Ahmet Arman

600 total citations
38 papers, 442 citations indexed

About

Ahmet Arman is a scholar working on Molecular Biology, Immunology and Genetics. According to data from OpenAlex, Ahmet Arman has authored 38 papers receiving a total of 442 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 11 papers in Immunology and 9 papers in Genetics. Recurrent topics in Ahmet Arman's work include Growth Hormone and Insulin-like Growth Factors (5 papers), Genetic Syndromes and Imprinting (3 papers) and Adipokines, Inflammation, and Metabolic Diseases (3 papers). Ahmet Arman is often cited by papers focused on Growth Hormone and Insulin-like Growth Factors (5 papers), Genetic Syndromes and Imprinting (3 papers) and Adipokines, Inflammation, and Metabolic Diseases (3 papers). Ahmet Arman collaborates with scholars based in Türkiye, United States and Germany. Ahmet Arman's co-authors include Ajda Çoker Gürkan, Philip E. Auron, Arvind Kumar, Yasuhiro Yoshida, Haibing Peng, Jason A. Boch, Yoshinobu Koyama, Tuna Tezel, Nevsun İnanç and Haner Di̇reskeneli̇ and has published in prestigious journals such as Journal of Biological Chemistry, SHILAP Revista de lepidopterología and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Ahmet Arman

36 papers receiving 428 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ahmet Arman Türkiye 12 166 152 127 72 66 38 442
Sofia Töyrä Silfverswärd Sweden 11 105 0.6× 128 0.8× 57 0.4× 84 1.2× 37 0.6× 25 341
Burçak Vural Türkiye 12 251 1.5× 56 0.4× 92 0.7× 42 0.6× 47 0.7× 38 566
Taiki Morohashi Japan 9 178 1.1× 192 1.3× 61 0.5× 29 0.4× 57 0.9× 21 451
Sherryline Jogie‐Brahim United States 8 213 1.3× 121 0.8× 28 0.2× 63 0.9× 58 0.9× 10 563
Anthony Rousselle Germany 10 285 1.7× 282 1.9× 65 0.5× 40 0.6× 48 0.7× 16 703
Stefanie Tippmer Germany 9 271 1.6× 141 0.9× 166 1.3× 27 0.4× 65 1.0× 12 648
Makoto Hase Japan 8 321 1.9× 42 0.3× 80 0.6× 40 0.6× 56 0.8× 8 481
Hilmi Tozkır Türkiye 12 90 0.5× 99 0.7× 66 0.5× 47 0.7× 62 0.9× 43 371
Sara Rattik Sweden 13 159 1.0× 313 2.1× 52 0.4× 33 0.5× 31 0.5× 25 560
Anna Rogers United States 13 236 1.4× 83 0.5× 89 0.7× 25 0.3× 36 0.5× 15 679

Countries citing papers authored by Ahmet Arman

Since Specialization
Citations

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

Fields of papers citing papers by Ahmet Arman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ahmet Arman

This figure shows the co-authorship network connecting the top 25 collaborators of Ahmet Arman. A scholar is included among the top collaborators of Ahmet Arman 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 Ahmet Arman. Ahmet Arman 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.
Eltan, Sevgi Bilgiç, Asena Pınar Sefer, Tülay Güran, et al.. (2024). Expanding the Clinical Features of Schimke Immuno-Osseous Dysplasia: A New Patient with a Novel Variant and Novel Clinical Findings. Journal of Clinical Research in Pediatric Endocrinology. 17(2). 126–135. 1 indexed citations
2.
Abalı, Zehra Yavaş, et al.. (2023). Two new cases with novel pathogenic variants reflecting the clinical diversity of Schaaf‐Yang syndrome. Clinical Genetics. 104(1). 127–132. 1 indexed citations
3.
Geçkinli, Bilgen Bilge, et al.. (2022). Whole-exome sequencing reveals new potential genes and variants in patients with premature ovarian insufficiency. Journal of Assisted Reproduction and Genetics. 39(3). 695–710. 12 indexed citations
4.
Arman, Ahmet, et al.. (2022). Vitamin D receptor polymorphisms among the Turkish population are associated with multiple sclerosis. SHILAP Revista de lepidopterología. 25(1). 41–50. 5 indexed citations
5.
Arman, Ahmet, et al.. (2022). First Patient Diagnosed as Feingold Syndrome Type 2 with Alport Syndrome and Review of the Current Literature. Molecular Syndromology. 13(5). 447–453.
6.
Geçkinli, Bilgen Bilge, et al.. (2021). Meckel-Gruber Syndrome: Clinical and Molecular Genetic Profiles in Two Fetuses and Review of the Current Literature. Genetic Testing and Molecular Biomarkers. 25(6). 445–451. 6 indexed citations
7.
Abalı, Zehra Yavaş, İbrahim Gökçe, Saygın Abalı, et al.. (2021). Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis Due to CLDN16 Gene Mutations: Novel Findings in Two Cases with Diverse Clinical Features. Calcified Tissue International. 110(4). 441–450. 1 indexed citations
8.
Geçkinli, Bilgen Bilge, et al.. (2021). Biallelic Mutations in <b><i>DNAJB11</i></b>are Associated with Prenatal Polycystic Kidney Disease in a Turkish Family. Molecular Syndromology. 12(3). 179–185. 1 indexed citations
9.
List, Edward O., et al.. (2018). Association Between IL7R Promoter Polymorphisms and Multiple Sclerosis in Turkish Population. Journal of Molecular Neuroscience. 67(1). 38–47. 2 indexed citations
10.
Arman, Ahmet, Abdullah Bereket, Ajda Çoker Gürkan, et al.. (2014). Cathepsin K analysis in a pycnodysostosis cohort: demographic, genotypic and phenotypic features. Orphanet Journal of Rare Diseases. 9(1). 60–60. 34 indexed citations
11.
Arman, Ahmet, et al.. (2014). Novel Growth Hormone-Releasing Hormone Receptor Gene Mutations in Turkish Children with Isolated Growth Hormone Deficiency. Journal of Clinical Research in Pediatric Endocrinology. 6(4). 202–208. 6 indexed citations
12.
Gürkan, Ajda Çoker, et al.. (2011). Lack of association between IL-1 and IL-6 gene polymorphisms and myocardial infarction in Turkish population. International Journal of Immunogenetics. 38(3). 201–208. 31 indexed citations
13.
Arman, Ahmet, et al.. (2011). Lack of association between IL-6 gene polymorphisms and rheumatoid arthritis in Turkish population. Rheumatology International. 32(7). 2199–2201. 24 indexed citations
14.
Arman, Ahmet, et al.. (2010). Novel Growth Hormone Receptor Gene Mutation in a Patient with Laron Syndrome. Journal of Pediatric Endocrinology and Metabolism. 23(4). 407–14. 4 indexed citations
15.
Arman, Ahmet, et al.. (2008). Novel Splice Site Mutation in the Growth Hormone Receptor Gene in Turkish Patients with Laron-type Dwarfism. Journal of Pediatric Endocrinology and Metabolism. 21(1). 47–58. 8 indexed citations
16.
Arman, Ahmet, et al.. (2008). O polimorfismo VNTR no gene codificador do antagonista do receptor da interleucina-1 está associado com a doença arterial coronariana. Arquivos Brasileiros de Cardiologia. 91(5). 293–298. 18 indexed citations
17.
Arman, Ahmet, Mehmet Birhan Yılmaz, Ajda Çoker Gürkan, Nevsun İnanç, & Haner Di̇reskeneli̇. (2007). Interleukin-1 receptor antagonist (IL-1RN) and interleukin-1B gene polymorphisms in Turkish patients with rheumatoid arthritis.. PubMed. 24(6). 643–8. 27 indexed citations
18.
Yoshida, Yasuhiro, Arvind Kumar, Yoshinobu Koyama, et al.. (2004). Interleukin 1 Activates STAT3/Nuclear Factor-κB Cross-talk via a Unique TRAF6- and p65-dependent Mechanism. Journal of Biological Chemistry. 279(3). 1768–1776. 122 indexed citations
19.
Geçkil, Hikmet, Ahmet Arman, Salih Gencer, Burhan Ateş, & H. Ramazan Yılmaz. (2004). Vitreoscilla hemoglobin renders Enterobacter aerogenes highly susceptible to heavy metals. BioMetals. 17(6). 715–723. 3 indexed citations
20.
Arman, Ahmet & Philip E. Auron. (2003). Interleukin 1 (IL-1) Induces the Activation of Stat3. Advances in experimental medicine and biology. 534. 297–307. 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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