Gönül Oğur
Impact in
- Nephrology top 10%
- Gout, Hyperuricemia, Uric Acid
- Reproductive Medicine top 10%
- Sperm and Testicular Function
Papers in
-
- Congenital limb and hand anomalies 4
- Genetics 21
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 6
- Connective tissue disorders research 4
- Genomic variations and chromosomal abnormalities 4
- Co-authors
- Nathan Fischel‐GhodsianYehuda L. DanonMordechai ShohatMehmet Eren YükselPierre HeimannNurit MagalHerman TournayeM Bonduelle
- Journals
- Prenatal Diagnosis (2 papers)Journal of Medical Genetics (2 papers)Human Mutation (2 papers)Andrologia (2 papers)Clinical Genetics (2 papers)
- Partner nations
- TürkiyeBelgiumUnited States
In The Last Decade
Gönül Oğur
48 papers receiving 654 citations
Peers
Comparison fields: 5 of 63
- Nephrology 64
- Reproductive Medicine 68
- Genetics 210
- Immunology 151
- Molecular Biology 468
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-authorship network
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
| # | Work | ||
|---|---|---|---|
| 1 | 2019 | 29 | |
| 2 | Correlation of phenotype with the CYP21 gene mutation analysis of classic type congenital adrenal hyperplasia due to 21-Hydroxylase deficiency | 2019 | 1 |
| 3 | 2019 | 2 | |
| 4 | 2018 | 1 | |
| 5 | 2017 | 1 | |
| 6 | 2017 | 1 | |
| 7 | 2016 | 2 | |
| 8 | 2016 | 33 | |
| 9 | 2013 | 17 | |
| 10 | 2012 | 6 | |
| 11 | 2012 | 15 | |
| 12 | 2006 | 20 | |
| 13 | 2006 | 86 | |
| 14 | 2002 | 4 | |
| 15 | 2001 | 5 | |
| 16 | 1999 | 167 | |
| 17 | 1998 | 6 | |
| 18 | 1998 | 6 | |
| 19 | 1997 | 7 | |
| 20 | 1990 | 12 |
About Gönül Oğur
Gönül Oğur is a scholar working on Developmental Biology, Genetics, Hematology, Pediatrics, Perinatology and Child Health and Immunology, having authored 51 papers that have together received 700 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (7 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers), Sexual Differentiation and Disorders (6 papers), Inflammasome and immune disorders (5 papers), Fetal and Pediatric Neurological Disorders (5 papers), Connective tissue disorders research (4 papers), Congenital limb and hand anomalies (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). The work is most often cited by research in Nephrology (64 citations), Reproductive Medicine (68 citations), Genetics (210 citations), Immunology (151 citations) and Molecular Biology (468 citations). Gönül Oğur has collaborated with scholars based in Türkiye, Belgium and United States. Frequent co-authors include Nathan Fischel‐Ghodsian, Yehuda L. Danon, Mordechai Shohat, Mehmet Eren Yüksel, Pierre Heimann, Nurit Magal, Herman Tournaye, M Bonduelle, Tami Shohat and Walter Vegetti. Their work appears in journals such as Prenatal Diagnosis, Journal of Medical Genetics, Human Mutation, Andrologia and Clinical 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.