Genomic Medicine and the Future of Health Care
Embracing all the myriad variations of the human genome should, in theory, lead to rewards that all can share.
Embracing all the myriad variations of the human genome should, in theory, lead to rewards that all can share.
The authors explored whether valproate (VPA) treatment effects vary by catechol-O-methyltransferase (COMT) genotype.
It is hypothesized that multiple single nucleotide polymorphisms (SNPs) work together to influence risk of complex neuropsychiatric disorders such as depression.
Genetic variation can increase the predisposition to major depressive disorder.
Genetic factors and the environment patients share with their partner or spouse may determine their risk of developing chronic pain and help explain the association between chronic pain and depression.
Compared with men, women diagnosed with AUD have higher rates of premature death due to alcohol abuse.
Investigators used decomposition methods to examine the relative importance of genetic and environmental components to the burden of ADHD.
Early life trauma interacts with FKBP5 genotype to predict heavy alcohol consumption in college students.
Appropriate study planning from the outset is one step that can help improve interpretability.
To date, there are no validated biomarkers to independently assess Parkinson Disease diagnosis and prognosis, or to measure disease severity.