Ainoon Othman
Impact in
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- Neonatal Health and Biochemistry
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- Hemoglobinopathies and Related Disorders
Papers in
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- Neonatal Health and Biochemistry 12
- Genetics 11
- Hemoglobinopathies and Related Disorders 11
- Co-authors
- Fook‐Choe Cheah (3 shared papers)Lesley J. Bruce (1 shared paper)N Y Boo (4 shared papers)Graham D. Ogle (1 shared paper)Sarah Hart (1 shared paper)Oliver Wrong (1 shared paper)Gerard B. Nash (1 shared paper)Paddy McMaster (1 shared paper)
- Journals
- PLoS ONE (2 papers)Frontiers in Genetics (1 paper)Frontiers in Pediatrics (1 paper)Annals of Human Genetics (1 paper)Biochemical Journal (1 paper)
- Partner nations
- MalaysiaPortugalNew Zealand
In The Last Decade
Ainoon Othman
20 papers receiving 307 citations
Peers
Comparison fields: 5 of 50
- Pediatrics, Perinatology and Child Health 136
- Genetics 66
- Nephrology 32
- Hematology 49
- Physiology 81
Countries citing papers authored by Ainoon Othman
This map shows the geographic impact of Ainoon Othman'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 Ainoon Othman with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ainoon Othman more than expected).
Fields of papers citing papers by Ainoon Othman
This network shows the impact of papers produced by Ainoon Othman. 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 Ainoon Othman. The network helps show where Ainoon Othman may publish in the future.
Co-authors
The 25 scholars most cited alongside Ainoon Othman, 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 23 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2000 | 143 | |
| 2 | 2022 | 44 | |
| 3 | Complete molecular characterisation of glucose-6-phosphate dehydrogenase (G6PD) deficiency in a group of Malaysian Chinese neonates. | 2004 | 24 |
| 4 | 2017 | 13 | |
| 5 | 2014 | 12 | |
| 6 | 2009 | 11 | |
| 7 | 2017 | 11 | |
| 8 | 2014 | 9 | |
| 9 | 2014 | 8 | |
| 10 | 2017 | 7 | |
| 11 | 2016 | 7 | |
| 12 | Variants of organic anion transporter polypeptide 2 gene are not risk factors associated with severe neonatal hyperbilirubinemia. | 2009 | 6 |
| 13 | 2023 | 6 | |
| 14 | 2023 | 4 | |
| 15 | Co-inheritance of compound heterozygous Hb Constant Spring and a single -alpha(3.7) gene deletion with heterozygous deltabeta thalassaemia: a diagnostic challenge. | 2012 | 4 |
| 16 | 2015 | 2 | |
| 17 | A family study of HbS in a Malay family by molecular analysis. | 2010 | 2 |
| 18 | Detection of Homozygous Haemoglobin Constant Spring by Capillary Electrophoresis Method | 2016 | 2 |
| 19 | 2012 | 1 | |
| 20 | 2019 | 1 |
About Ainoon Othman
Ainoon Othman is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Hematology, Pulmonary and Respiratory Medicine and Clinical Biochemistry, having authored 23 papers that have together received 318 indexed citations. Recurring topics across this work include Neonatal Health and Biochemistry (12 papers), Hemoglobinopathies and Related Disorders (11 papers), Iron Metabolism and Disorders (7 papers), Blood groups and transfusion (5 papers), Metabolism and Genetic Disorders (4 papers), Erythrocyte Function and Pathophysiology (4 papers), Methemoglobinemia and Tumor Lysis Syndrome (4 papers) and Heme Oxygenase-1 and Carbon Monoxide (2 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (136 citations), Genetics (66 citations), Nephrology (32 citations), Hematology (49 citations) and Physiology (81 citations). Ainoon Othman has collaborated with scholars based in Malaysia, Portugal and New Zealand. Frequent co-authors include Fook‐Choe Cheah, Lesley J. Bruce, N Y Boo, Graham D. Ogle, Sarah Hart, Oliver Wrong, Gerard B. Nash, Paddy McMaster, Zulkifli Ismail and Evelyn Lavu. Their work appears in journals such as PLoS ONE, Frontiers in Genetics, Frontiers in Pediatrics, Annals of Human Genetics and Biochemical Journal.
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.