Variation in the Plasma Membrane Monoamine Transporter (PMAT) (Encoded by SLC29A4 ) and Organic Cation Transporter 1 (OCT1) (Encoded by SLC22A1 ) and Gastrointestinal Intolerance t... von Dawed, Adem Y, Zhou, Kaixin, van Leeuwen, Nienke, Mahajan, Anubha, Robertson, Neil, Koivula, Robert, Elders, Petra J M, Rauh, Simone P, Jones, Angus G, Holl, Reinhard W, Stingl, Julia C, Franks, Paul W, McCarthy, Mark I, 't Hart, Leen M, Pearson, Ewan R

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Genetic analysis of blood molecular phenotypes reveals common properties in the regulatory networks affecting complex traits von Hong, M.G., Davtian, D., Michalettou, T.D., Forgie, I.M., Adam, J., Allin, K.H., Caiazzo, R., Cederberg, H., Haid, M., Hansen, T.H., Hattersley, A.T., Heggie, A.J., Howald, C., Jones, A.G., Laakso, M., Mari, A., McEvoy, D., Mourby, M., Musholt, P.B., Pattou, F., Penet, D., Raverdy, V., Ridderstråle, M., Romano, L., Rutters, F., Sharma, S., Teare, H., Hart, L. 't, Vangipurapu, J., Vestergaard, H., Brunak, S., Franks, P.W., Grallert, H., Jablonka, B., McCarthy, M., Pedersen, O., Schwenk, J.M., Pearson, E.R., Adragni, K., Allesoe, R.L.L., Artati, A.A., Atabaki-Pasdar, N., Barnett, A.L., Baum, P., Bianzano, S.B., Bizzotto, R., Cabrelli, L., Preville, N. de, Dekkers, K.F., Deshmukh, H.A., Donnelly, L., Dutta, A., Ehrhardt, B., Fan, Y., Ferrer, J., Forman, A., Fritsche, A., Froguel, P., Gassenhuber, J., Grempler, R., Groeneveld, L., Groop, L., Gudmundsdóttir, V., Gupta, R., Hennige, A.M.H., Hill, A.V., Holl, R.W., Hudson, M., Jacobsen, U.P., Kaye, J., Klintenberg, M., Kuulasmaa, T., Loftus, H., Lundgaard, A.T.T., McRobert, N., McVittie, I., Nice, R., Nicolay, C., Palmer, C.N., Pedersen, H.K., Perry, M.H., Prehn, C.P., Ramisch, A., Scherer, N., Sihinevich, I., Slieker, R.C., Sondertoft, N.B., Steckel-Hamann, B., Thomas, M.K., Thomas, E.L.L., Thorand, B., Thorne, C.E., Tura, A., Uhlen, M., Oort, S. van, Vogt, J., Sackett, P.W.W., Wesolowska-Andersen, A., Whitcher, B., White, M.W.

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Four groups of type 2 diabetes contribute to the etiological and clinical heterogeneity in newly diagnosed individuals: an IMI DIRECT study von Wesolowska-Andersen, A., Brorsson, C.A., Bizzotto, R., Mari, A., Tura, A., Koivula, R., Mahajan, A., Vinuela, A., Tajes, J.F., Sharma, S., Haid, M., Prehn, C., Artati, A., Hong, M.G., Musholt, P.B., Kurbasic, A., Masi, F. de, Tsirigos, K., Pedersen, H.K., Gudmundsdottir, V., Thomas, C.E., Banasik, K., Jennison, C., Jones, A., Kennedy, G., Bell, J., Thomas, L., Frost, G., Thomsen, H., Allin, K., Hansen, T.H., Vestergaard, H., Hansen, T., Rutters, F., Elders, P., T'Hart, L., Bonnefond, A., Canouil, M., Brage, S., Kokkola, T., Heggie, A., McEvoy, D., Hattersley, A., McDonald, T., Teare, H., Ridderstrale, M., Walker, M., Forgie, I., Giordano, G.N., Froguel, P., Pavo, I., Ruetten, H., Pedersen, O., Dermitzakis, E., Franks, P.W., Schwenk, J.M., Adamski, J., Pearson, E., McCarthy, M.I., Brunak, S.

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