Arda Çetinkaya

494 total citations
15 papers, 202 citations indexed

About

Arda Çetinkaya is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Arda Çetinkaya has authored 15 papers receiving a total of 202 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Surgery. Recurrent topics in Arda Çetinkaya's work include Attention Deficit Hyperactivity Disorder (2 papers), Connective tissue disorders research (2 papers) and Folate and B Vitamins Research (2 papers). Arda Çetinkaya is often cited by papers focused on Attention Deficit Hyperactivity Disorder (2 papers), Connective tissue disorders research (2 papers) and Folate and B Vitamins Research (2 papers). Arda Çetinkaya collaborates with scholars based in Türkiye, Netherlands and Canada. Arda Çetinkaya's co-authors include Mehmet Alikaşifoğlu, Gülen Eda Ütine, Koray Boduroğlu, Ali̇ Karaman, Pelin Özlem Şimşek‐Kiper, Hatip Aydın, Bilge Volkan Salancı, Göknur Haliloğlu, Ekim Z. Taşkıran and Dilek Aktaş and has published in prestigious journals such as Journal of Cellular Biochemistry, European Journal of Human Genetics and Mutation Research/Genetic Toxicology and Environmental Mutagenesis.

In The Last Decade

Arda Çetinkaya

11 papers receiving 200 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Arda Çetinkaya Türkiye 8 110 48 38 21 20 15 202
Yuval Yogev Israel 9 138 1.3× 51 1.1× 19 0.5× 15 0.7× 23 1.1× 28 243
Ohad Wormser Israel 11 173 1.6× 65 1.4× 20 0.5× 15 0.7× 23 1.1× 28 275
Wen Gu China 9 144 1.3× 33 0.7× 38 1.0× 31 1.5× 17 0.8× 16 330
Heiko Brennenstuhl Germany 11 180 1.6× 74 1.5× 47 1.2× 25 1.2× 16 0.8× 25 315
Yngve Sejersted Norway 9 203 1.8× 42 0.9× 35 0.9× 13 0.6× 34 1.7× 16 381
Hideaki Ohtsubo Japan 10 192 1.7× 20 0.4× 41 1.1× 18 0.9× 36 1.8× 14 305
Maki Asada Japan 8 87 0.8× 31 0.6× 10 0.3× 21 1.0× 36 1.8× 15 214
Mayuko Ishikawa Japan 10 124 1.1× 45 0.9× 43 1.1× 32 1.5× 96 4.8× 22 352
Arthur Sorlin France 8 115 1.0× 86 1.8× 19 0.5× 6 0.3× 11 0.6× 23 224

Countries citing papers authored by Arda Çetinkaya

Since Specialization
Citations

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

Fields of papers citing papers by Arda Çetinkaya

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Arda Çetinkaya

This figure shows the co-authorship network connecting the top 25 collaborators of Arda Çetinkaya. A scholar is included among the top collaborators of Arda Çetinkaya 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 Arda Çetinkaya. Arda Çetinkaya is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

15 of 15 papers shown
1.
Gümrük, Fatma, et al.. (2024). Alu‐Mediated Deletion of FANCA in Turkish Families With Fanconi Anemia: Evidence of a Founder Effect. American Journal of Medical Genetics Part A. 197(4). e63945–e63945.
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Bekircan‐Kurt, Can Ebru, Arda Çetinkaya, Rahşan Göçmen, et al.. (2021). One Disease with two Faces: Semidominant Inheritance of a Novel HTRA1 Mutation in a Consanguineous Family. Journal of Stroke and Cerebrovascular Diseases. 30(9). 105997–105997. 4 indexed citations
4.
Bekircan‐Kurt, Can Ebru, Sevim Erdem‐Özdamar, Arda Çetinkaya, et al.. (2020). Comprehensive clinical, biochemical, radiological and genetic analysis of 28 Turkish cases with suspected metachromatic leukodystrophy and their relatives. Molecular Genetics and Metabolism Reports. 25. 100688–100688. 6 indexed citations
5.
Ünal, Fatih, et al.. (2018). Neuropsychological correlates of ADRA2A(rs1800544) and COMT(rs4680) polymorphisms in Turkish ADHD patients. European Neuropsychopharmacology. 28. S63–S64.
6.
Çetinkaya, Arda, Ekim Z. Taşkıran, Tutku Soyer, et al.. (2017). Dermal fibroblast transcriptome indicates contribution of WNT signaling pathways in the pathogenesis of Apert syndrome. The Turkish Journal of Pediatrics. 59(6). 619–624. 9 indexed citations
7.
Çetinkaya, Arda, et al.. (2017). Novel FBN1 mutation in a family with inherited Marfan Syndrome: p.Cys2672Arg. Congenital Anomalies. 58(1). 41–43. 2 indexed citations
8.
Aydın, Hatip, et al.. (2016). Anensefalide Gebelerin Folat ve Vitamin B12 Düzeyleri ile Faktör V Leiden, Faktör II G20210A, MTHFR C667T ve MTHFR A1298C Polimorfizlerinin Önemi. DergiPark (Istanbul University). 3(3). 112–116.
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Ünal, Fatih, et al.. (2016). Genetic Variations in Attention Deficit Hyperactivity Disorder Subtypes and Treatment Resistant Cases. Psychiatry Investigation. 13(4). 427–427. 9 indexed citations
11.
KILIÇ, Esra KAYA, Arda Çetinkaya, Gülen Eda Ütine, & Koray Boduroğlu. (2016). A Diagnosis to Consider in Intellectual Disability. Journal of Child Neurology. 31(7). 913–917. 8 indexed citations
12.
Karaman, Ali̇, et al.. (2015). DNA damage is increased in lymphocytes of patients with metabolic syndrome. Mutation Research/Genetic Toxicology and Environmental Mutagenesis. 782. 30–35. 43 indexed citations
13.
Ütine, Gülen Eda, Göknur Haliloğlu, Bilge Volkan Salancı, et al.. (2014). Etiological yield of SNP microarrays in idiopathic intellectual disability. European Journal of Paediatric Neurology. 18(3). 327–337. 23 indexed citations
14.
Ütine, Gülen Eda, Göknur Haliloğlu, Bilge Volkan Salancı, et al.. (2013). A Homozygous Deletion in GRID2 Causes a Human Phenotype With Cerebellar Ataxia and Atrophy. Journal of Child Neurology. 28(7). 926–932. 55 indexed citations
15.
Taşkıran, Ekim Z., et al.. (2012). The effect of colchicine on pyrin and pyrin interacting proteins. Journal of Cellular Biochemistry. 113(11). 3536–3546. 34 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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