Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry

- Mueller, Stefanie H., Lai, Alvina G., Andrulis, Irene L., Anton-Culver, Hoda, Antonenkova, Natalia N., Arndt, Volker, Aronson, Kristan J., Augustinsson, Annelie, Baert, Thais, Freeman, Laura E. Beane, Beckmann, Matthias W., Behrens, Sabine, Valkovskaya, Maria, Benitez, Javier, Bermisheva, M, Blomqvist, C, Bogdanova, NV, Bojesen, SE, Bonanni, B, Brenner, H, Brucker, SY, Buys, SS, Castelao, JE, Michailidou, Kyriaki, Chan, TL, Chang-Claude, J, Chanock, SJ, Choi, JY, Chung, WK, Sahlberg, KK, Børresen-Dale, AL, Ottestad, L, Kåresen, R, Schlichting, E, Bolla, Manjeet K., Holmen, MM, Sauer, T, Haakensen, V, Engebråten, O, Naume, B, Fosså, A, Kiserud, CE, Reinertsen, KV, Helland, Å, Riis, M, Wang, Qin, Geisler, J, Grenaker Alnaes, GI, Colonna, SV, Cornelissen, S, Couch, FJ, Czene, K, Daly, MB, Devilee, P, Dörk, T, Dossus, L, Dennis, Joe, Dwek, M, Eccles, DM, Ekici, AB, Eliassen, AH, Engel, C, Evans, DG, Fasching, PA, Fletcher, O, Flyger, H, Gago-Dominguez, M, Lush, Michael, Gao, YT, García-Closas, M, García-Sáenz, JA, Genkinger, J, Gentry-Maharaj, A, Grassmann, F, Guénel, P, Gündert, M, Haeberle, L, Hahnen, E, Abu-Ful, Zomoruda, Haiman, CA, Håkansson, N, Hall, P, Harkness, EF, Harrington, PA, Hartikainen, JM, Hartman, M, Hein, A, Ho, WK, Hooning, MJ, Ahearn, Thomas U., Hoppe, R, Hopper, JL, Houlston, RS, Howell, A, Hunter, DJ, Huo, D, Marsh, D, Scott, Rodney, Baxter, R, Yip, D

Rare variant analysis in eczema identifies exonic variants in DUSP1, NOTCH4 and SLC9A4

- Grosche, Sarah, Marenholz, Ingo, Bisgaard, Hans, Bønnelykke, Klaus, Brown, Sara J., Bustamante, Mariona, Curtin, John A., Custovic, Adnan, Dharmage, Shyamali C., Esplugues, Ana, Falchi, Mario, Fernandez-Orth, Dietmar, Esparza-Gordillo, Jorge, Ferreira, Manuel A. R., Franke, A, Gerdes, S, Gieger, C, Hakonarson, H, Holt, PG, Homuth, G, Hubner, N, Hysi, PG, Jarvelin, M-R, Arnau-Soler, Aleix, Karlsson, R, Koppelman, GH, Lau, S, Lutz, M, Magnusson, PKE, Marks, GB, Mueller-Nurasyid, M, Noethen, MM, Paternoster, L, Pennell, Craig E., Pairo-Castineira, Erola, Peters, A, Rawlik, K, Robertson, CF, Rodriguez, E, Sebert, S, Simpson, A, Sleiman, PMA, Standl, M, Stoelzl, D, Strauch, K, Rüschendorf, Franz, Szwajda, A, Tenesa, A, Thompson, PJ, Ullemar, V, Visconti, A, Vonk, JM, Wang, CA, Weidinger, S, Wielscher, M, Worth, CL, Ahluwalia, Tarunveer S., Xu, C-J, Lee, Y-A, Almqvist, Catarina, Arnold, Andreas, Baurecht, Hansjörg

Population-based identity-by-descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia

- Harold, Denise, Connolly, Siobhan, Riley, Brien P., Kendler, Kenneth S., McCarthy, Shane E., McCombie, William R., Richards, Alex, Owen, Michael J., O'Donovan, Michael C., Walters, James, Donnelly, Peter, Bates, Lesley, Barroso, Ines, Blackwell, Jenefer M., Bramon, Elvira, Brown, Matthew A., Casas, Juan P., Corvin, Aiden, Deloukas, Panos, Duncanson, Audrey, Henskens, Frans A., Loughland, Carmel M., Michie, Patricia T., Schall, Ulrich, Scott, Rodney J.