Edinburgh Research Explorer

Yanick Crow

Chair of Genomic Medicine

  1. 2013
  2. Systemic lupus erythematosus due to C1q deficiency with progressive encephalopathy, intracranial calcification and acquired moyamoya cerebral vasculopathy

    Troedson, C., Wong, M., Dalby-Payne, J., Wilson, M., Dexter, M., Rice, G. I., Crow, Y. J. & Dale, R. C., May 2013, In : Lupus. 22, 6, p. 639-43 5 p.

    Research output: Contribution to journalArticle

  3. 2011
  4. HIV-1 restriction factor SAMHD1 is a deoxynucleoside triphosphate triphosphohydrolase

    Goldstone, D. C., Ennis-Adeniran, V., Hedden, J. J., Groom, H. C. T., Rice, G. I., Christodoulou, E., Walker, P. A., Kelly, G., Haire, L. F., Yap, M. W., de Carvalho, L. P. S., Stoye, J. P., Crow, Y. J., Taylor, I. A. & Webb, M., 6 Nov 2011, In : Nature. 480, 7377, p. 379-82 4 p.

    Research output: Contribution to journalArticle

  5. Type I interferonopathies: a novel set of inborn errors of immunity

    Crow, Y. J., Nov 2011, In : Annals of the New York Academy of Sciences. 1238, p. 91-8 8 p.

    Research output: Contribution to journalArticle

  6. Tartrate-resistant acid phosphatase deficiency causes a bone dysplasia with autoimmunity and a type I interferon expression signature

    Briggs, T. A., Rice, G. I., Daly, S., Urquhart, J., Gornall, H., Bader-Meunier, B., Baskar, K., Baskar, S., Baudouin, V., Beresford, M. W., Black, G. C. M., Dearman, R. J., de Zegher, F., Foster, E. S., Francès, C., Hayman, A. R., Hilton, E., Job-Deslandre, C., Kulkarni, M. L., Le Merrer, M. & 20 others, Linglart, A., Lovell, S. C., Maurer, K., Musset, L., Navarro, V., Picard, C., Puel, A., Rieux-Laucat, F., Roifman, C. M., Scholl-Bürgi, S., Smith, N., Szynkiewicz, M., Wiedeman, A., Wouters, C., Zeef, L. A. H., Casanova, J-L., Elkon, K. B., Janckila, A., Lebon, P. & Crow, Y. J., Feb 2011, In : Nature Genetics. 43, 2, p. 127-31 5 p.

    Research output: Contribution to journalArticle

  7. 2010
  8. Recessive mutations in the gene encoding the tight junction protein occludin cause band-like calcification with simplified gyration and polymicrogyria

    O'Driscoll, M. C., Daly, S. B., Urquhart, J. E., Black, G. C. M., Pilz, D. T., Brockmann, K., McEntagart, M., Abdel-Salam, G., Zaki, M., Wolf, N. I., Ladda, R. L., Sell, S., D'Arrigo, S., Squier, W., Dobyns, W. B., Livingston, J. H. & Crow, Y. J., 10 Sep 2010, In : American Journal of Human Genetics. 87, 3, p. 354-64 11 p.

    Research output: Contribution to journalArticle

  9. 2009
  10. Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune response

    Rice, G. I., Bond, J., Asipu, A., Brunette, R. L., Manfield, I. W., Carr, I. M., Fuller, J. C., Jackson, R. M., Lamb, T., Briggs, T. A., Ali, M., Gornall, H., Couthard, L. R., Aeby, A., Attard-Montalto, S. P., Bertini, E., Bodemer, C., Brockmann, K., Brueton, L. A., Corry, P. C. & 31 others, Desguerre, I., Fazzi, E., Cazorla, A. G., Gener, B., Hamel, B. C. J., Heiberg, A., Hunter, M., van der Knaap, M. S., Kumar, R., Lagae, L., Landrieu, P. G., Lourenco, C. M., Marom, D., McDermott, M. F., van der Merwe, W., Orcesi, S., Prendiville, J. S., Rasmussen, M., Shalev, S. A., Soler, D. M., Shinawi, M., Spiegel, R., Tan, T. Y., Vanderver, A., Wakeling, E. L., Wassmer, E., Whittaker, E., Lebon, P., Stetson, D. B., Bonthron, D. T. & Crow, Y. J., Jul 2009, In : Nature Genetics. 41, 7, p. 829-32 4 p.

    Research output: Contribution to journalArticle

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