Murat Derbent
Impact in
- Urology top 10%
- Urological Disorders and Treatments
-
- Congenital Ear and Nasal Anomalies
- Craniofacial Disorders and Treatments
- Genomic variations and chromosomal abnormalities
Papers in
-
- Congenital heart defects research 6
- Protein Tyrosine Phosphatases 4
- Surgery 13
- Vascular Malformations and Hemangiomas 3
- Congenital Diaphragmatic Hernia Studies 3
- Co-authors
- U Saatçi (8 shared papers)Esra Baskın (7 shared papers)Birgül Varan (6 shared papers)Zerrin Yılmaz (7 shared papers)Namık Yaşar Özbek (8 shared papers)Pınar Işık Ağras (5 shared papers)Figen Özçay (6 shared papers)Füsun Alehan (3 shared papers)
- Journals
- Pediatric Nephrology (3 papers)The American Journal of Human Genetics (2 papers)European Journal of Pediatrics (1 paper)Prenatal Diagnosis (1 paper)Journal of Child Neurology (1 paper)
- Partner nations
- TürkiyeUnited StatesUnited Kingdom
In The Last Decade
Murat Derbent
44 papers receiving 546 citations
Peers
Comparison fields: 5 of 68
- Urology 45
- Genetics 52
- Genetics 107
- Nephrology 22
- Molecular Biology 209
Countries citing papers authored by Murat Derbent
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
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-authors
The 25 scholars most cited alongside Murat Derbent, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 46 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2010 | 73 | |
| 2 | 2015 | 61 | |
| 3 | 2002 | 56 | |
| 4 | 2004 | 39 | |
| 5 | Propranolol for infantile hemangiomas: a preliminary report on efficacy and safety in very low birth weight infants. | 2011 | 36 |
| 6 | 2003 | 23 | |
| 7 | 2004 | 22 | |
| 8 | 2002 | 22 | |
| 9 | 2012 | 21 | |
| 10 | 2003 | 17 | |
| 11 | 2007 | 17 | |
| 12 | 2007 | 16 | |
| 13 | 2010 | 15 | |
| 14 | 2006 | 15 | |
| 15 | 2002 | 12 | |
| 16 | 2001 | 11 | |
| 17 | Thoracoschisis associated with diaphragmatic hernia in a 31-week-old stillbirth. | 2001 | 11 |
| 18 | 2004 | 10 | |
| 19 | Severe iron deficiency anemia in a child with idiopathic pulmonary hemosiderosis: a case report. | 2002 | 8 |
| 20 | 2015 | 7 |
About Murat Derbent
Murat Derbent is a scholar working on Molecular Biology, Surgery, Genetics, Pulmonary and Respiratory Medicine and Genetics, having authored 46 papers that have together received 562 indexed citations. Recurring topics across this work include Congenital heart defects research (6 papers), Protein Tyrosine Phosphatases (4 papers), Tracheal and airway disorders (4 papers), Congenital Ear and Nasal Anomalies (4 papers), Neurofibromatosis and Schwannoma Cases (3 papers), Vascular Malformations and Hemangiomas (3 papers), Congenital Diaphragmatic Hernia Studies (3 papers) and Urological Disorders and Treatments (3 papers). The work is most often cited by research in Urology (45 citations), Genetics (52 citations), Genetics (107 citations), Nephrology (22 citations) and Molecular Biology (209 citations). Murat Derbent has collaborated with scholars based in Türkiye, United States and United Kingdom. Frequent co-authors include U Saatçi, Esra Baskın, Birgül Varan, Zerrin Yılmaz, Namık Yaşar Özbek, Pınar Işık Ağras, Figen Özçay, Füsun Alehan, Volkan Baltacı and Arda Saygılı. Their work appears in journals such as Pediatric Nephrology, The American Journal of Human Genetics, European Journal of Pediatrics, Prenatal Diagnosis and Journal of Child Neurology.
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.