using LDSC (P=0.01), while oligodendrocytes did not replicate in this dataset, perhaps because they were not sampled from the regions affected by the disorder (i.e. spinal cord, pons, medulla or midbrain). A within-neuron analysis again found that projecting excitatory (i.e. pyramidal CA1) and projecting inhibitory neurons (i.e. medium spiny neurons) can be prioritized for multiple traits (schizophrenia, bipolar, intelligence, educational attainment, BMI). In addition, we found that neuroblasts could be prioritized for MDD and that neural progenitors could be prioritized for intracranial volume (Figure S18) in this dataset.
