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CGRG - Publications
2000-2010
2010
- Morris,
C.M. & Jewell, U.R. Array of hope for high-resolution genetic
screening services in New Zealand. New Zealand Medical Journal
(NZMJ) 123 (1318), 6-11, (2010) [Lead Editorial] ISSN
1175 8716
2009
- Benjes,
S.M. & Morris, C.M. L1 Elements. In Encyclopedia
of Cancer, 2nd
Ed. (Ed: M. Schwab). Springer, New York, print + eReference, ISBN:
978-3-540-47649-8 (2009) [Essay Contribution]
- Morris,
C.M. & Benjes, S.M. BCR-ABL1. In Encyclopedia of
Cancer, 2nd Ed. (Ed: M. Schwab). Springer, New York, print +
eReference, ISBN: 978-3-540-47649-8 (2009) [Essay Contribution]
- Morris,
C.M. Alu Elements. In Encyclopedia of Cancer, 2nd Ed.
(Ed: M. Schwab). Springer, New York, print + eReference, ISBN: 978-3-540-47649-8
(2009) [Essay Contribution]
- Morris,
C.M. Blast crisis. In Encyclopedia of Cancer, 2nd Ed.
(Ed: M. Schwab). Springer, New York, print + eReference, ISBN: 978-3-540-47649-8
(2009) [Essay Contribution]
2008
2007
- Walker,
L.C., Harris, G.C., Holloway, A.J., McKenzie, G.W., Wells, J.E.,
Robinson, B.A. & Morris, C.M. Cytokeratin KRT8/18 expression
differentiates distinct subtypes of grade 3 invasive ductal carcinoma
of the breast. Cancer Genetics & Cytogenetics 178, 94-103
(2007). [Journal]
- Sheen,
C.R., Jewell, U.R., Morris, C.M., Brennan, S.O., Ferec, C., George,
P.M., Smith, M.P. & Chen, J.M. Double complex mutations involving
F8 and FUNDC2 caused by distinct break-induced replication. Human
Mutation 28, 1198-206 (2007). [Journal]
2006
2005
- Chee, L., Spearing,
R.L., Morris, C.M., McDonald, M., Hanrahan, V., Ebbett, A., Scott,
R., Florkowski, C., Walmsley, T. & Patton, W.N. Acquired
myeloma-associated Type III hyperlipidaemia treated by nonmyeloablative
HLA-identical sibling allogeneic stem cell transplant using a donor
with essential thrombocythaemia (ET): evidence of engraftment without
manifestation of ET in recipient. Bone Marrow Transplantation 35,
1213-4 (2005). [Journal]
2004
- Ganly,
P., McDonald, M., Spearing, R. & Morris, C.M. Constitutional
t(5;7)(q11;p15) rearranged to acquire monosomy 7q and trisomy 1q
in a patient with myelodysplastic syndrome transforming to acute
myelocytic leukemia. Cancer Genetics & Cytogenetics 149,
125-30 (2004). [Journal]
- Ganly,P.S.,
Walker, L.C. & Morris, C.M. Familial mutations of the transcription
factor RUNX1 (AML1, CBFA2) predispose to acute myeloid leukemia. Leukemia & Lymphoma 45,
1-10 (2004). [Journal]
2003
- Gough,
S.M., McDonald, M., Chen, X.N., Korenberg, J.R., Neri, A., Kahn,
T., Eccles, M.R. & Morris, C.M. Refined physical map of the
human PAX2/HOX11/NFKB2 cancer gene region at 10q24 and relocalization
of the HPV6AI1 viral integration site to 14q13.3-q21.1. BMC Genomics 4-9,
1-12 (2003). [Journal]
2002
- Walker,
L.C., Stevens, J., Campbell, H., Corbett, R., Spearing, R., Heaton,
D., Macdonald, D.H., Morris, C.M. & Ganly, P. A novel inherited
mutation of the transcription factor RUNX1 causes thrombocytopenia
and may predispose to acute myeloid leukaemia. British Journal
Haematology 117, 878-81 (2002). [Journal]
2001
- Benjes,
S.M. & Morris, C.M. A full-length and potentially active
LINE element is integrated polymorphically within the IGL locus in
a genomically unstable region of chromosome 22. Human Genetics 109,
628-37 (2001). [Journal]
- Kearns,
M., Morris, C. & Whitelaw, E. Spontaneous germline amplification
and translocation of a transgene array. Mutation Research 486,
125-36 (2001). [Journal]
- Jeffs,
A.R., Wells, E. & Morris, C.M. Nonrandom distribution of
interspersed repeat elements in the BCR and ABL1 genes and its relation
to breakpoint cluster regions. Genes Chromosomes & Cancer 32,
144-54 (2001). [Journal]
- Morris, C.M. BCR-ABL1. In Cancer Research: An Encyclopedic Reference,
pp106-111 (ed. Schwab, M.) (Springer, New York, 2001). [Essay Contribution]
2000
- Sutherland,
H.G., Kearns, M., Morgan, H.D., Headley, A.P., Morris, C., Martin,
D.I. & Whitelaw, E. Reactivation of heritably silenced gene
expression in mice. Mammalian Genome 11, 347-55 (2000).
[Journal]
- Morris,
C.M., Haataja, L., McDonald, M., Gough, S., Markie, D., Groffen,
J. & Heisterkamp, N. The small GTPase RAC3 gene is located
within chromosome band 17q25.3 outside and telomeric of a region
commonly deleted in breast and ovarian tumours. Cytogenetics
Cell Genetics 89, 18-23 (2000). [Journal]
- Llewellyn,
I.E., Morris, C.M., Stanworth, S., Heaton, D.C. & Spearing, R.L. Trisomy
10 in acute myeloid leukemia: three new cases. Cancer Genetics & Cytogenetics 118,
148-50 (2000). [Journal]
- Kearns,
M., Preis, J., McDonald, M., Morris, C. & Whitelaw, E. Complex
patterns of inheritance of an imprinted murine transgene suggest
incomplete germline erasure. Nucleic Acids Research 28,
3301-3309 (2000). [Journal]
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