Hereditary C1q deficiency and systemic lupus erythematosus. by Bowness, P, Davies, K, Norsworthy, P, Athanassiou, P, Taylor-Wiedeman, J, Borysiewicz, L, Meyer, P, Walport, M

Malaria susceptibility and CD36 mutation. by Aitman, T, Cooper, L, Norsworthy, P, Wahid, F, Gray, J, Curtis, B, McKeigue, P, Kwiatkowski, D, Greenwood, B, Snow, R, Hill, A, Scott, J

FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunity. by Fanciulli, M, Norsworthy, P, Petretto, E, Dong, R, Harper, L, Kamesh, L, Heward, J, Gough, S, de Smith, A, Blakemore, A, Froguel, P, Owen, C, Pearce, S, Teixeira, L, Guillevin, L, Graham, D, Pusey, C, Cook, H, Vyse, T, Aitman, T

Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans. by Aitman, T, Dong, R, Vyse, T, Norsworthy, P, Johnson, MD, Smith, J, Mangion, J, Roberton-Lowe, C, Marshall, A, Petretto, E, Hodges, MD, Bhangal, G, Patel, S, Sheehan-Rooney, K, Duda, M, Cook, P, Evans, D, Domin, J, Flint, J, Boyle, J, Pusey, C, Cook, H

Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association study by Jones, E, Hummerich, H, Viré, E, Uphill, J, Dimitriadis, A, Speedy, H, Campbell, T, Norsworthy, P, Quinn, L, Whitfield, J, Linehan, J, Jaunmuktane, Z, Brandner, S, Jat, P, Nihat, A, How Mok, T, Ahmed, P, Collins, S, Stehmann, C, Sarros, S, Kovacs, GG, Geschwind, MD, Golubjatnikov, A, Frontzek, K, Budka, H, Aguzzi, A, Karamujić-Čomić, H, van der Lee, SJ, Ibrahim-Verbaas, CA, van Duijn, CM, Sikorska, B, Golanska, E, Liberski, PP, Calero, M, Calero, O, Sanchez-Juan, P, Salas, A, Martinón-Torres, F, Bouaziz-Amar, E, Haïk, S, Laplanche, J-L, Brandel, J-P, Amouyel, P, Lambert, J-C, Parchi, P, Bartoletti-Stella, A, Capellari, S, Poleggi, A, Ladogana, A, Pocchiari, M