Ainoon Othman

417 total citations
22 papers, 287 citations indexed

About

Ainoon Othman is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Hematology. According to data from OpenAlex, Ainoon Othman has authored 22 papers receiving a total of 287 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 11 papers in Pediatrics, Perinatology and Child Health and 10 papers in Hematology. Recurrent topics in Ainoon Othman's work include Hemoglobinopathies and Related Disorders (12 papers), Neonatal Health and Biochemistry (11 papers) and Iron Metabolism and Disorders (7 papers). Ainoon Othman is often cited by papers focused on Hemoglobinopathies and Related Disorders (12 papers), Neonatal Health and Biochemistry (11 papers) and Iron Metabolism and Disorders (7 papers). Ainoon Othman collaborates with scholars based in Malaysia, New Zealand and Portugal. Ainoon Othman's co-authors include Raja Zahratul Azma Raja Sabudin, Fook‐Choe Cheah, Zulkifli Ismail, Robert J. Unwin, Minna Tanner, Mark T. Young, N Y Boo, Oliver Wrong, Gerard B. Nash and Paddy McMaster and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Biochemical Journal.

In The Last Decade

Ainoon Othman

19 papers receiving 282 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Ainoon Othman Malaysia 9 137 133 100 69 66 22 287
Kimberley Veraar Netherlands 7 54 0.4× 126 0.9× 54 0.5× 25 0.4× 11 0.2× 9 395
Jean D. Ross United States 9 123 0.9× 63 0.5× 81 0.8× 82 1.2× 77 1.2× 14 329
María Helena Vaisbich Brazil 9 69 0.5× 107 0.8× 22 0.2× 39 0.6× 10 0.2× 34 282
Elisa Seneca Italy 4 94 0.7× 40 0.3× 35 0.3× 50 0.7× 59 0.9× 8 204
Ahmet Yeşilyurt Türkiye 11 55 0.4× 95 0.7× 14 0.1× 37 0.5× 17 0.3× 34 251
Shinya Ishiko Japan 11 16 0.1× 195 1.5× 32 0.3× 44 0.6× 20 0.3× 31 343
Weizhen Tan United States 8 78 0.6× 190 1.4× 27 0.3× 120 1.7× 36 0.5× 12 418
Reza Alibakhshi Iran 10 39 0.3× 98 0.7× 14 0.1× 87 1.3× 86 1.3× 47 326
A Karaklis Greece 10 127 0.9× 63 0.5× 150 1.5× 48 0.7× 251 3.8× 18 423
Nazlisadat Seyed Khoei Austria 7 130 0.9× 129 1.0× 28 0.3× 38 0.6× 21 0.3× 10 224

Countries citing papers authored by Ainoon Othman

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Ainoon Othman

This figure shows the co-authorship network connecting the top 25 collaborators of Ainoon Othman. A scholar is included among the top collaborators of Ainoon Othman 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 Ainoon Othman. Ainoon Othman 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.
Sabudin, Raja Zahratul Azma Raja, et al.. (2023). Prevalence and molecular heterogeneity of glucose-6-phosphate dehydrogenase (G6PD) deficiency in the Senoi Malaysian Orang Asli population. PLoS ONE. 18(12). e0294891–e0294891. 3 indexed citations
2.
Sabudin, Raja Zahratul Azma Raja, et al.. (2023). Population screening for glucose-6-phosphate dehydrogenase deficiency using quantitative point-of-care tests: a systematic review. Frontiers in Genetics. 14. 1098828–1098828. 4 indexed citations
3.
Sabudin, Raja Zahratul Azma Raja, et al.. (2022). Glucose-6-Phosphate Dehydrogenase Deficiency and Neonatal Hyperbilirubinemia: Insights on Pathophysiology, Diagnosis, and Gene Variants in Disease Heterogeneity. Frontiers in Pediatrics. 10. 875877–875877. 37 indexed citations
4.
Othman, Ainoon, et al.. (2019). Team-Based Learning: Benefits on Learning and Students’ Perception. Education in Medicine Journal. 14(4). 61–69. 1 indexed citations
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Sathar, Jameela, et al.. (2017). Importance of extended blood group genotyping in multiply transfused patients. Transfusion and Apheresis Science. 56(3). 410–416. 12 indexed citations
8.
Othman, Ainoon, et al.. (2017). Glucose‐6‐phosphate dehydrogenase (G6PD)‐deficient infants: Enzyme activity and gene variants as risk factors for phototherapy in the first week of life. Journal of Paediatrics and Child Health. 53(7). 705–710. 7 indexed citations
9.
Sabudin, Raja Zahratul Azma Raja, et al.. (2017). Molecular Characterisation of α‐ and β‐Thalassaemia among Indigenous Senoi Orang Asli Communities in Peninsular Malaysia. Annals of Human Genetics. 81(5). 205–212. 8 indexed citations
10.
Alias, Hamidah, et al.. (2016). Detection of Homozygous Haemoglobin Constant Spring by Capillary Electrophoresis Method. 1(1). 28–32. 2 indexed citations
11.
Sabudin, Raja Zahratul Azma Raja, et al.. (2015). Hemoglobinopathies and thalassemia screening among Senoi Orang Asli in Peninsular Malaysia. AIP conference proceedings. 1678. 30033–30033. 2 indexed citations
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Sabudin, Raja Zahratul Azma Raja, et al.. (2014). Immature reticulocyte fraction is an early predictor of bone marrow recovery post chemotherapy in patients with acute leukemia.. PubMed. 35(4). 346–9. 9 indexed citations
14.
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Boo, N Y, et al.. (2012). Genotyping of OATP2 Variants in a Group of Malaysian Neonates Using High-Resolution Melting Analysis. SHILAP Revista de lepidopterología. 1(2). 92–96. 1 indexed citations
16.
Sabudin, Raja Zahratul Azma Raja, et al.. (2012). Co-inheritance of compound heterozygous Hb Constant Spring and a single -alpha(3.7) gene deletion with heterozygous deltabeta thalassaemia: a diagnostic challenge.. PubMed. 34(1). 57–62. 4 indexed citations
17.
Othman, Ainoon, et al.. (2010). A family study of HbS in a Malay family by molecular analysis.. PubMed. 32(2). 137–41. 2 indexed citations
18.
Boo, N Y, et al.. (2009). Homozygous variant of UGT1A1 gene mutation and severe neonatal hyperbilirubinemia. Pediatrics International. 51(4). 488–493. 11 indexed citations
19.
Boo, N Y, et al.. (2009). Variants of organic anion transporter polypeptide 2 gene are not risk factors associated with severe neonatal hyperbilirubinemia.. PubMed. 31(2). 99–104. 6 indexed citations
20.
Othman, Ainoon, et al.. (2004). Complete molecular characterisation of glucose-6-phosphate dehydrogenase (G6PD) deficiency in a group of Malaysian Chinese neonates.. PubMed. 26(2). 89–98. 23 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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