(Q47895165)

6 February 2018

title

The implications of the shared genetics of psychiatric disorders (English)

1 reference

6 February 2018

author

Michael C O'Donovan

series ordinal

2

1

object named as

Michael C O'Donovan

1 reference

6 February 2018

language of work or name

English

0 references

publication date

26 October 2016

1 reference

6 February 2018

published in

Nature Medicine

1 reference

6 February 2018

volume

22

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6 February 2018

issue

11

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6 February 2018

page(s)

1214-1219

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6 February 2018

Global burden of disease attributable to mental and substance use disorders: findings from the Global Burden of Disease Study 2010.

cites work

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1 reference

Why has it taken so long for biological psychiatry to develop clinical tests and what to do about it?

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Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci

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Most genetic risk for autism resides with common variation

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Biological insights from 108 schizophrenia-associated genetic loci

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1 reference

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21 January 2018

1 reference

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A polygenic burden of rare disruptive mutations in schizophrenia

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Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders.

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1 reference

Copy number variation in bipolar disorder

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1 reference

The many faces of pleiotropy

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1 reference

Pleiotropy in complex traits: challenges and strategies

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1 reference

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1 reference

Analysis of Intellectual Disability Copy Number Variants for Association With Schizophrenia

21 January 2018

1 reference

Disruption of the neurexin 1 gene is associated with schizophrenia

21 January 2018

1 reference

Large-scale discovery of novel genetic causes of developmental disorders

21 January 2018

1 reference

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

21 January 2018

1 reference

LD Score regression distinguishes confounding from polygenicity in genome-wide association studies

21 January 2018

1 reference

Shared polygenic contribution between childhood attention-deficit hyperactivity disorder and adult schizophrenia

21 January 2018

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A framework for the interpretation of de novo mutation in human disease

21 January 2018

1 reference

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

21 January 2018

1 reference

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CNVs conferring risk of autism or schizophrenia affect cognition in controls

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1 reference

Common alleles contribute to schizophrenia in CNV carriers.

21 January 2018

1 reference

Evidence that duplications of 22q11.2 protect against schizophrenia

21 January 2018

1 reference

Pathogenic rare copy number variants in community-based schizophrenia suggest a potential role for clinical microarrays

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1 reference

New ethical issues for genetic counseling in common mental disorders

21 January 2018

1 reference

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21 January 2018

1 reference

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21 January 2018

1 reference

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21 January 2018

1 reference

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21 January 2018

1 reference

Assessing the utility of intermediate phenotypes for genetic mapping of psychiatric disease

21 January 2018

1 reference

Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept

21 January 2018

1 reference

The RDoC framework: facilitating transition from ICD/DSM to dimensional approaches that integrate neuroscience and psychopathology

21 January 2018

1 reference

An atlas of genetic correlations across human diseases and traits

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/27783064

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/27783064

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Analysis of shared heritability in common disorders of the brain

1 reference

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/NM.4196

1 reference

6 February 2018

1 reference

6 February 2018