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20112020

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  • The pseudo-caspase FLIP(L) regulates cell fate following p53 activation

    Lees, A., McIntyre, A. J., Crawford, N. T., Falcone, F., McCann, C., Holohan, C., Quinn, G. P., Roberts, J. Z., Sessler, T., Gallagher, P. F., Gregg, G. M. A., McAllister, K., McLaughlin, K. M., Allen, W. L., Egan, L. J., Ryan, A. E., Labonte-Wilson, M. J., Dunne, P. D., Wappett, M., Coyle, V. M. & 4 others, Johnston, P. G., Kerr, E. M., Longley, D. B. & McDade, S. S., Jul 2020, In: Proceedings of the National Academy of Sciences of the United States of America. 117, 30, p. 17808

    Research output: Contribution to journalArticlepeer-review

    2 Citations (Scopus)
  • A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease

    Holmans, P., Moskvina, V., Jones, L., Sharma, M., Vedernikov, A., Buchel, F., Sadd, M., Bras, J. M., Bettella, F., Nicolaou, N., Simon-Sanchez, J., Mittag, F., Gibbs, J. R., Schulte, C., Durr, A., Guerreiro, R., Hernandez, D., Brice, A., Stefansson, H., Majamaa, K. & 117 others, Gasser, T., Heutink, P., Wood, N. W., Martinez, M., Singleton, A. B., Nalls, M. A., Hardy, J., Morris, H. R., Williams, N. M., Arepalli, S., Barker, R., Barrett, J., Ben-Shlomo, Y., Berendse, H. W., Berg, D., Bhatia, K., de Bie, R. M. A., Biffi, A., Bloem, B., Bochdanovits, Z., Bonin, M., Brockmann, K., Brooks, J., Burn, D. J., Charlesworth, G., Chen, H., Chinnery, P. F., Chong, S., Clarke, C. E., Cookson, M. R., Cooper, J. M., Corvol, J-C., Counsell, C., Damier, P., Dartigues, J. F., Deloukas, P., Deuschl, G., Dexter, D. T., van Dijk, K. D., Dillman, A., Durif, F., Edkins, S., Evans, J. R., Foltynie, T., Gao, J., Gardner, M., Goate, A., Gray, E., Gustafsson, O., Harris, C., Hernandez, D. G., van Hilten, J. J., Hofman, A., Hollenbeck, A., Holton, J., Hu, M., Huber, H., Hudson, G., Hunt, S. E., Huttenlocher, J., Illig, T., Langford, C., Lees, A., Lesage, S., Lichtner, P., Limousin, P., Lopez, G., Lorenz, D., McNeill, A., Moorby, C., Moore, M., Morris, H. R., Morrison, K. E., Mudanohwo, E., Nalls, M. A., Pearson, J., Perlmutter, J. S., Petursson, H., Plagnol, V., Pollak, P., Post, B., Potter, S., Ravina, B., Revesz, T., Riess, O., Rivadeneira, F., Rizzu, P., Ryten, M., Saad, M., Sawcer, S., Schapira, A., Scheffer, H., Shaw, K., Sheerin, U-M., Shoulson, I., Sidransky, E., Smith, C., Stefansson, K., Steinberg, S., Stockton, J. D., Sveinbjornsdottir, S., Talbot, K., Tanner, C. M., Tashakkori-Ghanbaria, A., Tison, F., Trabzuni, D., Traynor, B. J., Uitterlinden, A. G., Velseboer, D., Vidailhet, M., Walker, R., van de Warrenburg, B., Wickremaratchi, M., Williams, N., Williams-Gray, C. H., Winder-Rhodes, S. & Wood, N., 01 Mar 2013, In: Human Molecular Genetics. 22, 5, p. 1039-1049 11 p.

    Research output: Contribution to journalArticlepeer-review

    72 Citations (Scopus)
  • Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21

    Spencer, C. C. A., Plagnol, V., Strange, A., Gardner, M., Paisan-Ruiz, C., Band, G., Barker, R. A., Bellenguez, C., Bhatia, K., Blackburn, H., Blackwell, J. M., Bramon, E., Brown, M. A., Burn, D., Casas, J-P., Chinnery, P. F., Clarke, C. E., Corvin, A., Craddock, N., Deloukas, P. & 29 others, Edkins, S., Evans, J., Freeman, C., Gray, E., Hardy, J., Hudson, G., Hunt, S., Jankowski, J., Langford, C., Lees, A. J., Markus, H. S., Mathew, C. G., McCarthy, M. I., Morrison, K. E., Palmer, C. N. A., Pearson, J. P., Peltonen, L., Pirinen, M., Plomin, R., Potter, S., Rautanen, A., Sawcer, S. J., Su, Z., Trembath, R. C., Viswanathan, A. C., Williams, N. W., Morris, H. R., Donnelly, P. & Wood, N. W., 15 Jan 2011, In: Human Molecular Genetics. 20, 2, p. 345-353 9 p.

    Research output: Contribution to journalArticlepeer-review

    161 Citations (Scopus)
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