ASD and schizophrenia show distinct developmental profiles in common genetic overlap with population-based social communication difficulties von St Pourcain, B, Robinson, E B, Anttila, V, Sullivan, B B, Maller, J, Golding, J, Skuse, D, Ring, S, Evans, D M, Zammit, S, Fisher, S E, Neale, B M, Anney, R J L, Ripke, S, Hollegaard, M V, Werge, T, Ronald, A, Grove, J, Hougaard, D M, Børglum, A D, Mortensen, P B, Daly, M J, Davey Smith, G

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Does vitamin D mediate the protective effects of time outdoors on myopia? Findings from a prospective birth cohort von Guggenheim, Jeremy A, Williams, Cathy, Northstone, Kate, Howe, Laura D, Tilling, Kate, St Pourcain, Beate, McMahon, George, Lawlor, Debbie A

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Genome‐wide association study of shared components of reading disability and language impairment von Eicher, J. D., Powers, N. R., Miller, L. L., Akshoomoff, N., Amaral, D. G., Bloss, C. S., Libiger, O., Schork, N. J., Darst, B. F., Casey, B. J., Chang, L, Ernst, T., Frazier, J., Kaufmann, W. E., Keating, B., Kenet, T., Kennedy, D., Mostofsky, S., Murray, S. S., Sowell, E. R., Bartsch, H., Kuperman, J. M., Brown, T. T., Hagler, D. J., Dale, A. M., Jernigan, T. L., St. Pourcain, B., Davey Smith, G., Ring, S. M., Gruen, J. R.

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Novel Functionalized Biodegradable Polymers for Nanoparticle Drug Delivery Systems von Kallinteri, Paraskevi, Higgins, Sean, Hutcheon, Gillian A, St. Pourçain, Christopher B, Garnett, Martin C

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Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia von Gialluisi, Alessandro, Andlauer, Till F. M., Mirza-Schreiber, Nazanin, Moll, Kristina, Becker, Jessica, Hoffmann, Per, Ludwig, Kerstin U., Czamara, Darina, Pourcain, Beate St, Honbolygó, Ferenc, Tóth, Dénes, Csépe, Valéria, Huguet, Guillaume, Chaix, Yves, Iannuzzi, Stephanie, Demonet, Jean-Francois, Morris, Andrew P., Hulslander, Jacqueline, Willcutt, Erik G., DeFries, John C., Olson, Richard K., Smith, Shelley D., Pennington, Bruce F., Vaessen, Anniek, Maurer, Urs, Lyytinen, Heikki, Peyrard-Janvid, Myriam, Leppänen, Paavo H. T., Brandeis, Daniel, Bonte, Milene, Stein, John F., Talcott, Joel B., Fauchereau, Fabien, Wilcke, Arndt, Kirsten, Holger, Müller, Bent, Francks, Clyde, Bourgeron, Thomas, Monaco, Anthony P., Ramus, Franck, Landerl, Karin, Kere, Juha, Scerri, Thomas S., Paracchini, Silvia, Fisher, Simon E., Schumacher, Johannes, Nöthen, Markus M., Müller-Myhsok, Bertram, Schulte-Körne, Gerd

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Discovery of 42 genome-wide significant loci associated with dyslexia von Doust, Catherine, Fontanillas, Pierre, Eising, Else, Gordon, Scott D., Wang, Zhengjun, Alagöz, Gökberk, Molz, Barbara, Pourcain, Beate St, Francks, Clyde, Marioni, Riccardo E., Zhao, Jingjing, Paracchini, Silvia, Talcott, Joel B., Monaco, Anthony P., Stein, John F., Gruen, Jeffrey R., Olson, Richard K., Willcutt, Erik G., DeFries, John C., Pennington, Bruce F., Smith, Shelley D., Wright, Margaret J., Martin, Nicholas G., Auton, Adam, Bates, Timothy C., Fisher, Simon E., Luciano, Michelle

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Childhood intelligence is heritable, highly polygenic and associated with FNBP1L von Benyamin, B, Pourcain, BSt, Davis, O S, Davies, G, Hansell, N K, Brion, M-JA, Kirkpatrick, R M, Cents, R A M, Franić, S, Miller, M B, Haworth, C M A, Meaburn, E, Price, T S, Evans, D M, Timpson, N, Kemp, J, Ring, S, McArdle, W, Medland, S E, Yang, J, Harris, S E, Liewald, D C, Scheet, P, Xiao, X, Hudziak, J J, de Geus, E J C, Jaddoe, V W V, Starr, J M, Verhulst, F C, Pennell, C, Tiemeier, H, Iacono, W G, Palmer, L J, Montgomery, G W, Martin, N G, Boomsma, D I, Posthuma, D, McGue, M, Wright, M J, Davey Smith, G, Deary, I J, Plomin, R, Visscher, P M

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A genome-wide association meta-analysis and mouse gene deletion identify WNT16 as a regulator of cortical bone thickness von Tobias, J, Ohlsson, C, Paternoster, L, Lehtimaki, T, Raitakari, O, Viikari, J, Lyytikainen, L.-P, Sievanen, H, Mellström, D, Movérare-Skrtic, S, Eriksson, J, St Pourcain, B, Timpson, N.J, Smith, G.D, Ring, S.M, Karlsson, M, Kemp, J, Sayers, A, Nethander, M, Vandenput, L, Brommage, R, Lui, J, Evans, D, Lorentzon, M

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Meta-analysis of genome-wide scans for total body BMD in children and adults reveals allelic heterogeneity, pleiotropy and age-specific effects at the WNT16 locus von Medina-Gomez, C, Kemp, J.P, Estrada, K, Eriksson, J, Liu, J, Reppe, S, Evans, D.M, Heppe, D, van den Put, L, Herrera, L, Ring, S.M, Kruithof, C, Timpson, N.J, Zillikens, M.C, Olstad, O.K, St Pourcain, B, Hofman, A, Jaddoe, V.W, Smith, G.D, Lorentzon, M, Gautvik, K.M, Uitterlinden, A.G, Brommage, R, Ohlsson, C, Tobias, J.H, Rivadeneira, F

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Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia von Gialluisi, Alessandro, Andlauer, Till F. M., Mirza-Schreiber, Nazanin, Moll, Kristina, Becker, Jessica, Hoffmann, Per, Ludwig, Kerstin U., Czamara, Darina, St Pourcain, Beate, Brandler, William, Honbolygó, Ferenc, Tóth, Dénes, Csépe, Valéria, Huguet, Guillaume, Morris, Andrew P., Hulslander, Jacqueline, Willcutt, Erik G., DeFries, John C., Olson, Richard K., Smith, Shelley D., Pennington, Bruce F., Vaessen, Anniek, Maurer, Urs, Lyytinen, Heikki, Peyrard-Janvid, Myriam, Leppänen, Paavo H. T., Brandeis, Daniel, Bonte, Milene, Stein, John F., Talcott, Joel B., Fauchereau, Fabien, Wilcke, Arndt, Francks, Clyde, Bourgeron, Thomas, Monaco, Anthony P., Ramus, Franck, Landerl, Karin, Kere, Juha, Scerri, Thomas S., Paracchini, Silvia, Fisher, Simon E., Schumacher, Johannes, Nöthen, Markus M., Müller-Myhsok, Bertram, Schulte-Körne, Gerd

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A genome-wide association study of total child psychiatric problems scores von Neumann, A, Nolte, IM, Pappa, I, Ahluwalia, TS, Pettersson, E, Rodriguez, A, Whitehouse, A, Van Beijsterveldt, CEM, Benyamin, B, Hammerschlag, AR, Helmer, Q, Karhunen, V, Krapohl, E, Lu, Y, Van der Most, PJ, Palviainen, T, St Pourcain, B, Seppälä, I, Suarez, A, Vilor-Tejedor, N, Tiesler, CMT, Wang, C, Wills, A, Zhou, A, Alemany, S, Bisgaard, H, Bønnelykke, K, Davies, GE, Hakulinen, C, Henders, AK, Hyppönen, E, Stokholm, J, Bartels, M, Hottenga, J-J, Heinrich, J, Hewitt, J, Keltikangas-Järvinen, L, Korhonen, T, Kaprio, J, Lahti, J, Lahti-Pulkkinen, M, Lehtimäki, T, Middeldorp, CM, Najman, JM, Pennell, C, Power, C, Oldehinkel, AJ, Plomin, R, Räikkönen, K, Raitakari, OT, Rimfeld, K, Sass, L, Snieder, H, Standl, M, Sunyer, J, Williams, GM, Bakermans-Kranenburg, MJ, Boomsma, DI, Van IJzendoorn, MH, Hartman, CA, Tiemeier, H

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Novel hydrophilic cyclic monomers in hydrogel synthesis von Jarvie, A.W.P., Lloyd, M.C., Pourcain, C.B.St

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Genetic association study of childhood aggression across raters, instruments, and age von Ip, HF, Krapohl, EML, Brikell, I, Sanchez-Mora, C, Nolte, IM, Bolhuis, K, Palviainen, T, Colodro-Conde, L, Jiang, C, Wang, CA, Saunders, G, Karhunen, V, Peterson, RE, Thiering, E, Seppala, I, Vilor-Tejedor, N, Day, FR, Hottenga, J-J, Allegrini, AG, Rimfeld, K, Chen, Q, Lu, Y, Martin, J, Rovira, P, Bosch, R, Espanol, G, Ramos Quiroga, JA, Neumann, A, Ensink, J, Morosoli, JJ, Marrington, S, Scott, JG, Vinkhuyzen, A, Corley, R, Sugden, K, Alemany, S, Sass, L, Ruth, K, Tyrrell, J, Ehli, EA, Hagenbeek, FA, Van Beijsterveldt, TCEM, Larsson, H, Snieder, H, Verhulst, FC, Amin, N, Whipp, AM, Rose, RJ, Uitterlinden, AG, Madden, P, Haavik, J, Harris, JR, Helgeland, O, Knudsen, GPS, Lu, Q, Henders, AK, Najman, JM, Brown, S, Krauter, K, Stallings, M, Silberg, JL, Pulkki-Raback, L, Havdahl, A, Magnus, P, Raitakari, OT, Perry, JRB, Llop, S, Lopez-Espinosa, M-J, Bonnelykke, K, Bisgaard, H, Sunyer, J, Lehtimaki, T, Arseneault, L, Standl, M, Heinrich, J, Boden, J, Pearson, J, Kennedy, M, Poulton, R, Hewitt, J, Copeland, WE, Costello, EJ, Williams, GM, Jarvelin, M-R, Iacono, W, Caspi, A, Moffitt, TE, Pennell, CE, Klump, KL, Dick, DM, Reichborn-Kjennerud, T, Martin, NG, Medland, SE, Kaprio, J, Tiemeier, H, Oldehinkel, AJ, Lichtenstein, P, Lundstrom, S, Nivard, MG, Boomsma, DI

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Whole-genome sequencing coupled to imputation discovers genetic signals for anthropometric traits von Tachmazidou, I, Suveges, D, Min, JL, Ritchie, GRS, Steinberg, J, Walter, K, Iotchkova, V, Schwartzentruber, J, Huang, J, Memari, Y, McCarthy, S, Crawford, AA, Bombieri, C, Cocca, M, Farmaki, A-E, Gaunt, TR, Jousilahti, P, Kooijman, MN, Lehne, B, Malerba, G, Mannisto, S, Matchan, A, Medina-Gomez, C, Metrustry, SJ, Nag, A, Ntalla, I, Paternoster, L, Rayner, NW, Sala, C, Scott, WR, Shihab, HA, Southam, L, St Pourcain, B, Traglia, M, Trajanoska, K, Zaza, G, Zhang, W, Artigas, MS, Bansal, N, Benn, M, Chen, Z, Danecek, P, Lin, W-Y, Locke, A, Luan, J, Manning, AK, Mulas, A, Sidore, C, Tybjaerg-Hansen, A, Varbo, A, Zoledziewska, M, Finan, C, Hendricks, AE, Kemp, JP, Moayyeri, A, Panoutsopoulou, K, Szpak, M, Wilson, SG, Boehnke, M, Cucca, F, Di Angelantonio, E, Langenberg, C, Lindgren, C, McCarthy, MI, Morris, AP, Nordestgaard, BG, Scott, RA, Tobin, MD, Wareham, NJ, Burton, P, Chambers, JC, Smith, GD, Dedoussis, G, Franco, OH, Gambaro, G, Gasparini, P, Hammond, CJ, Hofman, A, Jaddoe, VWV, Kooner, JS, Perola, M, Relton, C, Ring, SM, Rivadeneira, F, Salomaa, V, Spector, TD, Stegle, O, Toniolo, D, Uitterlinden, AG, Barroso, I, Greenwood, CMT, Perry, JRB, Walker, BR, Butterworth, AS, Xue, Y, Durbin, R, Small, KS, Soranzo, N, Timpson, NJ, Zeggini, E

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A genome-wide association study of body mass index across early life and childhood von Warrington, NM, Howe, LD, Paternoster, L, Kaakinen, M, Herrala, S, Huikari, V, Wu, YY, Kemp, JP, Timpson, NJ, St Pourcain, B, Smith, GD, Tilling, K, Jarvelin, M-R, Pennell, CE, Evans, DM, Lawlor, DA, Briollais, L, Palmer, LJ

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Hair cortisol in twins: heritability and genetic overlap with psychological variables and stress-system genes von Rietschel, L, Streit, F, Zhu, G, McAloney, K, Frank, J, Couvy-Duchesne, B, Witt, SH, Binz, TM, Bolton, JL, Hayward, C, Direk, N, Anderson, A, Huffman, J, Wilson, JF, Campbell, H, Rudan, I, Wright, A, Hastie, N, Wild, SH, Velders, FP, Hofman, A, Uitterlinden, AG, Lahti, J, Räikkönen, K, Kajantie, E, Widen, E, Palotie, A, Eriksson, JG, Kaakinen, M, Järvelin, MR, Timpson, NJ, Davey Smith, G, Ring, SM, Evans, DM, St Pourcain, B, Tanaka, T, Milaneschi, Y, Bandinelli, S, Ferrucci, L, Van Der Harst, P, Rosmalen, JG, Bakker, SJ, Verweij, N, Dullaart, RP, Mahajan, A, Lindgren, CM, Morris, A, Lind, L, Ingelsson, E, Anderson, LN, Pennell, CE, Lye, SJ, Matthews, SG, Eriksson, J, Mellstrom, D, Ohlsson, C, Price, JF, Strachan, MW, Reynolds, RM, Tiemeier, H, Ripke, S, Mattheisen, M, Abdellaoui, A, Adams, MJ, Agerbo, E, Air, TM, Andlauer, TF, Bacanu, SA, Bækvad-Hansen, M, Beekman, AT, Bennett, DA, Berger, K, Bigdeli, TB, Bybjerg-Grauholm, J

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Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances von Fatemifar, G, Hoggart, CJ, Paternoster, L, Kemp, JP, Prokopenko, I, Horikoshi, M, Wright, VJ, Tobias, JH, Richmond, S, Zhurov, AI, Toma, AM, Pouta, A, Taanila, A, Sipila, K, Lahdesmaki, R, Pillas, D, Geller, F, Feenstra, B, Melbye, M, Nohr, EA, Ring, SM, St Pourcain, B, Timpson, NJ, Smith, GD, Jarvelin, M-R, Evans, DM

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Common variation near ROBO2 is associated with expressive vocabulary in infancy von St Pourcain, B, Cents, RAM, Whitehouse, AJO, Haworth, CMA, Davis, OSP, O'Reilly, PF, Roulstone, S, Wren, Y, Ang, QW, Velders, FP, Evans, DM, Kemp, JP, Warrington, NM, Miller, L, Timpson, NJ, Ring, SM, Verhulst, FC, Hofman, A, Rivadeneira, F, Meaburn, EL, Price, TS, Dale, PS, Pillas, D, Yliherva, A, Rodriguez, A, Golding, J, Jaddoe, VWV, Jarvelin, M-R, Plomin, R, Pennell, CE, Tiemeier, H, Smith, GD

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A novel common variant in DCST2 is associated with length in early life and height in adulthood von Van der Valk, RJP, Kreiner-Moller, E, Kooijman, MN, Guxens, M, Saaf, A, Bradfield, JP, Hayes, MG, Cousminer, DL, Grallert, H, Custovic, A, Jacobsson, B, Jarvelin, M-R, Koppelman, GH, Pennell, CE, Niinikoski, H, Thiering, E, Frayling, TM, Sunyer, J, Timpson, NJ, Rivadeneira, F, Bonnelykke, K, Jaddoe, VWV, Curtin, JA, Myhre, R, Huikari, V, Joro, R, Kerkhof, M, Warrington, NM, Pitkanen, N, Horikoshi, M, Veijola, R, Teo, Y-Y, Barton, SJ, Kemp, JP, St Pourcain, B, Ring, SM, Smith, GD, Bergstrom, A, Kull, I, Hakonarson, H, Mentch, FD, Bisgaard, H, Chawes, B, Stokholm, J, Eriksen, P, Sevelsted, A, Melbye, M, Medina-Gomez, C, Hofman, A, De Jongste, JC, Taal, HR, Uitterlinden, AG, Armstrong, LL, Eriksson, J, Palotie, A, Bustamante, M, Estivill, X, Gonzalez, JR, Kiess, W, Mahajan, A, Flexeder, C, Tiesler, CMT, Murray, CS, Simpson, A, Sengpiel, V, Hartikainen, A-L, Lewin, A, Alves, ADSC, Blakemore, AI, Buxton, JL, Kaakinen, M, Rodriguez, A, Sebert, S, Vaarasmaki, M, Lakka, T, Lindi, V, Gehring, U, Postma, DS, Ang, W, Newnham, JP, Lyytikainen, L-P, Pahkala, K, Raitakari, OT, Panoutsopoulou, K, Zeggini, E, Boomsma, DI, Ilonen, J, Franke, L, Hirschhorn, JN, Pers, TH, Liang, L, Huang, J, Knip, M, Saw, S-M, Holloway, JW, Melen, E, Grant, SFA, Feenstra, B, Lowe, WL, Widen, E

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Genome Wide Association Identifies Common Variants at the SERPINA6/SERPINA1 Locus Influencing Plasma Cortisol and Corticosteroid Binding Globulin von Bolton, JL, Hayward, C, Direk, N, Lewis, JG, Hammond, GL, Hill, LA, Anderson, A, Huffman, J, Wilson, JF, Campbell, H, Rudan, I, Wright, A, Hastie, N, Wild, SH, Velders, FP, Hofman, A, Uitterlinden, AG, Lahti, J, Raikkonen, K, Kajantie, E, Widen, E, Palotie, A, Eriksson, JG, Kaakinen, M, Jarvelin, M-R, Timpson, NJ, Smith, GD, Ring, SM, Evans, DM, St Pourcain, B, Tanaka, T, Milaneschi, Y, Bandinelli, S, Ferrucci, L, Van der Harst, P, Rosmalen, JGM, Bakker, SJL, Verweij, N, Dullaart, RPF, Mahajan, A, Lindgren, CM, Morris, A, Lind, L, Ingelsson, E, Anderson, LN, Pennell, CE, Lye, SJ, Matthews, SG, Eriksson, J, Mellstrom, D, Ohlsson, C, Price, JF, Strachan, MWJ, Reynolds, RM, Tiemeier, H, Walker, BR

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