Ferda Özkınay
Impact in
- Periodontics top 2%
- Genetics top 5%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 83
- Genomic variations and chromosomal abnormalities 20
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 12
- Neurogenetic and Muscular Disorders Research 12
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- Prenatal Screening and Diagnostics 24
- Co-authors
- Hüseyin ÖnayÖzgür ÇoğuluCihangir ÖzkınayTahir AtıkBurak DurmazAyça AykutCumhur GündüzFadıl Vardar
- Journals
- European Journal of Medical Genetics (5 papers)Journal of Pediatric Hematology/Oncology (4 papers)Gene (4 papers)Clinical Genetics (4 papers)Journal of Child Neurology (3 papers)
- Partner nations
- TürkiyeUnited StatesGermany
In The Last Decade
Ferda Özkınay
253 papers receiving 2.8k citations
Peers
Comparison fields: 5 of 134
- Periodontics 107
- Genetics 635
- Genetics 213
- Immunology 392
- Cell Biology 240
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-authorship network
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
| # | Work | ||
|---|---|---|---|
| 1 | 2023 | 0 | |
| 2 | 2021 | 3 | |
| 3 | 2021 | 2 | |
| 4 | Izmir Mental Health Cohort for Gene-Environment Interaction in Psychosis (TürkSch): Assessment of the Extended and Transdiagnostic Psychosis Phenotype and Analysis of Attrition in a 6-Year Follow-Up of a Community-Based Sample : Assessment of the Extended and Transdiagnostic Psychosis Phenotype and Analysis of Attrition in a 6-Year Follow-Up of a Community-Based Sample | 2019 | 12 |
| 5 | 2017 | 2 | |
| 6 | Mannose-binding lectin may affect pregnancy outcome. | 2016 | 8 |
| 7 | Prevalence of Melanocortin 4 Receptor Mutations in Turkish Obese Children | 2016 | 1 |
| 8 | Omenn Sendromlu Bir Olgu | 2013 | 1 |
| 9 | Ventricular septal defect in Crouzon Syndrome: case report. | 2012 | 2 |
| 10 | Nöral Tüp Defektlerinde Annelerde MTHFR Gen Polimorfizmleri ve Diğer Risk Faktörlerinin Değerlendirilmesi | 2012 | 1 |
| 11 | 2012 | 3 | |
| 12 | Talasemi ve Hemoglobinopatilerin Moleküler Tanı Yöntemleri | 2010 | 1 |
| 13 | 2009 | 2 | |
| 14 | THE EPIDEMIOLOGY OF HEPATITIS A INFECTION IN THE POPULATION OF BORNOVA, IZMIR, TURKEY | 2007 | 6 |
| 15 | Duane anomaly, meningomyelocele, dextroposition of heart and localized vertebrocostal alterations with associated anomalies in a girl. | 2007 | 2 |
| 16 | 2007 | 1 | |
| 17 | 2006 | 1 | |
| 18 | 2000 | 0 | |
| 19 | 2000 | 1 | |
| 20 | 2000 | 11 |
About Ferda Özkınay
Ferda Özkınay is a scholar working on Genetics, Genetics, Pediatrics, Perinatology and Child Health, Hematology and Rheumatology, having authored 272 papers that have together received 2.9k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (24 papers), Genomic variations and chromosomal abnormalities (20 papers), Congenital Anomalies and Fetal Surgery (16 papers), Sexual Differentiation and Disorders (15 papers), RNA modifications and cancer (14 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (12 papers), Neurogenetic and Muscular Disorders Research (12 papers) and Lysosomal Storage Disorders Research (11 papers). The work is most often cited by research in Periodontics (107 citations), Genetics (635 citations), Genetics (213 citations), Immunology (392 citations) and Cell Biology (240 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, Journal of Pediatric Hematology/Oncology, Gene, Clinical Genetics 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.