Lauren Johnson

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4 Article

The C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founder
Smith, B. N., Newhouse, S., Shatunov, A., Vance, C., Topp, S., Johnson, L., Miller, J., Lee, Y., Troakes, C., Scott, K. M., Jones, A., Gray, I., Wright, J., Hortobágyi, T., Al-Sarraj, S., Rogelj, B., Powell, J., Lupton, M., Lovestone, S. & Sapp, P. C. & 26 others, Weber, M., Nestor, P. J., Schelhaas, H. J., Asbroek, A. A. T., Silani, V., Gellera, C., Taroni, F., Ticozzi, N., Van den Berg, L., Veldink, J., Van Damme, P., Robberecht, W., Shaw, P. J., Kirby, J., Pall, H., Morrison, K. E., Morris, A., de Belleroche, J., Vianney de Jong, J. M. B., Baas, F., Andersen, P. M., Landers, J., Brown, R. H., Weale, M. E., Al-Chalabi, A. & Shaw, C. E., Jan 2013, In: European Journal of Human Genetics. 21, 1, p. 102-108 7 p., N/A.
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193 Citations (Scopus)
An MND/ALS phenotype associated with C9orf72 repeat expansion: Abundant p62-positive, TDP-43-negative inclusions in cerebral cortex, hippocampus and cerebellum but without associated cognitive decline
Troakes, C., Maekawa, S., Wijesekera, L., Rogelj, B., Siklos, L., Bell, C., Smith, B., Newhouse, S., Vance, C., Johnson, L., Hortobagyi, T., Shatunov, A., Al-Chalabi, A., Leigh, N., Shaw, C. E., King, A. & Al-Sarraj, S., Oct 2012, In: Neuropathology. 32, 5, p. 505-514 10 p.
Research output: Contribution to journal › Article › peer-review
109 Citations (Scopus)
Screening for OPTN mutations in a cohort of British amyotrophic lateral sclerosis patients
Johnson, L., Miller, J. W., Gkazi, A. S., Vance, C., Topp, S. D., Newhouse, S. J., Al-Chalabi, A., Smith, B. N. & Shaw, C. E., Dec 2012, In: Neurobiology of Aging. 33, 12, p. - 3 p., 2948.e15.
Research output: Contribution to journal › Article › peer-review
17 Citations (Scopus)
Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study
Shatunov, A., Mok, K., Newhouse, S., Weale, M. E., Smith, B., Vance, C., Johnson, L., Veldink, J. H., van Es, M. A., van den Berg, L. H., Robberecht, W., Van Damme, P., Hardiman, O., Farmer, A. E., Lewis, C. M., Butler, A. W., Abel, O., Andersen, P. M., Fogh, I. & Silani, V. & 17 others, Chiò, A., Traynor, B. J., Melki, J., Meininger, V., Landers, J. E., McGuffin, P., Glass, J. D., Pall, H., Leigh, P. N., Hardy, J., Brown, R. H., Powell, J. F., Orrell, R. W., Morrison, K. E., Shaw, P. J., Shaw, C. E. & Al-Chalabi, A., Oct 2010, In: Lancet Neurology. 9, 10, p. 986-94 9 p.
Research output: Contribution to journal › Article › peer-review

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Lauren Johnson

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Research output

The C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founder

An MND/ALS phenotype associated with C9orf72 repeat expansion: Abundant p62-positive, TDP-43-negative inclusions in cerebral cortex, hippocampus and cerebellum but without associated cognitive decline

Screening for OPTN mutations in a cohort of British amyotrophic lateral sclerosis patients

Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study