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NEUROGENETICS, 1364-6745

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  1. Does genetic anticipation occur in familial Alexander disease?

    Hunt, C. K., Al Khleifat, A., burchill, E., Ederle, J., Al-Chalabi, A. & Sreedharan, J., Jul 2021, In: NEUROGENETICS. 22, 3, p. 215-219 5 p.

    Research output: Contribution to journalArticlepeer-review

  2. Novel GFM2 variants associated with early-onset neurological presentations of mitochondrial disease and impaired expression of OXPHOS subunits

    Glasgow, R. I. C., Thompson, K., Barbosa, I. A., He, L., Alston, C. L., Deshpande, C., Simpson, M. A., Morris, A. A. M., Neu, A., Löbel, U., Hall, J., Prokisch, H., Haack, T. B., Hempel, M., McFarland, R. & Taylor, R. W., 26 Oct 2017, In: NEUROGENETICS. p. 1-9 9 p.

    Research output: Contribution to journalArticlepeer-review

  3. Genes and Gene Networks Implicated in Aggression Related Behaviour

    Malki, K., Pain, O., Du Rietz, E., Tosto, M. G., Paya-cano, J., Sandnabba, K. N., De Boer, S., Schalkwyk, L. C. & Sluyter, F., 1 Oct 2014, In: NEUROGENETICS. 15, 4, p. 255-266 12 p.

    Research output: Contribution to journalArticlepeer-review

  4. Novel SPG11 mutations in Asian kindreds and disruption of spatacsin function in the zebrafish

    Southgate, L., Dafou, D., Hoyle, J., Li, N., Kinning, E., Critchley, P., Nemeth, A. H., Talbot, K., Bindu, P. S., Sinha, S., Taly, A. B., Raghavendra, S., Mueller, F., Maher, E. R. & Trembath, R. C., Oct 2010, In: NEUROGENETICS. 11, 4, p. 379 - 389 11 p.

    Research output: Contribution to journalArticlepeer-review

  5. Age at onset in sod1-mediated amyotrophic lateral sclerosis shows familiality

    Fogh, I., Rijsdijk, F., Andersen, P. M., Sham, P. C., Knight, J., Neale, B., Kenna-Yasek, D., Silani, V., Brown, R. H., Powell, J. F. & Al-Chalabi, A., Aug 2007, In: NEUROGENETICS. 8, 3, p. 235 - 236 2 p.

    Research output: Contribution to journalLetterpeer-review

  6. A novel NIPA1 mutation associated with a pure form of autosomal dominant hereditary spastic paraplegia

    Reed, J. A., Wilkinson, P. A., Patel, H., Simpson, M. A., Chatonnet, A., Robay, D., Patton, M. A., Crosby, A. H. & Warner, T. T., May 2005, In: NEUROGENETICS. 6, 2, p. 79-84 6 p.

    Research output: Contribution to journalArticlepeer-review

  7. Early onset autosomal dominant spastic paraplegia caused by novel mutations in SPG3A

    Abel, A., Fonknechten, N., Hofer, A., Durr, A., Cruaud, C., Voit, T., Weissenbach, J., Brice, A., Klimpe, S., Auburger, G. & Hazan, J., Dec 2004, In: NEUROGENETICS. 5, 4, p. 239 - 243 5 p.

    Research output: Contribution to journalArticlepeer-review

  8. Towards a transcriptome definition of microglial cells

    Moran, L. B., Duke, D. C., Turkheimer, F. E., Banati, R. B. & Graeber, M. B., Jun 2004, In: NEUROGENETICS. 5, 2, p. 95-108 14 p.

    Research output: Contribution to journalArticlepeer-review

  9. Variants in the ALS2 gene are not associated with sporadic amyotrophic lateral sclerosis

    Al-Chalabi, A., Hansen, V. K., Simpson, C. L., Xi, J., Hosler, B. A., Powell, J. F., McKenna-Yasek, D., Shaw, C. E., Leigh, P. N. & Brown, R. H., Aug 2003, In: NEUROGENETICS. 4, 4, p. 221 - 222 2 p.

    Research output: Contribution to journalLetterpeer-review

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