| Item Type | Name |
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Concept
|
Age Factors
|
|
Concept
|
Africa
|
|
Concept
|
Amino Acid Sequence
|
|
Concept
|
Animals
|
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Concept
|
Chromosomes, Human, Pair 11
|
|
Concept
|
Chromosomes, Human, Pair 6
|
|
Concept
|
Analysis of Variance
|
|
Concept
|
Anthropometry
|
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Concept
|
Chromosomes, Human, Pair 8
|
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Concept
|
Arthritis, Rheumatoid
|
|
Concept
|
Base Sequence
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|
Concept
|
Body Height
|
|
Concept
|
Choice Behavior
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|
Concept
|
Autistic Disorder
|
|
Concept
|
Birth Order
|
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Concept
|
Body Weight
|
|
Concept
|
Biological Evolution
|
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Concept
|
Chromosomes, Human, Pair 1
|
|
Concept
|
Chromosomes, Human, Pair 15
|
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Concept
|
Chromosomes, Human, Pair 21
|
|
Concept
|
Chromosomes, Human, Pair 3
|
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Concept
|
Chromosomes, Human, Pair 14
|
|
Concept
|
Chromosome Deletion
|
|
Concept
|
Chromosomes, Human, Pair 13
|
|
Concept
|
Chromosomes, Human, Pair 22
|
|
Concept
|
Chromosomes, Human, Pair 4
|
|
Concept
|
Cognition
|
|
Concept
|
Chromosomes, Human, Pair 5
|
|
Concept
|
Chromosomes, Human, Pair 7
|
|
Concept
|
United Kingdom
|
|
Concept
|
Chromosomes, Human, Pair 20
|
|
Concept
|
Crohn Disease
|
|
Concept
|
Europe
|
|
Concept
|
Chromosomes, Human, Pair 10
|
|
Concept
|
Chromosomes, Human, Pair 19
|
|
Concept
|
Chromosomes, Human, Pair 9
|
|
Concept
|
Cross-Sectional Studies
|
|
Concept
|
Disease Susceptibility
|
|
Concept
|
DNA
|
|
Concept
|
Introns
|
|
Concept
|
Environment
|
|
Concept
|
Decision Making
|
|
Concept
|
Genes, Dominant
|
|
Concept
|
Genes, Recessive
|
|
Concept
|
Obesity
|
|
Concept
|
Hippocampus
|
|
Concept
|
Genetic Carrier Screening
|
|
Concept
|
Factor Analysis, Statistical
|
|
Concept
|
Functional Laterality
|
|
Concept
|
Models, Genetic
|
|
Concept
|
Molecular Sequence Data
|
|
Concept
|
National Institute of Mental Health (U.S.)
|
|
Concept
|
Random Allocation
|
|
Concept
|
Repetitive Sequences, Nucleic Acid
|
|
Concept
|
Cricetinae
|
|
Concept
|
Nucleic Acid Conformation
|
|
Concept
|
Lung Neoplasms
|
|
Concept
|
Major Histocompatibility Complex
|
|
Concept
|
Parity
|
|
Concept
|
Nuclear Family
|
|
Concept
|
Sweden
|
|
Concept
|
Population Surveillance
|
|
Concept
|
Prader-Willi Syndrome
|
|
Concept
|
Rats, Inbred F344
|
|
Concept
|
Receptors, Thyrotropin
|
|
Concept
|
Recurrence
|
|
Concept
|
Receptors, Serotonin
|
|
Concept
|
Referral and Consultation
|
|
Concept
|
Risk Factors
|
|
Concept
|
Psychopharmacology
|
|
Concept
|
Receptors, LDL
|
|
Concept
|
Cohort Studies
|
|
Concept
|
Polymorphism, Restriction Fragment Length
|
|
Concept
|
Risk
|
|
Concept
|
RNA
|
|
Concept
|
Humans
|
|
Concept
|
Body Mass Index
|
|
Concept
|
Synapses
|
|
Concept
|
Statistics as Topic
|
|
Concept
|
Informed Consent
|
|
Concept
|
CHO Cells
|
|
Concept
|
United States
|
|
Concept
|
Behavior, Addictive
|
|
Concept
|
Twins
|
|
Concept
|
Angelman Syndrome
|
|
Concept
|
Risk Assessment
|
|
Concept
|
Reverse Transcriptase Polymerase Chain Reaction
|
|
Concept
|
Multifactorial Inheritance
|
|
Concept
|
Vacuolar Proton-Translocating ATPases
|
|
Concept
|
Principal Component Analysis
|
|
Concept
|
Cell Adhesion Molecules
|
|
Concept
|
Prevalence
|
|
Concept
|
Likelihood Functions
|
|
Concept
|
Matched-Pair Analysis
|
|
Concept
|
Case-Control Studies
|
|
Concept
|
Protein Structure, Tertiary
|
|
Concept
|
Mental Health
|
|
Concept
|
Genes, Reporter
|
|
Concept
|
Oligodeoxyribonucleotides
|
|
Concept
|
Sequence Deletion
|
|
Concept
|
Twin Studies as Topic
|
|
Concept
|
DNA, Complementary
|
|
Concept
|
Cell Proliferation
|
|
Concept
|
Waist-Hip Ratio
|
|
Concept
|
Evolution, Molecular
|
|
Concept
|
Databases as Topic
|
|
Concept
|
Genetic Pleiotropy
|
|
Concept
|
Receptors, G-Protein-Coupled
|
|
Concept
|
Inheritance Patterns
|
|
Concept
|
Receptor, Fibroblast Growth Factor, Type 2
|
|
Concept
|
Microarray Analysis
|
|
Concept
|
Genomic Imprinting
|
|
Concept
|
Homosexuality, Female
|
|
Concept
|
Amino Acid Substitution
|
|
Concept
|
5' Untranslated Regions
|
|
Concept
|
Patient Participation
|
|
Concept
|
Internet
|
|
Concept
|
Oligonucleotide Array Sequence Analysis
|
|
Concept
|
Heterosexuality
|
|
Concept
|
Databases, Genetic
|
|
Concept
|
Receptors, Dopamine D3
|
|
Concept
|
Promoter Regions, Genetic
|
|
Concept
|
Psychiatric Status Rating Scales
|
|
Concept
|
Sp4 Transcription Factor
|
|
Concept
|
Receptors, Dopamine
|
|
Concept
|
Receptors, Nicotinic
|
|
Concept
|
Surveys and Questionnaires
|
|
Concept
|
Self-Assessment
|
|
Concept
|
Severity of Illness Index
|
|
Concept
|
RNA, Messenger
|
|
Concept
|
Stress Disorders, Post-Traumatic
|
|
Concept
|
Receptors, Vascular Endothelial Growth Factor
|
|
Concept
|
General Practitioners
|
|
Concept
|
Rats
|
|
Concept
|
Kruppel-Like Transcription Factors
|
|
Concept
|
Sex Factors
|
|
Concept
|
Dystrophin-Associated Proteins
|
|
Concept
|
Sulfurtransferases
|
|
Concept
|
Models, Statistical
|
|
Concept
|
Logistic Models
|
|
Concept
|
DNA Copy Number Variations
|
|
Concept
|
Electronic Health Records
|
|
Concept
|
Meta-Analysis as Topic
|
|
Concept
|
Codon, Nonsense
|
|
Concept
|
Homosexuality, Male
|
|
Concept
|
Odds Ratio
|
|
Concept
|
Polymerase Chain Reaction
|
|
Concept
|
Metabolic Networks and Pathways
|
|
Concept
|
Receptors, Metabotropic Glutamate
|
|
Concept
|
Statistics, Nonparametric
|
|
Concept
|
Microsatellite Repeats
|
|
Concept
|
Williams Syndrome
|
|
Concept
|
Neuregulin-1
|
|
Concept
|
Receptor, Serotonin, 5-HT1B
|
|
Concept
|
Genome-Wide Association Study
|
|
Concept
|
Siblings
|
|
Concept
|
Chromosome Duplication
|
|
Concept
|
Molecular Sequence Annotation
|
|
Concept
|
Adolescent Development
|
|
Concept
|
Endothelial Cells
|
|
Concept
|
Body Size
|
|
Concept
|
Induced Pluripotent Stem Cells
|
|
Concept
|
Alzheimer Disease
|
|
Concept
|
Calcium
|
|
Concept
|
Canada
|
|
Concept
|
Catechol O-Methyltransferase
|
|
Concept
|
Chromatin
|
|
Concept
|
Chromosomes, Human
|
|
Concept
|
Chromosomes, Human, Pair 16
|
|
Concept
|
Chromosomes, Human, Pair 18
|
|
Concept
|
Enhancer Elements, Genetic
|
|
Concept
|
Family Health
|
|
Concept
|
Follow-Up Studies
|
|
Concept
|
Gender Identity
|
|
Concept
|
Longitudinal Studies
|
|
Concept
|
Mothers
|
|
Concept
|
Nicotine
|
|
Concept
|
Oligonucleotides
|
|
Concept
|
Personality Assessment
|
|
Concept
|
Hydroxymethylbilane Synthase
|
|
Concept
|
Prospective Studies
|
|
Concept
|
Databases, Factual
|
|
Concept
|
Receptors, Dopamine D2
|
|
Concept
|
Age of Onset
|
|
Concept
|
Dopamine Antagonists
|
|
Concept
|
Quantitative Trait, Heritable
|
|
Concept
|
Genetic Predisposition to Disease
|
|
Concept
|
Polymorphism, Single Nucleotide
|
|
Concept
|
MicroRNAs
|
|
Concept
|
Chromosomes, Human, X
|
|
Concept
|
Neurogenesis
|
|
Academic Article
|
Affected-sib-pair analyses reveal support of prior evidence for a susceptibility locus for bipolar disorder, on 21q.
|
|
Academic Article
|
Association study of schizophrenia and the dopamine D3 receptor gene locus in two independent samples.
|
|
Academic Article
|
Isolation of chromosome 18-specific brain transcripts as positional candidates for bipolar disorder.
|
|
Academic Article
|
An integrated physical map of 18p11.2: a susceptibility region for bipolar disorder.
|
|
Academic Article
|
Initial genome scan of the NIMH genetics initiative bipolar pedigrees: chromosomes 4, 7, 9, 18, 19, 20, and 21q.
|
|
Academic Article
|
Suggestive evidence for a schizophrenia susceptibility locus on chromosome 6q and a confirmation in an independent series of pedigrees.
|
|
Academic Article
|
Multiple transcriptional variants and RNA editing in C18orf1, a novel gene with LDLRA and transmembrane domains on 18p11.2.
|
|
Academic Article
|
Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: schizophrenia linkage collaborative group III.
|
|
Academic Article
|
Closing in on genes for manic-depressive illness and schizophrenia.
|
|
Academic Article
|
A high-density genome scan detects evidence for a bipolar-disorder susceptibility locus on 13q32 and other potential loci on 1q32 and 18p11.2.
|
|
Academic Article
|
Follow-up study on a susceptibility locus for schizophrenia on chromosome 6q.
|
|
Academic Article
|
Linkage analysis of schizophrenia to chromosome 15.
|
|
Academic Article
|
No major schizophrenia locus detected on chromosome 1q in a large multicenter sample.
|
|
Academic Article
|
Genetic diversity of the human serotonin receptor 1B (HTR1B) gene.
|
|
Academic Article
|
DNA variation and psychopharmacology of the human serotonin receptor 1B (HTR1B) gene.
|
|
Academic Article
|
Major corrections are indicated for 'Comparative proteome analysis of the hippocampus implicates chromosome 6q in schizophrenia'.
|
|
Academic Article
|
Polymorphisms in the 5'-untranslated region of the human serotonin receptor 1B (HTR1B) gene affect gene expression.
|
|
Academic Article
|
Polymorphisms in the trace amine receptor 4 (TRAR4) gene on chromosome 6q23.2 are associated with susceptibility to schizophrenia.
|
|
Academic Article
|
Neuregulin 1 (NRG1 ) and schizophrenia: analysis of a US family sample and the evidence in the balance.
|
|
Academic Article
|
Multicenter linkage study of schizophrenia loci on chromosome 22q.
|
|
Academic Article
|
Haplotypic association spanning the 22q11.21 genes COMT and ARVCF with schizophrenia.
|
|
Academic Article
|
No significant association of 14 candidate genes with schizophrenia in a large European ancestry sample: implications for psychiatric genetics.
|
|
Academic Article
|
Identification of loci associated with schizophrenia by genome-wide association and follow-up.
|
|
Academic Article
|
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.
|
|
Academic Article
|
Genomewide linkage scan of schizophrenia in a large multicenter pedigree sample using single nucleotide polymorphisms.
|
|
Academic Article
|
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.
|
|
Academic Article
|
Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications.
|
|
Academic Article
|
Genetics of schizophrenia: new findings and challenges.
|
|
Academic Article
|
Common variants on chromosome 6p22.1 are associated with schizophrenia.
|
|
Academic Article
|
Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2.
|
|
Academic Article
|
Hundreds of variants clustered in genomic loci and biological pathways affect human height.
|
|
Academic Article
|
Meta-analysis of 32 genome-wide linkage studies of schizophrenia.
|
|
Academic Article
|
Smoking and genetic risk variation across populations of European, Asian, and African American ancestry--a meta-analysis of chromosome 15q25.
|
|
Academic Article
|
A novel human myo-inositol monophosphatase gene, IMP.18p, maps to a susceptibility region for bipolar disorder.
|
|
Academic Article
|
Implication of a rare deletion at distal 16p11.2 in schizophrenia.
|
|
Academic Article
|
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.
|
|
Academic Article
|
Reciprocal duplication of the Williams-Beuren syndrome deletion on chromosome 7q11.23 is associated with schizophrenia.
|
|
Academic Article
|
A rare functional noncoding variant at the GWAS-implicated MIR137/MIR2682 locus might confer risk to schizophrenia and bipolar disorder.
|
|
Academic Article
|
Transcriptome study of differential expression in schizophrenia.
|
|
Academic Article
|
Genome-wide association analysis identifies 13 new risk loci for schizophrenia.
|
|
Academic Article
|
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs.
|
|
Academic Article
|
Genome-wide scan demonstrates significant linkage for male sexual orientation.
|
|
Academic Article
|
Contamination of sequence databases with adaptor sequences.
|
|
Academic Article
|
Transcriptome outlier analysis implicates schizophrenia susceptibility genes and enriches putatively functional rare genetic variants.
|
|
Academic Article
|
New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis.
|
|
Academic Article
|
Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders.
|
|
Academic Article
|
Genome-wide association study identifies 74 loci associated with educational attainment.
|
|
Academic Article
|
Does training general practitioners result in more shared decision making during consultations?
|
|
Academic Article
|
Further data concerning Blanchard's (2011) "Fertility in the mothers of firstborn homosexual and heterosexual men".
|
|
Academic Article
|
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.
|
|
Academic Article
|
Genome-Wide Association Study of Male Sexual Orientation.
|
|
Academic Article
|
Familiality of Gender Nonconformity Among Homosexual Men.
|
|
Academic Article
|
Allele-specific open chromatin in human iPSC neurons elucidates functional disease variants.
|
|
Academic Article
|
Sex-specific nicotine sensitization and imprinting of self-administration in rats inform GWAS findings on human addiction phenotypes.
|
|
Academic Article
|
Genome-Wide Linkage Study Meta-Analysis of Male Sexual Orientation.
|
|
Academic Article
|
Genome-Wide Linkage and Association Study of Childhood Gender Nonconformity in Males.
|
|
Academic Article
|
Mapping genomic loci implicates genes and synaptic biology in schizophrenia.
|
|
Concept
|
Paternal Inheritance
|
|
Concept
|
Dysbindin
|
|
Concept
|
Population Health
|
|
Concept
|
Patient Outcome Assessment
|
|
Concept
|
Datasets as Topic
|
|
Grant
|
Meta-Analysis of Male Sexual Orientation
|
|
Grant
|
Molecular Genetic Study of Sexual Orientation
|
|
Grant
|
Familial Female Sexual Orientation Phenotypes
|
|
Grant
|
2/2 Targeted Sequencing and Functional Evaluation of Mutations in Schizophrenia
|