Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people von Eising, Else, Mirza-Schreiber, Nazanin, de Zeeuw, Eveline L, Wang, Carol A, Truong, Dongnhu T, Allegrini, Andrea G, Shapland, Chin Yang, Zhu, Gu, Wigg, Karen G, Gerritse, Margot L, Molz, Barbara, Alagöz, Gökberk, Gialluisi, Alessandro, Abbondanza, Filippo, Rimfeld, Kaili, van Donkelaar, Marjolein, Liao, Zhijie, Jansen, Philip R, Andlauer, Till F M, Bates, Timothy C, Bernard, Manon, Blokland, Kirsten, Bonte, Milene, Børglum, Anders D, Bourgeron, Thomas, Brandeis, Daniel, Ceroni, Fabiola, Csépe, Valéria, Dale, Philip S, de Jong, Peter F, DeFries, John C, Démonet, Jean-François, Demontis, Ditte, Feng, Yu, Gordon, Scott D, Guger, Sharon L, Hayiou-Thomas, Marianna E, Hernández-Cabrera, Juan A, Hottenga, Jouke-Jan, Hulme, Charles, Kere, Juha, Kerr, Elizabeth N, Koomar, Tanner, Landerl, Karin, Leonard, Gabriel T, Lovett, Maureen W, Lyytinen, Heikki, Martin, Nicholas G, Martinelli, Angela, Maurer, Urs, Michaelson, Jacob J, Moll, Kristina, Monaco, Anthony P, Morgan, Angela T, Nöthen, Markus M, Pausova, Zdenka, Pennell, Craig E, Pennington, Bruce F, Price, Kaitlyn M, Rajagopal, Veera M, Ramus, Franck, Richer, Louis, Simpson, Nuala H, Smith, Shelley D, Snowling, Margaret J, Stein, John, Strug, Lisa J, Talcott, Joel B, Tiemeier, Henning, van der Schroeff, Marc P, Verhoef, Ellen, Watkins, Kate E, Wilkinson, Margaret, Wright, Margaret J, Barr, Cathy L, Boomsma, Dorret I, Carreiras, Manuel, Franken, Marie-Christine J, Gruen, Jeffrey R, Luciano, Michelle, Müller-Myhsok, Bertram, Newbury, Dianne F, Olson, Richard K, Paracchini, Silvia, Paus, Tomáš, Plomin, Robert, Reilly, Sheena, Schulte-Körne, Gerd, Tomblin, J Bruce, van Bergen, Elsje, Whitehouse, Andrew J O, Willcutt, Erik G, St Pourcain, Beate, Francks, Clyde, Fisher, Simon E

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Mendelian randomization incorporating uncertainty about pleiotropy von Thompson, JR, Minelli, C, Bowden, J, Del Greco, FM, Gill, D, Jones, EM, Shapland, CY, Sheehan, NA

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Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities von Price, Kaitlyn M., Wigg, Karen G., Eising, Else, Feng, Yu, Blokland, Kirsten, Wilkinson, Margaret, Kerr, Elizabeth N., Guger, Sharon L., Fisher, Simon E., Lovett, Maureen W., Strug, Lisa J., Barr, Cathy L.

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Structural Models of Genome-Wide Covariance Identify Multiple Genetic Influences Across ASD Symptoms von de Hoyos, L, Barendse, MT, Schlag, F, van Donkelaar, MMJ, Verhoef, E, Shapland, CY, Buitelaar, J, Verhulst, B, Fischer, SE, Rai, D, St Pourcain, B

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Disentangling polygenic associations between attention-deficit/hyperactivity disorder, educational attainment, literacy and language von Verhoef, Ellen, Demontis, Ditte, Burgess, Stephen, Shapland, Chin Yang, Dale, Philip S., Okbay, Aysu, Neale, Benjamin M., Faraone, Stephen V., Stergiakouli, Evie, Davey Smith, George, Fisher, Simon E., Børglum, Anders D., St Pourcain, Beate

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Mendelian randomization incorporating uncertainty about pleiotropy von Thompson, JR, Minelli, C, Bowden, J, Del Greco, FM, Gill, D, Jones, EM, Shapland, CY, Sheehan, NA

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The genetic architecture of the human cerebral cortex von Grasby, KL, Jahanshad, N, Lind, PA, Pizzagalli, F, Zsembik, LCP, Agartz, I, Alhusaini, S, Atkins, JR, Cannon, DM, Chen, Q, Couvy-Duchesne, B, de Zwarte, SMC, den Braber, A, Doan, NT, Dohm, K, Fukunaga, M, Giddaluru, S, Grotegerd, D, Gurholt, TP, Hansell, NK, Harrison, MB, Hauser, M, Ho, NF, Hoogman, M, Jockwitz, C, Knapp, M, Lancaster, TM, Lee, PH, Lopes-Cendes, I, Müller-Myhsok, B, Nho, K, Pitcher, TL, Reinbold, CS, Repple, J, Schlag, F, Schofield, PR, Shen, L, Sønderby, IE, Sprooten, E, Tansey, KE, Teumer, A, van Haren, NEM, Verhoef, E, Walton, E, Wang, M, Wang, Y, Wittfeld, K, Wolf, C, Ayesa-Arriola, R, Brandt, CL, Degenhardt, F, Doherty, CP, Espiritu, R, Garijo, D, Gil, Y, Ho, B-C, Holsboer, F, Hosten, N, Jang, M, Kolskår, K, Krug, A, O'Leary, DS, Opel, N, Pike, GB, Preda, A, Whelan, R, Launer, L, Roshchupkin, GV, Parkinson’s Progression Markers Initiative, Ames, D, Andreassen, OA, Blangero, J, Boomsma, DI, Cahn, W, Cairns, MJ, Calhoun, V, Carr, VJ, Cavalleri, GL, Cendes, F, Dalrymple-Alford, JC, de Geus, EJC, Francks, C, Glahn, DC, Gollub, RL, Hashimoto, R, Heinz, A, Henskens, FA, Hulshoff Pol, HE, Jönsson, EG, Kircher, TTJ, Martinot, J-L, Meyer-Lindenberg, A, Michie, PT, Rowland, LM, Schall, U, Toga, AW, Trollor, JN, Völzke, H, Walter, H, Weinberger, DR

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Low-frequency variation in TP53 has large effects on head circumference and intracranial volume von Hayward, C, Felix, JF, Wang, C, Ahluwalia, TS, Sunyer, J, Walter, K, Cleal, L, Huffmann, J, Sass, L, Antony, D, Artigas, MS, Bala, S, Bentham, J, Blackwood, D, Cirak, S, Clapham, P, Coates, G, Cocca, M, Cox, T, Crooks, L, Curran, S, Curtis, D, Daly, A, Day, INM, Day-Williams, A, Dunham, I, Evans, DM, Franklin, CS, Geihs, M, Geschwind, D, Greenwood, CMT, Guo, X, Gurling, H, Huang, L, Hubbard, T, Humphries, SE, Hysi, P, Kent, A, van Kogelenberg, M, Kolb-Kokocinski, A, Langford, C, Li, Y, Lonnqvist, J, Lopes, LR, Lopes, M, MacArthur, DG, McCarthy, S, McGuffin, P, McIntosh, AM, McKechanie, AG, Metrustry, S, Mitchison, HM, Morris, A, Muddyman, D, Oualkacha, K, Palotie, A, Parker, V, Parr, JR, Paunio, T, Perry, JRB, Pietilainen, O, Quail, MA, Raymond, FL, Richards, JB, Ridout, CK, Robinson, RL, Savage, DB, Scambler, P, Schoenmakers, N, Serra, E, Shaw, A, Shin, S-Y, Small, KS, Smith, BH, Soranzo, N, Stevens, E, Suvisaari, J, Taylor, R, Tian, J, Tobin, MD, Valdes, AM, Vijayarangakannan, P, Visscher, PM, Wain, LV, Ward, K, Wheeler, E, Whyte, T, Williams, HJ, Williamson, KA, Wilson, C, Wilson, SG, Zhang, P, Cole, TJ, Bisgaard, H, Pennell, CE, Dedoussis, G, Timpson, N, Zeggini, E, Vitart, V, St Pourcain, B

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