Macquarie University, Sydney Macquarie University ResearchOnline

Bahlo, Melanie

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The Advantages of dense marker sets for linkage analysis with very large families 98 77 0
Multiple sclerosis susceptibility-associated SNPs do not influence disease severity measures in a cohort of Australian MS patients 258 526 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 158 372 2
Detecting genome wide haplotype sharing using SNP or microsatellite haplotype data 99 111 0
Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20 1893 7027 2
Apolipoprotein genotype does not influence MS severity, cognition, or brain atrophy 123 311 0
SNP mapping and candidate gene sequencing in the class I region of the HLA complex : searching for multiple sclerosis susceptibility genes in Tasmanians 447 1036 1
Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci 488 1150 0
Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosis 1786 3526 0
Mapping of the Plasmodium chabaudi resistance locus char2 170 107 0
On the utility of data from the international HapMap project for Australian association studies 140 177 0
A Polymorphism in the HLA-DPB1 gene is associated with susceptibility to multiple sclerosis 556 1769 0
Comparing genotyping algorithms for Illumina's Infinium whole-genome SNP BeadChips 484 868 25
Identity-by-descent mapping to detect rare variants conferring susceptibility to Multiple Sclerosis 712 846 151
Replication of KIAA0350, IL2RA, RPL5 and CD58 as multiple sclerosis susceptibility genes in Australians 197 355 1
Saliva-derived DNA performs well in large-scale, high-density single-nucleotide polymorphism microarray studies 4135 3926 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 480 272 0
Evidence for a common genetic aetiology in high-risk families with multiple haematological malignancy subtypes 160 172 0
Heterogeneity at the HLA-DRB1 allelic variation locus does not influence multiple sclerosis disease severity, brain atrophy or cognition 460 469 0
A Transcription factor map as revealed by a genome-wide gene expression analysis of whole-blood mRNA transcriptome in multiple sclerosis 1004 4438 42
The Multiple sclerosis whole blood mRNA transcriptome and genetic associations indicate dysregulation of specific T cell pathways in pathogenesis 576 523 0
MicroRNAs miR-17 and miR-20a inhibit T cell activation genes and are under-expressed in MS whole blood 425 1948 20
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