(Q45908246)

17 December 2017

title

Clinical and parental age characteristics of rare copy number variant burden in patients with schizophrenia. (English)

1 reference

17 December 2017

1 reference

1

1 reference

17 December 2017

David C. Reutens

object named as

David Reutens

series ordinal

3

0 references

author name string

Gail Robinson

series ordinal

2

1 reference

17 December 2017

Bryan Mowry

series ordinal

4

1 reference

17 December 2017

publication date

5 May 2015

1 reference

17 December 2017

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

published in

1 reference

17 December 2017

volume

168B

1 reference

17 December 2017

issue

5

1 reference

17 December 2017

page(s)

374-382

1 reference

17 December 2017

Increased paternal age and the influence on burden of genomic copy number variation in the general population.

cites work

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32321

Genome-wide analysis shows increased frequency of copy number variation deletions in Dutch schizophrenia patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32321

Advanced parental age and the risk of autism spectrum disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32321

Paternal and maternal age as risk factors for psychosis: findings from Denmark, Sweden and Australia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32321

Genome-wide association study of clinical dimensions of schizophrenia: polygenic effect on disorganized symptoms

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32321

A controlled family study of chronic psychoses. Schizophrenia and schizoaffective disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32321

Recurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32321

De novo copy number variants associated with intellectual disability have a paternal origin and age bias.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32321

Rare chromosomal deletions and duplications increase risk of schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32321

Mapping and sequencing of structural variation from eight human genomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32321

Rate of de novo mutations and the importance of father's age to disease risk

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32321

Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32321

Delayed fathering and risk of mental disorders in adult offspring.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32321

Best estimate of lifetime psychiatric diagnosis: a methodological study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32321

Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32321

The Lifetime Dimensions of Psychosis Scale (LDPS): description and interrater reliability.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32321

Paternal factors and schizophrenia risk: de novo mutations and imprinting

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32321

Advancing paternal age and the risk of schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32321

Cannabis abuse and age at onset in schizophrenia patients with large, rare copy number variants.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32321

Copy number deletion burden is associated with cognitive, structural, and resting-state network differences in patients with schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32321

Teen-aged mothers in contemporary Britain

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32321

The emerging spectrum of allelic variation in schizophrenia: current evidence and strategies for the identification and functional characterization of common and rare variants

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32321

Diagnostic interview for genetic studies. Rationale, unique features, and training. NIMH Genetics Initiative

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32321

PLINK: a tool set for whole-genome association and population-based linkage analyses

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32321

Maternal and paternal age are jointly associated with childhood autism in Jamaica

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32321

Analysis of copy number variations at 15 schizophrenia-associated loci.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32321

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32321

CNVs conferring risk of autism or schizophrenia affect cognition in controls

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32321

Large recurrent microdeletions associated with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32321

Genomewide linkage scan of 409 European-ancestry and African American families with schizophrenia: suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sample

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32321

The health and development of children born to older mothers in the United Kingdom: observational study using longitudinal cohort data

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32321

Copy number variation in schizophrenia in Sweden

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32321

Schizophrenia genetic variants are not associated with intelligence

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32321

PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32321

Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32321

The impact of copy number deletions on general cognitive ability and ventricle size in patients with schizophrenia and healthy control subjects

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32321

Paternal age and risk for schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32321

21 January 2018

Identifiers

DOI

10.1002/AJMG.B.32321

1 reference

17 December 2017

PubMed ID

25943776

1 reference

17 December 2017