Matt W. Wright
Impact in
- Genetics top 1%
- Genomics and Rare Diseases
- Genetic Associations and Epidemiology
- Molecular Biology top 1%
- Genomics and Phylogenetic Studies
- Bioinformatics and Genomic Networks
- Biomedical Text Mining and Ontologies
Papers in
- Genetics 20
- Genomics and Rare Diseases 14
- Genomic variations and chromosomal abnormalities 3
- Race, Genetics, and Society 3
-
- Genomics and Phylogenetic Studies 16
- Biomedical Text Mining and Ontologies 8
- Bioinformatics and Genomic Networks 8
- Co-authors
- Elspeth A. Bruford (14 shared papers)Michael J. Lush (7 shared papers)Sue Povey (5 shared papers)Ruth C. Lovering (3 shared papers)Hester Wain (3 shared papers)Ruth L. Seal (6 shared papers)Kristian A. Gray (4 shared papers)Bethan Yates (1 shared paper)
- Journals
- Human Genomics (7 papers)Nucleic Acids Research (7 papers)Human Mutation (3 papers)Mammalian Genome (3 papers)The American Journal of Human Genetics (3 papers)
- Partner nations
- United StatesUnited KingdomGermany
In The Last Decade
Matt W. Wright
46 papers receiving 10.9k citations
Matt W. Wright's Hit Papers
Peers
Comparison fields: 5 of 157
- Genetics 2.4k
- Molecular Biology 4.2k
- Cancer Research 733
- Cell Biology 409
- Molecular Medicine 167
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 47 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Reference sequence (RefSeq) database at NCBI: current status, taxonomic expansion, and functional annotation Hit paper breakdown → | 2015 | 4460 |
| 2 | Gene map of the extended human MHC Hit paper breakdown → | 2004 | 927 |
| 3 | 2006 | 599 | |
| 4 | Evaluating the Clinical Validity of Gene-Disease Associations: An Evidence-Based Framework Developed by the Clinical Genome Resource Hit paper breakdown → | 2017 | 452 |
| 5 | Recommendations for application of the functional evidence PS3/BS3 criterion using the ACMG/AMP sequence variant interpretation framework Hit paper breakdown → | 2019 | 428 |
| 6 | 2014 | 410 | |
| 7 | 2001 | 406 | |
| 8 | 2015 | 400 | |
| 9 | 2002 | 345 | |
| 10 | 2013 | 210 | |
| 11 | 2012 | 209 | |
| 12 | 2008 | 193 | |
| 13 | 2010 | 186 | |
| 14 | 2007 | 181 | |
| 15 | 2010 | 161 | |
| 16 | 2011 | 151 | |
| 17 | 2018 | 120 | |
| 18 | 2014 | 106 | |
| 19 | 2014 | 99 | |
| 20 | 2008 | 84 |
About Matt W. Wright
Matt W. Wright is a scholar working on Genetics, Molecular Biology, Cancer Research, Pharmacology and Urology, having authored 47 papers that have together received 11.1k indexed citations. Recurring topics across this work include Genomics and Phylogenetic Studies (16 papers), Genomics and Rare Diseases (14 papers), Biomedical Text Mining and Ontologies (8 papers), Bioinformatics and Genomic Networks (8 papers), Cancer-related molecular mechanisms research (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Race, Genetics, and Society (3 papers) and Pharmacogenetics and Drug Metabolism (3 papers). The work is most often cited by research in Genetics (2.4k citations), Molecular Biology (4.2k citations), Cancer Research (733 citations), Cell Biology (409 citations) and Molecular Medicine (167 citations). Matt W. Wright has collaborated with scholars based in United States, United Kingdom and Germany. Frequent co-authors include Elspeth A. Bruford, Michael J. Lush, Sue Povey, Ruth C. Lovering, Hester Wain, Ruth L. Seal, Kristian A. Gray, Bethan Yates, Lois J. Maltais and Varsha Khodiyar. Their work appears in journals such as Human Genomics, Nucleic Acids Research, Human Mutation, Mammalian Genome and The American Journal of Human Genetics.
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.