Caleb Webber
Impact in
- Genetics top 1%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Developmental Neuroscience top 5%
Papers in
-
- Congenital heart defects research 10
- Single-cell and spatial transcriptomics 6
- Genomics and Phylogenetic Studies 6
- Genetics 27
- Genomic variations and chromosomal abnormalities 18
- Genomics and Rare Diseases 16
- Genetic Associations and Epidemiology 6
- Genetics and Neurodevelopmental Disorders 5
- Co-authors
- Chris P. Ponting (16 shared papers)Viola Volpato (5 shared papers)Duc-Quang Nguyen (3 shared papers)Julia Steinberg (6 shared papers)Richard Wade‐Martins (7 shared papers)Jimena Monzón‐Sandoval (8 shared papers)Andreas Heger (4 shared papers)Rory Bowden (5 shared papers)
- Journals
- PLoS Genetics (8 papers)Genome Research (7 papers)Bioinformatics (4 papers)Human Molecular Genetics (3 papers)PLoS Computational Biology (3 papers)
- Partner nations
- United KingdomNetherlandsUnited States
In The Last Decade
Caleb Webber
58 papers receiving 3.0k citations
Peers
Comparison fields: 5 of 136
- Genetics 1.1k
- Developmental Neuroscience 130
- Neurology 251
- Molecular Biology 1.6k
- Neurology 286
Countries citing papers authored by Caleb Webber
This map shows the geographic impact of Caleb Webber'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 Caleb Webber with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Caleb Webber more than expected).
Fields of papers citing papers by Caleb Webber
This network shows the impact of papers produced by Caleb Webber. 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 Caleb Webber. The network helps show where Caleb Webber may publish in the future.
Co-authors
The 25 scholars most cited alongside Caleb Webber, 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 59 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2020 | 241 | |
| 2 | 2006 | 203 | |
| 3 | 2020 | 198 | |
| 4 | 2016 | 198 | |
| 5 | 2011 | 179 | |
| 6 | 2013 | 160 | |
| 7 | 2013 | 115 | |
| 8 | 2018 | 109 | |
| 9 | 2019 | 108 | |
| 10 | 2014 | 101 | |
| 11 | 2013 | 91 | |
| 12 | 2015 | 88 | |
| 13 | 2008 | 82 | |
| 14 | 2013 | 79 | |
| 15 | 2008 | 68 | |
| 16 | 2019 | 55 | |
| 17 | 2016 | 51 | |
| 18 | 2020 | 47 | |
| 19 | 2014 | 47 | |
| 20 | 2013 | 47 |
About Caleb Webber
Caleb Webber is a scholar working on Molecular Biology, Genetics, Cellular and Molecular Neuroscience, Neurology and Neurology, having authored 59 papers that have together received 3.0k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (18 papers), Genomics and Rare Diseases (16 papers), Congenital heart defects research (10 papers), Single-cell and spatial transcriptomics (6 papers), Genomics and Phylogenetic Studies (6 papers), Parkinson's Disease Mechanisms and Treatments (6 papers), Genetic Associations and Epidemiology (6 papers) and Genetics and Neurodevelopmental Disorders (5 papers). The work is most often cited by research in Genetics (1.1k citations), Developmental Neuroscience (130 citations), Neurology (251 citations), Molecular Biology (1.6k citations) and Neurology (286 citations). Caleb Webber has collaborated with scholars based in United Kingdom, Netherlands and United States. Frequent co-authors include Chris P. Ponting, Viola Volpato, Duc-Quang Nguyen, Julia Steinberg, Richard Wade‐Martins, Jimena Monzón‐Sandoval, Andreas Heger, Rory Bowden, Cynthia Sandor and Geoffrey J. Barton. Their work appears in journals such as PLoS Genetics, Genome Research, Bioinformatics, Human Molecular Genetics and PLoS Computational Biology.
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.