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 99 78 0
Multiple sclerosis susceptibility-associated SNPs do not influence disease severity measures in a cohort of Australian MS patients 261 529 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 160 374 2
Detecting genome wide haplotype sharing using SNP or microsatellite haplotype data 101 113 0
Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20 1901 7035 2
Apolipoprotein genotype does not influence MS severity, cognition, or brain atrophy 125 313 0
SNP mapping and candidate gene sequencing in the class I region of the HLA complex : searching for multiple sclerosis susceptibility genes in Tasmanians 452 1041 1
Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci 501 1163 0
Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosis 1799 3539 0
Mapping of the Plasmodium chabaudi resistance locus char2 173 110 0
On the utility of data from the international HapMap project for Australian association studies 142 179 0
A Polymorphism in the HLA-DPB1 gene is associated with susceptibility to multiple sclerosis 562 1775 0
Comparing genotyping algorithms for Illumina's Infinium whole-genome SNP BeadChips 488 872 25
Identity-by-descent mapping to detect rare variants conferring susceptibility to Multiple Sclerosis 713 847 151
Replication of KIAA0350, IL2RA, RPL5 and CD58 as multiple sclerosis susceptibility genes in Australians 200 358 1
Saliva-derived DNA performs well in large-scale, high-density single-nucleotide polymorphism microarray studies 4147 3938 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 483 275 0
Evidence for a common genetic aetiology in high-risk families with multiple haematological malignancy subtypes 161 173 0
Heterogeneity at the HLA-DRB1 allelic variation locus does not influence multiple sclerosis disease severity, brain atrophy or cognition 462 471 0
A Transcription factor map as revealed by a genome-wide gene expression analysis of whole-blood mRNA transcriptome in multiple sclerosis 1017 4452 43
The Multiple sclerosis whole blood mRNA transcriptome and genetic associations indicate dysregulation of specific T cell pathways in pathogenesis 579 526 0
MicroRNAs miR-17 and miR-20a inhibit T cell activation genes and are under-expressed in MS whole blood 428 1951 20
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