Christopher A. Cassa

4.1k citations
38 papers · 1.9k · 2 hit papers · h-index 19

Impact in

Papers in

    • Genomics and Rare Diseases 16
    • Genetic Associations and Epidemiology 14
    • Genomic variations and chromosomal abnormalities 6
    • Evolution and Genetic Dynamics 4
    • CRISPR and Genetic Engineering 6
    • RNA and protein synthesis mechanisms 4

Christopher A. Cassa

38 papers receiving 1.9k citations

Christopher A. Cassa's Hit Papers

Polygenic background modifies penetrance of monogenic variants for tier 1 genomic conditions 2020 · 252 citations
2520+2+5Years since publication100200300

Peers

Christopher A. Cassa
Comparison fields: 5 of 147
  • Aging 56
  • Business and International Management 51
  • Genetics 727
  • Molecular Biology 882
  • Cancer Research 136
Replace Xiya Zhang with:
Xiya Zhang China
Paul Higgins United States
Shuhua Xu China
David King United States
Upasna Sharma India
Y. Miyake Japan
Colin S. Gillespie United Kingdom
Enrique Vidal Spain
Asaf Madi Israel
Johanna Hardin United States
Christopher A. Cassa relative to Xiya Zhang China Xiya Zhang's profile →
Citations per field
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Xiya Zhang · 1×
Citations per year

Countries citing papers authored by Christopher A. Cassa

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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.

Border = papers with Christopher A. Cassa Line = papers co-authored together Christopher A. Cassa links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

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 →
2018380
2
Polygenic background modifies penetrance of monogenic variants for tier 1 genomic conditions
Hit paper breakdown →
2020252
3 2020185
4 2002146
5 201386
6 201779
7 200574
8 201170
9 201567
10 201365
11 202063
12 202260
13 201553
14 200852
15 200438
16 200634
17 200830
18 200822
19 202021
20 201117

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.

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