Copy number variation: What is it and what has it told us about child psychiatric disorders?

Journal of the American Academy of Child and Adolescent Psychiatry

Volumn 52, Issue 8, 2013, Pages 772-774

  Thapar, Anita ^a   Cooper, Miriam ^a  

^a CARDIFF UNIVERSITY SCHOOL OF MEDICINE   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ATTENTION DEFICIT DISORDER; AUTISM; CHILD PSYCHIATRY; CHROMOSOME ABERRATION; COPY NUMBER VARIATION; COUNSELING; DNA SEQUENCE; GENE MUTATION; GENERALIZED EPILEPSY; GENETIC RISK; GENOTYPE ENVIRONMENT INTERACTION; HUMAN; INTELLECTUAL IMPAIRMENT; MENTAL DISEASE; NOTE; PATHOGENICITY; PRADER WILLI SYNDROME; PRIORITY JOURNAL; RISK ASSESSMENT; SCHIZOPHRENIA; SINGLE NUCLEOTIDE POLYMORPHISM; SMITH MAGENIS SYNDROME;

EID: 84880599004     PISSN: 08908567     EISSN: 15275418     Source Type: Journal    
DOI: 10.1016/j.jaac.2013.05.013     Document Type: Article

References (5)

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3. S. Girirajan, Z. Brkanac, and B.P. Coe Relative burden of large CNVs on a range of neurodevelopmental phenotypes PLoS Genet 7 2011 e1002334
4. N.M. Williams, I. Zaharieva, and A. Martin Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis Lancet 376 2010 1401 1408
5. N.M. Williams, B. Franke, and E. Mick Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3 Am J Psychiatry 169 2012 195 204