Tau gene mutation in familial progressive subcortical gliosis von Goedert, M, Gambetti, P, Spillantini, M.G, Crowther, R.A, Chen, S.G, Parchi, P, Tabaton, M, Lanska, D.J, Markesbery, W.R, Wilhelmsen, K.C, Dickson, D.W, Petersen, R.B

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Associations Between Genomic Variants in Alcohol Dehydrogenase Genes and Alcohol Symptomatology in American Indians and European Americans: Distinctions and Convergence von Peng, Qian, Gizer, Ian R., Wilhelmsen, Kirk C., Ehlers, Cindy L.

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Antipsychotic-induced vacuous chewing movements and extrapyramidal side effects are highly heritable in mice von Crowley, J J, Adkins, D E, Pratt, A L, Quackenbush, C R, van den Oord, E J, Moy, S S, Wilhelmsen, K C, Cooper, T B, Bogue, M A, McLeod, H L, Sullivan, P F

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Supplementary Material for: Association of Predicted Expression and Multimodel Association Analysis of Substance Abuse Traits von D.M., Bost, C., Bizon, J.L., Tilson, D.L., Filer, I.R., Gizer, K.C., Wilhelmsen

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Nucleic acid sequences of the oncogene v-rel in reticuloendotheliosis virus strain T and its cellular homolog, the proto-oncogene c-rel von Wilhelmsen, K.C, Eggleton, K, Temin, H.M

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Familial Primary Pulmonary Hypertension Locus Mapped to Chromosome 2q31-q32 von Morse, Jane H., Jones, A.C., Barst, R.J., Hodge, S.E., Wilhelmsen, K.C., Nygaard, T.G.

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Pore domain sequence of a voltage-sensitive K + channel from Dendroaspis angusticeps Elapidae von Takacs, Z., Wilhelmsen, K.C., Sorota, S.

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Large-scale pharmacogenomic study of sulfonylureas and the QT, JT and QRS intervals: CHARGE Pharmacogenomics Working Group von Floyd, J.S., Sitlani, C.M., Avery, C.L., Noordam, R., Li, X., Smith, A.V., Gogarten, S.M., Li, J., Broer, L., Evans, D.S., Trompet, S., Brody, J.A., Stewart, J.D., Eicher, J.D., Seyerle, A.A., Roach, J., Lange, L.A., Lin, H.J., Kors, J.A., Harris, T.B., Li-Gao, R., Sattar, N., Cummings, S.R., Wiggins, K.L., Napier, M.D., Sturmer, T., Bis, J.C., Kerr, K., Uitterlinden, A.G., Taylor, K.D., Stott, D.J., Mutsert, R. de, Launer, L.J., Busch, E.L., Mendez-Giraldez, R., Sotoodehnia, N., Soliman, E.Z., Li, Y., Duan, Q., Rosendaal, F.R., Slagboom, P.E., Wilhelmsen, K.C., Reiner, A.P., Chen, Y.D., Heckbert, S.R., Kaplan, R.C., Rice, K.M., Jukema, J.W., Johnson, A.D., Liu, Y., Mook-Kanamori, D.O., Gudnason, V., Wilson, J.G., Rotter, J.I., Laurie, C.C., Psaty, B.M., Whitsel, E.A., Cupples, L.A., Stricker, B.H.

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Characterization of microsatellite polymorphisms DXS691 and DXS692: Genetic mapping to Xq26. 2-Xq27 and Xq25-Xq26. 2 von Lasser, D.M., Tantravahi, U., Wilhelmsen, K.C., Mygaard, T.G.

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Genetic loci associated with heart rate variability and their effects on cardiac disease risk von Munoz, M.L., Tragante, V., Amare, A.T., Heyde, B. von der, Avery, C.L., Dierckx, B., Dongen, J. van, Gogarten, S.M., Goyette, P., Hernesniemi, J., Huikari, V., Hwang, S.J., Jaju, D., Kerr, K.F., Lyytikainen, L.P., Maihofer, A.X., Most, P.J. van der, Muller-Nurasyid, M., Nivard, M., Thayer, J.F., Wong, A., Zafarmand, M.H., Abdellaoui, A., Albert, C., Auvinen, J., Baker, D.G., Bayoumi, R., Boomsma, D., Boucher, G., Dietrich, A., Ehret, G.B., Ellinor, P.T., Felix, J.F., Floras, J.S., Geyer, M.A., Giedraitis, V., Hartman, C.A., Hofman, A., Hottenga, J.J., Huikuri, H., Kors, J.A., Kumari, M., Kuznetsova, T., Li, Y., Lin, H.J., Lindgren, C.M., Lubitz, S.A., Mahajan, A., McKnight, B., Milaneschi, Y., Mononen, N., Morris, A.P., Nalls, M.A., Navis, G., Nikus, K., O'Connor, D.T., Ormel, J., Perz, S., Peters, A., Psaty, B.M., Risbrough, V.B., Siscovick, D., Smit, J.H., Smith, N.L., Stilp, A.M., Stolarz-Skrzypek, K., Strauch, K., Sundstrom, J., Syvanen, A.C., Tardif, J.C., Taylor, K.D., Teumer, A., Thornton, T.A., Voss, A., Wilhelmsen, K.C., Willemsen, G., Wong, Q.N., Zhang, Z.M., Zonderman, A.B., Cusi, D., Evans, M.K., Hassan, M., Ingelsson, E., Kahonen, M., Kooperberg, C., Lehtimaki, T., Lind, L., Nievergelt, C.M., Oldehinkel, A.J., Penninx, B., Roon, A.M. van, Rioux, J.D., Rotter, J.I., Stricker, B.H., Tiemeier, H., Asselbergs, F.W., Brundel, B.J.J.M., Heckbert, S.R., Hoed, M. den, Geus, E.J.C. de

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Structure and expression of c-rel, the cellular homolog to the oncogene of reticuloendotheliosis virus strain T [Causes rapidly fatal leukemia in newly hatched chicks and turkey po... von Chen, I S, Wilhelmsen, K C, Temin, H M

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