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Paraoxonase gene cluster is a genetic marker for early microvascular complications in Type 1 diabetes

Diabetic medicine, 2002-03, Vol.19 (3), p.212-215

2002

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A genome screen for linkage in Australian sibling-pairs with multiple sclerosis

Genes and immunity, 2002-12, Vol.3 (8), p.464-469

2002

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An investigation of polymorphisms in the 4q13.3-21.1 CXC chemokine gene cluster for association with multiple sclerosis in Australians

Multiple sclerosis, 2006-12, Vol.12 (6), p.710-722

2006

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A genome-wide screen for linkage disequilibrium in Australian HLA-DRB11501 positive multiple sclerosis patients

Journal of neuroimmunology, 2003-10, Vol.143 (1), p.60-64

2003

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CCR5 Genotyping in an Australian and New Zealand Type 1 Diabetes Cohort

Autoimmunity (Chur, Switzerland), 2002-01, Vol.35 (7), p.457-461

2002

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Lack of restriction of T cell receptor β variable gene usage in cerebrospinal fluid lymphocytes in acute optic neuritis

Journal of neurology, neurosurgery and psychiatry, 1999-11, Vol.67 (5), p.585-590

1999

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Association of common T cell activation gene polymorphisms with multiple sclerosis in Australian patients

Journal of neuroimmunology, 2004-03, Vol.148 (1), p.218-230

2004

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T cell receptor β chain genotyping in Australian relapsing-remitting multiple sclerosis patients

Multiple sclerosis, 2000-06, Vol.6 (3), p.140-147

2000

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The CCR5 Deletion Mutation Fails to Protect Against Multiple Sclerosis

Human immunology, 1997-11, Vol.58 (1), p.52-59

1997

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HLA-DQA1 AND -DQB1 GENOTYPING BY PCR-RFLP, HETERODUPLEX AND HOMODUPLEX ANALYSIS

European journal of immunogenetics, 1996-04, Vol.23 (2), p.107-120

1996

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Increased frequency of CCR-5 Delta 32 heterozygotes among long-term non-progressors with HIV-1 infection

AIDS (London), 1997-12, Vol.11 (15), p.1833-1838

1997

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Evaluation of the Apo-1/Fas promoter Mva 1 polymorphism in multiple sclerosis

Multiple sclerosis, 2000-02, Vol.6 (1), p.14-18

2000

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The usefulness of a rapid PCR methodology to detect rearranged Ig heavy chain genes in lymphoproliferative disease in a diagnostic setting

Pathology, 1995-10, Vol.27 (4), p.352-357

1995

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Evaluation of the Apo-I/Fas promoter Mva I polymorphism in multiple sclerosis

Multiple sclerosis, 2000-02, Vol.6 (1), p.14-18

2000

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HLA-DMB gene and HLA-DRA promoter region polymorphisms in Australian multiple sclerosis patients

Human immunology, 1999-09, Vol.60 (9), p.886-893

1999

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Assessment of HIV status using the polymerase chain reaction in antibody-positive patients and high-risk antibody-negative haemophiliacs

AIDS (London), 1991-02, Vol.5 (2), p.221-224

1991

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HLA-DR, -DQA1 and -DQB1 associations in Australian multiple sclerosis patients

European journal of immunogenetics, 1997-04, Vol.24 (2), p.81-92

1997

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Primary structure of a human glandular kallikrein gene

DNA (New York, N.Y.), 1987-10, Vol.6 (5), p.429-437

1987

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Identification of 11 novel and common single nucleotide polymorphisms in the interleukin-7 receptor-α gene and their associations with multiple sclerosis

European journal of human genetics : EJHG, 2003-07, Vol.11 (7), p.509-515

2003

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TAP2 polymorphisms in Australian multiple sclerosis patients

Journal of neuroimmunology, 1995-06, Vol.59 (1), p.113-121

1995

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An investigation of polymorphisms in the 4q1 3.3-21.1 CXC chemokine gene cluster for association with multiple sclerosis in Australians

Multiple sclerosis, 2006-12, Vol.12 (6), p.710-722

2006

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Increased frequency of CCR-5 Δ32 heterozygotes among long-term non-progressors with HIV-1 infection

AIDS (London), 1997-12, Vol.11 (15), p.1833-1838

1997

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A case of periodic fever and persistent splenomegaly in a 2-year-old boy

BMJ case reports, 2009, Vol.2009 (may25 1), p.bcr0620080098-bcr0620080098

2009

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Analysis of the CCL3-L1 gene for association with HIV-1 susceptibility and disease progression

AIDS (London), 2004-04, Vol.18 (7), p.1069-1071

2004

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Investigation of Epistasis Between the Serotonin Transporter and Norepinephrine Transporter Genes in Anorexia Nervosa

Neuropsychopharmacology, 2003-07, Vol.28 (7), p.1351-1355

2003

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Paraoxonase gene cluster is a genetic marker for early microvascular complications in Type 1 diabetes

A genome screen for linkage in Australian sibling-pairs with multiple sclerosis

An investigation of polymorphisms in the 4q13.3-21.1 CXC chemokine gene cluster for association with multiple sclerosis in Australians

A genome-wide screen for linkage disequilibrium in Australian HLA-DRB11501 positive multiple sclerosis patients

CCR5 Genotyping in an Australian and New Zealand Type 1 Diabetes Cohort

Lack of restriction of T cell receptor β variable gene usage in cerebrospinal fluid lymphocytes in acute optic neuritis

Association of common T cell activation gene polymorphisms with multiple sclerosis in Australian patients

T cell receptor β chain genotyping in Australian relapsing-remitting multiple sclerosis patients

The CCR5 Deletion Mutation Fails to Protect Against Multiple Sclerosis

HLA-DQA1 AND -DQB1 GENOTYPING BY PCR-RFLP, HETERODUPLEX AND HOMODUPLEX ANALYSIS

Increased frequency of CCR-5 Delta 32 heterozygotes among long-term non-progressors with HIV-1 infection

Evaluation of the Apo-1/Fas promoter Mva 1 polymorphism in multiple sclerosis

The usefulness of a rapid PCR methodology to detect rearranged Ig heavy chain genes in lymphoproliferative disease in a diagnostic setting

Evaluation of the Apo-I/Fas promoter Mva I polymorphism in multiple sclerosis

HLA-DMB gene and HLA-DRA promoter region polymorphisms in Australian multiple sclerosis patients

Assessment of HIV status using the polymerase chain reaction in antibody-positive patients and high-risk antibody-negative haemophiliacs

HLA-DR, -DQA1 and -DQB1 associations in Australian multiple sclerosis patients

Primary structure of a human glandular kallikrein gene

Identification of 11 novel and common single nucleotide polymorphisms in the interleukin-7 receptor-α gene and their associations with multiple sclerosis

TAP2 polymorphisms in Australian multiple sclerosis patients

An investigation of polymorphisms in the 4q1 3.3-21.1 CXC chemokine gene cluster for association with multiple sclerosis in Australians

Increased frequency of CCR-5 Δ32 heterozygotes among long-term non-progressors with HIV-1 infection

A case of periodic fever and persistent splenomegaly in a 2-year-old boy

Analysis of the CCL3-L1 gene for association with HIV-1 susceptibility and disease progression

Investigation of Epistasis Between the Serotonin Transporter and Norepinephrine Transporter Genes in Anorexia Nervosa

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