Browse By Person: Clout, Mhairi

Huang, Xiaomin, Leo, Paul, Clout, Mhairi, Fink, Lynn, Ellis, Jonathan, Hughes, Brett G.M., Kenny, Lizbeth, Vasani, Sarju, & Punyadeera, Chamindie (2025) Tumour-informed workflow to use ctDNA as a biomarker for risk of recurrence in head and neck cancer patients post-treatment. VIEW, Article number: 20250112.

Fink, J. Lynn, Jaradi, Binny, Stone, Nathan, Anderson, Lisa, Leo, Paul J., Marshall, Mhairi, Ellis, Jonathan, Waring, Paul M., & O'Byrne, Kenneth (2023) Minimizing Sample Failure Rates for Challenging Clinical Tumor Samples. Journal of Molecular Diagnostics, 25(5), pp. 263-273.

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Fink, Lynn, Waring, Paul Michael, Jaradi, Binny, Stone, Nathan, Anderson, Lisa, Leo, Paul, Marshall, Mhairi, Ellis, Jonathan, & O'Byrne, Kenneth (2022) Reducing pre-analytical sample QC failure rates for cancer molecular genetic assays with SLIMamp technology. Journal of Clinical Oncology, 40(16 Suppl), e15034.

McInerney-Leo, Aideen M., Chew, Hui Yi, Inglis, Po Ling, Leo, Paul J., Joseph, Shannon R., Cooper, Caroline L., Okano, Satomi, Hassall, Tim, Anderson, Lisa K., Bowman, Rayleen V., Gattas, Michael, Harris, Jessica E., Marshall, Mhairi S., Shaw, Janet G., Wheeler, Lawrie, Yang, Ian A., Brown, Matthew A., Fong, Kwun M., Simpson, Fiona, & Duncan, Emma L. (2021) Germline ERBB3 mutation in familial non-small-cell lung carcinoma: Expanding ErbB's role in oncogenesis. Human Molecular Genetics, 30(24), pp. 2393-2401.

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Graff, Sarah M., Johnson, Stephanie R., Leo, Paul J., Dadi, Prasanna K., Dickerson, Matthew T., Nakhe, Arya Y., McInerney-Leo, Aideen M., Marshall, Mhairi, Zaborska, Karolina E., Schaub, Charles M., Brown, Matthew A., Jacobson, David A., & Duncan, Emma L. (2021) A KCNK16 mutation causing TALK-1 gain of function is associated with maturity-onset diabetes of the young. JCI Insight, 6(13), Article number: e138057.

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Seabrook, Amanda J., Harris, Jessica E., Velosa, Sofia B., Kim, Edward, McInerney-Leo, Aideen M., Dwight, Trisha, Hockings, Jason I., Hockings, Nicholas G., Kirk, Judy, Leo, Paul J., Love, Amanda J., Luxford, Catherine, Marshall, Mhairi, Mete, Ozgur, Pennisi, David J., Brown, Matthew A., Gill, Anthony J., Hockings, Gregory I., Clifton-Bligh, Roderick J., & Duncan, Emma 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.

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Gregson, Celia L., Bergen, Dylan J.M., Leo, Paul, Sessions, Richard B., Wheeler, Lawrie, Hartley, April, Youlten, Scott, Croucher, Peter I., McInerney-Leo, Aideen M., Fraser, William, Tang, Jonathan C.Y., Anderson, Lisa, Marshall, Mhairi, Sergot, Leon, Paternoster, Lavinia, Davey Smith, George, Brown, Matthew A., Hammond, Chrissy, Kemp, John P., Tobias, Jon H., Duncan, Emma L., & other, and (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), pp. 92-105.

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Gorvin, Caroline M., Loh, Nellie Y., Stechman, Michael J., Falcone, Sara, Hannan, Fadil M., Ahmad, Bushra N., Piret, Sian E., Reed, Anita A.C., Jeyabalan, Jeshmi, Leo, Paul, Marshall, Mhairi, Sethi, Siddharth, Bass, Paul, Roberts, Ian, Sanderson, Jeremy, Wells, Sara, Hough, Tertius A., Bentley, Liz, Christie, Paul T., Simon, Michelle M., Mallon, Ann Marie, Schulz, Herbert, Cox, Roger D., Brown, Matthew A., Huebner, Norbert, Brown, Steve D., & Thakker, Rajesh V. (2019) Mice with a Brd4 Mutation Represent a New Model of Nephrocalcinosis. Journal of Bone and Mineral Research, 34(7), pp. 1324-1335.

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Gorvin, Caroline, Ahmad, Bushra, Stechman, Michael, Loh, Nellie, Hough, Tertius, Leo, Paul, Clout, Mhairi, Sethi, Siddharth, Bentley, Liz, Piret, Sian, Reed, Anita, Jeyabalan, Jeshmi, Christie, Paul, Wells, Sara, Simon, Michelle, Mallon, Ann-Marie, Schulz, Herbert, Huebner, Norbert, Brown, Matt, Cox, Roger, Brown, Steve, & Thakker, Rajesh (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), pp. 497-507.

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Asquith, Mark, Sternes, Peter, Costello, Mary-Ellen, Karstens, Lisa, Diamond, Sarah, Martin, Tammy, Li, Zhixiu, Clout, Mhairi, Spector, Timothy, Le Cao, Kim-Anh, Rosenbaum, James, & Brown, Matt (2019) HLA alleles associated with risk of ankylosing spondylitis and rheumatoid arthritis influence the gut microbiome. Arthritis and Rheumatology, 71(10), pp. 1642-1650.

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Gregson, Celia, Newell, Felicity, Leo, Paul, Clark, Graeme, Paternoster, Lavinia, Clout, Mhairi, Forgetta, Vincenzo, Morris, John, Ge, Bing, Bao, Xiao, Bassett, J.H. Duncan, Williams, Graham, Youlten, Scott, Croucher, Peter, Smith, George Davey, Evans, David, Kemp, John, Brown, Matt, Tobias, Jonathan, & Duncan, Emma (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, pp. 62-71.

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Bao, Xiao, Hanson, Aimee, Madeleine, Margaret, Wang, Sophia, Schwartz, Stephen, Newell, Felicity, Pettersson-Kymmer, Ulrika, Hemminki, Kari, Tiews, Sven, Steinberg, Winfried, Clout, Mhairi, Brown, Matt, Duncan, Emma, & Leo, Paul (2018) HLA and KIR associations of cervical neoplasia. Journal of Infectious Diseases, 218(12), pp. 2003-2015.

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Ze Ya Maung, Kyaw, Leo, Paul, Bassal, Mahmoud, Casolari, Debora, Gray, James, Bray, Sarah, Pederson, Stephen, Singhal, Deepak, Samaraweera, Saumya, Nguyen, Tran, Cildir, Gokhan, Clout, Mhairi, Ewing, Adam, Duncan, Emma, Brown, Matt, Saal, Russell, & other, and (2018) Rare variants in Fanconi anemia genes are enriched in acute myeloid leukemia. Blood Cancer Journal, 8, Article number: 50 1-5.

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Johnson, Stephanie, Leo, Paul, McInerney-Leo, Aideen, Anderson, Lisa, Clout, Mhairi, McGown, Ivan, Newell, Felicity, Brown, Matt, Conwell, Louise, Harris, Mark, & Duncan, Emma (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), pp. 656-662.

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Gratten, Jake, Zhao, Qiongyi, Benyamin, Beben, Garton, Fleur, He, Ji, Leo, Paul, Mangelsdorf, Marie, Anderson, Lisa, Zhang, Zong-Hong, Chen, Lu, Cremin, Katie, Harris, Jessica, Clout, Mhairi, Song, Sharon, Wheeler, Lawrie, Brown, Matt, & other, and (2017) Whole-exome sequencing in amyotrophic lateral sclerosis suggests NEK1 is a risk gene in Chinese. Genome Medicine, 9, Article number: 97 1-9.

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