Hakan Gürkan

878 total citations
104 papers, 544 citations indexed

About

Hakan Gürkan is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Hakan Gürkan has authored 104 papers receiving a total of 544 indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Genetics, 39 papers in Molecular Biology and 18 papers in Surgery. Recurrent topics in Hakan Gürkan's work include Genomic variations and chromosomal abnormalities (16 papers), Genomics and Rare Diseases (10 papers) and Prenatal Screening and Diagnostics (9 papers). Hakan Gürkan is often cited by papers focused on Genomic variations and chromosomal abnormalities (16 papers), Genomics and Rare Diseases (10 papers) and Prenatal Screening and Diagnostics (9 papers). Hakan Gürkan collaborates with scholars based in Türkiye, Cyprus and Germany. Hakan Gürkan's co-authors include Hilmi Tozkır, Emine İkbal Atlı, Selma Demır, Ömer Nurı Pamuk, Gülsüm Emel Pamuk, Ahmet Muzaffer Demir, Ceyhun Numanoğlu, Özgür Akbayır, Ali Gedikbaşı and Filiz Aydın and has published in prestigious journals such as Journal of Clinical Investigation, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Hakan Gürkan

88 papers receiving 518 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hakan Gürkan Türkiye 13 212 134 78 73 71 104 544
Bhoom Suktitipat Thailand 18 273 1.3× 160 1.2× 61 0.8× 78 1.1× 103 1.5× 48 842
Müge Sayitoğlu Türkiye 13 326 1.5× 76 0.6× 47 0.6× 98 1.3× 80 1.1× 49 605
Yutaka Harita Japan 19 427 2.0× 156 1.2× 87 1.1× 52 0.7× 124 1.7× 66 934
Wanda E. Filipiak United States 8 407 1.9× 234 1.7× 77 1.0× 39 0.5× 85 1.2× 11 906
Shin Fukuda Japan 15 208 1.0× 123 0.9× 111 1.4× 58 0.8× 58 0.8× 25 750
Ilse Scroyen Belgium 17 272 1.3× 52 0.4× 87 1.1× 56 0.8× 81 1.1× 38 699
Godfrey T. Gillett United Kingdom 13 286 1.3× 138 1.0× 31 0.4× 88 1.2× 50 0.7× 20 677
Yuan-Yuan Ho Hong Kong 12 325 1.5× 275 2.1× 59 0.8× 60 0.8× 83 1.2× 18 785
F. Scatena Italy 13 231 1.1× 78 0.6× 104 1.3× 74 1.0× 202 2.8× 34 701
Amanda A. Hill United States 9 226 1.1× 64 0.5× 220 2.8× 83 1.1× 40 0.6× 17 638

Countries citing papers authored by Hakan Gürkan

Since Specialization
Citations

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

Fields of papers citing papers by Hakan Gürkan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hakan Gürkan

This figure shows the co-authorship network connecting the top 25 collaborators of Hakan Gürkan. A scholar is included among the top collaborators of Hakan Gürkan 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 Gürkan. Hakan Gürkan 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.
Gürkan, Hakan, et al.. (2025). The Importance of Genetic Diagnosis in Rare Diseases. Balkan Medical Journal. 42(2). 92–93.
2.
Demır, Selma, et al.. (2024). Investigation of Targeted Genes and Identification of Novel Variants with Next Generation Sequencing Method in Hearing Loss. The Journal of International Advanced Otology. 20(4). 312–324.
3.
Atlı, Emine İkbal, et al.. (2024). Next-Generation Sequencing Infertility Panel in Turkey: First Results. SHILAP Revista de lepidopterología. 27(2). 49–57. 1 indexed citations
4.
5.
Gürkan, Hakan, et al.. (2024). The Phenotypic Spectrum of Desanto–Shinawi Syndrome: A Comparative Report of the First Reported Case in Turkey. Genetic Testing and Molecular Biomarkers. 28(5). 213–217.
6.
Saïd, Mariem Ben, Saber Masmoudi, Angela Brieger, et al.. (2024). Functional analysis of MMR gene VUS from potential Lynch syndrome patients. PLoS ONE. 19(6). e0304141–e0304141. 1 indexed citations
7.
Eren, Erdal, et al.. (2023). A Novel PHEX Mutation in A Case Followed Up with A Diagnosis of X-linked Hypophosphatemic Rickets. Güncel Pediatri. 21(1). 98–101.
8.
Gürkan, Hakan, et al.. (2022). Investigating the Genetic Etiology of Pediatric Patients with Peripheral Hypotonia Using the Next-Generation Sequencing Method. SHILAP Revista de lepidopterología. 9(3). 200–207. 1 indexed citations
9.
10.
11.
Demır, Selma, et al.. (2021). RETROSPECTIVE ANALYSIS OF ALPHA GLOBIN COPY NUMBER VARIATIONS DETERMINED BY MLPA IN THE TRAKYA REGION. SHILAP Revista de lepidopterología. 84(3). 348–353. 1 indexed citations
12.
Gürkan, Hakan, et al.. (2021). TRAKYA BÖLGESİ ERKEK İNFERTİLİTE OLGULARINDA Y KROMOZOM MİKRODELESYONLARI VE SİTOGENETİK ANOMALİLERİN SIKLIĞI: TEK MERKEZ DENEYİMİ. SHILAP Revista de lepidopterología. 84(1). 27–33. 1 indexed citations
13.
Gürkan, Hakan, et al.. (2021). The Application of Next Generation Sequencing Maturity Onset Diabetes of the Young Gene Panel in Turkish Patients from Trakya Region. Journal of Clinical Research in Pediatric Endocrinology. 13(3). 320–331. 7 indexed citations
14.
Atlı, Emine İkbal, et al.. (2020). Pros and cons for fluorescent in situ hybridization, karyotyping and next generation sequencing for diagnosis and follow-up of multiple myeloma. SHILAP Revista de lepidopterología. 23(2). 59–64. 3 indexed citations
15.
Varol, Füsun, et al.. (2019). Placental and serum levels of human Klotho in severe preeclampsia: A potential sensitive biomarker. Placenta. 85. 49–55. 15 indexed citations
16.
Çelik, Mehmet, Semra Aytürk, Hakan Gürkan, et al.. (2019). The relation between BRAFV600E mutation and clinicopathological characteristics of papillary thyroid cancer. Medicinski Glasnik. 17(1). 30–34. 24 indexed citations
17.
Gürkan, Hakan. (2019). Y Kromozomu Mikrodelesyonu ve Fertiliteyi Etkileyen Y Kromozomu Genleri. 4(3). 25–31. 1 indexed citations
18.
Arslan, Selçuk, Hakan Gürkan, Selma Demır, et al.. (2017). Novel EYA1 variants causing Branchio-oto-renal syndrome. International Journal of Pediatric Otorhinolaryngology. 98. 59–63. 15 indexed citations
19.
Can, Güray, et al.. (2016). Investigation of IL23R, JAK2, and STAT3 gene polymorphisms and gene–gene interactions in Crohn’s disease and ulcerative colitis in a Turkish population. The Turkish Journal of Gastroenterology. 27(6). 525–536. 10 indexed citations
20.
Gürkan, Hakan, et al.. (2014). An Investigation of the Relationship Between the Enos Gene Polymorphism and Diagnosed Migraine. Balkan Journal of Medical Genetics. 17(2). 49–59. 11 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