Robin Forbes

551 total citations
22 papers, 360 citations indexed

About

Robin Forbes is a scholar working on Surgery, Genetics and Molecular Biology. According to data from OpenAlex, Robin Forbes has authored 22 papers receiving a total of 360 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Surgery, 8 papers in Genetics and 6 papers in Molecular Biology. Recurrent topics in Robin Forbes's work include Congenital Anomalies and Fetal Surgery (6 papers), Neurogenetic and Muscular Disorders Research (5 papers) and Prenatal Screening and Diagnostics (5 papers). Robin Forbes is often cited by papers focused on Congenital Anomalies and Fetal Surgery (6 papers), Neurogenetic and Muscular Disorders Research (5 papers) and Prenatal Screening and Diagnostics (5 papers). Robin Forbes collaborates with scholars based in Australia, United States and Malaysia. Robin Forbes's co-authors include Carol Bower, Monique M. Ryan, Fiona Stanley, Ivan Francis, Zornitza Stark, George McGillivray, Trent Burgess, Veronica Collins, Leslie J. Sheffield and Jane Halliday and has published in prestigious journals such as SHILAP Revista de lepidopterología, Journal of Neurology Neurosurgery & Psychiatry and BJOG An International Journal of Obstetrics & Gynaecology.

In The Last Decade

Robin Forbes

21 papers receiving 353 citations

Peers

Robin Forbes
M. McLimont Canada
Tai Ju Hwang South Korea
B. Boudailliez France
Estelle Dubruc Switzerland
S. Ota Canada
Huanmin Wang China
Elena Palmisani Italy
Antonio Marzollo Italy
Ghada El‐Kamah Egypt
Koki Fujiwara Japan
M. McLimont Canada
Robin Forbes
Citations per year, relative to Robin Forbes Robin Forbes (= 1×) peers M. McLimont

Countries citing papers authored by Robin Forbes

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Robin Forbes

This figure shows the co-authorship network connecting the top 25 collaborators of Robin Forbes. A scholar is included among the top collaborators of Robin Forbes based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Robin Forbes. Robin Forbes is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Petway, Adam, et al.. (2025). Examining prior injury relative to Achilles tendon ruptures in National Basketball Association players. Research in Sports Medicine. 33(5). 525–536.
2.
Li, Limin, Manoj P. Menezes, Melanie Smith, et al.. (2024). Rare homozygous disease-associated sequence variants in children with spinal muscular atrophy: a phenotypic description and review of the literature. Neuromuscular Disorders. 37. 29–35. 2 indexed citations
3.
Boggs, Kirsten, Fiona Lynch, Michelle C. Ward, et al.. (2024). Rapid genomic testing in critically ill pediatric patients: Genetic counseling lessons from a national program. SHILAP Revista de lepidopterología. 2(Suppl 2). 101878–101878. 2 indexed citations
4.
Forbes, Robin, et al.. (2023). Psychosocial and supportive care needs of individuals with advanced myeloma. Canadian Oncology Nursing Journal. 33(2). 215–222. 2 indexed citations
5.
Carroll, Kate, Robin Forbes, Rachel A. Kennedy, et al.. (2022). Delivering multidisciplinary neuromuscular care for children via telehealth. Muscle & Nerve. 66(1). 31–38. 9 indexed citations
6.
Houweling, Peter J., Robin Forbes, Monique M. Ryan, et al.. (2021). Generating an iPSC line (with isogenic control) from the PBMCs of an ACTA1 (p.Gly148Asp) nemaline myopathy patient. Stem Cell Research. 54. 102429–102429. 3 indexed citations
7.
Baker, Emma K., Marta Arpone, Robin Forbes, et al.. (2019). Clinical and Molecular Differences between 4-Year-Old Monozygous Male Twins Mosaic for Normal, Premutation and Fragile X Full Mutation Alleles. Genes. 10(4). 279–279. 4 indexed citations
8.
Farrar, Michelle A., Kate A. Carey, Anita Cairns, et al.. (2018). Nusinersen for SMA: expanded access programme. Journal of Neurology Neurosurgery & Psychiatry. 89(9). 937–942. 50 indexed citations
9.
Higgs, Emily, Belinda McClaren, Margaret Sahhar, Monique M. Ryan, & Robin Forbes. (2015). ‘A short time but a lovely little short time’: Bereaved parents' experiences of having a child with spinal muscular atrophy type 1. Journal of Paediatrics and Child Health. 52(1). 40–46. 30 indexed citations
10.
Brown, Natasha J., Trent Burgess, Robin Forbes, et al.. (2013). 5q31.3 Microdeletion syndrome: Clinical and molecular characterization of two further cases. American Journal of Medical Genetics Part A. 161(10). 2604–2608. 27 indexed citations
11.
Howell, Katherine B., Robin Forbes, Trent Burgess, et al.. (2012). D.O.2 Microarray testing for developmental delay reveals an expanded clinical spectrum of dystrophinopathies. Neuromuscular Disorders. 22(9-10). 805–806. 1 indexed citations
12.
Tan, Tiong Yang, Amanda Collins, Paul A. James, et al.. (2011). Phenotypic variability of distal 22q11.2 copy number abnormalities. American Journal of Medical Genetics Part A. 155(7). 1623–1633. 54 indexed citations
13.
Dimasi, David P., Alex W. Hewitt, Sonja Klebe, et al.. (2009). Novel quantitative trait loci for central corneal thickness identified by candidate gene analysis of osteogenesis imperfecta genes. Human Genetics. 127(1). 33–44. 29 indexed citations
14.
Nisselle, Amy, et al.. (2008). Consumer contribution to the delivery of genetic health services. American Journal of Medical Genetics Part A. 146A(17). 2266–2274. 6 indexed citations
15.
Massie, John, et al.. (2007). Community‐wide screening for cystic fibrosis carriers could replace newborn screening for the diagnosis of cystic fibrosis. Journal of Paediatrics and Child Health. 43(11). 721–723. 13 indexed citations
16.
Halliday, J., et al.. (2007). Follow up and evaluation of the Victorian first‐trimester combined screening programme for Down syndrome and trisomy 18. BJOG An International Journal of Obstetrics & Gynaecology. 114(7). 812–818. 21 indexed citations
17.
Jaques, Alice M., Veronica Collins, Kerry Haynes, et al.. (2006). Using record linkage and manual follow-up to evaluate the Victorian maternal serum screening quadruple test for Down's syndrome, trisomy 18 and neural tube defects. Journal of Medical Screening. 13(1). 8–13. 41 indexed citations
18.
Bower, Carol, et al.. (1990). VALIDATION STUDIES FROM THE WESTERN AUSTRALIAN CONGENITAL MALFORMATIONS REGISTRY. Community Health Studies. 14(3). 274–278. 11 indexed citations
19.
Bower, Carol, et al.. (1989). Congenital malformations in Aborigines and non‐Aborigines in Western Australia, 1980–1987 (for editorial comment see page 241). The Medical Journal of Australia. 151(5). 245–248. 18 indexed citations
20.
Bower, Carol, et al.. (1989). Congenital malformations in aborigines and non-aborigines in Western Australia, 1980-1987.. PubMed. 151(5). 245–8. 24 indexed citations

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.

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