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Christine Morris

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Campbell R Sheen; Margaret A McDonald; Peter M George; Mark P Smith; Christine Morris
Genotyping the factor VIII intron 22 inversion locus using fluorescent in situ hybridization.
Christine Morris
Chronic myeloid leukemia: cytogenetic methods and applications for diagnosis and treatment.
Christine Morris; Ursula R Jewell
Array of hope for high-resolution genetic screening services in New Zealand.

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All Publications

2011: Campbell R Sheen; Margaret A McDonald; Peter M George; Mark P Smith; Christine Morris
Genotyping the factor VIII intron 22 inversion locus using fluorescent in situ hybridization.
Blood cells, molecules & diseases 2011;46(2):151-8.
2011: Christine Morris
Chronic myeloid leukemia: cytogenetic methods and applications for diagnosis and treatment.
Methods in molecular biology (Clifton, N.J.) 2011;730():33-61.
2010: Christine Morris; Ursula R Jewell
Array of hope for high-resolution genetic screening services in New Zealand.
The New Zealand medical journal 2010;123(1318):6-11.
2008: Logan C Walker; Gavin C Harris; J Elisabeth Wells; Bridget A Robinson; Christine Morris
Association of chromosome band 8q22 copy number gain with high grade invasive breast carcinomas by assessment of core needle biopsies.
Genes, chromosomes & cancer 2008;47(5):405-17.
2007: Campbell R Sheen; Ursula R Jewell; Christine Morris; Stephen O Brennan; Claude Férec; Peter M George; Mark P Smith; Jian-Min Chen
Double complex mutations involving F8 and FUNDC2 caused by distinct break-induced replication.
Human mutation 2007;28(12):1198-206.
2007: Logan C Walker; Gavin C Harris; Andrew J Holloway; Grant W McKenzie; J Elisabeth Wells; Bridget A Robinson; Christine Morris
Cytokeratin KRT8/18 expression differentiates distinct subtypes of grade 3 invasive ductal carcinoma of the breast.
Cancer genetics and cytogenetics 2007;178(2):94-103.
2006: Sheryl M Gough; Suzanne M Benjes; Margaret McDonald; David Heaton; Peter Ganly; Christine Morris
Translocation (5;10)(q22;q24) in a case of acute lymphoblastic leukemia.
Cancer genetics and cytogenetics 2006;165(1):36-40.
2005: L Chee; Ruth Spearing; Christine Morris; M McDonald; V Hanrahan; A Ebbett; R Scott; C Florkowski; Trevor Walmsley; William Nigel Patton
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 2005;35(12):1213-4.
2004: Peter Ganly; Margaret McDonald; Ruth Spearing; Christine Morris
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 and cytogenetics 2004;149(2):125-30.
2004: Peter Ganly; Logan C Walker; Christine Morris
Familial mutations of the transcription factor RUNX1 (AML1, CBFA2) predispose to acute myeloid leukemia.
Leukemia & lymphoma 2004;45(1):1-10.
2003: Sheryl M Gough; Margaret McDonald; Xiao-Ning Chen; Julie R Korenberg; Antonino Neri; Tomas Kahn; Michael Eccles; Christine Morris
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 2003;4(1):9.
2002: Logan C Walker; Jane Stevens; Hamish Campbell; Rob Corbett; Ruth Spearing; David Heaton; Donald H Macdonald; Christine Morris; Peter Ganly
A novel inherited mutation of the transcription factor RUNX1 causes thrombocytopenia and may predispose to acute myeloid leukaemia.
British journal of haematology 2002;117(4):878-81.
2001: Suzanne M Benjes; Christine Morris
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 2001;109(6):628-37.
2001: AR Jeffs; E Wells; Christine Morris
Nonrandom distribution of interspersed repeat elements in the BCR and ABL1 genes and its relation to breakpoint cluster regions.
Genes, chromosomes & cancer 2001;32(2):144-54.
2001: M Kearns; Christine Morris; Emma Whitelaw
Spontaneous germline amplification and translocation of a transgene array.
Mutation research 2001;486(2):125-36.
2000: M Kearns; Jost Preis; M McDonald; Christine Morris; Emma Whitelaw
Complex patterns of inheritance of an imprinted murine transgene suggest incomplete germline erasure.
Nucleic acids research 2000;28(17):3301-9.
2000: HG Sutherland; M Kearns; Hugh D Morgan; A P Headley; Christine Morris; David I K Martin; Emma Whitelaw
Reactivation of heritably silenced gene expression in mice.
Mammalian genome : official journal of the International Mammalian Genome Society 2000;11(5):347-55.
2000: I E Llewellyn; Christine Morris; S Stanworth; David Heaton; Ruth Spearing
Trisomy 10 in acute myeloid leukemia: three new cases.
Cancer genetics and cytogenetics 2000;118(2):148-50.
2000: Christine Morris; Leena Haataja; M McDonald; S Gough; D Markie; John Groffen; Nora Heisterkamp
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 and cell genetics 2000;89(1-2):18-23.
1999: Suzanne M Benjes; L J Millow; AR Jeffs; Stephen J Sowerby; A E Reeve; Christine Morris
3' BCR recombines with IGL locus in BCR-ABL-positive philadelphia-negative chronic myeloid leukemia.
Genes, chromosomes & cancer 1999;26(4):366-71.
1999: Klaus Lehnert; Jian Ni; Euphemia Leung; SM Gough; A Weaver; WP Yao; D Liu; SX Wang; Christine Morris; Geoffrey W Krissansen
Cloning, sequence analysis, and chromosomal localization of the novel human integrin alpha11 subunit (ITGA11).
Genomics 1999;60(2):179-87.
1999: PE Crossen; MJ Morrison; P Rodley; J Cochrane; Christine Morris
Identification of amplified genes in a patient with acute myeloid leukemia and double minute chromosomes.
Cancer genetics and cytogenetics 1999;113(2):126-33.
1999: Christine Morris; Mario Luppi; M McDonald; Patrizia Barozzi; G Torelli
Fine mapping of an apparently targeted latent human herpesvirus type 6 integration site in chromosome band 17p13.3.
Journal of medical virology 1999;58(1):69-75.
1999: Randy W Berg; Euphemia Leung; SM Gough; Christine Morris; WP Yao; SX Wang; Jian Ni; Geoffrey W Krissansen
Cloning and characterization of a novel beta integrin-related cDNA coding for the protein TIED ("ten beta integrin EGF-like repeat domains") that maps to chromosome band 13q33: A divergent stand-alone integrin stalk structure.
Genomics 1999;56(2):169-78.
1999: Klaus Lehnert; Jian Ni; Euphemia Leung; SM Gough; Christine Morris; D Liu; SX Wang; Ries Langley; Geoffrey W Krissansen
The integrin alpha10 subunit: expression pattern, partial gene structure, and chromosomal localization.
Cytogenetics and cell genetics 1999;87(3-4):238-44.
1999: R Manley; J Cochrane; M McDonald; S Rigby; A Moore; A Kirk; S Clarke; PE Crossen; Christine Morris; William Nigel Patton
Clonally unrelated BCR-ABL-negative acute myeloblastic leukemia masquerading as blast crisis after busulphan and interferon therapy for BCR-ABL-positive chronic myeloid leukemia.
Leukemia 1999;13(1):126-9.
1999: Mario Luppi; Patrizia Barozzi; Christine Morris; Antonio Maiorana; R Garber; Goretta Bonacorsi; Amedea Donelli; Marasca Roberto; A Tabilio; Giuseppe Torelli
Human herpesvirus 6 latently infects early bone marrow progenitors in vivo.
Journal of virology 1999;73(1):754-9.
1998: M Luppi; Patrizia Barozzi; Christine Morris; Elisa Merelli; G Torelli
Integration of human herpesvirus 6 genome in human chromosomes.
Lancet 1998;352(9141):1707-8.
1998: Ries Langley; Euphemia Leung; Christine Morris; R Berg; M McDonald; A Weaver; D A Parry; Jian Ni; J Su; R Gentz; N Spurr; Geoffrey W Krissansen
Identification of multiple forms of 180-kDa ribosome receptor in human cells.
DNA and cell biology 1998;17(5):449-60.
1998: Masato Kato; TK Neil; Georgina J Clark; Christine Morris; RV Sorg; Derek N J Hart
cDNA cloning of human DEC-205, a putative antigen-uptake receptor on dendritic cells.
Immunogenetics 1998;47(6):442-50.
1998: AR Jeffs; Suzanne M Benjes; T L Smith; Stephen J Sowerby; Christine Morris
The BCR gene recombines preferentially with Alu elements in complex BCR-ABL translocations of chronic myeloid leukaemia.
Human molecular genetics 1998;7(5):767-76.
1998: Christine Morris; M McDonald; E Leung; A Weaver; Geoffrey W Krissansen
Assignment of the murine kinectin gene (Ktn1) to mouse chromosome 14C2 by fluorescence in situ hybridization.
Cytogenetics and cell genetics 1998;81(1):87-8.
1997: P Rodley; M McDonald; B Price; R Fright; Christine Morris
Comparative genomic hybridization reveals previously undescribed amplifications and deletions in the chronic myeloid leukemia-derived K-562 cell line.
Genes, chromosomes & cancer 1997;19(1):36-42.
1996: M A Kennedy; S A Rowland; A L Miller; Christine Morris; L A Neville; A Dodd; W J Fifield; Donald R Love
Structure and location of the murine adrenoleukodystrophy gene.
Genomics 1996;32(3):395-400.
1996: Christine Morris; A Jeffs; T Smith; M McDonald; P Board; M Kennedy; P Fitzgerald
BCR gene recombines with genomically distinct sites on band 11Q13 in complex BCR-ABL translocations of chronic myeloid leukemia.
Oncogene 1996;12(3):677-85.
1996: J Borrow; A M Shearman; V P Stanton; R Becher; T Collins; A J Williams; I Dubé; F Katz; Y L Kwong; Christine Morris; K Ohyashiki; K Toyama; J Rowley; David E Housman
The t(7;11)(p15;p15) translocation in acute myeloid leukaemia fuses the genes for nucleoporin NUP98 and class I homeoprotein HOXA9.
Nature genetics 1996;12(2):159-67.
1996: G R Hill; D N Hart; A F Moore; Christine Morris
Donor leukocyte infusions in the treatment of chronic myeloid leukemia in relapse post bone marrow transplantation.
Pathology 1996;28(1):51-3.
1996: P H Fitzgerald; Christine Morris
A greater incidence of complex translocations in myeloid leukemias than in lymphomas and lymphoid leukemias associated with IGH rearrangement.
Cancer genetics and cytogenetics 1996;86(1):8-12.
1996: C G Print; Christine Morris; N K Spurr; L Rooke; Geoffrey W Krissansen
The CG-1 gene, a member of the kinectin and ES/130 family, maps to human chromosome band 14q22.
Immunogenetics 1996;43(4):227-9.
1995: Christine Morris; Suzanne M Benjes; Leena Haataja; David Ledbetter; Nora Heisterkamp; John Groffen
Spatial organization of ABR and CRK genes on human chromosome band 17p13.3.
Oncogene 1995;10(5):1009-11.
1994: M A Kennedy; J C Rayner; Christine Morris
Genomic structure, promoter sequence, and revised translation of human homeobox gene HLX1.
Genomics 1994;22(2):348-55.
1994: Kathryn E Crosier; L R Hall; P M Lewis; Christine Morris; Clive R Wood; J C Morris; Philip S Crosier
Isolation and characterization of the human DTK receptor tyrosine kinase.
Growth factors (Chur, Switzerland) 1994;11(2):137-44.
1994: Philip S Crosier; P M Lewis; L R Hall; Maria R Vitas; Christine Morris; David Beier; Clive R Wood; Kathryn E Crosier
Isolation of a receptor tyrosine kinase (DTK) from embryonic stem cells: structure, genetic mapping and analysis of expression.
Growth factors (Chur, Switzerland) 1994;11(2):125-36.
1993: J ten Hoeve; Christine Morris; A Poustka; John Groffen; Nora Heisterkamp
Isolation of NotI sites from chromosome 22q11.
Genomics 1993;18(3):588-97.
1993: T Fioretos; Nora Heisterkamp; John Groffen; Suzanne M Benjes; Christine Morris
CRK proto-oncogene maps to human chromosome band 17p13.
Oncogene 1993;8(10):2853-5.
1993: J ten Hoeve; Christine Morris; Nora Heisterkamp; John Groffen
Isolation and chromosomal localization of CRKL, a human crk-like gene.
Oncogene 1993;8(9):2469-74.
1993: Stephen J Sowerby; M A Kennedy; P H Fitzgerald; Christine Morris
DNA sequence analysis of the major breakpoint cluster region of the BCR gene rearranged in Philadelphia-positive human leukemias.
Oncogene 1993;8(6):1679-83.
1993: Christine Morris; C Courtay; A Geurts van Kessel; J ten Hoeve; Nora Heisterkamp; John Groffen
Localization of a gamma-glutamyl-transferase-related gene family on chromosome 22.
Human genetics 1993;91(1):31-6.
1993: Christine Morris; M P Bodger
Localization of the human poly(A)-binding protein gene (PAB1) to chromosomal regions 3q22-q25, 12q13-q14, and 13q12-q13 by in situ hybridization.
Genomics 1993;15(1):209-11.
1993: John Groffen; JW Voncken; Vesa Kaartinen; Christine Morris; Nora Heisterkamp
Ph-positive leukemia: a transgenic mouse model.
Leukemia & lymphoma 1993;11 Suppl 1():19-24.
1992: Christine Morris; P H Fitzgerald
Assignments of polymorphic loci on chromosome 13 refined by in situ hybridization.
Genomics 1992;12(4):852-3.
1992: JW Voncken; Christine Morris; Paul K Pattengale; G Dennert; C Kikly; John Groffen; Nora Heisterkamp
Clonal development and karyotype evolution during leukemogenesis of BCR/ABL transgenic mice.
Blood 1992;79(4):1029-36.
1992: Christine Morris; N Heisterkamp; J Groffen; J C Williams; I Mononen
Chromosomal localization of the human glycoasparaginase gene to 4q32-q33.
Human genetics 1992;88(3):295-7.
1991: P H Fitzgerald; Christine Morris
Complex chromosomal translocations in the Philadelphia chromosome leukemias. Serial translocations or a concerted genomic rearrangement?
Cancer genetics and cytogenetics 1991;57(2):143-51.
1991: Christine Morris; J M Cochrane; Suzanne M Benjes; PE Crossen; P H Fitzgerald
Molecular definition of interstitial deletions of chromosome 13 in leukemic cells.
Genes, chromosomes & cancer 1991;3(6):455-60.
1991: Christine Morris; Nora Heisterkamp; John Groffen; P H Fitzgerald
Entire ABL gene is joined with 5'-BCR in some patients with Philadelphia-positive leukemia.
Blood 1991;78(4):1078-84.
1991: Christine Morris; M Kennedy; Nora Heisterkamp; L Columbano-Green; K Romeril; John Groffen; P Fitzgerald
A complex chromosome rearrangement forms the BCR-ABL fusion gene in leukemic cells with a normal karyotype.
Genes, chromosomes & cancer 1991;3(4):263-71.
1991: Christine Morris; Q L Hao; Nora Heisterkamp; P H Fitzgerald; John Groffen
Localization of the TRK proto-oncogene to human chromosome bands 1q23-1q24.
Oncogene 1991;6(6):1093-5.
1990: Christine Morris; Nora Heisterkamp; M A Kennedy; P H Fitzgerald; John Groffen
Ph-negative chronic myeloid leukemia: molecular analysis of ABL insertion into M-BCR on chromosome 22.
Blood 1990;76(9):1812-8.
1990: D DiSilvestre; Christine Morris; Nora Heisterkamp; John Groffen
A second hypervariable RFLP within the ABR gene.
Nucleic acids research 1990;18(19):5925.
1990: D DiSilvestre; Christine Morris; Nora Heisterkamp; John Groffen
A hypervariable RFLP within the ABR gene.
Nucleic acids research 1990;18(19):5924.
1990: N Heisterkamp; Christine Morris; L Sender; E Knoppel; L Uribe; M Y Cui; J Groffen
Rearrangement of the human ABL oncogene in a glioblastoma.
Cancer research 1990;50(11):3429-34.
1990: Christine Morris; N Heisterkamp; Q L Hao; J R Testa; J Groffen
The human tyrosine kinase gene (FER) maps to chromosome 5 and is deleted in myeloid leukemias with a del(5q).
Cytogenetics and cell genetics 1990;53(4):196-200.
1989: Nora Heisterkamp; Christine Morris; John Groffen
ABR, an active BCR-related gene.
Nucleic acids research 1989;17(21):8821-31.
1989: P H Fitzgerald; Christine Morris
The variable hematologic expression of the BCR-ABL genomic mutation and its possible determinants.
Cancer genetics and cytogenetics 1989;42(1):9-25.
1989: Christine Morris; L M Honeybone; P E Hollings; P H Fitzgerald
Localization of the SRC oncogene to chromosome band 20q11.2 and loss of this gene with deletion (20q) in two leukemic patients.
Blood 1989;74(5):1768-73.
1989: Christine Morris; P H Fitzgerald; M A Kennedy; P E Hollings; M Garry; G M Corbett
HRAS1 and INS genes are relocated but not structurally altered as a result of the t(7;11)(p15;p15) in a clone from a patient with acute myeloid leukaemia (M4).
British journal of haematology 1989;71(4):481-6.
1989: Christine Morris; J Bowen; P H Fitzgerald
Localization of human c-mos to chromosome band 8q11 in leukemic cells with the t(8;21) (q22;q22).
Human genetics 1989;81(4):339-42.
1989: M P Bodger; Christine Morris; M A Kennedy; J A Bowen; J M Hilton; P H Fitzgerald
Basophils (Bsp-1+) derive from the leukemic clone in human myeloid leukemias involving the chromosome breakpoint 9q34.
Blood 1989;73(3):777-81.
1989: M A Kennedy; Christine Morris; P H Fitzgerald
A sequence homologous to kappa-deleting element is located 5' to the human JK locus.
Nucleic acids research 1989;17(2):809.
1989: M A Kennedy; Christine Morris; P H Fitzgerald
The oncogene ETS1 is distant from the chromosome 11 breakpoint in leukaemic cells with the t(11;19)(q23;p13).
Leukemia research 1989;13(6):459-63.
1989: M A Kennedy; Christine Morris; P E Hollings; P H Fitzgerald
Involvement of immunoglobulin heavy- and light-chain (kappa) gene clusters in a human B-cell translocation, t(2;14).
Cytogenetics and cell genetics 1989;52(1-2):50-6.
1988: Christine Morris; I Rosman; S A Archer; J M Cochrane; P H Fitzgerald
A cytogenetic and molecular analysis of five variant Philadelphia translocations in chronic myeloid leukemia.
Cancer genetics and cytogenetics 1988;35(2):179-97.
1988: Christine Morris; P H Fitzgerald; P E Hollings; S A Archer; I Rosman; M E Beard; D C Heaton; C J Newhook
Essential thrombocythaemia and the Philadelphia chromosome.
British journal of haematology 1988;70(1):13-9.
1988: A E Reeve; Christine Morris; P H Fitzgerald
Acquired homozygosity of the rearranged bcr allele during the acute leukemic phase of a patient with Ph-negative chronic myeloid leukemia.
Blood 1988;72(1):24-8.
1988: Christine Morris; S E Whitham; P H Fitzgerald
Transposition of the oncogene c-ets-1 in a t(11;19)(q23;p13) cell line transient during clonal evolution of blast crisis chronic myeloid leukemia.
Leukemia 1988;2(2):74-8.
1987: P H Fitzgerald; M E Beard; Christine Morris; D C Heaton; A E Reeve
Ph-negative chronic myeloid leukaemia.
British journal of haematology 1987;66(3):311-4.
1987: P H Fitzgerald; Christine Morris; I Rosman; S A Archer; P E Hollings
Karyotypic evolution in a B-cell lymphoma.
Cancer genetics and cytogenetics 1987;24(2):271-9.
1987: Christine Morris; A E Reeve; P H Fitzgerald; P E Hollings; D C Heaton; M E Beard
Philadelphia chromosome negative CGL.
American journal of clinical pathology 1987;87(2):299-300.
1987: Christine Morris; P H Fitzgerald
Complexity of an apparently simple variant Ph translocation in chronic myeloid leukemia.
Leukemia research 1987;11(2):163-9.
1986: Christine Morris; A E Reeve; P H Fitzgerald; P E Hollings; M E Beard; D C Heaton
Genomic diversity correlates with clinical variation in Ph'-negative chronic myeloid leukaemia.
Nature 1986;320(6059):281-3.
1986: P H Fitzgerald; S A Archer; Christine Morris
Evidence for the repeated primary non-disjunction of chromosome 21 as a result of premature centromere division (PCD).
Human genetics 1986;72(1):58-62.
1985: Christine Morris; P H Fitzgerald
An evaluation of high resolution chromosome banding of hematologic cells by methotrexate synchronization and thymidine release.
Cancer genetics and cytogenetics 1985;14(3-4):275-84.
1984: Christine Morris; P H Fitzgerald; M A Neville; P J Wyld; M E Beard
Does multisomy of chromosome 1q confer a proliferative advantage in B-cell acute lymphoblastic leukemia?
Cancer 1984;54(1):48-53.
1984: Christine Morris; P H Fitzgerald
Karyotypic evolution in patients with acute myeloid leukemia.
Cancer genetics and cytogenetics 1984;11(2):143-52.
1984: P H Fitzgerald; Christine Morris
Telomeric association of chromosomes in B-cell lymphoid leukemia.
Human genetics 1984;67(4):385-90.
1983: P H Fitzgerald; Christine Morris; G J Fraser; L M Giles; J W Hamer; D C Heaton; M E Beard
Nonrandom cytogenetic changes in New Zealand patients with acute myeloid leukemia.
Cancer genetics and cytogenetics 1983;8(1):51-66.
1982: P H Fitzgerald; L M Giles; Christine Morris; D C Heaton; M E Beard
Cytogenetic studies of acute promyelocytic leukemia.
Cancer genetics and cytogenetics 1982;7(4):299-305.
1982: P H Fitzgerald; Christine Morris; L M Giles
Direct versus cultured preparation of bone marrow cells from 22 patients with acute myeloid leukemia.
Human genetics 1982;60(3):281-3.