Gönül Oğur
Impact in
- Nephrology top 10%
- Gout, Hyperuricemia, Uric Acid
- Genetics top 10%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genomic variations and chromosomal abnormalities
Papers in
-
- Sexual Differentiation and Disorders 5
- Inflammasome and immune disorders 5
- Genetics 21
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 6
- Genomic variations and chromosomal abnormalities 4
- Connective tissue disorders research 4
- Co-authors
- Nathan Fischel‐Ghodsian (4 shared papers)Yehuda L. Danon (4 shared papers)Mordechai Shohat (2 shared papers)Mehmet Eren Yüksel (2 shared papers)Pierre Heimann (5 shared papers)Nurit Magal (2 shared papers)Tami Shohat (2 shared papers)Arthur D. Schwabe (2 shared papers)
- Journals
- Prenatal Diagnosis (2 papers)Andrologia (2 papers)Human Mutation (2 papers)Clinical Genetics (2 papers)Journal of Medical Genetics (2 papers)
- Partner nations
- TürkiyeUnited StatesBelgium
In The Last Decade
Gönül Oğur
48 papers receiving 659 citations
Peers
Comparison fields: 5 of 62
- Nephrology 46
- Genetics 187
- Reproductive Medicine 51
- Molecular Biology 434
- Immunology 110
Countries citing papers authored by Gönül Oğur
This map shows the geographic impact of Gönül Oğur'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 Gönül Oğur with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Gönül Oğur more than expected).
Fields of papers citing papers by Gönül Oğur
This network shows the impact of papers produced by Gönül Oğur. 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 Gönül Oğur. The network helps show where Gönül Oğur may publish in the future.
Co-authors
The 25 scholars most cited alongside Gönül Oğur, 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 51 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1999 | 167 | |
| 2 | 2006 | 86 | |
| 3 | Fusion of a novel gene, RCC17, to the TFE3 gene in t(X;17)(p11.2;q25.3)-bearing papillary renal cell carcinomas. | 2001 | 61 |
| 4 | 1998 | 39 | |
| 5 | 2016 | 34 | |
| 6 | 2019 | 31 | |
| 7 | 2015 | 24 | |
| 8 | 1988 | 23 | |
| 9 | 2006 | 20 | |
| 10 | 2012 | 19 | |
| 11 | 2013 | 17 | |
| 12 | 2012 | 15 | |
| 13 | 2000 | 15 | |
| 14 | 1990 | 12 | |
| 15 | 1995 | 11 | |
| 16 | 2018 | 10 | |
| 17 | 1986 | 10 | |
| 18 | 1994 | 8 | |
| 19 | 2002 | 7 | |
| 20 | 1993 | 7 |
About Gönül Oğur
Gönül Oğur is a scholar working on Molecular Biology, Genetics, Surgery, Pediatrics, Perinatology and Child Health and Hematology, having authored 51 papers that have together received 705 indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers), Sexual Differentiation and Disorders (5 papers), Inflammasome and immune disorders (5 papers), Prenatal Screening and Diagnostics (5 papers), Congenital limb and hand anomalies (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Connective tissue disorders research (4 papers) and interferon and immune responses (3 papers). The work is most often cited by research in Nephrology (46 citations), Genetics (187 citations), Reproductive Medicine (51 citations), Molecular Biology (434 citations) and Immunology (110 citations). Gönül Oğur has collaborated with scholars based in Türkiye, United States and Belgium. Frequent co-authors include Nathan Fischel‐Ghodsian, Yehuda L. Danon, Mordechai Shohat, Mehmet Eren Yüksel, Pierre Heimann, Nurit Magal, Tami Shohat, Arthur D. Schwabe, Elvire Van Assche and Greta Verheyen. Their work appears in journals such as Prenatal Diagnosis, Andrologia, Human Mutation, Clinical Genetics 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.