Matt W. Wright
Impact in
- Urology top 1%
- Hair Growth and Disorders
- Cancer Research top 5%
- Cancer-related molecular mechanisms research
Papers in
- Genetics 17
- Genomics and Rare Diseases 11
- BRCA gene mutations in cancer 3
- Genomic variations and chromosomal abnormalities 2
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- Genomics and Phylogenetic Studies 11
- Biomedical Text Mining and Ontologies 8
- Bioinformatics and Genomic Networks 3
- Co-authors
- Elspeth A. Bruford (13 shared papers)Michael Lush (7 shared papers)Ruth C. Lovering (3 shared papers)Hester Wain (3 shared papers)Ruth L. Seal (5 shared papers)Sue Povey (3 shared papers)Kristian Gray (3 shared papers)Bethan Yates (1 shared paper)
- Journals
- Human Genomics (5 papers)Nucleic Acids Research (4 papers)Mammalian Genome (3 papers)The American Journal of Human Genetics (2 papers)Human Mutation (2 papers)
- Partner nations
- United KingdomUnited StatesUnited Arab Emirates
In The Last Decade
Matt W. Wright
29 papers receiving 4.6k citations
Matt W. Wright's Hit Papers
Peers
Comparison fields: 5 of 146
- Urology 231
- Cancer Research 502
- Immunology 684
- Genetics 916
- Cell Biology 526
Countries citing papers authored by Matt W. Wright
This map shows the geographic impact of Matt W. Wright'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 W. Wright with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Matt W. Wright more than expected).
Fields of papers citing papers by Matt W. Wright
This network shows the impact of papers produced by Matt W. Wright. 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 W. Wright. The network helps show where Matt W. Wright may publish in the future.
Co-authors
The 25 scholars most cited alongside Matt W. Wright, 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 31 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Gene map of the extended humanMHC Hit paper breakdown → | 2004 | 882 |
| 2 | New consensus nomenclature for mammalian keratins Hit paper breakdown → | 2006 | 586 |
| 3 | 2001 | 398 | |
| 4 | 2014 | 390 | |
| 5 | Recommendations for application of the functional evidence PS3/BS3 criterion using the ACMG/AMP sequence variant interpretation framework Hit paper breakdown → | 2019 | 333 |
| 6 | 2002 | 333 | |
| 7 | 2013 | 196 | |
| 8 | 2012 | 196 | |
| 9 | 2010 | 182 | |
| 10 | 2007 | 170 | |
| 11 | 2010 | 157 | |
| 12 | 2011 | 148 | |
| 13 | 2018 | 100 | |
| 14 | 2008 | 83 | |
| 15 | 2011 | 74 | |
| 16 | 2005 | 71 | |
| 17 | 2016 | 64 | |
| 18 | 2012 | 63 | |
| 19 | 2006 | 61 | |
| 20 | 2020 | 51 |
About Matt W. Wright
Matt W. Wright is a scholar working on Genetics, Molecular Biology, Public Health, Environmental and Occupational Health, Cell Biology and Cancer Research, having authored 31 papers that have together received 4.7k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (11 papers), Genomics and Phylogenetic Studies (11 papers), Biomedical Text Mining and Ontologies (8 papers), BRCA gene mutations in cancer (3 papers), Bioinformatics and Genomic Networks (3 papers), Advanced Proteomics Techniques and Applications (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Skin and Cellular Biology Research (2 papers). The work is most often cited by research in Urology (231 citations), Cancer Research (502 citations), Immunology (684 citations), Genetics (916 citations) and Cell Biology (526 citations). Matt W. Wright has collaborated with scholars based in United Kingdom, United States and United Arab Emirates. Frequent co-authors include Elspeth A. Bruford, Michael Lush, Ruth C. Lovering, Hester Wain, Ruth L. Seal, Sue Povey, Kristian Gray, Bethan Yates, Lois J. Maltais and Susan M. Gordon. Their work appears in journals such as Human Genomics, Nucleic Acids Research, Mammalian Genome, The American Journal of Human Genetics and Human Mutation.
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.