Comparing genotyping algorithms for Illumina's Infinium whole-genome SNP BeadChips

- Ritchie, Matthew E., Ruijie, Liu, Kilpatrick, Trevor J., Lechner-Scott, Jeannette, Moscato, Pablo, Perreau, Victoria M., Rubio, Justin P., Scott, Rodney J., Stankovich, Jim, Stewart, Graeme J., Taylor, Bruce V., Wiley, James, Carvalho, Benilton S., Booth, David R., Clarke, Glynnis, Cox, Mathew B., Csurhes, Peter A., Danoy, Patrick, Dickinson, Joanne L., Drysdale, Karen, Field, Judith, Greer, Judith M., Griffiths, Lyn R., Irizarry, Rafael A., Guru, Preethi, Hadler, Johanna, Hoban, Ella, McMorran, Brendan J., Jensen, Cathy J., Johnson, Laura J., McCallum, Ruth, Merriman, Marilyn, Merriman, Tony, Polanowski, Andrea, Bahlo, Melanie, Pryce, Karena, Tajouri, Lotfi, Whittock, Lucy, Wilkins, Ella J., Browning, Brian L., Browning, Sharon R., Perera, Devindri, Butzkueven, Helmut, Carroll, William M., Chapman, Caron, Kermode, Allan G., Marriott, Mark, Mason, Deborah, Heard, Robert N., Pender, Michael P., Slee, Mark, Tubridy, Niall, Willoughby, Ernest, Broadley, Simon A., Brown, Matthew A., Foote, Simon J.

Microwaves for chromogenic in situ hybridization

- Leong, Anthony S. -Y., Haffajee, Zenobia

P53 in human melanoma fails to regulate target genes associated with apoptosis and the cell cycle and may contribute to proliferation

- Avery-Kiejda, Kelly A., Bowden, Nikola A., Hersey, Peter, Croft, Amanda J., Scurr, Lyndee L., Kairupan, Carla F., Ashton, Katie A., Talseth-Palmer, Bente A., Rizos, Helen, Zhang, Xu D., Scott, Rodney J.

A transcription factor map as revealed by a genome-wide gene expression analysis of whole-blood mRNA transcriptome in multiple sclerosis

- Riveros, Carlos, Mellor, Drew, Vucic, Stephen, Stewart, Graeme J., Williams, David W., Scott, Rodney J., Lechner-Scott, Jeannette, Booth, David R., Moscato, Pablo, ANZgene Multiple Sclerosis Genetics Consortium, Gandhi, Kaushal S., McKay, Fiona C., Cox, Mathew B., Berretta, Regina, Vaezpour, S. Yahya, Inostroza-Ponta, Mario, Broadley, Simon A., Heard, Robert N.

Application of serial analysis of gene expression to the study of human genetic disease

- Horan, Martin P.

Phenotypic expansion and further characterisation of the 17q21.31 microdeletion syndrome

- Tan, T. Y., Aftimos, S., Slavotinek, A., Hogue, J., Moeschler, J. B., Ozmore, J., Widmer, R., Savarirayan, R., Peters, G., Worgan, L., Susman, R., Wilson, M., Ghedia, S., Kirk, E. P., Love, D., Ronan, A., Darmanian, A.

RNA modulators of complex phenotypes in mammalian cells

- Lai, Angela, Cairns, Murray J., Tran, Nham, Zhang, Hong-Ping, Cullen, Lara, Arndt, Greg M.

The nutrigenomics of asthma: molecular mechanisms of airway neutrophilia following dietary antioxidant withdrawal

- Baines, Katherine J., Wood, Lisa G., Gibson, Peter G.

Electrochemical detection of short DNA sequences related to the Escherichia coli pathogen using a zirconia-modified screen-printed DNA biosensor

- Zuo, Shao-Hua, Zhang, Ling-Fan, Zhao, Yan-Hui, Yuan, Hui-Hui, Lan, Min-Bo, Lawrance, Geoffrey A., Wei, Gang

Selection of discriminative genes in microarray experiments using mathematical programming

- Berretta, Regina, Mendes, Alexandre, Moscato, Pablo

Genes related with Alzheimer's disease: a comparison of evolutionary search, statistical and integer programming approaches

- Moscato, Pablo Alberto, Berretta, Regina Esther, Hourani, Mou'ath, Mendes, Alexandre, Cotta, Carlos

Gene profiling in the amygdala in schizophrenia

- Weidenhofer, J., Bowden, N. A., Scott, R. J., Tooney, P. A.