Christopher A. Cassa
Impact in
- Aging top 5%
Papers in
- Genetics 21
- Genomics and Rare Diseases 16
- Genetic Associations and Epidemiology 14
- Genomic variations and chromosomal abnormalities 6
- Evolution and Genetic Dynamics 4
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- CRISPR and Genetic Engineering 6
- RNA and protein synthesis mechanisms 4
- Co-authors
- Kenneth D. Mandl (11 shared papers)Max W. Shen (3 shared papers)Mandana Arbab (2 shared papers)David R. Liu (2 shared papers)Richard I. Sherwood (6 shared papers)Daniel M. Jordan (6 shared papers)David K. Gifford (2 shared papers)Sannie J. Culbertson (1 shared paper)
- Journals
- Nature Genetics (3 papers)Cell Genomics (2 papers)Nature Communications (2 papers)Bioinformatics (2 papers)Genetics in Medicine (2 papers)
- Partner nations
- United StatesCanadaAustralia
In The Last Decade
Christopher A. Cassa
38 papers receiving 1.9k citations
Christopher A. Cassa's Hit Papers
Peers
Comparison fields: 5 of 147
- Aging 56
- Business and International Management 51
- Genetics 727
- Molecular Biology 882
- Cancer Research 136
Countries citing papers authored by Christopher A. Cassa
This map shows the geographic impact of Christopher A. Cassa'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 Christopher A. Cassa with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Christopher A. Cassa more than expected).
Fields of papers citing papers by Christopher A. Cassa
This network shows the impact of papers produced by Christopher A. Cassa. 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 Christopher A. Cassa. The network helps show where Christopher A. Cassa may publish in the future.
Co-authors
The 25 scholars most cited alongside Christopher A. Cassa, 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 38 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Predictable and precise template-free CRISPR editing of pathogenic variants Hit paper breakdown → | 2018 | 380 |
| 2 | Polygenic background modifies penetrance of monogenic variants for tier 1 genomic conditions Hit paper breakdown → | 2020 | 252 |
| 3 | 2020 | 185 | |
| 4 | 2002 | 146 | |
| 5 | 2013 | 86 | |
| 6 | 2017 | 79 | |
| 7 | 2005 | 74 | |
| 8 | 2011 | 70 | |
| 9 | 2015 | 67 | |
| 10 | 2013 | 65 | |
| 11 | 2020 | 63 | |
| 12 | 2022 | 60 | |
| 13 | 2015 | 53 | |
| 14 | 2008 | 52 | |
| 15 | 2004 | 38 | |
| 16 | 2006 | 34 | |
| 17 | 2008 | 30 | |
| 18 | 2008 | 22 | |
| 19 | 2020 | 21 | |
| 20 | 2011 | 17 |
About Christopher A. Cassa
Christopher A. Cassa is a scholar working on Genetics, Molecular Biology, Epidemiology, Cancer Research and Public Health, Environmental and Occupational Health, having authored 38 papers that have together received 1.9k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (16 papers), Genetic Associations and Epidemiology (14 papers), Data-Driven Disease Surveillance (8 papers), CRISPR and Genetic Engineering (6 papers), Genomic variations and chromosomal abnormalities (6 papers), Cancer Genomics and Diagnostics (5 papers), Evolution and Genetic Dynamics (4 papers) and RNA and protein synthesis mechanisms (4 papers). The work is most often cited by research in Aging (56 citations), Business and International Management (51 citations), Genetics (727 citations), Molecular Biology (882 citations) and Cancer Research (136 citations). Christopher A. Cassa has collaborated with scholars based in United States, Canada and Australia. Frequent co-authors include Kenneth D. Mandl, Max W. Shen, Mandana Arbab, David R. Liu, Richard I. Sherwood, Daniel M. Jordan, David K. Gifford, Sannie J. Culbertson, Jonathan Y. Hsu and Shamil Sunyaev. Their work appears in journals such as Nature Genetics, Cell Genomics, Nature Communications, Bioinformatics 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.