(Q37834132)

PubMed publication ID

24 August 2017

1 reference

title

After GWAS: searching for genetic risk for schizophrenia and bipolar disorder (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6760656&resulttype=core&format=json

genome-wide association study

12 May 2020

main subject

0 references

0 references

1 reference

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6760656&resulttype=core&format=json

12 May 2020

author name string

Elliot S Gershon

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6760656&resulttype=core&format=json

12 May 2020

Ney Alliey-Rodriguez

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6760656&resulttype=core&format=json

12 May 2020

language of work or name

English

0 references

publication date

1 February 2011

1 reference

PubMed publication ID

21285144

American Journal of Psychiatry

24 August 2017

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6760656&resulttype=core&format=json

12 May 2020

volume

168

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6760656&resulttype=core&format=json

12 May 2020

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6760656&resulttype=core&format=json

12 May 2020

page(s)

253-256

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6760656&resulttype=core&format=json

Are rare variants responsible for susceptibility to complex diseases?

12 May 2020

cites work

1 reference

12 December 2020

On the allelic spectrum of human disease

1 reference

12 December 2020

Large-scale copy number polymorphism in the human genome

1 reference

12 December 2020

Detection of large-scale variation in the human genome

1 reference

12 December 2020

Rare chromosomal deletions and duplications increase risk of schizophrenia

1 reference

12 December 2020

Personal genomes: The case of the missing heritability

1 reference

12 December 2020

Genetic mapping in human disease

1 reference

12 December 2020

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

1 reference

12 December 2020

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

1 reference

12 December 2020

Copy number variation in human health, disease, and evolution

1 reference

12 December 2020

Origins and functional impact of copy number variation in the human genome

1 reference

12 December 2020

Finding the missing heritability of complex diseases

1 reference

12 December 2020

Microduplications of 16p11.2 are associated with schizophrenia

1 reference

12 December 2020

Genetic overlap between autism, schizophrenia and bipolar disorder

1 reference

12 December 2020

A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay

1 reference

12 December 2020

Trait-associated SNPs are more likely to be eQTLs: annotation to enhance discovery from GWAS

1 reference

12 December 2020

Genetic heterogeneity in human disease

1 reference

12 December 2020

Penetrance for copy number variants associated with schizophrenia.

1 reference

12 December 2020

Phenotypic variability and genetic susceptibility to genomic disorders

1 reference

12 December 2020

10.1176/APPI.AJP.2010.10091340

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6760656&resulttype=core&format=json

release_f4cjdkig2jdufhzjdazjjsxuza

12 May 2020

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/f4cjdkig2jdufhzjdazjjsxuza

24 November 2022

mapped directly with Wikidata item

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6760656&resulttype=core&format=json

12 May 2020

PubMed publication ID

21285144

1 reference