(Q50305811)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16077734%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

title

Analysis of four neuroligin genes as candidates for autism (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16077734%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

0 references

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16077734%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

Irma Järvelä

14

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16077734%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

author name string

Tero Ylisaukko-oja

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16077734%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

Karola Rehnström

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16077734%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

Mari Auranen

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16077734%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

Raija Vanhala

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16077734%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

Reija Alen

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16077734%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

Elli Kempas

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16077734%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

Pekka Ellonen

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16077734%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

Ismo Makkonen

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16077734%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

Raili Riikonen

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16077734%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

Taina Nieminen-von Wendt

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16077734%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

Lennart von Wendt

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16077734%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

Leena Peltonen

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16077734%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

publication date

1 December 2005

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16077734%20AND%20SRC:MED&resulttype=core&format=json

European Journal of Human Genetics

5 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16077734%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

volume

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16077734%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

issue

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16077734%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

page(s)

1285-1292

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16077734%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5201474

5 January 2020

exact match

0 references

cites work

Pervasive Developmental Disorders in Preschool Children

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201474

The prevalence of autism spectrum disorders. Recent evidence and future challenges

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201474

Prevalence of autism in a US metropolitan area

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201474

Autism as a strongly genetic disorder: evidence from a British twin study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201474

A case-control family history study of autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201474

A genomic screen of autism: evidence for a multilocus etiology

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201474

Molecular genetics of autism spectrum disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201474

Chromosomal disorders and autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201474

The behavioral phenotype in fragile X: symptoms of autism in very young children with fragile X syndrome, idiopathic autism, and other developmental disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201474

Autism in tuberous sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201474

Identification of MeCP2 mutations in a series of females with autistic disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201474

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201474

X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201474

Neuroligin 1: a splice site-specific ligand for beta-neurexins

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201474

Binding of neuroligins to PSD-95

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201474

Identification of a novel neuroligin in humans which binds to PSD-95 and has a widespread expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201474

A novel multiple PDZ domain-containing molecule interacting with N-methyl-D-aspartate receptors and neuronal cell adhesion proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201474

Neuroligin expressed in nonneuronal cells triggers presynaptic development in contacting axons

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201474

Neurexin mediates the assembly of presynaptic terminals

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201474

Disorder-associated mutations lead to functional inactivation of neuroligins

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201474

The Arg451Cys-neuroligin-3 mutation associated with autism reveals a defect in protein processing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201474

A genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201474

Genome-wide scan for loci of Asperger syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201474

The human genome browser at UCSC

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201474

BCM Search Launcher--an integrated interface to molecular biology data base search and analysis services available on the World Wide Web.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201474

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201474

A system for specific, high-throughput genotyping by allele-specific primer extension on microarrays

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201474

Construction of human linkage maps: likelihood calculations for multilocus linkage analysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201474

Haploview: analysis and visualization of LD and haplotype maps

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201474

Linkage analysis in the presence of errors IV: joint pseudomarker analysis of linkage and/or linkage disequilibrium on a mixture of pedigrees and singletons when the mode of inheritance cannot be accurately specified

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201474

The family based association test method: strategies for studying general genotype--phenotype associations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201474

Mutation screening of X-chromosomal neuroligin genes: no mutations in 196 autism probands

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201474

NLGN3/NLGN4 gene mutations are not responsible for autism in the Quebec population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201474

Analysis of the neuroligin 3 and 4 genes in autism and other neuropsychiatric patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201474

Haplotype analysis and identification of genes for a complex trait: examples from schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201474

Association of genetic loci: replication or not, that is the question

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201474

Model of autism: increased ratio of excitation/inhibition in key neural systems

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201474

A balance between excitatory and inhibitory synapses is controlled by PSD-95 and neuroligin

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201474