Filiz Özbas‐Gerçeker
- Molecular Biology
- Oncology
- Pediatrics, Perinatology and Child Health top 10%
- Psychiatry and Mental health top 10%
- Clinical Biochemistry top 5%
- Co-authors
- Eleonora AronicaMeral ÖzgüçMarja RamkemaSandra RedekerDirk TroostJan A. GorterJohannes C. BaayenPaul van der Valk
- Topics
- Forensic and Genetic Research (3 papers)Forensic Anthropology and Bioarchaeology Studies (2 papers)Ubiquitin and proteasome pathways (2 papers)
- Journals
- SHILAP Revista de lepidopterologíaHuman Molecular GeneticsEpilepsia
- Partner nations
- TürkiyeNetherlandsCyprus
In The Last Decade
Filiz Özbas‐Gerçeker
22 papers receiving 530 citations
Peers
Comparison fields: 5 of 73
- Molecular Biology 223
- Oncology 144
- Pediatrics, Perinatology and Child Health 125
- Psychiatry and Mental health 119
- Clinical Biochemistry 78
Countries citing papers authored by Filiz Özbas‐Gerçeker
This map shows the geographic impact of Filiz Özbas‐Gerçeker'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 Filiz Özbas‐Gerçeker with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Filiz Özbas‐Gerçeker more than expected).
Fields of papers citing papers by Filiz Özbas‐Gerçeker
This network shows the impact of papers produced by Filiz Özbas‐Gerçeker. 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 Filiz Özbas‐Gerçeker. The network helps show where Filiz Özbas‐Gerçeker may publish in the future.
Co-authorship network of co-authors of Filiz Özbas‐Gerçeker
This figure shows the co-authorship network connecting the top 25 collaborators of Filiz Özbas‐Gerçeker. A scholar is included among the top collaborators of Filiz Özbas‐Gerçeker 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 Filiz Özbas‐Gerçeker. Filiz Özbas‐Gerçeker is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 53 | |
| 2 | 0 | |
| 3 | 0 | |
| 4 | 1 | |
| 5 | 26 | |
| 6 | 12 | |
| 7 | 7 | |
| 8 | 3 | |
| 9 | 10 | |
| 10 | 14 | |
| 11 | Identification of an ancestral haplotype of the 35delG mutation in the GJB2 (connexin 26) gene responsible for autosomal recessive non-syndromic hearing loss in families from the Eastern Black Sea Region in Turkey. | 8 |
| 12 | 167 | |
| 13 | 101 | |
| 14 | 24 | |
| 15 | 22 | |
| 16 | Defective anti-polysaccharide antibody response in patients with ataxia-telangiectasia. | 12 |
| 17 | 32 | |
| 18 | 5 | |
| 19 | The effect of mannose-binding protein gene polymorphisms in recurrent respiratory system infections in children and lung tuberculosis. | 28 |
| 20 | Analysis of the modifying effects of TAP 1/2 genes on cystic fibrosis phenotype. | 3 |
About Filiz Özbas‐Gerçeker
Filiz Özbas‐Gerçeker is a scholar working on Developmental Neuroscience, Parasitology and Sensory Systems, having authored 25 papers that have together received 540 indexed citations. Recurring topics across this work include Forensic and Genetic Research (3 papers), Forensic Anthropology and Bioarchaeology Studies (2 papers) and Ubiquitin and proteasome pathways (2 papers). The work is most often cited by research in Clinical Biochemistry (78 citations), Psychiatry and Mental health (119 citations) and Pediatrics, Perinatology and Child Health (125 citations). Filiz Özbas‐Gerçeker has collaborated with scholars based in Türkiye, Netherlands and Cyprus. Frequent co-authors include Eleonora Aronica, Meral Özgüç, Marja Ramkema, Sandra Redeker, Dirk Troost, Jan A. Gorter, Johannes C. Baayen, Paul van der Valk, George L. Scheffer and Rik J. Scheper. Their work appears in journals such as SHILAP Revista de lepidopterología, Human Molecular Genetics and Epilepsia.
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.