Edip Ünal

666 total citations
43 papers, 272 citations indexed

About

Edip Ünal is a scholar working on Endocrinology, Diabetes and Metabolism, Molecular Biology and Genetics. According to data from OpenAlex, Edip Ünal has authored 43 papers receiving a total of 272 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Endocrinology, Diabetes and Metabolism, 21 papers in Molecular Biology and 15 papers in Genetics. Recurrent topics in Edip Ünal's work include Sexual Differentiation and Disorders (11 papers), Thyroid Disorders and Treatments (10 papers) and Diabetes and associated disorders (6 papers). Edip Ünal is often cited by papers focused on Sexual Differentiation and Disorders (11 papers), Thyroid Disorders and Treatments (10 papers) and Diabetes and associated disorders (6 papers). Edip Ünal collaborates with scholars based in Türkiye, United States and Germany. Edip Ünal's co-authors include Ruken Yıldırım, Mustafa Korman, Mehmet Nuri Özbek, Mustafa Taşkın, Kürşad Zengın, Hüseyin Demirbilek, Hüseyin Önay, İsmail Yıldız, Mehmet Türe and Serdar Ceylaner and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Journal of Clinical Endocrinology & Metabolism and Scientific Reports.

In The Last Decade

Edip Ünal

38 papers receiving 263 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Edip Ünal Türkiye 9 104 89 85 76 33 43 272
Jørgen Knudtzon Norway 7 94 0.9× 134 1.5× 117 1.4× 87 1.1× 12 0.4× 14 319
Antonia Dastamani United Kingdom 9 86 0.8× 67 0.8× 48 0.6× 202 2.7× 29 0.9× 31 263
Francesco Medici Italy 6 73 0.7× 137 1.5× 105 1.2× 116 1.5× 18 0.5× 17 272
Ruken Yıldırım Türkiye 9 98 0.9× 68 0.8× 26 0.3× 61 0.8× 6 0.2× 29 197
J. Douglas Smith United States 8 140 1.3× 100 1.1× 84 1.0× 66 0.9× 79 2.4× 10 418
Mallory L. Downie Canada 8 70 0.7× 27 0.3× 56 0.7× 24 0.3× 71 2.2× 22 259
V. Fattorusso Italy 9 38 0.4× 98 1.1× 58 0.7× 59 0.8× 23 0.7× 17 256
Stéphane Affenberger France 5 53 0.5× 48 0.5× 60 0.7× 46 0.6× 8 0.2× 7 339
Mohammed Didi United Kingdom 8 42 0.4× 58 0.7× 73 0.9× 214 2.8× 36 1.1× 19 271
Sa. Muntoni Italy 8 47 0.5× 100 1.1× 80 0.9× 116 1.5× 14 0.4× 12 255

Countries citing papers authored by Edip Ünal

Since Specialization
Citations

This map shows the geographic impact of Edip Ünal'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 Edip Ünal with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Edip Ünal more than expected).

Fields of papers citing papers by Edip Ünal

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Edip Ünal. 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 Edip Ünal. The network helps show where Edip Ünal may publish in the future.

Co-authorship network of co-authors of Edip Ünal

This figure shows the co-authorship network connecting the top 25 collaborators of Edip Ünal. A scholar is included among the top collaborators of Edip Ünal 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 Edip Ünal. Edip Ünal 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.
Ünal, Edip, Atilla Çayır, Esra Deniz Papatya Çakır, et al.. (2025). Phenotypes Linked to Duplication Upstream of SOX9: New Insights Into Presentation and Diagnosis. The Journal of Clinical Endocrinology & Metabolism. 110(10). e3482–e3488. 1 indexed citations
2.
Ünal, Edip, et al.. (2024). Retrospective evaluation of patients diagnosed with central precocious puberty who reached the final height. Journal of Pediatric Endocrinology and Metabolism. 37(8). 715–721. 1 indexed citations
3.
Yıldırım, Ruken, et al.. (2024). Clinical and molecular spectrum along with genotype–phenotype correlation of 25 patients diagnosed with 3 M syndrome: a study from Turkey. European Journal of Pediatrics. 184(1). 68–68. 1 indexed citations
4.
5.
Çayır, Atilla, et al.. (2022). A rare cause of primary amenorrhea: LHCGR gene mutations. European Journal of Obstetrics & Gynecology and Reproductive Biology. 272. 193–197. 3 indexed citations
6.
Yıldırım, Ruken, et al.. (2022). Revisiting the Annual Incidence of Type 1 Diabetes Mellitus in Children from the Southeastern Anatolian Region of Turkey: A Regional Report. Journal of Clinical Research in Pediatric Endocrinology. 14(2). 172–178. 3 indexed citations
7.
Bolu, Semih, et al.. (2021). A rare cause of delayed puberty and primary amenorrhea: 17α-hydroxylase enzyme deficiency. Endocrine. 75(3). 927–933. 6 indexed citations
8.
Türe, Mehmet, et al.. (2021). The association between electrocardiographic data and obesity in children and adolescents. Minerva Pediatrics. 2 indexed citations
9.
10.
Demirbilek, Hüseyin, Atilla Çayır, Doğuş Vurallı, et al.. (2020). Identification of Three Novel and One Known Mutation in the WFS1 Gene in Four Unrelated Turkish Families: The Role of Homozygosity Mapping in the Early Diagnosis. Journal of Clinical Research in Pediatric Endocrinology. 13(1). 34–43. 2 indexed citations
11.
Ünal, Edip, et al.. (2020). Validity of Six Month L-Thyroxine Dose for Differentiation of Transient or Permanent Congenital Hypothyroidism. Journal of Clinical Research in Pediatric Endocrinology. 12(3). 275–280. 15 indexed citations
12.
Ünal, Edip, et al.. (2020). Frequency of Celiac Disease and Spontaneous Normalization Rate of Celiac Serology in Children and Adolescent Patients with Type 1 Diabetes. Journal of Clinical Research in Pediatric Endocrinology. 13(1). 72–79. 20 indexed citations
13.
14.
Ünal, Edip, et al.. (2020). Incidence of Autoimmune Thyroid Disease in Patients with Type 1 Diabetes. Güncel Pediatri. 18(2). 251–262.
15.
16.
Erdeve, Şenay Savaş, Zehra Aycan, Semra Çeti̇nkaya, et al.. (2020). Clinical Characteristics of 46,XX Males with Congenital Adrenal Hyperplasia. Journal of Clinical Research in Pediatric Endocrinology. 13(2). 180–186. 2 indexed citations
17.
Demirbilek, Hüseyin, et al.. (2019). Ectopic Posterior Pituitary, Polydactyly, Midfacial Hypoplasia and Multiple Pituitary Hormone Deficiency due to a Novel Heterozygous IVS11-2A>C(c.1957-2A>C) Mutation in the <i>GLI2</i> Gene. Journal of Clinical Research in Pediatric Endocrinology. 12(3). 319–328. 6 indexed citations
18.
Ünal, Edip, et al.. (2018). A rare cause of neonatal hypoglycemia in two siblings: TBX19 gene mutation. HORMONES. 17(2). 269–273. 10 indexed citations
19.
Ullah, Asmat, Julián Nevado, Ruken Yıldırım, et al.. (2017). GLI1 inactivation is associated with developmental phenotypes overlapping with Ellis–van Creveld syndrome. Human Molecular Genetics. 26(23). 4556–4571. 39 indexed citations
20.
Ünal, Edip, et al.. (2016). Association of Subclinical Hypothyroidism with Dyslipidemia and Increased Carotid Intima-Media Thickness in Children. Journal of Clinical Research in Pediatric Endocrinology. 9(2). 144–149. 28 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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