Pages that link to "Q45101667"
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The following pages link to Evidence for a schizophrenia vulnerability locus on chromosome 8p in the Irish Study of High-Density Schizophrenia Families (Q45101667):
Displaying 50 items.
- Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia (Q24532517) (← links)
- Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23 (Q24536215) (← links)
- Neuregulin 1 transcripts are differentially expressed in schizophrenia and regulated by 5' SNPs associated with the disease (Q24546782) (← links)
- Association of neuregulin 1 with schizophrenia confirmed in a Scottish population (Q24561773) (← links)
- Neuregulin 1 and susceptibility to schizophrenia (Q24616921) (← links)
- Variations in the vesicular monoamine transporter 1 gene (VMAT1/SLC18A1) are associated with bipolar i disorder (Q24645725) (← links)
- Genetic association and brain morphology studies and the chromosome 8p22 pericentriolar material 1 (PCM1) gene in susceptibility to schizophrenia (Q24658441) (← links)
- Animal models of schizophrenia: a critical review (Q24674909) (← links)
- Evidence for association of schizophrenia with genetic variation in the 8p21.3 gene, PPP3CC, encoding the calcineurin gamma subunit (Q24678549) (← links)
- The glial growth factors deficiency and synaptic destabilization hypothesis of schizophrenia (Q24798030) (← links)
- No association between the dihydropyrimidinase-related protein 2 (DRP-2) gene and bipolar disorder in humans (Q28204591) (← links)
- From genomics to proteomics: new directions in molecular neuropsychiatry. (Q30385730) (← links)
- Deletion of PLCB1 gene in schizophrenia-affected patients (Q30415884) (← links)
- Evidence of missense mutations on the neuregulin 1 gene affecting function of prepulse inhibition (Q30458275) (← links)
- Prefrontal neurons and the genetics of schizophrenia (Q30666934) (← links)
- Genetic and non-genetic vulnerability factors in schizophrenia: the basis of the "two hit hypothesis". (Q33813156) (← links)
- Search for schizophrenia susceptibility genes (Q33842584) (← links)
- Susceptibility loci for bipolar disorder: overlap with inherited vulnerability to schizophrenia (Q33842595) (← links)
- Genomewide linkage analyses of bipolar disorder: a new sample of 250 pedigrees from the National Institute of Mental Health Genetics Initiative. (Q33905879) (← links)
- Genomewide linkage scan for schizophrenia susceptibility loci among Ashkenazi Jewish families shows evidence of linkage on chromosome 10q22. (Q33906350) (← links)
- The DTNBP1 (dysbindin-1) gene variant rs2619522 is associated with variation of hippocampal and prefrontal grey matter volumes in humans. (Q34031938) (← links)
- Genetic analyses of schizophrenia (Q34108332) (← links)
- The epidemiology of the genetic liability for schizophrenia (Q34113081) (← links)
- Genetics of schizophrenia and the new millennium: progress and pitfalls (Q34136656) (← links)
- Genomewide high-density SNP linkage analysis of 236 Japanese families supports the existence of schizophrenia susceptibility loci on chromosomes 1p, 14q, and 20p. (Q34137538) (← links)
- Linkage of familial schizophrenia to chromosome 13q32 (Q34145743) (← links)
- Genetic insights into schizophrenia (Q34203064) (← links)
- No association with the calcineurin A gamma subunit gene (PPP3CC) haplotype to Japanese schizophrenia (Q34412903) (← links)
- Recent advances in the genetics of schizophrenia. (Q34578115) (← links)
- Molecular genetics of schizophrenia: past, present and future (Q34584191) (← links)
- Biological phenotypes and genetic research on schizophrenia (Q34721909) (← links)
- Personalized medicine in psychiatry: problems and promises (Q34726454) (← links)
- Stigma and public health policy for schizophrenia (Q35102495) (← links)
- Molecular genetics of schizophrenia: a critical review. (Q35590435) (← links)
- Three independent lines of evidence suggest retinoids as causal to schizophrenia (Q36067304) (← links)
- Unravelling the genome: a review of molecular genetic research in schizophrenia (Q36938089) (← links)
- Methionine sulfoxide reductase: a novel schizophrenia candidate gene (Q37192367) (← links)
- Neurodevelopmental Perspectives on Wnt Signaling in Psychiatry (Q38917986) (← links)
- Genome-wide scan of homogeneous subtypes of NIMH genetics initiative schizophrenia families. (Q40452223) (← links)
- A novel permutation testing method implicates sixteen nicotinic acetylcholine receptor genes as risk factors for smoking in schizophrenia families (Q40504359) (← links)
- The genetics of schizophrenia: past, present, and future concepts (Q40869587) (← links)
- Implications of genetic research for child psychiatry (Q40885221) (← links)
- Neurodevelopmental and neuroprogressive processes in schizophrenia. Antithetical or complementary, over a lifetime trajectory of disease? (Q41743488) (← links)
- Gene expression of neuregulin-1 isoforms in different brain regions of elderly schizophrenia patients (Q43135420) (← links)
- Phenomic, convergent functional genomic, and biomarker studies in a stress-reactive genetic animal model of bipolar disorder and co-morbid alcoholism (Q43459376) (← links)
- Neuregulin 1 in schizophrenia: out of Iceland (Q43530887) (← links)
- A genome-wide association study for quantitative traits in schizophrenia in China. (Q44395308) (← links)
- The genetic epidemiology of psychiatric disorders: a current perspective (Q45102836) (← links)
- Linkage evidence of schizophrenia to loci near neuregulin 1 gene on chromosome 8p21 in Taiwanese families. (Q45259986) (← links)
- Relative risk for cognitive impairments in siblings of patients with schizophrenia (Q46692838) (← links)