Eda Ütine
Impact in
-
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Connective tissue disorders research
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- Moyamoya disease diagnosis and treatment
Papers in
- Genetics 11
- Genomic variations and chromosomal abnormalities 4
- Connective tissue disorders research 2
- Craniofacial Disorders and Treatments 2
- Co-authors
- Yasemin Alanay (8 shared papers)Koray Boduroğlu (10 shared papers)Dilek Aktaş (3 shared papers)Pelin Özlem Şimşek‐Kiper (7 shared papers)Ergül Tunçbılek (3 shared papers)Ekim Z. Taşkıran (7 shared papers)Melda Çaǧlar (1 shared paper)Esra KAYA KILIÇ (3 shared papers)
- Journals
- Journal of Intellectual Disability Research (1 paper)Molecular Cytogenetics (1 paper)PEDIATRICS (1 paper)Neuropediatrics (1 paper)Journal of Medical Genetics (1 paper)
- Partner nations
- TürkiyeUnited KingdomUnited States
In The Last Decade
Eda Ütine
22 papers receiving 213 citations
Peers
Comparison fields: 5 of 57
- Genetics 99
- Rheumatology 28
- Gastroenterology 8
- Molecular Biology 96
- Neurology 21
Countries citing papers authored by Eda Ütine
This map shows the geographic impact of Eda Ütine'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 Eda Ütine with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Eda Ütine more than expected).
Fields of papers citing papers by Eda Ütine
This network shows the impact of papers produced by Eda Ütine. 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 Eda Ütine. The network helps show where Eda Ütine may publish in the future.
Co-authors
The 25 scholars most cited alongside Eda Ütine, 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 24 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2016 | 32 | |
| 2 | 2007 | 30 | |
| 3 | 2005 | 28 | |
| 4 | 2013 | 23 | |
| 5 | 2013 | 15 | |
| 6 | 2021 | 12 | |
| 7 | 2012 | 12 | |
| 8 | 2010 | 10 | |
| 9 | Arterial tortuosity and aneurysm in a case of Loeys-Dietz syndrome type IB with a mutation p.R537P in the TGFBR2 gene. | 2012 | 8 |
| 10 | 2007 | 7 | |
| 11 | 2020 | 7 | |
| 12 | 2016 | 6 | |
| 13 | 2021 | 5 | |
| 14 | 2013 | 5 | |
| 15 | 2022 | 4 | |
| 16 | 2009 | 3 | |
| 17 | 2016 | 3 | |
| 18 | 2020 | 3 | |
| 19 | 2014 | 2 | |
| 20 | 2024 | 1 |
About Eda Ütine
Eda Ütine is a scholar working on Genetics, Molecular Biology, Surgery, Pulmonary and Respiratory Medicine and Genetics, having authored 24 papers that have together received 218 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (4 papers), Medical Imaging and Pathology Studies (2 papers), Cerebrovascular and genetic disorders (2 papers), Neurological Complications and Syndromes (2 papers), Connective tissue disorders research (2 papers), Moyamoya disease diagnosis and treatment (2 papers), Craniofacial Disorders and Treatments (2 papers) and Prenatal Screening and Diagnostics (2 papers). The work is most often cited by research in Genetics (99 citations), Rheumatology (28 citations), Gastroenterology (8 citations), Molecular Biology (96 citations) and Neurology (21 citations). Eda Ütine has collaborated with scholars based in Türkiye, United Kingdom and United States. Frequent co-authors include Yasemin Alanay, Koray Boduroğlu, Dilek Aktaş, Pelin Özlem Şimşek‐Kiper, Ergül Tunçbılek, Ekim Z. Taşkıran, Melda Çaǧlar, Esra KAYA KILIÇ, Beril Talim and Lütfü Önderoğlu. Their work appears in journals such as Journal of Intellectual Disability Research, Molecular Cytogenetics, PEDIATRICS, Neuropediatrics and Journal of Medical Genetics.
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.