| Item Type | Name |
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Concept
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Adoption
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Concept
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Chromosomes, Human, Pair 11
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Concept
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Chromosomes, Human, Pair 6
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Concept
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Analysis of Variance
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Concept
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Chromosomes, Human, Pair 8
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Concept
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Arthritis, Rheumatoid
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Concept
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Cell Differentiation
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Concept
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Attention Deficit Disorder with Hyperactivity
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Concept
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Birth Order
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Concept
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Chromosomes, Human, Pair 1
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Concept
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Chromosomes, Human, Pair 15
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Concept
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Chromosomes, Human, Pair 21
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Concept
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Chromosomes, Human, Pair 3
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Concept
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Chromosomes, Human, Pair 14
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Concept
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Chromosome Deletion
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Concept
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Chromosomes, Human, Pair 13
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Concept
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Chromosomes, Human, Pair 22
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Concept
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Chromosomes, Human, Pair 4
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Concept
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Chromosomes, Human, Pair 5
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Concept
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Chromosomes, Human, Pair 7
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Concept
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Chromosomes, Human, Pair 20
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Concept
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Chromosomes, Human, Pair 10
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Concept
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Chromosomes, Human, Pair 19
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Concept
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Chromosomes, Human, Pair 9
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Concept
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Exons
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Concept
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Family
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Concept
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Introns
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Concept
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Genetics, Behavioral
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Concept
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Genetics, Population
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Concept
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Cricetinae
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Concept
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Nuclear Family
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Concept
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Prader-Willi Syndrome
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Concept
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Rats, Inbred F344
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Concept
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Psychopharmacology
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|
Concept
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Humans
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Concept
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Angelman Syndrome
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Concept
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Deoxyribonuclease EcoRI
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Concept
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Vacuolar Proton-Translocating ATPases
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Concept
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Deoxyribonucleases, Type II Site-Specific
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Concept
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5' Untranslated Regions
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Concept
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Patient Participation
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Concept
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Receptors, Dopamine D3
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Concept
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Promoter Regions, Genetic
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Concept
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Receptors, Dopamine
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Concept
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Receptors, Nicotinic
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Concept
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Rats
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Concept
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Williams Syndrome
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Concept
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Receptor, Serotonin, 5-HT1B
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Concept
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Siblings
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Concept
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Chromosomes, Human
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|
Concept
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Chromosomes, Human, Pair 16
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|
Concept
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Chromosomes, Human, Pair 18
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Concept
|
Enhancer Elements, Genetic
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|
Concept
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Mothers
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Concept
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Nicotine
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Concept
|
Receptors, Dopamine D2
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|
Concept
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Dopamine Antagonists
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|
Concept
|
Computational Biology
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|
Concept
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Genomics
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|
Concept
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MicroRNAs
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Concept
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Chromosomes, Human, X
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Concept
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Neurogenesis
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Concept
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HapMap Project
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Academic Article
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Affected-sib-pair analyses reveal support of prior evidence for a susceptibility locus for bipolar disorder, on 21q.
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Academic Article
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Isolation of chromosome 18-specific brain transcripts as positional candidates for bipolar disorder.
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Academic Article
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Images in neuroscience. Clinical genetics, VII. From genetics to pathophysiology: positional cloning.
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Academic Article
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Images in neuroscience. Clinical Genetics, VIII. From genetics to pathophysiology--candidate genes.
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|
Academic Article
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An integrated physical map of 18p11.2: a susceptibility region for bipolar disorder.
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|
Academic Article
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Initial genome scan of the NIMH genetics initiative bipolar pedigrees: chromosomes 4, 7, 9, 18, 19, 20, and 21q.
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Academic Article
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Suggestive evidence for a schizophrenia susceptibility locus on chromosome 6q and a confirmation in an independent series of pedigrees.
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Academic Article
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Multiple transcriptional variants and RNA editing in C18orf1, a novel gene with LDLRA and transmembrane domains on 18p11.2.
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Academic Article
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Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: schizophrenia linkage collaborative group III.
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|
Academic Article
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A high-density genome scan detects evidence for a bipolar-disorder susceptibility locus on 13q32 and other potential loci on 1q32 and 18p11.2.
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Academic Article
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Follow-up study on a susceptibility locus for schizophrenia on chromosome 6q.
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|
Academic Article
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Linkage analysis of schizophrenia to chromosome 15.
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Academic Article
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No major schizophrenia locus detected on chromosome 1q in a large multicenter sample.
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Academic Article
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Genetic diversity of the human serotonin receptor 1B (HTR1B) gene.
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|
Academic Article
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Influential ideas and experimental progress in schizophrenia genetics research.
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|
Academic Article
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Major corrections are indicated for 'Comparative proteome analysis of the hippocampus implicates chromosome 6q in schizophrenia'.
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|
Academic Article
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Polymorphisms in the trace amine receptor 4 (TRAR4) gene on chromosome 6q23.2 are associated with susceptibility to schizophrenia.
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Academic Article
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Neuregulin 1 (NRG1 ) and schizophrenia: analysis of a US family sample and the evidence in the balance.
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Academic Article
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Multicenter linkage study of schizophrenia loci on chromosome 22q.
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|
Academic Article
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Haplotypic association spanning the 22q11.21 genes COMT and ARVCF with schizophrenia.
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Academic Article
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Genomewide linkage scan of 409 European-ancestry and African American families with schizophrenia: suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sample.
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|
Academic Article
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Genomewide linkage scan of schizophrenia in a large multicenter pedigree sample using single nucleotide polymorphisms.
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|
Academic Article
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Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications.
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Academic Article
|
Common variants on chromosome 6p22.1 are associated with schizophrenia.
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|
Academic Article
|
Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2.
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|
Academic Article
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Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies.
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Academic Article
|
Hundreds of variants clustered in genomic loci and biological pathways affect human height.
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Academic Article
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Meta-analysis of 32 genome-wide linkage studies of schizophrenia.
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|
Academic Article
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Smoking and genetic risk variation across populations of European, Asian, and African American ancestry--a meta-analysis of chromosome 15q25.
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Academic Article
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Linkage and association in complex genetic diseases.
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Academic Article
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A novel human myo-inositol monophosphatase gene, IMP.18p, maps to a susceptibility region for bipolar disorder.
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Academic Article
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Genome-wide survey of interindividual differences of RNA stability in human lymphoblastoid cell lines.
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Academic Article
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Genome-wide association study of clinical dimensions of schizophrenia: polygenic effect on disorganized symptoms.
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Academic Article
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Implication of a rare deletion at distal 16p11.2 in schizophrenia.
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Academic Article
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Reciprocal duplication of the Williams-Beuren syndrome deletion on chromosome 7q11.23 is associated with schizophrenia.
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|
Academic Article
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Transcriptome study of differential expression in schizophrenia.
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|
Academic Article
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Genome-wide association analysis identifies 13 new risk loci for schizophrenia.
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|
Academic Article
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Genome-wide scan demonstrates significant linkage for male sexual orientation.
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Academic Article
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Transcriptome outlier analysis implicates schizophrenia susceptibility genes and enriches putatively functional rare genetic variants.
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Academic Article
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Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders.
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Academic Article
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Genome-Wide Association Study of Male Sexual Orientation.
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Academic Article
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Transcriptomic signatures of schizophrenia revealed by dopamine perturbation in an ex vivo model.
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|
Academic Article
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Dopamine perturbation of gene co-expression networks reveals differential response in schizophrenia for translational machinery.
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|
Academic Article
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Genome-wide Burden of Rare Short Deletions Is Enriched in Major Depressive Disorder in Four Cohorts.
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Academic Article
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Loss of function of OTUD7A in the schizophrenia- associated 15q13.3 deletion impairs synapse development and function in human neurons.
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|
Academic Article
|
Excitatory Dysfunction Drives Network and Calcium Handling Deficits in 16p11.2 Duplication Schizophrenia Induced Pluripotent Stem Cell-Derived Neurons.
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|
Grant
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Meta-Analysis of Male Sexual Orientation
|
|
Academic Article
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Multiple genes in a single GWAS risk locus synergistically mediate aberrant synaptic development and function in human neurons.
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|
Academic Article
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Brain Lipids and Lipid Droplet Dysregulation in Alzheimer's Disease and Neuropsychiatric Disorders.
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Academic Article
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Personalized medicine in a community health system: the NorthShore experience.
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