Bowling aid with ball engaging detent means von SKUSE SAMUEL J

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A Genetics-First Approach to Dissecting the Heterogeneity of Autism: Phenotypic Comparison of Autism Risk Copy Number Variants von Chawner, Samuel J.R.A, Doherty, Joanne L, Anney, Richard J. L, Antshel, Kevin M, Bearden, Carrie E, Bernier, Raphael, Chung, Wendy K, Clements, Caitlin C, Curran, Sarah R, Cuturilo, Goran, Fiksinski, Ania M, Gallagher, Louise, Goin-Kochel, Robin P, Gur, Raquel E, Hanson, Ellen, Jacquemont, Sebastien, Kates, Wendy R, Kushan, Leila, Maillard, Anne M, McDonald-McGinn, Donna M, Mihaljevic, Marina, Miller, Judith S, Moss, Hayley, Pejovic-Milovancevic, Milica, Schultz, Robert T, Green-Snyder, LeeAnne, Vorstman, Jacob A, Wenger, Tara L, Hall, Jeremy, Owen, Michael J, van den Bree, Marianne B.M

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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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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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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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The psychiatric phenotypes of 1q21 distal deletion and duplication von Linden, Stefanie C., Watson, Cameron J., Smith, Jacqueline, Chawner, Samuel J. R. A., Lancaster, Thomas M., Evans, Ffion, Williams, Nigel, Skuse, David, Raymond, F. Lucy, Hall, Jeremy, Owen, Michael J., Linden, David E. J., Green-Snyder, LeeAnne, Chung, Wendy K., Maillard, Anne M., Jacquemont, Sébastien, van den Bree, Marianne B. M.

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Genotype–phenotype associations in children with copy number variants associated with high neuropsychiatric risk in the UK (IMAGINE-ID): a case-control cohort study von Chawner, Samuel J R A, Owen, Michael J, Holmans, Peter, Raymond, F Lucy, Skuse, David, Hall, Jeremy, van den Bree, Marianne B M

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Correction: The psychiatric phenotypes of 1q21 distal deletion and duplication von Linden, Stefanie C., Watson, Cameron J., Smith, Jacqueline, Chawner, Samuel J. R. A., Lancaster, Thomas M., Evans, Ffion, Williams, Nigel, Skuse, David, Raymond, F. Lucy, Hall, Jeremy, Owen, Michael J., Linden, David E. J., Green-Snyder, LeeAnne, Chung, Wendy K., Maillard, Anne M., Jacquemont, Sébastien, van den Bree, Marianne B. M.

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Neuropsychiatric risk in children with intellectual disability of genetic origin: IMAGINE, a UK national cohort study von Wolstencroft, Jeanne, Wicks, Francesca, Srinivasan, Ramya, Wynn, Sarah, Ford, Tamsin, Baker, Kate, Chawner, Samuel J R A, Hall, Jeremy, van den Bree, Marianne B M, Owen, Michael J, Wolstencroft, Jeanne, Wicks, Francesca, Srinivasan, Ramya, Erwood, Marie, Lafont, Amy, Timur, Husne, Ye, Zheng, Walker, Susan, Printzlau, Frida, Juj, Manoj, Davies, Sarah, Denyer, Hayley, Watkins, Alice, Kerry, Eleanor, Coscini, Nadia, Fatih, Nasrtullah, Lucock, Anna, Denaxas, Spiros, Mandy, William, Walker, Neil, Wallwork, Sarah, Dewhurst, Eleanor, Cuthbert, Andrew, Challenger, Aimee, Andrews, Sophie, Holmans, Peter, Bowen, Samantha, Bradley, Karen, Birch, Philippa, Tong, Molly, Lewis, Nicola, Ray, Sinead, Sopp, Matthew, Moss, Hayley, Wynn, Sarah, Searle, Beverley, Robertson, Lisa, Berg, Jonathan, Lampe, Anne, Joss, Shelagh, Brennan, Paul, Kraus, Alison, Lahiri, Nayana, Weber, Astrid, Rawson, Myfanwy, Johnson, Diana, Vasudevan, Pradeep, Harrison, Rachel, Williams, Denise, Maher, Eamonn, Kini, Usha, Van Dijk, Fleur, Clowes, Virginia, Gurasashvilli, Jana, Mansour, Sahar, Holder-Espinasse, Muriel, Watford, Amy, Rankin, Julia, Baralle, Diana, Procter, Annie, Ford, Tamsin, Baker, Kate, Chawner, Samuel, Hall, Jeremy, Van den Bree, Marianne B M, Owen, Michael J, Skuse, David, Raymond, F Lucy, Skuse, David, Raymond, F Lucy

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Neurodevelopmental dimensional assessment of young children at high genomic risk of neuropsychiatric conditions von Chawner, Samuel J. R. A., Paine, Amy L., Dunn, Matt J., Walsh, Alice, Sloane, Poppy, Thomas, Megan, Evans, Alexandra, Hopkins‐Jones, Lucinda, Struik, Siske, Hall, Jeremy, Erichsen, Jonathan T., Leekam, Susan R., Owen, Michael J., Hay, Dale, Bree, Marianne B. M., Raymond, F. Lucy, Dewhurst, Eleanor, Lafont, Amy, Timur, Husniye, Wicks, Francesca, Ye, Zheng, Baker, Kate, Walker, Neil, Wallwork, Sarah, Skuse, David, Denaxas, Spiros, Mandy, William, Wolstencroft, Jeanne, Davies, Sarah, Erwood, Marie, Juj, Manoj, Kerry, Eleanor, Lucock, Anna, Printzlau, Frida, Srinivasan, Ramya, Walker, Susan, Coscini, Nadia, Fatih, Nasrtullah, Denyer, Hayley, Andrews, Sophie, Chawner, Samuel, Cuthbert, Andrew, Challenger, Aimee, Hall, Jeremy, Lewis, Nicola, Owen, Michael, Ray, Sinead, Sopp, Matthew, Moss, Hayley, Bree, Marianne, Holmans, Peter, Bowen, Samantha, Bradley, Karen, Birch, Philippa, Tong, Molly, Ford, Tasmin, Searle, Beverly, Wynn, Sarah, Robertson, Lisa, Berg, Jonathan, Lampe, Anne, Joss, Shelagh, Brennan, Paul, Kraus, Alison, Weber, Astrid, Rawson, Myfanwy, Quarrell, Oliver, Vasudevan, Pradeep, Harrison, Rachel, Williams, Denise, Maher, Eamonn, Kini, Usha, Clowes, Virginia, Van Dijk, Fleur, Gurasashvilli, Jana, Mansour, Sahar, Holder‐Espinasse, Muriel, Watford, Amy, Rankin, Julia, Baralle, Diana, Procter, Annie

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Correction: 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., van den Bree, Marianne B. M.

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

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Neuropsychiatric risk in children with intellectual disability of genetic origin: IMAGINE, a UK national cohort study von Wolstencroft, Jeanne, Wicks, Francesca, Srinivasan, Ramya, Wynn, Sarah, Ford, Tamsin, Baker, Kate, Chawner, Samuel JRA, Hall, Jeremy, van den Bree, Marianne BM, Owen, Michael J, IMAGINE Study, Skuse, David, Raymond, F Lucy

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The psychiatric phenotypes of 1q21 distal deletion and duplication von Linden, Stefanie C, Watson, Cameron J, Smith, Jacqueline, Chawner, Samuel J. R. A, Lancaster, Thomas M, Evans, Ffion, Williams, Nigel, Skuse, David, Raymond, F. Lucy, Hall, Jeremy, Owen, Michael J, Linden, David E. J, Green-Snyder, LeeAnne, Chung, Wendy K, Maillard, Anne M, Jacquemont, Sébastien, van den Bree, Marianne B. M

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The psychiatric phenotypes of 1q21 distal deletion and duplication von Linden, Stefanie C, Watson, Cameron J, Smith, Jacqueline, Chawner, Samuel J. R. A, Lancaster, Thomas M, Evans, Ffion, Williams, Nigel, Skuse, David, Raymond, F. Lucy, Hall, Jeremy, Owen, Michael J, Linden, David E. J, Green-Snyder, LeeAnne, Chung, Wendy K, Maillard, Anne M, Jacquemont, Sébastien, van den Bree, Marianne B. M

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The psychiatric phenotypes of 1q21 distal deletion and duplication von Linden, Stefanie C, Watson, Cameron J, Smith, Jacqueline, Chawner, Samuel JRA, Lancaster, Thomas M, Evans, Ffion, Williams, Nigel, Skuse, David, Raymond, F Lucy, Hall, Jeremy, Owen, Michael J, Linden, David EJ, Green-Snyder, LeeAnne, Chung, Wendy K, Maillard, Anne M, Jacquemont, Sébastien, van den Bree, Marianne BM

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Psychiatric disorders in children with 16p11.2 deletion and duplication von Niarchou, Maria, Chawner, Samuel JRA, 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 EJ, Linden, Stefanie C, Raymond, F Lucy, Skuse, David, Hall, Jeremy, Owen, Michael J, Bree, Marianne BM van den

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Correction: The psychiatric phenotypes of 1q21 distal deletion and duplication von Linden, Stefanie C, Watson, Cameron J, Smith, Jacqueline, Chawner, Samuel J. R. A, Lancaster, Thomas M, Evans, Ffion, Williams, Nigel, Skuse, David, Raymond, F. Lucy, Hall, Jeremy, Owen, Michael J, Linden, David E. J, Green-Snyder, LeeAnne, Chung, Wendy K, Maillard, Anne M, Jacquemont, Sébastien, van den Bree, Marianne B. M

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Correction: The psychiatric phenotypes of 1q21 distal deletion and duplication von Linden, Stefanie C, Watson, Cameron J, Smith, Jacqueline, Chawner, Samuel JRA, Lancaster, Thomas M, Evans, Ffion, Williams, Nigel, Skuse, David, Raymond, F Lucy, Hall, Jeremy, Owen, Michael J, Linden, David EJ, Green-Snyder, LeeAnne, Chung, Wendy K, Maillard, Anne M, Jacquemont, Sébastien, van den Bree, Marianne BM

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