Braden E. Boone
Impact in
Papers in
- Genetics 15
- Genomics and Rare Diseases 8
- Genetics and Neurodevelopmental Disorders 5
- Genomic variations and chromosomal abnormalities 3
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- RNA and protein synthesis mechanisms 4
- Mitochondrial Function and Pathology 3
- RNA modifications and cancer 2
- Co-authors
- Shawn Levy (7 shared papers)Joseph A. Gogos (2 shared papers)Maria Karayiorgou (2 shared papers)Bin Xu (2 shared papers)Johannes Lodewikus Roos (2 shared papers)Phillip J. Dexheimer (2 shared papers)Iuliana Ionita‐Laza (1 shared paper)Yan Sun (1 shared paper)
- Journals
- The American Journal of Human Genetics (8 papers)Cell Systems (3 papers)Nature Genetics (2 papers)Cancer Research (2 papers)Journal of Biological Chemistry (2 papers)
- Partner nations
- United StatesUnited KingdomSouth Africa
In The Last Decade
Braden E. Boone
42 papers receiving 6.0k citations
Braden E. Boone's Hit Papers
Peers
Comparison fields: 5 of 167
- Genetics 2.0k
- Neurology 931
- Genetics 496
- Neurology 333
- Molecular Biology 2.7k
Countries citing papers authored by Braden E. Boone
This map shows the geographic impact of Braden E. Boone'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 Braden E. Boone with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Braden E. Boone more than expected).
Fields of papers citing papers by Braden E. Boone
This network shows the impact of papers produced by Braden E. Boone. 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 Braden E. Boone. The network helps show where Braden E. Boone may publish in the future.
Co-authors
The 25 scholars most cited alongside Braden E. Boone, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 42 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Patterns and rates of exonic de novo mutations in autism spectrum disorders Hit paper breakdown → | 2012 | 1378 |
| 2 | Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways Hit paper breakdown → | 2015 | 801 |
| 3 | Genome-wide Analyses Identify KIF5A as a Novel ALS Gene Hit paper breakdown → | 2018 | 526 |
| 4 | 2011 | 366 | |
| 5 | 2012 | 343 | |
| 6 | 2007 | 302 | |
| 7 | 2015 | 246 | |
| 8 | 2017 | 223 | |
| 9 | 2017 | 162 | |
| 10 | 2006 | 157 | |
| 11 | 2007 | 147 | |
| 12 | 2017 | 133 | |
| 13 | 2021 | 109 | |
| 14 | 2018 | 108 | |
| 15 | 2018 | 84 | |
| 16 | 2001 | 83 | |
| 17 | 2018 | 80 | |
| 18 | 1999 | 78 | |
| 19 | 2019 | 76 | |
| 20 | 2018 | 70 |
About Braden E. Boone
Braden E. Boone is a scholar working on Genetics, Molecular Biology, Clinical Biochemistry, Genetics and Public Health, Environmental and Occupational Health, having authored 42 papers that have together received 6.1k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (8 papers), Genetics and Neurodevelopmental Disorders (5 papers), RNA and protein synthesis mechanisms (4 papers), Mitochondrial Function and Pathology (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Zoonotic diseases and public health (2 papers), NF-κB Signaling Pathways (2 papers) and RNA modifications and cancer (2 papers). The work is most often cited by research in Genetics (2.0k citations), Neurology (931 citations), Genetics (496 citations), Neurology (333 citations) and Molecular Biology (2.7k citations). Braden E. Boone has collaborated with scholars based in United States, United Kingdom and South Africa. Frequent co-authors include Shawn Levy, Joseph A. Gogos, Maria Karayiorgou, Bin Xu, Johannes Lodewikus Roos, Phillip J. Dexheimer, Iuliana Ionita‐Laza, Yan Sun, Shirley B. Russell and Joan C. Smith. Their work appears in journals such as The American Journal of Human Genetics, Cell Systems, Nature Genetics, Cancer Research and Journal of Biological Chemistry.
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.