Replication of bipolar disorder susceptibility alleles and identification of two novel genome-wide significant associations in a new bipolar disorder case–control sample von Green, E K, Hamshere, M, Forty, L, Gordon-Smith, K, Fraser, C, Russell, E, Grozeva, D, Kirov, G, Holmans, P, Moran, J L, Purcell, S, Sklar, P, Owen, M J, O'Donovan, M C, Jones, L, Jones, I R, Craddock, N

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The bipolar disorder risk allele at CACNA1C also confers risk of recurrent major depression and of schizophrenia von Green, E K, Grozeva, D, Jones, I, Jones, L, Kirov, G, Caesar, S, Gordon-Smith, K, Fraser, C, Forty, L, Russell, E, Hamshere, M L, Moskvina, V, Nikolov, I, Farmer, A, McGuffin, P, Holmans, P A, Owen, M J, O'Donovan, M C, Craddock, N

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Association at SYNE1 in both bipolar disorder and recurrent major depression von Green, E K, Grozeva, D, Forty, L, Gordon-Smith, K, Russell, E, Farmer, A, Hamshere, M, Jones, I R, Jones, L, McGuffin, P, Moran, J L, Purcell, S, Sklar, P, Owen, M J, O'Donovan, M C, Craddock, N

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Evidence that duplications of 22q11.2 protect against schizophrenia von Rees, E, Kirov, G, Sanders, A, Walters, J T R, Chambert, K D, Shi, J, Szatkiewicz, J, O'Dushlaine, C, Richards, A L, Green, E K, Jones, I, Davies, G, Legge, S E, Moran, J L, Pato, C, Pato, M, Genovese, G, Levinson, D, Duan, J, Moy, W, Göring, H H H, Morris, D, Cormican, P, Kendler, K S, O'Neill, F A, Riley, B, Gill, M, Corvin, A, Craddock, N, Sklar, P, Hultman, C, Sullivan, P F, Gejman, P V, McCarroll, S A, O'Donovan, M C, Owen, M J

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Genetic utility of broadly defined bipolar schizoaffective disorder as a diagnostic concept von Hamshere, M. L., Green, E. K., Jones, I. R., Jones, L., Moskvina, V., Kirov, G., Grozeva, D., Nikolov, I., Vukcevic, D., Caesar, S., Gordon-Smith, K., Fraser, C., Russell, E., Breen, G., Clair, D. St, Collier, D. A., Young, A. H., Ferrier, I. N., Farmer, A., McGuffin, P., Holmans, P. A., Owen, M. J., O'Donovan, M. C., Craddock, N.

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Efficient Markov Chain Monte Carlo for combined Subset Simulation and nonlinear finite element analysis von Green, David K.E.

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Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorder von Song, J, Bergen, S E, Di Florio, A, Karlsson, R, Charney, A, Ruderfer, D M, Stahl, E A, Chambert, K D, Moran, J L, Gordon-Smith, K, Forty, L, Green, E K, Jones, I, Jones, L, Scolnick, E M, Sklar, P, Smoller, J W, Lichtenstein, P, Hultman, C, Craddock, N, Landén, M

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Copy number variation in bipolar disorder von Green, E K, Rees, E, Walters, J T R, Smith, K-G, Forty, L, Grozeva, D, Moran, J L, Sklar, P, Ripke, S, Chambert, K D, Genovese, G, McCarroll, S A, Jones, I, Jones, L, Owen, M J, O'Donovan, M C, Craddock, N, Kirov, G

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Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorder von Song, J, Bergen, S E, Di Florio, A, Karlsson, R, Charney, A, Ruderfer, D M, Stahl, E A, Chambert, K D, Moran, J L, Gordon-Smith, K, Forty, L, Green, E K, Jones, I, Jones, L, Scolnick, E M, Sklar, P, Smoller, J W, Lichtenstein, P, Hultman, C, Craddock, N, Landén, M, Smoller, Jordan W, Perlis, Roy H, Lee, Phil Hyoun, Castro, Victor M, Hoffnagle, Alison G, Sklar, Pamela, Stahl, Eli A, Purcell, Shaun M, Ruderfer, Douglas M, Charney, Alexander W, Roussos, Panos, Michele Pato, Carlos Pato, Medeiros, Helen, Sobel, Janet, Craddock, Nick, Jones, Ian, Forty, Liz, Florio, Arianna Di, Green, Elaine, Jones, Lisa, Gordon-Smith, Katherine, Landen, Mikael, Hultman, Christina, Jureus, Anders, Bergen, Sarah, McCarroll, Steven, Moran, Jennifer, Chambert, Kimberly, Belliveau, Richard A

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DISC1 exon 11 rare variants found more commonly in schizoaffective spectrum cases than controls von Green, E.K., Grozeva, D., Sims, R., Raybould, R., Forty, L., Gordon-Smith, K., Russell, E., St. Clair, D., Young, A.H., Ferrier, I.N., Kirov, G., Jones, I., Jones, L, Owen, M.J., O'Donovan, M.C., Craddock, N.

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Evidence for familial cosegregation of major affective disorder and genetic markers flanking the gene for Darier's disease von JONES, I, JACOBSEN, N, GREEN, E. K, ELVIDGE, G. P, OWEN, M. J, CRADDOCK, N

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A polymorphic variation in the interleukin 1A gene increases brain microglial cell activity in Alzheimer’s disease von Hayes, A, Green, E K, Pritchard, A, Harris, J M, Zhang, Y, Lambert, J C, Chartier-Harlin, M C, Pickering-Brown, S M, Lendon, C L, Mann, D M A

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Decay rates of attractive and repellent pheromones in an ant foraging trail network von Robinson, E. J. H, Green, K. E, Jenner, E. A, Holcombe, M, Ratnieks, F. L. W

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Are interleukin-1 gene polymorphisms risk factors or disease modifiers in AD? von GREEN, E. K, HARRIS, J. M, LEMMON, H, LAMBERT, J. C, CHARTIER-HARLIN, M. C, CLAIR, D. St, MANN, D. M. A, IWATSUBO, T, LENDON, C. L

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No support for association between Dyslexia Susceptibility 1 Candidate 1 and developmental dyslexia von Cope, N A, Hill, G, van den Bree, M, Harold, D, Moskvina, V, Green, E K, Owen, M J, Williams, J, O'Donovan, M C

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Calcitonin gene-related peptide stimulates human villous trophoblast cell differentiation in vitro von Green, K.E., Thota, C., Hankins, G.D.V., Yallampalli, C., Dong, Yuan-Lin

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Rasch Analysis of the Geriatric Depression Scale–Short Form von Chiang, Karl S., Green, Kathy E., Cox, Enid O.

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Polygenic dissection of the bipolar phenotype von Hamshere, M L, O'Donovan, M C, Jones, I R, Jones, L, Kirov, G, Green, E K, Moskvina, V, Grozeva, D, Bass, N, McQuillin, A, Gurling, H, St Clair, D, Young, A H, Ferrier, I N, Farmer, A, McGuffin, P, Sklar, P, Purcell, S, Holmans, P A, Owen, M J, Craddock, N

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The Consistent Association Between Epstein-Barr Virus and Hodgkin's Disease in Children in Kenya von Weinreb, M., Day, P.J.R., Niggli, F., Green, E.K., Nyong'o, A.O., Othieno-Abinya, N.A., Riyat, M.S., Raafat, F., Mann, J.R.

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Detailed mapping of a congenital heart disease gene in chromosome 3p25 von Green, Elaine K, Priestley, Matthew D, Waters, Jonathan, Maliszewska, Chris, Latif, Farida, Maher, Eamonn R

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