Roger E. Stevenson
Impact in
- Genetics top 0.2%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Developmental Biology top 1%
Papers in
- Genetics 106
- Genetics and Neurodevelopmental Disorders 72
- Genomic variations and chromosomal abnormalities 15
- Genomics and Rare Diseases 11
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- Congenital limb and hand anomalies 7
- Co-authors
- Charles E. Schwartz (93 shared papers)Richard J. Simensen (28 shared papers)Herbert A. Lubs (29 shared papers)Richard J. Schroer (22 shared papers)Cindy D. Skinner (28 shared papers)Mary C. Phelan (12 shared papers)Jane H. Dean (15 shared papers)Michael J. Friez (27 shared papers)
- Journals
- The American Journal of Human Genetics (15 papers)Journal of Medical Genetics (11 papers)PEDIATRICS (10 papers)Clinical Genetics (8 papers)Human Molecular Genetics (6 papers)
- Partner nations
- United StatesCanadaUnited Kingdom
In The Last Decade
Roger E. Stevenson
246 papers receiving 13.0k citations
Roger E. Stevenson's Hit Papers
Peers
Comparison fields: 5 of 122
- Genetics 3.8k
- Developmental Biology 183
- Clinical Biochemistry 272
- Cognitive Neuroscience 678
- Developmental Neuroscience 89
Countries citing papers authored by Roger E. Stevenson
This map shows the geographic impact of Roger E. Stevenson'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 Roger E. Stevenson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Roger E. Stevenson more than expected).
Fields of papers citing papers by Roger E. Stevenson
This network shows the impact of papers produced by Roger E. Stevenson. 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 Roger E. Stevenson. The network helps show where Roger E. Stevenson may publish in the future.
Co-authors
The 25 scholars most cited alongside Roger E. Stevenson, 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 253 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2002 | 660 | |
| 2 | Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes Hit paper breakdown → | 2008 | 629 |
| 3 | 2008 | 476 | |
| 4 | 1994 | 343 | |
| 5 | 1998 | 319 | |
| 6 | 2005 | 315 | |
| 7 | 1997 | 309 | |
| 8 | 1994 | 247 | |
| 9 | 2020 | 231 | |
| 10 | 2007 | 230 | |
| 11 | 1996 | 203 | |
| 12 | 2007 | 197 | |
| 13 | 1986 | 193 | |
| 14 | 2012 | 191 | |
| 15 | 2008 | 189 | |
| 16 | 1994 | 180 | |
| 17 | 2005 | 174 | |
| 18 | 2000 | 169 | |
| 19 | 2007 | 169 | |
| 20 | 2011 | 168 |
About Roger E. Stevenson
Roger E. Stevenson is a scholar working on Genetics, Developmental Biology, Public Health, Environmental and Occupational Health, Physiology and Cognitive Neuroscience, having authored 253 papers that have together received 13.7k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (72 papers), Spinal Dysraphism and Malformations (16 papers), Genomic variations and chromosomal abnormalities (15 papers), Lysosomal Storage Disorders Research (11 papers), Genomics and Rare Diseases (11 papers), Autism Spectrum Disorder Research (8 papers), Congenital limb and hand anomalies (7 papers) and Congenital Anomalies and Fetal Surgery (5 papers). The work is most often cited by research in Genetics (3.8k citations), Developmental Biology (183 citations), Clinical Biochemistry (272 citations), Cognitive Neuroscience (678 citations) and Developmental Neuroscience (89 citations). Roger E. Stevenson has collaborated with scholars based in United States, Canada and United Kingdom. Frequent co-authors include Charles E. Schwartz, Richard J. Simensen, Herbert A. Lubs, Richard J. Schroer, Cindy D. Skinner, Mary C. Phelan, Jane H. Dean, Michael J. Friez, R. Curtis Rogers and R. Rodney Howell. Their work appears in journals such as The American Journal of Human Genetics, Journal of Medical Genetics, PEDIATRICS, Clinical Genetics and Human Molecular 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.