Derya Erçal
Impact in
-
- Neonatal Health and Biochemistry
- Prenatal Screening and Diagnostics
- Periodontics top 10%
Papers in
- Genetics 18
- Genomic variations and chromosomal abnormalities 6
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 4
- Congenital Ear and Nasal Anomalies 3
- Genomics and Rare Diseases 3
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- Sexual Differentiation and Disorders 4
- Co-authors
- Semra Gürsoy (9 shared papers)Abdullah Kumral (2 shared papers)Nuray Duman (2 shared papers)Hasan Özkan (5 shared papers)Ece Böber (5 shared papers)İlhan Tezcan (1 shared paper)Fügen Ersoy (1 shared paper)Ferda Özkınay (4 shared papers)
- Journals
- Pediatric Neurology (3 papers)HORMONES (2 papers)Cytogenetic and Genome Research (2 papers)Child s Nervous System (1 paper)Journal of Assisted Reproduction and Genetics (1 paper)
- Partner nations
- TürkiyeUnited StatesGermany
In The Last Decade
Derya Erçal
40 papers receiving 344 citations
Peers
Comparison fields: 5 of 63
- Pediatrics, Perinatology and Child Health 98
- Periodontics 23
- Genetics 114
- Endocrine and Autonomic Systems 15
- Genetics 22
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 45 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2015 | 55 | |
| 2 | 2009 | 36 | |
| 3 | 2003 | 28 | |
| 4 | 2010 | 28 | |
| 5 | 1993 | 28 | |
| 6 | 2014 | 22 | |
| 7 | 2015 | 17 | |
| 8 | 2018 | 15 | |
| 9 | 2008 | 12 | |
| 10 | 2019 | 11 | |
| 11 | 2021 | 10 | |
| 12 | 1998 | 9 | |
| 13 | 2012 | 9 | |
| 14 | 1996 | 8 | |
| 15 | 2002 | 7 | |
| 16 | 2017 | 7 | |
| 17 | 2018 | 6 | |
| 18 | Deletion analysis and clinical correlations in patients with Xp21 linked muscular dystrophy. | 2005 | 6 |
| 19 | Goldston syndrome: report of a case. | 2001 | 6 |
| 20 | 2011 | 5 |
About Derya Erçal
Derya Erçal is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Pulmonary and Respiratory Medicine and Genetics, having authored 45 papers that have together received 369 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (6 papers), Genomic variations and chromosomal abnormalities (6 papers), Chromosomal and Genetic Variations (5 papers), Sexual Differentiation and Disorders (4 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers), Tumors and Oncological Cases (4 papers), Congenital Ear and Nasal Anomalies (3 papers) and Genomics and Rare Diseases (3 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (98 citations), Periodontics (23 citations), Genetics (114 citations), Endocrine and Autonomic Systems (15 citations) and Genetics (22 citations). Derya Erçal has collaborated with scholars based in Türkiye, United States and Germany. Frequent co-authors include Semra Gürsoy, Abdullah Kumral, Nuray Duman, Hasan Özkan, Ece Böber, İlhan Tezcan, Fügen Ersoy, Ferda Özkınay, Cihangir Özkınay and A Büyükgebiz. Their work appears in journals such as Pediatric Neurology, HORMONES, Cytogenetic and Genome Research, Child s Nervous System and Journal of Assisted Reproduction and 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.