Bekir Ergüner

941 citations
14 papers · 164 · h-index 7

Impact in

    • Genomics and Rare Diseases
    • Genomic variations and chromosomal abnormalities
    • Genetics and Neurodevelopmental Disorders
    • Glycogen Storage Diseases and Myoclonus

Papers in

    • Glycosylation and Glycoproteins Research 2
    • Genomics and Phylogenetic Studies 2
    • Genomic variations and chromosomal abnormalities 2

Bekir Ergüner

12 papers receiving 163 citations

Peers

Bekir Ergüner
Comparison fields: 5 of 56
  • Genetics 56
  • Rheumatology 15
  • Cell Biology 17
  • Molecular Biology 70
  • Cellular and Molecular Neuroscience 15
Replace Samantha Penney with:
Samantha Penney United States
Daphné Lehalle France
Minal Menezes Australia
Sebastian Röner Germany
Birutė Burnytė Lithuania
James Fasham United Kingdom
Adisak Trinavarat Thailand
Charu Kaiwar United States
Craig Chinault United States
Lucile Pinson France
Bekir Ergüner relative to Samantha Penney United States Samantha Penney's profile →
Citations per field
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Citations per year

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-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.

Border = papers with Bekir Ergüner Line = papers co-authored together Bekir Ergüner links everyone, so they are left out of the graph.

All Works

14 of 14 papers shown
#Work
1 201343
2 201439
3 201323
4 201517
5 201710
6 20188
7 20157
8 20166
9 20205
10 20213
11 20202
12 20161
13 20100
14 20140

About Bekir Ergüner

Bekir Ergüner is a scholar working on Molecular Biology, Genetics, Cancer Research, Surgery and Rheumatology, having authored 14 papers that have together received 164 indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (3 papers), Glycosylation and Glycoproteins Research (2 papers), Lysosomal Storage Disorders Research (2 papers), Genomics and Phylogenetic Studies (2 papers), Neurological diseases and metabolism (2 papers), Glycogen Storage Diseases and Myoclonus (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Autism Spectrum Disorder Research (1 paper). The work is most often cited by research in Genetics (56 citations), Rheumatology (15 citations), Cell Biology (17 citations), Molecular Biology (70 citations) and Cellular and Molecular Neuroscience (15 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, Can Alkan, Tayfun Özçelık, Cengiz Yakıcıer, Fatih Bayraklı, Hatice Balaban, Bülent Güçlü and Duran Üstek. Their work appears in journals such as Neuromuscular Disorders, BMC Genetics, The Journal of Gene Medicine, Journal of Medical Genetics and Bioinformatics.

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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