Phenomics: the systematic study of phenotypes on a genome-wide scale von Bilder, R.M, Sabb, F.W, Cannon, T.D, London, E.D, Jentsch, J.D, Parker, D. Stott, Poldrack, R.A, Evans, C, Freimer, N.B

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Challenges in phenotype definition in the whole-genome era: multivariate models of memory and intelligence von Sabb, F.W, Burggren, A.C, Higier, R.G, Fox, J, He, J, Parker, D.S, Poldrack, R.A, Chu, W, Cannon, T.D, Freimer, N.B, Bilder, R.M

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A phenome-wide examination of neural and cognitive function von Poldrack, R.A., Congdon, E., Triplett, W., Gorgolewski, K.J., Karlsgodt, K.H., Mumford, J.A., Sabb, F.W., Freimer, N.B., London, E.D., Cannon, T.D., Bilder, R.M.

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Genome-Wide Linkage Scan of Bipolar Disorder in a Colombian Population Isolate Replicates Loci on Chromosomes 7p21–22, 1p31, 16p12 and 21q21–22 and Identifies a Novel Locus on Chro... von Kremeyer, B., García, J., Müller, H., Burley, M.W., Herzberg, I., Parra, M.V., Duque, C., Vega, J., Montoya, P., López, M.C., Bedoya, G., Reus, V., Palacio, C., López, C., Ospina-Duque, J., Freimer, N.B., Ruiz-Linares, A.

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99 – Predicting schizophrenia spectrum disorders with psychological scales – The Northern Finland 1966 Birth Cohort von Miettunen, J, Veijola, J, Isohanni, M.K, Paunio, T, Freimer, N.B, Lauronen, E, Ekelund, J, Peltonen, L, Joukamaa, M, Lichtermann, D

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Polygenic Hyperlipidemia Increases Coronary Artery Disease Risk In The Uk Biobank von Ripatti, P., Rämö, J.T., Söderlund, S., Surakka, I., Havulinna, A.S., Widén, E., Palta, P., Freimer, N.B., Salomaa, V., Pirinen, M., Palotie, A., Taskinen, M.R., Ripatti, S.

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Results of a genome-wide genetic screen for panic disorder von Knowles, J.A., Fyer, A.J., Vieland, V.J., Weissman, M.M., Hodge, S.E., Heiman, G.A., Haghighi, F., de Jesus, G.M., Rassnick, H., Preud'homme-Rivelli, X., Austin, T., Cunjak, J., Mick, S., Fine, L.D., Woodley, K.A., Das, K., Maier, W., Adams, P.B., Freimer, N.B., Klein, D.F., Gilliam, T.C.

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Allele Frequencies at Microsatellite Loci: The Stepwise Mutation Model Revisited von Valdes, A. M, Slatkin, M, Freimer, N. B

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Subcortical volumetric abnormalities in bipolar disorder von Hibar, D.P, Westlye, L.T, van Erp, T.G.M, Rasmussen, J, Leonardo, C.D, Faskowitz, J, Haukvik, U.K, Hartberg, C.B, Doan, N.T, Agartz, I, Dale, A.M, Gruber, O, Krämer, B, Trost, S, Liberg, B, Abé, C, Ekman, C.J, Ingvar, M, Landén, M, Fears, S.C, Freimer, N.B, Bearden, C.E, Sprooten, E, Glahn, D.C, Pearlson, G.D, Emsell, Louise, Kenney, J, Scanlon, C, McDonald, C, Cannon, D.M, Almeida, J, Versace, A, Caseras, X, Lawrence, N.S, Phillips, M.L, Bou Mosleh, D, Delvecchio, G, Frangou, S, Satterthwaite, T.D, Wolf, D, Houenou, J, Henry, C, Malt, U.F, Bøen, E, Elvsåshagen, T, Young, A.H, Lloyd, A.J, Goodwin, G.M, Mackay, C.E, Bourne, C, Bilderbeck, A, Abramovic, L, Boks, M.P, van Haren, N.E.M, Ophoff, R.A, Kahn, R.S, Bauer, M, Pfennig, A, Alda, M, Hajek, T, Mwangi, B, Soares, J.C, Nickson, T, Dimitrova, R, Sussmann, J.E, Hagenaars, S, Whalley, H.C, McIntosh, A.M, Thompson, P.M, Andreassen, O.A

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Linkage-Disequilibrium Mapping of Disease Genes by Reconstruction of Ancestral Haplotypes in Founder Populations von Service, S.K., Lang, D.W. Temple, Freimer, N.B., Sandkuijl, L.A.

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The best of times, the worst of times for psychiatric disease von Karayiorgou, Maria, Flint, Jonathan, Gogos, Joseph A, Malenka, Robert C, Bargmann, C.I, Boyden, E.S, Bullmore, E.T, Chan, A.W, Davis, M, Deisseroth, K, Dolmetch, R.E, Eggan, K, Fears, S.C, Freimer, N.B, Geschwind, D.H, Gordon, J, Nickerson, D.A, Vanderhaeghen, Pierre, Axel, R, Zuker, C.S, Fischbach, G.D

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A narrow and highly significant linkage signal for severe bipolar disorder in the chromosome 5q33 region in Latin American pedigrees von Jasinska, A.J., Service, S., Jawaheer, D., DeYoung, J., Levinson, M., Zhang, Z., Kremeyer, B., Muller, H., Aldana, I., Garcia, J., Restrepo, G., Lopez, C., Palacio, C., Duque, C., Parra, M., Vega, J., Ortiz, D., Bedoya, G., Mathews, C., Davanzo, P., Fournier, E., Bejarano, J., Ramirez, M., Araya Ortiz, C., Araya, X., Molina, J., Sabatti, C., Reus, V., Ospina, J., Macaya, G., Ruiz-Linares, A., Freimer, N.B.

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Expanding the range of ZNF804A variants conferring risk of psychosis von Steinberg, S, Mors, O, Børglum, A.D, Gustafsson, O, Werge, T, Mortensen, P.B, Andreassen, O.A, Sigurdsson, E, Thorgeirsson, T.E, Böttcher, Y, Olason, P, Ophoff, R.A, Cichon, S, Gudjonsdottir, I.H, Pietiläinen, O.P.H, Nyegaard, M, Tuulio-Henriksson, A, Ingason, A, Hansen, T, Athanasiu, L, Suvisaari, J, Lonnqvist, J, Paunio, T, Hartmann, A, Jürgens, G, Nordentoft, M, Hougaard, D, Norgaard-Pedersen, B, Breuer, R, Möller, H.-J, Giegling, I, Glenthøj, B, Rasmussen, H.B, Mattheisen, M, Bitter, I, Réthelyi, J.M, Sigmundsson, T, Fossdal, R, Thorsteinsdottir, U, Ruggeri, M, Tosato, S, Strengman, E, Genetic Risk and Outcome In Psychosis (GROUP), Kiemeney, L.A, Melle, I, Djurovic, S, Abramova, L, Kaleda, V, Walshe, M, Bramon, E, Vassos, E, Li, Ting, Fraser, G, Walker, N, Toulopoulou, T, Yoon, J, Freimer, N.B, Cantor, R.M, Murray, R, Kong, A, Golimbet, V, Jönsson, E.G, Terenius, L, Agartz, I, Petursson, H, Nöthen, M.M, Rietschel, M, Peltonen, L, Rujescu, D, Collier, D.A, Stefansson, H, St Clair, D, Stefansson, K

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Incorrect specification of marker allele frequencies : effects on linkage analysis von FREIMER, N. B, SANDKUIJL, L. A, BLOWER, S. M

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A Minimalist Approach to Gene Mapping: Locating the Gene for Acheiropodia, by Homozygosity Analysis von Escamilla, M.A., DeMille, M.C., Benavides, E., Roche, E., Almasy, L., Pittman, S., Hauser, J., Lew, D.F., Freimer, N.B., Whittle, M.R.

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Results of a genome‐wide genetic screen for panic disorder von Knowles, J.A., Fyer, A.J., Vieland, V.J., Weissman, M.M., Hodge, S.E., Heiman, G.A., Haghighi, F., de Jesus, G.M., Rassnick, H., Preud'homme‐Rivelli, X., Austin, T., Cunjak, J., Mick, S., Fine, L.D., Woodley, K.A., Das, K., Maier, W., Adams, P.B., Freimer, N.B., Klein, D.F., Gilliam, T.C.

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