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Large-scale sequencing identifies multiple genes and rare variants associated with Crohn's disease susceptibility

by Sazonovs, Aleksejs, Stevens, Christine R, Venkataraman, Guhan R, Yuan, Kai, Avila, Brandon, Ahmad, Tariq, Ananthakrishnan, Ashwin N, Atzmon, Gil, Baras, Aris, Barrett, Jeffrey C, Barzilai, Nir, Beaugerie, Laurent, Bernstein, Charles N, Bitton, Alain, Bokemeyer, Bernd, Cosnes, Jacques, Cutler, David J, Daly, Allan, Damas, Oriana M, Devoto, Marcella, Ellinghaus, Eva, Farkkila, Martti, Ferreira, Manuel, Franchimont, Denis, Ge, Tian, Georges, Michel, Giri, Mamta, Glaser, Benjamin, Goyette, Philippe, Graham, Daniel, Hämäläinen, Eija, Haritunians, Talin, Heap, Graham A, Hiltunen, Mikko, Hoeppner, Marc, Horowitz, Julie E, Irving, Peter, Iyer, Vivek, Jalas, Chaim, Kelsen, Judith, Khalili, Hamed, Kirschner, Barbara S, Kontula, Kimmo, Kugathasan, Subra, Kupcinskas, Juozas, Lamb, Christopher A, Laudes, Matthias, Lévesque, Chloé, Levine, Adam P, Lewis, James D, Liefferinckx, Claire, Loescher, Britt-Sabina, Louis, Edouard, Mansfield, John, McCauley, Jacob L, Mengesha, Emebet, Moran, Christopher J, O'Charoen, Sirimon, Oldenburg, Bas, Ostrer, Harry, Palotie, Aarno, Paquette, Jean, Pekow, Joel, Peter, Inga, Ponsioen, Cyriel Y, Prescott, Natalie, Pulver, Ann E, Rahmouni, Souad, Saavalainen, Päivi, Sands, Bruce, Sartor, R Balfour, Schiff, Elena R, Schreiber, Stefan, Segal, Anthony W, Seksik, Philippe, Silverberg, Mark S, Simmons, Alison, Skeiceviciene, Jurgita, Solomonson, Matthew, Somineni, Hari, Turner, Dan, Uhlig, Holm H, van der Meulen, Andrea E, Vermeire, Séverine, Verstockt, Sare, Winter, Harland S, Young, Justine, Duerr, Richard H, Franke, Andre, Brant, Steven R, Cho, Judy, Weersma, Rinse K, Parkes, Miles, Xavier, Ramnik J, Rivas, Manuel A, Rioux, John D, McGovern, Dermot P B, Huang, Hailiang, Anderson, Carl A, Daly, Mark J
Published in Nature genetics (01.09.2022)

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