Mert Sozen

1.8k total citations · 1 hit paper
20 papers, 1.3k citations indexed

About

Mert Sozen is a scholar working on Genetics, Surgery and Molecular Biology. According to data from OpenAlex, Mert Sozen has authored 20 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 5 papers in Surgery and 3 papers in Molecular Biology. Recurrent topics in Mert Sozen's work include Lipoproteins and Cardiovascular Health (4 papers), Genomics and Rare Diseases (2 papers) and Genetic Associations and Epidemiology (2 papers). Mert Sozen is often cited by papers focused on Lipoproteins and Cardiovascular Health (4 papers), Genomics and Rare Diseases (2 papers) and Genetic Associations and Epidemiology (2 papers). Mert Sozen collaborates with scholars based in Türkiye, United Kingdom and United States. Mert Sozen's co-authors include Klaus Griewank, Boris C. Bastian, Michelle B. Crosby, Joan M. O’Brien, Igor Dolgalev, Raya Khanin, Gary Green, Ritu Roy, Catherine D. Van Raamsdonk and Nancy Bouvier and has published in prestigious journals such as New England Journal of Medicine, SHILAP Revista de lepidopterología and Clinical Chemistry.

In The Last Decade

Mert Sozen

19 papers receiving 1.3k citations

Hit Papers

Mutations in GNA11 in Uveal Melanoma 2010 2026 2015 2020 2010 250 500 750 1000

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mert Sozen Türkiye 9 693 687 512 270 191 20 1.3k
Marjo Hahka‐Kemppinen Finland 18 275 0.4× 545 0.8× 651 1.3× 220 0.8× 77 0.4× 33 1.1k
Audrey Rapinat France 13 170 0.2× 425 0.6× 312 0.6× 180 0.7× 47 0.2× 17 896
Ergang Shi United States 12 594 0.9× 720 1.0× 183 0.4× 123 0.5× 222 1.2× 14 1.4k
Emma Rennel United Kingdom 13 149 0.2× 669 1.0× 125 0.2× 143 0.5× 54 0.3× 14 954
Kazuto Nakae Japan 11 213 0.3× 399 0.6× 579 1.1× 363 1.3× 33 0.2× 14 1.0k
Abdullah Mahmood Ali United States 20 70 0.1× 1.5k 2.2× 244 0.5× 116 0.4× 181 0.9× 60 2.0k
Hong-Ji Xu United States 15 101 0.1× 569 0.8× 401 0.8× 89 0.3× 60 0.3× 19 966
Charles Decraene France 22 78 0.1× 645 0.9× 596 1.2× 140 0.5× 72 0.4× 40 1.4k
Yongping Crawford United States 14 56 0.1× 1.1k 1.6× 581 1.1× 157 0.6× 100 0.5× 16 1.5k
Steven Pennock United States 11 205 0.3× 534 0.8× 149 0.3× 63 0.2× 235 1.2× 16 849

Countries citing papers authored by Mert Sozen

Since Specialization
Citations

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

Fields of papers citing papers by Mert Sozen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mert Sozen

This figure shows the co-authorship network connecting the top 25 collaborators of Mert Sozen. A scholar is included among the top collaborators of Mert Sozen 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 Mert Sozen. Mert Sozen 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.
Sozen, Mert & Şükrü Kartalcı. (2023). Association of a haplotype in the NRG1 gene with schizophrenia: a case-control study. SHILAP Revista de lepidopterología. 48(3). 246–256.
2.
Sozen, Mert, Ceren Acar, & Şükrü Kartalcı. (2020). Presence of a genetic association between NRG-3 SNP rs17101193 and schizophrenia. Annals of Medical Research. 27(5). 1419–1419. 1 indexed citations
3.
Kamışlı, Özden, et al.. (2019). Lipoid proteinosis and epilepsy: Molecular analysis. Annals of Medical Research. 1–1. 1 indexed citations
4.
Sozen, Mert. (2018). Association of the Human PPARY2 PRO12ALA Polymorphism with Obesity in a Population from Turkey. Acta Endocrinologica (Bucharest). 14(4). 459–465. 2 indexed citations
5.
Kamışlı, Özden, et al.. (2018). The association between vitamin D receptor polymorphisms and multiple sclerosis in a Turkish population. Multiple Sclerosis and Related Disorders. 20. 78–81. 22 indexed citations
6.
Kamışlı, Özden, et al.. (2018). Analysis of Vitamin D Receptor Polymorphisms in Patients with Familial Multiple Sclerosis. Medical Archives. 72(1). 58–58. 14 indexed citations
7.
Çiftçi, Osman, et al.. (2018). The Novel Synthesized Pyridazinone Derivates had the Antiproliferative and Apoptotic Effects in SHSY5Y and HEP3B Cancer Cell Line. Letters in Organic Chemistry. 15(4). 323–331. 4 indexed citations
8.
Çiftçi, Osman, et al.. (2017). The novel synthesized pyridazinone derivates had the antiproliferative and apoptotic effects in SHSY5Y and HEP3B cancer cell line. Letters in Organic Chemistry. 14. 3 indexed citations
9.
Acar, Ceren, et al.. (2015). Lack of association between catechol-Omethyltransferase and schizophrenia in a Turkish population. Turkish Journal of Biochemistry. 40(3). 205–209. 3 indexed citations
11.
Sozen, Mert, et al.. (2015). Allozyme variations in Anatolian populations and cytotypes of the blind mole rats (Nannospalax). Biochemical Systematics and Ecology. 59. 126–134. 9 indexed citations
12.
Griewank, Klaus, Xiaoxing Yu, Jahan S. Khalili, et al.. (2012). Genetic and molecular characterization of uveal melanoma cell lines. Pigment Cell & Melanoma Research. 25(2). 182–187. 92 indexed citations
13.
Raamsdonk, Catherine D. Van, Klaus Griewank, Michelle B. Crosby, et al.. (2010). Mutations in GNA11 in Uveal Melanoma. New England Journal of Medicine. 363(23). 2191–2199. 1053 indexed citations breakdown →
14.
Taylor, Alison, et al.. (2007). Multiplex ARMS analysis to detect 13 common mutations in familial hypercholesterolaemia. Clinical Genetics. 71(6). 561–568. 25 indexed citations
15.
Sozen, Mert, Ros Whittall, Cihan Öner, et al.. (2005). The molecular basis of familial hypercholesterolaemia in Turkish patients. Atherosclerosis. 180(1). 63–71. 34 indexed citations
16.
Sozen, Mert, Çağatay Karaaslan, R. Öner, et al.. (2004). Severe hemolytic anemia associated with Hb Volga [β27(B9)Ala→Asp]: GCC→GAC at codon 27 in a Turkish family. American Journal of Hematology. 76(4). 378–382. 8 indexed citations
18.
Stephens, Jeffrey W., Mert Sozen, Ros Whittall, et al.. (2004). Three Novel Mutations in the Apolipoprotein E Gene in a Sample of Individuals with Type 2 Diabetes Mellitus. Clinical Chemistry. 51(1). 119–124. 6 indexed citations
19.
Öner, R., C. Öner, Esra Birben, et al.. (2001). β‐Thalassaemia intermedia in a Turkish girl: homozygosity for G→A substitution at +22 relative to the β‐globin cap site. British Journal of Haematology. 115(1). 90–94. 4 indexed citations
20.
Koç, Ahmet, R. Öner, C. Öner, et al.. (1999). Myelodysplastic syndrome (MDS) associated with increased hemoglobin F and trisomy 8: presentation of a patient. PubMed. 41(4). 187–189. 2 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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