Robin Forbes
Impact in
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- Neurogenetic and Muscular Disorders Research
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 6
- Neurogenetic and Muscular Disorders Research 5
- Genetics and Neurodevelopmental Disorders 3
- Cleft Lip and Palate Research 3
- Genomic variations and chromosomal abnormalities 2
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- Prenatal Screening and Diagnostics 4
- Co-authors
- Monique M. Ryan (7 shared papers)Carol I Bower (3 shared papers)Ivan Francis (2 shared papers)Fiona J. Stanley (2 shared papers)Trent Burgess (3 shared papers)Zornitza Stark (4 shared papers)George McGillivray (2 shared papers)Emily J. Higgs (1 shared paper)
- Journals
- The Lancet Regional Health - Western Pacific (2 papers)Neuromuscular Disorders (2 papers)Journal of Neuromuscular Diseases (1 paper)Stem Cell Research (1 paper)Journal of Child Neurology (1 paper)
- Partner nations
- AustraliaUnited KingdomUnited States
In The Last Decade
Robin Forbes
26 papers receiving 419 citations
Peers
Comparison fields: 5 of 63
- Genetics 83
- Pediatrics, Perinatology and Child Health 80
- Genetics 112
- Ophthalmology 17
- Oncology 49
Countries citing papers authored by Robin Forbes
This map shows the geographic impact of Robin Forbes'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 Robin Forbes with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Robin Forbes more than expected).
Fields of papers citing papers by Robin Forbes
This network shows the impact of papers produced by Robin Forbes. 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 Robin Forbes. The network helps show where Robin Forbes may publish in the future.
Co-authors
The 25 scholars most cited alongside Robin Forbes, 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 27 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2011 | 57 | |
| 2 | 2018 | 56 | |
| 3 | 2006 | 44 | |
| 4 | 2007 | 38 | |
| 5 | 2015 | 34 | |
| 6 | 2013 | 34 | |
| 7 | 2009 | 33 | |
| 8 | Congenital malformations in aborigines and non-aborigines in Western Australia, 1980-1987. | 1989 | 25 |
| 9 | 2017 | 19 | |
| 10 | 1989 | 19 | |
| 11 | 2007 | 14 | |
| 12 | 2022 | 13 | |
| 13 | 1990 | 11 | |
| 14 | 2014 | 11 | |
| 15 | 1987 | 6 | |
| 16 | 2008 | 6 | |
| 17 | 2023 | 5 | |
| 18 | 2019 | 4 | |
| 19 | 2024 | 3 | |
| 20 | 2021 | 3 |
About Robin Forbes
Robin Forbes is a scholar working on Genetics, Genetics, Pediatrics, Perinatology and Child Health, Cardiology and Cardiovascular Medicine and Molecular Biology, having authored 27 papers that have together received 445 indexed citations. Recurring topics across this work include Neurogenetic and Muscular Disorders Research (5 papers), Prenatal Screening and Diagnostics (4 papers), Muscle Physiology and Disorders (3 papers), Genetics and Neurodevelopmental Disorders (3 papers), Congenital Anomalies and Fetal Surgery (3 papers), Cleft Lip and Palate Research (3 papers), Genomic variations and chromosomal abnormalities (2 papers) and Autism Spectrum Disorder Research (2 papers). The work is most often cited by research in Genetics (83 citations), Pediatrics, Perinatology and Child Health (80 citations), Genetics (112 citations), Ophthalmology (17 citations) and Oncology (49 citations). Robin Forbes has collaborated with scholars based in Australia, United Kingdom and United States. Frequent co-authors include Monique M. Ryan, Carol I Bower, Ivan Francis, Fiona J. Stanley, Trent Burgess, Zornitza Stark, George McGillivray, Emily J. Higgs, Margaret Sahhar and Belinda Dawson McClaren. Their work appears in journals such as The Lancet Regional Health - Western Pacific, Neuromuscular Disorders, Journal of Neuromuscular Diseases, Stem Cell Research and Journal of Child Neurology.
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.