(Q35069454)

6 August 2017

title

A quantitative association study of SLC25A12 and restricted repetitive behavior traits in autism spectrum disorders (English)

1 reference

6 August 2017

main subject

autism spectrum disorder

0 references

0 references

8

Edwin H Cook

1 reference

6 August 2017

Suma Jacob

4

0 references

author name string

Soo-Jeong Kim

1

1 reference

6 August 2017

Raquel M Silva

2

1 reference

6 August 2017

Cindi G Flores

3

1 reference

6 August 2017

Stephen Guter

5

1 reference

6 August 2017

Gregory Valcante

6

1 reference

6 August 2017

Annette M Zaytoun

7

1 reference

6 August 2017

Judith A Badner

9

1 reference

6 August 2017

language of work or name

1 reference

24 May 2011

1 reference

6 August 2017

1 reference

6 August 2017

volume

2

1 reference

6 August 2017

issue

1

1 reference

6 August 2017

page(s)

8

1 reference

https://scigraph.springernature.com/pub.10.1186/2040-2392-2-8

6 August 2017

exact match

0 references

cites work

The Simons Simplex Collection: a resource for identification of autism genetic risk factors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123633

Genetics in psychiatry: common variant association studies

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123633

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123633

Slc25a12 disruption alters myelination and neurofilaments: a model for a hypomyelination syndrome and childhood neurodevelopmental disorders

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123633

Failure to replicate a genetic association may provide important clues about genetic architecture

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123633

SLC25A12 expression is associated with neurite outgrowth and is upregulated in the prefrontal cortex of autistic subjects

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123633

No gene is an island: the flip-flop phenomenon

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123633

The Repetitive Behavior Scale-Revised: Independent Validation in Individuals with Autism Spectrum Disorders

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123633

Lack of association between autism and SLC25A12

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123633

Confirmation of association between autism and the mitochondrial aspartate/glutamate carrier SLC25A12 gene on chromosome 2q31

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123633

SLC25A12 and CMYA3 gene variants are not associated with autism in the IMGSAC multiplex family sample

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123633

Autism as a paradigmatic complex genetic disorder

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123633

Molecular genetics of autism spectrum disorder.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123633

Linkage and association of the mitochondrial aspartate/glutamate carrier SLC25A12 gene with autism

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123633

Genetics of austim: complex aetiology for a heterogeneous disorder

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123633

Varieties of repetitive behavior in autism: comparisons to mental retardation

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123633

The autism diagnostic observation schedule-generic: a standard measure of social and communication deficits associated with the spectrum of autism

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123633

Autism screening questionnaire: diagnostic validity.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123633

Annotation: Repetitive behaviour in autism: a review of psychological research

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123633

A genomic screen of autism: evidence for a multilocus etiology

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123633

Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123633

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

8 July 2018

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123633

8 July 2018

https://api.crossref.org/works/10.1186%2F2040-2392-2-8

Latent-class analysis of recurrence risks for complex phenotypes with selection and measurement error: a twin and family history study of autism

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123633

Diagnostic uses of the Vineland Adaptive Behavior Scales

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123633

The aberrant behavior checklist: a behavior rating scale for the assessment of treatment effects.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123633

A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123633

Complex segregation analysis of autism

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123633

Autism: searching for coherence.

8 July 2018

1 reference

https://api.crossref.org/works/10.1186%2F2040-2392-2-8

Mitochondrial aspartate/glutamate carrier SLC25A12 gene is associated with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F2040-2392-2-8

Brief report: High frequency of biochemical markers for mitochondrial dysfunction in autism: no association with the mitochondrial aspartate/glutamate carrier SLC25A12 gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F2040-2392-2-8

Association study of the SLC25A12 gene and autism in Han Chinese in Taiwan.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F2040-2392-2-8

AGC1 deficiency associated with global cerebral hypomyelination.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F2040-2392-2-8

Reduced N-acetylaspartate levels in mice lacking aralar, a brain- and muscle-type mitochondrial aspartate-glutamate carrier

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F2040-2392-2-8

Early features of autism: Repetitive behaviours in young children.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F2040-2392-2-8

An analysis of candidate autism loci on chromosome 2q24-q33: evidence for association to the STK39 gene

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123633

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123633

Lack of Association Between Autism and SLC25A12

27 September 2018

1 reference

https://api.crossref.org/works/10.1186%2F2040-2392-2-8

21 January 2018

Identifiers

DOI

10.1186/2040-2392-2-8

1 reference

Dimensions Publication ID

6 August 2017

0 references

1 reference

6 August 2017

1 reference