İlyas Okur

836 total citations
62 papers, 372 citations indexed

About

İlyas Okur is a scholar working on Rheumatology, Physiology and Molecular Biology. According to data from OpenAlex, İlyas Okur has authored 62 papers receiving a total of 372 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Rheumatology, 20 papers in Physiology and 17 papers in Molecular Biology. Recurrent topics in İlyas Okur's work include Lysosomal Storage Disorders Research (16 papers), Glycogen Storage Diseases and Myoclonus (16 papers) and Metabolism and Genetic Disorders (14 papers). İlyas Okur is often cited by papers focused on Lysosomal Storage Disorders Research (16 papers), Glycogen Storage Diseases and Myoclonus (16 papers) and Metabolism and Genetic Disorders (14 papers). İlyas Okur collaborates with scholars based in Türkiye, United States and United Kingdom. İlyas Okur's co-authors include Leyla Tümer, Alev Hasanoğlu, Fatih Süheyl Ezgü, Gürsel Biberoğlu, Fatma Tuba Eminoğlu, Çiğdem Seher Kasapkara, Patrizia Tarugi, M. Mahmood Hussain, Meghan T. Walsh and Enza Di Leo and has published in prestigious journals such as Journal of Clinical Investigation, SHILAP Revista de lepidopterología and Gene.

In The Last Decade

İlyas Okur

58 papers receiving 366 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
İlyas Okur Türkiye	12	136	124	86	78	46	62	372
Serap Sivri Türkiye	11	145 1.1×	120 1.0×	62 0.7×	182 2.3×	43 0.9×	53	342
François Labarthe France	11	185 1.4×	188 1.5×	67 0.8×	100 1.3×	21 0.5×	28	412
Roberta Taurisano Italy	14	257 1.9×	174 1.4×	107 1.2×	58 0.7×	63 1.4×	28	501
Veronica Pagliardini Italy	11	178 1.3×	65 0.5×	103 1.2×	41 0.5×	42 0.9×	16	346
Mahoko Furujo Japan	10	130 1.0×	99 0.8×	76 0.9×	59 0.8×	28 0.6×	27	319
Ebru Canda Türkiye	9	56 0.4×	105 0.8×	56 0.7×	77 1.0×	29 0.6×	55	326
Drago Bratkovic Australia	14	157 1.2×	200 1.6×	70 0.8×	131 1.7×	87 1.9×	48	419
Matthias Zielonka Germany	15	151 1.1×	195 1.6×	33 0.4×	127 1.6×	74 1.6×	29	451
Lénaïg Abily-Donval France	10	112 0.8×	157 1.3×	32 0.4×	104 1.3×	39 0.8×	22	311
Ayesha Ahmad United States	13	85 0.6×	151 1.2×	62 0.7×	120 1.5×	108 2.3×	37	392

Countries citing papers authored by İlyas Okur

Since Specialization

Citations

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

Fields of papers citing papers by İlyas Okur

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of İlyas Okur

This figure shows the co-authorship network connecting the top 25 collaborators of İlyas Okur. A scholar is included among the top collaborators of İlyas Okur 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 İlyas Okur. İlyas Okur is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Okur, İlyas, et al.. (2024). Pterin Profiling in Serum, Dried Blood Spot, and Urine Samples Using LC-MS/MS in Patients with Inherited Hyperphenylalaninemia. Molecular Syndromology. 15(3). 185–193. 1 indexed citations

Kılıç, Ayşe, Dilek Yapar, İlyas Okur, et al.. (2023). Long-Term Experience with Anaphylaxis and Desensitization to Alglucosidase Alfa in Pompe Disease. International Archives of Allergy and Immunology. 184(4). 370–375. 4 indexed citations

Muschol, Nicole, İlyas Okur, Fatih Süheyl Ezgü, et al.. (2022). A phase I/II study on intracerebroventricular tralesinidase alfa in patients with Sanfilippo syndrome type B. Journal of Clinical Investigation. 133(2). 9 indexed citations

Yıldırım, Deniz Gezgin, Leyla Tümer, Ödül Eğritaş Gürkan, et al.. (2022). A possibly new autoinflammatory disease due to compound heterozygous phosphomevalonate kinase gene mutation. Joint Bone Spine. 90(1). 105490–105490. 5 indexed citations

Ezgü, Fatih Süheyl, İlyas Okur, Ayşe Kılıç, et al.. (2022). Assessment of auditory functions in patients with hepatic glycogen storage diseases. The Turkish Journal of Pediatrics. 64(4). 658–670. 2 indexed citations

Okur, İlyas, et al.. (2021). The Evaluation of Skeletal Manifestations in Patients with Gaucher Disease. SHILAP Revista de lepidopterología. 8(3). 257–261.

Özaslan, Ahmet, Esra Güney, Mehmet Ali Ergün, İlyas Okur, & Dilek Yapar. (2020). CDH13 and LPHN3 Gene Polymorphisms in Attention-Deficit/Hyperactivity Disorder: Their Relation to Clinical Characteristics. Journal of Molecular Neuroscience. 71(2). 394–408. 5 indexed citations

Özmert, Elif Nursel, Orhan Derman, İlyas Okur, et al.. (2020). Nutritional Status of Syrian Refugees in Early Adolescence Living in Turkey. Journal of Immigrant and Minority Health. 22(6). 1149–1154. 7 indexed citations

Tümer, Leyla, İlyas Okur, Yasemin Erten, et al.. (2018). High incidence of co-existing factors significantly modifying the phenotype in patients with Fabry disease. Gene. 687. 280–288. 5 indexed citations

10.

Walsh, Meghan T., Enza Di Leo, İlyas Okur, Patrizia Tarugi, & M. Mahmood Hussain. (2016). Structure-function analyses of microsomal triglyceride transfer protein missense mutations in abetalipoproteinemia and hypobetalipoproteinemia subjects. Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids. 1861(11). 1623–1633. 19 indexed citations

11.

Tutar, Hakan, et al.. (2015). Audiologic evaluations of children with mucopolysaccharidosis. Brazilian Journal of Otorhinolaryngology. 82(3). 281–284. 18 indexed citations

12.

Leo, Enza Di, et al.. (2015). The Janus-faced manifestations of homozygous familial hypobetalipoproteinemia due to apolipoprotein B truncations. Journal of clinical lipidology. 9(3). 400–405. 4 indexed citations

13.

Kurt, İsmail, Erdim Sertoğlu, İlyas Okur, et al.. (2014). Serum dipeptidyl peptidase-IV: A better screening test for early detection of mucopolysaccharidosis?. Clinica Chimica Acta. 431. 250–254. 7 indexed citations

14.

Okur, İlyas, Fatih Süheyl Ezgü, Gürsel Biberoğlu, et al.. (2013). Screening for Fabry disease in patients undergoing dialysis for chronic renal failure in Turkey: Identification of new case with novel mutation. Gene. 527(1). 42–47. 30 indexed citations

15.

Régal, Luc, Halil İbrahim Aydın, Hilde Van Esch, et al.. (2012). Two novel deletions in hypotonia–cystinuria syndrome. Molecular Genetics and Metabolism. 107(3). 614–616. 12 indexed citations

16.

Tümer, Leyla, et al.. (2011). Very long-chain acyl CoA dehydrogenase deficiency which was accepted as infanticide. Forensic Science International. 210(1-3). e1–e3. 4 indexed citations

17.

Kasapkara, Çiğdem Seher, Fatih Süheyl Ezgü, İlyas Okur, et al.. (2011). N-carbamylglutamate treatment for acute neonatal hyperammonemia in isovaleric acidemia. European Journal of Pediatrics. 170(6). 799–801. 29 indexed citations

18.

Yenicesu, İdil, et al.. (2008). Lipid apheresis applications in childhood: Experience in the University Hospital of Gazi. Transfusion and Apheresis Science. 39(3). 235–240. 2 indexed citations

19.

Memış, Leyla, et al.. (2006). Giant Bronchogenic Cyst Mimicking Tension Pneumothorax. Asian Cardiovascular and Thoracic Annals. 14(3). 244–246. 1 indexed citations

20.

Ezgü, Fatih Süheyl, et al.. (2004). Vitamin D intoxication and hypercalcaemia in an infant treated with pamidronate infusions. European Journal of Pediatrics. 163(3). 163–165. 19 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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