检索结果 - Collier, D A

Transfer factor for carbon monoxide in patients with diabetes with and without microangiopathy. 由 Bell, D, Collier, D A

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Systematic meta-analyses and field synopsis of genetic association studies of violence and aggression 由 Vassos, E, Collier, D A, Fazel, S

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Site-specific intercalation at the triplex-duplex junction induces a conformational change which is detectable by hypersensitivity to diethylpyrocarbonate. 由 Collier, D A, Mergny, J L, Thuong, N T, Helene, C

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Establishing the characteristics of an effective pharmacogenetic test for clozapine-induced agranulocytosis 由 Verbelen, M, Collier, D A, Cohen, D, MacCabe, J H, Lewis, C M

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Linkage of Wolfram syndrome to chromosome 4p16.1 and evidence for heterogeneity. 由 Collier, D. A., Barrett, T. G., Curtis, D., Macleod, A., Arranz, M. J., Maassen, J. A., Bundey, S.

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Epilepsy-associated GRIN2A mutations reduce NMDA receptor trafficking and agonist potency – molecular profiling and functional rescue 由 Addis, L., Virdee, J. K., Vidler, L. R., Collier, D. A., Pal, D. K., Ursu, D.

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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... 由 Cannon, D M, Walshe, M, Dempster, E, Collier, D A, Marshall, N, Bramon, E, Murray, R M, McDonald, C

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Cytochrome P4502D6 genotype does not determine response to clozapine. 由 Arranz, M J, Dawson, E, Shaikh, S, Sham, P, Sharma, T, Aitchison, K, Crocq, M A, Gill, M, Kerwin, R, Collier, D A

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Awareness and use of glucagon in diabetics treated with insulin. 由 Matthews, D M, Patrick, A W, Collier, D A, Kellett, H A, Steel, J M, Clarke, B F, MacIntyre, C C

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Neurotrophic gene polymorphisms and response to psychological therapy 由 Lester, K J, Hudson, J L, Tropeano, M, Creswell, C, Collier, D A, Farmer, A, Lyneham, H J, Rapee, R M, Eley, T C

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

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

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

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

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

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

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

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

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