L. Johnson

发表

Genetic dissection of the human leukocyte antigen region by use of haplotypes of Tasmanians with multiple sclerosis.

Terence Dwyer, Bruce Taylor, Terence P Speed, 2002, American journal of human genetics.

Cladribine Treatment for MS Preserves the Differentiative Capacity of Subsequently Generated Monocytes, Whereas Its Administration In Vitro Acutely Influences Monocyte Differentiation but Not Microglial Activation

T. Kilpatrick, L. Johnson, M. Binder, 2022, Frontiers in Immunology.

Replication of KIAA0350, IL2RA, RPL5 and CD58 as multiple sclerosis susceptibility genes in Australians

T. Speed, T. Kilpatrick, H. Butzkueven, 2008, Genes and Immunity.

Extended haplotype analysis in the HLA complex reveals an increased frequency of the HFE-C282Y mutation in individuals with multiple sclerosis

T. Speed, T. Kilpatrick, H. Butzkueven, 2004, Human Genetics.

Identification and Characterisation of cis-Regulatory Elements Upstream of the Human Receptor Tyrosine Kinase Gene MERTK

T. Kilpatrick, A. Harvey, L. Johnson, 2020, Brain plasticity.

Common and Low Frequency Variants in MERTK Are Independently Associated with Multiple Sclerosis Susceptibility with Discordant Association Dependent upon HLA-DRB1*15:01 Status

A. Fox, T. Kilpatrick, H. Butzkueven, 2016, PLoS genetics.

Analysis of extended HLA haplotypes in multiple sclerosis and narcolepsy families confirms a predisposing effect for the class I region in Tasmanian MS patients

T. Speed, E. Mignot, T. Kilpatrick, 2007, Immunogenetics.

Common and Low Frequency Variants in Mertk Are Independently Associated with Multiple Sclerosis Susceptibility with Discordant Association Dependent upon Hla-drb1 Low Frequency Variants in Mertk Are Independently Associated with Multiple Sclerosis Susceptibility with Discordant Association Dependent

A. Fox, T. Kilpatrick, H. Butzkueven, 2022 .

A Polymorphism in the HLA-DPB1 Gene Is Associated with Susceptibility to Multiple Sclerosis

Sharon R. Browning, Patrick Danoy, Melanie Bahlo, 2010, PloS one.

SNP mapping and candidate gene sequencing in the class I region of the HLA complex: searching for multiple sclerosis susceptibility genes in Tasmanians.

T. Speed, G. Stewart, D. Booth, 2007, Tissue antigens.

The MS Risk Allele of CD40 Is Associated with Reduced Cell-Membrane Bound Expression in Antigen Presenting Cells: Implications for Gene Function

G. Stewart, T. Kilpatrick, H. Butzkueven, 2015, PloS one.

Multiple Sclerosis Susceptibility-Associated SNPs Do Not Influence Disease Severity Measures in a Cohort of Australian MS Patients

M. Brown, T. Kilpatrick, H. Butzkueven, 2010, PloS one.

Repository Common and Low Frequency Variants in MERTK Are Independently Associated with Multiple Sclerosis Susceptibility with Discordant Association Dependent upon HLA-DRB 1 * 15 : 01 Status

A. Fox, T. Kilpatrick, H. Butzkueven, 2016 .

Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20

Pablo Moscato, Rodney J. Scott, Brian L. Browning, 2009, Nature Genetics.

Multiple sclerosis risk variants regulate gene expression in innate and adaptive immune cells

T. Speed, M. Brown, H. Butzkueven, 2020, Life Science Alliance.

On the utility of data from the International HapMap Project for Australian association studies

Terence P. Speed, Melanie Bahlo, Helmut Butzkueven, 2006, Human Genetics.

Saliva-derived DNA performs well in large-scale, high-density SNP microarray studies

Marilyn, Merriman, Booth, 2017 .

CSL324, a G-CSF receptor antagonist, blocks neutrophil migration markers that are upregulated in hidradenitis suppurativa.

M. Ng, G. Varigos, J. Field, 2023, The British journal of dermatology.