Search results

• 2014

  CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1

  Rees, E., Walters, J. T. R., Chambert, K. D., O'dushlaine, C., Szatkiewicz, J., Richards, A. L., Georgieva, L., Mahoney-davies, G., Legge, S. E., Moran, J. L., Genovese, G., Levinson, D., Morris, D. W., Cormican, P., Kendler, K. S., O'neill, F. A., Riley, B., Gill, M., Corvin, A., Wellcome Trust Case Control Consortium, & 9 othersSklar, P., Hultman, C., Pato, C., Pato, M., Sullivan, P. F., Gejman, P. V., O'donovan, M. C., Owen, M. J. & Kirov, G., 15 Mar 2014, In: Human Molecular Genetics. 23, 6, p. 1669-1676 8 p.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  File

  • SLC1A1 100%
  • Gene 33%
  70 Citations (Scopus)

  304 Downloads (Pure)

• Common variant at 16p11.2 conferring risk of psychosis

  Steinberg, S., De Jong, S., Mattheisen, M., Costas, J., Demontis, D., Jamain, S., Pietilainen, O. P. H., Lin, K., Papiol, S., Huttenlocher, J., Sigurdsson, E., Vassos, E., Giegling, I., Breuer, R., Fraser, G., Walker, N., Melle, I., Djurovic, S., Agartz, I., Tuulio-henriksson, A., & 30 othersSuvisaari, J., Lonnqvist, J., Paunio, T., Olsen, L., Hansen, T., Ingason, A., Pirinen, M., Strengman, E., Hougaard, D. M., Orntoft, T., Didriksen, M., Hollegaard, M. V., Nordentoft, M., Abramova, L., Kaleda, V., Arrojo, M., Sanju??n, J., Arango, C., Etain, B., Curran, S., Bolton, P., Surguladze, S., Farmer, A., Martin, N. G., Van Os, J., Powell, J., Murray, R., O'Neill, F. A., Wellcome Trust Case Control Consortium 2 & Collier, D. A., Jan 2014, In: Molecular Psychiatry. 19, 1, p. 108-114 7 p.

  Research output: Contribution to journal › Article › peer-review

  • Bipolar Disorder 100%
  • Body Mass Index 66%
  83 Citations (Scopus)
• 2012

  Identification of new susceptibility loci for osteoarthritis (arcOGEN): a genome-wide association study

  Zeggini, E., Panoutsopoulou, K., Southam, L., Rayner, N. W., Day-Williams, A. G., Lopes, M. C., Boraska, V., Esko, T., Evangelou, E., Hofman, A., Houwing-Duistermaat, J. J., Ingvarsson, T., Jonsdottir, I., Jonsson, H., Kerkhof, H. J. M., Kloppenburg, M., Bos, S. D., Mangino, M., Metrustry, S., Slagboom, P. E., & 31 othersThorleifsson, G., Raine, E. V. A., Ratnayake, M., Ricketts, M., Beazley, C., Blackburn, H., Bumpstead, S., Elliott, K. S., Hunt, S. E., Potter, S. C., Shin, S-Y., Yadav, V. K., Zhai, G., Sherburn, K., Dixon, K., Arden, E., Aslam, N., Battley, P-K., Carluke, I., Doherty, S., Gordon, A., Joseph, J., Keen, R., Koller, N. C., Mitchell, S., O'Neill, F., Paling, E., Reed, M. R., Valdes, A. M., Spector, T. D. & arcOGEN Consortium & arcOGEN Colla, 1 Sept 2012, In: The Lancet. 380, 9844, p. 815-823 9 p.

  Research output: Contribution to journal › Article › peer-review

  • Genetics 100%
  • Single Nucleotide Polymorphism 33%
  • Gene 33%
  • Missense 33%
  • FTO Gene 33%
  315 Citations (Scopus)