QUT - Academic profiles - Mrs Mhairi Clout

Personal details

Positions

Bioinformatician
Faculty of Health,
School of Biomedical Sciences

mhairi.marshall@qut.edu.au

View location details(QUT staff and student access only)

Research field

Medical biochemistry and metabolomics, Medical microbiology

Field of Research code, Australian and New Zealand Standard Research Classification (ANZSRC), 2020

Qualifications

MSc in Information Technology (University of Glasgow)

Publications

QUT ePrints

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

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2023

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

2021

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
Graff, S. M., Johnson, S. R., Leo, P. J., Dadi, P. K., Dickerson, M. T., Nakhe, A. Y., McInerney-Leo, A. M., Marshall, M., Zaborska, K. E., Schaub, C. M., Brown, M. A., Jacobson, D. A. & Duncan, E. L. (2021). A KCNK16 mutation causing TALK-1 gain of function is associated with maturity-onset diabetes of the young. JCI Insight, Article e138057, 6(13). https://eprints.qut.edu.au/232781
Seabrook, A. J., Harris, J. E., Velosa, S. B., Kim, E., McInerney-Leo, A. M., Dwight, T., Hockings, J. I., Hockings, N. G., Kirk, J., Leo, P. J., Love, A. J., Luxford, C., Marshall, M., Mete, O., Pennisi, D. J., Brown, M. A., Gill, A. J., Hockings, G. I., Clifton-Bligh, R. J. & Duncan, E. L. (2021). Multiple Endocrine Tumors Associated with Germline MAX Mutations: Multiple Endocrine Neoplasia Type 5? Journal of Clinical Endocrinology and Metabolism, 106(4), e1163-e1182. https://eprints.qut.edu.au/232788

2020

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

2019

Gorvin, C., Ahmad, B., Stechman, M., Loh, N., Hough, T., Leo, P., Clout, M., Sethi, S., Bentley, L., Piret, S., Reed, A., Jeyabalan, J., Christie, P., Wells, S., Simon, M., Mallon, A., Schulz, H., Huebner, N., Brown, M., Cox, R., Brown, S. & Thakker, R. (2019). An N-ethyl-N-nitrosourea (ENU)-induced Tyr265Stop mutation of the DNA polymerase accessory subunit gamma 2 (Polg2) is associated with renal calcification in mice. Journal of Bone and Mineral Research, 34(3), 497–507. https://eprints.qut.edu.au/124004
Asquith, M., Sternes, P., Costello, M., Karstens, L., Diamond, S., Martin, T., Li, Z., Clout, M., Spector, T., Le Cao, K., Rosenbaum, J. & Brown, M. (2019). HLA alleles associated with risk of ankylosing spondylitis and rheumatoid arthritis influence the gut microbiome. Arthritis and Rheumatology, 71(10), 1642–1650. https://eprints.qut.edu.au/132047
Gorvin, C. M., Loh, N. Y., Stechman, M. J., Falcone, S., Hannan, F. M., Ahmad, B. N., Piret, S. E., Reed, A. A. C., Jeyabalan, J., Leo, P., Marshall, M., Sethi, S., Bass, P., Roberts, I., Sanderson, J., Wells, S., Hough, T. A., Bentley, L., Christie, P. T., Simon, M. M., Mallon, A. M., Schulz, H., Cox, R. D., Brown, M. A., Huebner, N., Brown, S. D. & Thakker, R. V. (2019). Mice with a Brd4 Mutation Represent a New Model of Nephrocalcinosis. Journal of Bone and Mineral Research, 34(7), 1324–1335. https://eprints.qut.edu.au/232799

2018

Gregson, C., Newell, F., Leo, P., Clark, G., Paternoster, L., Clout, M., Forgetta, V., Morris, J., Ge, B., Bao, X., Bassett, J. H. D., Williams, G., Youlten, S., Croucher, P., Smith, G. D., Evans, D., Kemp, J., Brown, M., Tobias, J. & Duncan, E. (2018). Genome-wide association study of extreme high bone mass: Contribution of common genetic variation to extreme BMD phenotypes and potential novel BMD-associated genes. Bone, 114, 62–71. https://eprints.qut.edu.au/120208
Bao, X., Hanson, A., Madeleine, M., Wang, S., Schwartz, S., Newell, F., Pettersson-Kymmer, U., Hemminki, K., Tiews, S., Steinberg, W., Clout, M., Brown, M., Duncan, E. & Leo, P. (2018). HLA and KIR associations of cervical neoplasia. Journal of Infectious Diseases, 218(12), 2003–2015. https://eprints.qut.edu.au/124013
Ze Ya Maung, K., Leo, P., Bassal, M., Casolari, D., Gray, J., Bray, S., Pederson, S., Singhal, D., Samaraweera, S., Nguyen, T., Cildir, G., Clout, M., Ewing, A., Duncan, E., Brown, M., Saal, R. & other (2018). Rare variants in Fanconi anemia genes are enriched in acute myeloid leukemia. Blood Cancer Journal, Article 50, 8, 1–5. https://eprints.qut.edu.au/124011
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.

2017

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/mhairi.marshall

Mrs Mhairi Clout