No bipolar family study (that was conducted in an optimal manner) reports increased risk for schizophrenia among RG7204 cost relatives of bipolar probands. Similarly, no schizophrenia family study reports increased risk for bipolar disorders among

relatives of schizophrenia probands. However, several schizophrenia family studies report increased risk for recurrent unipolar depression and schizoaffective disorders among relatives of schizophrenia probands.5-8 Family studies of bipolar illness show that a spectrum of mood disorders is found among the first-degree relatives of bipolar probands: bipolar I, bipolar II with major depression (hypomania and depressive episodes in the same Inhibitors,research,lifescience,medical person), schizoaffective disorders, and recurrent unipolar depression.8-13 These family studies are consistent with some degree of overlap in susceptibility to recurrent unipolar depression and schizoaffective disorders for relatives of bipolar probands and relatives of Inhibitors,research,lifescience,medical schizophrenia probands. Kendler et al7

specifically noted Inhibitors,research,lifescience,medical an increase in risk for psychotic affective disorders among the relatives of schizophrenia probands. Thus, from this family study perspective, some endophenotypes may be shared between schizophrenia and affective disorders. Similarly, there is molecular evidence for genetic overlap in susceptibility to schizophrenia and to affective disorders (for a review, see reference 4). One promising candidate gene is the G72 locus on chromosomal Inhibitors,research,lifescience,medical region 13q32, the site of a confirmed linkage in bipolar disorder and schizophrenia.4 G72 is a primate-specific, brainexpressed gene that activates D-amino acid oxidase.14 D-Amino acid oxidase may control levels of D-serine, which regulates glutamatergic receptors.15 Chumakov et al14 identified a haplotype from G72 single nucleotide polymorphisms (without obvious functional significance) that were in linkage disequilibrium Inhibitors,research,lifescience,medical with schizophrenia in a French-Canadian

sample. This has been confirmed in distinct schizophrenia populations, Cediranib (AZD2171) including Russian,14 German,16 Israeli,17 and Chinese,18 although different haplotypes have been associated in distinct ethnic populations. Similarly, in bipolar disorder, there have been several positive findings with distinct haplotypes in different populations, including American19,20 and German16 bipolar samples. Thus, from this molecular perspective, some endophenotypes may be shared between schizophrenic and affective disorders. Given what we know about the overlap in genetic susceptibility to schizophrenia and mood disorders,4 it is entirely possible that some endophenotypes may be characteristics of both types of disorder. Stability and heritability of an endophenotype: the P50 abnormalities as an example Ideally, an endophenotype should be a stable, state-independent parameter.