Robert A. Saul
Impact in
- Genetics top 2%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Cognitive Neuroscience top 5%
- Autism Spectrum Disorder Research
Papers in
- Genetics 19
- Genetics and Neurodevelopmental Disorders 6
- Genomic variations and chromosomal abnormalities 6
- BRCA gene mutations in cancer 5
- Genomics and Rare Diseases 4
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- Congenital heart defects research 7
- Co-authors
- Beth A. Tarini (4 shared papers)Emily Chen (2 shared papers)Marilyn C. Jones (2 shared papers)Debra Freedenberg (2 shared papers)Joan M. Stoler (1 shared paper)John B. Moeschler (1 shared paper)Michael Shevell (1 shared paper)Rizwan Hamid (1 shared paper)
- Journals
- PEDIATRICS (7 papers)Alzheimer s & Dementia (2 papers)The Journal of Pediatrics (1 paper)Prenatal Diagnosis (1 paper)Human Molecular Genetics (1 paper)
- Partner nations
- United StatesCanadaAustralia
In The Last Decade
Robert A. Saul
42 papers receiving 1.4k citations
Peers
Comparison fields: 5 of 104
- Genetics 728
- Cognitive Neuroscience 239
- Neurology 112
- Pediatrics, Perinatology and Child Health 131
- Molecular Biology 504
Countries citing papers authored by Robert A. Saul
This map shows the geographic impact of Robert A. Saul'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 A. Saul with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Robert A. Saul more than expected).
Fields of papers citing papers by Robert A. Saul
This network shows the impact of papers produced by Robert A. Saul. 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 A. Saul. The network helps show where Robert A. Saul may publish in the future.
Co-authors
The 25 scholars most cited alongside Robert A. Saul, 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 | 2014 | 363 | |
| 2 | 2001 | 207 | |
| 3 | 2013 | 135 | |
| 4 | 2011 | 75 | |
| 5 | 2007 | 72 | |
| 6 | 1998 | 65 | |
| 7 | 1992 | 42 | |
| 8 | 1993 | 38 | |
| 9 | 2013 | 34 | |
| 10 | 1982 | 31 | |
| 11 | FMR1-Related Disorders | 2012 | 31 |
| 12 | 2013 | 29 | |
| 13 | 2014 | 28 | |
| 14 | 1982 | 25 | |
| 15 | 2004 | 23 | |
| 16 | 1982 | 23 | |
| 17 | 2015 | 20 | |
| 18 | 2017 | 20 | |
| 19 | 2003 | 18 | |
| 20 | 1988 | 17 |
About Robert A. Saul
Robert A. Saul is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Nutrition and Dietetics and Surgery, having authored 42 papers that have together received 1.5k indexed citations. Recurring topics across this work include Congenital heart defects research (7 papers), Genetics and Neurodevelopmental Disorders (6 papers), Genomic variations and chromosomal abnormalities (6 papers), Food composition and properties (5 papers), BRCA gene mutations in cancer (5 papers), Autism Spectrum Disorder Research (4 papers), Prenatal Screening and Diagnostics (4 papers) and Genomics and Rare Diseases (4 papers). The work is most often cited by research in Genetics (728 citations), Cognitive Neuroscience (239 citations), Neurology (112 citations), Pediatrics, Perinatology and Child Health (131 citations) and Molecular Biology (504 citations). Robert A. Saul has collaborated with scholars based in United States, Canada and Australia. Frequent co-authors include Beth A. Tarini, Emily Chen, Marilyn C. Jones, Debra Freedenberg, Joan M. Stoler, John B. Moeschler, Michael Shevell, Rizwan Hamid, Joseph H. Hersh and Jack Tarleton. Their work appears in journals such as PEDIATRICS, Alzheimer s & Dementia, The Journal of Pediatrics, Prenatal Diagnosis 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.