Publications for Ronald Trent
Publications for Ronald Trent
2015
Yu, B., O'Toole, S., Trent, R. (2015). Somatic
DNA mutation analysis in targeted therapy of
solid tumours. Translational Pediatrics, 4(2),
125-138. <a
href="http://dx.doi.org/10.3978/j.issn.2224-4336.
2015.04.04">[More Information]</a>
2014
Hinchcliffe, M., Le, H., Fimmel, A., Molloy, L.,
Freeman, L., Sullivan, D., Trent, R. (2014).
Diagnostic validation of a familial
hypercholesterolaemia cohort provides a model
for using targeted next generation DNA
sequencing in the clinical setting. Pathology,
46(1), 60-68. <a
href="http://dx.doi.org/10.1097/PAT.000000000
0000026">[More Information]</a>
Trent, R. (2014). Direct-to-consumer DNA
genetic testing and the GP. Australian Family
Physician, 43(7), 436-439.
2013
Pamphlett, R., Cheong, P., Trent, R., Yu, B.
(2013). Can ALS-Associated C9orf72 Repeat
Expansions be Diagnosed on a Blood DNA Test
Alone? PloS One, 8(7), 1-6. <a
href="http://dx.doi.org/10.1371/journal.pone.007
0007">[More Information]</a>
Ramos, E., Latourelle, J., Gillis, T., Mysore, J.,
Squitieri, F., Di Pardo, A., Di Donato, S.,
Gellera, C., Hayden, M., Morrison, P., Trent, R.,
McCusker, E., et al (2013). Candidate
glutamatergic and dopaminergic pathway gene
variants do not influence Huntington's disease
motor onset. Neurogenetics, 14(3-4), 173-179.
<a
href="http://dx.doi.org/10.1007/s10048-013-036
4-y">[More Information]</a>
Trent, R. (2013). Direct-to-consumer genetic
testing - clinical considerations. Medical Journal
of Australia, 198(9), 496-498. <a
href="http://dx.doi.org/10.5694/mja12.11019">[
More Information]</a>
Cooper, W., Yu, B., Yip, P., Ng, C., Lum, T.,
Farzin, M., Trent, R., Mercorella, B., Clarkson,
A., Kohonen-Corish, M., Horvath, L., Kench, J.,
McCaughan, B., Gill, A., O'Toole, S. (2013).
EGFR mutant-specific immunohistochemistry
has high specificity and sensitivity for detecting
targeted activating EGFR mutations in lung
adenocarcinoma. Journal of Clinical Pathology,
66(9), 744-748. <a
href="http://dx.doi.org/10.1136/jclinpath-2013-2
01607">[More Information]</a>
Yip, P., Yu, B., Cooper, W., Selinger, C., Ng, C.,
Kennedy, C., Kohonen-Corish, M., McCaughan,
B., Trent, R., Boyer, M., Kench, J., Horvath, L.,
O'Toole, S. (2013). Patterns of DNA mutations
and ALK Rearrangement in Resected Node
Negative Lung Adenocarcinoma. Journal of
Thoracic Oncology, 8(4), 408-414. <a
href="http://dx.doi.org/10.1097/JTO.0b013e3182
83558e">[More Information]</a>
Trent, R., Cheong, P., Chua, E., Kennedy, M.
(2013). Progressing the utilisation of
pharmacogenetics and pharmacogenomics into
clinical care. Pathology, 45(4), 357-370. <a
href="http://dx.doi.org/10.1097/PAT.0b013e328
360b66e">[More Information]</a>
2012
Lee, J., Ramos, E., Lee, J., Gillis, T., Mysore, J.,
Hayden, M., Warby, S., Morrison, P., Nance, M.,
Ross, C., Trent, R., McCusker, E., et al (2012).
CAG repeat expansion in Huntington disease
determines age at onset in a fully dominant
fashion. Neurology, 78(10), 690-695. <a
href="http://dx.doi.org/10.1212/WNL.0b013e31
8249f683">[More Information]</a>
Lee, J., Gillis, T., Mysore, J., Ramos, E., Myers,
R., Hayden, M., Morrison, P., Nance, M., Ross,
C., Margolis, R., Trent, R., et al (2012).
Common SNP-Based Haplotype Analysis of the
4p16.3 Huntington Disease Gene Region.
American Journal of Human Genetics, 90(3),
434-444. <a
href="http://dx.doi.org/10.1016/j.ajhg.2012.01.0
05">[More Information]</a>
Poursoltana, P., Currey, N., Pangon, L., van
Kralingen, C., Selinger, C., Mahar, A., Cooper,
W., Kennedy, C., McCaughan, B., Trent, R., et al
(2012). Loss of heterozygosity of the Mutated in
Colorectal Cancer gene is not associated with
promoter methylation in non-small cell lung
cancer. Lung Cancer, 77(2), 272-276. <a
href="http://dx.doi.org/10.1016/j.lungcan.2012.0
4.001">[More Information]</a>
Ramos, E., Latourelle, J., Lee, J., Gillis, T.,
Mysore, J., Squitieri, F., Di Pardo, A., Di
Donato, S., Hayden, M., Morrison, P., Trent, R.,
McCusker, E., et al (2012). Population
stratification may bias analysis of PGC-1(alpha)
as a modifier of age at Huntington disease motor
onset. Human Genetics, 131(12), 1833-1840. <a
href="http://dx.doi.org/10.1007/s00439-012-120
5-z">[More Information]</a>
Lee, J., Lee, J., Ramos, E., Gillis, T., Mysore, J.,
Kishikawa, S., Hadzi, T., Hendricks, A., Hayden,
M., Morrison, P., Trent, R., McCusker, E., et al
(2012). TAA repeat variation in the GRIK2 gene
does not influence age at onset in Huntington's
disease. Biochemical and Biophysical Research
Communications, 424(3), 404-408. <a
href="http://dx.doi.org/10.1016/j.bbrc.2012.06.1
Publications for Ronald Trent
20">[More Information]</a>
Pamphlett, R., Cheong, P., Trent, R., Yu, B.
(2012). Transmission of C9orf72 hexanucleotide
repeat expansions in sporadic amyotrophic
lateral sclerosis: an Australian trio study.
NeuroReport, 23(9), 556-559. <a
href="http://dx.doi.org/10.1097/WNR.0b013e32
83544718">[More Information]</a>
2011
Watts, G., Sullivan, D., Poplawski, N., van
Bockxmeer, F., Hamilton-Craig, I., Clifton, P.,
O'Brien, R., Bishop, W., George, P., Barter, P.,
Freeman, L., Krass, I., Trent, R., et al (2011).
Familial hypercholesterolaemia: A model of care
for Australasia. Atherosclerosis Supplements, 12,
221-263. <a
href="http://dx.doi.org/10.1016/j.atherosclerosiss
up.2011.06.001">[More Information]</a>
2010
Wollstein, A., Lao, O., Becker, C., Brauer, S.,
Trent, R., Nurnberg, P., Stoneking, M., Kayser,
M. (2010). Demographic History of Oceania
Inferred from Genome-wide Data. Current
Biology, 20(22), 1983-1992. <a
href="http://dx.doi.org/10.1016/j.cub.2010.10.04
0">[More Information]</a>
Luquin, N., Yu, B., Trent, R., Pamphlett, R.
(2010). DHPLC can be used to detect low-level
mutations in amyotrophic lateral sclerosis.
Amyotrophic Lateral Sclerosis and
Frontotemporal Degeneration, 11(40210),
76-82. <a
href="http://dx.doi.org/10.3109/1748296080257
2699">[More Information]</a>
Yu, B., Trent, R. (2010). Genetics of Athletic
Performance. Encyclopedia of Life Sciences, (pp.
1-8).
Trent, R., Otlowski, M., Ralston, M., Lonsdale,
L., Young, M., Suthers, G., Griffiths, P.,
Delatycki, M., Christodoulou, J.,
Barlow-Stewart, K. (2010). Medical Genetic
Testing: Information for health professionals,
NHMRC Publication reference: E99, (pp. vi 94). Canberra, Australia: Australian Government
National Health and Medical Research Council.
Trent, R. (2010). Pathology practice and
pharmacogenomics. Pharmacogenomics, 11(1),
105-111. <a
href="http://dx.doi.org/10.2217/pgs.09.150">[M
ore Information]</a>
2009
Morahan, J., Morahan, J., Yu, B., Yu, B., Trent,
R., Trent, R., Pamphlett, R., Pamphlett, R.
(2009). A genome-wide analysis of brain DNA
methylation identifies new candidate genes for
sporadic amyotrophic lateral sclerosis.
Amyotrophic Lateral Sclerosis and
Frontotemporal Degeneration, 10(5-6), 418-429.
<a
href="http://dx.doi.org/10.3109/1748296080263
5397">[More Information]</a>
Luquin, N., Yu, B., Saunderson, R., Trent, R.,
Pamphlett, R. (2009). Genetic variants in the
promoter of TARDBP in sporadic amyotrophic
lateral sclerosis. Neuromuscular Disorders,
19(10), 696-700. <a
href="http://dx.doi.org/10.1016/j.nmd.2009.07.0
05">[More Information]</a>
Trent, R., Yu, B. (2009). The future of genetic
research in exercise science and sports medicine.
Medicine and Sport Science, 54, 187-195. <a
href="http://dx.doi.org/10.1159/000235705">[M
ore Information]</a>
2008
Luquin, N., Yu, B., Trent, R., Morahan, J.,
Pamphlett, R. (2008). An analysis of the entire
SOD1 gene in sporadic ALS. Neuromuscular
Disorders, 18(7), 545-552. <a
href="http://dx.doi.org/10.1016/j.nmd.2008.04.0
13">[More Information]</a>
Le, H., Hinchcliffe, M., Yu, B., Trent, R. (2008).
Computer-assisted reading of DNA sequences.
Methods in molecular medicine, 141(Clinical
Bioinformatics), 177-197. <a
href="http://www.ncbi.nlm.nih.gov/entrez/query.
fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract
&list_uids=18453090">[More Information]</a>
Kayser, M., Lao, O., Saar, K., Brauer, S., Wang,
X., Nurnberg, P., Trent, R., Stoneking, M.
(2008). Genome-wide Analysis Indicates More
Asian than Melanesian Ancestry of Polynesians.
American Journal of Human Genetics, 82(1),
194-198. <a
href="http://dx.doi.org/10.1016/j.ajhg.2007.09.0
10">[More Information]</a>
Kayser, M., Choi, Y., van Oven, M., Mona, S.,
Brauer, S., Trent, R., Suarkia, D., Schiefenhovel,
W., Stoneking, M. (2008). The impact of the
Austronesian expansion: Evidence from mtDNA
and Y chromosome diversity in the Admiralty
Islands of Melanesia. Molecular Biology and
Evolution, 25(7), 1362-1374. <a
href="http://dx.doi.org/10.1093/molbev/msn078"
>[More Information]</a>
2007
Saunderson, R., Yu, B., Trent, R., Pamphlett, R.
(2007). A comparison of the lengths of androgen
receptor triplet repeats in brain and blood in
motor neuron diseases. Journal of the
Neurological Sciences, 267, 125-128. <a
href="http://dx.doi.org/10.1016/j.jns.2007.10.006
">[More Information]</a>
Publications for Ronald Trent
Saunderson, R., Yu, B., Trent, R., Pamphlett, R.
(2007). Are enteroviral receptors different in
sporadic motor neuron disease? Amyotrophic
Lateral Sclerosis and Frontotemporal
Degeneration, 8(1), 26-30. <a
href="http://www.ncbi.nlm.nih.gov/entrez/query.
fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract
&list_uids=17364432">[More Information]</a>
Morahan, J., Yu, B., Trent, R., Pamphlett, R.
(2007). Genetic susceptibility to environmental
toxicants in ALS. American Journal of Medical
Genetics Part B: Neuropsychiatric Genetics,
144B (7), 885-890. <a
href="http://dx.doi.org/10.1002/ajmg.b.30543">[
More Information]</a>
Myles, S., Hradetzky, E., Engelken, J., Lao, O.,
Numberg, P., Trent, R., Wang, X., Kayser, M.,
Stoneking, M. (2007). Identification of a
candidate genetic variant for the high prevalence
of type II diabetes in Polynesians. European
Journal of Human Genetics, 15(5), 584-589. <a
href="http://www.ncbi.nlm.nih.gov/entrez/query.
fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract
&list_uids=17327880">[More Information]</a>
Saunderson, R., Yu, B., Trent, R., Pamphlett, R.
(2007). Low yield in screening patients with
sporadic motor neuron disease for Kennedy
disease. Internal Medicine Journal, 37(11),
772-774. <a
href="http://www.ncbi.nlm.nih.gov/entrez/query.
fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract
&list_uids=17908088">[More Information]</a>
Trent, R. (2007). NHMRC Human Genetics
Advisory Committee. In Mark Stranger (Eds.),
Human Biotechnology and Public Trust: Trends,
Perceptions and Regulation, (pp. 247-252).
Australia: University of Tasmania - Centre for
Law and Genetics.
2006
Morahan, J., Yu, B., Trent, R., Pamphlett, R.
(2006). A gene-environment study of the
paraoxonase 1 gene and pesticides in
amyotrophic lateral sclerosis. NeuroToxicology,
28(3), 532-540. <a
href="http://www.ncbi.nlm.nih.gov/entrez/query.
fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract
&list_uids=17204329">[More Information]</a>
Morahan, J., Yu, B., Trent, R., Pamphlett, R.
(2006). Are metallothionein genes silenced in
ALS? Toxicology Letters, 168(1), 83-87. <a
href="http://www.ncbi.nlm.nih.gov/entrez/query.
fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract
&list_uids=17156946">[More Information]</a>
Trent, R., Webster, B., Bowden, D., Gilbert, A.,
Ho, J., Lindeman, R., Lammi, A., Rowell, J.,
Hinchcliffe, M., Colley, A., et al (2006).
Complex phenotypes in the
haemoglobinopathies: recommendations on
screening and DNA testing. Pathology, 38(6),
507-519.
Trent, R. (2006). Diagnosis of the
haemoglobinopathies. Clinical Biochemist
Reviews, 27(1), 27-38. <a
href="http://www.ncbi.nlm.nih.gov/entrez/query.
fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract
&list_uids=16886045">[More Information]</a>
Trent, R., Alexander, I. (2006). Gene therapy in
sport. British Journal of Sports Medicine, 40(1),
4-5. <a
href="http://www.ncbi.nlm.nih.gov/entrez/query.
fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract
&list_uids=16371483">[More Information]</a>
Li, J., Hayden, M., Warby, S., Durr, A.,
Morrison, P., Nance, M., Ross, C., Margolis, R.,
Rosenblatt, A., Trent, R., McCusker, E., et al
(2006). Genome-wide significance for a modifier
of age at neurological onset in Huntington's
disease at 6q23-24: the HD MAPS study. BMC
Medical Genetics, 7, 71-71. <a
href="http://www.ncbi.nlm.nih.gov/entrez/query.
fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract
&list_uids=16914060">[More Information]</a>
Kayser, M., Brauer, S., Cordaux, R., Casto, A.,
Lao, O., Zhivotovsky, L., Moyse-Faurie, C.,
Rutledge, R., Schiefenhoevel, W., Gil, D., Trent,
R., et al (2006). Melanesian and Asian origins of
Polynesians: mtDNA and Y chromosome
gradients across the Pacific. Molecular Biology
and Evolution, 23(11), 2234-2244. <a
href="http://www.ncbi.nlm.nih.gov/entrez/query.
fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract
&list_uids=16923821">[More Information]</a>
Kohonen-Corish, M., Cooper, W., Saab, J.,
Thompson, J., Trent, R., Millward, M. (2006).
Promoter hypermethylation of the
O(6)-methylguanine DNA methyltransferase
gene and microsatellite instability in metastatic
melanoma. Journal of Investigative
Dermatology, 126(1), 167-171. <a
href="http://www.ncbi.nlm.nih.gov/entrez/query.
fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract
&list_uids=16417233">[More Information]</a>
Gopinath, B., Trent, R., Yu, B. (2006). The
unique expression profile of the androgen
receptor gene in a rat model of neonatal cardiac
hypertrophy. Pathology, 38(2), 142-144. <a
href="http://www.ncbi.nlm.nih.gov/entrez/query.
fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract
&list_uids=16581655">[More Information]</a>
2005
Yu, B., Sawyer, N., Caramins, M., Yuan, Z.,
Saunderson, R., Pamphlett, R., Richmond, D.,
Jeremy, R., Trent, R. (2005). Denaturing high
performance liquid chromatography: high
Publications for Ronald Trent
throughput mutation screening in familial
hypertrophic cardiomyopathy and SNP
genotyping in motor neurone disease. Journal of
Clinical Pathology, 58(5), 479-485. <a
href="http://www.ncbi.nlm.nih.gov/entrez/query.
fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract
&list_uids=15858117">[More Information]</a>
Kohonen-Corish, M., Daniel, J., Chan, C., Lin,
B., Kwun, S., Dent, O., Dhillon, V., Trent, R.,
Chapuis, P., Bokey, E. (2005). Low
Microsatellite Instability Is Associated With
Poor Prognosis in Stage C Colon Cancer.
Journal of Clinical Oncology, 23(10),
2318-2324. <a
href="http://www.ncbi.nlm.nih.gov/entrez/query.
fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract
&list_uids=15800322">[More Information]</a>
Trent, R. (2005). Molecular Medicine.
Burlington, Massachusetts: Academic Press.
Trent, R. (2005). Oversight and monitoring of
clinical research with gene therapy in Australia.
Medical Journal of Australia, 182(9), 441-442.
<a
href="http://www.ncbi.nlm.nih.gov/entrez/query.
fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract
&list_uids=15865585">[More Information]</a>
Morahan, J., Yu, B., Trent, R., Pamphlett, R.
(2005). Screening the metallothionein III gene in
sporadic amyotrophic lateral sclerosis.
Amyotrophic Lateral Sclerosis and
Frontotemporal Degeneration, 6(2), 115-117. <a
href="http://www.ncbi.nlm.nih.gov/entrez/query.
fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract
&list_uids=16036436">[More Information]</a>
Henderson, J., Withford-Cave, J., Duffy, D.,
Cole, S., Sawyer, N., Gulbin, J., Hahn, A., Trent,
R., Yu, B. (2005). The EPAS1 gene influences
the aerobic-anaerobic contribution in elite
endurance athletes. Human Genetics,
118(03-Apr), 416-423. <a
href="http://dx.doi.org/10.1007/s00439-005-006
6-0">[More Information]</a>
2004
Saunderson, R., Yu, B., Trent, R., Pamphlett, R.
(2004). A Polymorphism In The Poliovirus
Receptor Gene Differs In Motor Neuron Disease.
NeuroReport, 15(2), 383-386.
Trent, R., Yu, B., Caramins, M. (2004).
Challenges For Clinical Genetic DNA Testing.
Expert Review of Molecular Diagnostics, 4(2),
201-208.
Djousse, L., Knowlton, B., Hayden, M.,
Almqvist, E., Brinkman, R., Ross, C., Margolis,
R., Rosenblatt, A., Durr, A., Dode, C., Trent, R.,
et al (2004). Evidence For A Modifier Of Onset
Age In Huntington Disease Linked To The Hd
Gene In 4P16. Neurogenetics, 5, 109-14. <a
href="http://dx.doi.org/10.1007/s10048-004-017
5-2">[More Information]</a>
Trent, R., Alexander, I. (2004). Gene Therapy:
Applications And Progress Towards The Clinic.
Internal Medicine Journal, 34(11), 621-625.
Trent, R., Yu, B., Caramins, M. (2004).
Introduction of molecular genetics and genomics
into clinical practice. In Fuchs J, Podda M,
Goethe JW (Eds.), Encyclopedia of Diagnostic
Genomics and Proteomics. (pp. 676-681). New
York: Marcel Dekker.
Gopinath, B., Trent, R., Yu, B. (2004).
Molecular Characterisation Of Neonatal Cardiac
Hypertrophy And Its Regression. Cardiology in
the Young, 14(5), 498-505.
Yu, B., Trent, R. (2004). Present And
Prospective Applications Of Genetic Dna
Testing (Part I). Chinese Journal of
Contemporary Pediatrics, 6(5), 447-450.
Yu, B., Trent, R. (2004). Present And
Prospective Applications Of Genetic Dna
Testing (Part II). Chinese Journal of
Contemporary Pediatrics, 6(6), 538-541.
Trent, R., Caramins, M., Yu, B. (2004).
Separation techniques – Capillary
electrophoresis. In Fuchs J and Podda M,
Goethe JW (Eds.), Encyclopedia of Diagnostic
Genomics and Proteomics. (pp. 210-215). New
York: Marcel Dekker.
Jen, J., Wang, H., Lee, H., Sabatti, C., Trent, R.,
Hannigan, I., Brantberg, K., Halmagyi, G.,
Nelson, S., Baloh, R. (2004). Suggestive Linkage
To Chromosome 6Q In Families With Bilateral
Vestibulopathy. Neurology, 63(12), 2376-9.
2003
Li, J., Hayden, M., Almqvist, E., Brinkman, R.,
Durr, A., Dode, C., Morrison, P., Suchowersky,
O., Ross, C., Margolis, R., Trent, R. (2003). A
genome scan for modifiers of age at onset in
Huntington Disease: The HD MAPS Study.
American Journal of Human Genetics, 73(3),
682-687.
Caramins, M., Halliday, G., McCusker, E., Trent,
R. (2003). Genetically confirmed clinical
Huntington's disease with no observable cell
loss. Journal of Neurology, Neurosurgery and
Psychiatry, 74(7), 968-970.
Djousse, L., Knowlton, B., Hayden, M.,
Almqvist, E., Brinkman, R., Ross, C., Margolis,
R., Rosenblatt, A., Durr, A., Dode, C., Trent, R.,
et al (2003). Interaction of normal and expanded
CAG repeat sizes influences age at onset of
Huntington disease. American Journal of
Medical Genetics. Part A, 119A (3), 279-282.
Orange, S., Painter, D., Horvath, J., Yu, B.,
Trent, R., Hennessy, A. (2003). Placental
Publications for Ronald Trent
endothelial nitric oxide synthase localization and
expression in normal human pregnancy and
pre-eclampsia. Clinical and Experimental
Pharmacology and Physiology, 30(5-6),
376-381.
Trent, R., Williamson, R., Sutherland, A. (2003).
The "new genetics" and clinical practice.
Medical Journal of Australia, 11, 406-409.
2002
Brown, L., Singh, L., Sale, K., Yu, B., Trent, R.,
Fajer, P., Hambly, B. (2002). Functional and
spectroscopic studies of a familial hypertrophic
cardiomyopathy mutation in Motif X of cardiac
myosin binding protein-C. European Biophysics
Journal, 31(5), 400-408. <a
href="http://dx.doi.org/10.1007/s00249-002-023
6-0">[More Information]</a>
Huang, Q., Trevena, L., Kidd, M., Trent, R.,
Callen, J. (2002). The impact of the human
genetic research on primary care: a summary of
general practitioners on genetic counselling and
testing in general practice. Research from the
Ground Up, : British Medical Journal Publishing
Group.
2001
Dedic, J., Weiss, A., Yu, B., Trent, R., Katahira,
J., Urban, Z. (2001). A novel elastin gene
mutation (1281delC) in a family with
supravalvular aortic stenosis: a mutation cluster
within exon 20. Human Mutation, 17, 81-81.
2000
Trent, R., He, H., Yu, B., Young, G., Bowden,
D. (2000). DNA testing for haemochromatosis:
diagnostic, predictive and screening implications.
Pathology, 32, 274-279.
Rivory, L., Qin, H., Clarke, S., Eris, J., Duggin,
G., Ray, E., Trent, R., Bishop, J. (2000).
Frequency of cytochrome P450 3A4 variant
genotype in transplant population and lack of
association with cyclosporin clearance.
European Journal of Clinical Pharmacology, 56,
395-398.
McCusker, E., Richards, F., Sillence, D., Wilson,
M., Trent, R. (2000). Huntington's disease:
neurological assessment of potential gene
carriers presenting for predictive DNA testing.
Journal of Clinical Neuroscience.
Trent, R. (2000). Milestones in the human
genome project: genesis to postgenome. Medical
Journal of Australia, 173, 591-594.
Yu, S., Fimmel, A., Fung, D., Trent, R. (2000).
Polymorphisms in the CAG repeat- a source of
error in Huntington disease DNA testing.
Clinical Genetics, 58, 469-472.