E. Ferda Perçin
Impact in
- Developmental Biology top 1%
- Congenital limb and hand anomalies
- Genetics top 5%
- Ocular Disorders and Treatments
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Connective tissue disorders research
Papers in
- Genetics 54
- Genomics and Rare Diseases 17
- Genomic variations and chromosomal abnormalities 16
- Connective tissue disorders research 8
- Craniofacial Disorders and Treatments 5
- Genetics and Neurodevelopmental Disorders 5
- Genetic and rare skin diseases. 4
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- Congenital limb and hand anomalies 15
- Co-authors
- Nurten Ayse Akarsu (5 shared papers)Mehmet Ali Ergün (29 shared papers)Han G. Brunner (1 shared paper)M. Joseph Phillips (2 shared papers)Wim Brussel (1 shared paper)Elizabeth E. Capowski (2 shared papers)Hülya Kayserili (2 shared papers)Bronwyn A. Kerr (1 shared paper)
- Journals
- European Journal of Medical Genetics (5 papers)Nature Genetics (3 papers)The American Journal of Human Genetics (3 papers)Clinical Genetics (2 papers)Gene (2 papers)
- Partner nations
- TürkiyeGermanyUnited Kingdom
In The Last Decade
E. Ferda Perçin
86 papers receiving 1.8k citations
Peers
Comparison fields: 5 of 82
- Developmental Biology 212
- Genetics 599
- Molecular Biology 755
- Pharmacology 67
- Pediatrics, Perinatology and Child Health 89
Countries citing papers authored by E. Ferda Perçin
This map shows the geographic impact of E. Ferda Perçin'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 E. Ferda Perçin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites E. Ferda Perçin more than expected).
Fields of papers citing papers by E. Ferda Perçin
This network shows the impact of papers produced by E. Ferda Perçin. 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 E. Ferda Perçin. The network helps show where E. Ferda Perçin may publish in the future.
Co-authors
The 25 scholars most cited alongside E. Ferda Perçin, 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 92 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2000 | 239 | |
| 2 | 2000 | 214 | |
| 3 | 2012 | 172 | |
| 4 | 2010 | 147 | |
| 5 | 2014 | 100 | |
| 6 | 2017 | 86 | |
| 7 | 2015 | 73 | |
| 8 | 2016 | 53 | |
| 9 | 2010 | 51 | |
| 10 | 2007 | 43 | |
| 11 | 2014 | 39 | |
| 12 | 2014 | 37 | |
| 13 | 2008 | 35 | |
| 14 | 2019 | 32 | |
| 15 | 2013 | 28 | |
| 16 | 2014 | 28 | |
| 17 | 2013 | 23 | |
| 18 | 2016 | 20 | |
| 19 | 2010 | 19 | |
| 20 | 2005 | 18 |
About E. Ferda Perçin
E. Ferda Perçin is a scholar working on Genetics, Developmental Biology, Pharmacology, Pediatrics, Perinatology and Child Health and Genetics, having authored 92 papers that have together received 1.8k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (17 papers), Genomic variations and chromosomal abnormalities (16 papers), Congenital limb and hand anomalies (15 papers), Connective tissue disorders research (8 papers), Craniofacial Disorders and Treatments (5 papers), Genetics and Neurodevelopmental Disorders (5 papers), Pharmacogenetics and Drug Metabolism (5 papers) and Genetic and rare skin diseases. (4 papers). The work is most often cited by research in Developmental Biology (212 citations), Genetics (599 citations), Molecular Biology (755 citations), Pharmacology (67 citations) and Pediatrics, Perinatology and Child Health (89 citations). E. Ferda Perçin has collaborated with scholars based in Türkiye, Germany and United Kingdom. Frequent co-authors include Nurten Ayse Akarsu, Mehmet Ali Ergün, Han G. Brunner, M. Joseph Phillips, Wim Brussel, Elizabeth E. Capowski, Hülya Kayserili, Bronwyn A. Kerr, Sevim Balcı and Kyle A. Wallace. Their work appears in journals such as European Journal of Medical Genetics, Nature Genetics, The American Journal of Human Genetics, Clinical Genetics and Gene.
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.