Michelle McBean

663 total citations
21 papers, 262 citations indexed

About

Michelle McBean is a scholar working on Hematology, Molecular Biology and Clinical Biochemistry. According to data from OpenAlex, Michelle McBean has authored 21 papers receiving a total of 262 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Hematology, 7 papers in Molecular Biology and 6 papers in Clinical Biochemistry. Recurrent topics in Michelle McBean's work include Acute Myeloid Leukemia Research (10 papers), Metabolism and Genetic Disorders (6 papers) and Chronic Myeloid Leukemia Treatments (4 papers). Michelle McBean is often cited by papers focused on Acute Myeloid Leukemia Research (10 papers), Metabolism and Genetic Disorders (6 papers) and Chronic Myeloid Leukemia Treatments (4 papers). Michelle McBean collaborates with scholars based in Australia, United Kingdom and Canada. Michelle McBean's co-authors include J Stephenson, David Westerman, John B.P. Stephenson, L. I. Woolf, Piers Blombery, David Ritchie, Ella R. Thompson, Alexander Dobrovic, Kate Jones and W. I. Cranston and has published in prestigious journals such as The Lancet, Blood and International Journal of Molecular Sciences.

In The Last Decade

Michelle McBean

21 papers receiving 240 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Michelle McBean Australia 12 109 97 80 79 37 21 262
Arthavan Selvanathan Australia 7 98 0.9× 88 0.9× 32 0.4× 22 0.3× 21 0.6× 22 290
Yasuhiro Yamashiro Japan 9 136 1.2× 168 1.7× 8 0.1× 187 2.4× 9 0.2× 43 360
G. P. Tamagnini Portugal 11 232 2.1× 133 1.4× 9 0.1× 235 3.0× 9 0.2× 20 457
Rachel Stapleton Nigeria 5 26 0.2× 38 0.4× 19 0.2× 16 0.2× 7 0.2× 11 136
C. R. Greenberg Canada 8 13 0.1× 72 0.7× 51 0.6× 15 0.2× 34 0.9× 13 218
Francesca La Carpia United States 8 62 0.6× 124 1.3× 4 0.1× 48 0.6× 9 0.2× 15 281
Lene Hyldahl Ebbesen Denmark 8 152 1.4× 100 1.0× 5 0.1× 77 1.0× 6 0.2× 13 215
Sandra S. Pinhanços Netherlands 8 82 0.8× 150 1.5× 3 0.0× 20 0.3× 16 0.4× 18 260
Solomon Estren United States 9 69 0.6× 99 1.0× 9 0.1× 61 0.8× 77 2.1× 19 280
Yuya Aoto Japan 12 32 0.3× 199 2.1× 7 0.1× 20 0.3× 5 0.1× 29 324

Countries citing papers authored by Michelle McBean

Since Specialization
Citations

This map shows the geographic impact of Michelle McBean'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 Michelle McBean with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Michelle McBean more than expected).

Fields of papers citing papers by Michelle McBean

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Michelle McBean. 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 Michelle McBean. The network helps show where Michelle McBean may publish in the future.

Co-authorship network of co-authors of Michelle McBean

This figure shows the co-authorship network connecting the top 25 collaborators of Michelle McBean. A scholar is included among the top collaborators of Michelle McBean 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 Michelle McBean. Michelle McBean 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.
Gould, Clare, et al.. (2024). Observations from a national sample exchange program for molecular haematology testing. Pathology. 56(4). 540–547. 1 indexed citations
2.
Press, Richard D., Michelle McBean, Ing Soo Tiong, et al.. (2024). Evaluation of a New Closed-System Automated RT-qPCR Assay for the Rapid Detection and Monitoring of Common Nucleophosmin Mutations in Patients with Acute Myeloid Leukemia. International Journal of Molecular Sciences. 25(14). 7912–7912. 1 indexed citations
3.
Loo, Sun, Richard Dillon, Adam Ivey, et al.. (2022). Pretransplant FLT3-ITD MRD assessed by high-sensitivity PCR-NGS determines posttransplant clinical outcome. Blood. 140(22). 2407–2411. 42 indexed citations
4.
Tiong, Ing Soo, Phuong Dang, Kate E. Jones, et al.. (2022). Clinically relevant variation in FLT3-ITD quantitation as a result of PCR cycle number and ITD insertion size. Pathology. 55(1). 71–76. 1 indexed citations
5.
Ryland, Georgina L., Michelle McBean, Eric Wong, et al.. (2021). T cell receptor beta locus sequencing early post-allogeneic stem cell transplant identifies patients at risk of initial and recurrent cytomegalovirus infection. Bone Marrow Transplantation. 56(10). 2582–2590. 2 indexed citations
6.
Grigoriadis, George, David Westerman, Michelle McBean, et al.. (2021). Correlation between a 10‐color flow cytometric measurable residual disease (MRD) analysis and molecular MRD in adult B‐acute lymphoblastic leukemia. Cytometry Part B Clinical Cytometry. 102(2). 115–122. 6 indexed citations
7.
Blombery, Piers, Lucy C. Fox, Georgina L. Ryland, et al.. (2020). Utility of clinical comprehensive genomic characterization for diagnostic categorization in patients presenting with hypocellular bone marrow failure syndromes. Haematologica. 106(1). 64–73. 11 indexed citations
8.
Thompson, Ella R., Tamia Nguyen, Paul Yeh, et al.. (2020). Clonal independence of <i>JAK2</i> and <i>CALR</i> or <i>MPL</i> mutations in comutated myeloproliferative neoplasms demonstrated by single cell DNA sequencing. Haematologica. 106(1). 313–315. 14 indexed citations
9.
Thompson, Ella R., et al.. (2020). Detection of an IGH-BRAF fusion in a patient with BRAF Val600Glu negative hairy cell leukemia. Leukemia & lymphoma. 61(8). 2024–2026. 11 indexed citations
10.
Blombery, Piers, Ella R. Thompson, Tamia Nguyen, et al.. (2019). Detection of Multiple Recurrent Novel BCL2 Mutations Co-Occurring with BCL2 Gly101Val in Patients with Chronic Lymphocytic Leukemia on Long Term Venetoclax. Blood. 134(Supplement_1). 171–171. 3 indexed citations
11.
Blombery, Piers, Kate Jones, Ken Doig, et al.. (2018). Sensitive NPM1 Mutation Quantitation in Acute Myeloid Leukemia Using Ultradeep Next-Generation Sequencing in the Diagnostic Laboratory. Archives of Pathology & Laboratory Medicine. 142(5). 606–612. 7 indexed citations
12.
13.
Yannakou, Costas K., Kate Jones, Georgina L. Ryland, et al.. (2017). Incidental detection of germline variants of potential clinical significance by massively parallel sequencing in haematological malignancies. Journal of Clinical Pathology. 71(1). 84–87. 11 indexed citations
14.
Zapparoli, Giada V., Robert N. Jorissen, Chelsee Hewitt, et al.. (2013). Quantitative threefold allele-specific PCR (QuanTAS-PCR) for highly sensitive JAK2V617F mutant allele detection. BMC Cancer. 13(1). 206–206. 12 indexed citations
15.
Ritchie, David, et al.. (2007). Complete molecular response of e6a2 BCR-ABL–positive acute myeloid leukemia to imatinib then dasatinib. Blood. 111(5). 2896–2898. 17 indexed citations
16.
Crockett, David J., et al.. (1990). Birth Weight and Pathogenesis in Phenylketonuria. International Journal of Neuroscience. 54(3-4). 259–266. 3 indexed citations
17.
McBean, Michelle & John B.P. Stephenson. (1968). Treatment of classical phenylketonuria.. Archives of Disease in Childhood. 43(227). 1–7. 21 indexed citations
18.
Woolf, L. I., Brian L. Goodwin, W. I. Cranston, et al.. (1968). A THIRD ALLELE AT THE PHENYLALANINE-HYDROXYLASE LOCUS IN MILD PHENYLKETONURIA (HYPERPHENYLALANEWEMIA). The Lancet. 291(7534). 114–117. 24 indexed citations
19.
Stephenson, J & Michelle McBean. (1967). Diagnosis of Phenylketonuria (Phenylalanine Hydroxylase Deficiency, Temporary and Permanent). BMJ. 3(5565). 579–581. 20 indexed citations
20.
Stephenson, J & Michelle McBean. (1967). Phenylketonuria: A Reassessment of Mass Infant Screening by Napkin Test. BMJ. 3(5565). 582–582. 12 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Arthavan Selvanathan Breakdown of academic impact, for papers by Yasuhiro Yamashiro Breakdown of academic impact, for papers by G. P. Tamagnini Breakdown of academic impact, for papers by Rachel Stapleton Breakdown of academic impact, for papers by C. R. Greenberg Breakdown of academic impact, for papers by Francesca La Carpia Breakdown of academic impact, for papers by Lene Hyldahl Ebbesen Breakdown of academic impact, for papers by Sandra S. Pinhanços Breakdown of academic impact, for papers by Solomon Estren Breakdown of academic impact, for papers by Yuya Aoto
Rankless by CCL
2026