Erdal Kurnaz

420 total citations
39 papers, 242 citations indexed

About

Erdal Kurnaz is a scholar working on Molecular Biology, Genetics and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Erdal Kurnaz has authored 39 papers receiving a total of 242 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 10 papers in Genetics and 8 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Erdal Kurnaz's work include Sexual Differentiation and Disorders (8 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers) and Parathyroid Disorders and Treatments (4 papers). Erdal Kurnaz is often cited by papers focused on Sexual Differentiation and Disorders (8 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers) and Parathyroid Disorders and Treatments (4 papers). Erdal Kurnaz collaborates with scholars based in Türkiye, United Kingdom and United States. Erdal Kurnaz's co-authors include Zehra Aycan, Semra Çeti̇nkaya, Şenay Savaş Erdeve, Elvan Bayramoğlu, Merve İnanç, Mustafa Koç, Emre Aydemır, Kemal Tekin, Atilla Çayır and Hasan Kızıltoprak and has published in prestigious journals such as SHILAP Revista de lepidopterología, Human Molecular Genetics and American Journal of Ophthalmology.

In The Last Decade

Erdal Kurnaz

35 papers receiving 239 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Erdal Kurnaz Türkiye 10 91 62 48 48 40 39 242
Saygın Abalı Türkiye 11 95 1.0× 94 1.5× 40 0.8× 106 2.2× 42 1.1× 39 317
Ingrid Rietveld Netherlands 10 160 1.8× 65 1.0× 98 2.0× 198 4.1× 88 2.2× 12 414
Danyan Liu China 9 45 0.5× 26 0.4× 66 1.4× 7 0.1× 73 1.8× 30 280
Irene Weiss United States 11 53 0.6× 41 0.7× 46 1.0× 196 4.1× 34 0.8× 15 330
Anna Syreeni Australia 8 57 0.6× 63 1.0× 11 0.2× 45 0.9× 29 0.7× 15 172
B Mirkiewicz-Sieradzka Poland 7 53 0.6× 32 0.5× 46 1.0× 51 1.1× 70 1.8× 17 232
Mateusz Jagła Poland 10 76 0.8× 35 0.6× 35 0.7× 46 1.0× 4 0.1× 28 343
Kim Lawson United States 7 38 0.4× 80 1.3× 25 0.5× 57 1.2× 22 0.6× 9 263
P. Rampini Italy 9 32 0.4× 18 0.3× 60 1.3× 218 4.5× 11 0.3× 19 368
Radhika Susarla United Kingdom 8 44 0.5× 13 0.2× 24 0.5× 23 0.5× 42 1.1× 16 323

Countries citing papers authored by Erdal Kurnaz

Since Specialization
Citations

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

Fields of papers citing papers by Erdal Kurnaz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Erdal Kurnaz

This figure shows the co-authorship network connecting the top 25 collaborators of Erdal Kurnaz. A scholar is included among the top collaborators of Erdal Kurnaz 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 Erdal Kurnaz. Erdal Kurnaz 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.
2.
Kurnaz, Erdal, et al.. (2021). First Report of a de novo 10q23.31q23.33 Microdeletion: Obesity, Intellectual Disability and Microcephaly. Molecular Syndromology. 12(4). 258–262. 1 indexed citations
3.
Kurnaz, Erdal, et al.. (2021). The Spectrum of Low-Density Lipoprotein Receptor Mutations in a Large Turkish Cohort of Patients with Familial Hypercholesterolemia. Metabolic Syndrome and Related Disorders. 19(6). 340–346. 6 indexed citations
4.
Kurnaz, Erdal, Zehra Yavaş Abalı, Serap Turan, et al.. (2020). Genotypic Sex and Severity of the Disease Determine the Time of Clinical Presentation in Steroid 17α-Hydroxylase/17,20-Lyase Deficiency. Hormone Research in Paediatrics. 93(9-10). 558–566. 11 indexed citations
5.
Çayır, Atilla, et al.. (2019). Systemic Pseudohypoaldosteronism Type 1 due to 3 Novel Mutations in <b><i>SCNN1A</i></b>and <b><i>SCNN1B</i></b>Genes. Hormone Research in Paediatrics. 91(3). 175–185. 8 indexed citations
6.
Kurnaz, Erdal, et al.. (2019). Congenital long-QT syndrome in type 1 diabetes: a unique association. The Turkish Journal of Pediatrics. 61(5). 791–793. 2 indexed citations
7.
Kurnaz, Erdal, Semra Çeti̇nkaya, Şenay Savaş Erdeve, & Zehra Aycan. (2019). Detection of the SRY gene in patients with Turner Syndrome. Journal of Gynecology Obstetrics and Human Reproduction. 48(4). 265–267. 1 indexed citations
8.
Bayramoğlu, Elvan, H. Nursun Özcan, Erdal Kurnaz, et al.. (2019). Antimüllerian Hormone Levels of Infants with Premature Thelarche. Journal of Clinical Research in Pediatric Endocrinology. 11(3). 287–292. 3 indexed citations
9.
Erdeve, Şenay Savaş, et al.. (2018). Follow-up in children with non-obese and non-autoimmune subclinical hypothyroidism. Journal of Pediatric Endocrinology and Metabolism. 31(10). 1133–1138. 7 indexed citations
10.
Kurnaz, Erdal, Şenay Savaş Erdeve, Semra Çeti̇nkaya, & Zehra Aycan. (2018). SHOX gene deletion screening by FISH in children with short stature and Madelung deformity and their characteristics. Journal of Pediatric Endocrinology and Metabolism. 0(0). 1273–1278. 2 indexed citations
11.
Kurnaz, Erdal, Şenay Savaş Erdeve, Semra Çeti̇nkaya, & Zehra Aycan. (2018). Rare Cause of Infantile Hypercalcemia: A Novel Mutation in the SLC34A1 Gene. Hormone Research in Paediatrics. 91(4). 278–284. 9 indexed citations
12.
Aycan, Zehra, et al.. (2018). Investigation of MKRN3 Mutation in Patients with Familial Central Precocious Puberty. Journal of Clinical Research in Pediatric Endocrinology. 10(3). 223–229. 21 indexed citations
13.
14.
Kurnaz, Erdal, Zehra Aycan, Şenay Savaş Erdeve, et al.. (2017). Clinical and genetic characterisation of a series of patients with triple A syndrome. European Journal of Pediatrics. 177(3). 363–369. 17 indexed citations
15.
Çeti̇nkaya, Semra, Tülay Güran, Erdal Kurnaz, et al.. (2017). A Patient with Proopiomelanocortin Deficiency: An Increasingly Important Diagnosis to Make. Journal of Clinical Research in Pediatric Endocrinology. 10(1). 68–73. 12 indexed citations
16.
Kurnaz, Erdal, Yaşar Şen, & Süleyman Aydın. (2017). Plasma kisspeptin and ghrelin levels in puberty variant cases. Journal of Pediatric Endocrinology and Metabolism. 30(5). 569–573. 3 indexed citations
17.
İnanç, Merve, et al.. (2017). Evaluation of anterior segment parameters in patients with Turner syndrome using Scheimpflug imaging. Journal of American Association for Pediatric Ophthalmology and Strabismus. 22(1). 56–60. 1 indexed citations
18.
Erdeve, Şenay Savaş, Corinne Magdelaine, Anne Lienhardt-Roussie, et al.. (2016). Treatment Experience and Long-Term Follow-Up Data in Two Severe Neonatal Hyperparathyroidism Cases. 86. 2 indexed citations
19.
Erdeve, Şenay Savaş, et al.. (2016). The first childhood case with coexisting Hashimoto thyroiditis, vitiligo and autoimmune hepatitis. The Turkish Journal of Pediatrics. 58(4). 432–435. 2 indexed citations
20.
Kurnaz, Erdal, et al.. (2016). A case with atrophic autoimmune thyroiditis-related hypothyroidism causing multisystem involvement in early childhood. The Turkish Journal of Pediatrics. 58(4). 446–451. 3 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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