The Genetics of Adult-Onset Neuropsychiatric Disease: Complexities and Conundra?
- 31 October 2003
- journal article
- review article
- Published by American Association for the Advancement of Science (AAAS) in Science
- Vol. 302 (5646) , 822-826
- https://doi.org/10.1126/science.1092132
Abstract
Genetic factors play a major role in the etiology of adult-onset neurodegenerative and neuropsychiatric disorders. Several highly penetrant genes have been cloned for rare, autosomal-dominant, early-onset forms of neurodegenerative diseases. These genes have provided important insights into the mechanisms of these diseases (often altering neuronal protein processing). However, the genes associated with inherited susceptibility to late-onset neurodegenerative diseases, schizophrenia, and bipolar disorder appear to have smaller effects and are likely to interact with each other (and with nongenetic factors) to modulate susceptibility and/or disease phenotype. Several strategies have recently been applied to address this complexity, leading to the identification of a number of candidate susceptibility loci/genes.This publication has 55 references indexed in Scilit:
- Recent advances in the genetics of schizophreniaHuman Molecular Genetics, 2003
- Genome Scan Meta-Analysis of Schizophrenia and Bipolar Disorder, Part II: SchizophreniaAmerican Journal of Human Genetics, 2003
- Fine Mapping of Autistic Disorder to Chromosome 15q11-q13 by Use of Phenotypic SubtypesAmerican Journal of Human Genetics, 2003
- The future of genetic association studies in Alzheimer diseaseJournal Of Neural Transmission-Parkinsons Disease and Dementia Section, 2003
- The BDNF val66met Polymorphism Affects Activity-Dependent Secretion of BDNF and Human Memory and Hippocampal FunctionPublished by Elsevier ,2003
- Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common diseaseNature Genetics, 2003
- Three‐Axis Eye Movement Abnormalities with Cerebellar LesionsAnnals of the New York Academy of Sciences, 2002
- Additive Effects of PS1 and APP Mutations on Secretion of the 42-Residue Amyloid β-ProteinNeurobiology of Disease, 1998
- Tau is a candidate gene for chromosome 17 frontotemporal dementiaAnnals of Neurology, 1998
- Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's diseaseNature, 1991