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Email

yamuna.kankanige@unimelb.edu.au

Credentials


Position
Honorary (Fellow)
The Sir Peter MacCallum Department of Oncology

Dr Yamuna Kankanige

Honorary (Fellow)
The Sir Peter MacCallum Department of Oncology

17 Scholarly works
0 Projects

HIGHLIGHTS

  • 2026

    Journal article

    Refinement of the classification of DDX41 variants through analysis of aggregated clinical datasets
    DOI: 10.1038/s41375-026-02886-6
  • 2025

    Journal article

    Genomic variation in DDX41 identified through clinical sequencing
    DOI: 10.1111/bjh.70086
  • 2025

    Journal article

    Using artificial intelligence (AI) to model clinical variant reporting for next generation sequencing (NGS) oncology assays
    DOI: 10.1186/s13040-025-00489-y
  • 2023

    Journal article

    Computational flow cytometry provides accurate assessment of measurable residual disease in chronic lymphocytic leukaemia
    DOI: 10.1111/bjh.18802
  • 2022

    Journal article

    P1306: CLINICAL AND GENOMIC ANALYSIS OF HIGH-GRADE TRANSFORMATION OF MARGINAL ZONE LYMPHOMA
    DOI: 10.1097/01.hs9.0000848088.46359.81
  • 2022

    Journal article

    Single-cell sequencing demonstrates complex resistance landscape in CLL and MCL treated with BTK and BCL2 inhibitors
    DOI: 10.1182/bloodadvances.2021006211
  • 2021

    Journal article

    T cell receptor beta locus sequencing early post-allogeneic stem cell transplant identifies patients at risk of initial and recurrent cytomegalovirus infection
    DOI: 10.1038/s41409-021-01354-2
Yamuna Kankanige

RECENT SCHOLARLY WORKS

  • 2021

    Journal article

    Characterisation of immune checkpoints in Richter syndrome identifies LAG3 as a potential therapeutic target
    DOI: 10.1111/bjh.17789
  • 2021

    Journal article

    Clonal independence of JAK2 and CALR or MPL mutations in comutated myeloproliferative neoplasms demonstrated by single cell DNA sequencing
    DOI: 10.3324/haematol.2020.260448
  • 2020

    Conference Proceedings

    High Clonal Complexity of Resistance Mechanisms Occurring at Progression after Single-Agent Targeted Therapy Strategies in Chronic Lymphocytic Leukemia
    DOI: 10.1182/blood-2020-137411

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