Gene symbol | Ensemble ID | Log2-fold change | P value | Association to neurodevelopmental/neuropsychiatric disease | Ref. |
---|---|---|---|---|---|
RORA | ENSG00000069667 | 1.118 | 1.21E−05 | ASD candidate | [43] |
CPLX1 | ENSG00000168993 | 0.820 | 4.60E−04 | Wolf Hirschhorn syndrome | [44] |
TCF4 | ENSG00000196628 | 1.063 | 4.97E−04 | SCZ, Pitt-Hopkins syndrome | |
SIRT1 | ENSG00000096717 | 1.074 | 5.59E−04 | SCZ | [46] |
ESRRA | ENSG00000173153 | 0.888 | 2.72E−03 |  |  |
CDK6 | ENSG00000105810 | 1.087 | 3.86E−03 | Microcephaly | [47] |
XIAP | ENSG00000101966 | 1.060 | 4.68E−03 | SCZ | [48] |
ZNF804A | ENSG00000170396 | 1.108 | 5.29E−03 | SCZ, BD | [49] |
MET | ENSG00000105976 | 1.132 | 5.34E−03 |  |  |
CTBP1 | ENSG00000159692 | 0.936 | 5.77E−03 |  |  |
GRIA1 | ENSG00000155511 | 1.068 | 8.78E−03 | SCZ | |
KLF12 | ENSG00000118922 | 1.066 | 1.10E−02 |  |  |
MSI1 | ENSG00000135097 | 0.865 | 1.23E−02 |  |  |
KDM5B | ENSG00000117139 | 1.049 | 1.45E−02 | ID, ASD | [51] |
PAQR3 | ENSG00000163291 | 1.067 | 1.71E−02 |  |  |
TRIM13 | ENSG00000204977 | 1.050 | 2.28E−02 |  |  |