Bekir Ergüner

916 total citations
14 papers, 162 citations indexed

About

Bekir Ergüner is a scholar working on Genetics, Molecular Biology and Cancer Research. According to data from OpenAlex, Bekir Ergüner has authored 14 papers receiving a total of 162 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 6 papers in Molecular Biology and 4 papers in Cancer Research. Recurrent topics in Bekir Ergüner's work include Cancer Genomics and Diagnostics (4 papers), Genomics and Rare Diseases (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). Bekir Ergüner is often cited by papers focused on Cancer Genomics and Diagnostics (4 papers), Genomics and Rare Diseases (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). Bekir Ergüner collaborates with scholars based in Türkiye, United States and Germany. Bekir Ergüner's co-authors include Mahmut Şamil Sağıroğlu, Bayram Yüksel, Can Alkan, Onur Emre Onat, Tayfun Özçelık, Hatice Balaban, Fatih Bayraklı, Cengiz Yakıcıer, Bülent Güçlü and Duran Üstek and has published in prestigious journals such as Bioinformatics, Journal of Medical Genetics and Neuromuscular Disorders.

In The Last Decade

Bekir Ergüner

12 papers receiving 161 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Bekir Ergüner Türkiye 7 78 68 19 18 15 14 162
Birutė Burnytė Lithuania 7 103 1.3× 70 1.0× 18 0.9× 12 0.7× 10 0.7× 28 194
Shenela Lakhani United States 4 77 1.0× 87 1.3× 14 0.7× 32 1.8× 32 2.1× 6 185
Irén Haltrich Hungary 9 103 1.3× 93 1.4× 15 0.8× 15 0.8× 13 0.9× 33 239
Eda Ütine Türkiye 9 96 1.2× 99 1.5× 22 1.2× 16 0.9× 14 0.9× 24 218
Ayça Dilruba Aslanger Türkiye 7 126 1.6× 33 0.5× 25 1.3× 19 1.1× 13 0.9× 26 183
Minal Menezes Australia 10 195 2.5× 65 1.0× 17 0.9× 16 0.9× 10 0.7× 17 290
Resham Ejaz Canada 7 55 0.7× 42 0.6× 17 0.9× 12 0.7× 12 0.8× 16 132
Dmitriy Niyazov United States 7 140 1.8× 99 1.5× 13 0.7× 7 0.4× 11 0.7× 8 208
Samantha Penney United States 5 68 0.9× 76 1.1× 8 0.4× 22 1.2× 9 0.6× 5 157
Berardo Rinaldi Italy 7 99 1.3× 90 1.3× 10 0.5× 7 0.4× 10 0.7× 26 170

Countries citing papers authored by Bekir Ergüner

Since Specialization
Citations

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

Fields of papers citing papers by Bekir Ergüner

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bekir Ergüner

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

All Works

14 of 14 papers shown
1.
2.
Kılıç, Mustafa, Bekir Ergüner, Can Koşukçu, & Rıza Köksal Özgül. (2020). Detection of allele frequencies of common c. 511C>T and c.625G>A variants in the ACADS gene in the Turkish population. The Turkish Journal of Pediatrics. 62(1). 19–23. 2 indexed citations
3.
Akgün, Mete, et al.. (2020). Identifying disease-causing mutations with privacy protection. Bioinformatics. 36(21). 5205–5213. 5 indexed citations
4.
Yüksel, Bayram, et al.. (2018). GPR56 homozygous nonsense mutation p.R271* associated with phenotypic variability in bilateral frontoparietal polymicrogyria. The Turkish Journal of Pediatrics. 60(3). 229–237. 8 indexed citations
5.
Durmuş, Hacer, Bekir Ergüner, Hüseyin Demirci, et al.. (2017). Myophosphorylase ( PYGM ) mutations determined by next generation sequencing in a cohort from Turkey with McArdle disease. Neuromuscular Disorders. 27(11). 997–1008. 10 indexed citations
6.
Şahin, Yavuz, et al.. (2016). Exome sequencing identifies a novel homozygous CLN8 mutation in a Turkish family with Northern epilepsy. Acta Neurologica Belgica. 117(1). 159–167. 6 indexed citations
7.
Çakar, Zeynep Petek, Meral Yücel, Orhan Özcan, et al.. (2016). Draft Genome Sequences of Two Heat-Resistant Mutant Strains (A52 and B41) of the Photosynthetic Hydrogen-Producing Bacterium Rhodobacter capsulatus. Genome Announcements. 4(3). 1 indexed citations
8.
Bayraklı, Fatih, Hatice Gamze Poyrazoğlu, Cengiz Yakıcıer, et al.. (2015). Hereditary spastic paraplegia with recessive trait caused by mutation in KLC4 gene. Journal of Human Genetics. 60(12). 763–768. 17 indexed citations
9.
Ergüner, Bekir, Duran Üstek, & Mahmut Şamil Sağıroğlu. (2015). Performance comparison of Next Generation sequencing platforms. PubMed. 99. 6453–6456. 7 indexed citations
10.
Ergüner, Bekir, Mahmut Şamil Sağıroğlu, Bayram Yüksel, et al.. (2014). Early postzygotic mutations contribute to de novo variation in a healthy monozygotic twin pair. Journal of Medical Genetics. 51(7). 455–459. 38 indexed citations
11.
Akgün, Mete, et al.. (2014). Human Genome in a Smart Card. 310–316.
12.
Bayraklı, Fatih, Bülent Güçlü, Cengiz Yakıcıer, et al.. (2013). Mutation in MEOX1 gene causes a recessive Klippel-Feil syndrome subtype. BMC Genetics. 14(1). 95–95. 42 indexed citations
13.
Alanay, Yasemin, Bekir Ergüner, Eda Ütine, et al.. (2013). TMCO1 deficiency causes autosomal recessive cerebrofaciothoracic dysplasia. American Journal of Medical Genetics Part A. 164(2). 291–304. 23 indexed citations
14.
Ergüner, Bekir, Masahiro Hattori, Susumu Goto, & Minoru Kanehisa. (2010). CHARACTERIZING COMMON SUBSTRUCTURES OF LIGANDS FOR GPCR PROTEIN SUBFAMILIES. PubMed. 24. 31–41.

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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