Barry Moore
Impact in
- Genetics top 5%
- Genomics and Rare Diseases
- Molecular Biology top 5%
- Genomics and Phylogenetic Studies
- RNA and protein synthesis mechanisms
Papers in
- Genetics 20
- Genomics and Rare Diseases 16
- Genomic variations and chromosomal abnormalities 3
- Genetic Associations and Epidemiology 3
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- Genomics and Phylogenetic Studies 8
- RNA and protein synthesis mechanisms 6
- RNA modifications and cancer 4
- RNA Research and Splicing 4
- Biomedical Text Mining and Ontologies 3
- Co-authors
- Mark D. Yandell (19 shared papers)Carson Holt (2 shared papers)Michael S. Campbell (3 shared papers)Karen Eilbeck (6 shared papers)John F. Atkins (4 shared papers)Martin G. Reese (7 shared papers)Hao Yu Hu (5 shared papers)Raymond F. Gesteland (3 shared papers)
- Journals
- Genome biology (4 papers)The American Journal of Human Genetics (3 papers)Nucleic Acids Research (3 papers)npj Genomic Medicine (3 papers)The Journal of Clinical Endocrinology & Metabolism (2 papers)
- Partner nations
- United StatesPolandNorway
In The Last Decade
Barry Moore
45 papers receiving 2.8k citations
Barry Moore's Hit Papers
Peers
Comparison fields: 5 of 131
- Genetics 742
- Molecular Biology 1.4k
- Cancer Research 272
- Plant Science 657
- Cell Biology 201
Countries citing papers authored by Barry Moore
This map shows the geographic impact of Barry Moore'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 Barry Moore with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Barry Moore more than expected).
Fields of papers citing papers by Barry Moore
This network shows the impact of papers produced by Barry Moore. 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 Barry Moore. The network helps show where Barry Moore may publish in the future.
Co-authors
The 25 scholars most cited alongside Barry Moore, 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 46 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Genome Annotation and Curation Using MAKER and MAKER‐P Hit paper breakdown → | 2014 | 506 |
| 2 | An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge Hit paper breakdown → | 2014 | 406 |
| 3 | 2010 | 340 | |
| 4 | 2011 | 204 | |
| 5 | 2007 | 128 | |
| 6 | 2009 | 111 | |
| 7 | 2021 | 109 | |
| 8 | 2013 | 103 | |
| 9 | 2014 | 78 | |
| 10 | 2014 | 73 | |
| 11 | 2010 | 72 | |
| 12 | 2006 | 70 | |
| 13 | 2019 | 70 | |
| 14 | 2000 | 56 | |
| 15 | 2012 | 56 | |
| 16 | 2010 | 55 | |
| 17 | 2017 | 53 | |
| 18 | Exome sequencing and unrelated findings in the context of complex disease research: ethical and clinical implications. | 2011 | 49 |
| 19 | 1995 | 42 | |
| 20 | 2011 | 36 |
About Barry Moore
Barry Moore is a scholar working on Genetics, Molecular Biology, Cancer Research, Clinical Biochemistry and Pediatrics, Perinatology and Child Health, having authored 46 papers that have together received 2.9k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (16 papers), Genomics and Phylogenetic Studies (8 papers), RNA and protein synthesis mechanisms (6 papers), RNA modifications and cancer (4 papers), RNA Research and Splicing (4 papers), Genomic variations and chromosomal abnormalities (3 papers), Genetic Associations and Epidemiology (3 papers) and Biomedical Text Mining and Ontologies (3 papers). The work is most often cited by research in Genetics (742 citations), Molecular Biology (1.4k citations), Cancer Research (272 citations), Plant Science (657 citations) and Cell Biology (201 citations). Barry Moore has collaborated with scholars based in United States, Poland and Norway. Frequent co-authors include Mark D. Yandell, Carson Holt, Michael S. Campbell, Karen Eilbeck, John F. Atkins, Martin G. Reese, Hao Yu Hu, Raymond F. Gesteland, Steven D. Flygare and Chad Daniel Huff. Their work appears in journals such as Genome biology, The American Journal of Human Genetics, Nucleic Acids Research, npj Genomic Medicine and The Journal of Clinical Endocrinology & Metabolism.
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.