Search Results - Hummerich, H.

HECTD2 is associated with susceptibility to mouse and human prion disease by Lloyd, S., Maytham, E., Pota, H., Grizenkova, J., Molou, E., Uphill, J., Hummerich, H., Whitfield, J., Alpers, Michael Philip, Mead, S., Collinge, J.

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Genetic susceptibility, evolution and the kuru epidemic by Mead, S., Whitfield, Jerome, Poulter, M., Shah, P., Uphill, J., Beck, J., Campbell, T., Al-Dujaily, H., Hummerich, H., Alpers, Michael Philip, Collinge, J.

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Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study by Mead, S., Poulter, M., Uphill, J., Beck, J., Whitfield, Jerome, Webb, T., Campbell, T., Adamson, G., Deriziotis, P., Tabrizi, S., Hummerich, H., Verzilli, C., Alpers, Michael Philip, Whittaker, J., Collinge, J.

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A novel protective prion protein variant that colocalizes with Kuru exposure by Mead, S., Whitfield, Jerome, Poulter, M., Shah, P., Uphill, J., Campbell, T., Al-Dujaily, H., Hummerich, H., Beck, J., Mein, C., Verzilli, C., Whittaker, J., Alpers, Michael Philip, Collinge, J.

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Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP by Mead, S., Uphill, J., Beck, J., Poulter, M., Campbell, T., Lowe, J., Adamson, G., Hummerich, H., Klopp, N., Ruckert, I., Wichmann, H., Azazu, D., Plagnol, V., Pako, W., Whitfield, J., Alpers, Michael Philip, Whittaker, J., Balding, D., Zerr, I., Kretzschmar, H., Collinge, J.

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