Investigate the causal relationships between genetic variants and molecular phenotype changes in human complex diseases such as neuropsychiatric disorders (e.g., autism spectrum disorder (ASD), schizophrenia (SCZ), and Alzheimer's disease (AD)) and cancer (e.g., glioma and breast cancer)
Comparative & Evolutionary Genomics/Transcriptomics
Post-transcriptional Regulation
Genomic imprinting
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