Yeşim Kesim
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- Genetics and Neurodevelopmental Disorders 3
- Genomic variations and chromosomal abnormalities 2
- Ocular Disorders and Treatments 2
- Genomics and Rare Diseases 1
- Craniofacial Disorders and Treatments 1
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- Amino Acid Enzymes and Metabolism 1
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- Glycogen Storage Diseases and Myoclonus 1
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- Peptidase Inhibition and Analysis 1
Yeşim Kesim
7 papers receiving 36 citations
Peers
Comparison fields: 5 of 30
- Neurology 8
- Developmental Neuroscience 3
- Genetics 11
- Cognitive Neuroscience 7
- Orthopedics and Sports Medicine 3
Countries citing papers authored by Yeşim Kesim
This map shows the geographic impact of Yeşim Kesim'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 Yeşim Kesim with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Yeşim Kesim more than expected).
Fields of papers citing papers by Yeşim Kesim
This network shows the impact of papers produced by Yeşim Kesim. 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 Yeşim Kesim. The network helps show where Yeşim Kesim may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Yeşim Kesim, 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 | 2024 | 2 | |
| 2 | 2023 | 2 | |
| 3 | 2023 | 1 | |
| 4 | 2021 | 2 | |
| 5 | 2020 | 1 | |
| 6 | 2020 | 20 | |
| 7 | 2019 | 8 |
About Yeşim Kesim
Yeşim Kesim is a scholar working on Genetics, Clinical Biochemistry and Biochemistry, having authored 7 papers that have together received 36 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (3 papers), Genomic variations and chromosomal abnormalities (2 papers), Ocular Disorders and Treatments (2 papers), Amino Acid Enzymes and Metabolism (1 paper), Genomics and Rare Diseases (1 paper), Glycogen Storage Diseases and Myoclonus (1 paper), Craniofacial Disorders and Treatments (1 paper) and Peptidase Inhibition and Analysis (1 paper). The work is most often cited by research in Neurology (8 citations), Developmental Neuroscience (3 citations) and Genetics (11 citations). Yeşim Kesim has collaborated with scholars based in Türkiye, United Kingdom and Hungary. Frequent co-authors include Sı̇bel Aylı̇n Uğur İşerı̇, Ali Emre Öge, Zeliha Matur, Emrah Yücesan, Uğur Özbek, Mustafa Çalık, Sanaa Muheisen, Gülden Gökçay, Thomas Naert and Kathy Williamson. Their work appears in journals such as Nature Communications, Brain Research and European Journal of Human Genetics.
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.