Özgür Çoğulu
- Molecular Biology
- Genetics top 10%
- Immunology
- Pediatrics, Perinatology and Child Health top 10%
- Surgery
- Co-authors
- Ferda ÖzkınayEmin KaracaHüseyin ÖnayCumhur GündüzBurak DurmazAsude DurmazCihangir ÖzkınayAyça Aykut
- Topics
- Prenatal Screening and Diagnostics (20 papers)Genomic variations and chromosomal abnormalities (18 papers)Congenital Anomalies and Fetal Surgery (12 papers)
- Cited by
- GeneticsCancer Research
- Journals
- SHILAP Revista de lepidopterologíaBloodThe Journal of Clinical Endocrinology & Metabolism
- Partner nations
- TürkiyeUnited StatesGermany
In The Last Decade
Özgür Çoğulu
124 papers receiving 1.2k citations
Peers
Comparison fields: 5 of 120
- Molecular Biology 515
- Genetics 320
- Immunology 166
- Pediatrics, Perinatology and Child Health 153
- Surgery 129
Countries citing papers authored by Özgür Çoğulu
This map shows the geographic impact of Özgür Çoğulu'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 Özgür Çoğulu with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Özgür Çoğulu more than expected).
Fields of papers citing papers by Özgür Çoğulu
This network shows the impact of papers produced by Özgür Çoğulu. 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 Özgür Çoğulu. The network helps show where Özgür Çoğulu may publish in the future.
Co-authorship network of co-authors of Özgür Çoğulu
This figure shows the co-authorship network connecting the top 25 collaborators of Özgür Çoğulu. A scholar is included among the top collaborators of Özgür Çoğulu 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 Özgür Çoğulu. Özgür Çoğulu is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 0 | |
| 2 | 0 | |
| 3 | 1 | |
| 4 | 4 | |
| 5 | 5 | |
| 6 | 3 | |
| 7 | 10 | |
| 8 | 3 | |
| 9 | 9 | |
| 10 | 4 | |
| 11 | 10 | |
| 12 | 15 | |
| 13 | 2 | |
| 14 | 0 | |
| 15 | Duane anomaly, meningomyelocele, dextroposition of heart and localized vertebrocostal alterations with associated anomalies in a girl. | 2 |
| 16 | 11 | |
| 17 | 1 | |
| 18 | 35 | |
| 19 | 0 | |
| 20 | 1 |
About Özgür Çoğulu
Özgür Çoğulu is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Hematology, having authored 133 papers that have together received 1.2k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (20 papers), Genomic variations and chromosomal abnormalities (18 papers) and Congenital Anomalies and Fetal Surgery (12 papers). The work is most often cited by research in Genetics (320 citations), Genetics (92 citations) and Cancer Research (120 citations). Özgür Çoğulu has collaborated with scholars based in Türkiye, United States and Germany. Frequent co-authors include Ferda Özkınay, Emin Karaca, Hüseyin Önay, Cumhur Gündüz, Burak Durmaz, Asude Durmaz, Cihangir Özkınay, Ayça Aykut, Tahir Atık and Haluk Akın. Their work appears in journals such as SHILAP Revista de lepidopterología, Blood and The Journal of Clinical Endocrinology & Metabolism.
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.