(Q48221004)

http://europepmc.org/abstract/PMC/5443344

14 June 2018

title

The Cognitive and Behavioral Phenotypes of Individuals with CHRNA7 Duplications. (English)

1 reference

http://europepmc.org/abstract/PMC/5443344

14 June 2018

corrigendum / erratum

Erratum to: The Cognitive and Behavioral Phenotypes of Individuals with CHRNA7 Duplications.

0 references

author

Brett H Graham

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27853923%20AND%20SRC:MED&resulttype=core&format=json

5 June 2020

Marwan Shinawi

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27853923%20AND%20SRC:MED&resulttype=core&format=json

5 June 2020

Christian P Schaaf

21

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27853923%20AND%20SRC:MED&resulttype=core&format=json

5 June 2020

author name string

M A Gillentine

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27853923%20AND%20SRC:MED&resulttype=core&format=json

5 June 2020

L N Berry

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27853923%20AND%20SRC:MED&resulttype=core&format=json

5 June 2020

R P Goin-Kochel

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27853923%20AND%20SRC:MED&resulttype=core&format=json

5 June 2020

M A Ali

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27853923%20AND%20SRC:MED&resulttype=core&format=json

5 June 2020

J Ge

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27853923%20AND%20SRC:MED&resulttype=core&format=json

5 June 2020

D Guffey

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27853923%20AND%20SRC:MED&resulttype=core&format=json

5 June 2020

J A Rosenfeld

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27853923%20AND%20SRC:MED&resulttype=core&format=json

5 June 2020

V Hannig

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27853923%20AND%20SRC:MED&resulttype=core&format=json

5 June 2020

P Bader

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27853923%20AND%20SRC:MED&resulttype=core&format=json

5 June 2020

M Proud

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27853923%20AND%20SRC:MED&resulttype=core&format=json

5 June 2020

A Lin

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27853923%20AND%20SRC:MED&resulttype=core&format=json

5 June 2020

S R Lalani

14

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27853923%20AND%20SRC:MED&resulttype=core&format=json

5 June 2020

J Reynolds

15

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27853923%20AND%20SRC:MED&resulttype=core&format=json

5 June 2020

M Chen

16

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27853923%20AND%20SRC:MED&resulttype=core&format=json

5 June 2020

T Grebe

17

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27853923%20AND%20SRC:MED&resulttype=core&format=json

5 June 2020

C G Minard

18

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27853923%20AND%20SRC:MED&resulttype=core&format=json

5 June 2020

P Stankiewicz

19

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27853923%20AND%20SRC:MED&resulttype=core&format=json

5 June 2020

A L Beaudet

20

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27853923%20AND%20SRC:MED&resulttype=core&format=json

5 June 2020

language of work or name

English

0 references

publication date

1 March 2017

1 reference

http://europepmc.org/abstract/PMC/5443344

14 June 2018

published in

Journal of Autism and Developmental Disorders

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27853923%20AND%20SRC:MED&resulttype=core&format=json

5 June 2020

volume

47

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27853923%20AND%20SRC:MED&resulttype=core&format=json

5 June 2020

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27853923%20AND%20SRC:MED&resulttype=core&format=json

5 June 2020

page(s)

549-562

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27853923%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/s10803-016-2961-8

5 June 2020

exact match

0 references

cites work

The human clinical phenotypes of altered CHRNA7 copy number

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5443344

Clinical phenotype of the recurrent 1q21.1 copy-number variant

14 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5443344

Copy number variations and cognitive phenotypes in unselected populations

14 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5443344

The human CHRNA7 and CHRFAM7A genes: A review of the genetics, regulation, and function

14 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5443344

Delineating the 15q13.3 microdeletion phenotype: a case series and comprehensive review of the literature

14 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5443344

CHRNA7 triplication associated with cognitive impairment and neuropsychiatric phenotypes in a three-generation pedigree.

14 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5443344

CNVs conferring risk of autism or schizophrenia affect cognition in controls

14 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5443344

Association study of the 2-bp deletion polymorphism in exon 6 of the CHRFAM7A gene with idiopathic generalized epilepsy.

14 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5443344

Phenotypic heterogeneity of genomic disorders and rare copy-number variants

14 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5443344

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

14 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5443344

Phenotypic variability and genetic susceptibility to genomic disorders

14 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5443344

Cognitive and behavioral characterization of 16p11.2 deletion syndrome

14 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5443344

Structures and molecular mechanisms for common 15q13.3 microduplications involving CHRNA7: benign or pathological?

14 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5443344

A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypes

14 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5443344

15q13.3 microdeletions increase risk of idiopathic generalized epilepsy

14 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5443344

Assortative mating in the affective disorders: a systematic review and meta-analysis.

14 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5443344

Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3.

14 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5443344

The complex behavioral phenotype of 15q13.3 microdeletion syndrome.

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5443344

Association study of CHRFAM7A copy number and 2bp deletion polymorphisms with schizophrenia and bipolar affective disorder

14 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/27853923

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S10803-016-2961-8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27853923%20AND%20SRC:MED&resulttype=core&format=json

5 June 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27853923%20AND%20SRC:MED&resulttype=core&format=json

5 June 2020

1 reference