiye

Necmettin Kırtak Türkiye

Tobias Moser Austria

Bárbara Alonso Spain

Ljiljana Luković Serbia

Alberto Hidalgo‐Bravo Mexico

F. Cailotto France

Ahmėt Çolak Türkiye

Tarnjit K. Khera United Kingdom

Saori Yaguchi Japan

Hilmi Tozkır Türkiye

Nela Maksimović

90 ×0.6

47 ×0.5

RHEUM

26 ×0.4

PHEOH

15 ×0.3

GENET

36 ×0.9

HEMAT

Citations per year, relative to Nela Maksimović Nela Maksimović (= 1×) peers Hilmi Tozkır

Countries citing papers authored by Nela Maksimović

Since Specialization

Citations

This map shows the geographic impact of Nela Maksimović's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Nela Maksimović with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Nela Maksimović more than expected).

Fields of papers citing papers by Nela Maksimović

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Nela Maksimović. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Nela Maksimović. The network helps show where Nela Maksimović may publish in the future.

Co-authorship network of co-authors of Nela Maksimović

This figure shows the co-authorship network connecting the top 25 collaborators of Nela Maksimović. A scholar is included among the top collaborators of Nela Maksimović based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Nela Maksimović. Nela Maksimović is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Maksimović, Nela, et al.. (2025). Association of NOS Gene Polymorphisms with Sepsis-Related Complications in Secondary Peritonitis. International Journal of Molecular Sciences. 26(21). 10306–10306. 1 indexed citations

Novaković, Ivana, et al.. (2024). Genetic and epigenetic mechanisms of aging. SHILAP Revista de lepidopterología. 75(5). 6–12. 1 indexed citations

Jekić, Biljana, et al.. (2024). Chromosomal Microarray in Children Born Small for Gestational Age – Single Center Experience. SHILAP Revista de lepidopterología. 27(2). 13–21.

Todorović, Jovana, et al.. (2023). Association of IL-6 rs1800795, but not TNF-α rs1800629, and IL-1β rs16944 polymorphisms’ genotypes with recovery of ischemic stroke patients following thrombolysis. Neurological Research. 46(2). 157–164. 1 indexed citations

Novaković, Ivana, et al.. (2023). Galectin 3 rs4644 gene polymorphism is associated with metabolic traits in Serbian adolescent population. Journal of Medical Biochemistry. 43(4). 445–450. 1 indexed citations

Jekić, Biljana, et al.. (2022). Chromosomal microarray in postnatal diagnosis of congenital anomalies and neurodevelopmental disorders in Serbian patients. Journal of Clinical Laboratory Analysis. 36(6). e24441–e24441. 8 indexed citations

Kovačević, Zoran, Tatjana Lazarević, Nela Maksimović, et al.. (2022). Galectin 3 (LGALS3) Gene Polymorphisms Are Associated with Biochemical Parameters and Primary Disease in Patients with End-Stage Renal Disease in Serbian Population. Journal of Clinical Medicine. 11(13). 3874–3874. 2 indexed citations

Maksimović, Nela, et al.. (2022). PPARGC1A gene polymorphism and its association with obesity-related metabolic traits in Serbian adolescent population. Genetika. 54(3). 1375–1384.

Škrbić, Ranko, et al.. (2021). Prevalence of five pharmacologically most important CYP2C9 and CYP2C19 allelic variants in the population from the Republic of Srpska in Bosnia and Herzegovina. Archives of Industrial Hygiene and Toxicology. 72(2). 129–134. 4 indexed citations

10.

Maksimović, Nela, et al.. (2021). Association between isolated mild symmetrical ventriculomegaly and fetal chromosomal aberrations. Genetika. 53(3). 1007–1015.

11.

Jekić, Biljana, et al.. (2021). TT genotype of the MMP‐9‐1562C/T polymorphism may be a risk factor for thrombolytic therapy‐induced hemorrhagic complications after acute ischemic stroke. Pharmacotherapy The Journal of Human Pharmacology and Drug Therapy. 41(7). 562–571. 6 indexed citations

12.

Milić, Vera, Vita Dolžan, Nela Maksimović, et al.. (2020). Analysis of association of ADORA2A and ADORA3 polymorphisms genotypes/haplotypes with efficacy and toxicity of methotrexate in patients with Rheumatoid arthritis. The Pharmacogenomics Journal. 20(6). 784–791. 6 indexed citations

13.

Izrael-Živković, Lidija, Vladimir Beškoski, Milena Rikalović, et al.. (2019). High-quality draft genome sequence of Pseudomonas aeruginosa san ai, an environmental isolate resistant to heavy metals. Extremophiles. 23(4). 399–405. 10 indexed citations

14.

Maksimović, Nela, Biljana Jekić, Vera Milić, et al.. (2015). Polymorphisms of the eNOS gene are associated with disease activity in rheumatoid arthritis. Rheumatology International. 36(4). 597–602. 8 indexed citations

15.

Vojinović, Dina, Jovan Pešović, Vesna Lukić, et al.. (2014). Intellectual Ability in the Duchenne Muscular Dystrophy and Dystrophin Gene Mutation Location. Balkan Journal of Medical Genetics. 17(2). 25–35. 32 indexed citations

16.

Jekić, Biljana, Ljiljana Luković, Vera Milić, et al.. (2012). Association of the TYMS 3G/3G genotype with poor response and GGH 354GG genotype with the bone marrow toxicity of the methotrexate in RA patients. European Journal of Clinical Pharmacology. 69(3). 377–383. 41 indexed citations

17.

Maksimović, Nela, et al.. (2012). Quantitative analysis of the dystrophin gene by real-time PCR. Archives of Biological Sciences. 64(2). 787–792. 3 indexed citations

18.

Jekić, Biljana, Valerija Dobričić, Ivana Novaković, et al.. (2011). NPM1 gene mutations in children with Myelodysplastic syndromes. Archives of Biological Sciences. 63(3). 649–653. 1 indexed citations

19.

Langmann, Thomas, Silvio Alessandro Di Gioia, Isabella Rau, et al.. (2010). Nonsense Mutations in FAM161A Cause RP28-Associated Recessive Retinitis Pigmentosa. The American Journal of Human Genetics. 87(3). 376–381. 64 indexed citations

20.

Nikolić, Dejan, et al.. (2010). Degree of genetic homozygosity and distribution of AB0 blood types among patients with spina bifida occulta and spina bifida aperta. Archives of Medical Science. 6(6). 854–859. 10 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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