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  1. Gauging NOTCH1 activation in cancer using immunohistochemistry

    Leigh, I. M. & 29 others Kluk, M. J., Ashworth, T., Wang, H., Knoechel, B., Mason, E. F., Morgan, E. A., Dorfman, D., Pinkus, G., Weigert, O., Hornick, J. L., Chirieac, L. R., Hirsch, M., Oh, D. J., South, A. P., Pourreyron, C., Cassidy, A. J., DeAngelo, D. J., Weinstock, D. M., Krop, I. E., Dillon, D., Brock, J. E., Lazar, A. J. F., Peto, M., Cho, R. J., Stoeck, A., Haines, B. B., Sathayanrayanan, S., Rodig, S. & Aster, J. C. 2013 In : PLoS ONE. 8, 6, 14 p.e67306

    Research output: Contribution to journalArticle

  2. The C134W (402 C > G) FOXL2 mutation is absent in ovarian gynandroblastoma: insights into the genesis of an unusual tumour

    Oparka, R., Cassidy, A., Reilly, S., Stenhouse, A., McCluggage, W. G. & Herrington, C. S. Apr 2012 In : Histopathology. 60, 5, p. 838-842 5 p.

    Research output: Contribution to journalArticle

  3. Epithelial IgG and its relationship to the loss of F508 in the common mutant form of the cystic fibrosis transmembrane conductance regulator

    Treharne, K. J., Cassidy, D., Goddard, C., Colledge, W. H., Cassidy, A. & Mehta, A. 6 Aug 2009 In : FEBS Letters. 583, 15, p. 2493-2499 7 p.

    Research output: Contribution to journalArticle

  4. MDM2 SNP309 is associated with high grade node positive breast tumours and is in linkage disequilibrium with a novel MDM2 intron 1 polymorphism

    Paulin, F. E. M., O'Neill, M., McGregor, G., Cassidy, A., Ashfield, A., Ali, C. W., Munro, A. J., Baker, L., Purdie, C. A., Lane, D. P. & Thompson, A. M. 1 Oct 2008 In : BMC Cancer. 8, p. - 10 p.281

    Research output: Contribution to journalArticle

  5. The human intermediate filament database: Comprehensive information on a gene family involved in many human diseases

    Szeverenyi, I. , Cassidy, A. J. , Chung, C. W. , Lee, B. T. K. , Common, J. E. A. , Ogg, S. C. , Chen, H. , Sim, S. Y. , Goh, W. L. R. , Ng, K. W. , Simpson, J. A. , Chee, L. L. , Eng, G. H. , Li, B. , Lunny, D. P. , Chuon, D. , Venkatesh, A. , Khoo, K. H. , McLean, W. H. I. , Lim, Y. P. & 1 others Lane, E. B. Mar 2008 In : Human Mutation. 29, 3, p. 351-360 10 p.

    Research output: Contribution to journalArticle

  6. Novel Mdm2 intron 1 single nucleotide polymorphisms and their role in breast cancer

    Paulin, F., O'Neill, M., McGregor, G., Cassidy, A., Ashfield, A., Ali, C. W., Baker, L., Munro, A. J., Lane, D. & Thompson, A. M. Dec 2007 In : Breast Cancer Research and Treatment. 106, p. S285-S285 1 p.6114

    Research output: Contribution to journalBook/Film/Article review

  7. Prevalent and rare mutations in the gene encoding filaggrin cause ichthyosis vulgaris and predispose individuals to atopic dermatitis

    Sandilands, A., O'Regan, G. M., Liao, H., Zhao, Y., Terron-Kwiatkowski, A., Watson, R. M., Cassidy, A. J., Goudie, D. R., Smith, F. J. D., McLean, W. H. I. & Irvine, A. D. 2006 In : Journal of Investigative Dermatology. 126, 8, p. 1770-1775 6 p.

    Research output: Contribution to journalArticle

  8. A homozygous missense mutation in TGM5 abolishes epidermal transglutaminase 5 activity and causes acral peeling skin syndrome

    Cassidy, A., van Steensel, M. A. M., Steijlen, P. M., van Geel, M., van der Velden, J., Morley, S., Terrinoni, A., Melino, G., Candi, E. & McLean, I. Dec 2005 In : American Journal of Human Genetics. 77, 6, p. 909-917 9 p.

    Research output: Contribution to journalArticle

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