Approaches and advances in the genetic causes of autoimmune disease and their implications af Inshaw, JR, Cutler, AJ, Burren, OS, Stefana, MI, Todd, JA

Assessing the contribution of rare protein-coding germline variants to prostate cancer risk and severity in 37,184 cases af Mitchell, J, Camacho, N, Shea, P, Stopsack, KH, Joseph, V, Burren, OS, Dhindsa, RS, Nag, A, Berchuck, JE, O’Neill, A, Abbasi, A, Zoghbi, AW, Alegre-Díaz, J, Kuri-Morales, P, Berumen, J, Tapia-Conyer, R, Emberson, J, Torres, JM, Collins, R, Wang, Q, Goldstein, D, Matakidou, A, Haefliger, C, Anderson-Dring, L

Lineage-specific genome architecture links enhancers and non-coding disease variants to target gene promoters af Javierre, BM, Burren, OS, Wilder, SP, Kreuzhuber, R, Hill, SM, Sewitz, S, Cairns, J, Wingett, SW, Várnai, C, Thiecke, MJ, Burden, F, Farrow, S, Cutler, AJ, Rehnström, K, Downes, K, Grassi, L, Kostadima, M, Freire-Pritchett, P, Wang, F, BLUEPRINT Consortium, Stunnenberg, HG, Todd, JA, Zerbino, DR, Stegle, O, Ouwehand, WH, Frontini, M, Wallace, C, Spivakov, M, Fraser, P

Whole-genome sequencing of a sporadic primary immunodeficiency cohort af Thaventhiran, JED, Lango Allen, H, Burren, OS, Rae, W, Greene, D, Staples, E, Zhang, Z, Farmery, JHR, Simeoni, I, Rivers, E, Maimaris, J, Penkett, CJ, Stephens, J, Deevi, SVV, Sanchis-Juan, A, Gleadall, NS, Thomas, MJ, Sargur, RB, Gordins, P, Baxendale, HE, Brown, M, Tuijnenburg, P, Worth, A, Hanson, S, Linger, RJ, Buckland, MS, Rayner-Matthews, PJ, Gilmour, KC, Samarghitean, C, Seneviratne, SL, Sansom, DM, Lynch, AG, Megy, K, Ellinghaus, E, Ellinghaus, D, Jorgensen, SF, Karlsen, TH, Stirrups, KE, Cutler, AJ, Kumararatne, DS, Chandra, A, Edgar, JDM, Herwadkar, A, Cooper, N, Grigoriadou, S, Huissoon, AP, Goddard, S, Jolles, S, Schuetz, C, Boschann, F, Roberts, IAG