Sarah E. Brnich
Impact in
- Genetics top 10%
- Genomics and Rare Diseases
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
-
- Cancer Genomics and Diagnostics
Papers in
- Genetics 6
- Genomics and Rare Diseases 6
- Genetic Associations and Epidemiology 2
- BRCA gene mutations in cancer 1
-
- Cancer Genomics and Diagnostics 3
- Co-authors
- Jonathan S. Berg (6 shared papers)Dona Kanavy (2 shared papers)Shannon McNulty (2 shared papers)Lea M. Starita (2 shared papers)Marc S. Greenblatt (1 shared paper)Leslie G. Biesecker (1 shared paper)Matt W. Wright (1 shared paper)Ahmad Abou Tayoun (1 shared paper)
- Journals
- Genome Medicine (3 papers)Human Mutation (1 paper)Journal of Molecular Diagnostics (1 paper)Genetics in Medicine (1 paper)
- Partner nations
- United StatesUnited Arab EmiratesAustralia
In The Last Decade
Sarah E. Brnich
6 papers receiving 493 citations
Sarah E. Brnich's Hit Papers
Peers
Comparison fields: 5 of 58
- Genetics 275
- Cancer Research 53
- Molecular Biology 240
- Aging 5
- Pathology and Forensic Medicine 43
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 | 326 |
| 2 | 2019 | 50 | |
| 3 | 2018 | 46 | |
| 4 | 2018 | 36 | |
| 5 | 2019 | 34 | |
| 6 | 2021 | 2 |
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 494 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (6 papers), Cancer Genomics and Diagnostics (3 papers), Genetic Associations and Epidemiology (2 papers), DNA Repair Mechanisms (1 paper), BRCA gene mutations in cancer (1 paper) and Genetic factors in colorectal cancer (1 paper). The work is most often cited by research in Genetics (275 citations), Cancer Research (53 citations), Molecular Biology (240 citations), Aging (5 citations) and Pathology and Forensic Medicine (43 citations). Sarah E. Brnich has collaborated with scholars based in United States, United Arab Emirates and Australia. Frequent co-authors include Jonathan S. Berg, Dona Kanavy, Shannon McNulty, Lea M. Starita, Marc S. Greenblatt, Leslie G. Biesecker, Matt W. Wright, Ahmad Abou Tayoun, Xi Luo and Sean V. Tavtigian. Their work appears in journals such as Genome Medicine, Human Mutation, Journal of Molecular Diagnostics and Genetics in Medicine.
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.