Ferda Özkınay
Impact in
- Genetics top 5%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Neurogenetic and Muscular Disorders Research
- Immunology top 10%
- Complement system in diseases
Papers in
-
- Sexual Differentiation and Disorders 12
- RNA modifications and cancer 11
- Genetics 71
- Genomic variations and chromosomal abnormalities 16
- Neurogenetic and Muscular Disorders Research 12
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 10
- Co-authors
- Hüseyin Önay (116 shared papers)Özgür Çoğulu (97 shared papers)Cihangir Özkınay (41 shared papers)Tahir Atık (51 shared papers)Burak Durmaz (34 shared papers)Ayça Aykut (39 shared papers)Cumhur Gündüz (34 shared papers)Fadıl Vardar (15 shared papers)
- Journals
- European Journal of Medical Genetics (5 papers)Clinical Genetics (4 papers)Journal of Pediatric Hematology/Oncology (4 papers)Gene (4 papers)Journal of Child Neurology (3 papers)
- Partner nations
- TürkiyeUnited StatesGermany
In The Last Decade
Ferda Özkınay
255 papers receiving 2.8k citations
Peers
Comparison fields: 5 of 125
- Genetics 199
- Genetics 539
- Immunology 338
- Periodontics 68
- Hematology 145
Countries citing papers authored by Ferda Özkınay
This map shows the geographic impact of Ferda Özkınay'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 Ferda Özkınay with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ferda Özkınay more than expected).
Fields of papers citing papers by Ferda Özkınay
This network shows the impact of papers produced by Ferda Özkınay. 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 Ferda Özkınay. The network helps show where Ferda Özkınay may publish in the future.
Co-authors
The 25 scholars most cited alongside Ferda Özkınay, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 272 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2000 | 90 | |
| 2 | 2011 | 88 | |
| 3 | Rotavirus gastroenteritis among children under five years of age in Izmir, Turkey. | 2004 | 82 |
| 4 | 2005 | 68 | |
| 5 | 2013 | 55 | |
| 6 | 2005 | 52 | |
| 7 | 2015 | 49 | |
| 8 | 2014 | 48 | |
| 9 | 2009 | 48 | |
| 10 | 2002 | 47 | |
| 11 | 2019 | 45 | |
| 12 | 2013 | 42 | |
| 13 | 2009 | 36 | |
| 14 | 2015 | 35 | |
| 15 | 2008 | 35 | |
| 16 | 2015 | 34 | |
| 17 | 2005 | 33 | |
| 18 | 2018 | 33 | |
| 19 | 2000 | 33 | |
| 20 | 2016 | 33 |
About Ferda Özkınay
Ferda Özkınay is a scholar working on Molecular Biology, Genetics, Surgery, Pediatrics, Perinatology and Child Health and Genetics, having authored 272 papers that have together received 2.9k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (19 papers), Genomic variations and chromosomal abnormalities (16 papers), Congenital Anomalies and Fetal Surgery (12 papers), Sexual Differentiation and Disorders (12 papers), Neurogenetic and Muscular Disorders Research (12 papers), Lysosomal Storage Disorders Research (11 papers), RNA modifications and cancer (11 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (10 papers). The work is most often cited by research in Genetics (199 citations), Genetics (539 citations), Immunology (338 citations), Periodontics (68 citations) and Hematology (145 citations). Ferda Özkınay has collaborated with scholars based in Türkiye, United States and Germany. Frequent co-authors include Hüseyin Önay, Özgür Çoğulu, Cihangir Özkınay, Tahir Atık, Burak Durmaz, Ayça Aykut, Cumhur Gündüz, Fadıl Vardar, Zafer Kurugöl and Sacide Pehlıvan. Their work appears in journals such as European Journal of Medical Genetics, Clinical Genetics, Journal of Pediatric Hematology/Oncology, Gene and Journal of Child Neurology.
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.