Matthew Bower
Impact in
-
- melanin and skin pigmentation
-
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- BRCA gene mutations in cancer
Papers in
-
- RNA regulation and disease 4
- Genetics 11
- Genomics and Rare Diseases 5
- Genomic variations and chromosomal abnormalities 5
- Genetics and Neurodevelopmental Disorders 3
- Co-authors
- Bonnie S. LeRoy (3 shared papers)Patricia McCarthy Veach (3 shared papers)Dianne M. Bartels (1 shared paper)Bharat Thyagarajan (10 shared papers)Kevin A.T. Silverstein (5 shared papers)Getiria Onsongo (6 shared papers)Xinjing Wang (3 shared papers)Sophia Yohe (5 shared papers)
- Journals
- Human Mutation (2 papers)Archives of Pathology & Laboratory Medicine (2 papers)Pediatric Blood & Cancer (1 paper)European Journal of Human Genetics (1 paper)Genetics in Medicine (1 paper)
- Partner nations
- United StatesUnited KingdomCanada
In The Last Decade
Matthew Bower
28 papers receiving 527 citations
Peers
Comparison fields: 5 of 88
- Cell Biology 109
- Genetics 161
- Internal Medicine 18
- Molecular Biology 260
- Neurology 55
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 29 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2013 | 102 | |
| 2 | 2010 | 55 | |
| 3 | 2002 | 45 | |
| 4 | 2015 | 43 | |
| 5 | 2003 | 42 | |
| 6 | 2011 | 26 | |
| 7 | 2013 | 26 | |
| 8 | 2016 | 24 | |
| 9 | 2005 | 23 | |
| 10 | 2018 | 21 | |
| 11 | 2014 | 18 | |
| 12 | 2013 | 18 | |
| 13 | 2005 | 15 | |
| 14 | 2011 | 13 | |
| 15 | 2014 | 12 | |
| 16 | Criteria for Clinical Reporting of Variants from a Broad Target Capture NGS Assay without Sanger Verification | 2015 | 12 |
| 17 | 2018 | 11 | |
| 18 | 2011 | 5 | |
| 19 | 2020 | 5 | |
| 20 | 2012 | 3 |
About Matthew Bower
Matthew Bower is a scholar working on Molecular Biology, Genetics, Cancer Research, Cellular and Molecular Neuroscience and Information Systems and Management, having authored 29 papers that have together received 535 indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (5 papers), Genomics and Rare Diseases (5 papers), Genomic variations and chromosomal abnormalities (5 papers), RNA regulation and disease (4 papers), Scientific Computing and Data Management (3 papers), Neurological diseases and metabolism (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Hereditary Neurological Disorders (2 papers). The work is most often cited by research in Cell Biology (109 citations), Genetics (161 citations), Internal Medicine (18 citations), Molecular Biology (260 citations) and Neurology (55 citations). Matthew Bower has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include Bonnie S. LeRoy, Patricia McCarthy Veach, Dianne M. Bartels, Bharat Thyagarajan, Kevin A.T. Silverstein, Getiria Onsongo, Xinjing Wang, Sophia Yohe, Kevin J. Felice and Yuri V. Sergeev. Their work appears in journals such as Human Mutation, Archives of Pathology & Laboratory Medicine, Pediatric Blood & Cancer, European Journal of Human Genetics and Genetics in Medicine.
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.