Sarah E. Brnich
Impact in
- Genetics top 10%
- Genomics and Rare Diseases
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
- Genetic Associations and Epidemiology
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- Cancer Genomics and Diagnostics
Papers in
- Genetics 6
- Genomics and Rare Diseases 6
- Genetic Associations and Epidemiology 3
- BRCA gene mutations in cancer 1
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- Cancer Genomics and Diagnostics 4
- Co-authors
- Jonathan S. Berg (6 shared papers)Shannon McNulty (2 shared papers)Dona Kanavy (2 shared papers)Lea M. Starita (2 shared papers)Garry R. Cutting (1 shared paper)Christopher D. Heinen (1 shared paper)Xi Luo (1 shared paper)Leslie G. Biesecker (1 shared paper)
- Journals
- Genome Medicine (3 papers)Genetics in Medicine (1 paper)Human Mutation (1 paper)Journal of Molecular Diagnostics (1 paper)
- Partner nations
- United StatesAustraliaUnited Arab Emirates
In The Last Decade
Sarah E. Brnich
6 papers receiving 470 citations
Sarah E. Brnich's Hit Papers
Peers
Comparison fields: 5 of 62
- Genetics 302
- Cancer Research 79
- Molecular Biology 281
- Pathology and Forensic Medicine 55
- Aging 5
Countries citing papers authored by Sarah E. Brnich
This map shows the geographic impact of Sarah E. Brnich'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 Sarah E. Brnich with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sarah E. Brnich more than expected).
Fields of papers citing papers by Sarah E. Brnich
This network shows the impact of papers produced by Sarah E. Brnich. 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 Sarah E. Brnich. The network helps show where Sarah E. Brnich may publish in the future.
Co-authors
The 25 scholars most cited alongside Sarah E. Brnich, 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 | Recommendations for application of the functional evidence PS3/BS3 criterion using the ACMG/AMP sequence variant interpretation framework Hit paper breakdown → | 2019 | 310 |
| 2 | 2019 | 48 | |
| 3 | 2018 | 45 | |
| 4 | 2018 | 34 | |
| 5 | 2019 | 33 | |
| 6 | 2021 | 1 |
About Sarah E. Brnich
Sarah E. Brnich is a scholar working on Genetics, Cancer Research, Molecular Biology, Pathology and Forensic Medicine and Infectious Diseases, having authored 6 papers that have together received 471 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (6 papers), Cancer Genomics and Diagnostics (4 papers), Genetic Associations and Epidemiology (3 papers), Genetic factors in colorectal cancer (2 papers), BRCA gene mutations in cancer (1 paper), RNA modifications and cancer (1 paper) and DNA Repair Mechanisms (1 paper). The work is most often cited by research in Genetics (302 citations), Cancer Research (79 citations), Molecular Biology (281 citations), Pathology and Forensic Medicine (55 citations) and Aging (5 citations). Sarah E. Brnich has collaborated with scholars based in United States, Australia and United Arab Emirates. Frequent co-authors include Jonathan S. Berg, Shannon McNulty, Dona Kanavy, Lea M. Starita, Garry R. Cutting, Christopher D. Heinen, Xi Luo, Leslie G. Biesecker, Steven M. Harrison and Fergus J. Couch. Their work appears in journals such as Genome Medicine, Genetics in Medicine, Human Mutation and Journal of Molecular Diagnostics.
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.