Sam Novod
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 12
- Genomics and Rare Diseases 12
- Genetic Associations and Epidemiology 4
- Evolution and Genetic Dynamics 2
- Genomic variations and chromosomal abnormalities 1
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- Parkinson's Disease Mechanisms and Treatments 1
- Journals
- Nature (7 papers)Nature Communications (3 papers)Nature Medicine (1 paper)Nature Neuroscience (1 paper)Nature Genetics (1 paper)
- Partner nations
- United StatesFinlandUnited Kingdom
In The Last Decade
Sam Novod
13 papers receiving 9k citations
Sam Novod's Hit Papers
Peers
Comparison fields: 5 of 119
- Genetics 4.4k
- Clinical Biochemistry 217
- Cancer Research 415
- Molecular Biology 1.9k
- Neurology 373
Countries citing papers authored by Sam Novod
This map shows the geographic impact of Sam Novod'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 Sam Novod with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sam Novod more than expected).
Fields of papers citing papers by Sam Novod
This network shows the impact of papers produced by Sam Novod. 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 Sam Novod. The network helps show where Sam Novod may publish in the future.
No co-authors to show.
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 | 2020 | 135 | |
| 5 | 2020 | 130 | |
| 6 | 2020 | 130 | |
| 7 | 2020 | 111 | |
| 8 | 2020 | 100 | |
| 9 | 2021 | 38 | |
| 10 | 2024 | 33 | |
| 11 | 2023 | 22 | |
| 12 | 2025 | 8 | |
| 13 | The mutational constraint spectrum quantified from variation in 141,456 humans (vol 581, pg 434, 2020) | 2021 | 2 |
About Sam Novod
Sam Novod is a scholar working on Genetics, Neurology, Psychiatry and Mental health, Nuclear Energy and Engineering and Waste Management and Disposal, having authored 13 papers that have together received 9.1k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (12 papers), Genetic Associations and Epidemiology (4 papers), Evolution and Genetic Dynamics (2 papers), Epilepsy research and treatment (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 (4.4k citations), Clinical Biochemistry (217 citations), Cancer Research (415 citations), Molecular Biology (1.9k citations) and Neurology (373 citations). Sam Novod has collaborated with scholars based in United States, Finland and United Kingdom. Their work appears in journals such as Nature, Nature Communications, Nature Medicine, Nature Neuroscience 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.