Katelyn Payne
Impact in
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- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 4
- Genetics and Neurodevelopmental Disorders 4
- Genomics and Rare Diseases 2
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- Epigenetics and DNA Methylation 1
- Ion Transport and Channel Regulation 1
- DNA Repair Mechanisms 1
- Co-authors
- Stephen R. Dlouhy (2 shared papers)Joanne Wojcieszek (1 shared paper)Boris Keren (1 shared paper)Berivan Baskin (1 shared paper)Neda Zadeh (1 shared paper)Claudia M. Nicolae (1 shared paper)Jill A. Rosenfeld (1 shared paper)Zeynep Coban‐Akdemir (1 shared paper)
- Journals
- Journal of Child Neurology (1 paper)Annals of Clinical and Translational Neurology (1 paper)The American Journal of Human Genetics (1 paper)Medical Clinics of North America (1 paper)American Journal of Medical Genetics Part A (2 papers)
- Partner nations
- United StatesIsraelUnited Kingdom
In The Last Decade
Katelyn Payne
6 papers receiving 91 citations
Peers
Comparison fields: 5 of 31
- Genetics 42
- Neurology 6
- Molecular Biology 46
- Genetics 6
- Neurology 8
Countries citing papers authored by Katelyn Payne
This map shows the geographic impact of Katelyn Payne'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 Katelyn Payne with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Katelyn Payne more than expected).
Fields of papers citing papers by Katelyn Payne
This network shows the impact of papers produced by Katelyn Payne. 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 Katelyn Payne. The network helps show where Katelyn Payne may publish in the future.
Co-authors
The 25 scholars most cited alongside Katelyn Payne, 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 | 2017 | 35 | |
| 2 | 2019 | 32 | |
| 3 | 2018 | 10 | |
| 4 | 2019 | 9 | |
| 5 | 2018 | 4 | |
| 6 | 2024 | 3 |
About Katelyn Payne
Katelyn Payne is a scholar working on Genetics, Molecular Biology, Neurology, Cellular and Molecular Neuroscience and Neurology, having authored 6 papers that have together received 93 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (4 papers), Genomics and Rare Diseases (2 papers), Epigenetics and DNA Methylation (1 paper), Ion Transport and Channel Regulation (1 paper), DNA Repair Mechanisms (1 paper), Amyotrophic Lateral Sclerosis Research (1 paper), Parkinson's Disease Mechanisms and Treatments (1 paper) and Neurological diseases and metabolism (1 paper). The work is most often cited by research in Genetics (42 citations), Neurology (6 citations), Molecular Biology (46 citations), Genetics (6 citations) and Neurology (8 citations). Katelyn Payne has collaborated with scholars based in United States, Israel and United Kingdom. Frequent co-authors include Stephen R. Dlouhy, Joanne Wojcieszek, Boris Keren, Berivan Baskin, Neda Zadeh, Claudia M. Nicolae, Jill A. Rosenfeld, Zeynep Coban‐Akdemir, V. Reid Sutton and Richard H. Scott. Their work appears in journals such as Journal of Child Neurology, Annals of Clinical and Translational Neurology, The American Journal of Human Genetics, Medical Clinics of North America 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.