Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation

- Min, Josine L., Hemani, Gibran, Bretherick, Andrew D., Pennell, Craig E., Richardson, Tom G., Klughammer, Johanna, Iotchkova, Valentina, Sharp, Gemma, Al Khleifat, Ahmad, Shatunov, Aleksey, Iacoangeli, Alfredo, McArdle, Wendy L., Ho, Karen M., Hannon, Ellis, Kumar, Ashish, Söderhäll, C, Soriano-Tárraga, C, Giralt-Steinhauer, E, Kazmi, N, Mason, D, McRae, AF, Corcoran, DL, Sugden, K, Kasela, S, Dekkers, Koen F., Cardona, A, Day, FR, Cugliari, G, Viberti, C, Guarrera, S, Lerro, M, Gupta, R, Bollepalli, S, Mandaviya, P, Zeng, Y, Castillo-Fernandez, Juan, Clarke, TK, Walker, RM, Schmoll, V, Czamara, D, Ruiz-Arenas, C, Rezwan, FI, Marioni, RE, Lin, T, Awaloff, Y, Germain, M, Luijk, Rene, Aïssi, D, Zwamborn, R, van Eijk, K, Dekker, A, van Dongen, J, Hottenga, JJ, Willemsen, G, Xu, CJ, Barturen, G, Català-Moll, F, Carnero-Montoro, Elena, Kerick, M, Wang, Carol, Melton, P, Elliott, HR, Shin, J, Bernard, M, Yet, I, Smart, M, Gorrie-Stone, T, Shaw, C, Lawson, Daniel J., Al Chalabi, A, Ring, SM, Pershagen, G, Melén, E, Jiménez-Conde, J, Roquer, J, Lawlor, DA, Wright, J, Martin, NG, Montgomery, GW, Burrows, Kimberley, Moffitt, TE, Poulton, R, Esko, T, Milani, L, Metspalu, A, Perry, JRB, Ong, KK, Wareham, NJ, Matullo, G, Sacerdote, C, Suderman, Matthew, Panico, S, Caspi, A, Arseneault, L, Gagnon, F, Ollikainen, M, Kaprio, J, Felix, JF, Rivadeneira, F, Tiemeier, H, van IJzendoorn, MH

Investigating the causal relationship of C-reactive protein with 32 complex somatic and psychiatric outcomes: a large-scale cross-consortium mendelian randomization study

- Prins, Bram P., Abbasi, Ali, Valdes, Ana M., Bras, Jose, Shatunov, Aleksey, Lu, Chen, Han, Buhm, Raychaudhuri, Soumya, Bevan, Steve, Mayes, Maureen D., Tsoi, Lam C., Evangelou, Evangelos, Wong, Anson, Nair, Rajan P., Grant, Stuan F. A., Polychronakos, Constantin, Radstake, Timothy R. D., van Heel, David A., Dunstan, Melanie L., Wood, Nicholas W., Al-Chalabi, Ammar, Dehghan, Abbas, Hakonarson, Hakon, Vaez, Ahmad, Markus, Hugh S., Elder, James T., Knight, Jo, Arking, Dan E., Spector, Timothy D., Koeleman, Bobby P. C., van Duijn, Cornelia M., Martin, Javier, Morris, Andrew P., Weersma, Rinse K., Nolte, Ilja, Wijmenga, Cisca, Munroe, Patricia B., Perry, John R. B., Pouget, Jennie G., Jamshidi, Yalda, Snieder, Harold, Alizadeh, Behrooz Z., Tooney, Paul, Franceschini, Nora, Stuart, Philip E., Guterriez Achury, Javier, Mistry, Vanisha, Bradfield, Jonathan P.

No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis

- Goris, An, van Setten, Jessica, Diekstra, Frank, Ripke, Stephan, Patsopoulos, Nikolaos A., Sawcer, Stephen J., The International Multiple Sclerosis Genetics Consortium, van Es, Michael, The Australia and New Zealand MS Genetics Consortium, Andersen, Peter M., Melki, Judith, Meininger, Vincent, Hardiman, Orla, Landers, John E., Brown, Robert H., Shatunov, Aleksey, Leigh, Nigel, Al-Chalabi, Ammar, Shaw, Christopher E., Traynor, Bryan J., Chio, Adriano, Restagno, Gabriella, Mora, Gabriele, Ophoff, Roel A., Oksenberg, Jorge R., Van Damme, Philip, Compston, Alastair, Robberecht, Wim, Dubois, Bénédicte, van den Berg, Leonard H., De Jager, Philip L., Veldink, Jan H., de Bakker, Paul I. W.