Matt E. Hurles
Impact in
- Genetics top 0.5%
- Genetic Associations and Epidemiology
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetic Mapping and Diversity in Plants and Animals
- Genetic and phenotypic traits in livestock
- Cancer Research top 2%
- Cancer Genomics and Diagnostics
Papers in
- Genetics 14
- Genetic Associations and Epidemiology 8
- Genomics and Rare Diseases 6
- Genetic and Kidney Cyst Diseases 3
- Diabetes and associated disorders 2
- Genomic variations and chromosomal abnormalities 2
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- Liver Disease Diagnosis and Treatment 4
- Co-authors
- Andrew H. Crosby (2 shared papers)Barry A. Chioza (2 shared papers)Saeed Al-Turki (2 shared papers)Katy E Barwick (2 shared papers)Randy Blakely (1 shared paper)Timothy J. Mohun (1 shared paper)David J. Adams (1 shared paper)Alicia M. Ruggiero (1 shared paper)
- Journals
- Nature Communications (4 papers)Nature (3 papers)Scientific Reports (2 papers)The American Journal of Human Genetics (2 papers)Research and Practice in Thrombosis and Haemostasis (1 paper)
- Partner nations
- United KingdomUnited StatesSwitzerland
In The Last Decade
Matt E. Hurles
19 papers receiving 8.5k citations
Matt E. Hurles's Hit Papers
Peers
Comparison fields: 5 of 170
- Genetics 4.1k
- Cancer Research 778
- Molecular Biology 3.8k
- Immunology 504
- Infectious Diseases 411
Countries citing papers authored by Matt E. Hurles
This map shows the geographic impact of Matt E. Hurles'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 Matt E. Hurles with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Matt E. Hurles more than expected).
Fields of papers citing papers by Matt E. Hurles
This network shows the impact of papers produced by Matt E. Hurles. 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 Matt E. Hurles. The network helps show where Matt E. Hurles may publish in the future.
Co-authors
The 25 scholars most cited alongside Matt E. Hurles, 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 21 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | A map of human genome variation from population-scale sequencing Hit paper breakdown → | 2010 | 6317 |
| 2 | Mapping the human genetic architecture of COVID-19 Hit paper breakdown → | 2021 | 641 |
| 3 | Demographic history and rare allele sharing among human populations Hit paper breakdown → | 2011 | 475 |
| 4 | 2010 | 416 | |
| 5 | 2016 | 200 | |
| 6 | 2017 | 126 | |
| 7 | 2022 | 107 | |
| 8 | 2012 | 84 | |
| 9 | 2013 | 69 | |
| 10 | 2013 | 67 | |
| 11 | 2015 | 51 | |
| 12 | 2013 | 40 | |
| 13 | 2024 | 23 | |
| 14 | 2024 | 12 | |
| 15 | 2023 | 8 | |
| 16 | 2025 | 4 | |
| 17 | 2023 | 2 | |
| 18 | 2023 | 2 | |
| 19 | 2014 | 1 | |
| 20 | 2025 | 0 |
About Matt E. Hurles
Matt E. Hurles is a scholar working on Genetics, Epidemiology, Molecular Biology, Pediatrics, Perinatology and Child Health and Infectious Diseases, having authored 21 papers that have together received 8.6k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (8 papers), Genomics and Rare Diseases (6 papers), Liver Disease Diagnosis and Treatment (4 papers), Genetic and Kidney Cyst Diseases (3 papers), Diabetes and associated disorders (2 papers), SARS-CoV-2 and COVID-19 Research (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Congenital heart defects research (2 papers). The work is most often cited by research in Genetics (4.1k citations), Cancer Research (778 citations), Molecular Biology (3.8k citations), Immunology (504 citations) and Infectious Diseases (411 citations). Matt E. Hurles has collaborated with scholars based in United Kingdom, United States and Switzerland. Frequent co-authors include Andrew H. Crosby, Barry A. Chioza, Saeed Al-Turki, Katy E Barwick, Randy Blakely, Timothy J. Mohun, David J. Adams, Alicia M. Ruggiero, Richard Alan Baldock and Jane Wright. Their work appears in journals such as Nature Communications, Nature, Scientific Reports, The American Journal of Human Genetics and Research and Practice in Thrombosis and Haemostasis.
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.