(Q39848269)

15 September 2017

title

Analysis of a t(18;21)(p11.1;p11.1) translocation in a family with schizophrenia (English)

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15 September 2017

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3

Yoshimi Iwayama

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15 September 2017

Joanne M A Meerabux

1

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15 September 2017

Hisako Ohba

2

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15 September 2017

Motoko Maekawa

4

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15 September 2017

Sevilla D Detera-Wadleigh

5

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15 September 2017

Lynn E DeLisi

6

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15 September 2017

Takeo Yoshikawa

7

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15 September 2017

language of work or name

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22 May 2009

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Journal of Human Genetics

15 September 2017

published in

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15 September 2017

volume

54

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15 September 2017

issue

7

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15 September 2017

page(s)

386-391

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https://scigraph.springernature.com/pub.10.1038/jhg.2009.47

15 September 2017

exact match

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cites work

Chromosome 18 DNA markers and manic-depressive illness: evidence for a susceptibility gene

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.47

7 January 2021

A high-density genome scan detects evidence for a bipolar-disorder susceptibility locus on 13q32 and other potential loci on 1q32 and 18p11.2.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.47

7 January 2021

Support for a chromosome 18p locus conferring susceptibility to functional psychoses in families with schizophrenia, by association and linkage analysis

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.47

7 January 2021

Report of the chromosome 18 workshop

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.47

7 January 2021

Evidence for association of the myo-inositol monophosphatase 2 (IMPA2) gene with schizophrenia in Japanese samples.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.47

7 January 2021

A search for specific and common susceptibility loci for schizophrenia and bipolar disorder: a linkage study in 13 target chromosomes

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.47

7 January 2021

A genome-wide scan for linkage to chromosomal regions in 382 sibling pairs with schizophrenia or schizoaffective disorder

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.47

7 January 2021

Linkage disequilibrium analysis of G-olf alpha (GNAL) in bipolar affective disorder.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.47

7 January 2021

Analysis of polymorphisms in the olfactory G-protein Golf in major depression

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.47

7 January 2021

A promoter haplotype of the inositol monophosphatase 2 gene (IMPA2) at 18p11.2 confers a possible risk for bipolar disorder by enhancing transcription

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.47

7 January 2021

Two-step association analyses of the chromosome 18p11.2 region in schizophrenia detect a locus encompassing C18orf1

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.47

7 January 2021

Multiple transcriptional variants and RNA editing in C18orf1, a novel gene with LDLRA and transmembrane domains on 18p11.2

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.47

7 January 2021

Chromosomal abnormalities and mental illness.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.47

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.47

7 January 2021

Chromosome 18 translocation (18;21) (p11.1;p11.1) associated with psychosis in one family

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.47

7 January 2021

The DNA sequence of human chromosome 21

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.47

7 January 2021

Map of candidate genes and STSs on 18p11.2, a bipolar disorder and schizophrenia susceptibility region

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.47

7 January 2021

A testis-specific gene, TPTE, encodes a putative transmembrane tyrosine phosphatase and maps to the pericentromeric region of human chromosomes 21 and 13, and to chromosomes 15, 22, and Y

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.47

7 January 2021

Genomic and genetic definition of a functional human centromere

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.47

7 January 2021

Satellite III sequences on 14p and their relevance to Robertsonian translocation formation.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.47

7 January 2021

Repeated, protein-encoding heterochromatic genes cause inactivation of a juxtaposed euchromatic gene.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.47

7 January 2021

Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.47

7 January 2021

Identifiers

DOI

10.1038/JHG.2009.47

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15 September 2017

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