(Q51899107)

17 April 2018

title

Failure to confirm CNVs as of aetiological significance in twin pairs discordant for schizophrenia. (English)

1 reference

17 April 2018

0 references

Shinji Ono

1

1 reference

17 April 2018

Akira Imamura

2

1 reference

17 April 2018

Shinya Tasaki

3

1 reference

17 April 2018

Naohiro Kurotaki

4

1 reference

17 April 2018

Hiroki Ozawa

5

1 reference

17 April 2018

Koh-ichiro Yoshiura

6

1 reference

17 April 2018

Yuji Okazaki

7

1 reference

17 April 2018

language of work or name

English

0 references

publication date

1 October 2010

1 reference

17 April 2018

Twin Research and Human Genetics

published in

1 reference

17 April 2018

volume

13

1 reference

17 April 2018

issue

5

1 reference

17 April 2018

page(s)

455-460

1 reference

17 April 2018

Genomewide scan in families with schizophrenia from the founder population of Afrikaners reveals evidence for linkage and uniparental disomy on chromosome 1

cites work

1 reference

https://api.crossref.org/works/10.1375%2FTWIN.13.5.455

Chromatin alterations associated with down-regulated metabolic gene expression in the prefrontal cortex of subjects with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1375%2FTWIN.13.5.455

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

21 January 2018

1 reference

https://api.crossref.org/works/10.1375%2FTWIN.13.5.455

Dysregulation of olfactory receptor neuron lineage in schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1375%2FTWIN.13.5.455

Genome, epigenome and RNA sequences of monozygotic twins discordant for multiple sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1375%2FTWIN.13.5.455

Phenotypically concordant and discordant monozygotic twins display different DNA copy-number-variation profiles

21 January 2018

1 reference

https://api.crossref.org/works/10.1375%2FTWIN.13.5.455

Methods and strategies for analyzing copy number variation using DNA microarrays

21 January 2018

1 reference

https://api.crossref.org/works/10.1375%2FTWIN.13.5.455

Copy-number variations associated with neuropsychiatric conditions

21 January 2018

1 reference

https://api.crossref.org/works/10.1375%2FTWIN.13.5.455

Handedness, language lateralisation and anatomical asymmetry: relevance of protocadherin XY to hominid speciation and the aetiology of psychosis. Point of view

21 January 2018

1 reference

https://api.crossref.org/works/10.1375%2FTWIN.13.5.455

Methylation analysis of the fragile X syndrome by PCR.

21 January 2018

1 reference

https://api.crossref.org/works/10.1375%2FTWIN.13.5.455

Up-regulation of ADM and SEPX1 in the lymphoblastoid cells of patients in monozygotic twins discordant for schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1375%2FTWIN.13.5.455

DNA methylation profiles in monozygotic and dizygotic twins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1375%2FTWIN.13.5.455

Genetic or epigenetic difference causing discordance between monozygotic twins as a clue to molecular basis of mental disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1375%2FTWIN.13.5.455

Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1375%2FTWIN.13.5.455

Integrated detection and population-genetic analysis of SNPs and copy number variation

21 January 2018

1 reference

https://api.crossref.org/works/10.1375%2FTWIN.13.5.455

Microduplications of 16p11.2 are associated with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1375%2FTWIN.13.5.455

Copy-number variants in neurodevelopmental disorders: promises and challenges

21 January 2018

1 reference

https://api.crossref.org/works/10.1375%2FTWIN.13.5.455

Global variation in copy number in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1375%2FTWIN.13.5.455

Segmental uniparental isodisomy on 5q32-qter in a patient with childhood-onset schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1375%2FTWIN.13.5.455

Strong association of de novo copy number mutations with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1375%2FTWIN.13.5.455

Rare structural variants in schizophrenia: one disorder, multiple mutations; one mutation, multiple disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1375%2FTWIN.13.5.455

A review of the evidence from family, twin and adoption studies for a genetic contribution to adult psychiatric disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1375%2FTWIN.13.5.455

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

21 January 2018

1 reference

https://api.crossref.org/works/10.1375%2FTWIN.13.5.455

Strong association of de novo copy number mutations with sporadic schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1375%2FTWIN.13.5.455

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1375%2FTWIN.13.5.455

Paternal uniparental disomy in monozygotic twins discordant for hemihypertrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1375%2FTWIN.13.5.455

21 January 2018

Identifiers

DOI

10.1375/TWIN.13.5.455

1 reference

17 April 2018

1 reference

17 April 2018