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Publications & Outputs

  1. Genome-wide association study of bipolar disorder in Canadian and UK populations corroborates disease loci including SYNE1 and CSMD1

    Xu, W., Cohen-Woods, S., Chen, Q., Noor, A., Knight, J., Hosang, G., Parikh, S. V., De Luca, V., Tozzi, F., Muglia, P., Forte, J., McQuillin, A., Hu, P., Gurling, H. M. D., Kennedy, J. L., McGuffin, P., Farmer, A., Strauss, J. & Vincent, J. B., 4/01/2014, In : Journal of Medical Genetics. 15, 13 p., 2.

    Research output: Contribution to journalJournal article

  2. Mutations in IL36RN/IL1F5 are associated with the severe episodic inflammatory skin disease known as generalized pustular psoriasis

    Onoufriadis, A., Simpson, M. A., Pink, A. E., Di Meglio, P., Smith, C. H., Pullabhatla, V., Knight, J., Spain, S. L., Nestle, F. O., Burden, A. D., Capon, F., Trembath, R. C. & Barker, J. N. W. N., 9/09/2011, In : American Journal of Human Genetics. 89, 3, p. 432-437 6 p.

    Research output: Contribution to journalJournal article

  3. Software for generating liability distributions for pedigrees conditional on their observed disease states and covariates

    Campbell, D. D., Sham, P. C., Knight, J., Wickham, H. & Landau, S., 02/2010, In : Genetic Epidemiology. 34, 2, p. 159-170 12 p.

    Research output: Contribution to journalJournal article

  4. The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes

    Brookes, K., Xu, X., Chen, W., Zhou, K., Neale, B., Lowe, N., Anney, R., Franke, B., Gill, M., Ebstein, R., Buitelaar, J., Sham, P., Campbell, D., Knight, J., Andreou, P., Altink, M., Arnold, R., Boer, F., Buschgens, C., Butler, L. & 42 others, Christiansen, H., Feldman, L., Fleischman, K., Fliers, E., Howe-Forbes, R., Goldfarb, A., Heise, A., Gabriëls, I., Korn-Lubetzki, I., Johansson, L., Marco, R., Medad, S., Minderaa, R., Mulas, F., Müller, U., Mulligan, A., Rabin, K., Rommelse, N., Sethna, V., Sorohan, J., Uebel, H., Psychogiou, L., Weeks, A., Barrett, R., Craig, I., Banaschewski, T., Sonuga-Barke, E., Eisenberg, J., Kuntsi, J., Manor, I., McGuffin, P., Miranda, A., Oades, R. D., Plomin, R., Roeyers, H., Rothenberger, A., Sergeant, J., Steinhausen, H-C., Taylor, E., Thompson, M., Faraone, S. V. & Asherson, P., 10/2006, In : Molecular Psychiatry. 11, 10, p. 934-953 20 p.

    Research output: Contribution to journalJournal article

  5. A new method of linkage analysis using LOD scores for quantitative traits supports linkage of monoamine oxidase activity to D17S250 in the Collaborative Study on the Genetics of Alcoholism pedigrees

    Curtis, D., Knight, J. & Sham, P. C., 09/2005, In : Psychiatric Genetics. 15, 3, p. 181-187 7 p.

    Research output: Contribution to journalJournal article

  6. "They want to know where they came from": population genetics, identity, and family genealogy

    Tutton, R., 2004, In : New Genetics and Society. 23, 1, p. 105-120 16 p.

    Research output: Contribution to journalJournal article

  7. Mapping loci influencing blood pressure in the Framingham pedigrees using model-free LOD score analysis of a quantitative trait

    Knight, J., North, B. V., Sham, P. C. & Curtis, D., 31/12/2003, In : Genetics. 4 , Suppl. 1, 4 p., S74.

    Research output: Contribution to journalJournal article

  8. Assignment of the gene for dyskeratosis congenita to Xq28

    Connor, J. M., Gatherer, D., Gray, F. C., Pirrit, L. A. & Affara, N. A., 04/1986, In : Human Genetics. 72, 4, p. 348-351 4 p.

    Research output: Contribution to journalJournal article