Multicentric Origin of Hemochromatosis Gene ( HFE) Mutations by Rochette, J., Pointon, J.J., Fisher, C.A., Perera, G., Arambepola, M., Arichchi, D. S. Kodikara, De Silva, S., Vandwalle, J.L., Monti, J.P., Old, J.M., Merryweather-Clarke, A.T., Weatherall, D.J., Robson, K.J.H.

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Mutations in LRP5 and SOST are a rare cause of high bone mass in the general population by Duncan, E.L, Gregson, C.L, Addison, K, Brugmans, M, Pointon, J.J, Appleton, L.H, Tobias, J.H, Brown, M.A

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The genetic associations of acute anterior uveitis and their overlap with the genetics of ankylosing spondylitis by Robinson, P C, Leo, P J, Pointon, J J, Harris, J, Cremin, K, Bradbury, L A, Stebbings, S, Harrison, A A, Evans, D M, Duncan, E L, Wordsworth, B P, Brown, M A

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The 16189 variant of mitochondrial DNA occurs more frequently in C282Y homozygotes with haemochromatosis than those without iron loading by Livesey, K J, Wimhurst, V L C, Carter, K, Worwood, M, Cadet, E, Rochette, J, Roberts, A G, Pointon, J J, Merryweather-Clarke, A T, Bassett, M L, Jouanolle, A-M, Mosser, A, David, V, Poulton, J, Robson, K J H

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A novel human leucocyte antigen-DRB1 genotyping method based on multiplex primer extension reactions by Jaakkola, E., Herzberg, I., Crane, A.M., Pointon, J.J., Laiho, K., Kauppi, M., Kaarela, K., Wordsworth, B.P., Tuomilehto, J., Brown, M.A.

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