R.N. Simmers
Impact in
-
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
-
- Drug Transport and Resistance Mechanisms
Papers in
-
- Epigenetics and DNA Methylation 2
- Protein Degradation and Inhibitors 1
- Genetics 6
- Genetics and Neurodevelopmental Disorders 6
- Genomic variations and chromosomal abnormalities 2
- Co-authors
- David F. Callen (5 shared papers)G.R. Sutherland (7 shared papers)Elizabeth Baker (3 shared papers)Grant R. Sutherland (2 shared papers)Igor B. Roninson (1 shared paper)R. Seshadri (1 shared paper)V.J. Hyland (4 shared papers)Adrian K. West (1 shared paper)
- Journals
- Human Genetics (3 papers)Cytogenetic and Genome Research (2 papers)Journal of Medical Genetics (1 paper)Science (1 paper)Genomics (1 paper)
- Partner nations
- AustraliaUnited States
In The Last Decade
R.N. Simmers
10 papers receiving 379 citations
Peers
Comparison fields: 5 of 58
- Genetics 158
- Oncology 135
- Pediatrics, Perinatology and Child Health 70
- Hematology 37
- Molecular Biology 205
Countries citing papers authored by R.N. Simmers
This map shows the geographic impact of R.N. Simmers'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.N. Simmers with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites R.N. Simmers more than expected).
Fields of papers citing papers by R.N. Simmers
This network shows the impact of papers produced by R.N. Simmers. 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.N. Simmers. The network helps show where R.N. Simmers may publish in the future.
Co-authors
The 19 scholars most cited alongside R.N. Simmers, 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 | 1987 | 146 | |
| 2 | 1988 | 49 | |
| 3 | 1987 | 49 | |
| 4 | 1986 | 38 | |
| 5 | 1988 | 33 | |
| 6 | 1986 | 31 | |
| 7 | 1988 | 20 | |
| 8 | 1987 | 13 | |
| 9 | 1988 | 8 | |
| 10 | Linkage analysis of markers near fragile sites on human chromosome 16 | 1987 | 2 |
About R.N. Simmers
R.N. Simmers is a scholar working on Molecular Biology, Genetics, Oncology, Hematology and Surgery, having authored 10 papers that have together received 389 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (6 papers), Acute Myeloid Leukemia Research (2 papers), Epigenetics and DNA Methylation (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Pancreatic function and diabetes (1 paper), Protein Degradation and Inhibitors (1 paper), Bone health and treatments (1 paper) and Neonatal Health and Biochemistry (1 paper). The work is most often cited by research in Genetics (158 citations), Oncology (135 citations), Pediatrics, Perinatology and Child Health (70 citations), Hematology (37 citations) and Molecular Biology (205 citations). R.N. Simmers has collaborated with scholars based in Australia and United States. Frequent co-authors include David F. Callen, G.R. Sutherland, Elizabeth Baker, Grant R. Sutherland, Igor B. Roninson, R. Seshadri, V.J. Hyland, Adrian K. West, Robert I. Richards and Ieva Stupans. Their work appears in journals such as Human Genetics, Cytogenetic and Genome Research, Journal of Medical Genetics, Science and Genomics.
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.