Belinda Chong
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- Genomics and Rare Diseases 10
- Genomic variations and chromosomal abnormalities 7
- Neurogenetic and Muscular Disorders Research 3
- Genetics and Neurodevelopmental Disorders 3
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- Genetic factors in colorectal cancer 5
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- Genomics and Rare Diseases 10
- Genomic variations and chromosomal abnormalities 7
- Neurogenetic and Muscular Disorders Research 3
- Genetics and Neurodevelopmental Disorders 3
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- Cardiomyopathy and Myosin Studies 3
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- RNA modifications and cancer 4
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- Metabolism and Genetic Disorders 3
Belinda Chong
27 papers receiving 608 citations
Peers
Comparison fields: 5 of 57
- Genetics 79
- Cancer Research 98
- Pathology and Forensic Medicine 114
- Genetics 169
- Cardiology and Cardiovascular Medicine 118
Countries citing papers authored by Belinda Chong
This map shows the geographic impact of Belinda Chong'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 Belinda Chong with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Belinda Chong more than expected).
Fields of papers citing papers by Belinda Chong
This network shows the impact of papers produced by Belinda Chong. 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 Belinda Chong. The network helps show where Belinda Chong may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Belinda Chong, 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 | 2023 | 7 | |
| 2 | 2023 | 7 | |
| 3 | 2022 | 2 | |
| 4 | 2022 | 4 | |
| 5 | 2021 | 13 | |
| 6 | 2020 | 26 | |
| 7 | 2020 | 5 | |
| 8 | 2019 | 35 | |
| 9 | 2019 | 14 | |
| 10 | 2017 | 25 | |
| 11 | 2016 | 20 | |
| 12 | 2014 | 72 | |
| 13 | 2010 | 1 | |
| 14 | 2009 | 27 | |
| 15 | 2007 | 57 | |
| 16 | 2005 | 27 | |
| 17 | 2005 | 49 | |
| 18 | 2001 | 7 | |
| 19 | 2001 | 30 | |
| 20 | 2000 | 2 |
About Belinda Chong
Belinda Chong is a scholar working on Genetics, Clinical Biochemistry and Genetics, having authored 27 papers that have together received 617 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (10 papers), Genomic variations and chromosomal abnormalities (7 papers), Genetic factors in colorectal cancer (5 papers), RNA modifications and cancer (4 papers), Metabolism and Genetic Disorders (3 papers), Neurogenetic and Muscular Disorders Research (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Cardiomyopathy and Myosin Studies (3 papers). The work is most often cited by research in Genetics (79 citations), Cancer Research (98 citations) and Pathology and Forensic Medicine (114 citations). Belinda Chong has collaborated with scholars based in Australia, United States and New Zealand. Frequent co-authors include Madhuri Hegde, Desirée du Sart, Donald R. Love, Shannon Cowie, Melanie Smith, Sebastian Lunke, Zornitza Stark, Paul A. James, Ivan Macciocca and C. Sue Richards. Their work appears in journals such as Clinical Cancer Research, Journal of Bone and Mineral Research and BMJ Open.
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.