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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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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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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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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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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Shared genetic influences between dimensional ASD and ADHD symptoms during child and adolescent development von Stergiakouli, Evie, Davey Smith, George, Martin, Joanna, Skuse, David H, Viechtbauer, Wolfgang, Ring, Susan M, Ronald, Angelica, Evans, David E, Fisher, Simon E, Thapar, Anita, St Pourcain, Beate

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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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Genetic Clustering of Repetitive Symptoms, Oppositional Defiant Disorder and Language Disorder and Delay in People with Autism: A Multivariate Genetic Variance Analysis of Genetic... von de Hoyos, L, Barendse, M, van Donkelaar, MMJ, Verhoef, E, Fisher, SE, Rai, D, St Pourcain, B

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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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GENETIC CLUSTERING OF CO-OCCURRING SYMPTOMS IN PEOPLE WITH AUTISM: A MULTIVARIATE GENETIC VARIANCE ANALYSIS OF GENETIC RELATIONSHIP MATRICES IN THE SPARK SAMPLE von de Hoyos, L, Barendse, MT, Van Donkelaar, MMJ, Verhoef, E, Fisher, SE, Rai, D, St Pourcain, B

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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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