Robert F. Stratton
Impact in
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Developmental Biology top 5%
Papers in
- Genetics 33
- Genomic variations and chromosomal abnormalities 15
- Connective tissue disorders research 5
- Cleft Lip and Palate Research 5
- Craniofacial Disorders and Treatments 5
- Congenital Ear and Nasal Anomalies 4
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- Hedgehog Signaling Pathway Studies 5
- Co-authors
- William B. Dobyns (6 shared papers)Frank Greenberg (4 shared papers)David H. Ledbetter (4 shared papers)Robert L. Nussbaum (1 shared paper)Julie T. Parke (1 shared paper)Susan Airhart (1 shared paper)Charleen M. Moore (6 shared papers)Barbara R. DuPont (6 shared papers)
- Journals
- Human Genetics (4 papers)American Journal of Medical Genetics (27 papers)Nature Genetics (1 paper)The Journal of Pediatrics (1 paper)Pediatric Research (1 paper)
- Partner nations
- United StatesNetherlandsUnited Kingdom
In The Last Decade
Robert F. Stratton
41 papers receiving 1.3k citations
Peers
Comparison fields: 5 of 62
- Genetics 916
- Developmental Biology 39
- Pediatrics, Perinatology and Child Health 353
- Genetics 138
- Molecular Biology 736
Countries citing papers authored by Robert F. Stratton
This map shows the geographic impact of Robert F. Stratton'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 F. Stratton with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Robert F. Stratton more than expected).
Fields of papers citing papers by Robert F. Stratton
This network shows the impact of papers produced by Robert F. Stratton. 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 F. Stratton. The network helps show where Robert F. Stratton may publish in the future.
Co-authors
The 25 scholars most cited alongside Robert F. Stratton, 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 42 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2002 | 174 | |
| 2 | 1984 | 169 | |
| 3 | 1983 | 137 | |
| 4 | 1986 | 104 | |
| 5 | 1984 | 91 | |
| 6 | 1999 | 87 | |
| 7 | 1994 | 51 | |
| 8 | 2007 | 44 | |
| 9 | 2009 | 43 | |
| 10 | 2013 | 39 | |
| 11 | 1996 | 32 | |
| 12 | 2007 | 31 | |
| 13 | 1986 | 26 | |
| 14 | 1991 | 25 | |
| 15 | 1994 | 24 | |
| 16 | 1994 | 24 | |
| 17 | 1998 | 21 | |
| 18 | 1993 | 19 | |
| 19 | 2012 | 18 | |
| 20 | 2001 | 16 |
About Robert F. Stratton
Robert F. Stratton is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Surgery and Genetics, having authored 42 papers that have together received 1.4k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (15 papers), Prenatal Screening and Diagnostics (6 papers), Connective tissue disorders research (5 papers), Cleft Lip and Palate Research (5 papers), Craniofacial Disorders and Treatments (5 papers), Hedgehog Signaling Pathway Studies (5 papers), Congenital Ear and Nasal Anomalies (4 papers) and Chromosomal and Genetic Variations (4 papers). The work is most often cited by research in Genetics (916 citations), Developmental Biology (39 citations), Pediatrics, Perinatology and Child Health (353 citations), Genetics (138 citations) and Molecular Biology (736 citations). Robert F. Stratton has collaborated with scholars based in United States, Netherlands and United Kingdom. Frequent co-authors include William B. Dobyns, Frank Greenberg, David H. Ledbetter, Robert L. Nussbaum, Julie T. Parke, Susan Airhart, Charleen M. Moore, Barbara R. DuPont, Jannine D. Cody and Eva Sujansky. Their work appears in journals such as Human Genetics, American Journal of Medical Genetics, Nature Genetics, The Journal of Pediatrics and Pediatric Research.
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.