Hakan Cangül

2.0k total citations
30 papers, 596 citations indexed

About

Hakan Cangül is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Hakan Cangül has authored 30 papers receiving a total of 596 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 19 papers in Endocrinology, Diabetes and Metabolism and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Hakan Cangül's work include Thyroid Disorders and Treatments (17 papers), RNA modifications and cancer (8 papers) and Congenital heart defects research (7 papers). Hakan Cangül is often cited by papers focused on Thyroid Disorders and Treatments (17 papers), RNA modifications and cancer (8 papers) and Congenital heart defects research (7 papers). Hakan Cangül collaborates with scholars based in Türkiye, United Kingdom and United States. Hakan Cangül's co-authors include Max Costa, Konstantin Salnikow, Michaela Kendall, Herman Yee, Eamonn R. Maher, Veysel Nijat Baş, Zehra Aycan, Thérèse Commes, Timothy Barrett and David Zagzag and has published in prestigious journals such as The Lancet, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Hakan Cangül

30 papers receiving 586 citations

Peers

Hakan Cangül

EDM

PFM

Shilpa Thakur India

Yoko Sakuma Japan

Egbert Schulze Germany

H.A.P. Pols Netherlands

Aurora Aiello Italy

Xueying Zhou China

Liang Wu China

Tobias Linden Germany

Runxia Gu China

Abdelali Lehraiki France

Shilpa Thakur India

Hakan Cangül

291 ×0.7

146 ×0.7

EDM

132 ×1.7

17 ×0.2

36 ×0.5

PFM

Citations per year, relative to Hakan Cangül Hakan Cangül (= 1×) peers Shilpa Thakur

Countries citing papers authored by Hakan Cangül

Since Specialization

Citations

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

Fields of papers citing papers by Hakan Cangül

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hakan Cangül

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Saygı, Ceren, et al.. (2022). Computational analysis of missense filamin-A variants, including the novel p.Arg484Gln variant of two brothers with periventricular nodular heterotopia. PLoS ONE. 17(5). e0265400–e0265400. 1 indexed citations

Aycan, Zehra, Hakan Cangül, Marina Muzza, et al.. (2017). Digenic DUOX1 and DUOX2 Mutations in Cases With Congenital Hypothyroidism. The Journal of Clinical Endocrinology & Metabolism. 102(9). 3085–3090. 46 indexed citations

Güçlü, Metin, Hakan Cangül, & Canan Ersoy. (2015). Strong Similarities in Turkish and European Patients Diagnosed with APECED Syndrome. SHILAP Revista de lepidopterología. 19(3). 89–92. 1 indexed citations

Cangül, Hakan, Murat Doğan, & Duran Üstek. (2015). A Homozygous Nonsense Thyroid Peroxidase Mutation (R540X) Consistently Causes Congenital Hypothyroidism in Two Siblings Born to a Consanguineous Family. Journal of Clinical Research in Pediatric Endocrinology. 7(4). 323–328. 3 indexed citations

Cangül, Hakan, Veysel Nijat Baş, Michaela Kendall, et al.. (2014). A Nonsense Thyrotropin Receptor Gene Mutation (R609X) is Associated with Congenital Hypothyroidism and Heart Defects. 82. 1 indexed citations

Cangül, Hakan, Murat Doğan, Michaela Kendall, et al.. (2014). One Base Deletion (c.2422delT) in the TPO Gene Causes Severe Congenital Hypothyroidism. Journal of Clinical Research in Pediatric Endocrinology. 6(3). 169–173. 13 indexed citations

Cangül, Hakan, Feyza Darendelıler, Michaela Kendall, et al.. (2014). A truncating TPO mutation (Y55X) in patients with hypothyroidism and total iodide organification defect. Endocrine Research. 40(3). 146–150. 7 indexed citations

Schoenmakers, Nadia, Hakan Cangül, Adeline K. Nicholas, et al.. (2013). A comprehensive next generation sequencing-based strategy for genetic diagnosis in congenital hypothyroidism. 33. 8 indexed citations

Temel, Şehime Gülsün, Özlem Bostan, Hakan Cangül, & Ergün Çil. (2013). Turkish perspective of Jervell and Lange-Nielsen syndrome. Annals of Indian Academy of Neurology. 16(1). 129–129. 1 indexed citations

10.

Bostan, Özlem, et al.. (2013). Jervell and Lange–Nielsen Syndrome: Homozygous Missense Mutation of KCNQ1 in a Turkish Family. Pediatric Cardiology. 34(8). 2063–2067. 5 indexed citations

11.

Cangül, Hakan, Kristien Boelaert, Murat Doğan, et al.. (2013). Novel truncating thyroglobulin gene mutations associated with congenital hypothyroidism. Endocrine. 45(2). 206–212. 24 indexed citations

12.

Baş, Veysel Nijat, Hakan Cangül, Sebahat Yılmaz Ağladıoğlu, et al.. (2012). Mild and severe congenital primary hypothyroidism in two patients by thyrotropin receptor (TSHR) gene mutation. Journal of Pediatric Endocrinology and Metabolism. 25(11-12). 1153–6. 11 indexed citations

13.

Cangül, Hakan, Zehra Aycan, Álvaro Olivera‐Nappa, et al.. (2012). Thyroid dyshormonogenesis is mainly caused by TPO mutations in consanguineous community. Clinical Endocrinology. 79(2). 275–281. 44 indexed citations

14.

Güçlü, Metin, Lin Lin, Erdinç Ertürk, John C. Achermann, & Hakan Cangül. (2010). Puberty, stress, and sudden death. The Lancet. 376(9751). 1512–1512. 13 indexed citations

15.

Kordan, Yakup, Hakan Cangül, Hasan Serkan Doğan, et al.. (2008). Association of urokinase gene 3′-UTR T/C polymorphism with calcium oxalate urolithiasis in children. International Urology and Nephrology. 40(3). 563–568. 15 indexed citations

16.

Pirgon, Özgür, Mehmet Emre Atabek, Hacı Hasan Esen, & Hakan Cangül. (2007). Infantile Systemic Hyalinosis with Early Thyroid Dysfunction. Journal of Pediatric Endocrinology and Metabolism. 20(7). 833–6. 1 indexed citations

17.

Cangül, Hakan. (2004). Hypoxia upregulates the expression of the NDRG1 gene leading to its overexpression in various human cancers. BMC Genetics. 5(1). 27–27. 148 indexed citations

18.

Cangül, Hakan, Konstantin Salnikow, Herman Yee, et al.. (2002). Enhanced overexpression of an HIF-1/hypoxia-related protein in cancer cells.. Environmental Health Perspectives. 110(suppl 5). 783–788. 44 indexed citations

19.

Cangül, Hakan, Konstantin Salnikow, Herman Yee, et al.. (2002). Enhanced Expression of a Novel Protein in Human Cancer Cells: A Potential Aid to Cancer Diagnosis. Cell Biology and Toxicology. 18(2). 87–96. 37 indexed citations

20.

Cangül, Hakan, Limor Broday, Konstantin Salnikow, et al.. (2002). Molecular mechanisms of nickel carcinogenesis. Toxicology Letters. 127(1-3). 69–75. 84 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.

Explore authors with similar magnitude of impact