Matt Hurles
Impact in
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- Hereditary Neurological Disorders
- Neuroscience and Neuropharmacology Research
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- Cellular transport and secretion
Papers in
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- Congenital heart defects research 1
- Mitochondrial Function and Pathology 1
- RNA modifications and cancer 1
- Genetics 1
- Genomics and Rare Diseases 1
- Neurogenetic and Muscular Disorders Research 1
- Co-authors
- Barry A. Chioza (2 shared papers)Andrew H. Crosby (2 shared papers)Katy Barwick (2 shared papers)Saeed Al-Turki (2 shared papers)Randy Blakely (1 shared paper)Katherine Dick (1 shared paper)Alicia M. Ruggiero (1 shared paper)Jane Wright (1 shared paper)
- Partner nations
- United KingdomUnited StatesGermany
In The Last Decade
Matt Hurles
3 papers receiving 104 citations
Peers
Comparison fields: 5 of 41
- Cellular and Molecular Neuroscience 32
- Cell Biology 26
- Neurology 12
- Clinical Biochemistry 9
- Neurology 17
Countries citing papers authored by Matt Hurles
This map shows the geographic impact of Matt 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 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 Hurles more than expected).
Fields of papers citing papers by Matt Hurles
This network shows the impact of papers produced by Matt 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 Hurles. The network helps show where Matt Hurles may publish in the future.
Co-authors
The 25 scholars most cited alongside Matt 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
About Matt Hurles
Matt Hurles is a scholar working on Molecular Biology, Genetics, Cellular and Molecular Neuroscience, Neurology and Cell Biology, having authored 3 papers that have together received 107 indexed citations. Recurring topics across this work include Neurological diseases and metabolism (1 paper), Hereditary Neurological Disorders (1 paper), Congenital heart defects research (1 paper), Genomics and Rare Diseases (1 paper), Genetic Neurodegenerative Diseases (1 paper), Mitochondrial Function and Pathology (1 paper), Neurogenetic and Muscular Disorders Research (1 paper) and RNA modifications and cancer (1 paper). The work is most often cited by research in Cellular and Molecular Neuroscience (32 citations), Cell Biology (26 citations), Neurology (12 citations), Clinical Biochemistry (9 citations) and Neurology (17 citations). Matt Hurles has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Barry A. Chioza, Andrew H. Crosby, Katy Barwick, Saeed Al-Turki, Randy Blakely, Katherine Dick, Alicia M. Ruggiero, Jane Wright, Mary M. Reilly and A. Al‐Memar. Their work appears in journals such as The American Journal of Human Genetics and Neuromuscular Disorders.
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.