Common alleles contribute to schizophrenia in CNV carriers von Tansey, K E, Rees, E, Linden, D E, Ripke, S, Chambert, K D, Moran, J L, McCarroll, S A, Holmans, P, Kirov, G, Walters, J, Owen, M J, O'Donovan, M C

Volltext

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

Volltext

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

Volltext

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

Volltext

De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia von Kirov, G, Pocklington, A J, Holmans, P, Ivanov, D, Ikeda, M, Ruderfer, D, Moran, J, Chambert, K, Toncheva, D, Georgieva, L, Grozeva, D, Fjodorova, M, Wollerton, R, Rees, E, Nikolov, I, van de Lagemaat, L N, Bayés, À, Fernandez, E, Olason, P I, Böttcher, Y, Komiyama, N H, Collins, M O, Choudhary, J, Stefansson, K, Stefansson, H, Grant, S G N, Purcell, S, Sklar, P, O'Donovan, M C, Owen, M J

Volltext

Is the self-adhesive mesh a solution for chronic postoperative inguinal pain after TAPP: A single centre preliminary experience? von Kirov, Kiril G, Mihaylov, Diyan M, Arnaudov, Stefan Svilenov

Volltext

Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia von Kirov, George, Gumus, Dilihan, Chen, Wei, Norton, Nadine, Georgieva, Lyudmila, Sari, Murat, O’Donovan, Michael C, Erdogan, Fikret, Owen, Michael J, Ropers, Hans-Hilger, Ullmann, Reinhard

Volltext

A genome-wide association study in 574 schizophrenia trios using DNA pooling von Kirov, G, Zaharieva, I, Georgieva, L, Moskvina, V, Nikolov, I, Cichon, S, Hillmer, A, Toncheva, D, Owen, M J, O'Donovan, M C

Volltext

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

Volltext

Family-based association study of 76 candidate genes in bipolar disorder: BDNF is a potential risk locus von SKLAR, P, GABRIEL, S. B, CRADDOCK, N, DEPAULO, J. R, LANDER, E. S, MCINNIS, M. G, BENNETT, P, LIM, Y-M, TSAN, G, SCHAFFNER, S, KIROV, G, JONES, I, OWEN, M

Volltext

Schizophrenia susceptibility alleles are enriched for alleles that affect gene expression in adult human brain von Richards, A L, Jones, L, Moskvina, V, Kirov, G, Gejman, P V, Levinson, D F, Sanders, A R, Purcell, S, Visscher, P M, Craddock, N, Owen, M J, Holmans, P, O'Donovan, M C

Volltext

Association of Per1 and Npas2 with autistic disorder : support for the clock genes/social timing hypothesis von NICHOLAS, B, RUDRASINGHAM, V, NASH, S, KIROV, G, OWEN, M. J, WIMPORY, D. C

Volltext

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.

Volltext

Common alleles contribute to schizophrenia in CNV carriers von Tansey, K E, Rees, E, Linden, D E, Ripke, S, Chambert, K D, Moran, J L, McCarroll, S A, Holmans, P, Kirov, G, Walters, J, Owen, M J, O'Donovan, M C

Volltext

Structural interpretation of anion exchange in divalent copper hydroxysalt minerals von Stanimirova, Ts, Dencheva, S, Kirov, G

Volltext

Schizophrenia copy number variants and associative learning von Clifton, N E, Pocklington, A J, Scholz, B, Rees, E, Walters, J T R, Kirov, G, O'Donovan, M C, Owen, M J, Wilkinson, L S, Thomas, K L, Hall, J

Volltext

Mutation screening of the 3q29 microdeletion syndrome candidate genes DLG1 and PAK2 in schizophrenia von Carroll, L.S., Williams, H.J., Walters, J., Kirov, G., O'Donovan, M.C., Owen, M.J.

Volltext

Finding schizophrenia genes von Kirov, George, O'Donovan, Michael C, Owen, Michael J

Volltext

Erratum: Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia von Legge, S E, Hamshere, M L, Ripke, S, Pardinas, A F, Goldstein, J I, Rees, E, Richards, A L, Leonenko, G, Jorskog, L F, Chambert, K D, Collier, D A, Genovese, G, Giegling, I, Holmans, P, Jonasdottir, A, Kirov, G, McCarroll, S A, MacCabe, J H, Mantripragada, K, Moran, J L, Neale, B M, Stefansson, H, Rujescu, D, Daly, M J, Sullivan, P F, Owen, M J, O'Donovan, M C, Walters, J T R

Volltext

Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia von Legge, S E, Hamshere, M L, Ripke, S, Pardinas, A F, Goldstein, J I, Rees, E, Richards, A L, Leonenko, G, Jorskog, L F, Chambert, K D, Collier, D A, Genovese, G, Giegling, I, Holmans, P, Jonasdottir, A, Kirov, G, McCarroll, S A, MacCabe, J H, Mantripragada, K, Moran, J L, Neale, B M, Stefansson, H, Rujescu, D, Daly, M J, Sullivan, P F, Owen, M J, O'Donovan, M C, Walters, J T R

Volltext