Hasibe Verdi

616 total citations
46 papers, 484 citations indexed

About

Hasibe Verdi is a scholar working on Epidemiology, Cardiology and Cardiovascular Medicine and Hematology. According to data from OpenAlex, Hasibe Verdi has authored 46 papers receiving a total of 484 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Epidemiology, 9 papers in Cardiology and Cardiovascular Medicine and 9 papers in Hematology. Recurrent topics in Hasibe Verdi's work include Blood Coagulation and Thrombosis Mechanisms (7 papers), Renin-Angiotensin System Studies (5 papers) and Liver Disease Diagnosis and Treatment (4 papers). Hasibe Verdi is often cited by papers focused on Blood Coagulation and Thrombosis Mechanisms (7 papers), Renin-Angiotensin System Studies (5 papers) and Liver Disease Diagnosis and Treatment (4 papers). Hasibe Verdi collaborates with scholars based in Türkiye, United States and Tunisia. Hasibe Verdi's co-authors include Fatma Belgin Ataç, Namık Yaşar Özbek, Füsun Öner Eyüboğlu, Mehmet Haberal, Siren Sezer, Fatma Nurhan Özdemir, Ayşe Canan Yazıcı, Z. Arat, Remzi Erdem and Eli̇f Küpeli̇ and has published in prestigious journals such as SHILAP Revista de lepidopterología, Journal of Hepatology and Transplantation.

In The Last Decade

Hasibe Verdi

46 papers receiving 464 citations

Peers

Hasibe Verdi
Hasibe Verdi
Citations per year, relative to Hasibe Verdi Hasibe Verdi (= 1×) peers Hidetaka Ushigome

Countries citing papers authored by Hasibe Verdi

Since Specialization
Citations

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

Fields of papers citing papers by Hasibe Verdi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hasibe Verdi

This figure shows the co-authorship network connecting the top 25 collaborators of Hasibe Verdi. A scholar is included among the top collaborators of Hasibe Verdi 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 Hasibe Verdi. Hasibe Verdi 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.
Verdi, Hasibe, et al.. (2024). In vitro cellular uptake and insulin secretion studies on INS-1E cells of exendin-4-loaded self-nanoemulsifying drug delivery systems. Pharmaceutical Development and Technology. 29(10). 1101–1110. 1 indexed citations
2.
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Tütüncü, Neslihan Başçıl, et al.. (2022). Beta-Cell Golgi Stress Response to Lipotoxicity and Glucolipotoxicity: A Preliminary Study of a Potential Mechanism of Beta-Cell Failure in Posttransplant Diabetes and Intraportal Islet Transplant. Experimental and Clinical Transplantation. 20(6). 585–594. 5 indexed citations
4.
Verdi, Hasibe, et al.. (2021). Lack of association between MMP13 (rs3819089), ADAM12 (rs3740199-rs1871054) and ADAMTS14 (rs4747096) genotypes and advanced-stage knee osteoarthritis. Joint Diseases and Related Surgery. 32(2). 299–305. 6 indexed citations
5.
Verdi, Hasibe, et al.. (2020). Uncoupling protein gene UCP1-3826A/G, UCP2 Ins/Del and UCP3-55C/T polymorphisms in obese Turkish children. The Turkish Journal of Pediatrics. 62(6). 921–929. 1 indexed citations
6.
Verdi, Hasibe, et al.. (2015). β-3AR W64R Polymorphism and 30-Minute Post-Challenge Plasma Glucose Levels in Obese Children. Journal of Clinical Research in Pediatric Endocrinology. 7(1). 7–12. 5 indexed citations
7.
Zidi, Sabrina, Hasibe Verdi, Ayşe Canan Yazıcı, et al.. (2014). Involvement of Toll-like receptors in cervical cancer susceptibility among Tunisian women. Bulletin du Cancer. 101(10). E31–E35. 15 indexed citations
8.
Yılmaz, Ünsal, et al.. (2012). Atypical phenotypes of DYT1 dystonia in three children. Brain and Development. 35(4). 356–359. 4 indexed citations
9.
Verdi, Hasibe, Ayşe Canan Yazıcı, Ayşe Ecevit, et al.. (2011). Maternal–Fetal Proinflammatory Cytokine Gene Polymorphism and Preterm Birth. DNA and Cell Biology. 31(1). 92–97. 33 indexed citations
10.
Can, Ufuk, Hasibe Verdi, Fatma Belgin Ataç, et al.. (2010). The Frequency of Factor V Leiden, Prothrombin G20210A and Methylenetetrahydrofolate Reductase C677T Mutations in Migraine Patients. SHILAP Revista de lepidopterología. 1 indexed citations
11.
Ataç, Fatma Belgin, Deniz Anuk İnce, Hasibe Verdi, et al.. (2009). Lack of Association Between FXIII -Val34Leu, FVII -323 del/ins, and Transforming Growth Factor β1 (915G/T) Gene Polymorphisms and Bronchopulmonary Dysplasia: A Single-Center Study. DNA and Cell Biology. 29(1). 13–18. 7 indexed citations
12.
Yazıcı, Ayşe Canan, et al.. (2008). PAI-1 gene 4G/5G polymorphism, cytokine levels and their relations with metabolic parameters in obese children. Thrombosis and Haemostasis. 99(2). 352–356. 24 indexed citations
13.
Serin, Ender, Fatma Belgin Ataç, Hasibe Verdi, et al.. (2007). Methylenetetrahydrofolate Reductase C677T Mutation and Nonalcoholic Fatty Liver Disease. Digestive Diseases and Sciences. 52(5). 1183–1186. 16 indexed citations
14.
Peşkircioğlu, Levent, Fatma Belgin Ataç, Remzi Erdem, et al.. (2006). The association between intron 4 VNTR, E298A and IVF 23+10 G/T polymorphisms of ecNOS gene and sildenafil responsiveness in patients with erectile dysfunction. International Journal of Impotence Research. 19(2). 149–153. 29 indexed citations
15.
Yılmaz, İsmail, Fatma Belgin Ataç, Alper Nabi Erkan, et al.. (2006). No difference in polymorphism frequency in a Turkish population with allergic rhinitis. Acta Oto-Laryngologica. 126(10). 1110–1111. 2 indexed citations
16.
Özdemir, Fatma Nurhan, Siren Sezer, Fatma Belgin Ataç, et al.. (2005). Vitamin D Receptor BsmI and TagI Gene Polymorphisms in a Turkish ESRD Population: Influences on Parathyroid Hormone Response. Transplantation Proceedings. 37(7). 2922–2924. 9 indexed citations
17.
Özbek, Namık Yaşar, et al.. (2005). Analysis of prothrombotic mutations and polymorphisms in children who developed thrombosis in the perioperative period of congenital cardiac surgery. Cardiology in the Young. 15(1). 19–25. 16 indexed citations
18.
Özdemir, Fatma Nurhan, Hasan Mıcozkadıoğlu, Fatma Belgin Ataç, et al.. (2004). The renin-angiotensin system and endothelial nitric oxide synthase gene polymorphisms and cyclosporine toxicity in renal transplant patients. Transplantation Proceedings. 36(1). 128–130. 2 indexed citations
19.
Özbek, Namık Yaşar, Fatma Belgin Ataç, Hasibe Verdi, & Sinan Mahir Kayıran. (2003). Purpura fulminans in a child with combined heterozygous prothrombin G20210A and factor V Leiden mutations. Annals of Hematology. 82(2). 118–120. 25 indexed citations
20.
Bozdayı, Mithat, Hakan Bozkaya, A.R. Türkyilmaz, et al.. (1999). Polymorphism of Precore Region of Hepatitis B Virus DNA among Patients with Chronic HBV Infection in Turkey. Infection. 27(6). 357–360. 24 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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