Derya Erçal
Impact in
-
- Neonatal Health and Biochemistry
- Prenatal Screening and Diagnostics
- Periodontics top 10%
Papers in
- Genetics 17
- Genomic variations and chromosomal abnormalities 5
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 4
- Genomics and Rare Diseases 3
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- Sexual Differentiation and Disorders 5
- Co-authors
- Semra Gürsoy (8 shared papers)Hasan Özkan (4 shared papers)Nuray Duman (2 shared papers)Abdullah Kumral (2 shared papers)Cihangir Özkınay (3 shared papers)Ferda Özkınay (4 shared papers)Ece Böber (5 shared papers)İlhan Tezcan (1 shared paper)
- Journals
- Pediatric Neurology (3 papers)HORMONES (2 papers)Child s Nervous System (1 paper)The Journal of Pediatrics (1 paper)Neonatology (1 paper)
- Partner nations
- TürkiyeUnited StatesPoland
In The Last Decade
Derya Erçal
38 papers receiving 323 citations
Peers
Comparison fields: 5 of 71
- Pediatrics, Perinatology and Child Health 117
- Periodontics 24
- Genetics 123
- Genetics 28
- Psychiatry and Mental health 38
Countries citing papers authored by Derya Erçal
This map shows the geographic impact of Derya Erçal'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 Derya Erçal with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Derya Erçal more than expected).
Fields of papers citing papers by Derya Erçal
This network shows the impact of papers produced by Derya Erçal. 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 Derya Erçal. The network helps show where Derya Erçal may publish in the future.
Co-authors
The 25 scholars most cited alongside Derya Erçal, 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 41 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2015 | 49 | |
| 2 | 2009 | 36 | |
| 3 | 2003 | 27 | |
| 4 | 1993 | 27 | |
| 5 | 2010 | 26 | |
| 6 | 2014 | 19 | |
| 7 | 2015 | 16 | |
| 8 | 2018 | 13 | |
| 9 | 2008 | 12 | |
| 10 | 2021 | 10 | |
| 11 | 2019 | 10 | |
| 12 | 2012 | 9 | |
| 13 | 1996 | 7 | |
| 14 | 1998 | 7 | |
| 15 | 2017 | 7 | |
| 16 | Goldston syndrome: report of a case. | 2001 | 6 |
| 17 | Deletion analysis and clinical correlations in patients with Xp21 linked muscular dystrophy. | 2005 | 6 |
| 18 | 2018 | 5 | |
| 19 | 2002 | 5 | |
| 20 | 2011 | 5 |
About Derya Erçal
Derya Erçal is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Genetics and Pulmonary and Respiratory Medicine, having authored 41 papers that have together received 341 indexed citations. Recurring topics across this work include Sexual Differentiation and Disorders (5 papers), Genomic variations and chromosomal abnormalities (5 papers), Prenatal Screening and Diagnostics (5 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers), Chromosomal and Genetic Variations (4 papers), Tumors and Oncological Cases (3 papers), Epilepsy research and treatment (3 papers) and Genomics and Rare Diseases (3 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (117 citations), Periodontics (24 citations), Genetics (123 citations), Genetics (28 citations) and Psychiatry and Mental health (38 citations). Derya Erçal has collaborated with scholars based in Türkiye, United States and Poland. Frequent co-authors include Semra Gürsoy, Hasan Özkan, Nuray Duman, Abdullah Kumral, Cihangir Özkınay, Ferda Özkınay, Ece Böber, İlhan Tezcan, Barış Altay and Özgür Çoğulu. Their work appears in journals such as Pediatric Neurology, HORMONES, Child s Nervous System, The Journal of Pediatrics and Neonatology.
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.