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Pharmacogenomics of statin response.
Differential effects of ramipril on ambulatory blood pressure in African Americans and Caucasians.
Family history, environmental exposures in early life, and childhood asthma.
Disruption of sphingolipid metabolism elicits apoptosis-associated reproductive defects in Drosophila.
Mapping of deletion and translocation breakpoints in 1q44 implicates the serine/threonine kinase AKT3 in postnatal microcephaly and agenesis of the corpus callosum.
Polymorphisms in IL13, total IgE, eosinophilia, and asthma exacerbations in childhood.
Increased plasma concentrations of lipoprotein(a) during a low-fat, high-carbohydrate diet are associated with increased plasma concentrations of apolipoprotein C-III bound to apolipoprotein B-containing lipoproteins.
NFIA haploinsufficiency is associated with a CNS malformation syndrome and urinary tract defects.
CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders.
Genetic nondiscrimination legislation: a critical prerequisite for pharmacogenomics data sharing.