Alan Stuart
Impact in
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- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- BRCA gene mutations in cancer
- Myeloproliferative Neoplasms: Diagnosis and Treatment
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- Cancer Genomics and Diagnostics
Papers in
- Genetics 5
- Myeloproliferative Neoplasms: Diagnosis and Treatment 5
- Genomics and Rare Diseases 2
- Genomic variations and chromosomal abnormalities 2
- BRCA gene mutations in cancer 1
- Hemoglobinopathies and Related Disorders 1
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- Acute Myeloid Leukemia Research 3
- Co-authors
- Bekim Sadiković (15 shared papers)Jennifer Kerkhof (9 shared papers)Peter Ainsworth (5 shared papers)Hanxin Lin (11 shared papers)Laila C. Schenkel (4 shared papers)Jack Reilly (3 shared papers)Joan H.M. Knoll (2 shared papers)Erfan Aref‐Eshghi (2 shared papers)
In The Last Decade
Alan Stuart
16 papers receiving 238 citations
Peers
Comparison fields: 5 of 38
- Genetics 43
- Cancer Research 46
- Genetics 85
- Hematology 27
- Clinical Biochemistry 12
Countries citing papers authored by Alan Stuart
This map shows the geographic impact of Alan Stuart'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 Alan Stuart with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Alan Stuart more than expected).
Fields of papers citing papers by Alan Stuart
This network shows the impact of papers produced by Alan Stuart. 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 Alan Stuart. The network helps show where Alan Stuart may publish in the future.
Co-authors
The 25 scholars most cited alongside Alan Stuart, 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 | 2017 | 98 | |
| 2 | 2016 | 43 | |
| 3 | 2020 | 19 | |
| 4 | 2020 | 15 | |
| 5 | 2022 | 11 | |
| 6 | 2020 | 10 | |
| 7 | 2022 | 9 | |
| 8 | 2022 | 7 | |
| 9 | 2022 | 5 | |
| 10 | 2020 | 5 | |
| 11 | 2017 | 5 | |
| 12 | 2023 | 3 | |
| 13 | 2021 | 3 | |
| 14 | 2021 | 3 | |
| 15 | 2021 | 2 | |
| 16 | 2022 | 2 |
About Alan Stuart
Alan Stuart is a scholar working on Genetics, Hematology, Cancer Research, Molecular Biology and Genetics, having authored 16 papers that have together received 240 indexed citations. Recurring topics across this work include Myeloproliferative Neoplasms: Diagnosis and Treatment (5 papers), Acute Myeloid Leukemia Research (3 papers), Cancer Genomics and Diagnostics (3 papers), Genomics and Rare Diseases (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Vitamin K Research Studies (1 paper), BRCA gene mutations in cancer (1 paper) and Hemoglobinopathies and Related Disorders (1 paper). The work is most often cited by research in Genetics (43 citations), Cancer Research (46 citations), Genetics (85 citations), Hematology (27 citations) and Clinical Biochemistry (12 citations). Alan Stuart has collaborated with scholars based in Canada, Japan and France. Frequent co-authors include Bekim Sadiković, Jennifer Kerkhof, Peter Ainsworth, Hanxin Lin, Laila C. Schenkel, Jack Reilly, Joan H.M. Knoll, Erfan Aref‐Eshghi, Paul C. Adams and C. Anthony Rupar. Their work appears in journals such as Journal of Molecular Diagnostics, Frontiers in Genetics, British Journal of Haematology, Blood and Frontiers in Oncology.
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.