Bradley P. Coe
Impact in
- Genetics top 0.2%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Cancer Research top 2%
- Cancer Genomics and Diagnostics
Papers in
- Genetics 42
- Genomic variations and chromosomal abnormalities 40
- Genomics and Rare Diseases 11
- Genetics and Neurodevelopmental Disorders 8
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- Genomics and Chromatin Dynamics 10
- Gene expression and cancer classification 6
- Congenital heart defects research 6
- Co-authors
- Evan E. Eichler (24 shared papers)Can Alkan (2 shared papers)Wan L. Lam (34 shared papers)Calum MacAulay (22 shared papers)Niklas Krumm (5 shared papers)Jill A. Rosenfeld (2 shared papers)Raphael Bernier (7 shared papers)Tychele N. Turner (5 shared papers)
- Journals
- PLoS ONE (4 papers)The American Journal of Human Genetics (4 papers)Genes Chromosomes and Cancer (3 papers)BMC Bioinformatics (3 papers)Nature Genetics (3 papers)
- Partner nations
- United StatesCanadaItaly
In The Last Decade
Bradley P. Coe
63 papers receiving 5.7k citations
Bradley P. Coe's Hit Papers
Peers
Comparison fields: 5 of 138
- Genetics 3.0k
- Cancer Research 681
- Cognitive Neuroscience 863
- Molecular Biology 2.6k
- Pediatrics, Perinatology and Child Health 443
Countries citing papers authored by Bradley P. Coe
This map shows the geographic impact of Bradley P. Coe'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 Bradley P. Coe with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Bradley P. Coe more than expected).
Fields of papers citing papers by Bradley P. Coe
This network shows the impact of papers produced by Bradley P. Coe. 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 Bradley P. Coe. The network helps show where Bradley P. Coe may publish in the future.
Co-authors
The 25 scholars most cited alongside Bradley P. Coe, 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 64 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Genome structural variation discovery and genotyping Hit paper breakdown → | 2011 | 1054 |
| 2 | 2004 | 475 | |
| 3 | 2012 | 415 | |
| 4 | A Higher Mutational Burden in Females Supports a “Female Protective Model” in Neurodevelopmental Disorders Hit paper breakdown → | 2014 | 380 |
| 5 | Excess of rare, inherited truncating mutations in autism Hit paper breakdown → | 2015 | 348 |
| 6 | 2012 | 253 | |
| 7 | 2011 | 222 | |
| 8 | 2013 | 212 | |
| 9 | 2017 | 210 | |
| 10 | 2018 | 172 | |
| 11 | 2007 | 128 | |
| 12 | 2019 | 113 | |
| 13 | 2015 | 98 | |
| 14 | 2017 | 93 | |
| 15 | 2008 | 91 | |
| 16 | 2018 | 82 | |
| 17 | 2012 | 81 | |
| 18 | 2010 | 76 | |
| 19 | 2004 | 76 | |
| 20 | 2013 | 70 |
About Bradley P. Coe
Bradley P. Coe is a scholar working on Genetics, Molecular Biology, Plant Science, Cognitive Neuroscience and Cancer Research, having authored 64 papers that have together received 5.8k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (40 papers), Genomics and Rare Diseases (11 papers), Genomics and Chromatin Dynamics (10 papers), Chromosomal and Genetic Variations (9 papers), Genetics and Neurodevelopmental Disorders (8 papers), Cancer Genomics and Diagnostics (6 papers), Gene expression and cancer classification (6 papers) and Congenital heart defects research (6 papers). The work is most often cited by research in Genetics (3.0k citations), Cancer Research (681 citations), Cognitive Neuroscience (863 citations), Molecular Biology (2.6k citations) and Pediatrics, Perinatology and Child Health (443 citations). Bradley P. Coe has collaborated with scholars based in United States, Canada and Italy. Frequent co-authors include Evan E. Eichler, Can Alkan, Wan L. Lam, Calum MacAulay, Niklas Krumm, Jill A. Rosenfeld, Raphael Bernier, Tychele N. Turner, Santhosh Girirajan and Carl Baker. Their work appears in journals such as PLoS ONE, The American Journal of Human Genetics, Genes Chromosomes and Cancer, BMC Bioinformatics and Nature 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.