E. Ferda Perçin
Impact in
- Developmental Biology top 2%
- Congenital limb and hand anomalies
- Genetics top 5%
- Ocular Disorders and Treatments
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 48
- Genomic variations and chromosomal abnormalities 13
- Connective tissue disorders research 9
- Genetics and Neurodevelopmental Disorders 9
- Congenital Ear and Nasal Anomalies 6
- Genomics and Rare Diseases 5
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 4
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- Congenital limb and hand anomalies 9
- Co-authors
- Nurten Ayse Akarsu (5 shared papers)Mehmet Ali Ergün (25 shared papers)Hans van Bokhoven (1 shared paper)Han G. Brunner (1 shared paper)Kyle A. Wallace (2 shared papers)Sarah Dickerson (2 shared papers)Enio T. Perez (2 shared papers)Michael J. Miller (2 shared papers)
- Journals
- European Journal of Medical Genetics (4 papers)The American Journal of Human Genetics (3 papers)Nature Genetics (3 papers)Gene (2 papers)Clinical Genetics (2 papers)
- Partner nations
- TürkiyeGermanyUnited States
In The Last Decade
E. Ferda Perçin
80 papers receiving 1.7k citations
Peers
Comparison fields: 5 of 96
- Developmental Biology 127
- Genetics 590
- Molecular Biology 1.1k
- Genetics 108
- Aging 18
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 85 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2000 | 240 | |
| 2 | 2000 | 211 | |
| 3 | 2012 | 173 | |
| 4 | 2010 | 145 | |
| 5 | 2014 | 101 | |
| 6 | 2017 | 84 | |
| 7 | 2015 | 73 | |
| 8 | 2016 | 53 | |
| 9 | 2010 | 51 | |
| 10 | 2007 | 42 | |
| 11 | 2014 | 39 | |
| 12 | 2014 | 38 | |
| 13 | 2008 | 35 | |
| 14 | 2019 | 32 | |
| 15 | 2013 | 28 | |
| 16 | 2014 | 28 | |
| 17 | 2013 | 23 | |
| 18 | 2016 | 21 | |
| 19 | 2010 | 19 | |
| 20 | 2005 | 18 |
About E. Ferda Perçin
E. Ferda Perçin is a scholar working on Genetics, Developmental Biology, Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology, having authored 85 papers that have together received 1.8k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (13 papers), Prenatal Screening and Diagnostics (12 papers), Connective tissue disorders research (9 papers), Genetics and Neurodevelopmental Disorders (9 papers), Congenital limb and hand anomalies (9 papers), Congenital Ear and Nasal Anomalies (6 papers), Genomics and Rare Diseases (5 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers). The work is most often cited by research in Developmental Biology (127 citations), Genetics (590 citations), Molecular Biology (1.1k citations), Genetics (108 citations) and Aging (18 citations). E. Ferda Perçin has collaborated with scholars based in Türkiye, Germany and United States. Frequent co-authors include Nurten Ayse Akarsu, Mehmet Ali Ergün, Hans van Bokhoven, Han G. Brunner, Kyle A. Wallace, Sarah Dickerson, Enio T. Perez, Michael J. Miller, Wim Brussel and Jessica M. Martin. Their work appears in journals such as European Journal of Medical Genetics, The American Journal of Human Genetics, Nature Genetics, Gene and Clinical Genetics.
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.