Stephany Donze
- Genetics top 10%
- Pediatrics, Perinatology and Child Health top 10%
- Molecular Biology
- Surgery
- Social Psychology
- Co-authors
- Anita C. S. Hokken‐KoelegaRenske KuppensLayla DamenAnita Hokken-KoelegaNienke BakkerElbrich P. C. SiemensmaTheo StijnenLaura C. G. de Graaff
- Topics
- Genetic Syndromes and Imprinting (18 papers)Prenatal Screening and Diagnostics (14 papers)Genetics and Neurodevelopmental Disorders (6 papers)
- Partner nations
- NetherlandsUnited KingdomSwitzerland
In The Last Decade
Stephany Donze
21 papers receiving 435 citations
Peers
Comparison fields: 5 of 52
- Genetics 340
- Pediatrics, Perinatology and Child Health 124
- Molecular Biology 118
- Surgery 66
- Social Psychology 59
Countries citing papers authored by Stephany Donze
This map shows the geographic impact of Stephany Donze'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 Stephany Donze with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stephany Donze more than expected).
Fields of papers citing papers by Stephany Donze
This network shows the impact of papers produced by Stephany Donze. 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 Stephany Donze. The network helps show where Stephany Donze may publish in the future.
Co-authorship network of co-authors of Stephany Donze
This figure shows the co-authorship network connecting the top 25 collaborators of Stephany Donze. A scholar is included among the top collaborators of Stephany Donze 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 Stephany Donze. Stephany Donze is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 2 | |
| 2 | 4 | |
| 3 | 2 | |
| 4 | 4 | |
| 5 | 16 | |
| 6 | 18 | |
| 7 | 13 | |
| 8 | 37 | |
| 9 | 1 | |
| 10 | 14 | |
| 11 | 7 | |
| 12 | 18 | |
| 13 | 82 | |
| 14 | 24 | |
| 15 | 19 | |
| 16 | 34 | |
| 17 | 17 | |
| 18 | 21 | |
| 19 | 65 | |
| 20 | 23 |
About Stephany Donze
Stephany Donze is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Endocrinology, Diabetes and Metabolism, having authored 21 papers that have together received 438 indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (18 papers), Prenatal Screening and Diagnostics (14 papers) and Genetics and Neurodevelopmental Disorders (6 papers). The work is most often cited by research in Genetics (340 citations), Endocrine and Autonomic Systems (49 citations) and Pediatrics, Perinatology and Child Health (124 citations). Stephany Donze has collaborated with scholars based in Netherlands, United Kingdom and Switzerland. Frequent co-authors include Anita C. S. Hokken‐Koelega, Renske Kuppens, Layla Damen, Anita Hokken-Koelega, Nienke Bakker, Elbrich P. C. Siemensma, Theo Stijnen, Laura C. G. de Graaff, Garth W. Strohbehn and Sébastien G. Bouret. Their work appears in journals such as The Journal of Clinical Endocrinology & Metabolism, Cell Reports and Psychoneuroendocrinology.
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.