Brad Angle
Impact in
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Connective tissue disorders research
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Clinical Biochemistry top 2%
- Metabolism and Genetic Disorders
Papers in
- Genetics 24
- Genomic variations and chromosomal abnormalities 12
- Genomics and Rare Diseases 7
- Genetics and Neurodevelopmental Disorders 6
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- RNA modifications and cancer 5
- Cancer-related gene regulation 4
- Co-authors
- Barbara K. Burton (9 shared papers)Zsolt Urbán (1 shared paper)Katherine H. Kim (1 shared paper)Lihua Y. Marmorstein (1 shared paper)Nina Sausgruber (1 shared paper)Vishwanathan Hucthagowder (1 shared paper)Laurence I. Burd (1 shared paper)Joseph H. Hersh (10 shared papers)
- Journals
- Genetics in Medicine (5 papers)Molecular Genetics and Metabolism (3 papers)Prenatal Diagnosis (2 papers)American Journal of Medical Genetics (12 papers)European Journal of Human Genetics (1 paper)
- Partner nations
- United StatesNetherlandsFrance
In The Last Decade
Brad Angle
45 papers receiving 2.0k citations
Brad Angle's Hit Papers
Peers
Comparison fields: 5 of 100
- Genetics 1.1k
- Clinical Biochemistry 174
- Molecular Biology 828
- Pediatrics, Perinatology and Child Health 201
- Developmental Biology 24
Countries citing papers authored by Brad Angle
This map shows the geographic impact of Brad Angle'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 Brad Angle with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Brad Angle more than expected).
Fields of papers citing papers by Brad Angle
This network shows the impact of papers produced by Brad Angle. 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 Brad Angle. The network helps show where Brad Angle may publish in the future.
Co-authors
The 25 scholars most cited alongside Brad Angle, 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 47 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Phenotypic Heterogeneity of Genomic Disorders and Rare Copy-Number Variants Hit paper breakdown → | 2012 | 455 |
| 2 | 2006 | 233 | |
| 3 | 1995 | 140 | |
| 4 | 2011 | 117 | |
| 5 | 2013 | 113 | |
| 6 | 2016 | 82 | |
| 7 | 2014 | 60 | |
| 8 | 2018 | 59 | |
| 9 | 2014 | 55 | |
| 10 | 2016 | 54 | |
| 11 | 2007 | 51 | |
| 12 | 2000 | 50 | |
| 13 | 2007 | 46 | |
| 14 | 2012 | 39 | |
| 15 | 2011 | 37 | |
| 16 | 2014 | 34 | |
| 17 | 2020 | 34 | |
| 18 | 2016 | 31 | |
| 19 | 2013 | 30 | |
| 20 | 2016 | 29 |
About Brad Angle
Brad Angle is a scholar working on Genetics, Molecular Biology, Clinical Biochemistry, Pediatrics, Perinatology and Child Health and Cell Biology, having authored 47 papers that have together received 2.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (12 papers), Genomics and Rare Diseases (7 papers), Genetics and Neurodevelopmental Disorders (6 papers), RNA modifications and cancer (5 papers), Prenatal Screening and Diagnostics (5 papers), Metabolism and Genetic Disorders (4 papers), Cancer-related gene regulation (4 papers) and Chromosomal and Genetic Variations (4 papers). The work is most often cited by research in Genetics (1.1k citations), Clinical Biochemistry (174 citations), Molecular Biology (828 citations), Pediatrics, Perinatology and Child Health (201 citations) and Developmental Biology (24 citations). Brad Angle has collaborated with scholars based in United States, Netherlands and France. Frequent co-authors include Barbara K. Burton, Zsolt Urbán, Katherine H. Kim, Lihua Y. Marmorstein, Nina Sausgruber, Vishwanathan Hucthagowder, Laurence I. Burd, Joseph H. Hersh, Joel Charrow and Katherine M. Christensen. Their work appears in journals such as Genetics in Medicine, Molecular Genetics and Metabolism, Prenatal Diagnosis, American Journal of Medical Genetics and European Journal of Human 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.