Aria Setoodeh
Impact in
- Clinical Biochemistry top 5%
- Metabolism and Genetic Disorders
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- Diabetes Management and Research
Papers in
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- Biochemical and Molecular Research 5
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- Metabolism and Genetic Disorders 15
- Co-authors
- Ali Rabbani (16 shared papers)Farzaneh Abbasi (11 shared papers)Amirreza Haghighi (3 shared papers)Alireza Haghighi (3 shared papers)Nasrollah Saleh-Gohari (2 shared papers)Mohammad Taghi Haghi Ashtıani (2 shared papers)Bahareh Rabbani (2 shared papers)Parastoo Rostami (10 shared papers)
- Journals
- Gene (2 papers)Cytotherapy (1 paper)Orphanet Journal of Rare Diseases (1 paper)European Journal of Human Genetics (1 paper)Mutation research. Fundamental and molecular mechanisms of mutagenesis (1 paper)
- Partner nations
- IranUnited KingdomUnited States
In The Last Decade
Aria Setoodeh
39 papers receiving 405 citations
Peers
Comparison fields: 5 of 65
- Clinical Biochemistry 110
- Endocrinology, Diabetes and Metabolism 106
- Genetics 46
- Genetics 119
- Rheumatology 60
Countries citing papers authored by Aria Setoodeh
This map shows the geographic impact of Aria Setoodeh'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 Aria Setoodeh with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Aria Setoodeh more than expected).
Fields of papers citing papers by Aria Setoodeh
This network shows the impact of papers produced by Aria Setoodeh. 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 Aria Setoodeh. The network helps show where Aria Setoodeh may publish in the future.
Co-authors
The 25 scholars most cited alongside Aria Setoodeh, 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 44 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2022 | 78 | |
| 2 | 2012 | 26 | |
| 3 | 2018 | 25 | |
| 4 | 2016 | 20 | |
| 5 | 2013 | 19 | |
| 6 | 2018 | 18 | |
| 7 | 2019 | 18 | |
| 8 | 2011 | 16 | |
| 9 | 2017 | 15 | |
| 10 | 2016 | 15 | |
| 11 | 2017 | 15 | |
| 12 | 2018 | 15 | |
| 13 | Transient neonatal diabetes as a presentation of Fanconi- Bickel Syndrome. | 2012 | 13 |
| 14 | 2016 | 12 | |
| 15 | 2012 | 11 | |
| 16 | 2015 | 10 | |
| 17 | Female sex as a risk factor for glycemic control and complications in Iranian patients with type one diabetes mellitus. | 2011 | 10 |
| 18 | 2015 | 8 | |
| 19 | 2018 | 8 | |
| 20 | 2022 | 6 |
About Aria Setoodeh
Aria Setoodeh is a scholar working on Molecular Biology, Clinical Biochemistry, Genetics, Endocrinology, Diabetes and Metabolism and Rheumatology, having authored 44 papers that have together received 414 indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (15 papers), Diabetes and associated disorders (8 papers), Diabetes Management and Research (7 papers), Pancreatic function and diabetes (7 papers), Neonatal Health and Biochemistry (5 papers), Biochemical and Molecular Research (5 papers), Folate and B Vitamins Research (5 papers) and Lysosomal Storage Disorders Research (4 papers). The work is most often cited by research in Clinical Biochemistry (110 citations), Endocrinology, Diabetes and Metabolism (106 citations), Genetics (46 citations), Genetics (119 citations) and Rheumatology (60 citations). Aria Setoodeh has collaborated with scholars based in Iran, United Kingdom and United States. Frequent co-authors include Ali Rabbani, Farzaneh Abbasi, Amirreza Haghighi, Alireza Haghighi, Nasrollah Saleh-Gohari, Mohammad Taghi Haghi Ashtıani, Bahareh Rabbani, Parastoo Rostami, Farzad Kompani and Sian Ellard. Their work appears in journals such as Gene, Cytotherapy, Orphanet Journal of Rare Diseases, European Journal of Human Genetics and Mutation research. Fundamental and molecular mechanisms of mutagenesis.
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.