Excitement and confusion on chromosome 6q: the challenges of neuropsychiatric genetics in microcosm (Q36261628)

13 August 2017

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title

Excitement and confusion on chromosome 6q: the challenges of neuropsychiatric genetics in microcosm (English)

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13 August 2017

Kohn Y

1

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PubMed ID

16172614

13 August 2017

Lerer B

series ordinal

2

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PubMed ID

16172614

13 August 2017

language of work or name

English

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publication date

1 December 2005

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13 August 2017

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13 August 2017

10

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13 August 2017

12

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13 August 2017

1062-1073

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https://scigraph.springernature.com/pub.10.1038/sj.mp.4001738

13 August 2017

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cites work

Linkage and associated studies of schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

Molecular linkage studies of bipolar disorders

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

Genetic linkage in bipolar disorder

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

Meta-analysis of whole-genome linkage scans of bipolar disorder and schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

Genetic variation in the 6p22.3 gene DTNBP1, the human ortholog of the mouse dysbindin gene, is associated with schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

Neuregulin 1 and susceptibility to schizophrenia

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

A highly significant association between a COMT haplotype and schizophrenia.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

Genetic and physiological data implicating the new human gene G72 and the gene for D-amino acid oxidase in schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

Polymorphisms at the G72/G30 gene locus, on 13q33, are associated with bipolar disorder in two independent pedigree series

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

Positive association between synapsin II and schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

Polymorphisms in the trace amine receptor 4 (TRAR4) gene on chromosome 6q23.2 are associated with susceptibility to schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

Evidence that the gene encoding ZDHHC8 contributes to the risk of schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

Association analysis of NOTCH 4 polymorphisms with schizophrenia among two independent family based samples

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

The Epsin 4 gene on chromosome 5q, which encodes the clathrin-associated protein enthoprotin, is involved in the genetic susceptibility to schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

Linkage of familial schizophrenia to chromosome 13q32

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

Schizophrenia genetics and dysbindin: a corner turned?

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

Impaired feedback regulation of XBP1 as a genetic risk factor for bipolar disorder

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

Genetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

Evidence for shared susceptibility in bipolar disorder and schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

COMT: a common susceptibility gene in bipolar disorder and schizophrenia.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

Suggestive evidence for a schizophrenia susceptibility locus on chromosome 6q and a confirmation in an independent series of pedigrees

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

Follow-up study on a susceptibility locus for schizophrenia on chromosome 6q

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

NIMH Genetics Initiative Millenium Schizophrenia Consortium: linkage analysis of African-American pedigrees

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: schizophrenia linkage collaborative group III

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

Genome scan for susceptibility loci for schizophrenia.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

A systematic genomewide linkage study in 353 sib pairs with schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

A schizophrenia-susceptibility locus at 6q25, in one of the world's largest reported pedigrees.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

Genome scan of Arab Israeli families maps a schizophrenia susceptibility gene to chromosome 6q23 and supports a locus at chromosome 10q24.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

The trace amine receptor 4 gene is not associated with schizophrenia in a sample linked to chromosome 6q23

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

Comparative proteome analysis of the hippocampus implicates chromosome 6q in schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

Major corrections are indicated for 'Comparative proteome analysis of the hippocampus implicates chromosome 6q in schizophrenia'.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

The Wellcome trust UK–Irish bipolar affective disorder sibling-pair genome screen: first stage report

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

A genome-wide scan shows significant linkage between bipolar disorder and chromosome 12q24.3 and suggestive linkage to chromosomes 1p22–21, 4p16, 6q14–22, 10q26 and 16p13.3

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

Genome scan for susceptibility loci for schizophrenia and bipolar disorder

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

Genome-wide scan and conditional analysis in bipolar disorder: evidence for genomic interaction in the National Institute of Mental Health genetics initiative bipolar pedigrees.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

Initial genome scan of the NIMH genetics initiative bipolar pedigrees: chromosomes 1, 6, 8, 10, and 12.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

Genomewide linkage analyses of bipolar disorder: a new sample of 250 pedigrees from the National Institute of Mental Health Genetics Initiative.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

Loci on chromosomes 6q and 6p interact to increase susceptibility to bipolar affective disorder in the national institute of mental health genetics initiative pedigrees

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

Genome-wide scan in Portuguese Island families implicates multiple loci in bipolar disorder: fine mapping adds support on chromosomes 6 and 11

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

Genomewide linkage analysis of bipolar disorder by use of a high-density single-nucleotide-polymorphism (SNP) genotyping assay: a comparison with microsatellite marker assays and finding of significant linkage to chromosome 6q22.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

Linkage analysis of psychosis in bipolar pedigrees suggests novel putative loci for bipolar disorder and shared susceptibility with schizophrenia.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

Absence of psychosis may influence linkage results for bipolar disorder.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

Genomewide scan for affective disorder susceptibility Loci in families of a northern Swedish isolated population

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

A family-based and case–control association study of trace amine receptor genes on chromosome 6q23 in bipolar affective disorder

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

A genome screen for genes predisposing to bipolar affective disorder detects a new susceptibility locus on 8q

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

Genome-wide linkage survey for genetic loci that affect the risk of suicide attempts in families with recurrent, early-onset, major depression

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

A second-generation genomic screen for multiple sclerosis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

A genome scan for modifiers of age at onset in Huntington disease: The HD MAPS study.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

Evidence for a susceptibility locus on chromosome 6q influencing phonological coding dyslexia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

Abnormal cerebellar development and axonal decussation due to mutations in AHI1 in Joubert syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

Mutations in the AHI1 gene, encoding jouberin, cause Joubert syndrome with cortical polymicrogyria

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

Combined analysis from eleven linkage studies of bipolar disorder provides strong evidence of susceptibility loci on chromosomes 6q and 8q

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

The DNA sequence and analysis of human chromosome 6

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

Bipolarity from ancient to modern times: conception, birth and rebirth

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

A continuum of psychosis, one human gene, and not much else--the case for homogeneity

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

The endophenotype concept in psychiatry: etymology and strategic intentions

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

Association within a family of a balanced autosomal translocation with major mental illness

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

Disruption of two novel genes by a translocation co-segregating with schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

Mining for SNPs: putting the common variants--common disease hypothesis to the test

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

Genetic heterogeneity, modifier genes, and quantitative phenotypes in psychiatric illness: searching for a framework

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

The genetics of Hirschsprung disease

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

Mutations of the RET proto-oncogene in Hirschsprung's disease

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

A common sex-dependent mutation in a RET enhancer underlies Hirschsprung disease risk.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

A survey of haplotype variants at several disease candidate genes: the importance of rare variants for complex diseases.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001738

7 January 2021

Identifiers

DOI

10.1038/SJ.MP.4001738

1 reference

13 August 2017

1 reference

PubMed ID

16172614