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Campa, D, Pastore, M, Gentiluomo, M, Talar-Wojnarowska, R, Kupcinskas, J, Malecka-Panas, E, Neoptolemos, JP, Niesen, W, Vodicka, P, Delle Fave, G et al (show 51 more authors) , Bueno-de-Mesquita, HB, Gazouli, M, Pacetti, P, Di Leo, M, Ito, H, Klueter, H, Soucek, P, Corbo, V, Yamao, K, Hosono, S, Kaaks, R, Vashist, Y, Gioffreda, D, Strobel, O, Shimizu, Y, Dijk, F, Andriulli, A, Ivanauskas, A, Bugert, P, Tavano, F, Vodickova, L, Zambon, CF, Lovecek, M, Landi, S, Key, TJ, Boggi, U, Pezzilli, R, Jamroziak, K, Mohelnikova-Duchonova, B, Mambrini, A, Bambi, F, Busch, O, Pazienza, V, Valente, R, Theodoropoulos, GE, Hackert, T, Capurso, G, Cavestro, GM, Pasquali, C, Basso, D, Sperti, C, Matsuo, K, Buechler, M, Khaw, K-T, Izbicki, J, Costello, E, Katzke, V, Michalski, C, Stepien, A, Rizzato, C and Canzian, F (2016) Functional single nucleotide polymorphisms within the cyclin-dependent kinase inhibitor 2A/2B region affect pancreatic cancer risk. ONCOTARGET, 7 (35). pp. 57011-57020.

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Schormair, B, Zhao, C, Bell, S, Tilch, E, Salminen, AV, Putz, B, Dauvilliers, Y, Stefani, A, Hogl, B, Poewe, W et al (show 89 more authors) , Kemlink, D, Sonka, K, Bachmann, CG, Paulus, W, Trenkwalder, C, Oertel, WH, Hornyak, M, Teder-Laving, M, Metspalu, A, Hadjigeorgiou, GM, Polo, O, Fietze, I, Ross, OA, Wszolek, Z, Butterworth, AS, Soranzo, N, Ouwehand, WH, Roberts, DJ, Danesh, J, Allen, RP, Earley, CJ, Ondo, WG, Xiong, L, Montplaisir, J, Gan-Or, Z, Perola, M, Vodicka, P, Dina, C, Franke, A, Tittmann, L, Stewart, AFR, Shah, SH, Gieger, C, Peters, A, Rouleau, GA, Berger, K, Oexle, K, Di Angelantonio, E, Hinds, DA, Muller-Myhsok, B ORCID: 0000-0002-0719-101X, Winkelmann, J, Balkau, B, Ducimetiere, P, Eschwege, E, Ranciere, F, Alhenc-Gelas, F, Gallois, Y, Girault, A, Fumeron, F, Marre, M, Roussel, R, Bonnet, F, Bonnefond, A, Cauchi, S, Froguel, P, Cogneau, J, Born, C, Caces, E, Cailleau, M, Lantieri, O, Moreau, JG, Rakotozafy, F, Tichet, J, Vol, S, Agee, M, Alipanahi, B, Auton, A, Bell, RK, Bryc, K, Elson, SL, Fontanillas, P, Furlotte, NA, Hinds, DA, Hromatka, BS, Huber, KE, Kleinman, A, Litterman, NK, McIntyre, MH, Mountain, JL, Northover, CA, Pitts, SJ, Sathirapongsasuti, JF, Sazonova, OV, Shelton, JF, Shringarpure, S, Tian, C, Tung, JY, Vacic, V and Wilson, CH (2017) Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis. Lancet Neurol, 16 (11). pp. 898-907.