Matthew Mort
Impact in
- Genetics top 0.2%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Molecular Biology top 1%
- RNA and protein synthesis mechanisms
- RNA modifications and cancer
- RNA Research and Splicing
- Genomics and Phylogenetic Studies
- Bioinformatics and Genomic Networks
Papers in
-
- RNA and protein synthesis mechanisms 22
- RNA modifications and cancer 19
- RNA Research and Splicing 14
- Genomics and Phylogenetic Studies 14
- Bioinformatics and Genomic Networks 10
- Genetics 41
- Genomics and Rare Diseases 37
- Genomic variations and chromosomal abnormalities 10
- Genetic Associations and Epidemiology 9
- Co-authors
- D.N. Cooper (70 shared papers)Edward V. Ball (15 shared papers)Peter D. Stenson (18 shared papers)Andrew D. Phillips (8 shared papers)Nick Thomas (4 shared papers)Michael Krawczak (6 shared papers)Katy Shaw (3 shared papers)Sean D. Mooney (13 shared papers)
- Journals
- Human Mutation (15 papers)Bioinformatics (7 papers)Human Genetics (5 papers)Nature Communications (5 papers)Human Genomics (5 papers)
- Partner nations
- United KingdomUnited StatesGermany
In The Last Decade
Matthew Mort
78 papers receiving 9.2k citations
Matthew Mort's Hit Papers
Peers
Comparison fields: 5 of 135
- Genetics 3.2k
- Molecular Biology 5.4k
- Cancer Research 799
- Clinical Biochemistry 281
- Genetics 359
Countries citing papers authored by Matthew Mort
This map shows the geographic impact of Matthew Mort'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 Mort with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Matthew Mort more than expected).
Fields of papers citing papers by Matthew Mort
This network shows the impact of papers produced by Matthew Mort. 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 Mort. The network helps show where Matthew Mort may publish in the future.
Co-authors
The 25 scholars most cited alongside Matthew Mort, 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 79 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Human Gene Mutation Database (HGMD®): 2003 update Hit paper breakdown → | 2003 | 1367 |
| 2 | The Human Gene Mutation Database: building a comprehensive mutation repository for clinical and molecular genetics, diagnostic testing and personalized genomic medicine Hit paper breakdown → | 2013 | 967 |
| 3 | The Human Gene Mutation Database: towards a comprehensive repository of inherited mutation data for medical research, genetic diagnosis and next-generation sequencing studies Hit paper breakdown → | 2017 | 934 |
| 4 | The Human Gene Mutation Database: 2008 update Hit paper breakdown → | 2009 | 635 |
| 5 | Automated inference of molecular mechanisms of disease from amino acid substitutions Hit paper breakdown → | 2009 | 629 |
| 6 | Inferring the molecular and phenotypic impact of amino acid variants with MutPred2 Hit paper breakdown → | 2020 | 445 |
| 7 | An integrative approach to predicting the functional effects of non-coding and coding sequence variation Hit paper breakdown → | 2015 | 443 |
| 8 | The Human Gene Mutation Database (HGMD®): optimizing its use in a clinical diagnostic or research setting Hit paper breakdown → | 2020 | 435 |
| 9 | 2008 | 342 | |
| 10 | FATHMM-XF: accurate prediction of pathogenic point mutations via extended features Hit paper breakdown → | 2017 | 280 |
| 11 | 2006 | 273 | |
| 12 | 2008 | 253 | |
| 13 | 2012 | 188 | |
| 14 | 2012 | 177 | |
| 15 | 2011 | 136 | |
| 16 | 2014 | 128 | |
| 17 | 2010 | 119 | |
| 18 | 2014 | 114 | |
| 19 | 2010 | 104 | |
| 20 | 2010 | 92 |
About Matthew Mort
Matthew Mort is a scholar working on Molecular Biology, Genetics, Cancer Research, Cellular and Molecular Neuroscience and Pathology and Forensic Medicine, having authored 79 papers that have together received 9.3k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (37 papers), RNA and protein synthesis mechanisms (22 papers), RNA modifications and cancer (19 papers), RNA Research and Splicing (14 papers), Genomics and Phylogenetic Studies (14 papers), Genomic variations and chromosomal abnormalities (10 papers), Bioinformatics and Genomic Networks (10 papers) and Genetic Associations and Epidemiology (9 papers). The work is most often cited by research in Genetics (3.2k citations), Molecular Biology (5.4k citations), Cancer Research (799 citations), Clinical Biochemistry (281 citations) and Genetics (359 citations). Matthew Mort has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include D.N. Cooper, Edward V. Ball, Peter D. Stenson, Andrew D. Phillips, Nick Thomas, Michael Krawczak, Katy Shaw, Sean D. Mooney, Predrag Radivojac and Shaun S. Abeysinghe. Their work appears in journals such as Human Mutation, Bioinformatics, Human Genetics, Nature Communications and Human Genomics.
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.