CNVs in neuropsychiatric disorders (Q28083143)

published in

Human Molecular Genetics

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volume

24

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page(s)

R45-9

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issue

R1

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High rates of schizophrenia in adults with velo-cardio-facial syndrome.

cites work

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https://api.crossref.org/works/10.1093%2FHMG%2FDDV253

Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV253

Genome architecture, rearrangements and genomic disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV253

Genomic disorders ten years on.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV253

Phenotypic heterogeneity of genomic disorders and rare copy-number variants

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV253

Refinement and discovery of new hotspots of copy-number variation associated with autism spectrum disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV253

Rare chromosomal deletions and duplications increase risk of schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV253

Large recurrent microdeletions associated with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV253

Disruption of the neurexin 1 gene is associated with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV253

Reciprocal duplication of the Williams-Beuren syndrome deletion on chromosome 7q11.23 is associated with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV253

Maternally derived microduplications at 15q11-q13: implication of imprinted genes in psychotic illness

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV253

CNVs: harbingers of a rare variant revolution in psychiatric genetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV253

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/10.1093%2FHMG%2FDDV253

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

21 January 2018

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https://api.crossref.org/works/10.1093%2FHMG%2FDDV253

The penetrance of copy number variations for schizophrenia and developmental delay.

21 January 2018

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https://api.crossref.org/works/10.1093%2FHMG%2FDDV253

Copy number variation in bipolar disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV253

An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV253

Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes

21 January 2018

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https://api.crossref.org/works/10.1093%2FHMG%2FDDV253

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV253

Microduplications of 16p11.2 are associated with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV253

Molecular analysis of a deletion hotspot in the NRXN1 region reveals the involvement of short inverted repeats in deletion CNVs

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV253

Rare copy number variants: a point of rarity in genetic risk for bipolar disorder and schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV253

Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV253

CNVs conferring risk of autism or schizophrenia affect cognition in controls

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV253

Neurocognition in first-episode schizophrenia: a meta-analytic review

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV253

De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV253

High frequencies of de novo CNVs in bipolar disorder and schizophrenia

21 January 2018

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https://api.crossref.org/works/10.1093%2FHMG%2FDDV253

De novo rates and selection of schizophrenia-associated copy number variants

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV253

Reproductive patterns in psychotic patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV253

Fecundity of patients with schizophrenia, autism, bipolar disorder, depression, anorexia nervosa, or substance abuse vs their unaffected siblings.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV253

Sex differences in reproductive fitness contribute to preferential maternal transmission of 22q11.2 deletions.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV253

New ethical issues for genetic counseling in common mental disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV253

Penetrance for copy number variants associated with schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV253

Estimates of penetrance for recurrent pathogenic copy-number variations

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV253

NAHR-mediated copy-number variants in a clinical population: mechanistic insights into both genomic disorders and Mendelizing traits

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV253

Fertility of Patients With Schizophrenia, Their Siblings, and the General Population: A Cohort Study From 1950 to 1959 in Finland

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV253

21 January 2018

Identifiers

DOI

10.1093/HMG/DDV253

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Consolidated OpenCitations Corpus – April 2017

4747448

4747448

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

1 reference