Aimee L Davidson

ORCID

Publication Activity (10 Years)

Years Active: 2020-2023
Publications (10 Years): 4

Top Venues

Human mutation

Genome medicine

Journal of medical genetics

QIMR Berghofer Medical Research Institute

This page only lists publications with an associated author ORCID identifier.

Affiliation History

QIMR Berghofer Medical Research Institute Jul 31 2017

Australia

PhD Student :: Genetics and Computational Biology

Publications

Aimee L Davidson, Uwe Dressel, Sarah Norris, Daffodil M Canson, Dylan M Glubb, Cristina Fortuno, Georgina E Hollway, Michael T Parsons, Miranda E Vidgen, Oliver Holmes, Lambros T Koufariotis, Vanessa Lakis, Conrad Leonard, Scott Wood, Qinying Xu, Amy E McCart Reed, Hilda A Pickett, Mohammad K Al-Shinnag, Rachel L Austin, Jo Burke, Elisa J Cops, Cassandra B Nichols, Annabel Goodwin, Marion T Harris, Megan J Higgins, Emilia L Ip, Catherine Kiraly-Borri, Chiyan Lau, Julia L Mansour, Michael W Millward, Melissa J Monnik, Nicholas S Pachter, Abiramy Ragunathan, Rachel D Susman, Sharron L Townshend, Alison H Trainer, Simon L Troth, Katherine M Tucker, Mathew J Wallis, Maie Walsh, Rachel A Williams, Ingrid M Winship, Felicity Newell, Emma Tudini, John V Pearson, Nicola K Poplawski, Helen G Mar Fan, Paul A James, Amanda B Spurdle, Nicola Waddell, Robyn L Ward
The clinical utility and costs of whole-genome sequencing to detect cancer susceptibility variants-a multi-site prospective cohort study. Genome medicine 15 (1) (2023)
Aimee L Davidson, Olga Kondrashova, Conrad Leonard, Scott Wood, Emma Tudini, Georgina E Hollway, John V Pearson, Felicity Newell, Amanda B Spurdle, Nicola Waddell
Analysis of hereditary cancer gene variant classifications from ClinVar indicates a need for regular reassessment of clinical assertions. Human mutation (2022)
Aimee L Davidson, Conrad Leonard, Lambros T Koufariotis, Michael T Parsons, Georgina E Hollway, John V Pearson, Felicity Newell, Nicola Waddell, Amanda B Spurdle
Considerations for using population frequency data in germline variant interpretation: Cancer syndrome genes as a model. Human mutation 42 (5) (2021)
Emma Tudini, Aimee L Davidson, Uwe Dressel, Lesley Andrews, Yoland Antill, Ashley Crook, Michael J Field, Michael Gattas, Rebecca Harris, Bettina Meiser, Nicholas Pachter, Lucinda Salmon, Rachel Susman, Sharron Townshend, Alison H Trainer, Katherine M Tucker, Gillian Mitchell, Paul A James, Robyn L Ward, Helen Mar Fan, Nicola K Poplawski, Amanda B Spurdle
Implementing gene curation for hereditary cancer susceptibility in Australia: achieving consensus on genes with clinical utility. Journal of medical genetics 58 (12) (2020)

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Publication Activity (10 Years)

Top Topics

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Aimee L Davidson