Number of items: 2.
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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 49 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 and Wilson, Catherine H
(2019)
Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis.
NATURE COMMUNICATIONS, 10 (1).
4857-.
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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.
This list was generated on Thu Feb 8 05:08:32 2024 GMT.