Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome

Anne S. Bassett*, Chelsea Lowther, Daniele Merico, Gregory Costain, Eva W. C. Chow, Therese van Amelsvoort, Donna McDonald-McGinn, Raquel E. Gur, Ann Swillen, Marianne Van den Bree, Kieran Murphy, Doron Gothelf, Carrie E. Bearden, Stephan Eliez, Wendy Kates, Nicole Philip, Vandana Sashi, Linda Campbell, Jacob Vorstman, Joseph CubellsGabriela M. Repetto, Tony Simon, Erik Boot, Tracy Heung, Rens Evers, Claudia Vingerhoets, Esther van Duin, Elaine Zackai, Elfi Vergaelen, Koen Devriendt, Joris R. Vermeesch, Michael Owen, Clodagh Murphy, Elena Michaelovosky, Leila Kushan, Maude Schneider, Wanda Fremont, Tiffany Busa, Stephen Hooper, Kathryn McCabe, Sasja Duijff, Karin Isaev, Giovanna Pellecchia, John Wei, Matthew J. Gazzellone, Stephen W. Scherer, Beverly S. Emanuel, Tingwei Guo, Bernice E. Morrow, Christian R. Marshall, Int 22q11 2DS Brain Behav Conso

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Original languageEnglish
Pages (from-to)1054-1063
Number of pages10
JournalAmerican Journal of Psychiatry
Volume174
Issue number11
DOIs
Publication statusPublished - 1 Nov 2017

Keywords

  • CHROMOSOMAL MICROARRAY
  • VARIANTS
  • RISK
  • DISORDERS
  • MICRODUPLICATIONS
  • INTEGRATION
  • MECHANISMS
  • CHILDHOOD
  • MUTATIONS
  • BURDEN

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