Stephanie Newton
- Co-authors
- Jeff M. MilunskyTom A. MaherYing ZouAntony A. BoucardJaewon KoAlice S. CarterHelen Tager‐FlusbergChen Zhang
- Topics
- Genomic variations and chromosomal abnormalities (4 papers)Genetics and Neurodevelopmental Disorders (3 papers)Autism Spectrum Disorder Research (3 papers)
- Partner nations
- United StatesMexicoUnited Kingdom
In The Last Decade
Stephanie Newton
7 papers receiving 266 citations
Peers
Comparison fields: 5 of 44
- Genetics 169
- Molecular Biology 126
- Cognitive Neuroscience 91
- Cellular and Molecular Neuroscience 66
- Cell Biology 37
Countries citing papers authored by Stephanie Newton
This map shows the geographic impact of Stephanie Newton'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 Newton with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stephanie Newton more than expected).
Fields of papers citing papers by Stephanie Newton
This network shows the impact of papers produced by Stephanie Newton. 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 Newton. The network helps show where Stephanie Newton may publish in the future.
Co-authorship network of co-authors of Stephanie Newton
This figure shows the co-authorship network connecting the top 25 collaborators of Stephanie Newton. A scholar is included among the top collaborators of Stephanie Newton 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 Newton. Stephanie Newton is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 0 | |
| 2 | 28 | |
| 3 | 15 | |
| 4 | 35 | |
| 5 | 1 | |
| 6 | 45 | |
| 7 | 14 | |
| 8 | 143 |
About Stephanie Newton
Stephanie Newton is a scholar working on Genetics, Cognitive Neuroscience and Cellular and Molecular Neuroscience, having authored 8 papers that have together received 281 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (4 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Autism Spectrum Disorder Research (3 papers). The work is most often cited by research in Genetics (169 citations), Cognitive Neuroscience (91 citations) and Cellular and Molecular Neuroscience (66 citations). Stephanie Newton has collaborated with scholars based in United States, Mexico and United Kingdom. Frequent co-authors include Jeff M. Milunsky, Tom A. Maher, Ying Zou, Antony A. Boucard, Jaewon Ko, Alice S. Carter, Helen Tager‐Flusberg, Chen Zhang, Geping Zhao and Craig M. Powell. Their work appears in journals such as Journal of Neuroscience, Synapse and American Journal of Medical Genetics Part A.
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.