R Hubert
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
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- Cancer Genomics and Diagnostics
Papers in
- Surgery 1
- Diagnosis and Treatment of Venous Diseases 1
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- Systemic Sclerosis and Related Diseases 1
R Hubert
3 papers receiving 695 citations
R Hubert's Hit Papers
Peers
Comparison fields: 5 of 79
- Genetics 263
- Cancer Research 108
- Pediatrics, Perinatology and Child Health 125
- Molecular Biology 393
- Genetics 33
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 | 719 |
| 2 | Variable-message signs: symbol legibility and recognition | 1991 | 4 |
| 3 | 2023 | 1 |
About R Hubert
R Hubert is a scholar working on Surgery, Pathology and Forensic Medicine, Social Psychology, Pediatrics, Perinatology and Child Health and Genetics, having authored 3 papers that have together received 724 indexed citations. Recurring topics across this work include Diagnosis and Treatment of Venous Diseases (1 paper), Systemic Sclerosis and Related Diseases (1 paper), Genomic variations and chromosomal abnormalities (1 paper), Genetic Syndromes and Imprinting (1 paper), Prenatal Screening and Diagnostics (1 paper) and Safety Warnings and Signage (1 paper). The work is most often cited by research in Genetics (263 citations), Cancer Research (108 citations), Pediatrics, Perinatology and Child Health (125 citations), Molecular Biology (393 citations) and Genetics (33 citations). R Hubert has collaborated with scholars based in United States and India. Frequent co-authors include Lin Zhang, Xiufang Cui, Karin Schmitt, William Navidi, Norman Arnheim and Michèle Colomb. Their work appears in journals such as Proceedings of the National Academy of Sciences.
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.