Items where Subject is "Australian and New Zealand Standard Research Classification > MEDICAL AND HEALTH SCIENCES (110000) > CLINICAL SCIENCES (110300) > Medical Genetics (excl. Cancer Genetics) (110311)"
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Number of items at this level: 15.
Binder, M. D., Fox, A. D., Merlo, D., Johnson, L. J., Giuffrida, L., Calvert, S. E., et al. (2016) Common and low frequency variants in MERTK are independently associated with Multiple Sclerosis susceptibility with discordant association dependent upon HLA-DRB1*15:01 status. PLoS ONE, 12(3), e1005853.
Bodea, C. A., Neale, B. M., Ripke, S., Barclay, M., Peyrin-Biroulet, L., Chamaillard, M., et al. (2016) A method to exploit the structure of genetic ancestry space to enhance case-control studies. American Journal of Human Genetics, 98(5), pp. 857-868.
Briers, Stephanie, Crawford, Catherine, Bickmore, Wendy A., & Sutherland, Heidi G. (2009) KRAB zinc-finger proteins localise to novel KAP1-containing foci that are adjacent to PML nuclear bodies. Journal of Cell Science, 122(7), pp. 937-946.
Connor, Jason P., Young, Ross McD., Lawford, Bruce R., Saunders, John B., Ritchie, Terry L., & Noble, Ernest P. (2007) Heavy nicotine and alcohol use in alcohol dependence is associated with D2 dopamine receptor (DRD2) polymorphism. Addictive Behaviors, 32(2), pp. 310-319.
Ellinghaus, D., Jostins, L., Spain, S. L., Cortes, A., Bethune, J., Han, B., et al. (2016) Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. Nature Genetics, 48(5), pp. 510-518.
Gilmore, Linda, Good, Lisa, Leong, Eliza Weiqin, Heussler, Helen, & Bowling, Francis (2013) Variable phenotype in 16p duplication within a family. In 16th SSBP International Research Symposium, 12-14 September 2013, Stellenbosch, South Africa.
Graves, Nicholas, Weinhold, Diana, Tong, Edward, Birrell, Frances A., Doidge, Shane R., Ramritu, Prabha, et al. (2007) The Effect of Healthcare-Acquired Infection on Length of Hospital Stay and Cost. Infection Control and Hospital Epidemiology, 28(3), pp. 280-292.
Kenna, Tony J., Hanson, Aimee, Costello, Mary-Ellen, & Brown, Matthew A. (2016) Functional genomics and its bench-to-bedside translation pertaining to the identified susceptibility alleles and loci in Ankylosing Spondylitis. Current Rheumatology Reports, 18(63).
Lau, Max C., Keith, Patricia, Costello, Mary-Ellen, Bradbury, Linda, Hollis, Kelly A., Thomas, Ranjeny, et al. (2016) Genetic association of ankylosing spondylitis with TBX21 influences T-bet and pro-inflammatory cytokine expression in humans and SKG mice as a model of spondyloarthritis. Annals of the Rheumatic Diseases. (In Press)
Pecheniuk, Natalie Maria, Deguchi, Hiroshi, Elias, Darlene, Xu, Xiao, & Griffin, John (2006) Cholesteryl ester transfer protein genotypes associated with venous thrombosis and dyslipoproteinemia in males. Journal Of Thrombosis And Haemostasis, 4(9), pp. 2080-2082.
Pradeepa, Madapura M., Sutherland, Heidi G., Ule, Jernej, Grimes, Graeme R., & Bickmore, Wendy A. (2012) Psip1/Ledgf p52 binds methylated histone H3K36 and splicing factors and contributes to the regulation of alternative splicing. PLoS Genetics, 8(5), e1002717.
Rautanen, Anna, Pirinen, Matti, Mills, Tara C., Rockett, Kirk A., Strange, Amy, Ndungu, Anne W., et al. (2016) Polymorphism in a lincRNA associates with a doubled risk of pneumococcal bacteremia in Kenyan children. American Journal of Human Genetics, 98(6), pp. 1092-1100.
Sutherland, Heidi & Bickmore, Wendy A. (2009) Transcription factories : gene expression in unions? Nature Reviews Genetics, 10(7), pp. 457-466.
Thomas, G.P., Willner, D., Robinson, P.C., Cortes, A., Duan, R., Rudwaleit, M., et al. (2016) Genetic diagnostic profiling in axial spondyloarthritis: a real world study. Clinical and Experimental Rheumatology. (In Press)
Wagschal, Alexandre, Sutherland, Heidi G., Woodfine, Kathryn, Henckel, Amandine, Chebli, Karim, Schulz, Reiner, et al. (2008) G9a histone methyltransferase contributes to imprinting in the mouse placenta. Molecular and Cellular Biology, 28(3), pp. 1104-1113.