Brooke Smith
Impact in
-
- Hereditary Neurological Disorders
- Genetic Neurodegenerative Diseases
- Neurology top 2%
- Neurological diseases and metabolism
- Botulinum Toxin and Related Neurological Disorders
- Peripheral Neuropathies and Disorders
Papers in
- Genetics 3
- Genomic variations and chromosomal abnormalities 3
- Genetics and Neurodevelopmental Disorders 2
-
- Antifungal resistance and susceptibility 2
- Co-authors
- Thomas D. Bird (2 shared papers)Norisada Matsunami (2 shared papers)M. William Lensch (2 shared papers)Phillip F. Chance (2 shared papers)Christine M. Distèche (1 shared paper)Phillip D. Swanson (1 shared paper)Kathleen A. Leppig (1 shared paper)Shannon J. Odelberg (1 shared paper)
- Journals
- Frontiers in Microbiology (2 papers)The Journal of Rheumatology (1 paper)Nature Genetics (1 paper)Cell (1 paper)European Journal of Medical Genetics (1 paper)
- Partner nations
- United StatesCzechiaGermany
In The Last Decade
Brooke Smith
8 papers receiving 949 citations
Brooke Smith's Hit Papers
Peers
Comparison fields: 5 of 62
- Cellular and Molecular Neuroscience 719
- Neurology 302
- Neurology 256
- Cell Biology 141
- Genetics 66
Countries citing papers authored by Brooke Smith
This map shows the geographic impact of Brooke Smith'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 Brooke Smith with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Brooke Smith more than expected).
Fields of papers citing papers by Brooke Smith
This network shows the impact of papers produced by Brooke Smith. 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 Brooke Smith. The network helps show where Brooke Smith may publish in the future.
Co-authors
The 25 scholars most cited alongside Brooke Smith, 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 | DNA deletion associated with hereditary neuropathy with liability to pressure palsies Hit paper breakdown → | 1993 | 606 |
| 2 | 1992 | 246 | |
| 3 | 2016 | 42 | |
| 4 | 2019 | 29 | |
| 5 | 2016 | 20 | |
| 6 | 2015 | 18 | |
| 7 | 2021 | 11 | |
| 8 | 2009 | 3 |
About Brooke Smith
Brooke Smith is a scholar working on Genetics, Infectious Diseases, Molecular Biology, Cellular and Molecular Neuroscience and Epidemiology, having authored 8 papers that have together received 975 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (3 papers), Hereditary Neurological Disorders (2 papers), Antifungal resistance and susceptibility (2 papers), Genetics and Neurodevelopmental Disorders (2 papers), Fungal Infections and Studies (2 papers), Cellular Mechanics and Interactions (2 papers), Hemophilia Treatment and Research (1 paper) and Signaling Pathways in Disease (1 paper). The work is most often cited by research in Cellular and Molecular Neuroscience (719 citations), Neurology (302 citations), Neurology (256 citations), Cell Biology (141 citations) and Genetics (66 citations). Brooke Smith has collaborated with scholars based in United States, Czechia and Germany. Frequent co-authors include Thomas D. Bird, Norisada Matsunami, M. William Lensch, Phillip F. Chance, Christine M. Distèche, Phillip D. Swanson, Kathleen A. Leppig, Shannon J. Odelberg, Hans Albertsen and R. White. Their work appears in journals such as Frontiers in Microbiology, The Journal of Rheumatology, Nature Genetics, Cell and European Journal of Medical Genetics.
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.