Sleep problems and associations with psychopathology and cognition in young people with 22q11.2 deletion syndrome (22q11.2DS) von Moulding, H A, Bartsch, U, Hall, J, Jones, M W, Linden, D E, Owen, M J, van den Bree, M B M

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The inequity of education, health and care plan provision for children and young people with intellectual and developmental disabilities von Lee, I. O., Wolstencroft, J., Housby, H., Bree, M. B. M., Chawner, S. J. R. A., Hall, J., Skuse, D. H.

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A neurogenetic model for the study of schizophrenia spectrum disorders: the International 22q11.2 Deletion Syndrome Brain Behavior Consortium von Gur, R E, Bassett, A S, McDonald-McGinn, D M, Bearden, C E, Chow, E, Emanuel, B S, Owen, M, Swillen, A, Van den Bree, M, Vermeesch, J, Vorstman, J A S, Warren, S, Lehner, T, Morrow, B

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Novel High-Throughput Fluorescence-Based Assay for the Identification of Nematocidal Compounds That Target the Blood-Feeding Pathway von Marchand, Anthony, Van Bree, Joyce, Taki, Aya, Moyat, Mati, Turcatti, Gerardo, Chambon, Marc, Smith, Adam, Doolan, Rory, Gasser, Robin, Harris, Nicola, Bouchery, Tiffany

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16p11.2 Locus modulates response to satiety before the onset of obesity von Maillard, A M, Hippolyte, L, Rodriguez-Herreros, B, Chawner, S J R A, Dremmel, D, Agüera, Z, Fagundo, A B, Pain, A, Martin-Brevet, S, Hilbert, A, Kurz, S, Etienne, R, Draganski, B, Jimenez-Murcia, S, Männik, K, Metspalu, A, Reigo, A, Isidor, B, Le Caignec, C, David, A, Mignot, C, Keren, B, van den Bree, M B M, Munsch, S, Fernandez-Aranda, F, Beckmann, J S, Reymond, A, Jacquemont, S

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Developmental coordination disorder, psychopathology and IQ in 22q11.2 deletion syndrome von Cunningham, Adam C, Delport, Sue, Cumines, Wendy, Busse, Monica, Linden, David E J, Hall, Jeremy, Owen, Michael J, van den Bree, Marianne B M

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Sleep EEG in young people with 22q11.2 deletion syndrome: A cross-sectional study of slow-waves, spindles and correlations with memory and neurodevelopmental symptoms von Donnelly, Nicholas A, Bartsch, Ullrich, Moulding, Hayley A, Eaton, Christopher, Marston, Hugh, Hall, Jessica H, Hall, Jeremy, Owen, Michael J, van den Bree, Marianne B M, Jones, Matt W

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Psychiatric disorders in children with 16p11.2 deletion and duplication von Niarchou, Maria, Chawner, Samuel J. R. A., Doherty, Joanne L., Maillard, Anne M., Jacquemont, Sébastien, Chung, Wendy K., Green-Snyder, LeeAnne, Bernier, Raphael A., Goin-Kochel, Robin P., Hanson, Ellen, Linden, David E. J., Linden, Stefanie C., Raymond, F. Lucy, Skuse, David, Hall, Jeremy, Owen, Michael J., Bree, Marianne B. M. van den

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Assessment of emotions and behaviour by the Developmental Behaviour Checklist in young people with neurodevelopmental CNVs von Cunningham, Adam C., Hall, Jeremy, Einfeld, Stewart, Owen, Michael J., van den Bree, Marianne B. M.

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In vivo evidence of microstructural hypo-connectivity of brain white matter in 22q11.2 deletion syndrome von Raven, Erika P., Veraart, Jelle, Kievit, Rogier A., Genc, Sila, Ward, Isobel L., Hall, Jessica, Cunningham, Adam, Doherty, Joanne, van den Bree, Marianne B. M., Jones, Derek K.

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Genetic and non-genetic influences on the development of co-occurring alcohol problem use and internalizing symptomatology in adolescence: a review von Saraceno, Luca, Munafó, Marcus, Heron, Jon, Craddock, Nick, Van Den Bree, Marianne B. M.

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The links between prenatal stress and offspring development and psychopathology: disentangling environmental and inherited influences von Rice, F., Harold, G. T., Boivin, J., van den Bree, M., Hay, D. F., Thapar, A.

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Using kinematic analyses to explore sensorimotor control impairments in children with 22q11.2 deletion syndrome von Cunningham, Adam C, Hill, Liam, Mon-Williams, Mark, Peall, Kathryn J, Linden, David E J, Hall, Jeremy, Owen, Michael J, van den Bree, Marianne B M

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Candidate genes for anorexia nervosa in the 1p33-36 linkage region: serotonin 1D and delta opioid receptor loci exhibit significant association to anorexia nervosa von Bergen, A W, van den Bree, M B M, Yeager, M, Welch, R, Ganjei, J K, Haque, K, Bacanu, S, Berrettini, W H, Grice, D E, Goldman, D, Bulik, C M, Klump, K, Fichter, M, Halmi, K, Kaplan, A, Strober, M, Treasure, J, Woodside, B, Kaye, W H

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Psychopathology and cognition in children with 22q11.2 deletion syndrome von Niarchou, Maria, Zammit, Stanley, van Goozen, Stephanie H. M., Thapar, Anita, Tierling, Hayley M., Owen, Michael J., Van Den Bree, Marianne B. M.

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Author Correction: Using rare genetic mutations to revisit structural brain asymmetry von Kopal, Jakub, Kumar, Kuldeep, Shafighi, Kimia, Saltoun, Karin, Modenato, Claudia, Moreau, Clara A., Huguet, Guillaume, Jean-Louis, Martineau, Martin, Charles-Olivier, Saci, Zohra, Younis, Nadine, Douard, Elise, Jizi, Khadije, Beauchamp-Chatel, Alexis, Kushan, Leila, Silva, Ana I., van den Bree, Marianne B. M., Linden, David E. J., Owen, Michael J., Hall, Jeremy, Lippé, Sarah, Draganski, Bogdan, Sønderby, Ida E., Andreassen, Ole A., Glahn, David C., Thompson, Paul M., Bearden, Carrie E., Zatorre, Robert, Jacquemont, Sébastien, Bzdok, Danilo

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Horner's syndrome in a patient presenting with chest pain von van Bree, S H W, van Bree, M D R, Somsen, G A

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Irritability in young people with copy number variants associated with neurodevelopmental disorders (ND-CNVs) von Hall, Jessica H., Chawner, Samuel J. R. A., Wolstencroft, Jeanne, Skuse, David, Hall, Jeremy, Holmans, Peter, Owen, Michael J., van den Bree, Marianne B. M.

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Identifying the neurodevelopmental and psychiatric signatures of genomic disorders associated with intellectual disability: a machine learning approach von Donnelly, Nicholas, Cunningham, Adam, Salas, Sergio Marco, Bracher-Smith, Matthew, Chawner, Samuel, Stochl, Jan, Ford, Tamsin, Raymond, F Lucy, Escott-Price, Valentina, van den Bree, Marianne B M

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Sleep disturbance as a transdiagnostic marker of psychiatric risk in children with neurodevelopmental risk genetic conditions von Chawner, Samuel J. R. A., Evans, Alexandra, Williams, Nigel, Owen, Michael J., Hall, Jeremy, van den Bree, Marianne B. M.

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