Matthew E. Hurles
- Genetics top 0.05%
- Genomic variations and chromosomal abnormalities 56
- Genomics and Rare Diseases 54
- Genetic Associations and Epidemiology 14
- Forensic and Genetic Research 12
- Developmental Neuroscience top 0.5%
- Molecular Biology top 0.5%
- Genomics and Phylogenetic Studies 17
- Cancer Research top 1%
- Cancer Genomics and Diagnostics 20
- Aging top 2%
-
- Chromosomal and Genetic Variations 21
-
- Prenatal Screening and Diagnostics 12
- Co-authors
- Andrew P. JacksonLouise S. BicknellTessa HomfrayJosef PenningerJuergen A. KnoblichCarol-Anne MartinMadeline A. LancasterMagdalena Renner
- Journals
- The American Journal of Human Genetics (14 papers)Nature Communications (10 papers)Nature Genetics (10 papers)
- Partner nations
- United KingdomUnited StatesCanada
In The Last Decade
Matthew E. Hurles
125 papers receiving 16.0k citations
Hit Papers
Peers
Comparison fields: 5 of 186
- Genetics 8.9k
- Developmental Neuroscience 660
- Molecular Biology 8.8k
- Cancer Research 1.5k
- Aging 118
Countries citing papers authored by Matthew E. Hurles
This map shows the geographic impact of Matthew 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 Matthew 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 Matthew E. Hurles more than expected).
Fields of papers citing papers by Matthew E. Hurles
This network shows the impact of papers produced by Matthew 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 Matthew E. Hurles. The network helps show where Matthew E. Hurles may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Matthew 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 | 2025 | 0 | |
| 2 | 2024 | 0 | |
| 3 | 2024 | 8 | |
| 4 | 2023 | 8 | |
| 5 | 2020 | 13 | |
| 6 | 2019 | 53 | |
| 7 | 2019 | 78 | |
| 8 | 2018 | 184 | |
| 9 | 2017 | 38 | |
| 10 | 2010 | 214 | |
| 11 | 2010 | 67 | |
| 12 | 2009 | 384 | |
| 13 | 2007 | 127 | |
| 14 | 2006 | 48 | |
| 15 | Copy number variation: New insights in genome diversitybreakdown → | 2006 | 592 |
| 16 | 2006 | 113 | |
| 17 | 2004 | 64 | |
| 18 | 2003 | 25 | |
| 19 | 2001 | 53 | |
| 20 | 1998 | 95 |
About Matthew E. Hurles
Matthew E. Hurles is a scholar working on Genetics, Cancer Research, Molecular Biology, Geography, Planning and Development and Pediatrics, Perinatology and Child Health, having authored 128 papers that have together received 16.4k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (56 papers), Genomics and Rare Diseases (54 papers), Chromosomal and Genetic Variations (21 papers), Cancer Genomics and Diagnostics (20 papers), Genomics and Phylogenetic Studies (17 papers), Genetic Associations and Epidemiology (14 papers), Forensic and Genetic Research (12 papers) and Prenatal Screening and Diagnostics (12 papers). The work is most often cited by research in Genetics (8.9k citations), Developmental Neuroscience (660 citations), Molecular Biology (8.8k citations), Cancer Research (1.5k citations) and Aging (118 citations). Matthew E. Hurles has collaborated with scholars based in United Kingdom, United States and Canada. Frequent co-authors include Andrew P. Jackson, Louise S. Bicknell, Tessa Homfray, Josef Penninger, Juergen A. Knoblich, Carol-Anne Martin, Madeline A. Lancaster, Magdalena Renner, D. Wénzel and Donald F. Conrad. Their work appears in journals such as The American Journal of Human Genetics, Nature Communications, Nature Genetics, Genome Research and Nature.
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.