Lack of association of functional cathechol-O-methyltransferase gene polymorphism in schizophrenia
- 15 February 1997
- journal article
- research article
- Published by Elsevier in Biological Psychiatry
- Vol. 41 (4) , 493-495
- https://doi.org/10.1016/s0006-3223(96)00474-x
Abstract
No abstract availableThis publication has 25 references indexed in Scilit:
- Human catechol-O-methyltransferase pharmacogenetics: description of a functional polymorphism and its potential application to neuropsychiatric disordersPharmacogenetics, 1996
- No evidence for allelic association between schizophrenia and a polymorphism determining high or low catechol O-methyltransferase activityAmerican Journal of Psychiatry, 1996
- Dopamine D4 receptor (D4DR) exon III polymorphism associated with the human personality trait of Novelty SeekingNature Genetics, 1996
- Velo‐cardio‐facial syndrome and psychotic disorders: Implications for psychiatric geneticsAmerican Journal of Medical Genetics, 1994
- Genetic study of dopamine D1, D2, and D4 receptors in schizophreniaPsychiatry Research, 1994
- Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis.Journal of Medical Genetics, 1993
- Catechol O-methyltransferase pharmacogenetics: photoaffinity labelling and Western blot analysis of human liver samplesPharmacogenetics, 1993
- Chromosomal mapping of the human catechol-O-methyltransferase gene to 22q11.1→q11.2Genomics, 1992
- The current status of the dopamine hypothesis of schizophreniaNeuropsychopharmacology, 1988
- The decrease of erythrocyte catechol-O-methyltransferase activity in depressed patients and its diagnostic significanceActa Psychiatrica Scandinavica, 1987