King's College London

Structural variation analysis of 6,500 whole genome sequences in amyotrophic lateral sclerosis

Al Khleifat, A., Iacoangeli, A., Van Vugt, J. J. F. A., Bowles, H., Zwamborn, R. A. J., Moisse, M., Zwamborn, R. A. J., Cooper-Knock, J., Shatunov, A., Jones, A., van Rheenen, W., Opie-Martin, S., Fogh, I., Topp, S., Smith, B., Dobson, R., Shaw, C., Chiò, A., Panades, M. P., Mora, J. S., & 10 othersShaw, P. J., Landers, J. E., Glass, J. D., Başak, A. N., Hardiman, O., Robberecht, W., Van Damme, P., van den Berg, L. H., Veldink, J. H. & Al-Chalabi, A., 19 Oct 2021, In: NPJ Genomic medicine.

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

Ethnic-specific association of amylase gene copy number with adiposity traits in a large Middle Eastern biobank

Rossi, N., Aliyev, E., Visconti, A., Akil, A. S. A., Syed, N., Aamer, W., Padmajeya, S. S., Falchi, M. & Fakhro, K. A., 9 Feb 2021, In: NPJ Genomic medicine. 6, 1, p. 8 8.

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

Significant out-of-sample classification from methylation profile scoring for amyotrophic lateral sclerosis

Nabais, M. F., Lin, T., Benyamin, B., Williams, K. L., Garton, F. C., Vinkhuyzen, A. A. E., Zhang, F., Vallerga, C. L., Restuadi, R., Freydenzon, A., Zwamborn, R. A. J., Hop, P. J., Robinson, M. R., Gratten, J., Visscher, P. M., Hannon, E., Mill, J., Brown, M. A., Laing, N. G., Mather, K. A., & 17 othersSachdev, P. S., Ngo, S. T., Steyn, F. J., Wallace, L., Henders, A. K., Needham, M., Veldink, J. H., Mathers, S., Nicholson, G., Rowe, D. B., Henderson, R. D., McCombe, P. A., Pamphlett, R., Yang, J., Blair, I. P., McRae, A. F. & Wray, N. R., 1 Dec 2020, In: NPJ Genomic medicine. 5, 1, 10.

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

Incorporating epilepsy genetics into clinical practice: A 360° evaluation

Oates, S., Tang, S., Rosch, R., Lear, R., Hughes, E. F., Williams, R. E., Larsen, L. H. G., Hao, Q., Dahl, H. A., Møller, R. S. & Pal, D. K., 10 May 2018, In: NPJ Genomic medicine. 3, 1

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

Exome-wide study of ankylosing spondylitis demonstrates additional shared genetic background with inflammatory bowel disease

Robinson, P. C., Leo, P. J., Pointon, J. J., Harris, J., Cremin, K., Bradbury, L. A., Stebbings, S., Harrison, A. A., Duncan, E. L., Evans, D. M., Wordsworth, P. B. & Brown, M. A., 4 May 2016, In: NPJ Genomic medicine. 1, 16008.

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