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Decreased male reproductive success in association with mitochondrial dysfunction

European journal of human genetics : EJHG, 2017-10, Vol.25 (10), p.1162-1164

2017

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Dissecting the neuronal vulnerability underpinning Alpers’ syndrome: a clinical and neuropathological study

Brain pathology (Zurich, Switzerland), 2019-01, Vol.29 (1), p.97-113

2019

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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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Mitochondrial dysfunction in myofibrillar myopathy

Neuromuscular disorders : NMD, 2016-10, Vol.26 (10), p.691-701

2016

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Investigating complex I deficiency in Purkinje cells and synapses in patients with mitochondrial disease

Neuropathology and applied neurobiology, 2016-08, Vol.42 (5), p.477-492

2016

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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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Dysferlin mutations and mitochondrial dysfunction

Neuromuscular disorders : NMD, 2016-11, Vol.26 (11), p.782-788

2016

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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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Trastuzumab emtansine (T-DM1) in advanced cancers with HER2 mutations or amplification: Results from the Molecular Screening and Therapeutics (MoST) Program substudy

Journal of clinical oncology, 2023-06, Vol.41 (16_suppl), p.3127-3127

2023

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Genomic therapy matching in rare and refractory cancers: Updated results from a retrospective cohort study in the Molecular Screening and Therapeutic (MoST) program

Journal of clinical oncology, 2023-06, Vol.41 (16_suppl), p.1540-1540

2023

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Molecular therapy selection in treatment-refractory advanced cancers: A retrospective cohort study determining the utility of TOPOGRAPH knowledge base

Journal of clinical oncology, 2022-06, Vol.40 (16_suppl), p.3073-3073

2022

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Whole Exome Sequencing of Paired MGUS/SMM to MM Patients Reveals Novel Subclonal Tumour Evolution Models in Disease Progression of Multiple Myeloma

Blood, 2017-12, Vol.130, p.391-391

2017

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Molecular patterns in salivary duct carcinoma identify prognostic subgroups

Oral oncology, 2021-07, Vol.118, p.4-4

2021

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Investigating complex I deficiency in P urkinje cells and synapses in patients with mitochondrial disease

Neuropathology and applied neurobiology, 2016-08, Vol.42 (5), p.477-492

2016

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mt DNA heteroplasmy level and copy number indicate disease burden in m.3243A>G mitochondrial disease

EMBO molecular medicine, 2018-06, Vol.10 (6)

2018

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The prevalence of mitochondrial disease in the adult population

Mitochondrion, 2015-09, Vol.24, p.S16-S17

2015

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Accurate Measurement of Mitochondrial DNA Deletion Level and Copy Number Differences in Human Skeletal Muscle: e114462

PloS one, 2014-12, Vol.9 (12)

2014

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Sequential evaluation of the supine hypertension or 'roll-over' test in a high risk population

Gynecologic and obstetric investigation, 1977-01, Vol.8 (5-6), p.282-287

1977

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Decreased male reproductive success in association with mitochondrial dysfunction

Dissecting the neuronal vulnerability underpinning Alpers’ syndrome: a clinical and neuropathological study

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

Mitochondrial dysfunction in myofibrillar myopathy

Investigating complex I deficiency in Purkinje cells and synapses in patients with mitochondrial disease

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

Dysferlin mutations and mitochondrial dysfunction

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

Trastuzumab emtansine (T-DM1) in advanced cancers with HER2 mutations or amplification: Results from the Molecular Screening and Therapeutics (MoST) Program substudy

Genomic therapy matching in rare and refractory cancers: Updated results from a retrospective cohort study in the Molecular Screening and Therapeutic (MoST) program

Molecular therapy selection in treatment-refractory advanced cancers: A retrospective cohort study determining the utility of TOPOGRAPH knowledge base

Whole Exome Sequencing of Paired MGUS/SMM to MM Patients Reveals Novel Subclonal Tumour Evolution Models in Disease Progression of Multiple Myeloma

Molecular patterns in salivary duct carcinoma identify prognostic subgroups

Investigating complex I deficiency in P urkinje cells and synapses in patients with mitochondrial disease

mt DNA heteroplasmy level and copy number indicate disease burden in m.3243A>G mitochondrial disease

The prevalence of mitochondrial disease in the adult population

Accurate Measurement of Mitochondrial DNA Deletion Level and Copy Number Differences in Human Skeletal Muscle: e114462

Sequential evaluation of the supine hypertension or 'roll-over' test in a high risk population

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