Matthew E. Hurles
Impact in
- Genetics top 0.05%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genetic Associations and Epidemiology
- Developmental Neuroscience top 0.5%
Papers in
- Genetics 104
- Genomic variations and chromosomal abnormalities 51
- Genomics and Rare Diseases 47
- Genetic Associations and Epidemiology 14
- Forensic and Genetic Research 13
- Genetic diversity and population structure 12
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- Genomics and Phylogenetic Studies 13
- Co-authors
- Andrew P. Jackson (3 shared papers)Louise S. Bicknell (3 shared papers)Tessa Homfray (3 shared papers)Carol-Anne Martin (1 shared paper)Josef Penninger (1 shared paper)Madeline A. Lancaster (1 shared paper)Juergen A. Knoblich (1 shared paper)D. Wénzel (1 shared paper)
- Journals
- The American Journal of Human Genetics (15 papers)Nature Genetics (10 papers)Nature Communications (10 papers)Genome Research (8 papers)Nature (8 papers)
- Partner nations
- United KingdomUnited StatesGermany
In The Last Decade
Matthew E. Hurles
133 papers receiving 17.1k citations
Matthew E. Hurles's Hit Papers
Peers
Comparison fields: 5 of 187
- Genetics 8.8k
- Developmental Neuroscience 682
- Molecular Biology 8.3k
- Cancer Research 1.3k
- Aging 116
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-authors
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
Showing the 20 most-cited of 137 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Cerebral organoids model human brain development and microcephaly Hit paper breakdown → | 2013 | 3892 |
| 2 | Relative Impact of Nucleotide and Copy Number Variation on Gene Expression Phenotypes Hit paper breakdown → | 2007 | 1327 |
| 3 | Copy Number Variation in Human Health, Disease, and Evolution Hit paper breakdown → | 2009 | 909 |
| 4 | Copy number variation: New insights in genome diversity Hit paper breakdown → | 2006 | 636 |
| 5 | A high-resolution survey of deletion polymorphism in the human genome Hit paper breakdown → | 2005 | 509 |
| 6 | 2010 | 445 | |
| 7 | 2009 | 429 | |
| 8 | 2015 | 407 | |
| 9 | A brief history of human disease genetics Hit paper breakdown → | 2020 | 379 |
| 10 | 2007 | 300 | |
| 11 | 2002 | 284 | |
| 12 | 2004 | 283 | |
| 13 | 2007 | 234 | |
| 14 | 2013 | 234 | |
| 15 | 2010 | 224 | |
| 16 | 2010 | 224 | |
| 17 | 2012 | 210 | |
| 18 | 2018 | 202 | |
| 19 | 2018 | 199 | |
| 20 | 2008 | 180 |
About Matthew E. Hurles
Matthew E. Hurles is a scholar working on Genetics, Molecular Biology, Plant Science, Cancer Research and Pediatrics, Perinatology and Child Health, having authored 137 papers that have together received 17.6k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (51 papers), Genomics and Rare Diseases (47 papers), Chromosomal and Genetic Variations (20 papers), Cancer Genomics and Diagnostics (16 papers), Genetic Associations and Epidemiology (14 papers), Forensic and Genetic Research (13 papers), Genomics and Phylogenetic Studies (13 papers) and Genetic diversity and population structure (12 papers). The work is most often cited by research in Genetics (8.8k citations), Developmental Neuroscience (682 citations), Molecular Biology (8.3k citations), Cancer Research (1.3k citations) and Aging (116 citations). Matthew E. Hurles has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Andrew P. Jackson, Louise S. Bicknell, Tessa Homfray, Carol-Anne Martin, Josef Penninger, Madeline A. Lancaster, Juergen A. Knoblich, D. Wénzel, Magdalena Renner and Donald F. Conrad. Their work appears in journals such as The American Journal of Human Genetics, Nature Genetics, Nature Communications, 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.