Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions

Keyphrases

• Schizophrenia 100%
• Copy number Variation 100%
• NRXN1 100%
• ABCB11 100%
• Schizophrenia Risk 66%
• Mesolimbic 33%
• Genotype 33%
• Non-coding 33%
• Exon 33%
• Cis-regulatory Elements 33%
• Germ Cells 33%
• Intragenic Deletion 33%
• Allele-specific 33%
• Hi-C Maps 33%
• Mesocortical 33%
• Blood Disorders 33%
• Treatment-resistant Schizophrenia 33%
• Unmarked Deletion 33%
• Cryptic Promoters 33%
• Antipsychotic Response 33%

Biochemistry, Genetics and Molecular Biology

• NRXN1 100%
• ABCB11 100%
• Dopaminergic 33%
• Promoter Region 33%
• Genotyping 33%
• Allele 33%
• Exon 33%
• Germline 33%
• Germ Cell 33%
• Cis-Regulatory Element 33%