Abstract | BACKGROUND: METHODS: In a bid to examine this hypothesis, we examined seven SNPs spanning GRM3 in a UK case-control sample (schizophrenic cases n = 674, controls n = 716). These included all SNPs previously reported to be associated, alone or in haplotypes, with schizophrenia in European or European American samples. RESULTS: Our data showed no evidence for association with single markers, or 2, 3, 4 and 5 marker haplotypes, nor did any specific haplotypes show evidence for association according to previously observed patterns. CONCLUSION: Examination of our own data and those of other groups leads us to conclude that at present, GRM3 should not be viewed as a gene for which there is replicated evidence for association with schizophrenia.
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Authors | Nadine Norton, Hywel J Williams, Sarah Dwyer, Dobril Ivanov, Anna C Preece, Amy Gerrish, Nigel M Williams, Pamela Yerassimou, Stanley Zammit, Michael C O'Donovan, Michael J Owen |
Journal | BMC psychiatry
(BMC Psychiatry)
Vol. 5
Pg. 23
(May 13 2005)
ISSN: 1471-244X [Electronic] England |
PMID | 15892884
(Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Genetic Markers
- Receptor, Metabotropic Glutamate 5
- Receptors, Metabotropic Glutamate
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Topics |
- Adult
- Case-Control Studies
- Female
- Gene Frequency
- Genetic Markers
- Genetic Predisposition to Disease
(genetics)
- Genotype
- Haplotypes
(genetics)
- Humans
- Male
- Polymorphism, Single Nucleotide
(genetics)
- Receptor, Metabotropic Glutamate 5
- Receptors, Metabotropic Glutamate
(genetics)
- Schizophrenia
(genetics)
- White People
(genetics)
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