Emregül Işık

420 total citations
6 papers, 91 citations indexed

About

Emregül Işık is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Surgery. According to data from OpenAlex, Emregül Işık has authored 6 papers receiving a total of 91 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 4 papers in Endocrinology, Diabetes and Metabolism and 1 paper in Surgery. Recurrent topics in Emregül Işık's work include Hyperglycemia and glycemic control in critically ill and hospitalized patients (2 papers), Sexual Differentiation and Disorders (2 papers) and Diabetes Management and Research (2 papers). Emregül Işık is often cited by papers focused on Hyperglycemia and glycemic control in critically ill and hospitalized patients (2 papers), Sexual Differentiation and Disorders (2 papers) and Diabetes Management and Research (2 papers). Emregül Işık collaborates with scholars based in Türkiye, Qatar and United Kingdom. Emregül Işık's co-authors include Hüseyin Demirbilek, Ayfer Alikaşifoğlu, Nurgün Kandemir, Jayne Houghton, Sian Ellard, Sarah E. Flanagan, Nazlı Gönç, O. U. Soyer, Coşkun Kocabaş and Ersoy Civelek and has published in prestigious journals such as Pediatric Pulmonology, Clinical Genetics and Journal of Pediatric Endocrinology and Metabolism.

In The Last Decade

Emregül Işık

6 papers receiving 90 citations

Peers

Emregül Işık
Ron van Golde Netherlands
Nicole Sheanon United States
Roxanne Phillips United States
Astrid van Hylckama Vlieg Netherlands
Т. В. Моругова Russia
V. Reid Sutton United States
Akira Namba Japan
Henrike Krenz Germany
C. J. Weber United States
Yanning Song China
Ron van Golde Netherlands
Emregül Işık
Citations per year, relative to Emregül Işık Emregül Işık (= 1×) peers Ron van Golde

Countries citing papers authored by Emregül Işık

Since Specialization
Citations

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

Fields of papers citing papers by Emregül Işık

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Emregül Işık

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

All Works

6 of 6 papers shown
1.
Işık, Emregül, et al.. (2019). Congenital Hyperinsulinism and Evolution to Sulfonylurearesponsive Diabetes Later in Life due to a Novel Homozygous p.L171F <i>ABCC8</i> Mutation. Journal of Clinical Research in Pediatric Endocrinology. 11(1). 82–87. 20 indexed citations
2.
Kotan, Leman Damla, Emregül Işık, İhsan Turan, et al.. (2018). Prevalence and associated phenotypes of PLXNA1 variants in normosmic and anosmic idiopathic hypogonadotropic hypogonadism. Clinical Genetics. 95(2). 320–324. 21 indexed citations
3.
Işık, Emregül, Hüseyin Demirbilek, Jayne Houghton, et al.. (2018). Congenital hyperinsulinism and evolution to sulfonylurea-responsive diabetes later in life due to a novel homozygous p.L171F ABCC8 mutation. Journal of Clinical Research in Pediatric Endocrinology. 3 indexed citations
4.
Işık, Emregül, Paolo Beck Peccoz, Irene Campi, et al.. (2014). Thyroid hormone resistance: a novel mutation in thyroid hormone receptor beta (THRB) gene - case report.. PubMed. 55(3). 322–7. 13 indexed citations
5.
Alikaşifoğlu, Ayfer, Olaf Hiort, Nazlı Gönç, et al.. (2012). 17β-Hydroxysteroid dehydrogenase type 3 deficiency as a result of a homozygous 7 base pair deletion in 17βHSD3 gene. Journal of Pediatric Endocrinology and Metabolism. 25(5-6). 561–3. 13 indexed citations
6.
Soyer, O. U., Ersoy Civelek, Emregül Işık, et al.. (2010). Parental perspectives on influenza vaccination in children with asthma. Pediatric Pulmonology. 46(2). 139–144. 21 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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2026