Genome-wide association study of recurrent major depressive disorder in two European case-control cohorts von Muglia, P, Tozzi, F, Galwey, N W, Francks, C, Upmanyu, R, Kong, X Q, Antoniades, A, Domenici, E, Perry, J, Rothen, S, Vandeleur, C L, Mooser, V, Waeber, G, Vollenweider, P, Preisig, M, Lucae, S, Müller-Myhsok, B, Holsboer, F, Middleton, L T, Roses, A D

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α-5 α-3 nicotinic receptor subunit alleles increase risk for heavy smoking von Berrettini, W, Yuan, X, Tozzi, F, Song, K, Francks, C, Chilcoat, H, Waterworth, D, Muglia, P, Mooser, V

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Next-gen sequencing identifies non-coding variation disrupting miRNA-binding sites in neurological disorders von Devanna, P, Chen, X S, Ho, J, Gajewski, D, Smith, S D, Gialluisi, A, Francks, C, Fisher, S E, Newbury, D F, Vernes, S C

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Genome‐wide screening for DNA variants associated with reading and language traits von Gialluisi, A., Newbury, D. F., Wilcutt, E. G., Olson, R. K., DeFries, J. C., Brandler, W. M., Pennington, B. F., Smith, S. D., Scerri, T. S., Simpson, N. H., Luciano, M., Evans, D. M., Bates, T. C., Stein, J. F., Talcott, J. B., Monaco, A. P., Paracchini, S., Francks, C., Fisher, S. E.

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A genome‐wide search for quantitative trait loci affecting the cortical surface area and thickness of Heschl's gyrus von Cai, D.‐C., Fonteijn, H., Guadalupe, T., Zwiers, M., Wittfeld, K., Teumer, A., Hoogman, M., Arias‐Vásquez, A., Yang, Y., Buitelaar, J., Fernández, G., Brunner, H. G., van Bokhoven, H., Franke, B., Hegenscheid, K., Homuth, G., Fisher, S. E., Grabe, H. J., Francks, C., Hagoort, P.

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Genome‐wide association analyses of child genotype effects and parent‐of‐origin effects in specific language impairment von Nudel, R., Simpson, N. H., Baird, G., O'Hare, A., Conti‐Ramsden, G., Bolton, P. F., Hennessy, E. R., Ring, S. M., Davey Smith, G., Francks, C., Paracchini, S., Monaco, A. P., Fisher, S. E., Newbury, D. F.

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Population-based linkage analysis of schizophrenia and bipolar case-control cohorts identifies a potential susceptibility locus on 19q13 von Francks, C, Tozzi, F, Farmer, A, Vincent, J B, Rujescu, D, St Clair, D, Muglia, P

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Evaluation of results from genome‐wide studies of language and reading in a novel independent dataset von Carrion‐Castillo, A., van Bergen, E., Vino, A., van Zuijen, T., de Jong, P. F., Francks, C., Fisher, S. E.

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Bivariate linkage scan for reading disability and attention-deficit/hyperactivity disorder localizes pleiotropic loci von Gayán, J., Willcutt, E.G., Fisher, S.E., Francks, C., Cardon, L.R., Olson, R.K., Pennington, B.F., Smith, S.D., Monaco, A.P., DeFries, J.C.

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Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK von Scerri, T S, Fisher, S E, Francks, C, MacPhie, I L, Paracchini, S, Richardson, A J, Stein, J F, Monaco, A P

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Pooled genome-wide linkage data on 424 ADHD ASPs suggests genetic heterogeneity and a common risk locus at 5p13 von Ogdie, M N, Bakker, S C, Fisher, S E, Francks, C, Yang, M H, Cantor, R M, Loo, S K, van der Meulen, E, Pearson, P, Buitelaar, J, Monaco, A, Nelson, S F, Sinke, R J, Smalley, S L

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Genome-wide scan of reading ability in affected sibling pairs with attention-deficit hyperactivity disorder: unique and shared genetic effects von Loo, S K, Fisher, S E, Francks, C, Ogdie, M N, MacPhie, I L, Yang, M, McCracken, J T, McGough, J J, Nelson, S F, Monaco, A P, Smalley, S L

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Parent-of-origin effects on handedness and schizophrenia susceptibility on chromosome 2p12–q11 von Francks, Clyde, DeLisi, Lynn E., Shaw, Sarah H., Fisher, Simon E., Richardson, Alex J., Stein, John F., Monaco, Anthony P.

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GENOMIC FINDINGS IN SCHIZOPHRENIA, ANIMAL MODELS AND INTERMEDIATE PHENOTYPES von Rujescu, D, Giegling, I, Hartmann, A, Genius, J, Mulert, C, Hegerl, U, Ruppert, A, Grunze, H, Francks, C, Möller, H.J

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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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The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration von Paracchini, Silvia, Thomas, Ankur, Castro, Sandra, Lai, Cecilia, Paramasivam, Murugan, Wang, Yu, Keating, Brendan J., Taylor, Jennifer M., Hacking, Douglas F., Scerri, Thomas, Francks, Clyde, Richardson, Alex J., Wade-Martins, Richard, Stein, John F., Knight, Julian C., Copp, Andrew J., LoTurco, Joseph, Monaco, Anthony P.

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174 – Genomic findings in schizophrenia, animal models and intermediate phenotypes von Rujescu, D, Giegling, I, Hartmann, A.M, Genius, J, Mulert, C, Hegerl, U, Ruppert, A, Grunze, H, Francks, C, Muglia, P, Möller, H.J

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Copy number variations of chromosome 16p13.1 region associated with schizophrenia von Ingason, A, Rujescu, D, Cichon, S, Sigurdsson, E, Sigmundsson, T, Pietiläinen, O P H, Buizer-Voskamp, J E, Strengman, E, Francks, C, Muglia, P, Gylfason, A, Gustafsson, O, Olason, P I, Steinberg, S, Hansen, T, Jakobsen, K D, Rasmussen, H B, Giegling, I, Möller, H-J, Hartmann, A, Crombie, C, Fraser, G, Walker, N, Lonnqvist, J, Suvisaari, J, Tuulio-Henriksson, A, Bramon, E, Kiemeney, L A, Franke, B, Murray, R, Vassos, E, Toulopoulou, T, Mühleisen, T W, Tosato, S, Ruggeri, M, Djurovic, S, Andreassen, O A, Zhang, Z, Werge, T, Ophoff, R A, Rietschel, M, Nöthen, M M, Petursson, H, Stefansson, H, Peltonen, L, Collier, D, Stefansson, K, Clair, D M St

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Subtly altered topological asymmetry of brain structural covariance networks in autism spectrum disorder across 43 datasets from the ENIGMA consortium von Sha, Z, Van Rooij, D, Anagnostou, E, Arango, C, Auzias, G, Behrmann, M, Bernhardt, B, Bolte, S, Busatto, GF, Calderoni, S, Calvo, R, Daly, E, Deruelle, C, Duan, M, Duran, FLS, Durston, S, Ecker, C, Ehrlich, S, Fair, D, Fedor, J, Fitzgerald, J, Floris, DL, Franke, B, Freitag, CM, Gallagher, L, Glahn, DC, Haar, S, Hoekstra, L, Jahanshad, N, Jalbrzikowski, M, Janssen, J, King, JA, Lazaro, L, Luna, B, McGrath, J, Medland, SE, Muratori, F, Murphy, DGM, Neufeld, J, O'Hearn, K, Oranje, B, Parellada, M, Pariente, JC, Postema, MC, Remnelius, KL, Retico, A, Rosa, PGP, Rubia, K, Shook, D, Tammimies, K, Taylor, MJ, Tosetti, M, Wallace, GL, Zhou, F, Thompson, PM, Fisher, SE, Buitelaar, JK, Francks, C

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Altered structural brain asymmetry in autism spectrum disorder in a study of 54 datasets (Oct, 10.1038/s41467-019-13005-8, 2019) von Postema, MC, Van Rooij, D, Anagnostou, E, Arango, C, Auzias, G, Behrmann, M, Busatto Filho, G, Calderoni, S, Calvo, R, Daly, E, Deruelle, C, Di Martino, A, Dinstein, I, Duran, FLS, Durston, S, Ecker, C, Ehrlich, S, Fair, D, Fedor, J, Feng, X, Fitzgerald, J, Floris, DL, Freitag, CM, Gallagher, L, Glahn, DC, Gori, I, Haar, S, Hoekstra, L, Jahanshad, N, Jalbrzikowski, M, Janssen, J, King, JA, Kong, XZ, Lazaro, L, Lerch, JP, Luna, B, Martinho, MM, McGrath, J, Medland, SE, Muratori, F, Murphy, CM, Murphy, DGM, O'Hearn, K, Oranje, B, Parellada, M, Puig, O, Retico, A, Rosa, P, Rubia, K, Shook, D, Taylor, MJ, Tosetti, M, Wallace, GL, Zhou, F, Thompson, PM, Fisher, SE, Buitelaar, JK, Francks, C

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