| Item Type | Name |
|
Concept
|
Gene Expression Profiling
|
|
Concept
|
Gene Regulatory Networks
|
|
Concept
|
Epistasis, Genetic
|
|
Concept
|
Gene Expression
|
|
Concept
|
Genes
|
|
Concept
|
Amino Acid Sequence
|
|
Concept
|
Genes, Dominant
|
|
Concept
|
Genome, Human
|
|
Concept
|
Polymorphism, Single Nucleotide
|
|
Concept
|
Quantitative Trait Loci
|
|
Concept
|
Sequence Homology, Amino Acid
|
|
Concept
|
Sequence Homology, Nucleic Acid
|
|
Concept
|
Genetic Loci
|
|
Concept
|
Genome
|
|
Concept
|
Gene Frequency
|
|
Concept
|
Gene Duplication
|
|
Concept
|
Base Sequence
|
|
Concept
|
Alleles
|
|
Concept
|
Genes, Recessive
|
|
Concept
|
Molecular Sequence Data
|
|
Concept
|
Repetitive Sequences, Nucleic Acid
|
|
Concept
|
Gene Expression Regulation
|
|
Concept
|
Nucleic Acid Conformation
|
|
Concept
|
Gene Dosage
|
|
Academic Article
|
Genome-wide association of bipolar disorder suggests an enrichment of replicable associations in regions near genes.
|
|
Academic Article
|
Evidence for association of bipolar disorder to haplotypes in the 22q12.3 region near the genes stargazin, IFT27 and parvalbumin.
|
|
Academic Article
|
Waardenburg syndrome and Hirschsprung disease: evidence for pleiotropic effects of a single dominant gene.
|
|
Academic Article
|
Tests of linkage and heterogeneity in Mendelian diseases using identity by descent scores.
|
|
Academic Article
|
A test of nonrandom segregation.
|
|
Academic Article
|
Multipoint genetic linkage analysis of the m2 human muscarinic receptor gene.
|
|
Academic Article
|
No association detected between a D3 receptor gene-expressed variant and schizophrenia.
|
|
Academic Article
|
Use of exact and adjusted liability scores to detect genes affecting common traits.
|
|
Academic Article
|
No abnormality in the gene for the G protein stimulatory alpha subunit in patients with bipolar disorder.
|
|
Academic Article
|
Lack of linkage between the corticotropin-releasing hormone (CRH) gene and bipolar affective disorder.
|
|
Academic Article
|
Bipolar disorder and chromosome 18: an analysis of multiple data sets.
|
|
Academic Article
|
Closing in on genes for manic-depressive illness and schizophrenia.
|
|
Academic Article
|
Serotonin transporter (5-HTT) gene and bipolar affective disorder.
|
|
Academic Article
|
Genetic diversity of the human serotonin receptor 1B (HTR1B) gene.
|
|
Academic Article
|
Linkage analysis of schizophrenia to chromosome 15.
|
|
Academic Article
|
A mannosyltransferase gene at 11q23 is disrupted by a translocation breakpoint that co-segregates with bipolar affective disorder in a small family.
|
|
Academic Article
|
Additional, physically ordered markers increase linkage signal for bipolar disorder on chromosome 18q22.
|
|
Academic Article
|
Polymorphisms at the G72/G30 gene locus, on 13q33, are associated with bipolar disorder in two independent pedigree series.
|
|
Academic Article
|
Progress toward discovery of susceptibility genes for bipolar manic-depressive illness and schizophrenia.
|
|
Academic Article
|
Linkage disequilibrium of the brain-derived neurotrophic factor Val66Met polymorphism in children with a prepubertal and early adolescent bipolar disorder phenotype.
|
|
Academic Article
|
Linkage disequilibrium analysis in the LOC93081-KDELC1-BIVM region on 13q in bipolar disorder.
|
|
Academic Article
|
Family-based association study of the serotonin transporter gene polymorphisms in Korean ADHD trios.
|
|
Academic Article
|
Family-based association study of DAT1 and DRD4 polymorphism in Korean children with ADHD.
|
|
Academic Article
|
No evidence for association between 19 cholinergic genes and bipolar disorder.
|
|
Academic Article
|
Mapping genes that contribute to daunorubicin-induced cytotoxicity.
|
|
Academic Article
|
No association of trace amine receptor genes with bipolar disorder.
|
|
Academic Article
|
Allelic association of G72/G30 with schizophrenia and bipolar disorder: a comprehensive meta-analysis.
|
|
Academic Article
|
Recurrent 16p11.2 microdeletions in autism.
|
|
Academic Article
|
Clock genes may influence bipolar disorder susceptibility and dysfunctional circadian rhythm.
|
|
Academic Article
|
Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder.
|
|
Academic Article
|
Association study of Wnt signaling pathway genes in bipolar disorder.
|
|
Academic Article
|
Whole-genome approach implicates CD44 in cellular resistance to carboplatin.
|
|
Academic Article
|
Association and mutation analyses of 16p11.2 autism candidate genes.
|
|
Academic Article
|
Genetic control of individual differences in gene-specific methylation in human brain.
|
|
Academic Article
|
Strategies to identify genes for complex disorders: a focus on bipolar disorder and chromosome 16p.
|
|
Academic Article
|
Family-based association testing of glutamate transporter genes in autism.
|
|
Academic Article
|
Removing batch effects in analysis of expression microarray data: an evaluation of six batch adjustment methods.
|
|
Academic Article
|
Enrichment of cis-regulatory gene expression SNPs and methylation quantitative trait loci among bipolar disorder susceptibility variants.
|
|
Academic Article
|
Two gene co-expression modules differentiate psychotics and controls.
|
|
Academic Article
|
A rare mutation of CACNA1C in a patient with bipolar disorder, and decreased gene expression associated with a bipolar-associated common SNP of CACNA1C in brain.
|
|
Academic Article
|
Genome-wide association study implicates NDST3 in schizophrenia and bipolar disorder.
|
|
Academic Article
|
Pharmacogenetic associations of the type-3 metabotropic glutamate receptor (GRM3) gene with working memory and clinical symptom response to antipsychotics in first-episode schizophrenia.
|
|
Academic Article
|
Rare variants in neuronal excitability genes influence risk for bipolar disorder.
|
|
Academic Article
|
Antipsychotic pharmacogenomics in first episode psychosis: a role for glutamate genes.
|
|
Academic Article
|
The transcription factor POU3F2 regulates a gene coexpression network in brain tissue from patients with psychiatric disorders.
|
|
Academic Article
|
Rare variants implicate NMDA receptor signaling and cerebellar gene networks in risk for bipolar disorder.
|
|
Academic Article
|
Whole-genome association mapping of gene expression in the human prefrontal cortex.
|