Saša Ostojić

1.2k total citations
52 papers, 901 citations indexed

About

Saša Ostojić is a scholar working on Public Health, Environmental and Occupational Health, Immunology and Genetics. According to data from OpenAlex, Saša Ostojić has authored 52 papers receiving a total of 901 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Public Health, Environmental and Occupational Health, 16 papers in Immunology and 15 papers in Genetics. Recurrent topics in Saša Ostojić's work include Reproductive System and Pregnancy (16 papers), Endometriosis Research and Treatment (10 papers) and Pregnancy and preeclampsia studies (9 papers). Saša Ostojić is often cited by papers focused on Reproductive System and Pregnancy (16 papers), Endometriosis Research and Treatment (10 papers) and Pregnancy and preeclampsia studies (9 papers). Saša Ostojić collaborates with scholars based in Croatia, Slovenia and Serbia. Saša Ostojić's co-authors include Miljenko Kapović, Nina Pereza, Borut Peterlin, Nathalie Lédée, Sandrine Zourbas, Gérard Chaouat, Alena Buretić‐Tomljanović, Marija Volk, G. Chaouat and Sylvie Dubanchet and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and International Journal of Molecular Sciences.

In The Last Decade

Saša Ostojić

44 papers receiving 871 citations

Peers

Saša Ostojić

IMMUN

PHEOH

PPCH

Alíz Barakonyi Hungary

Vincenzo Pinto Italy

Nataki C. Douglas United States

Naoaki Kuji Japan

André Sollwedel Germany

Keisuke Sawai Japan

Leigh R. Guerin Australia

S. Michalas Greece

Kilian Vomstein Austria

Daljeet Banwatt Canada

Alíz Barakonyi Hungary

Saša Ostojić

1.1k ×1.9

IMMUN

396 ×1.2

PHEOH

306 ×1.1

319 ×1.4

71 ×0.6

PPCH

Citations per year, relative to Saša Ostojić Saša Ostojić (= 1×) peers Alíz Barakonyi

Countries citing papers authored by Saša Ostojić

Since Specialization

Citations

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

Fields of papers citing papers by Saša Ostojić

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Saša Ostojić

This figure shows the co-authorship network connecting the top 25 collaborators of Saša Ostojić. A scholar is included among the top collaborators of Saša Ostojić 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 Saša Ostojić. Saša Ostojić 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

Rački, Valentino, Mojca Čižek Sajko, Nada Starčević Čizmarević, et al.. (2025). Microbial diversity in drug-naïve Parkinson’s disease patients. PLoS ONE. 20(8). e0328761–e0328761. 1 indexed citations

Martinović, Lara Saftić, et al.. (2024). Decoding the Epigenetics of Infertility: Mechanisms, Environmental Influences, and Therapeutic Strategies. Epigenomes. 8(3). 34–34. 14 indexed citations

Rački, Valentino, Anja Kovanda, Nada Starčević Čizmarević, et al.. (2024). GiOPARK Project: The Genetic Study of Parkinson’s Disease in the Croatian Population. Genes. 15(2). 255–255.

Stanković, Aleksandra, et al.. (2024). MTHFR Gene Polymorphisms and DNA Methylation in Idiopathic Spontaneous Preterm Birth. Medicina. 60(12). 2028–2028. 2 indexed citations

Pereza, Nina, et al.. (2024). Second Case of Gonadal Mosaicism and a Novel Nonsense NR2F1 Gene Variant as the Cause of Bosch–Boonstra–Schaaf Optic Atrophy Syndrome. Clinical Genetics. 106(6). 786–787.

Aralica, Merica, et al.. (2024). Association of 25(OH)-Vitamin D3 Serum Concentrations and Vitamin D Receptor Gene Variants with the Risk of Idiopathic Spontaneous Preterm Birth in the Croatian Population. International Journal of Molecular Sciences. 25(21). 11712–11712. 2 indexed citations

Pereza, Nina, Saša Ostojić, Miljenko Kapović, & Borut Peterlin. (2016). Systematic review and meta-analysis of genetic association studies in idiopathic recurrent spontaneous abortion. Fertility and Sterility. 107(1). 150–159.e2. 111 indexed citations

Pereza, Nina, Borut Peterlin, Marija Volk, Miljenko Kapović, & Saša Ostojić. (2015). A critical update on endothelial nitric oxide synthase gene variations in women with idiopathic recurrent spontaneous abortion: genetic association study, systematic review and meta-analyses. Molecular Human Reproduction. 21(5). 466–478. 14 indexed citations

Pereza, Nina, et al.. (2015). The −2549 insertion/deletion polymorphism in the promoter region of the VEGFA gene in couples with idiopathic recurrent spontaneous abortion. Journal of Assisted Reproduction and Genetics. 32(12). 1789–1794. 10 indexed citations

10.

Pereza, Nina, et al.. (2013). Genetic variation in tissue inhibitors of metalloproteinases as a risk factor for idiopathic recurrent spontaneous abortion. Fertility and Sterility. 99(7). 1923–1929. 7 indexed citations

11.

Pereza, Nina, Saša Ostojić, Marija Volk, Miljenko Kapović, & Borut Peterlin. (2012). Matrix metalloproteinases 1, 2, 3 and 9 functional single-nucleotide polymorphisms in idiopathic recurrent spontaneous abortion. Reproductive BioMedicine Online. 24(5). 567–575. 36 indexed citations

12.

Pereza, Nina, Saša Ostojić, Marija Volk, et al.. (2012). Third case of 8q23.3‐q24.13 deletion in a patient with Langer–Giedion syndrome phenotype without TRPS1 gene deletion. American Journal of Medical Genetics Part A. 158A(3). 659–663. 15 indexed citations

13.

Novokmet, Natalija, Damir Marjanović, Vedrana Škaro, et al.. (2010). Genetic polymorphisms of 15 STR loci in the population of the island of Cres (Croatia). Annals of Human Biology. 38(1). 12–21. 3 indexed citations

14.

Medica, Igor, Saša Ostojić, Nina Pereza, Andrej Kastrin, & Borut Peterlin. (2009). Association between genetic polymorphisms in cytokine genes and recurrent miscarriage – a meta-analysis. Reproductive BioMedicine Online. 19(3). 406–414. 21 indexed citations

15.

Pereza, Nina & Saša Ostojić. (2008). Funkcionalna nejednakost roditeljskih genoma u etiologiji gestacijskih trofoblastičnih bolesti. University of Zagreb University Computing Centre (SRCE). 44(1). 22–37.

16.

Buretić‐Tomljanović, Alena, Saša Ostojić, & Miljenko Kapović. (2006). Secular change of craniofacial measures in Croatian younger adults. American Journal of Human Biology. 18(5). 668–675. 28 indexed citations

17.

Ostojić, Saša, et al.. (2005). [Controlled orthodontic extrusion with subsequent implantation].. PubMed. 115(3). 222–31. 5 indexed citations

18.

Chaouat, G., Nathalie Lédée, Sandrine Zourbas, et al.. (2003). Cytokines, implantation and early abortion: re‐examining the Th1/Th2 paradigm leads to question the single pathway, single therapy concept. American Journal of Reproductive Immunology. 50(3). 177–186. 88 indexed citations

19.

Chaouat, Gérard, et al.. (2002). A brief review of recent data on some cytokine expressions at the materno-foetal interface which might challenge the classical Th1/Th2 dichotomy. Journal of Reproductive Immunology. 53(1-2). 241–256. 221 indexed citations

20.

Chaouat, G., et al.. (2001). New insights into maternal-fetal interactions at implantation. Reproductive BioMedicine Online. 2(3). 198–203. 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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