Murat Derbent

862 total citations
43 papers, 480 citations indexed

About

Murat Derbent is a scholar working on Molecular Biology, Surgery and Genetics. According to data from OpenAlex, Murat Derbent has authored 43 papers receiving a total of 480 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 11 papers in Surgery and 11 papers in Genetics. Recurrent topics in Murat Derbent's work include Congenital heart defects research (6 papers), Congenital Ear and Nasal Anomalies (4 papers) and Tracheal and airway disorders (4 papers). Murat Derbent is often cited by papers focused on Congenital heart defects research (6 papers), Congenital Ear and Nasal Anomalies (4 papers) and Tracheal and airway disorders (4 papers). Murat Derbent collaborates with scholars based in Türkiye, United States and Austria. Murat Derbent's co-authors include Kürşad Tokel, U Saatçi, Birgül Varan, Esra Baskın, Namık Yaşar Özbek, Zerrin Yılmaz, Pınar Işık Ağras, Figen Özçay, Füsun Alehan and Arda Saygılı and has published in prestigious journals such as SHILAP Revista de lepidopterología, Acta Paediatrica and Journal of Pediatric Surgery.

In The Last Decade

Murat Derbent

42 papers receiving 463 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 Derbent Türkiye 13 185 121 103 101 68 43 480
Gaurav Tyagi India 11 88 0.5× 86 0.7× 107 1.0× 68 0.7× 50 0.7× 48 560
Katsuya Saito Japan 11 105 0.6× 75 0.6× 90 0.9× 76 0.8× 80 1.2× 44 456
P. S. N. Menon India 15 205 1.1× 142 1.2× 167 1.6× 51 0.5× 74 1.1× 67 672
Julia Zimmer Ireland 10 119 0.6× 48 0.4× 158 1.5× 140 1.4× 87 1.3× 34 569
David L. Zwick United States 14 106 0.6× 74 0.6× 117 1.1× 157 1.6× 79 1.2× 32 606
A. Fishman Israel 13 89 0.5× 64 0.5× 147 1.4× 51 0.5× 45 0.7× 34 507
C Scheiner France 13 103 0.6× 49 0.4× 115 1.1× 85 0.8× 53 0.8× 37 433
Kanshi Minamitani Japan 15 188 1.0× 186 1.5× 137 1.3× 76 0.8× 49 0.7× 42 678
Giuseppe De Santis Italy 13 213 1.2× 80 0.7× 143 1.4× 73 0.7× 53 0.8× 25 626
Annie Purvis United States 8 163 0.9× 64 0.5× 37 0.4× 136 1.3× 27 0.4× 12 532

Countries citing papers authored by Murat Derbent

Since Specialization
Citations

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

Fields of papers citing papers by Murat Derbent

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Murat Derbent

This figure shows the co-authorship network connecting the top 25 collaborators of Murat Derbent. A scholar is included among the top collaborators of Murat Derbent 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 Derbent. Murat Derbent 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.
Dikoglu, Esra, Ali Abdullah Alfaiz, Maria W. Górna, et al.. (2015). Mutations in LONP1, a mitochondrial matrix protease, cause CODAS syndrome. American Journal of Medical Genetics Part A. 167(7). 1501–1509. 60 indexed citations
2.
Denayer, Ellen, et al.. (2012). <b><i>NRAS</i></b> Mutations in Noonan Syndrome. Molecular Syndromology. 3(1). 34–38. 21 indexed citations
3.
Derbent, Murat, et al.. (2011). A patient with Keipert syndrome and isolated fibrous dysplasia of the sphenoid sinus. American Journal of Medical Genetics Part A. 155(6). 1496–1499. 2 indexed citations
4.
Derbent, Murat, Mehmet Yekta Öncel, Kürşad Tokel, et al.. (2010). Clinical and hematologic findings in Noonan syndrome patients with PTPN11 gene mutations. American Journal of Medical Genetics Part A. 152A(11). 2768–2774. 15 indexed citations
5.
Derbent, Murat, Engin Melek, Ayca Arman‐Özçırpıcı, Sina Uçkan, & Esra Baskın. (2009). Urofacial (Ochoa) Syndrome: Can a Facial Gestalt Represent Severe Voiding Dysfunction?. Renal Failure. 31(7). 589–592. 3 indexed citations
6.
Yılmaz, Zerrin, et al.. (2008). Greig syndrome based on a de novo translocation. Pediatrics International. 50(2). 248–250. 3 indexed citations
7.
Akkuzu, Babür, et al.. (2007). Congenital partial arhinia: a case report. Journal of Medical Case Reports. 1(1). 97–97. 17 indexed citations
8.
Gülcan, Hande, et al.. (2007). PHACES syndrome with small, late-onset hemangiomas. European Journal of Pediatrics. 166(12). 1293–1295. 16 indexed citations
9.
Balcı, Sibel Oğuzkan, et al.. (2006). Two neurofibromatosis type 1 cases associated with rhabdomyosarcoma of bladder, one with a large deletion in the NF1 gene. Cancer Genetics and Cytogenetics. 164(2). 159–163. 15 indexed citations
10.
Derbent, Murat, Esra Baskın, Ahmet Muhteşem Ağıldere, Pınar Işık Ağras, & U Saatçi. (2005). Brachydactyly short-stature hypertension syndrome: a case with associated vascular malformations. Pediatric Nephrology. 21(3). 390–393. 2 indexed citations
11.
Derbent, Murat, Pınar Işık Ağras, Şansal Gedik, et al.. (2004). Congenital cataract, microphthalmia, hypoplasia of corpus callosum and hypogenitalism: Report and review of Micro syndrome. American Journal of Medical Genetics Part A. 128A(3). 232–234. 22 indexed citations
12.
Özbek, Namık Yaşar, Murat Derbent, Lale Olcay, Zerrin Yılmaz, & Kürşad Tokel. (2004). Dysplastic changes in the peripheral blood of children with microdeletion 22q11.2. American Journal of Hematology. 77(2). 126–131. 10 indexed citations
13.
Lembet, Arda, et al.. (2003). Prenatal diagnosis of multiple pterygium syndrome associated with Klinefelter syndrome. Prenatal Diagnosis. 23(9). 728–730. 3 indexed citations
14.
Özçay, Figen, Murat Derbent, Derya Aldemir, et al.. (2003). Effect of iron deficiency anemia on renal tubular function in childhood. Pediatric Nephrology. 18(3). 254–256. 23 indexed citations
15.
Ağras, Pınar Işık, Esra Baskın, İrfan Serdar Arda, et al.. (2003). Neurofibromatosis—Noonan's Syndrome With Associated Rhabdomyosarcoma of the Urinary Bladder in an Infant: Case Report. Journal of Child Neurology. 18(1). 68–72. 17 indexed citations
16.
Derbent, Murat, et al.. (2002). A mild case of frontonasal dysplasia: the rhinologic perspective. International Journal of Pediatric Otorhinolaryngology. 65(1). 75–83. 12 indexed citations
17.
Derbent, Murat, Zerrin Yılmaz, Volkan Baltacı, et al.. (2002). Chromosome 22q11.2 deletion and phenotypic features in 30 patients with conotruncal heart defects. American Journal of Medical Genetics Part A. 116A(2). 129–135. 55 indexed citations
18.
Özçay, Figen, Murat Derbent, Beyhan Demirhan, Kürşad Tokel, & U Saatçi. (2001). A family with Jeune syndrome. Pediatric Nephrology. 16(8). 623–626. 11 indexed citations
19.
Derbent, Murat, et al.. (2001). Popliteal pterygium associated with neonatal Marfan syndrome: case report*. Clinical Dysmorphology. 10(3). 209–213. 4 indexed citations
20.
Derbent, Murat, et al.. (2001). Thoracoschisis associated with diaphragmatic hernia in a 31-week-old stillbirth.. PubMed. 43(3). 269–71. 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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