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Bahlo, Melanie

Bahlo, Melanie

Lin, Enmoore, Pappenfuss, Tony, Tan, Rachel B, Senyschyn, Danielle, Bahlo, Melanie, Speed, Terence P, Foote, Simon J, . American Society for Microbiology; 2006. Mapping of the Plasmodium chabaudi resistance locus char2.
Stankovich, Jim, Cox, Charles J, Speed, Terence P, Roses, Allen D, Bahlo, Melanie, Foote, Simon J, Tan, Rachel B, Montgomery, Douglas S, Huxtable, Stewart J, Rubio, Justin P, Ehm, Margaret G, Johnson, Laura J, Butzkueven, Helmut, Kilpatrick, Trevor J, . Springer; 2006. On the utility of data from the international HapMap project for Australian association studies.
Rubio, Justin P, Stankovich, Jim, Varney, Michael D, Speed, Terence P, Taylor, Bruce V, Foote, Simon J, Butzkueven, Helmut, Kilpatrick, Trevor J, Field, Judith, Tubridy, Niall, Marriott, Mark, Chapman, Caron, Bahlo, Melanie, Perera, Devindri, Johnson, Laura J, Tait, Brian D, . Nature Publishing Group; 2008. Replication of KIAA0350, IL2RA, RPL5 and CD58 as multiple sclerosis susceptibility genes in Australians.
Field, Judith, Browning, Sharon R, Stewart, Graeme J, Kilpatrick, Trevor J, Foote, Simon J, Bahlo, Melanie, Butzkueven, Helmut, Wiley, James, Booth, David R, Taylor, Bruce V, Brown, Matthew A, Rubio, Justin P, Johnson, Laura J, Stankovich, Jim, Danoy, Patrick, Varney, Michael D, Tait, Brian D, Gandhi, Kaushal S, Charlesworth, Jac C, Heard, Robert N, ANZgene MS Genetics Consortium,, . Public Library of Science; 2010. A Polymorphism in the HLA-DPB1 gene is associated with susceptibility to multiple sclerosis.
Rubio, Justin P, Bahlo, Melanie, Kilpatrick, Trevor J, Mignot, Emmanuel, Foote, Simon J, Stankovich, Jim, Burfoot, Rachel K, Johnson, Laura J, Huxtable, Stewart, Butzkueven, Helmut, Lin, Ling, Taylor, Bruce V, Speed, Terence P, . Springer; 2007. Analysis of extended HLA haplotypes in multiple sclerosis and narcolepsy families confirms a predisposing effect for the class I region in Tasmanian MS patients.
Thomson, Russell, Quinn, Stephen, McKay, James, Silver, Jeremy, Bahlo, Melanie, FitzGerald, Liesel, Foote, Simon J, Dickinson, Joanne, Stankovich, Jim, . Springer; 2007. The Advantages of dense marker sets for linkage analysis with very large families.
Burfoot, Rachel K, Jensen, Cathy J, Taylor, Bruce V, Speed, Terence P, Heard, R, Stewart, Graeme J, Foote, Simon J, Kilpatrick, Trevor J, Rubio, Justin P, Field, Judith, Stankovich, Jim, Varney, M. D, Johnson, Laura J, Butzkueven, Helmut, Booth, David R, Bahlo, Melanie, Tait, B. D, . Wiley-Blackwell Publishing; 2008. SNP mapping and candidate gene sequencing in the class I region of the HLA complex : searching for multiple sclerosis susceptibility genes in Tasmanians.
Powell, Kim L, Cain, Stuart M, Foote, Simon J, Snutch, Terrance P, O'Brien, Terence J, Ng, Caroline, Sirdesai, Shreerang, David, Laurence S, Kyi, Mervyn, Garcia, Esperanza, Tyson, John R, Reid, Christopher A, Bahlo, Melanie, . Society for Neuroscience; 2009. 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.
Bahlo, Melanie, Booth, David R, Rubio, Justin P, Scott, Rodney J, Stankovich, Jim, Stewart, Graeme J, Taylor, Bruce V, Wiley, James, Clarke, Glynnis, Cox, Mathew B, Csurhes, Peter A, Danoy, Patrick, Broadley, Simon A, Drysdale, Karen, Field, Judith, Greer, Judith M, Guru, Preethi, Hadler, Johanna, McMorran, Brendan J, Jensen, Cathy J, Johnson, Laura J, McCallum, Ruth, Merriman, Marilyn, Brown, Matthew A, Merriman, Tony, Pryce, Karen, Tajouri, Lotfi, Wilkins, Ella J, Browning, Brian L, Browning, Sharon R, Perera, Devindri, Willoughby, Ernest, Butzkueven, Helmut, Carroll, William M, Foote, Simon J, Chapman, Caron, Kermode, Allan G, Marriott, Mark, Mason, Deborah, Heard, Robert N, Pender, Michael P, Slee, Mark, Tubridy, Niall, Griffiths, Lyn R, Kilpatrick, Trevor J, Lechner-Scott, Jeanette, Moscato, Pablo, Perreau, Victoria M, . Nature Publishing Group; 2009. Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20.
Jensen, Cathy J, Stankovich, Jim, Field, Judith, Danoy, Patrick, Brown, Matthew A, Rubio, Justin P, Butzkueven, Helmut, Consortium, ANZgene MS Genetics, van der Walt , Anneke, Bahlo, Melanie, Taylor, Bruce V, van der Mei, Ingrid A. F, Foote, Simon J, Kilpatrick, Trevor J, Johnson, Laura J, Wilkins, Ella, . Public Library of Science; 2010. Multiple sclerosis susceptibility-associated SNPs do not influence disease severity measures in a cohort of Australian MS patients.
van der Walt, Anneke, Stankovich, Jim, Bahlo, Melanie, Taylor, Bruce V, Van Der Mei, Ingrid A. F, Foote, Simon J, Kilpatrick, Trevor J, Rubio, Justin P, Butzkueven, Helmut, . Lippincott Williams & Wilkins; 2009. Apolipoprotein genotype does not influence MS severity, cognition, or brain atrophy.
Tegg, Elizabeth M, Thomson, Russell J, Lowenthal, Ray M, Foote, Simon J, Dickinson, Joanne L, Stankovich, Jim, Banks, Annette, Flowers, Ceri, McWhirter, Rebekah, Panton, Jean, Piaszczyk, Anne, Bahlo, Melanie, Marsden, Katherine A, . Wiley-Blackwell Publishing; 2010. Evidence for a common genetic aetiology in high-risk families with multiple haematological malignancy subtypes.
van der Walt, Anneke, Stankovich, Jim, Bahlo, Melanie, Taylor, Bruce V, van der Mei, Ingrid A. F, Foote, Simon J, Rubio, Justin P, Kilpatrick, Trevor J, Butzkueven, Helmut, . Sage Publications; 2011. Heterogeneity at the HLA-DRB1 allelic variation locus does not influence multiple sclerosis disease severity, brain atrophy or cognition.
Bahlo, Melanie, Stankovich, Jim, Speed, Terence P, Rubio, Justin P, Burfoot, Rachel K, Foote, Simon J, . Springer Verlag; 2006. Detecting genome wide haplotype sharing using SNP or microsatellite haplotype data.