Publications for Bing Yu
Publications for Bing Yu
5.007">[More Information]</a>
2016
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>
Luk, P., Weston, J., Yu, B., Selinger, C.,
Ekmejian, R., Eviston, T., Lum, T., Gao, K.,
Boyer, M., O'Toole, S., Clark, J., Gupta, R.
(2016). Salivary duct carcinoma:
Clinicopathologic features, morphologic
spectrum, and somatic mutations. Head and
Neck, 38(Suppl 1), e1838-e1847. <a
href="http://dx.doi.org/10.1002/hed.24332">[Mo
re Information]</a>
Lyle, M., Haydu, L., Menzies, A., Thompson, J.,
Saw, R., Spillane, A., Kefford, R., Mann, G.,
Cooper, W., Yu, B., Scolyer, R., O'Toole, S.,
Long, G. (2016). The molecular profile of
metastatic melanoma in Australia. Pathology,
48(2), 188-193. <a
href="http://dx.doi.org/10.1016/j.pathol.2015.12.
008">[More Information]</a>
2015
Luk, P., Yu, B., Ng, C., Mercorella, B., Selinger,
C., Lum, T., Kao, S., O'Toole, S., Cooper, W.
(2015). BRAF mutations in non-small cell lung
cancer. Translational Lung Cancer Research,
4(2), 142-148. <a
href="http://dx.doi.org/10.3978/j.issn.2218-6751.
2014.08.08">[More Information]</a>
Steinberg, K., Yu, B., Koboldt, D., Mardis, E.,
Pamphlett, R. (2015). Exome sequencing of
case-unaffected-parents trios reveals
recessive and de novo genetic variants in
sporadic ALS. Scientific Reports, 5, 1-8. <a
href="http://dx.doi.org/10.1038/srep09124">[Mo
re Information]</a>
Li, B., Lee, A., O'Toole, S., Cooper, W., Yu, B.,
Chaft, J., Arcila, M., Kris, M., Pavlakis, N.
(2015). HER2 insertion YVMA mutant lung
cancer: Long natural history and response to
afatinib. Lung Cancer, 90(3), 617-619. <a
href="http://dx.doi.org/10.1016/j.lungcan.2015.1
0.025">[More Information]</a>
Luk, P., Selinger, C., Eviston, T., Lum, T., Yu,
B., O'Toole, S., Clark, J., Gupta, R. (2015).
Mammary analogue secretory carcinoma: an
evaluation of its clinicopathological and genetic
characteristics. Pathology, 47(7), 659-666. <a
href="http://dx.doi.org/10.1097/PAT.000000000
0000322">[More Information]</a>
Cooper, W., Tran, T., Vilain, R., Madore, J.,
Selinger, C., Kohonen-Corish, M., Yip, P., Yu,
B., O'Toole, S., McCaughan, B., Horvath, L.,
Kao, S., Boyer, M., Scolyer, R., et al (2015).
PD-L1 expression is a favorable prognostic
factor in early stage non-small cell carcinoma.
Lung Cancer, 89(2), 181-188. <a
href="http://dx.doi.org/10.1016/j.lungcan.2015.0
Wang, S., Yu, B., Ng, C., Mercorella, B.,
Selinger, C., O'Toole, S., Cooper, W. (2015).
The suitability of small biopsy and cytology
specimens for EGFR and other mutation testing
in non-small cell lung cancer. Translational
Lung Cancer Research, 4(2), 119-125. <a
href="http://dx.doi.org/10.3978/j.issn.2218-6751.
2015.01.05">[More Information]</a>
Steinberg, K., Nicholas, T., Koboldt, D., Yu, B.,
Mardis, E., Pamphlett, R. (2015). Whole genome
analyses reveal no pathogenetic single nucleotide
or structural differences between monozygotic
twins discordant for amyotrophic lateral
sclerosis. Amyotrophic Lateral Sclerosis and
Frontotemporal Degeneration, 16(5-6), 385-392.
<a
href="http://dx.doi.org/10.3109/21678421.2015.
1040029">[More Information]</a>
2014
Tran, T., Selinger, C., Yu, B., Ng, C.,
Kohonen-Corish, M., McCaughan, B., Kennedy,
C., O'Toole, S., Cooper, W. (2014). Alterations
of insulin-like growth factor-1 receptor gene
copy number and protein expression are common
in non-small cell lung cancer. Journal of Clinical
Pathology, 67(11), 985-991. <a
href="http://dx.doi.org/10.1136/jclinpath-2014-2
02347">[More Information]</a>
Carlino, M., Haydu, L., Kakavand, H., Menzies,
A., Hamilton, A., Yu, B., Ng, C., Cooper, W.,
Thompson, J., Kefford, R., O'Toole, S., Scolyer,
R., Long, G. (2014). Correlation of BRAF and
NRAS mutation status with outcome, site of
distant metastasis and response to chemotherapy
in metastatic melanoma. British Journal of
Cancer, 111(2), 292-299. <a
href="http://dx.doi.org/10.1038/bjc.2014.287">[
More Information]</a>
O'Toole, S., Yu, B., Cooper, W. (2014).
Molecular Diagnosis in Cytology and Its Place in
the New Classification: A Practical Guide. The
Journal of OncoPathology, 2(1), 63-73. <a
href="http://dx.doi.org/10.13032/tjop.2052-5931.
100080.">[More Information]</a>
Fox, G., Sy, D., Viet Nhung, N., Yu, B., Ellis,
M., Hung, N., Cuong, N., Lien, L., Marks, G.,
Saunders, B., Britton, W. (2014). Polymorphisms
of SP110 Are Associated with both Pulmonary
and Extra-Pulmonary Tuberculosis among the
Vietnamese. PloS One, 9(7), e99496. <a
Publications for Bing Yu
href="http://dx.doi.org/10.1371/journal.pone.009
9496">[More Information]</a>
fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract
&list_uids=23404800">[More Information]</a>
Yu, B. (2014). Setting Up Next-Generation
Sequencing in the Medical Laboratory. In
Ronald Trent (Eds.), Clinical Bioinformatics,
(pp. 195-206). New York, United States:
Humana Press.
2012
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>
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>
Yu, B. (2013). In silico interpretation of the
splicing code and estimating the abundance of
expressed mRNA isoforms. Human Mutation,
34(4). <a
href="http://dx.doi.org/10.1002/humu.22182">[
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>
Chan, K., O'Connell, R., Sullivan, D., Hoffmann,
L., Rajamani, K., Whiting, M., Donoghoe, M.,
Vanhala, M., Hamer, A., Yu, B., Stocker, R., Ng,
M., Keech, A. (2013). Plasma total bilirubin
levels predict amputation events in type 2
diabetes mellitus: the fenofibrate intervention
and event lowering in diabetes (field) study.
Diabetologia, 56(4), 724-736. <a
href="http://dx.doi.org/10.1007/s00125-012-281
8-4">[More Information]</a>
Karim, R., O'Toole, S., Scolyer, R., Cooper, C.,
Chan, B., Selinger, C., Yu, B., Carmalt, H., Mak,
C., Tse, G., Lee, C., et al (2013). Recent insights
into the molecular pathogenesis of mammary
phyllodes tumours. Journal of Clinical
Pathology, 66(6), 496-505. <a
href="http://www.ncbi.nlm.nih.gov/entrez/query.
Pamphlett, R., Morahan, J., Luquin, N., Yu, B.
(2012). An approach to finding brain-situated
mutations in sporadic Parkinson's disease.
Parkinsonism & Related Disorders, 18(1), 82-85.
<a
href="http://dx.doi.org/10.1016/j.parkreldis.2011
.08.024">[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
Yu, B., Zhang, C. (2011). In Silico PCR
Analysis. In Bing Yu & Marcus Hinchcliffe
(Eds.), In Silico Tools for Gene Discovery, (pp.
91-107). New York: Humana Press.
Yu, B., Hinchcliffe, M. (2011). In Silico Tools
for Gene Discovery. New York: Humana Press.
Pamphlett, R., Morahan, J., Luquin, N., Yu, B.
(2011). Looking for differences in copy number
between blood and brain in sporadic amyotrophic
lateral sclerosis. Muscle and Nerve, 44(4),
492-498. <a
href="http://dx.doi.org/10.1002/mus.22095">[M
ore Information]</a>
Dong, C., Yu, B. (2011). Mutation Surveyor: An
In Silico Tool for Sequencing Analysis. In Bing
Yu & Marcus Hinchcliffe (Eds.), In Silico Tools
for Gene Discovery, (pp. 223-237). New York:
Humana Press.
Sandhu, S., McKenzie, P., Yu, B., Chua, E.
(2011). Phaeochromocytoma, Neurofibromatosis
and Gastrointestinal stromal tumour: Just a
random event? Internal Medicine Journal, 41(2),
212-213. <a
href="http://dx.doi.org/10.1111/j.1445-5994.201
0.02412.x">[More Information]</a>
Yu, B., Fey, P., Kestin-Pilcher, K., Federov, A.,
Prakash, A., Chisholm, R., Wu, J. (2011).
Spliceosomal genes in the D. discoideum
genome: a comparison with those in H. sapiens,
D. melanogaster, A. thaliana and S. cerevisiae.
Protein and Cell, 2(5), 395-409. <a
href="http://dx.doi.org/10.1007/s13238-011-105
2-z">[More Information]</a>
Pamphlett, R., Morahan, J., Yu, B. (2011). Using
case-parent trios to look for rare de novo genetic
variants in adult-onset neurodegenerative
diseases. Journal of Neuroscience Methods,
197(2), 297-301. <a
Publications for Bing Yu
href="http://dx.doi.org/10.1016/j.jneumeth.2011.
02.028">[More Information]</a>
2010
Xu, M., Bi, Y., Xu, Y., Yu, B., Huang, Y., Gu,
L., Wu, Y., Zhu, X., Li, M., Wang, T., et al
(2010). Combined effects of 19 common
variations on type 2 diabetes in Chinese: results
from two community-based studies. PloS One,
5(11), e14022-1-e14022-10. <a
href="http://dx.doi.org/10.1371/journal.pone.001
4022">[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).
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>
Yu, B. (2008). In silico gene discovery. Methods
in molecular medicine, 141, 1-22. <a
href="http://www.ncbi.nlm.nih.gov/entrez/query.
fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract
&list_uids=18453081">[More Information]</a>
Yu, B. (2008). Role of In Silico Tools in Gene
Discovery. Molecular Biotechnology, 41(3),
296-306. <a
href="http://dx.doi.org/10.1007/s12033-008-913
4-8">[More Information]</a>
Xiang, J., Li, X., Xu, M., Hong, J., Huang, Y.,
Tan, J., Lu, X., Dai, M., Yu, B., Ning, G. (2008).
Zinc Transporter-8 Gene (SLC30A8) Is
Associated with Type 2 Diabetes in Chinese.
Journal of Clinical Endocrinology and
Metabolism, 93(10), 4107-4112. <a
href="http://dx.doi.org/10.1210/jc.2008-0161">[
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>
Sun, H., Wang, Y., Ma, X., Pei, F., Sun, H.,
Zhang, Y., Yu, B. (2007). A method of oligochip
for single nucleotide polymorphism genotyping
in the promoter region of the interleukin-1 beta
gene and its clinical application.
Oligonucleotides, 17(3), 336-344.
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>
Wang, B., Yu, B., Karim, M., Hu, H., Sun, Y.,
McGreevy, P., Petocz, P., Held, S., Brand-Miller,
J. (2007). Dietary sialic acid supplementation
improves learning and memory in piglets. The
American Journal of Clinical Nutrition, 85(2),
561-569. <a
href="http://www.ncbi.nlm.nih.gov/entrez/query.
fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract
&list_uids=17284758">[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
Publications for Bing Yu
href="http://dx.doi.org/10.1002/ajmg.b.30543">[
More Information]</a>
fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract
&list_uids=16026832">[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>
Wang, B., Yu, B., Karim, M., Hu, H., Sun, Y.,
McGreevy, P., Petocz, P., Held, S., Brand-Miller,
J. (2006). Sialic acid: a novel nutrient that
enhances learning and memory. Trends in
Glycoscience and Glycotechnology,
18(supplement), S23-S23.
Wang, B., Hu, H., Yu, B., Troy II, F. (2007).
Molecular characterization of pig
UDP-N-acetylglucosamine-2-epimerase/Nacetylmannosamine kinase (Gne) gene: Effect of
dietary sialic acid supplementation on gene
expression in piglets. Current Topics in
Nutraceutical Research: an international
scientific journal for decision makers in
nutraceutical industry, 5(4), 165-176.
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>
Yu, B., Sawyer, N., Chiu, C., Underhill, P.
(2006). DNA Mutation Detection Using UNIT
7.10 Denaturing High-Performance Liquid
Chromatography (DHPLC). In Dracopoli NC,
Haines JL, Korf BR, Morton CC, Seidman CE,
Seidman JG, and Smith D (Eds.), Current
Protocols in Human Genetics, (pp.
7.10.1-7.10.14). John Wiley & Sons.
Wang, B., Hu, H., Yu, B. (2006). Molecular
characterization of pig ST8Sia IV - a critical
gene for the formation of neural cell adhesion
molecule and its response to sialic acid
supplement in piglets. Nutritional Neuroscience,
9(3-4), 147-154. <a
href="http://www.ncbi.nlm.nih.gov/entrez/query.
fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract
&list_uids=17176637">[More Information]</a>
Makris, A., Xu, B., Yu, B., Thornton, C.,
Hennessy, A. (2006). Placental deficiency of
interleukin-10 (IL-10) in preeclampsia and its
relationship to an IL10 promoter polymorphism.
Placenta, 27, 445-451. <a
href="http://www.ncbi.nlm.nih.gov/entrez/query.
Wu, J., Kar, A., Kuo, D., Yu, B., Havlioglu, N.
(2006). SRp54 (SFRS11), a regulator for tau
exon 10 alternative splicing identified by an
expression cloning strategy. Molecular and
Cellular Biology, 26(18), 6739-6747. <a
href="http://www.ncbi.nlm.nih.gov/entrez/query.
fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract
&list_uids=16943417">[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
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>
Wang, Y., Ma, X., Sun, S., Sun, Y., Yu, B.
(2005). Development of an oligochip for
genotyping human leukocyte antigen-B51 and its
clinical application. Genetic Testing, 9(4),
292-296.
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
Publications for Bing Yu
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.
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.
Trent, R., Yu, B., Caramins, M. (2004).
Challenges For Clinical Genetic DNA Testing.
Expert Review of Molecular Diagnostics, 4(2),
201-208.
Yu, B., Handelsman, D. (2001).
Pharmacogenetic polymorphisms of the AR and
metabolism and susceptibility to
hormone-induced azoospermia. Journal of
Clinical Endocrinology and Metabolism, 86,
4406-4411.
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.
Yu, B. (2004). What Is The Value Of Mutation
Identification In Familial Hypertrophic
Cardiomyopathy? answer. IUBMB Life, 56(5),
281-283.
2003
Orange, S., Painter, D., Horvath, J., Yu, B.,
Trent, R., Hennessy, A. (2003). Placental
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.
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>
2001
Dedic, J., Weiss, A., Yu, B., Trent, R., Katahira,
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.