Dilek Aktaş
- Co-authors
- Mehmet AlikaşifoğluErgül TunçbılekYasemin AlanayKoray BoduroğluThomas LiehrGülen Eda ÜtineSevim BalcıSinan Sözen
- Topics
- Genomic variations and chromosomal abnormalities (17 papers)Genetics and Neurodevelopmental Disorders (9 papers)Prenatal Screening and Diagnostics (8 papers)
In The Last Decade
Dilek Aktaş
64 papers receiving 838 citations
Peers
Comparison fields: 5 of 96
- Genetics 455
- Molecular Biology 423
- Surgery 106
- Pediatrics, Perinatology and Child Health 104
- Oncology 70
Countries citing papers authored by Dilek Aktaş
This map shows the geographic impact of Dilek Aktaş'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 Dilek Aktaş with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Dilek Aktaş more than expected).
Fields of papers citing papers by Dilek Aktaş
This network shows the impact of papers produced by Dilek Aktaş. 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 Dilek Aktaş. The network helps show where Dilek Aktaş may publish in the future.
Co-authorship network of co-authors of Dilek Aktaş
This figure shows the co-authorship network connecting the top 25 collaborators of Dilek Aktaş. A scholar is included among the top collaborators of Dilek Aktaş 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 Dilek Aktaş. Dilek Aktaş is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 1 | |
| 2 | 6 | |
| 3 | 1 | |
| 4 | Dental Findings and Mutational Analysis of a Case with Ehlers-Danlos Syndrome | 2 |
| 5 | Bir Eğitim Araştırma Hastanesinde Hemşirelerin Kurumdan Ayrılmayı İsteme Nedenlerinin İncelenmesi | 1 |
| 6 | Body Image Perceptions of Persons With a Stoma and Their Partners: A Descriptive, Cross-sectional Study. | 19 |
| 7 | 23 | |
| 8 | 2 | |
| 9 | 101 | |
| 10 | 13 | |
| 11 | 30 | |
| 12 | 19 | |
| 13 | 13 | |
| 14 | 28 | |
| 15 | 38 | |
| 16 | 44 | |
| 17 | 29 | |
| 18 | 1 | |
| 19 | 8 | |
| 20 | 22 |
About Dilek Aktaş
Dilek Aktaş is a scholar working on Occupational Therapy, Genetics and Developmental Biology, having authored 68 papers that have together received 873 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (17 papers), Genetics and Neurodevelopmental Disorders (9 papers) and Prenatal Screening and Diagnostics (8 papers). The work is most often cited by research in Genetics (455 citations), Molecular Biology (423 citations) and Reproductive Medicine (49 citations). Dilek Aktaş has collaborated with scholars based in Türkiye, Germany and Belgium. Frequent co-authors include Mehmet Alikaşifoğlu, Ergül Tunçbılek, Yasemin Alanay, Koray Boduroğlu, Thomas Liehr, Gülen Eda Ütine, Sevim Balcı, Sinan Sözen, Haluk Özen and K. Yüce. Their work appears in journals such as The American Journal of Human Genetics, The American Journal of Gastroenterology and Journal of Periodontology.
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.