Additional file 1 of xWAS analysis in neuropsychiatric disorders by integrating multi-molecular phenotype quantitative trait loci and GWAS summary data

Additional file 1: Table S1. Basic information and used frequency of GWAS summary datasets of five diseases. Table S2. Basic information and used frequency of xQTL weight of five diseases for FUSION-like analyses. Table S3. Basic information and used frequency of xQTL sources of five diseases for SMR analyses. Table S4. Included literature information for SCZ. Table S5. Included literature information for BP. Table S6. Included literature information for ADHD. Table S7. Included literature information for ASD. Table S8. Included literature information for MDD. Table S9. Overview of novel genes in SCZ. Table S10. Overview of novel genes in BP. Table S11. Overview of novel genes in ADHD. Table S12. Overview of novel genes in ASD. Table S13. Overview of novel genes in MDD. Table S14. GO biological process (BP) functional enrichment results for the novel genes of five diseases with gProfiler. Table S15. Function enrichment of all reliable genes (novel reliable genes and non-novel reliable genes) of five diseases on GO-BP, GWAS Catalog, and KEGG using FUMA.