Feodora Stipoljev

484 total citations
33 papers, 244 citations indexed

About

Feodora Stipoljev is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, Feodora Stipoljev has authored 33 papers receiving a total of 244 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Pediatrics, Perinatology and Child Health, 16 papers in Genetics and 11 papers in Molecular Biology. Recurrent topics in Feodora Stipoljev's work include Prenatal Screening and Diagnostics (18 papers), Genomic variations and chromosomal abnormalities (9 papers) and Sexual Differentiation and Disorders (4 papers). Feodora Stipoljev is often cited by papers focused on Prenatal Screening and Diagnostics (18 papers), Genomic variations and chromosomal abnormalities (9 papers) and Sexual Differentiation and Disorders (4 papers). Feodora Stipoljev collaborates with scholars based in Croatia, Kosovo and Spain. Feodora Stipoljev's co-authors include A Kurjak, Berivoj Mišković, Tomislav Hafner, V Latin, Marina Kos, Milan Stanojević, Davor Ježek, Milan Kos, Tomislav Strinić and Damir Roje and has published in prestigious journals such as SHILAP Revista de lepidopterología, Human Reproduction and Reproductive Toxicology.

In The Last Decade

Feodora Stipoljev

29 papers receiving 218 citations

Peers

Feodora Stipoljev

PPCH

GENET

PHEOH

SURGE

Shilpa Chetty United States

Claudine Le Vaillant France

K.-Ph. Gloning Germany

M Nonomura Japan

Alicia Cervantes Mexico

Paula C. Cosper United States

Eita Mizutani Japan

Maria Carla Pittalis Italy

Molka Kammoun Tunisia

Shilpa Chetty United States

Feodora Stipoljev

177 ×1.4

PPCH

61 ×0.6

GENET

25 ×0.5

PHEOH

30 ×0.6

30 ×0.7

SURGE

Citations per year, relative to Feodora Stipoljev Feodora Stipoljev (= 1×) peers Shilpa Chetty

Countries citing papers authored by Feodora Stipoljev

Since Specialization

Citations

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

Fields of papers citing papers by Feodora Stipoljev

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Feodora Stipoljev

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

Stipoljev, Feodora, et al.. (2022). Susceptibility to chromosome instability and occurrence of the regular form of Down syndrome in young couples. Mutation Research/Genetic Toxicology and Environmental Mutagenesis. 881. 503511–503511. 1 indexed citations

Martić, Tamara Nikuševa, et al.. (2020). The Frequency of Follicle-Stimulating Hormone Receptor 2039A>G Gene Polymorphism and the Risk of Male Infertility in Albanian Population. SHILAP Revista de lepidopterología. 2 indexed citations

Stipoljev, Feodora, et al.. (2017). Prenatal diagnosis of complex phenotype in a 13-week-old fetus with an interstitial multigene deletion 20q13.13.-q13.2 by chromosomal microarray. European Journal of Medical Genetics. 60(11). 589–594. 2 indexed citations

Hafner, Tomislav, et al.. (2017). Prenatal diagnosis of Down syndrome: A 13-year retrospective study. Taiwanese Journal of Obstetrics and Gynecology. 56(6). 731–735. 12 indexed citations

Stipoljev, Feodora. (2016). Chorionic villus biopsy.

Hafner, Tomislav, et al.. (2014). Prenatal diagnosis of 18p deletion and isochromosome 18q mosaicism in a fetus with a cystic hygroma.. PubMed. 38(3). 1059–62. 1 indexed citations

Škrlec, Ivana, Jasenka Wagner, Silvija Pušeljić, Marija Heffer, & Feodora Stipoljev. (2014). De novo case of a partial trisomy 4p and a partial monosomy 8p.. PubMed. 38(1). 319–23. 7 indexed citations

Hafner, Tomislav, et al.. (2014). Prenatal diagnosis of sex chromosome aneuploidies and disorders of sex development – a retrospective analysis of 11-year data. Journal of Perinatal Medicine. 42(4). 529–534. 10 indexed citations

Ramadža, Danijela Petković, Feodora Stipoljev, Vladimir Sarnavka, et al.. (2009). Hypophosphatasia: phenotypic variability and possible Croatian origin of the c.1402g>A mutation of TNSALP gene.. PubMed. 33(4). 1255–8. 4 indexed citations

10.

Wagner, Jasenka, Feodora Stipoljev, Ivana Škrlec, et al.. (2009). Partial monosomy 4q and partial trisomy 13q: phenotype and molecular mapping of the breakpoints. Chromosome Research. 1 indexed citations

11.

Roje, Damir, et al.. (2008). Trisomy 1 in an early pregnancy failure. American Journal of Medical Genetics Part A. 146A(18). 2439–2441. 25 indexed citations

12.

Pavlinić, Dinko, et al.. (2008). Quantitative Fluorescent PCR – A Rapid Approach to Prenatal Diagnostics of Common Autosomal Aneuploidies. University of Zagreb University Computing Centre (SRCE). 81(1). 219–222. 2 indexed citations

13.

Juraški, Romana Gjergja, et al.. (2005). Knowledge and use of folic acid in Croatian pregnant women—a need for health care education initiative. Reproductive Toxicology. 21(1). 16–20. 17 indexed citations

14.

Stipoljev, Feodora, et al.. (2005). Pericentric inversion of chromosome 2 in a patient with the empty follicle syndrome: Case report. Human Reproduction. 20(9). 2552–2555. 28 indexed citations

15.

Stipoljev, Feodora, et al.. (2005). Cytogenetic analysis of azoospermic patients: karyotype comparison of peripheral blood lymphocytes and testicular tissue. European Journal of Obstetrics & Gynecology and Reproductive Biology. 124(2). 197–203. 2 indexed citations

16.

Stipoljev, Feodora, et al.. (2003). Antenatal detection of mosaic trisomy 9 by ultrasound: a case report and literature review. The Journal of Maternal-Fetal & Neonatal Medicine. 14(1). 65–69. 10 indexed citations

17.

Stanojević, Milan, et al.. (2001). Oculo-auriculo-vertebral (Goldenhar) spectrum associated with pericentric inversion 9: coincidental findings or etiologic factor?. PubMed. 20(3). 150–4. 29 indexed citations

18.

Stipoljev, Feodora, V Latin, Marina Kos, Berivoj Mišković, & A Kurjak. (2000). Correlation of Confined Placental Mosaicism with Fetal Intrauterine Growth Retardation. Fetal Diagnosis and Therapy. 16(1). 4–9. 30 indexed citations

19.

Kurjak, Asim, Milan Kos, Feodora Stipoljev, et al.. (1999). Ultrasonic markers of fetal chromosomal abnormalities. European Journal of Obstetrics & Gynecology and Reproductive Biology. 85(1). 105–108. 9 indexed citations

20.

Stipoljev, Feodora, et al.. (1999). Incidence of chromosomopathies and cystic fibrosis mutations in second trimester fetuses with isolated hyperechoic bowel. The Journal of Maternal-Fetal Medicine. 8(2). 44–47. 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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