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Paper Details

Rare coding variants as risk modifiers of the 22q11.2 deletion implicate postnatal cortical development in syndromic schizophrenia.
Mol Psychiatry
2
2023
110, 22q11, COMT, PI4KA, SCZ, SLC25A1, developmental disorders, gene coexpression modules, gene network, modifier genes, rare, rare coding variants, rare nonsynonymous variants, schizophrenia, syndromic schizophrenia
Author NameAffiliation
Michael J OwenDivision of Psychological Medicine and Clinical Neurosciences, Cardiff University
Anne S BassettUniversity of Toronto
Raquel E GurDepartment of Psychiatry and Lifespan Brain Institute, University of Pennsylvania
Raquel E GurDepartment of Psychiatry and Lifespan Brain Institute, University of Pennsylvania
Zhengdong D ZhangAlbert Einstein College of Medicine
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