Item Type | Name |
Concept
|
Chromosomes, Human, Pair 15
|
Concept
|
Chromosomes, Human, X
|
Concept
|
Chromosomes, Human, Pair 12
|
Concept
|
Chromosomes, Human, Pair 18
|
Concept
|
Chromosomes, Human, Pair 16
|
Concept
|
Chromosomes, Human, Pair 17
|
Concept
|
Chromosomes, Human
|
Concept
|
Chromosomes, Human, Pair 14
|
Concept
|
Chromosomes, Human, Pair 11
|
Concept
|
Chromosomes, Human, Pair 1
|
Concept
|
Chromosomes, Human, Pair 19
|
Concept
|
Chromosomes, Human, Pair 3
|
Concept
|
Chromosomes, Human, Pair 20
|
Concept
|
Chromosomes, Human, 6-12 and X
|
Concept
|
Chromosomes, Human, Pair 4
|
Concept
|
Chromosomes, Human, Pair 5
|
Concept
|
Chromosomes, Human, Pair 21
|
Concept
|
Chromosomes, Human, Pair 8
|
Concept
|
Chromosomes, Human, Pair 10
|
Concept
|
Chromosomes, Human, Pair 7
|
Concept
|
Chromosomes, Human, Pair 6
|
Concept
|
Chromosomes, Human, Pair 2
|
Concept
|
Chromosomes, Human, Pair 13
|
Concept
|
Chromosomes, Human, Pair 9
|
Concept
|
Chromosomes, Human, Pair 22
|
Academic Article
|
Loci on chromosomes 6q and 6p interact to increase susceptibility to bipolar affective disorder in the national institute of mental health genetics initiative pedigrees.
|
Academic Article
|
Evidence for association of bipolar disorder to haplotypes in the 22q12.3 region near the genes stargazin, IFT27 and parvalbumin.
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Academic Article
|
A test of nonrandom segregation.
|
Academic Article
|
Affected-sib-pair analyses reveal support of prior evidence for a susceptibility locus for bipolar disorder, on 21q.
|
Academic Article
|
Maternal inheritance and chromosome 18 allele sharing in unilineal bipolar illness pedigrees.
|
Academic Article
|
Analysis of DRPLA trinucleotide repeats in schizophrenia.
|
Academic Article
|
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
|
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
|
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
|
Serotonin transporter (5-HTT) gene and bipolar affective disorder.
|
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
|
Suggestive evidence of a locus on chromosome 10p using the NIMH genetics initiative bipolar affective disorder pedigrees.
|
Academic Article
|
Linkage of bipolar disorder to chromosome 18q and the validity of bipolar II disorder.
|
Academic Article
|
Regional meta-analysis of published data supports linkage of autism with markers on chromosome 7.
|
Academic Article
|
Linkage analysis of schizophrenia to chromosome 15.
|
Academic Article
|
An evaluation of the assembly of an approximately 15-Mb region on human chromosome 13q32-q33 linked to bipolar disorder and schizophrenia.
|
Academic Article
|
Can long-range microsatellite data be used to predict short-range linkage disequilibrium?
|
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
|
Genome-wide scan and conditional analysis in bipolar disorder: evidence for genomic interaction in the National Institute of Mental Health genetics initiative bipolar pedigrees.
|
Academic Article
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Linkage disequilibrium analysis in the LOC93081-KDELC1-BIVM region on 13q in bipolar disorder.
|
Academic Article
|
Attempted suicide in bipolar disorder pedigrees: evidence for linkage to 2p12.
|
Academic Article
|
Genome-wide linkage scan of 98 bipolar pedigrees and analysis of clinical covariates.
|
Academic Article
|
Recurrent 16p11.2 microdeletions in autism.
|
Academic Article
|
Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder.
|
Academic Article
|
PDLIM5 and susceptibility to bipolar disorder: a family-based association study and meta-analysis.
|
Academic Article
|
Association study of Wnt signaling pathway genes in bipolar disorder.
|
Academic Article
|
Genome-wide parametric linkage analyses of 644 bipolar pedigrees suggest susceptibility loci at chromosomes 16 and 20.
|
Academic Article
|
Association and mutation analyses of 16p11.2 autism candidate genes.
|
Academic Article
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Strategies to identify genes for complex disorders: a focus on bipolar disorder and chromosome 16p.
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Academic Article
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Genomewide linkage analysis in Costa Rican families implicates chromosome 15q14 as a candidate region for OCD.
|
Academic Article
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Genome-wide linkage analysis of obsessive-compulsive disorder implicates chromosome 1p36.
|
Academic Article
|
Genome-wide scan demonstrates significant linkage for male sexual orientation.
|
Academic Article
|
Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder.
|
Academic Article
|
Genome-Wide Association Study of Male Sexual Orientation.
|