Bekir Ergüner
Impact in
-
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Connective tissue disorders research
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- Congenital heart defects research
Papers in
- Genetics 8
- Genomics and Rare Diseases 3
- Genomic variations and chromosomal abnormalities 3
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- Genomics and Phylogenetic Studies 2
- Glycosylation and Glycoproteins Research 2
- Co-authors
- Mahmut Şamil Sağıroğlu (7 shared papers)Bayram Yüksel (4 shared papers)Onur Emre Onat (1 shared paper)Tayfun Özçelık (1 shared paper)Can Alkan (1 shared paper)Fatih Bayraklı (2 shared papers)Bülent Güçlü (1 shared paper)Cengiz Yakıcıer (2 shared papers)
- Journals
- BMC Genetics (1 paper)Neuromuscular Disorders (1 paper)Journal of Medical Genetics (1 paper)Bioinformatics (1 paper)The Journal of Gene Medicine (1 paper)
- Partner nations
- TürkiyeUnited StatesGermany
In The Last Decade
Bekir Ergüner
12 papers receiving 161 citations
Peers
Comparison fields: 5 of 57
- Genetics 68
- Molecular Biology 78
- Cell Biology 18
- Neurology 8
- Rheumatology 14
Countries citing papers authored by Bekir Ergüner
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
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-authors
The 25 scholars most cited alongside Bekir Ergüner, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2013 | 42 | |
| 2 | 2014 | 38 | |
| 3 | 2013 | 23 | |
| 4 | 2015 | 17 | |
| 5 | 2017 | 10 | |
| 6 | 2018 | 8 | |
| 7 | 2015 | 7 | |
| 8 | 2016 | 6 | |
| 9 | 2020 | 5 | |
| 10 | 2021 | 3 | |
| 11 | 2020 | 2 | |
| 12 | 2016 | 1 | |
| 13 | 2010 | 0 | |
| 14 | 2014 | 0 |
About Bekir Ergüner
Bekir Ergüner is a scholar working on Genetics, Molecular Biology, Cancer Research, Surgery and Rheumatology, having authored 14 papers that have together received 162 indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (4 papers), Genomics and Rare Diseases (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Neurological diseases and metabolism (2 papers), Lysosomal Storage Disorders Research (2 papers), Genomics and Phylogenetic Studies (2 papers), Glycosylation and Glycoproteins Research (2 papers) and Glycogen Storage Diseases and Myoclonus (2 papers). The work is most often cited by research in Genetics (68 citations), Molecular Biology (78 citations), Cell Biology (18 citations), Neurology (8 citations) and Rheumatology (14 citations). Bekir Ergüner has collaborated with scholars based in Türkiye, United States and Germany. Frequent co-authors include Mahmut Şamil Sağıroğlu, Bayram Yüksel, Onur Emre Onat, Tayfun Özçelık, Can Alkan, Fatih Bayraklı, Bülent Güçlü, Cengiz Yakıcıer, Hatice Balaban and Duran Üstek. Their work appears in journals such as BMC Genetics, Neuromuscular Disorders, Journal of Medical Genetics, Bioinformatics and The Journal of Gene Medicine.
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.