Hande Çağlayan
Impact in
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- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genetic Associations and Epidemiology
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- Epilepsy research and treatment
Papers in
- Genetics 4
- Genomics and Rare Diseases 3
- Genetics and Neurodevelopmental Disorders 2
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- Cancer-related gene regulation 2
- Ion channel regulation and function 1
- Co-authors
- Zühal Yapıcı (2 shared papers)Katherine L. Helbig (1 shared paper)Ingrid E. Scheffer (1 shared paper)Marta A. Bayly (1 shared paper)Saul A. Mullen (1 shared paper)André Franke (1 shared paper)Samuel F. Berkovic (1 shared paper)Heather C. Mefford (1 shared paper)
In The Last Decade
Hande Çağlayan
8 papers receiving 189 citations
Peers
Comparison fields: 5 of 22
- Genetics 133
- Psychiatry and Mental health 41
- Clinical Biochemistry 7
- Cellular and Molecular Neuroscience 18
- Molecular Biology 67
Countries citing papers authored by Hande Çağlayan
This map shows the geographic impact of Hande Çağlayan'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 Hande Çağlayan with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Hande Çağlayan more than expected).
Fields of papers citing papers by Hande Çağlayan
This network shows the impact of papers produced by Hande Çağlayan. 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 Hande Çağlayan. The network helps show where Hande Çağlayan may publish in the future.
Co-authors
The 25 scholars most cited alongside Hande Çağlayan, 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 | 2009 | 167 | |
| 2 | 2006 | 9 | |
| 3 | 2019 | 7 | |
| 4 | 2012 | 4 | |
| 5 | 2023 | 3 | |
| 6 | 2023 | 2 | |
| 7 | Dravet Sendromunda Kesin Sudep: Erişkin Bir Olgu Sunumu | 2015 | 1 |
| 8 | Intron 1 inversion mutation among Turkish hemophilia A patients. | 2006 | 1 |
About Hande Çağlayan
Hande Çağlayan is a scholar working on Genetics, Molecular Biology, Neurology, Hematology and Surgery, having authored 8 papers that have together received 194 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (3 papers), Genetics and Neurodevelopmental Disorders (2 papers), Hemophilia Treatment and Research (2 papers), Cancer-related gene regulation (2 papers), Platelet Disorders and Treatments (2 papers), Autoimmune Neurological Disorders and Treatments (1 paper), Ion channel regulation and function (1 paper) and Glycogen Storage Diseases and Myoclonus (1 paper). The work is most often cited by research in Genetics (133 citations), Psychiatry and Mental health (41 citations), Clinical Biochemistry (7 citations), Cellular and Molecular Neuroscience (18 citations) and Molecular Biology (67 citations). Hande Çağlayan has collaborated with scholars based in Türkiye, Germany and Australia. Frequent co-authors include Zühal Yapıcı, Katherine L. Helbig, Ingrid E. Scheffer, Marta A. Bayly, Saul A. Mullen, André Franke, Samuel F. Berkovic, Heather C. Mefford, Holger Trucks and John C. Mulley. Their work appears in journals such as Seizure, Haemophilia, Human Molecular Genetics, Epilepsia Open and Epileptic Disorders.
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.