Matthew Bower
Impact in
- Cell Biology top 10%
- melanin and skin pigmentation
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- Genomics and Rare Diseases
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
Papers in
-
- RNA regulation and disease 4
- Glycosylation and Glycoproteins Research 2
- DNA Repair Mechanisms 2
- Genetics 11
- Genomics and Rare Diseases 6
- Genomic variations and chromosomal abnormalities 3
- Genetics and Neurodevelopmental Disorders 2
- BRCA gene mutations in cancer 2
- Co-authors
- Patricia McCarthy Veach (3 shared papers)Bonnie S. LeRoy (3 shared papers)Dianne M. Bartels (1 shared paper)Bharat Thyagarajan (11 shared papers)Getiria Onsongo (6 shared papers)Kevin A.T. Silverstein (5 shared papers)Xinjing Wang (3 shared papers)Paul Tuite (2 shared papers)
- Journals
- Human Mutation (2 papers)Archives of Pathology & Laboratory Medicine (2 papers)Frontiers in Genetics (1 paper)Journal of Molecular Diagnostics (1 paper)PLoS ONE (1 paper)
- Partner nations
- United StatesUnited KingdomBrazil
In The Last Decade
Matthew Bower
29 papers receiving 571 citations
Peers
Comparison fields: 5 of 86
- Cell Biology 112
- Genetics 159
- Internal Medicine 17
- Pediatrics, Perinatology and Child Health 61
- Neurology 47
Countries citing papers authored by Matthew Bower
This map shows the geographic impact of Matthew Bower'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 Bower with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Matthew Bower more than expected).
Fields of papers citing papers by Matthew Bower
This network shows the impact of papers produced by Matthew Bower. 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 Bower. The network helps show where Matthew Bower may publish in the future.
Co-authors
The 25 scholars most cited alongside Matthew Bower, 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 | 2013 | 109 | |
| 2 | 2010 | 60 | |
| 3 | 2002 | 51 | |
| 4 | 2003 | 45 | |
| 5 | 2015 | 42 | |
| 6 | 2013 | 27 | |
| 7 | 2011 | 26 | |
| 8 | 2016 | 25 | |
| 9 | 2005 | 24 | |
| 10 | 2018 | 23 | |
| 11 | 2014 | 19 | |
| 12 | 2013 | 19 | |
| 13 | 2011 | 18 | |
| 14 | 2014 | 16 | |
| 15 | 2005 | 15 | |
| 16 | 2018 | 12 | |
| 17 | Criteria for Clinical Reporting of Variants from a Broad Target Capture NGS Assay without Sanger Verification | 2015 | 12 |
| 18 | 2011 | 9 | |
| 19 | 2011 | 7 | |
| 20 | 2020 | 5 |
About Matthew Bower
Matthew Bower is a scholar working on Molecular Biology, Genetics, Cellular and Molecular Neuroscience, Cognitive Neuroscience and Cancer Research, having authored 31 papers that have together received 588 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (6 papers), RNA regulation and disease (4 papers), Cancer Genomics and Diagnostics (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Genetics and Neurodevelopmental Disorders (2 papers), BRCA gene mutations in cancer (2 papers), Glycosylation and Glycoproteins Research (2 papers) and DNA Repair Mechanisms (2 papers). The work is most often cited by research in Cell Biology (112 citations), Genetics (159 citations), Internal Medicine (17 citations), Pediatrics, Perinatology and Child Health (61 citations) and Neurology (47 citations). Matthew Bower has collaborated with scholars based in United States, United Kingdom and Brazil. Frequent co-authors include Patricia McCarthy Veach, Bonnie S. LeRoy, Dianne M. Bartels, Bharat Thyagarajan, Getiria Onsongo, Kevin A.T. Silverstein, Xinjing Wang, Paul Tuite, Chen Wang and Dimitre R. Simeonov. Their work appears in journals such as Human Mutation, Archives of Pathology & Laboratory Medicine, Frontiers in Genetics, Journal of Molecular Diagnostics and PLoS ONE.
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.