Genomics, particularly high-throughput sequencing and characterization of e
xpressed human genes, has created new opportunities for drug discovery. Kno
wledge of all the human genes and their functions may allow effective preve
ntive measures, annd change drug research strategy and drug discovery devel
opment processes. Pharmacogenomics is the application of genomic technologi
es such as gene sequencing, statistical genetics, and gene expression analy
sis to drugs in clinical development and on the market. It applies the larg
e-scale systematic approaches of genomics to speed the discovery of drug re
sponse markers, whether they act at the level of the drug target, drug meta
bolism, or disease pathways. The potential implication of genomics and phar
macogenomics in clinical research and clinical medicine is that disease cou
ld be treated according to genetic and specific individual markers, selecti
ng medications and dosages that are optimized for individual patients. The
possibility of defining patient populations genetically may improve outcome
s by predicting individual responses to drugs, and could improve safety and
efficacy in therapeutic areas such as neuropsychiatry, cardiovascular medi
cine, endocrinology (diabetes and obesity) and oncology. Ethical questions
need to be addressed and guidelines established for the use of genomics in
clinical research and clinical medicine. Significant achievements are possi
ble with an interdisciplinary approach that includes genetic, technological
and therapeutic measures.