Amanda L. Bergner
- Neurology top 5%
- Neurofibromatosis and Schwannoma Cases 10
- Vascular Malformations Diagnosis and Treatment 4
- Genetics top 10%
- Genomics and Rare Diseases 11
- BRCA gene mutations in cancer 5
- Genetics and Neurodevelopmental Disorders 3
- Clinical Biochemistry top 10%
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- Epilepsy research and treatment 5
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- Meningioma and schwannoma management 7
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- Ethics in Clinical Research 3
- Co-authors
- Jaishri O. BlakeleyXiaobu YeJuli BollingerCynthia A. JamesVanessa L. MerkerScott R. PlotkinLouise BierThierry A.G.M. Huisman
- Partner nations
- United StatesCanadaUnited Kingdom
In The Last Decade
Amanda L. Bergner
31 papers receiving 625 citations
Peers
Comparison fields: 5 of 74
- Neurology 244
- Genetics 227
- Clinical Biochemistry 42
- Psychiatry and Mental health 63
- Epidemiology 138
Countries citing papers authored by Amanda L. Bergner
This map shows the geographic impact of Amanda L. Bergner'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 Amanda L. Bergner with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Amanda L. Bergner more than expected).
Fields of papers citing papers by Amanda L. Bergner
This network shows the impact of papers produced by Amanda L. Bergner. 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 Amanda L. Bergner. The network helps show where Amanda L. Bergner may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Amanda L. Bergner, 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 | 2025 | 0 | |
| 2 | 2024 | 3 | |
| 3 | 2023 | 1 | |
| 4 | 2023 | 3 | |
| 5 | 2023 | 1 | |
| 6 | 2023 | 1 | |
| 7 | 2023 | 10 | |
| 8 | 2023 | 5 | |
| 9 | 2021 | 67 | |
| 10 | 2021 | 5 | |
| 11 | 2020 | 15 | |
| 12 | 2018 | 16 | |
| 13 | 2017 | 27 | |
| 14 | 2016 | 86 | |
| 15 | 2016 | 17 | |
| 16 | 2015 | 7 | |
| 17 | 2014 | 2 | |
| 18 | 2012 | 74 | |
| 19 | 2010 | 30 | |
| 20 | 2008 | 46 |
About Amanda L. Bergner
Amanda L. Bergner is a scholar working on Health Informatics, Neurology and Genetics, having authored 32 papers that have together received 640 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (11 papers), Neurofibromatosis and Schwannoma Cases (10 papers), Meningioma and schwannoma management (7 papers), BRCA gene mutations in cancer (5 papers), Epilepsy research and treatment (5 papers), Vascular Malformations Diagnosis and Treatment (4 papers), Ethics in Clinical Research (3 papers) and Genetics and Neurodevelopmental Disorders (3 papers). The work is most often cited by research in Neurology (244 citations), Genetics (227 citations) and Clinical Biochemistry (42 citations). Amanda L. Bergner has collaborated with scholars based in United States, Canada and United Kingdom. Frequent co-authors include Jaishri O. Blakeley, Xiaobu Ye, Juli Bollinger, Cynthia A. James, Vanessa L. Merker, Scott R. Plotkin, Louise Bier, Thierry A.G.M. Huisman, Aylin Tekes and Lori C. Jordan.
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.