Below are links to publications from our collaborative research. Please feel free to contact us to discuss how we can assist with your research interests.

2016

• Anderson C, Khan MA, Catanzariti AM, Jack CA, Nemri A, Lawrence GJ, Upadhyaya NM, Hardham AR, Ellis JG, Dodds PN, Jones DA. 2016. Genome analysis and avirulence gene cloning using a high-density RADseq linkage map of the flax rust fungus, Melampsora lini. BMC Genomics 17:667.
• Fraser CI, McGaughran A, Chuah A, Waters JM. 2016. The importance of replicating genomic analyses to verify phylogenetic signal for recently evolved lineages. Molecular Ecology 25(15):3683-3695.
• Galgamuwa R, Hardy K, Dahlstrom JE, Blackburn AC, Wium E, Rooke M, Cappello JY, Tummala P, Patel HR, Chuah A, Tian L, McMorrow L, Board PG, Theodoratos A. 2016. Dichloroacetate Prevents Cisplatin-Induced Nephrotoxicity without Compromising Cisplatin Anticancer Properties. Journal of the American Society of Nephrology 27(11):3331-3344.
• Lamb TD, Patel H, Chuah A, Natoli RC, Davies WIL, Hart NS, Collin SP, Hunt DM. 2016. Evolution of Vertebrate Phototransduction: Cascade Activation. Molecular Biology and Evolution 33 (8): 2064-2087.
• Nicotra AB, Chong C, Bragg JG, Ong CR, Aitken NC, Chuah A, Lepschi B, Borevitz JO. 2016. Population and phylogenomic decomposition via genotyping-by-sequencing in Australian Pelargonium. Molecular Ecology 25(9):2000-2014.
• Onyango MG, Aitken NC, Jack C, Chuah A, Oguya J, Djikeng A, Kemp S, Bellis GA, Nicholas A, Walker PJ, Duchemin J-B. 2016. Genotyping of whole genome amplified reduced representation libraries reveals a cryptic population of Culicoides brevitarsis in the Northern Territory, Australia. BMC Genomics 17:769.
• Vélez JI, Lopera F, Sepulveda-Falla D, Patel HR, Johar AS, Chuah A, Tobón C, Rivera D, Villegas A, Cai Y, et al. 2016. APOE*E2 allele delays age of onset in PSEN1 E280A. Alzheimer's disease. Molecular Psychiatry 21(7):916-924.

2015

• Field MA, Cho V, Cook MC, Enders A, Vinuesa CG, Whittle B, Andrews TD, Goodnow CC. 2015. Reducing the search space for causal genetic variants with VASP: Variant Analysis of Sequenced Pedigrees. Bioinformatics 31(14):2377-2379.
• Johar AS, Mastronardi C, Rojas-Villarraga A, Patel HR, Chuah A, Peng K, Higgins A, Milburn P, Palmer S, Silva-Lara MF, et al. 2015. Novel and rare functional genomic variants in multiple autoimmune syndrome and Sjögren’s syndrome. Journal of Translational Medicine 13 (1): 173.
• Padovan A, Patel HR, Chuah A, Huttley GA, Krause ST, Degenhardt J, Foley WJ, Külheim C. 2015. Transcriptome Sequencing of Two Phenotypic Mosaic Eucalyptus Trees Reveals Large Scale Transcriptome Re-Modelling. PLoS One. 10(5):e0123226
• Trivedi S, Neeman T, Jackson RJ, Ranasinghe R, Jack C, Ranasinghe C. 2015. Identification of biomarkers to measure HIV-specific mucosal and systemic CD8(+) T-cell immunity using single cell Fluidigm 48.48 Dynamic arrays. Vaccine 33(51):7315-7327.
• Vélez  JI, Jack CA, Chuah A, Buckley B, Correa JC, Easteal S, Arcos-Burgos M. 2015. Cross validation of pooling/resampling GWAS using the WTCCC data. Molecular Biology and Genetic Engineering 3:1.

2014

• Clancy JL, Patel HR, Hussein SM, Tonge PD, Cloonan N, Corso AJ, Li M, Lee DS, Shin JY, Wong JJ, et al. 2014. Small RNA changes en route to distinct cellular states of induced pluripotency. Nature communications 5:5522.
• Paz-Filho G, Boguszewski MC, Mastronardi CA, Patel HR, Johar AS, Chuah A, Huttley GA, Boguszewski CL, Wong ML, Arcos-Burgos M, Licinio J. 2014. Whole exome sequencing of extreme morbid obesity patients: translational implications for obesity and related disorders. Genes 5 (3), 709-725

2013 and earlier

• Nekrasov M, Soboleva TA, Jack C, Tremethick DJ. 2013. Histone variant selectivity at the transcription start site: H2A. Z or H2A. Lap1. Nucleus 4 (6): 431-437.
• Nekrasov M, Amrichova J, Parker BJ, Soboleva TA, Jack C, Williams R, Huttley GA, Tremethick DJ. 2012. Histone H2A. Z inheritance during the cell cycle and its impact on promoter organization and dynamics. Nature structural & molecular biology 19 (11): 1076-1083.
• Redon R, Ishikawa S, Fitch KR, Feuk L, Perry GH, Andrews TD, Fiegler H, Shapero MH, Carson AR, et al. 2006. Global variation in copy number in the human genome. Nature 444 (7118): 444-454