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Bahlo, Melanie

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Replication of KIAA0350, IL2RA, RPL5 and CD58 as multiple sclerosis susceptibility genes in Australians 22 20 1
On the utility of data from the international HapMap project for Australian association studies 12 11 0
A Cav3.2 T-type calcium channel point mutation has splice-variant-specific effects on function and segregates with seizure expression in a polygenic rat model of absence epilepsy 53 53 0
The Advantages of dense marker sets for linkage analysis with very large families 11 11 0
A Polymorphism in the HLA-DPB1 gene is associated with susceptibility to multiple sclerosis 18 17 0
Multiple sclerosis susceptibility-associated SNPs do not influence disease severity measures in a cohort of Australian MS patients 27 25 0
SNP mapping and candidate gene sequencing in the class I region of the HLA complex : searching for multiple sclerosis susceptibility genes in Tasmanians 91 87 1
Evidence for a common genetic aetiology in high-risk families with multiple haematological malignancy subtypes 23 22 0
Heterogeneity at the HLA-DRB1 allelic variation locus does not influence multiple sclerosis disease severity, brain atrophy or cognition 19 19 0
Apolipoprotein genotype does not influence MS severity, cognition, or brain atrophy 24 24 0
Analysis of extended HLA haplotypes in multiple sclerosis and narcolepsy families confirms a predisposing effect for the class I region in Tasmanian MS patients 53 45 2
Mapping of the Plasmodium chabaudi resistance locus char2 12 11 0
Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20 29 28 1
Detecting genome wide haplotype sharing using SNP or microsatellite haplotype data 20 20 0
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Bahlo, Melanie

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