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Ion torrent high throughput mitochondrial genome sequencing (HTMGS)

PloS one, 2019-11, Vol.14 (11), p.e0224847-e0224847

2019

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Beyond amyloid and tau: rethinking Alzheimer’s disease through less explored avenues

Open biology, 2024-06, Vol.14 (6), p.240035

2024

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Pedigree derived mutation rate across the entire mitochondrial genome of the Norfolk Island population

Scientific reports, 2022-04, Vol.12 (1), p.6827-6827, Article 6827

2022

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Investigation of Mitochondrial Related Variants in a Cerebral Small Vessel Disease Cohort

Molecular neurobiology, 2022-09, Vol.59 (9), p.5366-5378

2022

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Investigating diagnostic sequencing techniques for CADASIL diagnosis

Human genomics, 2020-01, Vol.14 (1), p.2-2, Article 2

2020

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Evaluation of an ancestry prediction strategy for historical military remains using a World War II-era sample and pedigrees with family-level admixture

Australian journal of forensic sciences, 2023-07, Vol.55 (4), p.456-473

2023

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Development of an accurate genomic ancestry prediction strategy to enable the accounting of Australian and Japanese historical military remains

Australian journal of forensic sciences, 2022-06, Vol.54 (3), p.416-436

2022

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Association study of calcitonin gene-related polypeptide-alpha (CALCA) gene polymorphism with migraine

Brain research, 2011-03, Vol.1378, p.119-124

2011

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Association of a Notch 3 gene polymorphism with migraine susceptibility

Cephalalgia, 2011-02, Vol.31 (3), p.264-270

2011

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Mitochondrial DNA Analysis in Population Isolates: Challenges and Implications for Human Identification

Current molecular biology reports, 2024, Vol.10 (1), p.1-8

2024

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Association study of the calcitonin gene-related polypeptide-alpha (CALCA) and the receptor activity modifying 1 (RAMP1) genes with migraine

Gene, 2013-02, Vol.515 (1), p.187-192

2013

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Confirmation that Xq27 and Xq28 are susceptibility loci for migraine in independent pedigrees and a case-control cohort

Neurogenetics, 2012-02, Vol.13 (1), p.97-101

2012

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Analysis of 3 common polymorphisms in the KCNK18 gene in an Australian Migraine Case-control cohort

Gene, 2013-10, Vol.528 (2), p.343-346

2013

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Semaphorin–plexin signalling genes associated with human breast tumourigenesis

Gene, 2011-12, Vol.489 (2), p.63-69

2011

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Investigation of the 1758G > C and 2880A > G variants within the NCOA3 gene in a breast cancer affected Australian population

Gene, 2011-08, Vol.482 (1), p.68-72

2011

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BDNF and TNF-α polymorphisms in memory

Molecular biology reports, 2013-09, Vol.40 (9), p.5483-5490

2013

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Development of an eight gene expression profile implicating human breast tumours of all grade

Molecular biology reports, 2012-04, Vol.39 (4), p.3879-3892

2012

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Loss of chromosomal integrity in human mammary epithelial cells subsequent to escape from senescence

Journal of mammary gland biology and neoplasia, 2001-04, Vol.6 (2), p.235

2001

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An epigenetic clock for human skeletal muscle

Journal of cachexia, sarcopenia and muscle, 2020-08, Vol.11 (4), p.887-898

2020

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The human [mu]-opioid receptor gene polymorphism (A118G) is associated with head pain severity in a clinical cohort of female migraine with aura patients

Journal of headache and pain, 2012-10, Vol.13 (7), p.513

2012

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BDNF and TNF-[alpha] polymorphisms in memory

Molecular biology reports, 2013-09, Vol.40 (9), p.5483

2013

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Effects of electroconvulsive therapy on the autobiographical memory of depressed patients: A controlled study in 64 subjects

The international journal of neuropsychopharmacology, 2008-07, Vol.11, p.187

2008

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IS‐RT‐PCR assay detection of MT‐MMP in a human breast cancer cell line

Biochemistry and molecular biology international, 1996-06, Vol.39 (3), p.553-561

1996

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Genetic investigation of methylenetetrahydrofolate reductase (MTHFR) and catechol- O-methyl transferase (COMT) in multiple sclerosis

Brain research bulletin, 2006-04, Vol.69 (3), p.327-331

2006

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Ion torrent high throughput mitochondrial genome sequencing (HTMGS)

Beyond amyloid and tau: rethinking Alzheimer’s disease through less explored avenues

Pedigree derived mutation rate across the entire mitochondrial genome of the Norfolk Island population

Investigation of Mitochondrial Related Variants in a Cerebral Small Vessel Disease Cohort

Investigating diagnostic sequencing techniques for CADASIL diagnosis

Evaluation of an ancestry prediction strategy for historical military remains using a World War II-era sample and pedigrees with family-level admixture

Development of an accurate genomic ancestry prediction strategy to enable the accounting of Australian and Japanese historical military remains

Association study of calcitonin gene-related polypeptide-alpha (CALCA) gene polymorphism with migraine

Association of a Notch 3 gene polymorphism with migraine susceptibility

Mitochondrial DNA Analysis in Population Isolates: Challenges and Implications for Human Identification

Association study of the calcitonin gene-related polypeptide-alpha (CALCA) and the receptor activity modifying 1 (RAMP1) genes with migraine

Confirmation that Xq27 and Xq28 are susceptibility loci for migraine in independent pedigrees and a case-control cohort

Analysis of 3 common polymorphisms in the KCNK18 gene in an Australian Migraine Case-control cohort

Semaphorin–plexin signalling genes associated with human breast tumourigenesis

Investigation of the 1758G > C and 2880A > G variants within the NCOA3 gene in a breast cancer affected Australian population

BDNF and TNF-α polymorphisms in memory

Development of an eight gene expression profile implicating human breast tumours of all grade

Loss of chromosomal integrity in human mammary epithelial cells subsequent to escape from senescence

An epigenetic clock for human skeletal muscle

Exercise is associated with younger methylome and transcriptome profiles in human skeletal muscle

The human [mu]-opioid receptor gene polymorphism (A118G) is associated with head pain severity in a clinical cohort of female migraine with aura patients

BDNF and TNF-[alpha] polymorphisms in memory

Effects of electroconvulsive therapy on the autobiographical memory of depressed patients: A controlled study in 64 subjects

IS‐RT‐PCR assay detection of MT‐MMP in a human breast cancer cell line

Genetic investigation of methylenetetrahydrofolate reductase (MTHFR) and catechol- O-methyl transferase (COMT) in multiple sclerosis

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