Alterations in T and B cell receptor repertoires patterns in patients with IL10 signaling defects and history of infantile-onset IBD by Werner, L, Lee, YN, Rechavi, E, Lev, A, Yerushalmi, B, Ling, G, Shah, N, Uhlig, HH, Weiss, B, Somech, R, Snapper, SB, Shouval, DS

Human MD2 deficiency – an inborn error of immunity with pleiotropic features by Li, Y, Yu, Z, Schenk, M, Lagovsky, I, Illig, D, Walz, C, Rohlfs, M, Conca, R, Muise, AM, Snapper, SB, Uhlig, HH, Zion Garty, B, Klein, C, Kotlarz, D

Clinical genomics for the diagnosis of monogenic forms of inflammatory bowel disease by Uhlig, H, Charbit-Henrion, F, Kotlarz, D, Shouval, D, Schwerd, T, Strisciuglio, C, de Ridder, L, van Limbergen, J, Macchia, L, Snapper, SB, Rummele, FM, Wilson, DC, Travis, SPL, Griffiths, AM, Turner, D, Klein, C, Muise, AM, Russell, RK

Prevalence and clinical features of inflammatory bowel diseases associated with monogenetic variants, identified by whole-exome sequencing in 1000 children at a single center by Crowley, E, Warner, N, Pan, J, Khalouei, S, Elkadri, A, Fiedler, K, Foong, J, Turinsky, AL, Bronte-Tinkew, D, Zhang, S, Hu, J, Tian, D, Li, D, Horowitz, J, Siddiqui, I, Upton, J, Roifman, CM, Church, PC, Wall, DA, Ramani, AK, Kotlarz, D, Klein, C, Uhlig, H, Snapper, SB, Gonzaga-Jauregui, C, Paterson, AD, McGovern, PB, Brudno, M, Walters, TD, Griffiths, AM, Muise, AM

Somatic mosaicism and common genetic variation contribute to the risk of very-early-onset inflammatory bowel disease by Gonçalves Serra, E, Schwerd, T, Moutsianas, L, Cavounidis, A, Fachal, L, Pandey, S, Kammermeier, J, Croft, NM, Posovszky, C, Rodrigues, A, Russell, RK, Barakat, F, Auth, MKH, Heuschkel, R, Zilbauer, M, Fyderek, K, Braegger, C, Travis, SP, Satsangi, J, Parkes, M, Thapar, N, Ferry, H, Matte, JC, Gilmour, KC, Wedrychowicz, A, Sullivan, P, Moore, C, Sambrook, J, Ouwehand, W, Roberts, D, Danesh, J, Baeumler, TA, Fulga, TA, Karaminejadranjbar, M, Ahmed, A, Wilson, R, Barrett, JC, Elkadri, A, Griffiths, AM, COLORS in IBD group investigators, Oxford IBD cohort study investigators, INTERVAL Study, Swiss IBD cohort investigators, UK IBD Genetics Consortium, NIDDK IBD Genetics Consortium, Snapper, SB, Shah, N, Muise, AM, Wilson, DC, Et al