Eda Mengen

795 total citations
49 papers, 405 citations indexed

About

Eda Mengen is a scholar working on Molecular Biology, Genetics and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Eda Mengen has authored 49 papers receiving a total of 405 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 16 papers in Genetics and 15 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Eda Mengen's work include Hypothalamic control of reproductive hormones (9 papers), Connective tissue disorders research (5 papers) and Sexual Differentiation and Disorders (5 papers). Eda Mengen is often cited by papers focused on Hypothalamic control of reproductive hormones (9 papers), Connective tissue disorders research (5 papers) and Sexual Differentiation and Disorders (5 papers). Eda Mengen collaborates with scholars based in Türkiye, United States and Antigua and Barbuda. Eda Mengen's co-authors include Bilgin Yüksel, Fatih Gürbüz, A. Kemal Topaloğlu, Leman Damla Kotan, Seyit Ahmet Uçaktürk, B. Ian Hutchins, Susan Wray, İhsan Turan, Paul J. Cheng and Yusuf Özkan and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Journal of Clinical Endocrinology & Metabolism and Endocrinology.

In The Last Decade

Eda Mengen

40 papers receiving 403 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Eda Mengen Türkiye 11 165 161 161 65 39 49 405
Michaël W. Pankhurst New Zealand 16 85 0.5× 144 0.9× 400 2.5× 66 1.0× 17 0.4× 36 643
Jenny N. Fung Australia 21 79 0.5× 205 1.3× 369 2.3× 17 0.3× 32 0.8× 48 989
Margaret Au United States 14 348 2.1× 404 2.5× 478 3.0× 141 2.2× 85 2.2× 23 840
C. Foresta Italy 10 240 1.5× 261 1.6× 273 1.7× 69 1.1× 16 0.4× 16 479
Cecilia Martin United States 9 120 0.7× 171 1.1× 353 2.2× 82 1.3× 44 1.1× 10 517
Ali Al‐Odaib Saudi Arabia 15 171 1.0× 240 1.5× 19 0.1× 62 1.0× 22 0.6× 34 574
Leanne Wallace Australia 13 130 0.8× 118 0.7× 82 0.5× 15 0.2× 57 1.5× 21 591
Marietta Vértes Hungary 11 163 1.0× 148 0.9× 119 0.7× 57 0.9× 171 4.4× 45 495
Roberta B. Todd United States 12 164 1.0× 111 0.7× 198 1.2× 159 2.4× 49 1.3× 16 569
Delanie B. Macedo Brazil 15 354 2.1× 374 2.3× 432 2.7× 97 1.5× 15 0.4× 22 723

Countries citing papers authored by Eda Mengen

Since Specialization
Citations

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

Fields of papers citing papers by Eda Mengen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eda Mengen

This figure shows the co-authorship network connecting the top 25 collaborators of Eda Mengen. A scholar is included among the top collaborators of Eda Mengen 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 Eda Mengen. Eda Mengen 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.
Uçaktürk, Seyit Ahmet, et al.. (2025). Urinary plasminogen as an early marker of diabetic kidney disease in children with type 1 diabetes mellitus: a cross-sectional study. European Journal of Pediatrics. 184(7). 451–451. 1 indexed citations
2.
Turan, İhsan, et al.. (2025). Evaluation of the Relationship Between Thyroid Hormone Levels and Bisphenol A in Children Aged 6−14 Years. Clinical Endocrinology. 103(1). 97–105.
3.
Turan, İhsan, et al.. (2025). Optimal timing of repeat thyroid fine-needle aspiration biopsy. Journal of Pediatric Endocrinology and Metabolism. 38(5). 494–500.
4.
Mengen, Eda, et al.. (2025). A novel homozygous missense DNAJC3 variant in syndromic juvenile-onset diabetes. Journal of Pediatric Endocrinology and Metabolism. 38(9). 991–995.
5.
Ekinci, Rabia Miray Kışla, Sibel Balcı, Fatih Gürbüz, et al.. (2025). When it’s not juvenile idiopathic arthritis: unmasking monogenic mimickers in children. European Journal of Pediatrics. 184(12). 791–791.
6.
Uçar, Ahmet, Eda Mengen, & Zehra Aycan. (2024). Psychosocial Development, Sexuality and Quality of Life in Congenital Adrenal Hyperplasia. Journal of Clinical Research in Pediatric Endocrinology. 17(Suppl 1). 54–59. 1 indexed citations
7.
8.
Mengen, Eda, et al.. (2021). Tip 1 Diabetes Mellitus’lu Çocuk ve Adolesan Hastaların Retrospektif Olarak Değerlendirilmesi: Tek Merkez Deneyimi. Turkish Journal of Pediatric Disease. 15(2). 142–149.
9.
Mengen, Eda, et al.. (2019). A Duplication Upstream of SOX9 Associated with <i>SRY</i> Negative 46,XX Ovotesticular Disorder of Sex Development: A Case Report. Journal of Clinical Research in Pediatric Endocrinology. 12(3). 308–314. 6 indexed citations
10.
Mengen, Eda, et al.. (2019). A Rare Etiology of 46,XY Disorder of Sex Development and Adrenal Insufficiency: A Case of MIRAGE Syndrome Caused by Mutations in the <i>SAMD9</i> Gene. Journal of Clinical Research in Pediatric Endocrinology. 12(2). 206–211. 8 indexed citations
11.
Uçaktürk, Seyit Ahmet, et al.. (2019). Subclinical Myocardial Dysfunction Demonstrated by Speckle Tracking Echocardiography in Children with Euthyroid Hashimoto’s Thyroiditis. Journal of Clinical Research in Pediatric Endocrinology. 11(4). 410–418. 6 indexed citations
12.
Uçaktürk, Seyit Ahmet, et al.. (2019). Catecholamine-induced Myocarditis in a Child with Pheochromocytoma. Journal of Clinical Research in Pediatric Endocrinology. 12(2). 202–205. 2 indexed citations
13.
Uçaktürk, Seyit Ahmet, et al.. (2018). Dynamic Thiol/Disulphide Homeostasis in Children and Adolescents with Non-Autoimmune Subclinical Hypothyroidism. Medical Principles and Practice. 27(1). 44–48. 2 indexed citations
14.
Gürbüz, Fatih, et al.. (2017). Kronik karaciğer hastalığı olan çocukların D vitamini düzeyleri. SHILAP Revista de lepidopterología. 43(4). 1–1. 1 indexed citations
15.
Kotan, Leman Damla, Charlton Cooper, Şükran Darcan, et al.. (2016). Idiopathic Hypogonadotrophic Hypogonadism Caused by Inactivating Mutations in SRA1. 86. 1 indexed citations
16.
Kotan, Leman Damla, Charlton Cooper, Şükran Darcan, et al.. (2016). Idiopathic Hypogonadotropic Hypogonadism Caused by Inactivating Mutations in SRA1. Journal of Clinical Research in Pediatric Endocrinology. 8(2). 125–134. 21 indexed citations
17.
Akkuş, Gamze, Leman Damla Kotan, Erdem Durmaz, et al.. (2016). Hypogonadotropic Hypogonadism due to Novel FGFR1 Mutations. Journal of Clinical Research in Pediatric Endocrinology. 9(2). 95–100. 6 indexed citations
18.
Mungan, Neslihan Önenli, et al.. (2014). Evaluation of Two Different Pamidronate Treatment Protocols in Children with Osteogenesis Imperfecta. SHILAP Revista de lepidopterología. 1 indexed citations
19.
Mungan, Neslihan Önenli, et al.. (2013). Ostegenezis İmperfekta Olan Çocuklarda Pamidronat ve Kalsitonin Tedavilerinin Karşılaştırılması. SHILAP Revista de lepidopterología. 3 indexed citations
20.
Yüksel, Bilgin, Alexandra Kulle, Fatih Gürbüz, et al.. (2013). The Novel Mutation p.Trp147Arg of the Steroidogenic Acute Regulatory Protein Causes Classic Lipoid Congenital Adrenal Hyperplasia with Adrenal Insufficiency and 46,XY Disorder of Sex Development. Hormone Research in Paediatrics. 80(3). 163–169. 7 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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