TY - JOUR
T1 - Genetics in psychiatry
T2 - Common variant association studies
AU - Buxbaum, Joseph
AU - Baron-Cohen, Simon
AU - Devlin, Bernie
N1 - Funding Information:
During the period of this work, JDB was supported by the NIH, Autism Speaks, the Simons Foundation, and the Seaver Foundation; SBC was supported by the MRC UK, the Nancy Lurie Marks Family Foundation, and Target Autism Genome (TAG); BD was supported by the NIH, Autism Speaks, and the Simons Foundation.
PY - 2010
Y1 - 2010
N2 - Many psychiatric conditions and traits are associated with significant heritability. Genetic risk for psychiatric conditions encompass rare variants, identified due to major effect, as well as common variants, the latter analyzed by association analyses. We review guidelines for common variant association analyses, undertaking after assessing evidence of heritability. We highlight the importance of: suitably large sample sizes; an experimental design that controls for ancestry; careful data cleaning; correction for multiple testing; small P values for positive findings; assessment of effect size for positive findings; and, inclusion of an independent replication sample. We also note the importance of a critical discussion of any prior findings, biological follow-up where possible, and a means of accessing the raw data.
AB - Many psychiatric conditions and traits are associated with significant heritability. Genetic risk for psychiatric conditions encompass rare variants, identified due to major effect, as well as common variants, the latter analyzed by association analyses. We review guidelines for common variant association analyses, undertaking after assessing evidence of heritability. We highlight the importance of: suitably large sample sizes; an experimental design that controls for ancestry; careful data cleaning; correction for multiple testing; small P values for positive findings; assessment of effect size for positive findings; and, inclusion of an independent replication sample. We also note the importance of a critical discussion of any prior findings, biological follow-up where possible, and a means of accessing the raw data.
UR - https://www.scopus.com/pages/publications/77956381675
U2 - 10.1186/2040-2392-1-6
DO - 10.1186/2040-2392-1-6
M3 - Review article
AN - SCOPUS:77956381675
SN - 2040-2392
VL - 1
JO - Molecular Autism
JF - Molecular Autism
IS - 1
M1 - 6
ER -