Ergün Pınarbaşı

508 total citations
25 papers, 352 citations indexed

About

Ergün Pınarbaşı is a scholar working on Molecular Biology, Obstetrics and Gynecology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Ergün Pınarbaşı has authored 25 papers receiving a total of 352 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 8 papers in Obstetrics and Gynecology and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Ergün Pınarbaşı's work include Pregnancy and preeclampsia studies (8 papers), Birth, Development, and Health (5 papers) and Glutathione Transferases and Polymorphisms (3 papers). Ergün Pınarbaşı is often cited by papers focused on Pregnancy and preeclampsia studies (8 papers), Birth, Development, and Health (5 papers) and Glutathione Transferases and Polymorphisms (3 papers). Ergün Pınarbaşı collaborates with scholars based in Türkiye, United Kingdom and Yemen. Ergün Pınarbaşı's co-authors include D. Hornby, John F. Elliott, Filiz Özen, Yavuz Siliğ, Ertan Mahir Korkmaz, Ali Çetin, Meral Çetin, E. Ferda Perçin, Emine Gulsen Gunes and Asli Oztan and has published in prestigious journals such as Journal of Molecular Biology, Journal of Bacteriology and Gene.

In The Last Decade

Ergün Pınarbaşı

25 papers receiving 341 citations

Peers

Ergün Pınarbaşı

IMMUN

PPCH

Fuyan Sun Japan

Milad Khorasani Iran

Lkhagvasuren Munkhtulga Japan

Xiaohua Huang China

Mohamed Abou El Hassan Canada

Danial Jahantigh Iran

Marianne Rodrigues Fernandes Brazil

Nichole Peterson Canada

Yujuan Qi China

Ulrike Lisewski Germany

Fuyan Sun Japan

Ergün Pınarbaşı

204 ×1.0

110 ×1.5

IMMUN

28 ×0.5

36 ×0.7

PPCH

47 ×1.2

Citations per year, relative to Ergün Pınarbaşı Ergün Pınarbaşı (= 1×) peers Fuyan Sun

Countries citing papers authored by Ergün Pınarbaşı

Since Specialization

Citations

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

Fields of papers citing papers by Ergün Pınarbaşı

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ergün Pınarbaşı

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

Pınarbaşı, Ergün, et al.. (2024). Impact of IL-6 rs1800795 and rs1800796 polymorphisms on clinical outcomes of COVID-19: a study on severity of disease in Turkish population. Mammalian Genome. 36(1). 213–229. 1 indexed citations

Pınarbaşı, Ergün, et al.. (2023). Relationship between STOX1 gene variations and preeclampsia in Turkish population. Human Gene. 37. 201193–201193. 2 indexed citations

Doğan, Halef Okan, et al.. (2023). Dysregulated Leukotriene Metabolism in Patients with COVID-19. Japanese Journal of Infectious Diseases. 77(3). 129–136. 1 indexed citations

Pınarbaşı, Ergün, et al.. (2020). STOX1 gene Y153H polymorphism is associated with early-onset preeclampsia in Turkish population. Gene. 754. 144894–144894. 12 indexed citations

Korkmaz, Ertan Mahir, et al.. (2020). Computationally predicted SARS-COV-2 encoded microRNAs target NFKB, JAK/STAT and TGFB signaling pathways. Gene Reports. 22. 101012–101012. 63 indexed citations

Pınarbaşı, Ergün, et al.. (2019). The role of two common FOXP3 gene promoter polymorphisms in preeclampsia in a Turkish population: a case–control study. Journal of Obstetrics and Gynaecology. 40(4). 495–499. 7 indexed citations

Pınarbaşı, Ergün, et al.. (2018). FOXP3 rs3761548 polymorphism is associated with knee osteoarthritis in a Turkish population. International Journal of Rheumatic Diseases. 21(10). 1779–1786. 7 indexed citations

Pınarbaşı, Ergün, et al.. (2017). MEFV mutations and their relation to major clinical symptoms of Familial Mediterranean Fever. Gene. 626. 9–13. 49 indexed citations

Sarı, İsmail, et al.. (2017). Association between the soluble epoxide hydrolase gene and preeclampsia. Hypertension in Pregnancy. 36(4). 315–325. 9 indexed citations

10.

Balaban, Hatice, et al.. (2012). A Novel Locus for Restless Legs Syndrome on Chromosome 13q. European Neurology. 68(2). 111–116. 9 indexed citations

11.

Bayraklı, Fatih, et al.. (2012). Intracranial arachnoid cyst family with autosomal recessive trait mapped to chromosome 6q22.31-23.2. Acta Neurochirurgica. 154(7). 1287–1292. 13 indexed citations

12.

Pınarbaşı, Ergün, et al.. (2010). AXIN2 polymorphism and its association with prostate cancer in a Turkish population. Medical Oncology. 28(4). 1373–1378. 22 indexed citations

13.

Pınarbaşı, Ergün, et al.. (2007). Association of microsomal epoxide hydrolase gene polymorphism and pre‐eclampsia in Turkish women. Journal of obstetrics and gynaecology research. 33(1). 32–37. 17 indexed citations

14.

Çetin, Meral, et al.. (2005). No association of polymorphisms in the glutathione S‐transferase genes with pre‐eclampsia, eclampsia and HELLP syndrome in a Turkish population. Journal of obstetrics and gynaecology research. 31(3). 236–241. 12 indexed citations

15.

Perçin, E. Ferda, et al.. (2005). Lack of association between the CYP11B2 gene polymorphism and preeclampsia, eclampsia, and the HELLP syndrome in Turkish women. European Journal of Obstetrics & Gynecology and Reproductive Biology. 127(2). 213–217. 8 indexed citations

16.

Siliğ, Yavuz, et al.. (2003). Strong association between the GSTM1-null genotype and lung cancer in a Turkish population. Cancer Genetics and Cytogenetics. 146(2). 125–129. 32 indexed citations

17.

Pınarbaşı, Ergün, et al.. (2002). Recombinant α and β Subunits of M.AquI Constitute an Active DNA Methyltransferase. BMB Reports. 35(3). 348–351. 4 indexed citations

18.

Oztan, Asli, et al.. (2002). Molecular Characterization of a Full Genome Turkish Hepatitis C Virus 1b Isolate (HCV-TR1): A Predominant Viral Form in Turkey. Virus Genes. 25(2). 169–177. 18 indexed citations

19.

Eroğlu, Çağla & Ergün Pınarbaşı. (2000). Hepatitis C virus: genome organization, viral proteins and implications in disease pathogenesis.. TURKISH JOURNAL OF BIOLOGY. 24(2). 253–270. 2 indexed citations

20.

Pınarbaşı, Ergün, John F. Elliott, & D. Hornby. (1996). Activation of a Yeast Pseudo DNA Methyltransferase by Deletion of a Single Amino Acid. Journal of Molecular Biology. 257(4). 804–813. 56 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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