(Q34507615)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20479756%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

title

A novel frameshift mutation in UPF3B identified in brothers affected with childhood onset schizophrenia and autism spectrum disorders (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20479756%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

main subject

autism spectrum disorder

0 references

0 references

0 references

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20479756%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Amélie Piton

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20479756%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

14

G A Rouleau

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20479756%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

author name string

J Gauthier

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20479756%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

F F Hamdan

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20479756%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

A Raymond

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20479756%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

N Gogtay

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20479756%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

R Miller

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20479756%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

J Tossell

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20479756%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

J Bakalar

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20479756%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

G Inoff-Germain

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20479756%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

P Gochman

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20479756%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

R Long

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20479756%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

J L Rapoport

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20479756%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

language of work or name

English

0 references

publication date

18 May 2010

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20479756%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20479756%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

volume

16

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20479756%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20479756%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

page(s)

238-239

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20479756%20AND%20SRC:MED&resulttype=core&format=json

The genetics of childhood-onset schizophrenia: when madness strikes the prepubescent

2 February 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3024438

Autism spectrum disorders and childhood-onset schizophrenia: clinical and biological contributions to a relation revisited

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3024438

Population analysis of large copy number variants and hotspots of human genetic disease

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3024438

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3024438

Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3024438

The neurodevelopmental model of schizophrenia: update 2005.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3024438

Autism screening questionnaire: diagnostic validity.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3024438

Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3024438

Novel de novo SHANK3 mutation in autistic patients

7 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FMP.2010.59

21 January 2018

Identifiers

DOI

10.1038/MP.2010.59

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20479756%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20479756%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

PubMed publication ID

20479756

1 reference