Davut Gül

1.1k total citations
28 papers, 246 citations indexed

About

Davut Gül is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Davut Gül has authored 28 papers receiving a total of 246 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 9 papers in Genetics and 6 papers in Surgery. Recurrent topics in Davut Gül's work include Inflammasome and immune disorders (5 papers), interferon and immune responses (3 papers) and Gout, Hyperuricemia, Uric Acid (3 papers). Davut Gül is often cited by papers focused on Inflammasome and immune disorders (5 papers), interferon and immune responses (3 papers) and Gout, Hyperuricemia, Uric Acid (3 papers). Davut Gül collaborates with scholars based in Türkiye, Serbia and United States. Davut Gül's co-authors include Erkan Demirkaya, Bekir Sıtkı Şaylı, Faysal Gök, Çağatay Öktenli, Yusuf Tunca, Seza Özen, Erdal Gökçay, Ismail H. Kocar, Jennifer J. Johnston and Selçuk Işık and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Journal of Clinical Endocrinology & Metabolism and Progress in Neuro-Psychopharmacology and Biological Psychiatry.

In The Last Decade

Davut Gül

24 papers receiving 235 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Davut Gül Türkiye 10 121 58 55 53 47 28 246
J.P. Leroy France 12 112 0.9× 59 1.0× 18 0.3× 32 0.6× 67 1.4× 26 336
Pauline Krug France 8 53 0.4× 35 0.6× 42 0.8× 41 0.8× 73 1.6× 17 235
Toshinori Fujino Japan 10 77 0.6× 27 0.5× 65 1.2× 23 0.4× 48 1.0× 17 349
Jill Gianettoni United States 5 51 0.4× 43 0.7× 81 1.5× 23 0.4× 19 0.4× 8 188
Nisha A. McConnell United States 5 240 2.0× 61 1.1× 30 0.5× 11 0.2× 44 0.9× 6 387
Zhaotong Lin United States 7 95 0.8× 136 2.3× 22 0.4× 21 0.4× 20 0.4× 16 249
Francisco Lendínez Spain 9 105 0.9× 17 0.3× 51 0.9× 48 0.9× 20 0.4× 18 323
Oğuz Çilingir Türkiye 8 87 0.7× 47 0.8× 16 0.3× 12 0.2× 14 0.3× 39 166
James P. Kersey United Kingdom 9 56 0.5× 27 0.5× 12 0.2× 23 0.4× 31 0.7× 13 493
Gianfranco Ciboddo Italy 8 66 0.5× 27 0.5× 232 4.2× 77 1.5× 24 0.5× 17 376

Countries citing papers authored by Davut Gül

Since Specialization
Citations

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

Fields of papers citing papers by Davut Gül

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Davut Gül

This figure shows the co-authorship network connecting the top 25 collaborators of Davut Gül. A scholar is included among the top collaborators of Davut Gül 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 Davut Gül. Davut Gül 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.
Sarı, İ̇smail, İsmail Şimşek, Yusuf Tunca, et al.. (2015). Is there a relationship between gouty arthritis and Mediterranean fever gene mutations?. Revista Brasileira de Reumatologia (English Edition). 55(4). 325–329. 5 indexed citations
2.
Çeti̇nkaya, Rıza Aytaç, et al.. (2014). Bombay Blood Group in a Turkish Family: Serological and Molecular Analysis. Indian Journal of Hematology and Blood Transfusion. 31(3). 396–397. 1 indexed citations
3.
Sarı, İ̇smail, İsmail Şimşek, Yusuf Tunca, et al.. (2014). Existe uma relação entre a artrite gotosa e as mutações genéticas da febre familiar do Mediterrâneo?. Revista Brasileira de Reumatologia. 55(4). 325–329. 4 indexed citations
4.
Uyar, İbrahim, et al.. (2012). Heterotopic brain tissue on the face and neck in a neonate: A rare case report and literature review. The Journal of Maternal-Fetal & Neonatal Medicine. 26(6). 619–621. 4 indexed citations
5.
Vurucu, Sebahattin, Erkan Demirkaya, Mustafa Kul, et al.. (2008). Evaluation of the relationship between C677T variants of methylenetetrahydrofolate reductase gene and hyperhomocysteinemia in children receiving antiepileptic drug therapy. Progress in Neuro-Psychopharmacology and Biological Psychiatry. 32(3). 844–848. 29 indexed citations
6.
Çam, Fethi Sırrı, et al.. (2008). Analysis of the dermatoglyphics in Turkish patients with Klinefelter's syndrome. Hereditas. 145(4). 163–166. 3 indexed citations
7.
Ulucan, Hakan, et al.. (2008). Extending the spectrum of Ellis van Creveld syndrome: a large family with a mild mutation in the EVCgene. BMC Medical Genetics. 9(1). 92–92. 22 indexed citations
8.
Demirkaya, Erkan, Yusuf Tunca, Faysal Gök, Seza Özen, & Davut Gül. (2007). A very frequent mutation and remarkable association of R761H with M694V mutations in Turkish familial Mediterranean fever patients. Clinical Rheumatology. 27(6). 729–732. 31 indexed citations
9.
Öktenli, Çağatay, et al.. (2007). The rate of pyrin mutations in critically ill patients with systemic inflammatory response syndrome and sepsis: a pilot study.. PubMed. 34(10). 2070–5. 16 indexed citations
10.
Şengezer, Mustafa, et al.. (2005). The Correction of Auricular and Mandibular Deformities in Auriculo-Condylar Syndrome. Journal of Craniofacial Surgery. 16(3). 489–492. 16 indexed citations
11.
Sakallıoğlu, Onur, et al.. (2005). The phenotype–genotype correlations of FMF patients: a single center study. Rheumatology International. 26(7). 638–640. 7 indexed citations
12.
Bahçe, Muhterem, et al.. (2004). Partial trisomy 18q11.2→qter due to de novo unbalanced translocation of chromosomes 15 and 18 analyzed by fluorescence in situ hybridization. Annales de Génétique. 47(4). 393–398. 1 indexed citations
13.
Öztürk, Serdar, et al.. (2004). Situs Inversus Totalis With Accompanying Craniodiaphysial Dysplasia: A New Syndrome?. Journal of Craniofacial Surgery. 15(5). 865–869. 2 indexed citations
14.
Öktenli, Çağatay, Davut Gül, Mutlu Sağlam, et al.. (2004). Unusual features in a patient with neurofibromatosis type 1: Multiple subcutaneous lipomas, a juvenile polyp in ascending colon, congenital intrahepatic portosystemic venous shunt, and horseshoe kidney. American Journal of Medical Genetics Part A. 127A(3). 298–301. 20 indexed citations
15.
Öktenli, Çağatay, Zeki Yeşilova, Ismail H. Kocar, et al.. (2002). Study of Autoimmunity in Klinefelter's Syndrome and Idiopathic Hypogonadotropic Hypogonadism. Journal of Clinical Immunology. 22(3). 137–143. 24 indexed citations
16.
Öktenli, Çağatay, et al.. (2002). Saethre-Chotzen Syndrome Presenting with Incomplete Renal Fanconi Syndrome. ˜The œNephron journals/Nephron journals. 92(2). 463–465. 1 indexed citations
17.
Çağlayan, Sinan, Metin Özata, Gökhan Özışık, et al.. (2001). Plasma Melatonin Concentration before and during Testosterone Replacement in Klinefelter’s Syndrome: Relation to Hepatic Indolamine Metabolism and Sympathoadrenal Activity. The Journal of Clinical Endocrinology & Metabolism. 86(2). 738–743. 12 indexed citations
18.
Gül, Davut, Çağatay Öktenli, Mutlu Sağlam, & Üzeyir Erdem. (2000). Craniofacial anomalies, ocular findings, pigmented nevi, camptodactyly, and skeletal changes. Clinical Dysmorphology. 9(1). 61–62.
19.
Gül, Davut & Bekir Sıtkı Şaylı. (1994). Klinefelter Syndrome Associated with 13/14 Translocation Abnormality 46, XXY, t(13q;14q). Urologia Internationalis. 52(3). 166–168. 3 indexed citations
20.
Şaylı, Bekir Sıtkı & Davut Gül. (1993). GAPO syndrome in three relatives in a Turkish kindred. American Journal of Medical Genetics. 47(3). 342–345. 16 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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