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Demographic History of Oceania Inferred from Genome-wide Data

Current biology, 2010-11, Vol.20 (22), p.1983-1992

2010

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Can ALS-associated C9orf72 repeat expansions be diagnosed on a blood DNA test alone?

PloS one, 2013-07, Vol.8 (7), p.e70007

2013

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Genome-wide Analysis Indicates More Asian than Melanesian Ancestry of Polynesians

American journal of human genetics, 2008-01, Vol.82 (1), p.194-198

2008

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Moderation of baclofen response by a GABAB receptor polymorphism: results from the BacALD randomized controlled trial

Addiction (Abingdon, England), 2018-12, Vol.113 (12), p.2205-2213

2018

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Making good on the promise of genomics in healthcare: the NSW Health perspective

Australian health review, 2023-12, Vol.47 (6), p.631-633

2023

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The severity of hereditary porphyria is modulated by the porphyrin exporter and Lan antigen ABCB6

Nature communications, 2016-08, Vol.7 (1), p.12353-12353, Article 12353

2016

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Direct-to-consumer genetic testing: clinical considerations

Medical journal of Australia, 2013-05, Vol.198 (9), p.496-498

Trent, Ronald J

2013

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Melanesian and Asian origins of Polynesians: mtDNA and Y chromosome gradients across the Pacific

Molecular biology and evolution, 2006-11, Vol.23 (11), p.2234-2244

2006

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Moderation of baclofen response by a GABA B receptor polymorphism: results from the BacALD randomized controlled trial

Addiction (Abingdon, England), 2018-12, Vol.113 (12), p.2205-2213

2018

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Implementation of a primary-tertiary shared care model to improve the detection of familial hypercholesterolaemia (FH): a mixed methods pre-post implementation study protocol

BMJ open, 2024-05, Vol.14 (5), p.e082699-e082699

2024

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The Impact of the Austronesian Expansion: Evidence from mtDNA and Y Chromosome Diversity in the Admiralty Islands of Melanesia

Molecular biology and evolution, 2008-07, Vol.25 (7), p.1362-1374

2008

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Essentials of a new clinical practice guidance on familial hypercholesterolaemia for physicians

Internal medicine journal, 2021-05, Vol.51 (5), p.769-779

2021

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Patterns of DNA Mutations and ALK Rearrangement in Resected Node Negative Lung Adenocarcinoma

Journal of thoracic oncology, 2013-04, Vol.8 (4), p.408-414

2013

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Genetic susceptibility to environmental toxicants in ALS

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2007-10, Vol.144B (7), p.885-890

2007

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Corrigendum to Synopsis of an integrated guidance for enhancing the care of familial hypercholesterolaemia: An Australian perspective [American Journal of Preventive Cardiology 6 (2021) 100151]

American journal of preventive cardiology, 2022-03, Vol.9, p.100200-100200, Article 100200

2022

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Low Microsatellite Instability Is Associated With Poor Prognosis in Stage C Colon Cancer

Journal of clinical oncology, 2005-04, Vol.23 (10), p.2318-2324

2005

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Bioinformatics challenges in genome-wide association studies (GWAS)

Methods in molecular biology (Clifton, N.J.), 2014-01, Vol.1168, p.63

2014

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Diagnostic validation of a familial hypercholesterolaemia cohort provides a model for using targeted next generation DNA sequencing in the clinical setting

Pathology, 2014-01, Vol.46 (1), p.60-68

2014

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Pathology practice and pharmacogenomics

Pharmacogenomics, 2010-01, Vol.11 (1), p.105-111

Trent, Ronald JA

2010

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Topiramate versus naltrexone for alcohol use disorder: study protocol for a genotype-stratified, double-blind randomised controlled trial (TOP study)

Trials, 2018-08, Vol.19 (1), p.443-443, Article 443

2018

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Transmission of C9orf72 hexanucleotide repeat expansions in sporadic amyotrophic lateral sclerosis: an Australian trio study

Neuroreport, 2012-06, Vol.23 (9), p.556-559

2012

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Molecular Medicine: Genomics to Personalized Healthcare

Trent, R. J

4th ed., 2012

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A comparison of the lengths of androgen receptor triplet repeats in brain and blood in motor neuron diseases

Journal of the neurological sciences, 2008-04, Vol.267 (1), p.125-128

2008

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Genetic variants in the promoter of TARDBP in sporadic amyotrophic lateral sclerosis

Neuromuscular disorders : NMD, 2009-10, Vol.19 (10), p.696-700

2009

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Demographic History of Oceania Inferred from Genome-wide Data

Can ALS-associated C9orf72 repeat expansions be diagnosed on a blood DNA test alone?

Genome-wide Analysis Indicates More Asian than Melanesian Ancestry of Polynesians

Moderation of baclofen response by a GABAB receptor polymorphism: results from the BacALD randomized controlled trial

Making good on the promise of genomics in healthcare: the NSW Health perspective

The severity of hereditary porphyria is modulated by the porphyrin exporter and Lan antigen ABCB6

Direct-to-consumer genetic testing: clinical considerations

Melanesian and Asian origins of Polynesians: mtDNA and Y chromosome gradients across the Pacific

Moderation of baclofen response by a GABA B receptor polymorphism: results from the BacALD randomized controlled trial

Implementation of a primary-tertiary shared care model to improve the detection of familial hypercholesterolaemia (FH): a mixed methods pre-post implementation study protocol

Common SNP-Based Haplotype Analysis of the 4p16.3 Huntington Disease Gene Region

The Impact of the Austronesian Expansion: Evidence from mtDNA and Y Chromosome Diversity in the Admiralty Islands of Melanesia

Essentials of a new clinical practice guidance on familial hypercholesterolaemia for physicians

Patterns of DNA Mutations and ALK Rearrangement in Resected Node Negative Lung Adenocarcinoma

Genetic susceptibility to environmental toxicants in ALS

Corrigendum to Synopsis of an integrated guidance for enhancing the care of familial hypercholesterolaemia: An Australian perspective [American Journal of Preventive Cardiology 6 (2021) 100151]

Low Microsatellite Instability Is Associated With Poor Prognosis in Stage C Colon Cancer

Bioinformatics challenges in genome-wide association studies (GWAS)

Diagnostic validation of a familial hypercholesterolaemia cohort provides a model for using targeted next generation DNA sequencing in the clinical setting

Pathology practice and pharmacogenomics

Topiramate versus naltrexone for alcohol use disorder: study protocol for a genotype-stratified, double-blind randomised controlled trial (TOP study)

Transmission of C9orf72 hexanucleotide repeat expansions in sporadic amyotrophic lateral sclerosis: an Australian trio study

Molecular Medicine: Genomics to Personalized Healthcare

A comparison of the lengths of androgen receptor triplet repeats in brain and blood in motor neuron diseases

Genetic variants in the promoter of TARDBP in sporadic amyotrophic lateral sclerosis

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