Christopher Vittal
Impact in
- Genetics top 0.5%
- Genomics and Rare Diseases
- Genetic Associations and Epidemiology
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- BRCA gene mutations in cancer
- Clinical Biochemistry top 1%
- Metabolism and Genetic Disorders
Papers in
- Genetics 13
- Genomics and Rare Diseases 13
- Genetic Associations and Epidemiology 5
- Evolution and Genetic Dynamics 2
- Genomic variations and chromosomal abnormalities 1
-
- Parkinson's Disease Mechanisms and Treatments 1
- Co-authors
- Timothy Poterba (1 shared paper)Daniel J. Goldstein (1 shared paper)Konrad J. Karczewski (1 shared paper)Cotton Seed (1 shared paper)Daniel A. King (1 shared paper)Benjamin M. Neale (1 shared paper)Jacqueline I. Goldstein (1 shared paper)
- Journals
- Nature (7 papers)Nature Communications (3 papers)Bioinformatics (1 paper)Nature Medicine (1 paper)Nature Genetics (1 paper)
- Partner nations
- United StatesFinlandUnited Kingdom
In The Last Decade
Christopher Vittal
14 papers receiving 9.2k citations
Christopher Vittal's Hit Papers
Peers
Comparison fields: 5 of 119
- Genetics 4.5k
- Clinical Biochemistry 219
- Molecular Biology 2k
- Cancer Research 418
- Neurology 377
Countries citing papers authored by Christopher Vittal
This map shows the geographic impact of Christopher Vittal'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 Vittal with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Christopher Vittal more than expected).
Fields of papers citing papers by Christopher Vittal
This network shows the impact of papers produced by Christopher Vittal. 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 Vittal. The network helps show where Christopher Vittal may publish in the future.
Co-authors
The 7 scholars most cited alongside Christopher Vittal, 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 | The mutational constraint spectrum quantified from variation in 141,456 humans Hit paper breakdown → | 2020 | 6789 |
| 2 | A genomic mutational constraint map using variation in 76,156 human genomes Hit paper breakdown → | 2023 | 966 |
| 3 | A structural variation reference for medical and population genetics Hit paper breakdown → | 2020 | 650 |
| 4 | Systematic single-variant and gene-based association testing of thousands of phenotypes in 394,841 UK Biobank exomes Hit paper breakdown → | 2022 | 183 |
| 5 | 2020 | 135 | |
| 6 | 2020 | 130 | |
| 7 | 2020 | 130 | |
| 8 | 2020 | 111 | |
| 9 | 2020 | 100 | |
| 10 | 2021 | 38 | |
| 11 | 2023 | 22 | |
| 12 | 2025 | 8 | |
| 13 | 2024 | 6 | |
| 14 | The mutational constraint spectrum quantified from variation in 141,456 humans (vol 581, pg 434, 2020) | 2021 | 2 |
About Christopher Vittal
Christopher Vittal is a scholar working on Genetics, Neurology, Molecular Biology, Nuclear Energy and Engineering and Waste Management and Disposal, having authored 14 papers that have together received 9.3k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (13 papers), Genetic Associations and Epidemiology (5 papers), Evolution and Genetic Dynamics (2 papers), Genomics and Phylogenetic Studies (1 paper), Parkinson's Disease Mechanisms and Treatments (1 paper) and Genomic variations and chromosomal abnormalities (1 paper). The work is most often cited by research in Genetics (4.5k citations), Clinical Biochemistry (219 citations), Molecular Biology (2k citations), Cancer Research (418 citations) and Neurology (377 citations). Christopher Vittal has collaborated with scholars based in United States, Finland and United Kingdom. Frequent co-authors include Timothy Poterba, Daniel J. Goldstein, Konrad J. Karczewski, Cotton Seed, Daniel A. King, Benjamin M. Neale and Jacqueline I. Goldstein. Their work appears in journals such as Nature, Nature Communications, Bioinformatics, Nature Medicine and Nature 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.