Robert S. Young
Impact in
- Cancer Research top 5%
- Cancer-related molecular mechanisms research
- Molecular Biology top 5%
- RNA Research and Splicing
- RNA regulation and disease
- RNA modifications and cancer
- RNA and protein synthesis mechanisms
Papers in
-
- RNA Research and Splicing 8
- Genomics and Chromatin Dynamics 8
- CRISPR and Genetic Engineering 4
- Genetics 20
- Genomic variations and chromosomal abnormalities 13
- Dermatoglyphics and Human Traits 4
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3
- Co-authors
- Chris P. Ponting (3 shared papers)Robert P. Langlais (2 shared papers)Ronald J. Jorgenson (6 shared papers)John M. Opitz (6 shared papers)Liam P. Keegan (1 shared paper)James Brindle (1 shared paper)Christoffer Nellåker (1 shared paper)Julia R. Dorin (1 shared paper)
- Journals
- Human Genetics (2 papers)Nature Communications (2 papers)Genome biology (2 papers)American Journal of Medical Genetics (11 papers)Stem Cell Research & Therapy (1 paper)
- Partner nations
- United StatesUnited KingdomChina
In The Last Decade
Robert S. Young
49 papers receiving 2.0k citations
Robert S. Young's Hit Papers
Peers
Comparison fields: 5 of 104
- Cancer Research 341
- Molecular Biology 1.3k
- Developmental Biology 40
- Genetics 378
- Rheumatology 163
Countries citing papers authored by Robert S. Young
This map shows the geographic impact of Robert S. Young'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 Robert S. Young with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Robert S. Young more than expected).
Fields of papers citing papers by Robert S. Young
This network shows the impact of papers produced by Robert S. Young. 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 Robert S. Young. The network helps show where Robert S. Young may publish in the future.
Co-authors
The 25 scholars most cited alongside Robert S. Young, 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 50 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | The RNA-Editing Enzyme ADAR1 Controls Innate Immune Responses to RNA Hit paper breakdown → | 2014 | 500 |
| 2 | 2012 | 223 | |
| 3 | 2012 | 164 | |
| 4 | 1984 | 102 | |
| 5 | The pattern ERG in man following surgical resection of the optic nerve. | 1987 | 72 |
| 6 | 1988 | 71 | |
| 7 | 2020 | 69 | |
| 8 | 2010 | 66 | |
| 9 | 2017 | 62 | |
| 10 | 1985 | 60 | |
| 11 | 1984 | 58 | |
| 12 | 1982 | 53 | |
| 13 | 1985 | 49 | |
| 14 | 2015 | 47 | |
| 15 | 2013 | 42 | |
| 16 | 2020 | 40 | |
| 17 | 2017 | 40 | |
| 18 | 2015 | 39 | |
| 19 | 1983 | 34 | |
| 20 | 2017 | 34 |
About Robert S. Young
Robert S. Young is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Rheumatology and Cancer Research, having authored 50 papers that have together received 2.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (13 papers), RNA Research and Splicing (8 papers), Genomics and Chromatin Dynamics (8 papers), Prenatal Screening and Diagnostics (5 papers), Cancer-related molecular mechanisms research (4 papers), Dermatoglyphics and Human Traits (4 papers), CRISPR and Genetic Engineering (4 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers). The work is most often cited by research in Cancer Research (341 citations), Molecular Biology (1.3k citations), Developmental Biology (40 citations), Genetics (378 citations) and Rheumatology (163 citations). Robert S. Young has collaborated with scholars based in United States, United Kingdom and China. Frequent co-authors include Chris P. Ponting, Robert P. Langlais, Ronald J. Jorgenson, John M. Opitz, Liam P. Keegan, James Brindle, Christoffer Nellåker, Julia R. Dorin, David F. Read and Sam M. Greenwood. Their work appears in journals such as Human Genetics, Nature Communications, Genome biology, American Journal of Medical Genetics and Stem Cell Research & Therapy.
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.