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Chromosome arm aneuploidies shape tumour evolution and drug response

Nature communications, 2020-01, Vol.11 (1), p.449-14, Article 449

2020

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Phenotypic heterogeneity in m.3243A>G mitochondrial disease: The role of nuclear factors

Annals of clinical and translational neurology, 2018-03, Vol.5 (3), p.333-345

2018

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Comparison of mitochondrial mutation spectra in ageing human colonic epithelium and disease: absence of evidence for purifying selection in somatic mitochondrial DNA point mutations

PLoS genetics, 2012-11, Vol.8 (11), p.e1003082-e1003082

2012

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Triplex real-time PCR–an improved method to detect a wide spectrum of mitochondrial DNA deletions in single cells

Scientific reports, 2015-05, Vol.5 (1), p.9906, Article 9906

2015

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A signal-seeking phase 2 study of Trastuzumab emtansine in tumours harbouring HER2 amplification or mutation

NPJ precision oncology, 2024-09, Vol.8 (1), p.195-10, Article 195

2024

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Criteria-based curation of a therapy-focused compendium to support treatment recommendations in precision oncology

NPJ precision oncology, 2021-06, Vol.5 (1), p.58-58, Article 58

2021

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Subclonal evolution in disease progression from MGUS/SMM to multiple myeloma is characterised by clonal stability

Leukemia, 2019-02, Vol.33 (2), p.457-468

2019

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Oncogenic mutations in the TP53 and PI-3 kinase/AKT pathway are independent predictors of survival for advanced thyroid cancer: Analysis from the Molecular Screening and Therapeutics (MoST) program

Surgery, 2024-10

2024

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A signal-seeking Phase 2 study of olaparib and durvalumab in advanced solid cancers with homologous recombination repair gene alterations

British journal of cancer, 2023-08, Vol.129 (3), p.475-485

2023

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Skeletal muscle mitochondrial oxidative phosphorylation function in idiopathic pulmonary arterial hypertension: in vivo and in vitro study

Pulmonary circulation, 2018-04, Vol.8 (2), p.1-5

2018

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Mitochondrial and inflammatory changes in sporadic inclusion body myositis

Neuropathology and applied neurobiology, 2015-04, Vol.41 (3), p.288-303

2015

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Mitochondrial Donation — How Many Women Could Benefit?

The New England journal of medicine, 2015-02, Vol.372 (9), p.885-887

2015

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Mitochondrial dysfunction within the synapses of substantia nigra neurons in Parkinson’s disease

NPJ Parkinson's Disease, 2018-03, Vol.4 (1), p.9-10, Article 9

2018

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Sudden adult death syndrome in m.3243A>G-related mitochondrial disease: an unrecognized clinical entity in young, asymptomatic adults

European heart journal, 2016-08, Vol.37 (32), p.2552-2559

2016

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Cutting edge genomics reveal new insights into tumour development, disease progression and therapeutic impacts in multiple myeloma

British journal of haematology, 2017-07, Vol.178 (2), p.196-208

2017

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PTEN deletion drives acute myeloid leukemia resistance to MEK inhibitors

Oncotarget, 2019-10, Vol.10 (56), p.5755-5767

2019

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Inherited pathogenic mitochondrial DNA mutations and gastrointestinal stem cell populations

The Journal of pathology, 2018-12, Vol.246 (4), p.427-432

2018

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Clinical Response to Seribantumab, an Anti-Human Epidermal Growth Factor Receptor-3 Immunoglobulin 2 Monoclonal Antibody, in a Patient With Metastatic Pancreatic Ductal Adenocarcinoma Harboring an NRG1 Fusion

JCO precision oncology, 2022-11, Vol.6 (6), p.e2200263

2022

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Erratum: PTEN deletion drives acute myeloid leukemia resistance to MEK inhibitors

Oncotarget, 2020-01, Vol.11 (3), p.305-305

2020

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Translocation Breakpoints Preferentially Occur in Euchromatin and Acrocentric Chromosomes

Cancers, 2018-01, Vol.10 (1), p.13

2018

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Unique quadruple immunofluorescence assay demonstrates mitochondrial respiratory chain dysfunction in osteoblasts of aged and PolgA−/− mice

Scientific reports, 2016-08, Vol.6 (1), p.31907-31907, Article 31907

2016

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Spatial frequency bandwidth of surround suppression tuning curves

Journal of vision (Charlottesville, Va.), 2012-06, Vol.12 (6), p.24-24

2012

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Genomic alterations associated with response to immune checkpoint inhibitors in rare cancers: A biomarker exploration study from the Australian Molecular Screening and Therapeutics (MoST) Program

Journal of clinical oncology, 2023-06, Vol.41 (16_suppl), p.2594-2594

2023

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Translating potential germline findings from tumour profiling into routine clinical care

Journal of clinical oncology, 2024-08, Vol.42 (23_suppl), p.105-105

2024

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Genomic targetability and survival outcomes of biliary tract cancers (BTC): A retrospective cohort study of the Australian Molecular Screening and Therapeutics (MoST) program

Journal of clinical oncology, 2023-06, Vol.41 (16_suppl), p.4093-4093

2023

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Chromosome arm aneuploidies shape tumour evolution and drug response

Phenotypic heterogeneity in m.3243A>G mitochondrial disease: The role of nuclear factors

Comparison of mitochondrial mutation spectra in ageing human colonic epithelium and disease: absence of evidence for purifying selection in somatic mitochondrial DNA point mutations

Triplex real-time PCR–an improved method to detect a wide spectrum of mitochondrial DNA deletions in single cells

A signal-seeking phase 2 study of Trastuzumab emtansine in tumours harbouring HER2 amplification or mutation

Criteria-based curation of a therapy-focused compendium to support treatment recommendations in precision oncology

Subclonal evolution in disease progression from MGUS/SMM to multiple myeloma is characterised by clonal stability

Oncogenic mutations in the TP53 and PI-3 kinase/AKT pathway are independent predictors of survival for advanced thyroid cancer: Analysis from the Molecular Screening and Therapeutics (MoST) program

A signal-seeking Phase 2 study of olaparib and durvalumab in advanced solid cancers with homologous recombination repair gene alterations

Skeletal muscle mitochondrial oxidative phosphorylation function in idiopathic pulmonary arterial hypertension: in vivo and in vitro study

Mitochondrial and inflammatory changes in sporadic inclusion body myositis

Mitochondrial Donation — How Many Women Could Benefit?

Mitochondrial dysfunction within the synapses of substantia nigra neurons in Parkinson’s disease

Sudden adult death syndrome in m.3243A>G-related mitochondrial disease: an unrecognized clinical entity in young, asymptomatic adults

Cutting edge genomics reveal new insights into tumour development, disease progression and therapeutic impacts in multiple myeloma

PTEN deletion drives acute myeloid leukemia resistance to MEK inhibitors

Inherited pathogenic mitochondrial DNA mutations and gastrointestinal stem cell populations

Clinical Response to Seribantumab, an Anti-Human Epidermal Growth Factor Receptor-3 Immunoglobulin 2 Monoclonal Antibody, in a Patient With Metastatic Pancreatic Ductal Adenocarcinoma Harboring an NRG1 Fusion

Erratum: PTEN deletion drives acute myeloid leukemia resistance to MEK inhibitors

Translocation Breakpoints Preferentially Occur in Euchromatin and Acrocentric Chromosomes

Unique quadruple immunofluorescence assay demonstrates mitochondrial respiratory chain dysfunction in osteoblasts of aged and PolgA−/− mice

Spatial frequency bandwidth of surround suppression tuning curves

Genomic alterations associated with response to immune checkpoint inhibitors in rare cancers: A biomarker exploration study from the Australian Molecular Screening and Therapeutics (MoST) Program

Translating potential germline findings from tumour profiling into routine clinical care

Genomic targetability and survival outcomes of biliary tract cancers (BTC): A retrospective cohort study of the Australian Molecular Screening and Therapeutics (MoST) program

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