(Q28266762)

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Loci nominally associated with autism from genome-wide analysis show enrichment of brain expression quantitative trait loci but not lymphoblastoid cell line expression quantitative trait loci

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Europe PubMed Central

PubMed publication ID

23 June 2017

Loci nominally associated with autism from genome-wide analysis show enrichment of brain expression quantitative trait loci but not lymphoblastoid cell line expression quantitative trait loci (English)

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Europe PubMed Central

PubMed publication ID

23 June 2017

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quantitative trait locus

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James S. Sutcliffe

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James S Sutcliffe

7

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object named as

Chunyu Liu

5

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6

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Edwin H Cook

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Europe PubMed Central

PubMed publication ID

23 June 2017

Eric R. Gamazon

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Eric R Gamazon

2

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8

object named as

Nancy J Cox

1 reference

Europe PubMed Central

PubMed publication ID

23 June 2017

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Lea K Davis

1

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Europe PubMed Central

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23 June 2017

Emily Kistner-Griffin

3

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Europe PubMed Central

PubMed publication ID

23 June 2017

Judith A Badner

4

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Europe PubMed Central

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23 June 2017

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publication date

16 May 2012

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Europe PubMed Central

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23 June 2017

Molecular Autism

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Europe PubMed Central

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23 June 2017

3

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Europe PubMed Central

PubMed publication ID

23 June 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

23 June 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

23 June 2017

MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484025

20 March 2017

Trait-associated SNPs are more likely to be eQTLs: annotation to enhance discovery from GWAS

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20 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484025

20 March 2017

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484025

20 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484025

20 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484025

20 March 2017

Capturing heterogeneity in gene expression studies by surrogate variable analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484025

20 March 2017

PLINK: a tool set for whole-genome association and population-based linkage analyses

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484025

20 March 2017

Strong association of de novo copy number mutations with autism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484025

20 March 2017

PANTHER: a browsable database of gene products organized by biological function, using curated protein family and subfamily classification

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484025

20 March 2017

Isogenic pairs of wild type and mutant induced pluripotent stem cell (iPSC) lines from Rett syndrome patients as in vitro disease model

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484025

20 March 2017

Genome-wide association and meta-analysis in populations from Starr County, Texas, and Mexico City identify type 2 diabetes susceptibility loci and enrichment for expression quantitative trait loci in top signals

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484025

20 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484025

20 March 2017

Transcriptomic analysis of autistic brain reveals convergent molecular pathology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484025

7 April 2017

Genotype imputation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484025

7 April 2017

Adjusting batch effects in microarray expression data using empirical Bayes methods

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484025

7 April 2017

Enrichment of cis-regulatory gene expression SNPs and methylation quantitative trait loci among bipolar disorder susceptibility variants.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484025

29 September 2017

Using iPSC-derived neurons to uncover cellular phenotypes associated with Timothy syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484025

29 September 2017

Induced pluripotent stem cells (iPSCs) and neurological disease modeling: progress and promises

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484025

29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484025

29 September 2017

Gene-ontology enrichment analysis in two independent family-based samples highlights biologically plausible processes for autism spectrum disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484025

29 September 2017

Genetic analysis of biological pathway data through genomic randomization

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484025

29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484025

29 September 2017

SCAN: SNP and copy number annotation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484025

29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484025

29 September 2017

Genetic architecture of transcript-level variation in humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484025

29 September 2017

Pannexin1 and Pannexin2 expression in the developing and mature rat brain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484025

29 September 2017

Genetic influences and infantile autism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484025

2 June 2018

Allowing for sex differences increases power in a GWAS of multiplex Autism families

1 reference

https://api.crossref.org/works/10.1186%2F2040-2392-3-3

21 January 2018

Pannexin 2 is expressed by postnatal hippocampal neural progenitors and modulates neuronal commitment

1 reference

https://api.crossref.org/works/10.1186%2F2040-2392-3-3

21 January 2018

Activation of pannexin-1 hemichannels augments aberrant bursting in the hippocampus.

1 reference

https://api.crossref.org/works/10.1186%2F2040-2392-3-3

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1186%2F2040-2392-3-3

21 January 2018

No association between a common single nucleotide polymorphism, rs4141463, in the MACROD2 gene and autism spectrum disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484025

27 November 2018

Autism-related routines and rituals associated with a mitochondrial aspartate/glutamate carrier SLC25A12 polymorphism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484025

27 November 2018

Identifiers

10.1186/2040-2392-3-3

1 reference

Europe PubMed Central

PubMed publication ID

23 June 2017

Dimensions Publication ID

1 reference

9 September 2019

https://scigraph.springernature.com/pub.10.1186/2040-2392-3-3

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PMC publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

23 June 2017

ResearchGate publication ID

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