Stephanie Fehr
- Genetics top 5%
- Cognitive Neuroscience top 10%
- Molecular Biology
- Clinical Psychology top 10%
- Psychiatry and Mental health top 10%
- Co-authors
- Helen LeonardJenny DownsNicholas de KlerkSimon WilliamsJohn ChristodoulouGladys HoAmi BebbingtonDavid Forbes
- Topics
- Genetics and Neurodevelopmental Disorders (9 papers)Genomic variations and chromosomal abnormalities (6 papers)Autism Spectrum Disorder Research (4 papers)
- Partner nations
- AustraliaUnited KingdomCanada
In The Last Decade
Stephanie Fehr
10 papers receiving 633 citations
Peers
Comparison fields: 5 of 50
- Genetics 584
- Cognitive Neuroscience 235
- Molecular Biology 188
- Clinical Psychology 152
- Psychiatry and Mental health 103
Countries citing papers authored by Stephanie Fehr
This map shows the geographic impact of Stephanie Fehr'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 Stephanie Fehr with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stephanie Fehr more than expected).
Fields of papers citing papers by Stephanie Fehr
This network shows the impact of papers produced by Stephanie Fehr. 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 Stephanie Fehr. The network helps show where Stephanie Fehr may publish in the future.
Co-authorship network of co-authors of Stephanie Fehr
This figure shows the co-authorship network connecting the top 25 collaborators of Stephanie Fehr. A scholar is included among the top collaborators of Stephanie Fehr 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 Stephanie Fehr. Stephanie Fehr is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 74 | |
| 2 | 78 | |
| 3 | 73 | |
| 4 | The natural history of the CDKL5 disorder: development of an international database | 1 |
| 5 | 209 | |
| 6 | 117 | |
| 7 | 18 | |
| 8 | 5 | |
| 9 | 36 | |
| 10 | 30 |
About Stephanie Fehr
Stephanie Fehr is a scholar working on Genetics, Cognitive Neuroscience and Clinical Psychology, having authored 10 papers that have together received 641 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (9 papers), Genomic variations and chromosomal abnormalities (6 papers) and Autism Spectrum Disorder Research (4 papers). The work is most often cited by research in Genetics (584 citations), Cognitive Neuroscience (235 citations) and Clinical Psychology (152 citations). Stephanie Fehr has collaborated with scholars based in Australia, United Kingdom and Canada. Frequent co-authors include Helen Leonard, Jenny Downs, Nicholas de Klerk, Simon Williams, John Christodoulou, Gladys Ho, Ami Bebbington, David Forbes, Gabriel M. Ronen and Natasha Nassar. Their work appears in journals such as Neurology, Drug and Alcohol Dependence and Pediatric Research.
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.