Matt W. Wright

14.9k citations
47 papers · 11.1k · 4 hit papers · h-index 33

Impact in

  • Genetics top 1%
    • Genomics and Rare Diseases
    • Genetic Associations and Epidemiology
    • Genomics and Phylogenetic Studies
    • Bioinformatics and Genomic Networks
    • Receptor Mechanisms and Signaling
    • Biomedical Text Mining and Ontologies

Papers in

    • Genomics and Rare Diseases 10
    • Genomic variations and chromosomal abnormalities 2
    • Race, Genetics, and Society 2
    • Biomedical Text Mining and Ontologies 6
    • Genomics and Phylogenetic Studies 6
    • Receptor Mechanisms and Signaling 2

Matt W. Wright

46 papers receiving 10.9k citations

Matt W. Wright's Hit Papers

Recommendations for application of the functional evidence PS3/BS3 criterion using the ACMG/AMP sequence variant interpretation framework 2019 · 428 citations
4280+7+14Years since publication10002.0k3.0k4.0k

Peers

Matt W. Wright
Comparison fields: 5 of 135
  • Genetics 1.4k
  • Molecular Biology 2.6k
  • Cancer Research 418
  • Cell Biology 268
  • Molecular Medicine 131
Replace Wratko Hlavina with:
Wratko Hlavina United States
Emily Bowler-Barnett United Kingdom
Melissa Landrum United States
Sylvain Poux Switzerland
Emmanuel Boutet Switzerland
Damien Lieberherr Switzerland
Rossana Zaru United Kingdom
PAUL C. DENNY United Kingdom
Anne Estreicher Switzerland
Arnaud Gos Switzerland
Matt W. Wright relative to Wratko Hlavina United States Wratko Hlavina's profile →
Citations per field
00.5×1.5×2×2.3×
Wratko Hlavina · 1×
Citations per year

Countries citing papers authored by Matt W. Wright

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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.

Border = papers with Matt W. Wright Line = papers co-authored together Matt W. Wright links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

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 →
20154460
2
Gene map of the extended human MHC
Hit paper breakdown →
2004927
3 2006599
4
Evaluating the Clinical Validity of Gene-Disease Associations: An Evidence-Based Framework Developed by the Clinical Genome Resource
Hit paper breakdown →
2017452
5
Recommendations for application of the functional evidence PS3/BS3 criterion using the ACMG/AMP sequence variant interpretation framework
Hit paper breakdown →
2019428
6 2014410
7 2001406
8 2015400
9 2002345
10 2013210
11 2012209
12 2008193
13 2010186
14 2007181
15 2010161
16 2011151
17 2018120
18 2014106
19 201499
20 200884

About Matt W. Wright

Matt W. Wright is a scholar working on Genetics, Molecular Biology, Pharmacology, Cell Biology and Cancer Research, having authored 47 papers that have together received 11.1k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (10 papers), Biomedical Text Mining and Ontologies (6 papers), Genomics and Phylogenetic Studies (6 papers), Pharmacogenetics and Drug Metabolism (3 papers), Receptor Mechanisms and Signaling (2 papers), Skin and Cellular Biology Research (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Race, Genetics, and Society (2 papers). The work is most often cited by research in Genetics (1.4k citations), Molecular Biology (2.6k citations), Cancer Research (418 citations), Cell Biology (268 citations) and Molecular Medicine (131 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 Vikki Rand. 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.

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