Aylin Köseler

684 total citations
42 papers, 499 citations indexed

About

Aylin Köseler is a scholar working on Genetics, Hematology and Molecular Biology. According to data from OpenAlex, Aylin Köseler has authored 42 papers receiving a total of 499 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 11 papers in Hematology and 10 papers in Molecular Biology. Recurrent topics in Aylin Köseler's work include Hemoglobinopathies and Related Disorders (13 papers), Iron Metabolism and Disorders (11 papers) and COVID-19 Clinical Research Studies (5 papers). Aylin Köseler is often cited by papers focused on Hemoglobinopathies and Related Disorders (13 papers), Iron Metabolism and Disorders (11 papers) and COVID-19 Clinical Research Studies (5 papers). Aylin Köseler collaborates with scholars based in Türkiye, United Kingdom and United States. Aylin Köseler's co-authors include Ramazan Sabırlı, Özgür Kurt, İbrahim Türkçüer, Anzel Bahadır, Jun Yokota, M. Helena Vasconcelos, Andreia Palmeira, Gülseren Bağcı, Arzu Yaren and Madalena Pinto and has published in prestigious journals such as SHILAP Revista de lepidopterología, Life Sciences and Journal of Experimental Marine Biology and Ecology.

In The Last Decade

Aylin Köseler

38 papers receiving 487 citations

Peers

Aylin Köseler

GENET

NEURO

HEMAT

Hubert Martin Germany

Tusar Giri United States

L. М. Samokhodskaya Russia

Takuji Miyoshi Japan

Branka Zukić Serbia

Jonathan M. Keller United States

Fayhan Alroqi Saudi Arabia

Tsutomu Kodera Japan

Raquel Lorenzetti Germany

R Streuli Switzerland

Hubert Martin Germany

Aylin Köseler

168 ×1.0

163 ×1.4

93 ×1.0

GENET

115 ×1.6

NEURO

6 ×0.1

HEMAT

Citations per year, relative to Aylin Köseler Aylin Köseler (= 1×) peers Hubert Martin

Countries citing papers authored by Aylin Köseler

Since Specialization

Citations

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

Fields of papers citing papers by Aylin Köseler

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Aylin Köseler

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

Morselli, Marco, Colin Farrell, Dennis Montoya, et al.. (2022). DNA methylation profiles in pneumonia patients reflect changes in cell types and pneumonia severity. Epigenetics. 17(12). 1646–1660. 9 indexed citations

Yılmaz, Atakan, Ramazan Sabırlı, Mert Özen, et al.. (2022). The Correlation Between Peroxisome Proliferator-Activated Receptor Alpha and Gamma Polymorphisms and Acute Coronary Syndrome. Cureus. 14(6). e26147–e26147.

Yılmaz, Atakan, Ramazan Sabırlı, Murat Seyit, et al.. (2022). Investigation of Serum Angiotensin-Converting Enzyme (ACE) Concentration and ACE Gene Polymorphism in Patients With SARS-CoV-2 Pneumonia Admitted to the Emergency Department. Cureus. 14(11). e31201–e31201. 3 indexed citations

Sabırlı, Ramazan, et al.. (2021). Soluble P-selectin as a potential diagnostic and prognostic biomarker for COVID-19 disease: A case-control study. Life Sciences. 277. 119634–119634. 27 indexed citations

Palmeira, Andreia, Emı́lia Sousa, Aylin Köseler, et al.. (2020). Preliminary Virtual Screening Studies to Identify GRP78 Inhibitors Which May Interfere with SARS-CoV-2 Infection. Pharmaceuticals. 13(6). 132–132. 48 indexed citations

Köseler, Aylin, et al.. (2020). Molecular and Biochemical Parameters Related to Plasma Mannose Levels in Coronary Artery Disease Among Nondiabetic Patients. Genetic Testing and Molecular Biomarkers. 24(9). 562–568. 3 indexed citations

Köseler, Aylin, et al.. (2019). Genome-wide DNA Methylation Profiling of Blood from Monozygotic Twins Discordant for Myocardial Infarction. In Vivo. 34(1). 361–367. 12 indexed citations

Köseler, Aylin, et al.. (2013). An ancient anatomic variation: bilateral elongated styloid process of cranium. Italian Journal of Anatomy and Embryology. 118(2). 184–188. 5 indexed citations

Köseler, Aylin, et al.. (2012). Association of a Genetic Polymorphism of the Alcohol-Metabolizing Enzyme ADH1C with Alcohol Dependence: Results of a Case-Control Study. European Addiction Research. 18(4). 161–166. 5 indexed citations

10.

Köseler, Aylin, et al.. (2012). HbA2-Yokoshima (delta 25(B7)Gly >Asp) and Hb A2-Yialousa (delta 27(B9)Ala>Ser) in Turkey. SHILAP Revista de lepidopterología. 29(3). 289–290. 2 indexed citations

11.

Köseler, Aylin, et al.. (2012). Molecular Studies on the Origin of the Hb G-Coushatta Mutation in Denizli Province of Turkey. Biochemical Genetics. 51(1-2). 71–75. 1 indexed citations

12.

Köseler, Aylin, et al.. (2010). Frequencies of ADH1C alleles and genotypes in a Turkish head andneck cancer population. Methods and Findings in Experimental and Clinical Pharmacology. 32(3). 187–187. 6 indexed citations

13.

Köseler, Aylin, et al.. (2010). First observation of Hb Tunis [beta124(H2)Pro>Ser] in Turkey. Turkish Journal of Hematology. 27(2). 120–122. 5 indexed citations

14.

Köseler, Aylin, et al.. (2010). Screening for G71R mutation of the UDP-glucuronosyltransferase 1 (UGT1A1) gene in neonates with pathologic and prolonged hyperbilirubinemia in Turkey. International Journal of Clinical Pharmacology and Therapeutics. 48(8). 504–508. 9 indexed citations

15.

Köseler, Aylin, et al.. (2009). Allele Frequency of VNTR Locus D1S80 Observed in Denizli Province of Turkey. Biochemical Genetics. 47(7-8). 540–546. 4 indexed citations

16.

Köseler, Aylin, et al.. (2008). Rare Hemoglobin Variant Hb Yaizu Observed in Turkey. Medical Principles and Practice. 17(4). 321–324. 10 indexed citations

17.

Köseler, Aylin, Yeşim Özarda İlçöl, & İsmail H. Ulus. (2007). Frequency of Mutated Allele CYP2D6*4 in the Turkish Population. Pharmacology. 79(4). 203–206. 13 indexed citations

18.

Köseler, Aylin, et al.. (2007). Hb Beograd [β121(GH4)Glu→Val, GAA→GTA] in the Turkish Population. Hemoglobin. 31(4). 491–493. 3 indexed citations

19.

Köseler, Aylin, et al.. (2007). Genetic Origin of Hb D-Los Angeles [β121(GH4)Glu→Gln,GAA→CAA] According to the β-Globin Gene Cluster Haplotypes. Hemoglobin. 31(3). 387–391. 18 indexed citations

20.

Bahadır, Anzel, et al.. (2005). High Incidence of Hb D-Los Angeles [β121(GH4)Glu→Gln] in Denizli Province, Aegean Region of Turkey. Hemoglobin. 29(4). 307–310. 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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