Derya Erçal

515 total citations
41 papers, 341 citations indexed

About

Derya Erçal is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Derya Erçal has authored 41 papers receiving a total of 341 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 16 papers in Molecular Biology and 10 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Derya Erçal's work include Sexual Differentiation and Disorders (5 papers), Prenatal Screening and Diagnostics (5 papers) and Genomic variations and chromosomal abnormalities (5 papers). Derya Erçal is often cited by papers focused on Sexual Differentiation and Disorders (5 papers), Prenatal Screening and Diagnostics (5 papers) and Genomic variations and chromosomal abnormalities (5 papers). Derya Erçal collaborates with scholars based in Türkiye, United States and Spain. Derya Erçal's co-authors include Semra Gürsoy, Hasan Özkan, Nuray Duman, Abdullah Kumral, İlhan Tezcan, Ece Böber, Ferda Özkınay, Cihangir Özkınay, Özgür Çoğulu and Erol Tavmergen and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Journal of Pediatrics and Acta Paediatrica.

In The Last Decade

Derya Erçal

38 papers receiving 323 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Derya Erçal Türkiye 11 135 123 117 38 37 41 341
Linda Gailīte Latvia 12 155 1.1× 142 1.2× 68 0.6× 16 0.4× 36 1.0× 67 437
Giuseppina Zirilli Italy 16 90 0.7× 125 1.0× 74 0.6× 14 0.4× 84 2.3× 48 589
Lokesh Lingappa India 10 132 1.0× 86 0.7× 77 0.7× 43 1.1× 25 0.7× 44 366
Nidhi Shah United States 12 96 0.7× 136 1.1× 59 0.5× 23 0.6× 23 0.6× 40 339
Alba Pilotta Italy 15 229 1.7× 268 2.2× 86 0.7× 15 0.4× 63 1.7× 26 586
Pooja Singh India 8 67 0.5× 35 0.3× 20 0.2× 36 0.9× 43 1.2× 58 280
Lilien Chertkoff Argentina 14 165 1.2× 194 1.6× 76 0.6× 13 0.3× 85 2.3× 31 479
Doman K. Keele United States 11 206 1.5× 123 1.0× 50 0.4× 18 0.5× 33 0.9× 20 441
Frédérique Tihy Canada 11 120 0.9× 215 1.7× 146 1.2× 14 0.4× 30 0.8× 18 384
Lucila Sandoval Mexico 10 53 0.4× 118 1.0× 68 0.6× 20 0.5× 22 0.6× 18 308

Countries citing papers authored by Derya Erçal

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Derya Erçal

This figure shows the co-authorship network connecting the top 25 collaborators of Derya Erçal. A scholar is included among the top collaborators of Derya Erçal based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Derya Erçal. Derya Erçal is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Arslan, Nur, et al.. (2021). Serum motilin levels and motilin gene polymorphisms in children with functional constipation. Minerva Pediatrics. 73(5). 420–425. 10 indexed citations
2.
Gürsoy, Semra, Pınar Gençpınar, Uluç Yiş, et al.. (2020). Identification of PCDH19 gene mutations/deletions in patients with early onset epilepsy. Annals of Indian Academy of Neurology. 23(2). 206–206. 1 indexed citations
3.
Urreizti, Roser, Semra Gürsoy, Raquel Rabionet, et al.. (2018). The ASXL1 mutation p.Gly646Trpfs*12 found in a Turkish boy with Bohring‐Opitz Syndrome. Clinical Case Reports. 6(8). 1452–1456. 5 indexed citations
4.
Gürsoy, Semra & Derya Erçal. (2018). Genetic Evaluation of Common Neurocutaneous Syndromes. Pediatric Neurology. 89. 3–10. 13 indexed citations
5.
Çankaya, Tufan, Semra Gürsoy, Altuğ Koç, et al.. (2017). Two Cases with Ring Chromosome 13 at either End of the Phenotypic Spectrum. Cytogenetic and Genome Research. 153(4). 175–180. 2 indexed citations
6.
Gürsoy, Semra, et al.. (2017). Expanding spectrum of SCN1A-related phenotype with novel mutations. The Turkish Journal of Pediatrics. 59(5). 570–575. 1 indexed citations
7.
Karaca, İrfan, et al.. (2014). Surgical management of complete penile duplication accompanied by multiple anomalies. Canadian Urological Association Journal. 8(9-10). 741–741. 4 indexed citations
8.
Şımşek, İlkay, et al.. (2013). Alpha-2-adrenergic receptor gene polymorphism in Turkish population with irritable bowel syndrome. The Turkish Journal of Gastroenterology. 24(6). 483–488. 3 indexed citations
9.
Uzuner, Nevin, et al.. (2012). Plasminogen activator inhibitor-1 and angiotensin converting enzyme gene polymorphisms in Turkish asthmatic children. Allergologia et Immunopathologia. 41(1). 11–16. 9 indexed citations
10.
Akıncı, Gülçin, et al.. (2011). Multi-cystic white matter enlarged Virchow Robin spaces in a 5-year-old boy. Child s Nervous System. 28(5). 743–746. 5 indexed citations
11.
Kumral, Abdullah, et al.. (2010). Prolonged unconjugated hyperbilirubinaemia associated with the haem oxygenase‐1 gene promoter polymorphism. Acta Paediatrica. 99(5). 679–683. 26 indexed citations
12.
Özkınay, Ferda, Derya Erçal, Özgür Çoğulu, et al.. (2009). Cytogenetic abnormalities in 179 cases with male infertility in Western Region of Turkey: Report and review. Journal of Assisted Reproduction and Genetics. 26(2-3). 119–122. 36 indexed citations
13.
Ünalp, Aycan, et al.. (2008). Role of Apolipoprotein E in Febrile Convulsion. Pediatric Neurology. 39(4). 241–244. 4 indexed citations
14.
Türkmen, Mehmet, Belde Kasap, Sezgin Güneş, et al.. (2008). Growth in Familial Mediterranean Fever: Effect of Attack Rate, Genotype and Colchicine Treatment. Journal of Pediatric Endocrinology and Metabolism. 21(8). 789–92. 12 indexed citations
15.
Ünalp, Aycan, et al.. (2007). A Case of Wolf-Hirschhorn Syndrome Progressing to Resistant Epilepsy. Pediatric Neurology. 37(2). 140–143. 3 indexed citations
16.
Erçal, Derya, et al.. (2005). Çocuk Sağlığı ve Prenatal Tanı. 1(2). 68–72. 1 indexed citations
17.
Duman, Nuray, Frederick V. Schaefer, Hande Gülcan, et al.. (2003). Analyses of Polymorphism for UGT1*1 Exon 1 Promoter in Neonates with Pathologic and Prolonged Jaundice. Neonatology. 83(4). 258–262. 27 indexed citations
18.
Dündar, Bumin Nuri, Derya Erçal, Ece Böber, Till Berk, & A Büyükgebiz. (2002). Amelogenesis Imperfecta with Growth Hormone Deficiency in a 12 Year-Old Boy. Journal of Pediatric Endocrinology and Metabolism. 15(5). 659–62. 5 indexed citations
19.
Öner, F. Hakan, et al.. (2002). Electroretinographic findings in Duchenne/Becker muscular dystrophy and correlation with genotype. Ophthalmic Genetics. 23(3). 157–165. 3 indexed citations
20.
Tezcan, İlhan, et al.. (1993). Neutrophil Chemotaxis and Periodontal Status in Down's Syndrome Patients.. The Journal of Nihon University School of Dentistry. 35(2). 91–95. 27 indexed citations

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.

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