Nina Pereza

529 total citations
37 papers, 388 citations indexed

About

Nina Pereza is a scholar working on Public Health, Environmental and Occupational Health, Genetics and Immunology. According to data from OpenAlex, Nina Pereza has authored 37 papers receiving a total of 388 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Public Health, Environmental and Occupational Health, 11 papers in Genetics and 11 papers in Immunology. Recurrent topics in Nina Pereza's work include Reproductive System and Pregnancy (11 papers), Pregnancy and preeclampsia studies (9 papers) and Genetic Syndromes and Imprinting (5 papers). Nina Pereza is often cited by papers focused on Reproductive System and Pregnancy (11 papers), Pregnancy and preeclampsia studies (9 papers) and Genetic Syndromes and Imprinting (5 papers). Nina Pereza collaborates with scholars based in Croatia, Slovenia and Serbia. Nina Pereza's co-authors include Saša Ostojić, Borut Peterlin, Miljenko Kapović, Marija Volk, Alenka Hodžić, Igor Medica, Andrej Kastrin, Nataša Tul, Martina Mavrinac and Aleš Maver and has published in prestigious journals such as International Journal of Molecular Sciences, Gene and Fertility and Sterility.

In The Last Decade

Nina Pereza

31 papers receiving 378 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nina Pereza Croatia 11 189 136 123 100 74 37 388
S.‐T. Joseph Huang United States 7 156 0.8× 135 1.0× 73 0.6× 72 0.7× 78 1.1× 7 340
K.E. Humphrey Australia 6 182 1.0× 132 1.0× 96 0.8× 84 0.8× 73 1.0× 7 357
Se-Te Joseph Huang United States 7 238 1.3× 205 1.5× 62 0.5× 94 0.9× 79 1.1× 7 380
Ritsuo Honda Japan 10 87 0.5× 88 0.6× 118 1.0× 52 0.5× 109 1.5× 23 323
Johanna Prast Austria 7 149 0.8× 224 1.6× 47 0.4× 91 0.9× 70 0.9× 7 328
Ruhul Choudhury United Kingdom 11 205 1.1× 216 1.6× 41 0.3× 113 1.1× 41 0.6× 21 403
Silke Mark Germany 7 88 0.5× 138 1.0× 43 0.3× 93 0.9× 51 0.7× 8 329
Rebeca Caze United States 6 274 1.4× 228 1.7× 96 0.8× 59 0.6× 253 3.4× 9 464
Hasida Orenstein Israel 13 314 1.7× 149 1.1× 201 1.6× 78 0.8× 49 0.7× 22 474
Kadri Haller‐Kikkatalo Estonia 16 228 1.2× 155 1.1× 192 1.6× 92 0.9× 298 4.0× 22 648

Countries citing papers authored by Nina Pereza

Since Specialization
Citations

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

Fields of papers citing papers by Nina Pereza

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nina Pereza

This figure shows the co-authorship network connecting the top 25 collaborators of Nina Pereza. A scholar is included among the top collaborators of Nina Pereza 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 Nina Pereza. Nina Pereza 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
1.
2.
Pereza, Nina, et al.. (2024). Epigenetics of oogenesis. Archives of Gynecology and Obstetrics. 311(2). 183–190. 2 indexed citations
3.
Stanković, Aleksandra, et al.. (2024). MTHFR Gene Polymorphisms and DNA Methylation in Idiopathic Spontaneous Preterm Birth. Medicina. 60(12). 2028–2028. 2 indexed citations
4.
5.
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
6.
Mavrinac, Martina, et al.. (2023). Non-genetic physicians’ knowledge, attitudes and behavior towards medical genetics. Wiener klinische Wochenschrift. 136(5-6). 137–145. 4 indexed citations
7.
Pereza, Nina, Rifet Terzić, Dijana Plaseska‐Karanfilska, et al.. (2022). Current State of Compulsory Basic and Clinical Courses in Genetics for Medical Students at Medical Faculties in Balkan Countries With Slavic Languages. Frontiers in Genetics. 12. 793834–793834. 2 indexed citations
8.
9.
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
10.
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
11.
12.
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
13.
Pereza, Nina, Alena Buretić‐Tomljanović, Marija Volk, et al.. (2013). Y chromosome azoospermia factor region microdeletions are not associated with idiopathic recurrent spontaneous abortion in a Slovenian population: association study and literature review. Fertility and Sterility. 99(6). 1663–1667. 9 indexed citations
14.
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
15.
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
16.
Pereza, Nina, Saša Ostojić, Marija Volk, et al.. (2011). The insulin-like growth factor 2 receptor gene Gly1619Arg polymorphism and idiopathic recurrent spontaneous abortion. The Journal of Maternal-Fetal & Neonatal Medicine. 25(4). 429–431. 4 indexed citations
17.
18.
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
19.
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.
20.
Ostojić, Saša, Nina Pereza, Marija Volk, Miljenko Kapović, & Borut Peterlin. (2008). ORIGINAL ARTICLE: Genetic Predisposition to Idiopathic Recurrent Spontaneous Abortion: Contribution of Genetic Variations in IGF‐2 and H19 Imprinted Genes. American Journal of Reproductive Immunology. 60(2). 111–117. 21 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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