(Q43079380)

13 November 2017

0 references

Association study between autistic-like traits and polymorphisms in the autism candidate regions RELN, CNTNAP2, SHANK3, and CDH9/10. (English)

1 reference

13 November 2017

0 references

5

Henrik Anckarsäter

1 reference

13 November 2017

7

Paul Lichtenstein

1 reference

13 November 2017

Erik Pettersson

3

1 reference

ORCID Public Data File 2021

author name string

Lina Jonsson

1

1 reference

13 November 2017

Anna Zettergren

2

1 reference

13 November 2017

Daniel Hovey

4

1 reference

13 November 2017

Lars Westberg

6

1 reference

13 November 2017

Sebastian Lundström

8

1 reference

13 November 2017

Jonas Melke

9

1 reference

13 November 2017

16 December 2014

1 reference

13 November 2017

1 reference

13 November 2017

5

1 reference

13 November 2017

1

1 reference

13 November 2017

55

1 reference

The co-occurrence of autism and attention deficit hyperactivity disorder in children - what do we know?

13 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4276093

Genome-wide association study of autistic-like traits in a general population study of young adults.

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4276093

Different neurodevelopmental symptoms have a common genetic etiology

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4276093

The conundrums of understanding genetic risks for autism spectrum disorders

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4276093

CNTNAP2 variants affect early language development in the general population

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4276093

The genetics of autism spectrum disorders and related neuropsychiatric disorders in childhood

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4276093

A genome-wide scan for common alleles affecting risk for autism

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4276093

Association between a high-risk autism locus on 5p14 and social communication spectrum phenotypes in the general population

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4276093

The autism--tics, AD/HD and other comorbidities inventory (A-TAC): further validation of a telephone interview for epidemiological research

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4276093

A genome-wide association study of social and non-social autistic-like traits in the general population using pooled DNA, 500 K SNP microarrays and both community and diagnosed autism replication samples

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4276093

A genome-wide linkage and association scan reveals novel loci for autism

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4276093

Association study of SHANK3 gene polymorphisms with autism in Chinese Han population

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4276093

A genome-wide association study of autism reveals a common novel risk locus at 5p14.1

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4276093

Common genetic variants on 5p14.1 associate with autism spectrum disorders

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4276093

A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4276093

Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4276093

Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4276093

Genetic heterogeneity between the three components of the autism spectrum: a twin study

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4276093

Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4276093

Association of Reelin gene polymorphisms with autism

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4276093

Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4276093

Reelin gene variants and risk of autism spectrum disorders: an integrated meta-analysis

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4276093

The Child and Adolescent Twin Study in Sweden (CATSS).

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4276093

Autism spectrum disorders and autistic like traits: similar etiology in the extreme end and the normal variation

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4276093

Psychiatric telephone interview with parents for screening of childhood autism - tics, attention-deficit hyperactivity disorder and other comorbidities (A-TAC): preliminary reliability and validity

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4276093

Sample size requirements for association studies of gene-gene interaction

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4276093

15 August 2018

Identifiers

DOI

10.1186/2040-2392-5-55

1 reference

Dimensions Publication ID

13 November 2017

1 reference

9 September 2019

https://scigraph.springernature.com/pub.10.1186/2040-2392-5-55

1 reference

13 November 2017

PubMed publication ID

25540679

1 reference