Who can join: Anyone with GWAS and good quality phenotypic data on substance use, preferably including detailed assessments of quantity, frequency and problematic use (e.g. abuse/dependence, or proxies). We strongly encourage the sharing of individual-level genotypes and phenotypes. However, we also welcome effect size/summary data as well.
How to join: Email one of the co-chairs and we will set up a time to introduce you to our group. We suggest you review the PGC2 MOU.