Mahmut Akyol

1.0k total citations
11 papers, 332 citations indexed

About

Mahmut Akyol is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Endocrine and Autonomic Systems. According to data from OpenAlex, Mahmut Akyol has authored 11 papers receiving a total of 332 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 3 papers in Cardiology and Cardiovascular Medicine and 2 papers in Endocrine and Autonomic Systems. Recurrent topics in Mahmut Akyol's work include Ion channel regulation and function (3 papers), Cardiac electrophysiology and arrhythmias (3 papers) and Cardiac Arrhythmias and Treatments (2 papers). Mahmut Akyol is often cited by papers focused on Ion channel regulation and function (3 papers), Cardiac electrophysiology and arrhythmias (3 papers) and Cardiac Arrhythmias and Treatments (2 papers). Mahmut Akyol collaborates with scholars based in Türkiye, Germany and United States. Mahmut Akyol's co-authors include Thomas Meitinger, Arne Pfeufer, Siegfried Perz, Martha Merrow, Irene Pichler, Bertram Müller-Myhsok, Michael Näbauer, Stefan Kääb, Martin Hinterseer and Thomas Illig and has published in prestigious journals such as SHILAP Revista de lepidopterología, Circulation Research and Biological Psychiatry.

In The Last Decade

Mahmut Akyol

10 papers receiving 325 citations

Peers

Mahmut Akyol

CCM

EAS

ECP

Shai Marcu United States

Naoki Kubota Japan

Antoine Weihs Germany

Thomas G. Brooks United States

Jeff Zhang United States

Daniel E. Roach Canada

Weiyun Qian China

Juan Shu United States

Ray Masuda Japan

Liisa Tomppo Finland

Shai Marcu United States

Mahmut Akyol

30 ×0.2

CCM

34 ×0.2

41 ×0.5

EAS

24 ×0.3

ECP

11 ×0.2

Citations per year, relative to Mahmut Akyol Mahmut Akyol (= 1×) peers Shai Marcu

Countries citing papers authored by Mahmut Akyol

Since Specialization

Citations

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

Fields of papers citing papers by Mahmut Akyol

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mahmut Akyol

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

All Works

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11 of 11 papers shown

Balkarlı, Ayşe, et al.. (2016). MEFV gene variation R202Q is associated with metabolic syndrome.. PubMed. 20(15). 3255–61. 2 indexed citations

Akyol, Mahmut, Muhammet Kazım Erol, Özdemir Özdemir, et al.. (2015). A novel mutation of sgk-1 gene in central serous chorioretinopathy.. SHILAP Revista de lepidopterología. 8(1). 23–8. 9 indexed citations

Akyol, Mahmut, et al.. (2013). Investigation of the serum glucocorticoid kinase 1 gene in patients with transient tachypnea of the newborn. The Journal of Maternal-Fetal & Neonatal Medicine. 26(10). 990–994. 3 indexed citations

Akyol, Mahmut, et al.. (2013). Evaluation of gene SCNN1A responsible for the synthesis of alpha subunit of epithelial sodium channel in transient tachypnea of newborn. Türk Pediatri Arşivi. 48(1). 35–39. 2 indexed citations

Bilgin, Ahmet Burak, Mustafa Ünal, Mahmut Akyol, et al.. (2012). Keratoconus presenting with bilateral simultaneous acute corneal hydrops. Contact Lens and Anterior Eye. 36(2). 98–100. 2 indexed citations

Allebrandt, Karla V., Maris Teder‐Laving, Mahmut Akyol, et al.. (2010). CLOCK Gene Variants Associate with Sleep Duration in Two Independent Populations. Biological Psychiatry. 67(11). 1040–1047. 110 indexed citations

Sinner, Moritz F., Arne Pfeufer, Mahmut Akyol, et al.. (2008). The non-synonymous coding IKr-channel variant KCNH2-K897T is associated with atrial fibrillation: results from a systematic candidate gene-based analysis of KCNH2 (HERG). European Heart Journal. 29(7). 907–914. 73 indexed citations

Akyol, Mahmut, Shapour Jalilzadeh, Moritz F. Sinner, et al.. (2007). The common non-synonymous variant G38S of the KCNE1-(minK)-gene is not associated to QT interval in Central European Caucasians: results from the KORA study. European Heart Journal. 28(3). 305–309. 23 indexed citations

Kääb, Stefan, Arne Pfeufer, Mahmut Akyol, et al.. (2007). Association mapping of QT interval in a 500k genome-wide scan: confirmation of NOS1AP and identification of a spectrum of additional QTLS. Journal of Electrocardiology. 40(4). S2–S2. 1 indexed citations

10.

Pfeufer, Arne, Dan E. Arking, Siegfried Perz, et al.. (2006). CAPON is a Novel QT-Interval Modifier Gene with Gender Dependent Effect Identified through Genomewide Association Analysis in Individuals from the General Population. Journal of Electrocardiology. 40(1). S75–S75. 1 indexed citations

11.

Pfeufer, Arne, Shapour Jalilzadeh, Siegfried Perz, et al.. (2005). Common Variants in Myocardial Ion Channel Genes Modify the QT Interval in the General Population. Circulation Research. 96(6). 693–701. 106 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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