Author Correction: Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases von An, Jiyuan, Gharahkhani, Puya, Law, Matthew H., Ong, Jue-Sheng, Han, Xikun, Olsen, Catherine M., Neale, Rachel E., Lai, John, Vaughan, Tom L., Gockel, Ines, Thieme, René, Böhmer, Anne C., Jankowski, Janusz, Fitzgerald, Rebecca C., Schumacher, Johannes, Palles, Claire, Whiteman, David C., MacGregor, Stuart

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The Parkinson’s phenome—traits associated with Parkinson’s disease in a broadly phenotyped cohort von Heilbron, Karl, Noyce, Alastair J., Fontanillas, Pierre, Alipanahi, Babak, Nalls, Mike A., Cannon, Paul

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Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways von Jansen, Philip R., Watanabe, Kyoko, Stringer, Sven, Skene, Nathan, Bryois, Julien, Hammerschlag, Anke R., de Leeuw, Christiaan A., Benjamins, Jeroen S., Muñoz-Manchado, Ana B., Nagel, Mats, Savage, Jeanne E., Tiemeier, Henning, White, Tonya, Tung, Joyce Y., Hinds, David A., Vacic, Vladimir, Wang, Xin, Sullivan, Patrick F., van der Sluis, Sophie, Polderman, Tinca J. C., Smit, August B., Hjerling-Leffler, Jens, Van Someren, Eus J. W., Posthuma, Danielle

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Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions von Howard, David M., Adams, Mark J., Clarke, Toni-Kim, Hafferty, Jonathan D., Gibson, Jude, Shirali, Masoud, Coleman, Jonathan R. I., Hagenaars, Saskia P., Ward, Joey, Wigmore, Eleanor M., Alloza, Clara, Shen, Xueyi, Barbu, Miruna C., Xu, Eileen Y., Whalley, Heather C., Marioni, Riccardo E., Porteous, David J., Davies, Gail, Deary, Ian J., Hemani, Gibran, Berger, Klaus, Teismann, Henning, Rawal, Rajesh, Arolt, Volker, Baune, Bernhard T., Dannlowski, Udo, Domschke, Katharina, Tian, Chao, Hinds, David A., Trzaskowski, Maciej, Byrne, Enda M., Ripke, Stephan, Smith, Daniel J., Sullivan, Patrick F., Wray, Naomi R., Breen, Gerome, Lewis, Cathryn M., McIntosh, Andrew M.

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Large-scale GWAS reveals insights into the genetic architecture of same-sex sexual behavior von Ganna, Andrea, Verweij, Karin J H, Nivard, Michel G, Maier, Robert, Wedow, Robbee, Busch, Alexander S, Abdellaoui, Abdel, Guo, Shengru, Sathirapongsasuti, J Fah, Lichtenstein, Paul, Lundström, Sebastian, Långström, Niklas, Auton, Adam, Harris, Kathleen Mullan, Beecham, Gary W, Martin, Eden R, Sanders, Alan R, Perry, John R B, Neale, Benjamin M, Zietsch, Brendan P

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Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis von Schormair, Barbara, Zhao, Chen, Bell, Steven, Tilch, Erik, Salminen, Aaro V, Pütz, Benno, Dauvilliers, Yves, Stefani, Ambra, Högl, Birgit, Poewe, Werner, Kemlink, David, Sonka, Karel, Bachmann, Cornelius G, Paulus, Walter, Trenkwalder, Claudia, Oertel, Wolfgang H, Hornyak, Magdolna, Teder-Laving, Maris, Metspalu, Andres, Hadjigeorgiou, Georgios M, Polo, Olli, Fietze, Ingo, Ross, Owen A, Wszolek, Zbigniew, Butterworth, Adam S, Soranzo, Nicole, Ouwehand, Willem H, Roberts, David J, Danesh, John, Allen, Richard P, Earley, Christopher J, Ondo, William G, Xiong, Lan, Montplaisir, Jacques, Gan-Or, Ziv, Perola, Markus, Vodicka, Pavel, Dina, Christian, Franke, Andre, Tittmann, Lukas, Stewart, Alexandre F R, Shah, Svati H, Gieger, Christian, Peters, Annette, Rouleau, Guy A, Berger, Klaus, Oexle, Konrad, Di Angelantonio, Emanuele, Hinds, David A, Müller-Myhsok, Bertram, Winkelmann, Juliane, Balkau, B, Ducimetière, P, Eschwège, E, Rancière, 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, Michelle, Alipanahi, Babak, Auton, Adam, Bell, Robert K, Bryc, Katarzyna, Elson, Sarah L, Fontanillas, Pierre, Furlotte, Nicholas A, Hinds, David A, Hromatka, Bethann S, Huber, Karen E, Kleinman, Aaron, Litterman, Nadia K, McIntyre, Matthew H, Mountain, Joanna L, Northover, Carrie AM, Pitts, Steven J, Sathirapongsasuti, J Fah, Sazonova, Olga V, Shelton, Janie F, Shringarpure, Suyash, Tian, Chao, Tung, Joyce Y, Vacic, Vladimir, Wilson, Catherine H

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A comprehensive re-assessment of the association between vitamin D and cancer susceptibility using Mendelian randomization von Ong, Jue-Sheng, Dixon-Suen, Suzanne C., Han, Xikun, An, Jiyuan, Liyanage, Upekha, Dusingize, Jean-Cluade, Schumacher, Johannes, Gockel, Ines, Böhmer, Anne, Jankowski, Janusz, Palles, Claire, O’Mara, Tracy, Spurdle, Amanda, Law, Matthew H., Iles, Mark M., Pharoah, Paul, Berchuck, Andrew, Zheng, Wei, Thrift, Aaron P., Olsen, Catherine, Neale, Rachel E., Gharahkhani, Puya, Webb, Penelope M., MacGregor, Stuart

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Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases von An, Jiyuan, Gharahkhani, Puya, Law, Matthew H., Ong, Jue-Sheng, Han, Xikun, Olsen, Catherine M., Neale, Rachel E., Lai, John, Vaughan, Tom L., Gockel, Ines, Thieme, René, Böhmer, Anne C., Jankowski, Janusz, Fitzgerald, Rebecca C., Schumacher, Johannes, Palles, Claire, Whiteman, David C., MacGregor, Stuart

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The Population Reference Sample, POPRES: A Resource for Population, Disease, and Pharmacological Genetics Research von Nelson, Matthew R., Bryc, Katarzyna, King, Karen S., Indap, Amit, Boyko, Adam R., Novembre, John, Briley, Linda P., Maruyama, Yuka, Waterworth, Dawn M., Waeber, Gérard, Vollenweider, Peter, Oksenberg, Jorge R., Hauser, Stephen L., Stirnadel, Heide A., Kooner, Jaspal S., Chambers, John C., Jones, Brendan, Mooser, Vincent, Bustamante, Carlos D., Roses, Allen D., Burns, Daniel K., Ehm, Margaret G., Lai, Eric H.

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Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis von Gallagher, CS, Makinen, N, Harris, HR, Rahmioglu, N, Uimari, O, Cook, JP, Shigesi, N, Ferreira, T, Velez-Edwards, DR, Edwards, TL, 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, M, Alipanahi, B, Auton, A, Bell, RK, Bryc, K, Elson, SL, Fontanillas, P, Furlotte, NA, Huber, KE, Kleinman, A, Litterman, NK, McIntyre, MH, Mountain, JL, Noblin, ES, Northover, CAM, Pitts, SJ, Sathirapongsasuti, JF, Sazonova, OV, Shelton, JF, Shringarpure, S, Tian, C, Vacic, V, Wilson, CH

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An atlas of genetic influences on osteoporosis in humans and mice von Morris, JA, Kemp, JP, Youlten, SE, Laurent, L, Logan, JG, Chai, RC, Vulpescu, NA, Forgetta, V, Kleinman, A, Mohanty, ST, Sergio, CM, Quinn, J, Nguyen-Yamamoto, L, Luco, A-L, Vijay, J, Simon, M-M, Pramatarova, A, Medina-Gomez, C, Trajanoska, K, Ghirardello, EJ, Butterfield, NC, Curry, KF, Leitch, VD, Sparkes, PC, Adoum, A-T, Mannan, NS, Komla-Ebri, DSK, Pollard, AS, Dewhurst, HF, Hassall, TAD, Beltejar, M-JG, Agee, M, Alipanahi, B, Auton, A, Bell, RK, Bryc, K, Elson, SL, Fontanillas, P, Furlotte, NA, McCreight, JC, Huber, KE, Litterman, NK, McIntyre, MH, Mountain, JL, Noblin, ES, Northover, CAM, Pitts, SJ, Sathirapongsasuti, JF, Sazonova, OV, Shelton, JF, Shringarpure, S, Tian, C, Tung, JY, Vacic, V, Wilson, CH, Adams, DJ, Vaillancourt, SM, Kaptoge, S, Baldock, P, Cooper, C, Reeve, J, Ntzani, EE, Evangelou, E, Ohlsson, C, Karasik, D, Rivadeneira, F, Kiel, DP, Tobias, JH, Gregson, CL, Harvey, NC, Grundberg, E, Goltzman, D, Lelliott, CJ, Hinds, DA, Ackert-Bicknell, CL, Hsu, Y-H, Maurano, MT, Croucher, PI, Williams, GR, Bassett, JHD, Evans, DM, Richards, JB

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Genomewide Association Studies of LRRK2 Modifiers of Parkinson's Disease von Lai, D, Alipanahi, B, Fontanillas, P, Schwantes-An, TH, Aasly, J, Alcalay, RN, Beecham, GW, Berg, D, Bressman, S, Brice, A, Brockman, K, Clark, L, Cookson, M, Das, S, Van Deerlin, V, Follett, J, Farrer, MJ, Trinh, J, Gasser, T, Goldwurm, S, Gustavsson, E, Klein, C, Lang, AE, Langston, JW, Latourelle, J, Lynch, T, Marder, K, Marras, C, Martin, ER, McLean, CY, Mejia-Santana, H, Molho, E, Myers, RH, Nuytemans, K, Ozelius, L, Payami, H, Raymond, D, Rogaeva, E, Rogers, MP, Ross, OA, Samii, A, Saunders-Pullman, R, Schüle, B, Schulte, C, Scott, WK, Tanner, C, Tolosa, E, Tomkins, JE, Vilas, D, Trojanowski, JQ, Uitti, R, Vance, JM, Visanji, NP, Wszolek, ZK, Zabetian, CP, Mirelman, A, Giladi, N, Orr Urtreger, A, Cannon, P, Fiske, B, Foroud, T, Agee, M, Auton, A, Bell, RK, Bryc, K, Elson, SL, Furlotte, NA, Hinds, DA, Huber, KE, Kleinman, A, Litterman, NK, McIntyre, MH, Mountain, JL, Noblin, ES, Northover, CAM, Pitts, SJ, Fah Sathirapongsasuti, J, Sazonova, OV, Shelton, JF, Shringarpure, S, Tian, C, Tung, JY, Vacic, V, Wilson, CH

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A comprehensive re-assessment of the association between vitamin D and cancer susceptibility using Mendelian randomization von Ong, Jue-Sheng, Dixon-Suen, Suzanne C, Han, Xikun, An, Jiyuan, Liyanage, Upekha, Dusingize, Jean-Cluade, Schumacher, Johannes, Gockel, Ines, Böhmer, Anne, Jankowski, Janusz, Palles, Claire, O’Mara, Tracy, Spurdle, Amanda, Law, Matthew H, Iles, Mark M, Pharoah, Paul, Berchuck, Andrew, Zheng, Wei, Thrift, Aaron P, Olsen, Catherine, Neale, Rachel E, Gharahkhani, Puya, Webb, Penelope M, MacGregor, Stuart, Fitzgerald, Rebecca, Buas, Matt, Gammon, Marilie D, Corley, Douglas A, Shaheen, Nicholas J, Hardie, Laura J, Bird, Nigel C, Reid, Brian J, Chow, Wong-Ho, Risch, Harvey A, Ye, Weimin, Liu, Geoffrey, Romero, Yvonne, Bernstein, Leslie, Wu, Anna H, Whiteman, David E, Vaughan, Thomas, Agee, M, Alipanahi, B, Auton, A, Bell, R. K, Bryc, K, Elson, S. L, Fontanillas, P, Furlotte, N. A, Hinds, D. A, Huber, K. E, Kleinman, A, Litterman, N. K, McIntyre, M. H, Mountain, J. L, Noblin, E. S, Northover, C. A. M, Pitts, S. J, Sathirapongsasuti, J. Fah, Sazonova, O. V, Shelton, J. F, Shringarpure, S, Tian, C, Tung, J. Y, Vacic, V, Wilson, C. H

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A comprehensive re-assessment of the association between vitamin D and cancer susceptibility using Mendelian randomization von Ong, JS, Dixon-Suen, SC, Han, X, An, J, Fitzgerald, R, Buas, M, Gammon, MD, Corley, DA, Shaheen, NJ, Hardie, LJ, Bird, NC, Reid, BJ, Chow, WH, Risch, HA, Ye, W, Liu, G, Romero, Y, Bernstein, L, Wu, AH, Whiteman, DE, Vaughan, T, Agee, M, Alipanahi, B, Auton, A, Bell, RK, Bryc, K, Elson, SL, Fontanillas, P, Furlotte, NA, Hinds, DA, Huber, KE, Kleinman, A, Litterman, NK, McIntyre, MH, Mountain, JL, Noblin, ES, Northover, CAM, Pitts, SJ, Sathirapongsasuti, JF, Sazonova, OV, Shelton, JF, Shringarpure, S, Tian, C, Tung, JY, Vacic, V, Wilson, CH, Liyanage, U, Dusingize, JC, Schumacher, J, Gockel, I, Böhmer, A, Jankowski, J, Palles, C, O’Mara, T, Spurdle, A, Law, MH, Iles, MM, Pharoah, P, Berchuck, A, Zheng, W, Thrift, AP, Olsen, C, Neale, RE, Gharahkhani, P, Webb, PM, MacGregor, S

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Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases von An, Jiyuan, Gharahkhani, Puya, Law, Matthew H, Ong, Jue-Sheng, Han, Xikun, Olsen, Catherine M, Neale, Rachel E, Lai, John, Vaughan, Tom L, Gockel, Ines, Thieme, René, Böhmer, Anne C, Jankowski, Janusz, Fitzgerald, Rebecca C, Schumacher, Johannes, Palles, Claire, Whiteman, David C, MacGregor, Stuart, Gammon, Marilie D, Corley, Douglas A, Shaheen, Nicholas J, Bird, Nigel C, Hardie, Laura J, Murray, Liam J, Reid, Brian J, Chow, Wong-Ho, Risch, Harvey A, Ye, Weimin, Liu, Geoffrey, Romero, Yvonne, Bernstein, Leslie, Wu, Anna H, Agee, M, Alipanahi, B, Auton, A, Bell, R. K, Bryc, K, Elson, S. L, Fontanillas, P, Furlotte, N. A, Hinds, D. A, Huber, K. E, Kleinman, A, Litterman, N. K, McIntyre, M. H, Mountain, J. L, Noblin, E. S, Northover, C. A. M, Pitts, S. J, Sathirapongsasuti, J. Fah, Sazonova, O. V, Shelton, J. F, Shringarpure, S, Tian, C, Tung, J. Y, Vacic, V, Wilson, C. H

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Overlapping genetic architecture between Parkinson disease and melanoma von Dube, U., Budde, J.P., Benitez, B.A., Davis, A.A., Harari, O., Iles, M.M., Brown, K.M., Agee, M., Alipanahi, B., Auton, A., Bell, R.K., Bryc, K., Elson, S.L., Fontanillas, P., Furlotte, N.A., Hinds, D.A., Kleinman, A., Litterman, N.K., McCreight, J.C., McIntyre, M.H., Mountain, J.L., Noblin, E.S., Northover, C.A.M., Sathirapongsasuti, J.F., Sazonova, O.V., Shelton, J.F., Tian, C., Tung, J.C.Y., Vacic, V., Wilson, C.H., Bishop, D.T., Brossard, M., Martin, N.G., Moses, E.K., Song, F., Barrett, J.H., Kumar, R., Easton, D.F., Pharoah, P.D., Swerdlow, A.J., Kypreou, K.P., Taylor, J.C., Harland, M., Randerson-Moor, J., Akslen, L.A., Andresen, P.A., Avril, M.F., Azizi, E., Scarra, G.B., Debniak, T., Duffy, D.L., Elder, D.E., Fang, S., Friedman, E., Galan, P., Gillanders, E.M., Goldstein, A.M., Gruis, N.A., Hansson, J., Helsing, P., Hocevar, M., Ingvar, C., Kanetsky, P.A., Chen, W.V., Landi, M.T., Lang, J., Lathrop, G.M., Lubinski, J., Mackie, R.M., Mann, G.J., Molven, A., Montgomery, G.W., Novakovic, S., Olsson, H., Puig, S., Puig-Butille, J.A., Wu, W., Qureshi, A.A., Radford-Smith, G.L., Stoep, N. van der, Doorn, R. van, Whiteman, D.C., Craig, J.E., Schadendorf, E., Burdon, K.P., Nyholt, D.R., Pooley, K.A., Orr, N., Stratigos, A.J., Cust, A.E., Ward, S.V., Hayward, N.K., Han, J., Schulze, H.J., Dunning, A.M., Bishop, J.A., Demenais, F., Amos, C.I., MacGregor, S., Cruchaga, C.

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Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways von Nagel, M, Jansen, PR, Stringer, S, Watanabe, K, De Leeuw, CA, Bryois, J, Savage, JE, Hammerschlag, AR, Skene, NG, Muñoz-Manchado, AB, 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, Noblin, ES, Northover, CAM, Pitts, SJ, Sathirapongsasuti, JF, Sazonova, OV, Shelton, JF, Shringarpure, S, Tian, C, Tung, JY, Vacic, V, Wilson, CH, White, T, Tiemeier, H, Linnarsson, S, Hjerling-Leffler, J, Polderman, TJC, Sullivan, PF, Van Der Sluis, S, Posthuma, D

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Disease risk scores for skin cancers von Fontanillas, Pierre, Alipanahi, Babak, Furlotte, Nicholas A., Johnson, Michaela, Wilson, Catherine H., Pitts, Steven J., Gentleman, Robert, Auton, Adam

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Genetic determinants of daytime napping and effects on cardiometabolic health von Dashti, Hassan S., Daghlas, Iyas, Lane, Jacqueline M., Huang, Yunru, Udler, Miriam S., Wang, Heming, Ollila, Hanna M., Jones, Samuel E., Kim, Jaegil, Wood, Andrew R., Weedon, Michael N., Aslibekyan, Stella, Garaulet, Marta, Saxena, Richa

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Multi-trait analysis of genome-wide association summary statistics using MTAG von Turley, Patrick, Walters, Raymond K., Maghzian, Omeed, Okbay, Aysu, Lee, James J., Fontana, Mark Alan, Nguyen-Viet, Tuan Anh, Wedow, Robbee, Zacher, Meghan, Furlotte, Nicholas A., Magnusson, Patrik, Oskarsson, Sven, Johannesson, Magnus, Visscher, Peter M., Laibson, David, Cesarini, David, Neale, Benjamin M., Benjamin, Daniel J.

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