Alan Stuart

1.3k total citations
16 papers, 224 citations indexed

About

Alan Stuart is a scholar working on Genetics, Hematology and Genetics. According to data from OpenAlex, Alan Stuart has authored 16 papers receiving a total of 224 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 7 papers in Hematology and 4 papers in Genetics. Recurrent topics in Alan Stuart's work include Myeloproliferative Neoplasms: Diagnosis and Treatment (6 papers), Acute Myeloid Leukemia Research (4 papers) and Hemoglobinopathies and Related Disorders (4 papers). Alan Stuart is often cited by papers focused on Myeloproliferative Neoplasms: Diagnosis and Treatment (6 papers), Acute Myeloid Leukemia Research (4 papers) and Hemoglobinopathies and Related Disorders (4 papers). Alan Stuart collaborates with scholars based in Canada, Japan and Poland. Alan Stuart's co-authors include Bekim Sadiković, Jennifer Kerkhof, Peter Ainsworth, Hanxin Lin, Laila C. Schenkel, Jack Reilly, Joan H.M. Knoll, Paul C. Adams, Erfan Aref‐Eshghi and Robert A. Hegele and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and The FASEB Journal.

In The Last Decade

Alan Stuart

15 papers receiving 222 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Alan Stuart Canada 7 96 95 59 46 36 16 224
Weiyue Gu China 11 101 1.1× 139 1.5× 23 0.4× 52 1.1× 19 0.5× 50 317
S. Bahl India 3 37 0.4× 125 1.3× 64 1.1× 51 1.1× 51 1.4× 4 217
Emine İkbal Atlı Türkiye 8 46 0.5× 119 1.3× 33 0.6× 51 1.1× 9 0.3× 48 212
Nagarajan Paramasivam Germany 13 165 1.7× 239 2.5× 43 0.7× 11 0.2× 54 1.5× 41 408
Sandy Laue Germany 12 123 1.3× 191 2.0× 65 1.1× 25 0.5× 19 0.5× 12 452
Omar Soukarieh France 10 72 0.8× 197 2.1× 45 0.8× 30 0.7× 36 1.0× 15 303
Sarah E. Brnich United States 5 302 3.1× 281 3.0× 79 1.3× 17 0.4× 55 1.5× 6 471
Renan Paulo Martin Brazil 12 66 0.7× 172 1.8× 15 0.3× 76 1.7× 19 0.5× 39 314
Abdulsalam Soofi United States 5 132 1.4× 303 3.2× 20 0.3× 19 0.4× 35 1.0× 5 523
Connie C. Weng United States 16 83 0.9× 138 1.5× 19 0.3× 17 0.4× 23 0.6× 25 435

Countries citing papers authored by Alan Stuart

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Alan Stuart

This figure shows the co-authorship network connecting the top 25 collaborators of Alan Stuart. A scholar is included among the top collaborators of Alan Stuart 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 Alan Stuart. Alan Stuart is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

16 of 16 papers shown
1.
Turowec, Jacob P., Jennifer Kerkhof, Aidin Foroutan, et al.. (2023). Molecular profiling of solid tumors by next-generation sequencing: an experience from a clinical laboratory. Frontiers in Oncology. 13. 1208244–1208244. 3 indexed citations
2.
Chin‐Yee, Benjamin, Ian Cheong, Michael A. Levy, et al.. (2022). Mutational Landscape of Patients Referred for Elevated Hemoglobin Level. Current Oncology. 29(10). 7209–7217.
3.
Hsia, Cyrus C., Laila C. Schenkel, Benjamin D. Hedley, et al.. (2022). Clinical Utility of Implementing a Frontline NGS-Based DNA and RNA Fusion Panel Test for Patients with Suspected Myeloid Malignancies. Molecular Diagnosis & Therapy. 26(3). 333–343. 8 indexed citations
4.
Chin‐Yee, Benjamin, Ian Cheong, Cyrus C. Hsia, et al.. (2022). A Rational Approach to JAK2 Mutation Testing in Patients with Elevated Hemoglobin: Results from the JAK2 Prediction Cohort (JAKPOT) Study. Journal of General Internal Medicine. 38(8). 1828–1833. 6 indexed citations
5.
Chin‐Yee, Benjamin, Ian Cheong, Alejandro Lazo‐Langner, et al.. (2022). Secondary causes of elevated hemoglobin in patients undergoing molecular testing for suspected polycythemia vera in southwestern Ontario: a chart review. CMAJ Open. 10(4). E988–E992. 9 indexed citations
6.
Chin‐Yee, Benjamin, Benjamin D. Hedley, Christopher J. Howlett, et al.. (2022). T‐cell clonality testing for the diagnosis of T‐cell large granular lymphocytic leukemia: Are we identifying pathology or incidental clones?. International Journal of Laboratory Hematology. 44(6). 1115–1120. 5 indexed citations
7.
Stuart, Alan, et al.. (2021). A case of congenital prothrombin deficiency with two concurrent mutations in the prothrombin gene. Research and Practice in Thrombosis and Haemostasis. 5(4). e12510–e12510. 1 indexed citations
8.
Levy, Michael A., Kathleen Rooney, Deanna Alexis Carere, et al.. (2021). Analysis of Sequence and Copy Number Variants in Canadian Patient Cohort With Familial Cancer Syndromes Using a Unique Next Generation Sequencing Based Approach. Frontiers in Genetics. 12. 698595–698595. 2 indexed citations
9.
Chin‐Yee, Benjamin, Ian Cheong, Alan Stuart, et al.. (2021). Investigating Erythrocytosis: Changing Practice Patterns in the Era of Molecular Diagnostics. Blood. 138(Supplement 1). 4630–4630. 2 indexed citations
10.
Kawata, Eri, Alejandro Lazo‐Langner, Anargyros Xenocostas, et al.. (2020). Clinical value of next‐generation sequencing compared to cytogenetics in patients with suspected myelodysplastic syndrome. British Journal of Haematology. 192(4). 729–736. 8 indexed citations
11.
Volodarsky, Michael, Jennifer Kerkhof, Alan Stuart, et al.. (2020). Comprehensive genetic sequence and copy number analysis for Charcot-Marie-Tooth disease in a Canadian cohort of 2517 patients. Journal of Medical Genetics. 58(4). 284–288. 19 indexed citations
12.
Aref‐Eshghi, Erfan, Jacob McGee, Jennifer Kerkhof, et al.. (2020). Genetic and epigenetic profiling of BRCA1/2 in ovarian tumors reveals additive diagnostic yield and evidence of a genomic BRCA1/2 DNA methylation signature. Journal of Human Genetics. 65(10). 865–873. 14 indexed citations
13.
Tarnopolsky, Mark A., Jennifer Kerkhof, Alan Stuart, et al.. (2020). Bone marrow‐derived mitochondrial DNA has limited capacity for inter‐tissue transfer in vivo. The FASEB Journal. 34(7). 9297–9306. 5 indexed citations
14.
Kerkhof, Jennifer, Laila C. Schenkel, Jack Reilly, et al.. (2017). Clinical Validation of Copy Number Variant Detection from Targeted Next-Generation Sequencing Panels. Journal of Molecular Diagnostics. 19(6). 905–920. 94 indexed citations
15.
Stuart, Alan, et al.. (2017).  GNPAT variant (D519G) is not associated with an elevated serum ferritin or iron removed by phlebotomy in patients referred for C282Y-linked hemochromatosis.. SHILAP Revista de lepidopterología. 15(6). 907–910. 5 indexed citations
16.
Schenkel, Laila C., Jennifer Kerkhof, Alan Stuart, et al.. (2016). Clinical Next-Generation Sequencing Pipeline Outperforms a Combined Approach Using Sanger Sequencing and Multiplex Ligation-Dependent Probe Amplification in Targeted Gene Panel Analysis. Journal of Molecular Diagnostics. 18(5). 657–667. 43 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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