Autism: A model of neurodevelopmental diversity informed by genomics

por Chawner, Samuel J. R. A., Owen, Michael J.
Publicado 2022

Neurodevelopmental Trajectories and Psychiatric Morbidity: Lessons Learned From the 22q11.2 Deletion Syndrome

por Fiksinski, Ania M., Schneider, Maude, Zinkstok, Janneke, Baribeau, Danielle, Chawner, Samuel J. R. A., Vorstman, Jacob A. S.
Publicado 2021

Sleep disturbance as a transdiagnostic marker of psychiatric risk in children with neurodevelopmental risk genetic conditions

por Chawner, Samuel J. R. A., Evans, Alexandra, Williams, Nigel, Owen, Michael J., Hall, Jeremy, van den Bree, Marianne B. M.
Publicado 2023

The emergence of psychotic experiences in the early adolescence of 22q11.2 Deletion Syndrome

por Chawner, Samuel J.R.A., Niarchou, Maria, Doherty, Joanne L., Moss, Hayley, Owen, Michael J., van den Bree, Marianne B.M.
Publicado 2019

Childhood cognitive development in 22q11.2 deletion syndrome: case–control study

por Chawner, Samuel J. R. A., Doherty, Joanne L., Moss, Hayley, Niarchou, Maria, Walters, James T. R., Owen, Michael J., van den Bree, Marianne B. M.
Publicado 2017

Psychopathology in mothers of children with pathogenic Copy Number Variants

por Niarchou, Maria, Cunningham, Adam C., Chawner, Samuel J. R. A., Moulding, Hayley, Sopp, Matthew, Hall, Jeremy, Owen, Michael J., van den Bree, Marianne B.M.
Publicado 2023

Neuropsychiatric risk in children with intellectual disability of genetic origin: IMAGINE, a UK national cohort study

por 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, Skuse, David, Raymond, F Lucy
Publicado 2022

Cognitive deficits in childhood, adolescence and adulthood in 22q11.2 deletion syndrome and association with psychopathology

por Morrison, Sinead, Chawner, Samuel J. R. A., van Amelsvoort, Therese A. M. J., Swillen, Ann, Vingerhoets, Claudia, Vergaelen, Elfi, Linden, David E. J., Linden, Stefanie, Owen, Michael J., van den Bree, Marianne B. M.
Publicado 2020

Copy number variants (CNVs): a powerful tool for iPSC-based modelling of ASD

por Drakulic, Danijela, Djurovic, Srdjan, Syed, Yasir Ahmed, Trattaro, Sebastiano, Caporale, Nicolò, Falk, Anna, Ofir, Rivka, Heine, Vivi M., Chawner, Samuel J. R. A., Rodriguez-Moreno, Antonio, van den Bree, Marianne B. M., Testa, Giuseppe, Petrakis, Spyros, Harwood, Adrian J.
Publicado 2020

Neurodevelopmental dimensional assessment of young children at high genomic risk of neuropsychiatric conditions

por 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, van den Bree, Marianne B. M.
Publicado 2023

The psychiatric phenotypes of 1q21 distal deletion and duplication

por 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.
Publicado 2021

Correction: The psychiatric phenotypes of 1q21 distal deletion and duplication

por 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.
Publicado 2021

Psychiatric disorders in children with 16p11.2 deletion and duplication

por 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
Publicado 2019

Correction: Psychiatric disorders in children with 16p11.2 deletion and duplication

por 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.
Publicado 2019

Attention deficit hyperactivity disorder symptoms as antecedents of later psychotic outcomes in 22q11.2 deletion syndrome

por Niarchou, Maria, Chawner, Samuel J.R.A., Fiksinski, Ania, Vorstman, Jacob A.S., Maeder, Johanna, Schneider, Maude, Eliez, Stephan, Armando, Marco, Pontillo, Maria, Vicari, Stefano, McDonald-McGinn, Donna M., Emanuel, Beverly S., Zackai, Elaine H., Bearden, Carrie E., Shashi, Vandana, Hooper, Stephen R., Owen, Michael J., Gur, Raquel E., Wray, Naomi R., van den Bree, Marianne B.M., Thapar, Anita
Publicado 2019

DRAGON-Data: a platform and protocol for integrating genomic and phenotypic data across large psychiatric cohorts

por Lynham, Amy J., Knott, Sarah, Underwood, Jack F. G., Hubbard, Leon, Agha, Sharifah S., Bisson, Jonathan I., van den Bree, Marianne B. M., Chawner, Samuel J. R. A., Craddock, Nicholas, O'Donovan, Michael, Jones, Ian R., Kirov, George, Langley, Kate, Martin, Joanna, Rice, Frances, Roberts, Neil P., Thapar, Anita, Anney, Richard, Owen, Michael J., Hall, Jeremy, Pardiñas, Antonio F., Walters, James T. R.
Publicado 2023