Aimee Davidson

Employment

• QIMR Berghofer Medical Research Institute Research Officer
  2022 - Present
• QIMR Berghofer Medical Research Institute Research Assistant
  2021 - 2022
• QIMR Berghofer Medical Research Institute PhD Student
  2017 - 2021

Education

Education history is unavailable.

Projects & Funding

Projects & funding information is unavailable.

Publications (14)

• Unrecognised actionability for breast cancer risk variants identified in a national-level review of Australian familial cancer centres
  European Journal of Human Genetics 2024 DOI: 10.1038/s41431-024-01705-9
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• Co-observation of germline pathogenic variants in breast cancer predisposition genes: Results from analysis of the BRIDGES sequencing dataset
  Aimee L. Davidson, Kyriaki Michailidou, Michael T. Parsons +97 more
  The American Journal of Human Genetics 2024 DOI: 10.1016/j.ajhg.2024.07.004
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• Unrecognised actionability for breast cancer risk variants identified in a national-level review of Australian familial cancer centres
  2024 DOI: 10.21203/rs.3.rs-4352556/v1
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• Regional-specific calibration enables application of bioinformatic evidence for clinical classification of 5’ cis-regulatory variants in Mendelian disease
  2023 DOI: 10.1101/2023.12.21.23300413
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• The clinical utility and costs of whole-genome sequencing to detect cancer susceptibility variants—a multi-site prospective cohort study
  Aimee L. Davidson, Uwe Dressel, Sarah Norris +48 more
  Genome Medicine 2023 DOI: 10.1186/s13073-023-01223-1
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• SpliceAI-10k calculator for the prediction of pseudoexonization, intron retention, and exon deletion
  Bioinformatics 2023 DOI: 10.1093/bioinformatics/btad179
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• Germline pathogenicSMARCA4variants in neuroblastoma
  Leora Witkowski, Kim E. Nichols, Marjolijn C.J. Jongmans +12 more
  Journal of Medical Genetics 2023 DOI: 10.1136/jmg-2022-108854
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• Analysis of hereditary cancer gene variant classifications from ClinVar indicates a need for regular reassessment of clinical assertions
  Aimee L. Davidson, Olga Kondrashova, Conrad Leonard +7 more
  Human Mutation 2022 DOI: 10.1002/humu.24468
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• Comprehensive genomic and tumour immune profiling reveals potential therapeutic targets in malignant pleural mesothelioma
  Jenette Creaney, Ann‐Marie Patch, Venkateswar Addala +27 more
  Genome Medicine 2022 DOI: 10.1186/s13073-022-01060-8
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• Patient-derived xenograft models capture genomic heterogeneity in endometrial cancer
  Vanessa Bonazzi, Olga Kondrashova, Deborah S. Smith +20 more
  Genome Medicine 2022 DOI: 10.1186/s13073-021-00990-z
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• The splicing effect of variants at branchpoint elements in cancer genes
  Genetics in Medicine 2022 DOI: 10.1016/j.gim.2021.09.020
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• Considerations for using population frequency data in germline variant interpretation: Cancer syndrome genes as a model
  Aimee L. Davidson, Conrad Leonard, Lambros T. Koufariotis +6 more
  Human Mutation 2021 DOI: 10.1002/humu.24183
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• Implementing gene curation for hereditary cancer susceptibility in Australia: achieving consensus on genes with clinical utility
  Journal of Medical Genetics 2020 DOI: 10.1136/jmedgenet-2020-107140
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• Whole-genome sequencing reveals clinically relevant insights into the aetiology of familial breast cancers
  Kátia Nones, Julie Johnson, Felicity Newell +29 more
  Annals of Oncology 2019 DOI: 10.1093/annonc/mdz132
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