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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

Nicholas C. M. Hearle

Section of Cancer Genetics

Institute of Cancer Research


United Kingdom


Name/email consistency: high



  • Section of Cancer Genetics, Institute of Cancer Research, Sutton, United Kingdom. 2004 - 2005


  1. Sequence changes in predicted promoter elements of STK11/LKB1 are unlikely to contribute to Peutz-Jeghers syndrome. Hearle, N.C., Tomlinson, I., Lim, W., Murday, V., Swarbrick, E., Lim, G., Phillips, R., Lee, P., O'Donohue, J., Trembath, R.C., Morrison, P.J., Norman, A., Taylor, R., Hodgson, S., Lucassen, A., Houlston, R.S. BMC. Genomics (2005) [Pubmed]
  2. Mapping of a translocation breakpoint in a Peutz-Jeghers hamartoma to the putative PJS locus at 19q13.4 and mutation analysis of candidate genes in polyp and STK11-negative PJS cases. Hearle, N., Lucassen, A., Wang, R., Lim, W., Ross, F., Wheeler, R., Moore, I., Shipley, J., Houlston, R. Genes. Chromosomes. Cancer (2004) [Pubmed]
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