Phenome-wide analysis of genome-wide polygenic scores von Krapohl, E, Euesden, J, Zabaneh, D, Pingault, J-B, Rimfeld, K, von Stumm, S, Dale, P S, Breen, G, O'Reilly, P F, Plomin, R

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Polygenic interactions with environmental adversity in the aetiology of major depressive disorder von Mullins, N., Power, R. A., Fisher, H. L., Hanscombe, K. B., Euesden, J., Iniesta, R., Levinson, D. F., Weissman, M. M., Potash, J. B., Shi, J., Uher, R., Cohen-Woods, S., Rivera, M., Jones, L., Jones, I., Craddock, N., Owen, M. J., Korszun, A., Craig, I. W., Farmer, A. E., McGuffin, P., Breen, G., Lewis, C. M.

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36P In-vitro tonic signalling profiling of CAR-T cells generated to support pre-clinical studies for solid tumour targets von Hunjan, S.S., Sampson, R., Evans, J., Chenoweth, H., Garrobo-Calleja, I., Lekomtsev, S., Zhang, J., Zona, S., Breuning, J., Oren, R., Davies, M., Di-Tullio, A., Euesden, J., Kennedy, J., Kay, C., Colebrook, J., Kloke, B.P., Southgate, T., Lee, J.

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NY-ESO-1 and LAGE1A: An emerging target for cell therapies in solid tumours von Eleftheriadou, I., Brett, S., Domogala, A., Patasic, L., Kijewska, M.A., Soor, K., Georgouli, M., Dopierala, J., Fisher, P., Jing, J., Euesden, J., Auger, K.R., Roberts, R., O’Sullivan, S., Castelletti, L., Damm, M., Pankov, D., Johnson, L.A., Shalabi, A., Britten, C.

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1229P - NY-ESO-1 and LAGE1A: An emerging target for cell therapies in solid tumours von Eleftheriadou, I., Brett, S., Domogala, A., Patasic, L., Kijewska, M.A., Soor, K., Georgouli, M., Dopierala, J., Fisher, P., Jing, J., Euesden, J., Auger, K.R., Roberts, R., O’Sullivan, S., Castelletti, L., Damm, M., Pankov, D., Johnson, L.A., Shalabi, A., Britten, C.

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P2.04-91 Target Antigen Levels in NSCLC Define a Clinically Relevant Activation Threshold for NY-ESO-1c259 TCR T-Cell Therapy von Eleftheriadou, I., Brett, S., Domogala, A., Patasic, L., Kijewska, M., Soor, K., Jing, J., Euesden, J., Auger, K., Roberts, R., O’sullivan, S., Castelletti, L., Damm, M., Klapwijk, J., Spaull, J., Pankov, D., Johnsons, L., Shalabi, A., Britten, C.

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1229PNY-ESO-1 and LAGE1A: An emerging target for cell therapies in solid tumours von Eleftheriadou, I, Brett, S, Domogala, A, Patasic, L, Kijewska, M A, Soor, K, Georgouli, M, Dopierala, J, Fisher, P, Jing, J, Euesden, J, Auger, K R, Roberts, R, O’Sullivan, S, Castelletti, L, Damm, M, Pankov, D, Johnson, L A, Shalabi, A, Britten, C

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An Examination of Polygenic Score Risk Prediction in Individuals With First-Episode Psychosis von Vassos, E, Di Forti, M, Coleman, J, Iyegbe, C, Prata, D, Euesden, J, O'Reilly, P, Curtis, C, Kolliakou, A, Patel, H, Newhouse, S, Traylor, M, Ajnakina, O, Mondelli, V, Marques, TR, Gardner-Sood, P, Aitchison, KJ, Powell, J, Atakan, Z, Greenwood, KE, Smith, S, Ismail, K, Pariante, C, Gaughran, F, Dazzan, P, Markus, HS, David, AS, Lewis, CM, Murray, RM, Breen, G

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Fourteen sequence variants that associate with multiple sclerosis discovered by meta-analysis informed by genetic correlations von Olafsson, S., Stridh, P., Bos, Steffan Daniel, Ingason, Andrés, Euesden, J, Sulem, Patrick, Thorleifsson, Gudmar, Gustafsson, O, Geirsson, AJ, Jóhannesson, Ari J., Thorsson, AV, Ludviksson, BR, Sigurgeirsson, Bardur, Jonasson, JG, Olafsson, E, Kristjansdottir, H, Olafsson, JH, Orvar, KB, Benediktsson, Rafn, Bjarnason, Ragnar, Kristjansdottir, Sjofn, Gislason, Thorarin, Valdimarsson, T, Mikaelsdottir, E, Sigurdsson, S, Jonsson, S, Rafnar, Thorunn, Aarsland, Dag, Djurovic, Srdjan, Fladby, Tormod, Knudsen, Gun Peggy S., Celius, Elisabeth Gulowsen, Myhr, Kjell-Morten, Gröndal, Gerdur, Steinsson, K, Valdimarsson, Helgi, Bjornsson, Sigurdur, Bjornsdottir, US, Bjornsson, Einar S., Nilsson, B, Andreassen, Ole Andreas, Alfredsson, Lars, Hillert, Jan, Kockum, Ingrid, Másson, Gísli, Thorsteinssdottir, U, Gudbjartsson, Daniel F., Stefansson, H, Hjaltason, H, Harbo, Hanne Flinstad, Olsson, T, Jonsdottir, I, Stefansson, K

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Classical Human Leukocyte Antigen Alleles and C4 Haplotypes Are Not Significantly Associated With Depression von Glanville, KP, Coleman, JRI, Hanscombe, KB, Euesden, J, Choi, SW, Purves, KL, Breen, G, Air, TM, Andlauer, TFM, Baune, BT, Binder, EB, Blackwood, DHR, Boomsma, DI, Buttenschøn, HN, Colodro-Conde, L, Dannlowski, U, Direk, N, Dunn, EC, Forstner, AJ, de Geus, EJC, Grabe, HJ, Hamilton, SP, Jones, I, Jones, LA, Knowles, JA, Kutalik, Z, Levinson, DF, Lewis, G, Lind, PA, Lucae, S, Magnusson, PK, McGuffin, P, McIntosh, AM, Milaneschi, Y, Mors, O, Mostafavi, S, Müller-Myhsok, B, Pedersen, NL, Penninx, BWJH, Potash, JB, Preisig, M, Ripke, S, Shi, J, Shyn, SI, Smoller, JW, Streit, F, Sullivan, PF, Tiemeier, H, Uher, R, Van der Auwera, S, Weissman, MM, Major Depressive Disorder Working Group of the Psychiatric Genom, O'Reilly, PF, Lewis, CM

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Phenome-wide analysis of genome-wide polygenic scores von Krapohl, E, Euesden, J, Zabaneh, D, Pingault, J. B, Rimfeld, K, Von Stumm, S, Dale, P. S, Breen, G, O'Reilly, P. F, Plomin, R

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An Examination of Polygenic Score Risk Prediction in Individuals With First-Episode Psychosis von Vassos, E, Di Forti, M, Coleman, J, Iyegbe, C, Prata, D, Euesden, J, O'Reilly, P, Curtis, C, Kolliakou, A, Patel, H, Newhouse, S, Traylor, M, Ajnakina, O, Mondelli, V, Marques, TR, Gardner-Sood, P, Aitchison, KJ, Powell, J, Atakan, Z, Greenwood, KE, Smith, S, Ismail, K, Pariante, C, Gaughran, F, Dazzan, P, Markus, HS, David, AS, Lewis, CM, Murray, RM, Breen, G

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Fourteen sequence variants that associate with multiple sclerosis discovered by meta-analysis informed by genetic correlations von Olafsson, S, Stridh, P, Bos, Steffan Daniel, Ingason, Andrés, Euesden, J, Sulem, Patrick, Thorleifsson, Gudmar, Gustafsson, O, Geirsson, AJ, Jóhannesson, Ari J, Thorsson, AV, Ludviksson, BR, Sigurgeirsson, Bardur, Jonasson, JG, Olafsson, E, Kristjansdottir, H, Olafsson, JH, Orvar, KB, Benediktsson, Rafn, Bjarnason, Ragnar, Kristjansdottir, Sjofn, Gislason, Thorarin, Valdimarsson, T, Mikaelsdottir, E, Sigurdsson, S, Jonsson, S, Rafnar, Thorunn, Aarsland, Dag, Djurovic, Srdjan, Fladby, Tormod, Knudsen, Gun Peggy S, Celius, Elisabeth Gulowsen, Myhr, Kjell-Morten, Gröndal, Gerdur, Steinsson, K, Valdimarsson, Helgi, Bjornsson, Sigurdur, Bjornsdottir, US, Bjornsson, Einar S, Nilsson, B, Andreassen, Ole Andreas, Alfredsson, Lars, Hillert, Jan, Kockum, Ingrid, Másson, Gísli, Thorsteinssdottir, U, Gudbjartsson, Daniel F, Stefansson, H, Hjaltason, H, Harbo, Hanne Flinstad, Olsson, T, Jonsdottir, I, Stefansson, K

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Fourteen sequence variants that associate with multiple sclerosis discovered by meta-analysis informed by genetic correlations von Olafsson, S, Stridh, P, Bos, Steffan Daniel, Ingason, Andrés, Euesden, J, Sulem, Patrick, Thorleifsson, Gudmar, Gustafsson, O, Geirsson, AJ, Jóhannesson, Ari J, Thorsson, AV, Ludviksson, BR, Sigurgeirsson, Bardur, Jonasson, JG, Olafsson, E, Kristjansdottir, H, Olafsson, JH, Orvar, KB, Benediktsson, Rafn, Bjarnason, Ragnar, Kristjansdottir, Sjofn, Gislason, Thorarin, Valdimarsson, T, Mikaelsdottir, E, Sigurdsson, S, Jonsson, S, Rafnar, Thorunn, Aarsland, Dag, Djurovic, Srdjan, Fladby, Tormod, Knudsen, Gun Peggy S, Celius, Elisabeth Gulowsen, Myhr, Kjell-Morten, Gröndal, Gerdur, Steinsson, K, Valdimarsson, Helgi, Bjornsson, Sigurdur, Bjornsdottir, US, Bjornsson, Einar S, Nilsson, B, Andreassen, Ole Andreas, Alfredsson, Lars, Hillert, Jan, Kockum, Ingrid, Másson, Gísli, Thorsteinssdottir, U, Gudbjartsson, Daniel F, Stefansson, H, Hjaltason, H, Harbo, Hanne Flinstad, Olsson, T, Jonsdottir, I, Stefansson, K

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Fourteen sequence variants that associate with multiple sclerosis discovered by meta-analysis informed by genetic correlations von Olafsson, S, Stridh, P, Bos, Steffan Daniel, Ingason, Andrés, Euesden, J, Sulem, Patrick, Thorleifsson, Gudmar, Gustafsson, O, Geirsson, AJ, Jóhannesson, Ari J, Thorsson, AV, Ludviksson, BR, Sigurgeirsson, Bardur, Jonasson, JG, Olafsson, E, Kristjansdottir, H, Olafsson, JH, Orvar, KB, Benediktsson, Rafn, Bjarnason, Ragnar, Kristjansdottir, Sjofn, Gislason, Thorarin, Valdimarsson, T, Mikaelsdottir, E, Sigurdsson, S, Jonsson, S, Rafnar, Thorunn, Aarsland, Dag, Djurovic, Srdjan, Fladby, Tormod, Knudsen, Gun Peggy S, Celius, Elisabeth Gulowsen, Myhr, Kjell-Morten, Gröndal, Gerdur, Steinsson, K, Valdimarsson, Helgi, Bjornsson, Sigurdur, Bjornsdottir, US, Bjornsson, Einar S, Nilsson, B, Andreassen, Ole Andreas, Alfredsson, Lars, Hillert, Jan, Kockum, Ingrid, Másson, Gísli, Thorsteinssdottir, U, Gudbjartsson, Daniel F, Stefansson, H, Hjaltason, H, Harbo, Hanne Flinstad, Olsson, T, Jonsdottir, I, Stefansson, K

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Understanding the environmentally assisted cracking (EAC) initiation and propagation of new generation 7xxx alloys using slow strain rate testing von Aboura, Y., Garner, A.J., Euesden, R., Barrett, Z., Engel, C., Holroyd, N.J.H., Prangnell, P.B., Burnett, T.L.

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Computational studies into urea formation in the interstellar medium von Slate, Eren C. S., Barker, Rory, Euesden, Ryan T., Revels, Max R., Meijer, Anthony J. H. M.

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In-situ observation of environmentally assisted crack initiation and short crack growth behaviour of new-generation 7xxx series alloys in humid air von Euesden, R.T., Aboura, Y., Garner, A.J., Jailin, T., Grant, C., Barrett, Z., Engel, C., Shanthraj, P., Holroyd, N.J.H., Prangnell, P.B., Burnett, T.L.

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Exploring the association of genetic factors with participation in the Avon Longitudinal Study of Parents and Children von Taylor, Amy E, Jones, Hannah J, Sallis, Hannah, Euesden, Jack, Stergiakouli, Evie, Davies, Neil M, Zammit, Stanley, Lawlor, Debbie A, Munafò, Marcus R, Davey Smith, George, Tilling, Kate

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Identification of novel genetic variants and biomarkers for cognitive decline in Alzheimer’s disease von Ali, Muhammad, Wang, Fengxian, Mafimoghaddam, Samira, Euesden, Jack, Robins, Chloe, Pulford, David J., Cruchaga, Carlos

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