Oliver Stojković

1.7k total citations · 1 hit paper
46 papers, 1.2k citations indexed

About

Oliver Stojković is a scholar working on Genetics, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Oliver Stojković has authored 46 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Genetics, 16 papers in Molecular Biology and 6 papers in Cellular and Molecular Neuroscience. Recurrent topics in Oliver Stojković's work include Forensic and Genetic Research (12 papers), Genetic Neurodegenerative Diseases (6 papers) and Insect and Arachnid Ecology and Behavior (5 papers). Oliver Stojković is often cited by papers focused on Forensic and Genetic Research (12 papers), Genetic Neurodegenerative Diseases (6 papers) and Insect and Arachnid Ecology and Behavior (5 papers). Oliver Stojković collaborates with scholars based in Serbia, United States and Belgium. Oliver Stojković's co-authors include Nobuaki Kawamura, Ikuya Tsuge, Masako Saitō, Tadashi Ariga, Yoshiyuki Minegishi, Ayşe Metìn, Hajime Karasuyama, Toshiro Hara, Hidetoshi Takada and Srdjan Pašić and has published in prestigious journals such as Nature, Analytical Biochemistry and Scientific Reports.

In The Last Decade

Oliver Stojković

44 papers receiving 1.2k citations

Hit Papers

Dominant-negative mutations in the DNA-binding domain of ... 2007 2026 2013 2019 2007 200 400 600

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Oliver Stojković Serbia 15 607 458 231 128 124 46 1.2k
Benjamin M. Matta United States 15 932 1.5× 141 0.3× 131 0.6× 54 0.4× 171 1.4× 21 1.4k
Weiping Zhou China 14 299 0.5× 180 0.4× 574 2.5× 27 0.2× 179 1.4× 38 1.1k
Kenneth B. Hoehn United States 16 360 0.6× 123 0.3× 273 1.2× 20 0.2× 71 0.6× 27 757
Roger B. Slee United States 16 257 0.4× 321 0.7× 526 2.3× 21 0.2× 91 0.7× 21 1.1k
Jun Kusuda Japan 18 964 1.6× 179 0.4× 581 2.5× 43 0.3× 783 6.3× 44 1.7k
Andrew King United States 20 373 0.6× 136 0.3× 658 2.8× 15 0.1× 243 2.0× 55 1.5k
Z. Runlin China 22 304 0.5× 427 0.9× 517 2.2× 13 0.1× 175 1.4× 45 1.3k
Anirban Chakraborty United States 24 347 0.6× 169 0.4× 1.5k 6.5× 150 1.2× 206 1.7× 47 2.0k
Kati J. Buckingham United States 15 190 0.3× 951 2.1× 999 4.3× 17 0.1× 51 0.4× 29 1.9k
Xianhua Yi United States 13 100 0.2× 331 0.7× 1.3k 5.5× 92 0.7× 169 1.4× 13 1.7k

Countries citing papers authored by Oliver Stojković

Since Specialization
Citations

This map shows the geographic impact of Oliver Stojković'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 Oliver Stojković with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Oliver Stojković more than expected).

Fields of papers citing papers by Oliver Stojković

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Oliver Stojković. 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 Oliver Stojković. The network helps show where Oliver Stojković may publish in the future.

Co-authorship network of co-authors of Oliver Stojković

This figure shows the co-authorship network connecting the top 25 collaborators of Oliver Stojković. A scholar is included among the top collaborators of Oliver Stojković 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 Oliver Stojković. Oliver Stojković is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
2.
Džoljić, Eleonora, et al.. (2023). Vitamin D Serum Levels and Vitamin D Receptor Genotype in Patients with Parkinson’s Disease. Neuroscience. 533. 53–62. 2 indexed citations
3.
Zdravković, Marija, et al.. (2022). Influence of ACE and ACTN3 genes polymorphisms on cardiovascular adaptation in female football players. Genetika. 54(3). 1035–1047. 1 indexed citations
4.
Atanasijević, Tatjana, et al.. (2021). Case Report: Post-mortem Histopathological and Molecular Analyses of the Very First Documented COVID-19-Related Death in Europe. Frontiers in Medicine. 8. 612758–612758. 11 indexed citations
5.
Stojković, Oliver, et al.. (2016). On the Bantu expansion. Gene. 593(1). 48–57. 3 indexed citations
6.
Preković, Stefan, Dušica Filipović Đurđević, Gábor Csifcsák, et al.. (2016). Multidisciplinary investigation links backward-speech trait and working memory through genetic mutation. Scientific Reports. 6(1). 20369–20369. 7 indexed citations
7.
Pajnič, Irena Zupanič, et al.. (2016). Prediction of autosomal STR typing success in ancient and Second World War bone samples. Forensic Science International Genetics. 27. 17–26. 27 indexed citations
8.
Gayden, Tenzin, et al.. (2011). Y-STR profiling in two Afghanistan populations. Legal Medicine. 13(2). 103–108. 16 indexed citations
9.
Mirabal, Sheyla, Tenzin Gayden, María Regueiro, et al.. (2010). Human Y‐chromosome short tandem repeats: A tale of acculturation and migrations as mechanisms for the diffusion of agriculture in the Balkan Peninsula. American Journal of Physical Anthropology. 142(3). 380–390. 26 indexed citations
10.
Gayden, Tenzin, et al.. (2010). Y-STR diversity in the Himalayas. International Journal of Legal Medicine. 125(3). 367–375. 14 indexed citations
11.
Regueiro, María, Aleksandar Stanojević, Shilpa Chennakrishnaiah, et al.. (2010). Divergent patrilineal signals in three Roma populations. American Journal of Physical Anthropology. 144(1). 80–91. 12 indexed citations
12.
Minegishi, Yoshiyuki, Masako Saitō, Shigeru Tsuchiya, et al.. (2007). Dominant-negative mutations in the DNA-binding domain of STAT3 cause hyper-IgE syndrome. Nature. 448(7157). 1058–1062. 704 indexed citations breakdown →
13.
Stojković, Oliver, et al.. (2007). Allele frequencies and population data for 17 Y-chromosome STR loci in a Serbian population sample from Vojvodina province. Forensic Science International. 176(2-3). e23–e28. 32 indexed citations
14.
Čuljković, Biljana, Dušanka Savić‐Pavićević, Oliver Stojković, & Stanka Romac. (2003). Poly(A) tailing of ancient DNA: a method for reproducible microsatellite genotyping. Analytical Biochemistry. 318(1). 124–131. 2 indexed citations
15.
Major, Tamara, Biljana Čuljković, Oliver Stojković, et al.. (2003). PREVALENCE OF THE FRAGILE X SYNDROME IN YUGOSLAV PATIENTS WITH NON-SPECIFIC MENTAL RETARDATION. Journal of Neurogenetics. 17(2-3). 223–230. 8 indexed citations
16.
Čuljković, Biljana, et al.. (2002). CTG repeat polymorphism in DMPK gene in healthy Yugoslav population. Acta Neurologica Scandinavica. 105(1). 55–58. 12 indexed citations
17.
Savić‐Pavićević, Dušanka, Ivan Topisirović, Tamara Major, et al.. (2001). Is the 31 CAG repeat allele of the spinocerebellar ataxia 1 (SCA1) gene locus non-specifically associated with trinucleotide expansion diseases?. Psychiatric Genetics. 11(4). 201–205. 4 indexed citations
18.
Stojković, Oliver, et al.. (2001). Yugoslav population data on nine STR loci. Forensic Science International. 115(3). 239–240. 2 indexed citations
19.
Čuljković, Biljana, Dušanka Savić‐Pavićević, Oliver Stojković, et al.. (2000). The Status of SCA1, MJD/SCA3, FRDA, DRPLA and MD Triplet Containing Genes in Patients with Huntington Disease and Healthy Controls. Journal of Neurogenetics. 14(4). 257–263. 10 indexed citations
20.
Čuljković, Biljana, Oliver Stojković, Nikola Vojvodić, et al.. (1999). Correlation between triplet repeat expansion and computed tomography measures of caudate nuclei atrophy in Huntington's disease. Journal of Neurology. 246(11). 1090–1093. 7 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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