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Cancer Genetics Research
Group - Dr Peter Ganly
Publications
Ganly, P.S., Keeman, H., R.L., S., Smith, M.P., Patton, N., Merriman,
E.G. & Gibbons, S.S. Written advice can provide a safe and acceptable
alternative to a new patient assessment for selected referrals to haematologists Med
J Aust 188:9-12 (2008).
Ganly, P., Hanrahan, V., Baker, B. & Romeril, K. Identification
of JAK2V617F in patients with polycythemia is highly correlated with
conventional criteria for diagnosis of polycythemia vera. Am J Hematol 82,
80-2 (2007).
Gough, S.M., Benjes, S.M., McDonald, M., Heaton, D., Ganly, P. & Morris,
C.M. Translocation (5;10)(q22;q24) in a case of acute lymphoblastic leukemia. Cancer
Genet Cytogenet 165, 36-40 (2006).
Ganly, P. & Spearing, R. Treatment with intravenous immunoglobulin
is not a panacea but should be limited to those who can benefit. N
Z Med J 119, U2335 (2006).
Chambers, S.T., Sanders, J., Patton, W.N., Ganly, P., Birch, M., Crump,
J.A. & Spearing, R.L. Reduction of exit-site infections of tunnelled
intravascular catheters among neutropenic patients by sustained-release
chlorhexidine dressings: results from a prospective randomized controlled
trial. J Hosp Infect 61, 53-61 (2005).
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 Genet Cytogenet 149, 125-30. (2004).
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).
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. Br J Haematol 117,
878-81. (2002).
Mullin, J.L., Brennan, S.O., Ganly, P.S. & George, P.M. Fibrinogen
Hillsborough: a novel gammaGly309Asp dysfibrinogen with impaired clotting. Blood 99,
3597-601. (2002).
Carradice, D., Austin, N., Bayston, K. & Ganly, P.S. Successful
treatment of acute promyelocytic leukaemia during pregnancy. Clin
Lab Haematol 24, 307-11. (2002).
Whittle, A.T., Davis, M., Shovlin, C.L., Ganly, P.S., Haslett, C. & Greening,
A.P. Alveolar macrophage activity and the pulmonary complications of
haematopoietic stem cell transplantation. Thorax 56, 941-6.
(2001).
Jackson, G., Taylor, P., Smith, G.M., Marcus, R., Smith, A., Chu, P.,
Littlewood, T.J., Duncombe, A., Hutchinson, M., Mehta, A.B., Johnson,
S.A., Carey, P., MacKie, M.J., Ganly, P.S., Turner, G.E., Deane, M.,
Schey, S., Brookes, J., Tollerfield, S.M. & Wilson, M.P. A multicentre,
open, non-comparative phase II study of a combination of fludarabine
phosphate, cytarabine and granulocyte colony-stimulating factor in relapsed
and refractory acute myeloid leukaemia and de novo refractory anaemia
with excess of blasts in transformation. Br J Haematol 112,
127-37. (2001).
Ganly, P. & Beard, M. Osteoclasts in Paget's disease of bone. Br
J Haematol 113, 259. (2001).
McMullin, M.F., Hillmen, P., Jackson, J., Ganly, P. & Luzzatto,
L. Tissue plasminogen activator for hepatic vein thrombosis in paroxysmal
nocturnal haemoglobinuria. J Intern Med 235, 85-9 (1994).
Sundaresan, V., Ganly, P., Hasleton, P., Bleehen, N.M. & Rabbitts,
P. Paraffin wax-embedded material as a source of DNA for the detection
of somatic genetic changes. J Pathol 169, 43-52 (1993).
Rabbitts, P., Daly, M., Douglas, J., Ganly, P., Heppell-Parton, A. & Sundaresan,
V. Deletion mapping of chromosome 3 in lung tumours. Lung Cancer 9,
69-74 (1993).
Sundaresan, V., Ganly, P., Hasleton, P., Rudd, R., Sinha, G., Bleehen,
N.M. & Rabbitts, P. p53 and chromosome 3 abnormalities, characteristic
of malignant lung tumours, are detectable in preinvasive lesions of the
bronchus. Oncogene 7, 1989-97 (1992).
Ganly, P.S., Jarad, N., Rudd, R.M. & Rabbitts, P.H. PCR-based RFLP
analysis allows genotyping of the short arm of chromosome 3 in small
biopsies from patients with lung cancer. Genomics 12, 221-8
(1992).
Ganly, P.S. & Rabbitts, P.H. Polymerase chain reaction (PCR) for
detection of BamHI polymorphism at the THRB gene. Nucleic Acids Res 19,
3757 (1991).
Ganly, P.S. & Rabbitts, P.H. Polymerase chain reaction (PCR) for
detection of EcoRI polymorphism at the THRB gene. Nucleic Acids Res 19,
3760 (1991).
Ganly, P.S. & Rabbitts, P.H. PCR detection of the HindIII polymorphism
at the thyroid hormone receptor, beta, gene (THRB). Nucleic Acids
Res 19, 3761 (1991).
Ganly, P.S. & Rabbitts, P.H. Polymerase chain reaction (PCR) for
detection of MspI polymorphism at the D3S30 locus. Nucleic Acids
Res 19, 3757 (1991).
Ganly, P.S., Douglas, J. & Rabbitts, P.H. Polymerase chain reaction
(PCR) for detection of MspI polymorphism at the D3S3 locus. Nucleic
Acids Res 19, 3759 (1991).
Ganly, P.S., Douglas, J. & Rabbitts, P.H. Polymerase chain reaction
(PCR) for detection of MspI polymorphism at the D3S6 locus. Nucleic
Acids Res 19, 3759 (1991).
Ganly, P.S. & Rabbitts, P.H. Polymerase chain reaction (PCR) for
detection of MspI and DraI polymorphism at the THRB gene. Nucleic
Acids Res 19, 3760 (1991).
Ganly, P.S. & Rabbitts, P.H. Polymerase chain reaction (PCR) for
detection of MspI polymorphism at the D3S2 locus. Nucleic Acids Res 19,
3761 (1991).
Ganly, P.S. & Rabbitts, P.H. Polymerase chain reaction (PCR) for
detection of HindIII polymorphism at the D3F15S2 locus. Nucleic Acids
Res 19, 3758 (1991).
Ganly, P.S. & Rabbitts, P.H. Polymerase chain reaction (PCR) for
detection of RsaI polymorphism at the D3S32 locus. Nucleic Acids
Res 19, 3758 (1991).
Gibbons, B., Katz, F.E., Ganly, P. & Chessells, J.M. Infant acute
lymphoblastic leukaemia with t(11; 19). Br J Haematol 74, 264-9
(1990).
Dokal, I., Ganly, P., Riebero, I., Marsh, J., Steed, A., Kendra, J.,
Drysdale, C. & Hows, J. Late onset bone marrow failure associated
with proximal fusion of radius and ulna: a new syndrome. Br J Haematol 71,
277-80 (1989).
Ganly, P.S., Arthur, C., Goldman, J.M. & Schulenburg, W.E. Foscarnet
as treatment for cytomegalovirus retinitis following bone marrow transplantation. Postgrad
Med J 64, 389-91 (1988).
Ganly, P.S., Laffan, M.A., Owen, I. & Hows, J.M. Auto-anti-Jka
in Evans' syndrome with negative direct antiglobulin test. Br J Haematol 69,
537-9 (1988).
Ganly, P.S., Isaacs, J.D., Laffan, M.A., Haslett, C. & Hows, J.M.
Acquired factor VIII inhibitor associated with lung abscess. Br Med
J (Clin Res Ed) 295, 811 (1987
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