QUT - Academic profiles - Ms Lisa Anderson

Personal details

Senior Technologist (Sequencing)
Academic Division,
Research Portfolio,
Central Analytical Research Facility (CARF)

View location details(QUT staff and student access only)

For more publications by Lisa, explore their research in QUT ePrints (our digital repository).

Filter publications:

Fink, J. L., Jaradi, B., Stone, N., Anderson, L., Leo, P. J., Marshall, M., Ellis, J., Waring, P. M. & O'Byrne, K. (2023). Minimizing Sample Failure Rates for Challenging Clinical Tumor Samples. Journal of Molecular Diagnostics, 25(5), 263–273. https://eprints.qut.edu.au/244558

Li, Z., Wu, X., Leo, P. J., De Guzman, E., Akkoc, N., Breban, M., MacFarlane, G. J., Mahmoudi, M., Marzo-Ortega, H., Anderson, L. K., Wheeler, L., Chou, C. T., Harrison, A. A., Stebbings, S., Jones, G. T., Bang, S. Y., Wang, G., Jamshidi, A., Farhadi, E., Song, J., Lin, L., Li, M., Wei, J. C. C., Martin, N. G., Wright, M. J., Lee, M. J., Wang, Y., Zhan, J., Zhang, J. S., Wang, X., Jin, Z. B., Weisman, M. H., Gensler, L. S., Ward, M. M., Rahbar, M. H., Diekman, L., Kim, T. H., Reveille, J. D., Wordsworth, B. P., Xu, H. & Brown, M. A. (2021). Polygenic Risk Scores have high diagnostic capacity in ankylosing spondylitis. Annals of the Rheumatic Diseases, 80(9), 1168–1174. https://eprints.qut.edu.au/230168
McInerney-Leo, A. M., Chew, H. Y., Inglis, P. L., Leo, P. J., Joseph, S. R., Cooper, C. L., Okano, S., Hassall, T., Anderson, L. K., Bowman, R. V., Gattas, M., Harris, J. E., Marshall, M. S., Shaw, J. G., Wheeler, L., Yang, I. A., Brown, M. A., Fong, K. M., Simpson, F. & Duncan, E. L. (2021). Germline ERBB3 mutation in familial non-small-cell lung carcinoma: Expanding ErbB's role in oncogenesis. Human Molecular Genetics, 30(24), 2393–2401. https://eprints.qut.edu.au/232780

Watad, A., Rowe, H., Russell, T., Zhou, Q., Anderson, L. K., Khan, A., Dunsmuir, R., Loughenbury, P., Borse, V., Rao, A., Millner, P. A., Bragazzi, N. L., Amital, H., Cuhtbert, R., Wittmann, M., Sharif, K., Kenna, T., Brown, M. A., Newton, D., Bridgewood, C. & Mcgonagle, D. G. (2020). Normal human enthesis harbours conventional CD4+ and CD8+ T cells with regulatory features and inducible IL-17A and TNF expression. Annals of the Rheumatic Diseases, 79(8), 1044–1054. https://eprints.qut.edu.au/201824
McInerney-Leo, A. M., West, J., Wheeler, L., Leo, P. J., Summers, K. M., Anderson, L., Brown, M. A., West, M. & Duncan, E. L. (2020). Compound heterozygous mutations in FBN1 in a large family with Marfan syndrome. Molecular Genetics and Genomic Medicine, Article e1116, 8(3). https://eprints.qut.edu.au/232790
Gregson, C. L., Bergen, D. J. M., Leo, P., Sessions, R. B., Wheeler, L., Hartley, A., Youlten, S., Croucher, P. I., McInerney-Leo, A. M., Fraser, W., Tang, J. C. Y., Anderson, L., Marshall, M., Sergot, L., Paternoster, L., Davey Smith, G., Brown, M. A., Hammond, C., Kemp, J. P., Tobias, J. H., Duncan, E. L. & other (2020). A Rare Mutation in SMAD9 Associated With High Bone Mass Identifies the SMAD-Dependent BMP Signaling Pathway as a Potential Anabolic Target for Osteoporosis. Journal of Bone and Mineral Research, 35(1), 92–105. https://eprints.qut.edu.au/232797

Johnson, S., Ellis, J., Leo, P., Anderson, L., Ganti, U., Harris, J., Curran, J., McInerney-Leo, A., Paramalingam, N., Song, S., Conwell, L., Harris, M., Jones, T., Brown, M., Davis, E. & Duncan, E. (2019). Comprehensive genetic screening: The prevalence of maturity-onset diabetes of the young gene variants in a population-based childhood diabetes cohort. Pediatric Diabetes, 20(1), 57–64. https://eprints.qut.edu.au/124018

De Smit, E., Lukowski, S., Anderson, L., Senabouth, A., Dauyey, K., Song, S., Wyse, B., Wheeler, L., Chen, C., Cao, K., Brown, M. & other (2018). Longitudinal expression profiling of CD4+ and CD8+ cells in patients with active to quiescent giant cell arteritis. BMC Medical Genomics, Article 61, 11, 1–16. https://eprints.qut.edu.au/121734
McInerney-Leo, A., Wheeler, L., Sturm, R., Tan, J., Harris, J., Anderson, L., Jagirdar, K., Brown, M., Leo, P., Soyer, H. P. & Duncan, E. (2018). Point mutation in p14ARF-specific exon 1Beta of CDKN2A causing familial melanoma and astrocytoma (Research Letter). British Journal of Dermatology, 178(4), e263-e264. https://eprints.qut.edu.au/117537
Johnson, S., Leo, P., McInerney-Leo, A., Anderson, L., Clout, M., McGown, I., Newell, F., Brown, M., Conwell, L., Harris, M. & Duncan, E. (2018). Whole-exome sequencing for mutation detection in pediatric disorders of insulin secretion: Maturity onset diabetes of the young and congenital hyperinsulinism. Pediatric Diabetes, 19(4), 656–662.

Benyamin, B., He, J., Zhao, Q., Gratten, J., Garton, F., Leo, P., Liu, Z., Mangelsdorf, M., Al-Chalabi, A., Anderson, L., Cremin, K., Harris, J., Song, S., Wheeler, L., Brown, M. & other (2017). Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis. Nature Communications, Article 611, 8, 1–7. https://eprints.qut.edu.au/108267
Li, Z., Haynes, K., Pennisi, D., Anderson, L., Song, X., Thomas, G., Kenna, T., Leo, P. & Brown, M. (2017). Epigenetic and gene expression analysis of ankylosing spondylitis-associated loci implicate immune cells and the gut in the disease pathogenesis. Genes and Immunity, 18(3), 135–143. https://eprints.qut.edu.au/108118
Gratten, J., Zhao, Q., Benyamin, B., Garton, F., He, J., Leo, P., Mangelsdorf, M., Anderson, L., Zhang, Z., Chen, L., Cremin, K., Harris, J., Clout, M., Song, S., Wheeler, L., Brown, M. & other (2017). Whole-exome sequencing in amyotrophic lateral sclerosis suggests NEK1 is a risk gene in Chinese. Genome Medicine, Article 97, 9, 1–9. https://eprints.qut.edu.au/130240

A complete list of publications is available at: https://www.qut.edu.au/about/our-people/academic-profiles/lisa.anderson