Systematic meta-analyses and field synopsis of genetic association studies of violence and aggression

por Vassos, E, Collier, D A, Fazel, S
Publicado 2014

Marconi: Beherrscher des Äthers

por Jacot, B L, Collier, D M B
Publicado 1937

Characterization of the complications associated with plasma exchange for thrombotic thrombocytopaenic purpura and related thrombotic microangiopathic anaemias: a single institutio...

por McGuckin, S, Westwood, J-P, Webster, H, Collier, D, Leverett, D, Scully, M
Publicado 2014

Establishing the characteristics of an effective pharmacogenetic test for clozapine-induced agranulocytosis

por Verbelen, M, Collier, D A, Cohen, D, MacCabe, J H, Lewis, C M
Publicado 2015

Epilepsy-associated GRIN2A mutations reduce NMDA receptor trafficking and agonist potency – molecular profiling and functional rescue

por Addis, L., Virdee, J. K., Vidler, L. R., Collier, D. A., Pal, D. K., Ursu, D.
Publicado 2017

The association of white matter volume in psychotic disorders with genotypic variation in NRG1, MOG and CNP: a voxel-based analysis in affected individuals and their unaffected rel...

por Cannon, D M, Walshe, M, Dempster, E, Collier, D A, Marshall, N, Bramon, E, Murray, R M, McDonald, C
Publicado 2012

Neurotrophic gene polymorphisms and response to psychological therapy

por Lester, K J, Hudson, J L, Tropeano, M, Creswell, C, Collier, D A, Farmer, A, Lyneham, H J, Rapee, R M, Eley, T C
Publicado 2012

Identification of increased genetic risk scores for schizophrenia in treatment-resistant patients

por Frank, J, Lang, M, Witt, S H, Strohmaier, J, Rujescu, D, Cichon, S, Degenhardt, F, Nöthen, M M, Collier, D A, Ripke, S, Naber, D, Rietschel, M
Publicado 2015

Evidence-informed policy making at country level: lessons learned from the South African Tuberculosis Think Tank

por White, R. G., Charalambous, S., Cardenas, V., Hippner, P., Sumner, T., Bozzani, F., Mudzengi, D., Houben, R. M. G. J., Collier, D., Kimerling, M. E., Vassall, A., Pillay, Y., Churchyard, G.
Publicado 2018

Expression analysis in a rat psychosis model identifies novel candidate genes validated in a large case–control sample of schizophrenia

por Ingason, A, Giegling, I, Hartmann, A M, Genius, J, Konte, B, Friedl, M, Ripke, S, Sullivan, P F, St. Clair, D, Collier, D A, O'Donovan, M C, Mirnics, K, Rujescu, D
Publicado 2015

Genetic utility of broadly defined bipolar schizoaffective disorder as a diagnostic concept

por 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., St Clair, D., 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.
Publicado 2009

Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia

por 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
Publicado 2017

Erratum: Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia

por 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
Publicado 2016

Erratum: Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia

por 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
Publicado 2017

Correction: Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosa

por Huckins, L M, Hatzikotoulas, K, Southam, L, Thornton, L M, Steinberg, J, Aguilera-McKay, F, Treasure, J, Schmidt, U, Gunasinghe, C, Romero, A, Curtis, C, Rhodes, D, Moens, J, Kalsi, G, Dempster, D, Leung, R, Keohane, A, Burghardt, R, Ehrlich, S, Hebebrand, J, Hinney, A, Ludolph, A, Walton, E, Deloukas, P, Hofman, A, Palotie, A, Palta, P, van Rooij, F J A, Stirrups, K, Adan, R, Boni, C, Cone, R, Dedoussis, G, van Furth, E, Gonidakis, F, Gorwood, P, Hudson, J, Kaprio, J, Kas, M, Keski-Rahonen, A, Kiezebrink, K, Knudsen, G-P, Maj, M, Monteleone, A M, Monteleone, P, Raevuori, A H, Reichborn-Kjennerud, T, Tozzi, F, Tsitsika, A, van Elburg, A, Collier, D A, Sullivan, P F, Breen, G, Bulik, C M, Zeggini, E
Publicado 2017

Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosa

por Huckins, L M, Hatzikotoulas, K, Southam, L, Thornton, L M, Steinberg, J, Aguilera-McKay, F, Treasure, J, Schmidt, U, Gunasinghe, C, Romero, A, Curtis, C, Rhodes, D, Moens, J, Kalsi, G, Dempster, D, Leung, R, Keohane, A, Burghardt, R, Ehrlich, S, Hebebrand, J, Hinney, A, Ludolph, A, Walton, E, Deloukas, P, Hofman, A, Palotie, A, Palta, P, van Rooij, F J A, Stirrups, K, Adan, R, Boni, C, Cone, R, Dedoussis, G, van Furth, E, Gonidakis, F, Gorwood, P, Hudson, J, Kaprio, J, Kas, M, Keski-Rahonen, A, Kiezebrink, K, Knudsen, G-P, Slof-Op 't Landt, M C T, Maj, M, Monteleone, A M, Monteleone, P, Raevuori, A H, Reichborn-Kjennerud, T, Tozzi, F, Tsitsika, A, van Elburg, A, Collier, D A, Sullivan, P F, Breen, G, Bulik, C M, Zeggini, E
Publicado 2018