R Hubert
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
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- Cancer Genomics and Diagnostics
Papers in
- Software 1
- Software Reliability and Analysis Research 1
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- Prenatal Screening and Diagnostics 1
R Hubert
3 papers receiving 717 citations
R Hubert's Hit Papers
Peers
Comparison fields: 5 of 85
- Genetics 269
- Cancer Research 111
- Pediatrics, Perinatology and Child Health 137
- Molecular Biology 409
- Genetics 34
Countries citing papers authored by R Hubert
This map shows the geographic impact of R Hubert'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 R Hubert with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites R Hubert more than expected).
Fields of papers citing papers by R Hubert
This network shows the impact of papers produced by R Hubert. 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 R Hubert. The network helps show where R Hubert may publish in the future.
Co-authors
The 6 scholars most cited alongside R Hubert, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | Whole genome amplification from a single cell: implications for genetic analysis. Hit paper breakdown → | 1992 | 759 |
| 2 | Variable-message signs: symbol legibility and recognition | 1991 | 3 |
| 3 | 2017 | 1 |
About R Hubert
R Hubert is a scholar working on Software, Pediatrics, Perinatology and Child Health, Social Psychology, Control and Systems Engineering and Genetics, having authored 3 papers that have together received 763 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (1 paper), Robot Manipulation and Learning (1 paper), Safety Warnings and Signage (1 paper), Genomic variations and chromosomal abnormalities (1 paper), Reinforcement Learning in Robotics (1 paper), Software Reliability and Analysis Research (1 paper) and Genetic Syndromes and Imprinting (1 paper). The work is most often cited by research in Genetics (269 citations), Cancer Research (111 citations), Pediatrics, Perinatology and Child Health (137 citations), Molecular Biology (409 citations) and Genetics (34 citations). R Hubert has collaborated with scholars based in Germany and United States. Frequent co-authors include Karin Schmitt, Lin Zhang, Xiufang Cui, William C. Navidi, Norman Arnheim and Michèle Colomb. Their work appears in journals such as Proceedings of the National Academy of Sciences and IFAC-PapersOnLine.
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.