(Q34593018)

3 August 2017

title

The copy number variant involving part of the alpha7 nicotinic receptor gene contains a polymorphic inversion (English)

1 reference

3 August 2017

Robin Murray

6

0 references

author name string

Rachel H Flomen

1

1 reference

3 August 2017

Angela F Davies

2

1 reference

3 August 2017

Marta Di Forti

3

1 reference

3 August 2017

Caterina La Cascia

4

1 reference

3 August 2017

Caroline Mackie-Ogilvie

5

1 reference

3 August 2017

Andrew J Makoff

7

1 reference

3 August 2017

language of work or name

1 reference

11 June 2008

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European Journal of Human Genetics

3 August 2017

published in

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3 August 2017

volume

16

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3 August 2017

issue

11

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3 August 2017

page(s)

1364-1371

1 reference

Centrotemporal spikes in families with rolandic epilepsy: linkage to chromosome 15q14.

3 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.112

Linkage of a neurophysiological deficit in schizophrenia to a chromosome 15 locus

21 January 2018

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https://api.crossref.org/works/10.1038%2FEJHG.2008.112

7 January 2021

Further investigation of a chromosome 15 locus in schizophrenia: Analysis of affected sibpairs from the NIMH genetics initiative

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https://api.crossref.org/works/10.1038%2FEJHG.2008.112

7 January 2021

Diminished Suppression of the P50 Auditory Evoked Potential in Bipolar Disorder Subjects With a History of Psychosis

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.112

7 January 2021

P50 auditory evoked potential suppression in bipolar disorder patients with psychotic features and their unaffected relatives

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.112

7 January 2021

Neuronal nicotinic acetylcholine receptors: from the gene to the disease

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.112

7 January 2021

Mapping susceptibility genes for bipolar disorder: a pharmacogenetic approach based on excellent response to lithium

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.112

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.112

7 January 2021

Haplotype transmission disequilibrium and evidence for linkage of the CHRNA7 gene region to schizophrenia in Southern African Bantu families

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.112

7 January 2021

Schizophrenia and smoking: evidence for a common neurobiological basis?

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.112

7 January 2021

Genetic mapping of a major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.112

7 January 2021

Genomic organization and partial duplication of the human alpha7 neuronal nicotinic acetylcholine receptor gene (CHRNA7)

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.112

7 January 2021

A 3-Mb map of a large Segmental duplication overlapping the alpha7-nicotinic acetylcholine receptor gene (CHRNA7) at human 15q13-q14

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.112

7 January 2021

Detailed analysis of 15q11-q14 sequence corrects errors and gaps in the public access sequence to fully reveal large segmental duplications at breakpoints for Prader-Willi, Angelman, and inv dup(15) syndromes

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.112

7 January 2021

Refinement of a chimpanzee pericentric inversion breakpoint to a segmental duplication cluster

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.112

7 January 2021

Association study of CHRFAM7A copy number and 2bp deletion polymorphisms with schizophrenia and bipolar affective disorder

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.112

7 January 2021

Delineation of two distinct 6p deletion syndromes

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.112

7 January 2021

Program Report: GENECOUNTING Support Programs

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.112

7 January 2021

2LD, GENECOUNTING and HAP: Computer programs for linkage disequilibrium analysis

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.112

7 January 2021

Recent duplication, domain accretion and the dynamic mutation of the human genome

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.112

7 January 2021

Analysis of the DNA sequence and duplication history of human chromosome 15

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.112

7 January 2021

A common inversion under selection in Europeans

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.112

7 January 2021

Linkage disequilibrium and heritability of copy-number polymorphisms within duplicated regions of the human genome

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.112

7 January 2021

Common deletion polymorphisms in the human genome.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.112

7 January 2021

Common deletions and SNPs are in linkage disequilibrium in the human genome

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.112

7 January 2021

High-throughput genotyping of intermediate-size structural variation

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.112

7 January 2021

Genomic inversions of human chromosome 15q11-q13 in mothers of Angelman syndrome patients with class II (BP2/3) deletions

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.112

7 January 2021

Structural variation of the human genome

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.112

7 January 2021

The inv dup(15) or idic(15) syndrome: a clinically recognisable neurogenetic disorder

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.112

7 January 2021

High-resolution molecular characterization of 15q11-q13 rearrangements by array comparative genomic hybridization (array CGH) with detection of gene dosage

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.112

7 January 2021

A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.112

7 January 2021

Mice deficient in the alpha7 neuronal nicotinic acetylcholine receptor lack alpha-bungarotoxin binding sites and hippocampal fast nicotinic currents

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.112

7 January 2021

Identification of novel deletions of 15q11q13 in Angelman syndrome by array-CGH: molecular characterization and genotype-phenotype correlations.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.112

7 January 2021

Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.112

7 January 2021

Global variation in copy number in the human genome

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.112

7 January 2021

The -2 bp deletion in exon 6 of the 'alpha 7-like' nicotinic receptor subunit gene is a risk factor for the P50 sensory gating deficit

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.112

7 January 2021

Episodic memory performance predicted by the 2bp deletion in exon 6 of the "alpha 7-like" nicotinic receptor subunit gene

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.112

7 January 2021

Association study of a nicotinic receptor variant with schizophrenic disorders

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.112

7 January 2021

Association study of the human partially duplicated alpha7 nicotinic acetylcholine receptor genetic variant with bipolar disorder

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.112

7 January 2021

Identifiers

DOI

10.1038/EJHG.2008.112

1 reference

Dimensions Publication ID

3 August 2017

1026092455

0 references

1 reference