The neuregulin 1 (NRG1) gene has been the subject of considerable excitement within the psychiatric genetics literature since it was originally identified as a potential susceptibility locus for schizophrenia. Here we provide an update of our first meta-analysis of this association. Case-control and family-based genetic association studies of the NRG1 gene in healthy control groups and clinically diagnosed schizophrenia patients were included. We re-peated the search strategy in our earlier meta-analysis for studies published between December 31, 2005, and Sep-tember 30, 2007, and updated the results of our original meta-analysis accordingly. Superficially, the results of our updated meta-analysis are consistent with those in our previous r...
Chromosome 8p22–p11 has been identified as a locus for schizophrenia in several genome-wide scans, w...
The cause of schizophrenia is unknown, but it has a significant genetic component. Pharmacologic stu...
To access publisher full text version of this article. Please click on the hyperlink in Additional L...
The neuregulin 1 (NRG1) gene has been the subject of considerable excitement within the psychiatric ...
Genetic, post-mortem and neuroimaging studies repeatedly implicate neuregulin-1 (NRG1) as a critical...
Genetic, post-mortem and neuroimaging studies repeatedly implicate neuregulin-1 (NRG1) as a critical...
Clinical and pre-clinical evidence has implicated neuregulin 1 (NRG1) as a critical component in the...
Neuregulin 1 (NRG1) is a leading schizophrenia susceptibility gene. The NRG1 locus on chromosome 8p ...
Chromosome 8p22-p11 has been identified as a locus for schizophrenia in several genome-wide scans, w...
A number of studies have indicated that 8p22-p12 is likely to harbor schizophrenia susceptibility lo...
Recently, we identified neuregulin 1 (NRG1) as a susceptibility gene for schizophrenia in the Icelan...
Recent work shows potentially promising associations between schizophrenia and polymorphisms in Neur...
<p><strong>Objective: </strong>Although the etiology of schizophrenia is unknown, it has a significa...
We investigated the association of the NRG1 gene and schizophrenia using meta-analytic techniques, c...
Schizophrenia is a serious and disabling mental disorder with a high heritability rate. The human ne...
Chromosome 8p22–p11 has been identified as a locus for schizophrenia in several genome-wide scans, w...
The cause of schizophrenia is unknown, but it has a significant genetic component. Pharmacologic stu...
To access publisher full text version of this article. Please click on the hyperlink in Additional L...
The neuregulin 1 (NRG1) gene has been the subject of considerable excitement within the psychiatric ...
Genetic, post-mortem and neuroimaging studies repeatedly implicate neuregulin-1 (NRG1) as a critical...
Genetic, post-mortem and neuroimaging studies repeatedly implicate neuregulin-1 (NRG1) as a critical...
Clinical and pre-clinical evidence has implicated neuregulin 1 (NRG1) as a critical component in the...
Neuregulin 1 (NRG1) is a leading schizophrenia susceptibility gene. The NRG1 locus on chromosome 8p ...
Chromosome 8p22-p11 has been identified as a locus for schizophrenia in several genome-wide scans, w...
A number of studies have indicated that 8p22-p12 is likely to harbor schizophrenia susceptibility lo...
Recently, we identified neuregulin 1 (NRG1) as a susceptibility gene for schizophrenia in the Icelan...
Recent work shows potentially promising associations between schizophrenia and polymorphisms in Neur...
<p><strong>Objective: </strong>Although the etiology of schizophrenia is unknown, it has a significa...
We investigated the association of the NRG1 gene and schizophrenia using meta-analytic techniques, c...
Schizophrenia is a serious and disabling mental disorder with a high heritability rate. The human ne...
Chromosome 8p22–p11 has been identified as a locus for schizophrenia in several genome-wide scans, w...
The cause of schizophrenia is unknown, but it has a significant genetic component. Pharmacologic stu...
To access publisher full text version of this article. Please click on the hyperlink in Additional L...