sameAs
Genome-wide association identifies a common variant in the reelin gene that increases the risk of schizophrenia only in womenHigh levels of RNA-editing site conservation amongst 15 laboratory mouse strainsPower failure: why small sample size undermines the reliability of neuroscienceMutations in the beta-tubulin gene TUBB2B result in asymmetrical polymicrogyriaGenome-wide generation and systematic phenotyping of knockout mice reveals new roles for many genes5-HTTLPR genotype and anxiety-related personality traits: a meta-analysis and new data.SW-ARRAY: a dynamic programming solution for the identification of copy-number changes in genomic DNA using array comparative genome hybridization dataGenetics and genomics of psychiatric diseaseThe genetics of major depressionIs there an excess of significant findings in published studies of psychotherapy for depression?Elusive copy number variation in the mouse genomeMutation of the diamond-blackfan anemia gene Rps7 in mouse results in morphological and neuroanatomical phenotypesSubtle chromosomal rearrangements in children with unexplained mental retardationSequence, structure and pathology of the fully annotated terminal 2 Mb of the short arm of human chromosome 16Characterization of a widely expressed gene (LUC7-LIKE; LUC7L) defining the centromeric boundary of the human alpha-globin domainThe genetic basis of emotional behaviour in miceSocial adversity, the serotonin transporter (5-HTTLPR) polymorphism and major depressive disorderThe IL-9 receptor gene (IL9R): genomic structure, chromosomal localization in the pseudoautosomal region of the long arm of the sex chromosomes, and identification of IL9R pseudogenes at 9qter, 10pter, 16pter, and 18pterGene X environment interactions at the serotonin transporter locusAssociation of the NRG1 gene and schizophrenia: a meta-analysisThe relationship between chromosome structure and function at a human telomeric regionNeurogenomic evidence for a shared mechanism of the antidepressant effects of exercise and chronic fluoxetine in miceNew semidominant mutations that affect mouse developmentPower failure: why small sample size undermines the reliability of neuroscienceMouse genomic variation and its effect on phenotypes and gene regulationMolecular signatures of major depression.Effects of environmental and physiological covariates on sex differences in unconditioned and conditioned anxiety and fear in a large sample of genetically heterogeneous (N/Nih-HS) rats.Cytoarchitectural disruption of the superior colliculus and an enlarged acoustic startle response in the Tuba1a mutant mouse.A quantitative trait locus influencing anxiety in the laboratory rat.Genomes and phenomes of a population of outbred rats and its progenitorsA genetic and functional relationship between T cells and cellular proliferation in the adult hippocampusAssociation of the dopamine D4 receptor (DRD4) gene and approach-related personality traits: meta-analysis and new data.Childhood sexual abuse and the development of recurrent major depression in Chinese women.Del(18p) shown to be a cryptic translocation using a multiprobe FISH assay for subtelomeric chromosome rearrangements.A high-resolution single nucleotide polymorphism genetic map of the mouse genomeHeterozygosity increases microsatellite mutation rate, linking it to demographic history.Genetic interactions with sex make a relatively small contribution to the heritability of complex traits in miceIdentifying genes for neurobehavioural traits in rodents: progress and pitfallsMolecular-cytogenetic detection of a deletion of 1p36.3.Commercially available outbred mice for genome-wide association studies.
P50
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