Matt E. Hurles
Impact in
- Genetics top 0.5%
- Genetic Associations and Epidemiology
- Genomics and Rare Diseases
- Forensic and Genetic Research
- Genetic diversity and population structure
- Evolution and Genetic Dynamics
- Genomic variations and chromosomal abnormalities
- Molecular Biology top 5%
- Genomics and Phylogenetic Studies
Papers in
- Genetics 15
- Genetic Associations and Epidemiology 9
- Genetic and Kidney Cyst Diseases 3
- Forensic and Genetic Research 2
- Genomics and Rare Diseases 2
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- Genomics and Phylogenetic Studies 2
- 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)James C. Smith (1 shared paper)Shoumo Bhattacharya (1 shared paper)A. Al‐Memar (1 shared paper)Timothy J. Mohun (1 shared paper)
- Journals
- Nature Communications (4 papers)Nature (3 papers)The American Journal of Human Genetics (2 papers)Scientific Reports (2 papers)Disease Models & Mechanisms (1 paper)
- Partner nations
- United KingdomUnited StatesSwitzerland
In The Last Decade
Matt E. Hurles
19 papers receiving 8.6k citations
Matt E. Hurles's Hit Papers
Peers
Comparison fields: 5 of 149
- Genetics 4.8k
- Molecular Biology 2.1k
- Cancer Research 348
- Infectious Diseases 443
- Pharmacology 186
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
| # | Work | ||
|---|---|---|---|
| 1 | A map of human genome variation from population-scale sequencing Hit paper breakdown → | 2010 | 6377 |
| 2 | Mapping the human genetic architecture of COVID-19 Hit paper breakdown → | 2021 | 656 |
| 3 | Demographic history and rare allele sharing among human populations Hit paper breakdown → | 2011 | 487 |
| 4 | 2010 | 424 | |
| 5 | 2016 | 205 | |
| 6 | 2017 | 126 | |
| 7 | 2022 | 124 | |
| 8 | 2012 | 84 | |
| 9 | 2013 | 70 | |
| 10 | 2013 | 67 | |
| 11 | 2015 | 50 | |
| 12 | 2013 | 40 | |
| 13 | 2024 | 26 | |
| 14 | 2024 | 12 | |
| 15 | 2023 | 8 | |
| 16 | 2023 | 4 | |
| 17 | 2025 | 4 | |
| 18 | 2023 | 2 | |
| 19 | 2025 | 1 | |
| 20 | 2026 | 0 |
About Matt E. Hurles
Matt E. Hurles is a scholar working on Genetics, Molecular Biology, Genetics, Obstetrics and Gynecology and Pediatrics, Perinatology and Child Health, having authored 20 papers that have together received 8.8k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (9 papers), Genetic and Kidney Cyst Diseases (3 papers), Forensic and Genetic Research (2 papers), Genomics and Phylogenetic Studies (2 papers), Genomics and Rare Diseases (2 papers), Pregnancy and Medication Impact (1 paper), Pregnancy and preeclampsia studies (1 paper) and Neonatal Health and Biochemistry (1 paper). The work is most often cited by research in Genetics (4.8k citations), Molecular Biology (2.1k citations), Cancer Research (348 citations), Infectious Diseases (443 citations) and Pharmacology (186 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, James C. Smith, Shoumo Bhattacharya, A. Al‐Memar, Timothy J. Mohun, Andrew J. Copp and Wolfgang J. Weninger. Their work appears in journals such as Nature Communications, Nature, The American Journal of Human Genetics, Scientific Reports and Disease Models & Mechanisms.
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.