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Gallagher, CS, Makinen, N, Harris, HR, Rahmioglu, N, Uimari, O, Cook, JP, Shigesi, N, Ferreira, T, Velez-Edwards, DR, Edwards, TL et al (show 50 more authors) , Mortlock, S, Ruhioglu, Z, Day, F, Becker, CM, Karhunen, V, Martikainen, H, Jarvelin, M-R, Cantor, RM, Ridker, PM, Terry, KL, Buring, JE, Gordon, SD, Medland, SE, Montgomery, GW, Nyholt, DR, Hinds, DA, Tung, JY, Perry, JRB, Lind, PA, Painter, JN, Martin, NG, Morris, AP, Chasman, DI, Missmer, SA, Zondervan, KT, Morton, CC, Agee, Michelle, Alipanahi, Babak, Auton, Adam, Bell, Robert K, Bryc, Katarzyna, Elson, Sarah L, Fontanillas, Pierre, Furlotte, Nicholas A, Huber, Karen E, Kleinman, Aaron, Litterman, Nadia K, McIntyre, Matthew H, Mountain, Joanna L, Noblin, Elizabeth S, Northover, Carrie AM, Pitts, Steven J, Sathirapongsasuti, J Fah, Sazonova, Olga V, Shelton, Janie F, Shringarpure, Suyash, Tian, Chao, Vacic, Vladimir, Wilson, Catherine H and Team, 23andMe Res (2019) Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis. NATURE COMMUNICATIONS, 10.

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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). 898 - 907.

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Gormley, P, Anttila, V, Winsvold, BS, Palta, P, Esko, T, Pers, TH, Farh, KH, Cuenca-Leon, E, Muona, M, Furlotte, NA et al (show 67 more authors) , Kurth, T, Ingason, A, McMahon, G, Ligthart, L, Terwindt, GM, Kallela, M, Freilinger, TM, Ran, C, Gordon, SG, Stam, AH, Steinberg, S, Borck, G, Koiranen, M, Quaye, L, Adams, HHH, Lehtimäki, T, Sarin, AP, Wedenoja, J, Hinds, DA, Buring, JE, Schürks, M, Ridker, PM, Hrafnsdottir, MG, Stefansson, H, Ring, SM, Hottenga, JJ, Penninx, BWJH, Färkkilä, M, Artto, V, Kaunisto, M, Vepsäläinen, S, Malik, R, Heath, AC, Madden, PAF, Martin, NG, Montgomery, GW, Kurki, MI, Kals, M, Mägi, R, Pärn, K, Hämäläinen, E, Huang, H, Byrnes, AE, Franke, L, Huang, J, Stergiakouli, E, Lee, PH, Sandor, C, Webber, C, Cader, Z, Muller-Myhsok, B ORCID: 0000-0002-0719-101X, Schreiber, S, Meitinger, T, Eriksson, JG, Salomaa, V, Heikkilä, K, Loehrer, E, Uitterlinden, AG, Hofman, A, Van Duijn, CM, Cherkas, L, Pedersen, LM, Stubhaug, A, Nielsen, CS, Männikkö, M, Mihailov, E and Milani, L (2016) Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. Nature Genetics, 48 (8). 856 - 866.