Family-based linkage disequilibrium mapping using SNP marker haplotypes: application to a potential locus for schizophrenia at chromosome 22q11 (Q57403416)

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scientific article published on 01 January 2000

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English	Family-based linkage disequilibrium mapping using SNP marker haplotypes: application to a potential locus for schizophrenia at chromosome 22q11	scientific article published on 01 January 2000

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4 November 2019

Family-based linkage disequilibrium mapping using SNP marker haplotypes: application to a potential locus for schizophrenia at chromosome 22q11 (English)

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4 November 2019

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linkage disequilibrium

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4 November 2019

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4 November 2019

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Ball D

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4 November 2019

Zhao J

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4 November 2019

Liu X

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Sham PC

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4 November 2019

Collier DA

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1 January 2000

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4 November 2019

Molecular Psychiatry

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4 November 2019

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4 November 2019

77-84

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4 November 2019

Genetic dissection of complex traits

1 reference

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21 January 2018

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

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The future of genetic studies of complex human diseases

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Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus

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Possible role for COMT in psychosis associated with velo-cardio-facial syndrome.

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Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.

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Chromosome 22q11.2 interstitial deletions among childhood-onset schizophrenics and "multidimensionally impaired".

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Dissecting the genetic complexity of schizophrenia

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Linkage studies suggest a possible locus for bipolar disorder near the velo-cardio-facial syndrome region on chromosome 22.

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A genome-wide search for schizophrenia susceptibility genes

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Erythrocyte catechol O-methyltransferase activity in schizophrenia: analysis of family data

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Kinetics of human soluble and membrane-bound catechol O-methyltransferase: a revised mechanism and description of the thermolabile variant of the enzyme

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Identification of Sequence Variants and Analysis of the Role of the Catechol-O-Methyl-Transferase Gene in Schizophrenia Susceptibility

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21 January 2018

Low activity allele of catechol-O-methyltransferase gene associated with rapid cycling bipolar disorder

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21 January 2018

Catechol-O-methyltransferase-deficient mice exhibit sexually dimorphic changes in catecholamine levels and behavior

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Analysis of a functional catechol-O-methyltransferase gene polymorphism in schizophrenia: evidence for association with aggressive and antisocial behavior

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21 January 2018

Genomic organization of the human catechol O-methyltransferase gene and its expression from two distinct promoters

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Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms

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Optimization of the single-strand conformation polymorphism (SSCP) technique for detection of point mutations.

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Identification of a new human catenin gene family member (ARVCF) from the region deleted in velo-cardio-facial syndrome

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An extended transmission/disequilibrium test (TDT) for multi-allele marker loci.

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Fine genetic mapping using haplotype analysis and the missing data problem

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Applications of DNA chips for genomic analysis

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No Association between Parkinson's Disease and Low-Activity Alleles of CatecholO-Methyltransferase

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21 January 2018

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The new genomics: global views of biology

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Variations on a theme: cataloging human DNA sequence variation

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Analysis of the CD3 gene region and type 1 diabetes: application of fluorescence-based technology to linkage disequilibrium mapping

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It's raining SNPs, hallelujah?

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Late‐Onset psychosis in the velo‐cardio‐facial syndrome

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Initial genomic scan of the NIMH genetics initiative bipolar pedigrees: Chromosomes 3, 5, 15, 16, 17, and 22

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Human catechol-O-methyltransferase pharmacogenetics: description of a functional polymorphism and its potential application to neuropsychiatric disorders.

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Preferential transmission of the high activity allele of COMT in schizophrenia

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No evidence for allelic association between schizophrenia and a polymorphism determining high or low catechol O-methyltransferase activity

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No association between bipolar disorder and alleles at a functional polymorphism in the COMT gene. Biomed European Bipolar Collaborative Group

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Ultra-ultra rapid cycling bipolar disorder is associated with the low activity catecholamine-O-methyltransferase allele

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Catechol-O-methyltransferase polymorphisms and schizophrenia: a transmission disequilibrium study in multiply affected families

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10.1038/SJ.MP.4000638

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10673772 AND SRC:MED&resulttype=core&format=json

4 November 2019

PubMed publication ID

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Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10673772 AND SRC:MED&resulttype=core&format=json

4 November 2019

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