Murat Erdoğan

818 total citations
41 papers, 533 citations indexed

About

Murat Erdoğan is a scholar working on Surgery, Molecular Biology and Genetics. According to data from OpenAlex, Murat Erdoğan has authored 41 papers receiving a total of 533 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Surgery, 11 papers in Molecular Biology and 11 papers in Genetics. Recurrent topics in Murat Erdoğan's work include Cystic Fibrosis Research Advances (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers). Murat Erdoğan is often cited by papers focused on Cystic Fibrosis Research Advances (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers). Murat Erdoğan collaborates with scholars based in Türkiye, United Kingdom and United States. Murat Erdoğan's co-authors include Katheryne Downes, Roy Sanders, Zachary M. Vaupel, Ahmet Köç, Mustafa Karaoğlanoğlu, Yaşar Cesur, Mustafa Kösecik, H. Claude Sagi, Yunus İmren and James A. Blair and has published in prestigious journals such as SHILAP Revista de lepidopterología, Journal of Biotechnology and Journal of Orthopaedic Trauma.

In The Last Decade

Murat Erdoğan

37 papers receiving 520 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Murat Erdoğan Türkiye 12 296 166 93 68 64 41 533
Tsuyoshi Saga Japan 13 263 0.9× 25 0.2× 43 0.5× 39 0.6× 37 0.6× 43 632
Michał Szpinda Poland 15 328 1.1× 52 0.3× 138 1.5× 8 0.1× 90 1.4× 106 811
Patrick Sunday Igbigbi Nigeria 13 159 0.5× 92 0.6× 49 0.5× 48 0.7× 53 0.8× 71 513
Márcio Antônio Babinski Brazil 15 347 1.2× 17 0.1× 72 0.8× 39 0.6× 38 0.6× 93 689
Emine Kızılkanat Türkiye 8 243 0.8× 31 0.2× 103 1.1× 16 0.2× 9 0.1× 16 472
Indar Jit India 18 271 0.9× 27 0.2× 120 1.3× 32 0.5× 67 1.0× 45 926
Joseph B. Slakey United States 7 387 1.3× 31 0.2× 33 0.4× 26 0.4× 12 0.2× 9 478
Murat Üzel Türkiye 13 190 0.6× 120 0.7× 61 0.7× 57 0.8× 48 0.8× 46 514
B C Didia Nigeria 11 60 0.2× 38 0.2× 20 0.2× 20 0.3× 28 0.4× 33 316
Neslihan Boyan Türkiye 7 145 0.5× 30 0.2× 100 1.1× 16 0.2× 16 0.3× 26 385

Countries citing papers authored by Murat Erdoğan

Since Specialization
Citations

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

Fields of papers citing papers by Murat Erdoğan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Murat Erdoğan

This figure shows the co-authorship network connecting the top 25 collaborators of Murat Erdoğan. A scholar is included among the top collaborators of Murat Erdoğan 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 Murat Erdoğan. Murat Erdoğan 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.
Erdoğan, Murat, Hakan Gümüş, Ahmet Sami Güven, et al.. (2025). A case series of joubert syndrome evaluated with whole exome sequencing and the utility of optical genome mapping in the diagnosis. Neurogenetics. 26(1). 47–47.
2.
Çiçek, Dilek, et al.. (2024). Congenital Adrenal Hyperplasia with Combined 21-hydroxylase deficiency and 17α-hydroxylase/17,20-lyase deficiency: An undervirilized male. European Journal of Medical Genetics. 69. 104952–104952. 1 indexed citations
3.
Erdoğan, Murat, et al.. (2022). Assessing humoral immune response after two doses of an inactivated SARS-CoV-2 vaccine (CoronaVac) in healthcare workers. Public Health. 205. 1–5. 5 indexed citations
4.
Erdoğan, Murat, Mehmet Canpolat, Hakan Gümüş, et al.. (2022). Congenital Myasthenic Syndromes in Turkey: Clinical and Molecular Characterization of 16 Cases With Three Novel Mutations. Pediatric Neurology. 136. 43–49. 5 indexed citations
5.
Erdoğan, Murat, Mehmet Köse, Sevgi Pekcan, et al.. (2021). The Genetic Analysis of Cystic Fibrosis Patients With Seven Novel Mutations in the CFTR Gene in the Central Anatolian Region of Turkey. Balkan Medical Journal. 38(6). 357–364. 6 indexed citations
6.
Baştuğ, Funda, et al.. (2021). Tubulopathy and hepatomegaly in a 2-year-old boy: Answers. Pediatric Nephrology. 36(7). 2083–2084. 2 indexed citations
7.
Erdoğan, Murat, et al.. (2020). The Role of Chromosome Analysis in Patients with Recurrent Pregnancy Loss. SHILAP Revista de lepidopterología.
8.
Hangül, Melih, Murat Erdoğan, Nihal Hatipoğlu, & Mehmet Köse. (2020). Maturity‐onset diabetes of the young: Different diabetes in an infant with cystic fibrosis. Pediatric Pulmonology. 55(5). E5–E7. 3 indexed citations
9.
Hangül, Melih, Sevgi Pekcan, Mehmet Köse, et al.. (2019). The Incidence of Cystic Fibrosis in the Central Region of Anatolia in Turkey Between 2015 and 2016. Balkan Medical Journal. 36(3). 179–183. 11 indexed citations
10.
Erdoğan, Murat, et al.. (2018). Decreased disulphide/thiol ratio in patients with autosomal recessive non-syndromic hearing loss. International Journal of Pediatric Otorhinolaryngology. 112. 188–192.
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13.
Erdoğan, Murat, et al.. (2017). Does thiol–disulphide balance show oxidative stress in different MEFV mutations?. Rheumatology International. 38(1). 97–104. 3 indexed citations
14.
İmren, Yunus, et al.. (2015). Quality of Life Following Treatment of Trochanteric Fractures with Proximal Femoral Nail versus Cementless Bipolar Hemiarthroplasty in Elderly. Clinical and investigative medicine. 38(1). 63–63. 29 indexed citations
15.
Sanders, Roy, Zachary M. Vaupel, Murat Erdoğan, & Katheryne Downes. (2014). Operative Treatment of Displaced Intraarticular Calcaneal Fractures. Journal of Orthopaedic Trauma. 28(10). 551–563. 146 indexed citations
16.
Erdoğan, Murat, et al.. (2014). Is Attention Deficit and Hyperactivity Disorder a Risk Factor for Sustaining Fractures of Proximal Humerus?. Acta chirurgiae orthopaedicae et traumatologiae Cechoslovaca. 81(3). 221–226. 7 indexed citations
17.
Chan, Daniel Shiu‐Hin, et al.. (2013). The Insertion of Intramedullary Nail Locking Screws Without Fluoroscopy. Journal of Orthopaedic Trauma. 27(7). 363–366. 24 indexed citations
18.
Erdoğan, Murat, et al.. (2012). Evaluation of nasal airway alterations associated with septorhinoplasty by both objective and subjective methods. European Archives of Oto-Rhino-Laryngology. 270(1). 99–106. 17 indexed citations
19.
Erdoğan, Murat, et al.. (2010). Gitelman syndrome with mental retardation: a case report. Journal of Nephrology. 23(5). 617–618. 4 indexed citations
20.
Erdoğan, Murat. (2003). Thiocyanate overload and thyroid disease. BioFactors. 19(3-4). 107–111. 37 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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