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A computational model for quantifying instability of tandem repeats across the genome
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Identifying disease-causing mechanisms and fundamental biology of neuromuscular disorder genes through genomic feature analysis
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Short tandem repeats significantly contribute to the genetic architecture of metabolic and sensory age-related hearing loss phenotypes
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Unbiased human genomic characterization of polyglutamine disorder genes to guide biological understanding and therapeutic strategies
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Genomic characterization of Huntington's disease genetic modifiers informs drug target tractability
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A multi-centre, tolerability study of a cannabidiol-enriched Cannabis Herbal Extract for chronic headaches in adolescents: The CAN-CHA protocol
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Characterization of CYP2B6 and CYP2A6 pharmacogenetic variation in sub-Saharan African populations
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A cross-sectional study of the relationship between CYP2D6 and CYP2C19 variations and depression symptoms, for women taking SSRIs during pregnancy
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A pharmacogenomic investigation of the cardiac safety profile of ondansetron in children and pregnant women
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A systematic review and analysis of the use of polygenic scores in pharmacogenomics
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