Bryce A. Seifert
Impact in
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- Cancer Genomics and Diagnostics
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- Genomics and Rare Diseases
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
Papers in
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- RNA modifications and cancer 2
- RNA Research and Splicing 2
- DNA Repair Mechanisms 1
- Genetics 4
- Neurogenetic and Muscular Disorders Research 2
- Genomic variations and chromosomal abnormalities 2
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 1
- Genomics and Rare Diseases 1
- Co-authors
- Daniel S. Marchuk (2 shared papers)Jonathan S. Berg (2 shared papers)Kirk C. Wilhelmsen (2 shared papers)James P. Evans (2 shared papers)Kristy Lee (2 shared papers)Deborah Ritter (2 shared papers)Norman E. Sharpless (1 shared paper)Yassmine Akkari (1 shared paper)
- Journals
- Genetics in Medicine (7 papers)JAMA Dermatology (1 paper)Clinical Cancer Research (1 paper)Circulation Cardiovascular Genetics (1 paper)Journal of Pediatric Genetics (1 paper)
- Partner nations
- United StatesAustraliaBelarus
In The Last Decade
Bryce A. Seifert
14 papers receiving 242 citations
Peers
Comparison fields: 5 of 36
- Cancer Research 62
- Genetics 116
- Pathology and Forensic Medicine 49
- Oncology 37
- Molecular Biology 76
Countries citing papers authored by Bryce A. Seifert
This map shows the geographic impact of Bryce A. Seifert'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 Bryce A. Seifert with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Bryce A. Seifert more than expected).
Fields of papers citing papers by Bryce A. Seifert
This network shows the impact of papers produced by Bryce A. Seifert. 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 Bryce A. Seifert. The network helps show where Bryce A. Seifert may publish in the future.
Co-authors
The 25 scholars most cited alongside Bryce A. Seifert, 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 | 2016 | 66 | |
| 2 | 2018 | 42 | |
| 3 | 2017 | 30 | |
| 4 | 2021 | 30 | |
| 5 | 2022 | 27 | |
| 6 | 2018 | 17 | |
| 7 | 2017 | 10 | |
| 8 | 2024 | 7 | |
| 9 | 2020 | 5 | |
| 10 | 2024 | 4 | |
| 11 | 2020 | 4 | |
| 12 | 2024 | 1 | |
| 13 | 2022 | 1 | |
| 14 | 2022 | 1 | |
| 15 | 2025 | 0 |
About Bryce A. Seifert
Bryce A. Seifert is a scholar working on Molecular Biology, Genetics, Genetics, Pathology and Forensic Medicine and Oncology, having authored 15 papers that have together received 245 indexed citations. Recurring topics across this work include Neurogenetic and Muscular Disorders Research (2 papers), Polyomavirus and related diseases (2 papers), RNA modifications and cancer (2 papers), Genomic variations and chromosomal abnormalities (2 papers), RNA Research and Splicing (2 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (1 paper), DNA Repair Mechanisms (1 paper) and Genomics and Rare Diseases (1 paper). The work is most often cited by research in Cancer Research (62 citations), Genetics (116 citations), Pathology and Forensic Medicine (49 citations), Oncology (37 citations) and Molecular Biology (76 citations). Bryce A. Seifert has collaborated with scholars based in United States, Australia and Belarus. Frequent co-authors include Daniel S. Marchuk, Jonathan S. Berg, Kirk C. Wilhelmsen, James P. Evans, Kristy Lee, Deborah Ritter, Norman E. Sharpless, Yassmine Akkari, Alan P. Hoyle and Lina Shao. Their work appears in journals such as Genetics in Medicine, JAMA Dermatology, Clinical Cancer Research, Circulation Cardiovascular Genetics and Journal of Pediatric 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.