(Q35304267)

English

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

scientific article published on 27 April 2011

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

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

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

autism spectrum disorder

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based on heuristic

inferred from title

Brian L. Yaspan

object named as

Brian L Yaspan

4

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Ellen M. Wijsman

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Joseph Glessner

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ORCID Public Data File 2021

6

object named as

Joseph D Buxbaum

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Europe PubMed Central

PubMed publication ID

7 August 2017

11

object named as

Joseph D Buxbaum

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Europe PubMed Central

PubMed publication ID

7 August 2017

author name string

Richard J L Anney

1

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Europe PubMed Central

PubMed publication ID

7 August 2017

Elaine M Kenny

2

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Europe PubMed Central

PubMed publication ID

7 August 2017

Colm O'Dushlaine

3

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Europe PubMed Central

PubMed publication ID

7 August 2017

Elena Parkhomenka

5

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Europe PubMed Central

PubMed publication ID

7 August 2017

James Sutcliffe

7

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Europe PubMed Central

PubMed publication ID

7 August 2017

Michael Gill

8

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Europe PubMed Central

PubMed publication ID

7 August 2017

Louise Gallagher

9

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Europe PubMed Central

PubMed publication ID

7 August 2017

Autism Genome Project

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Europe PubMed Central

PubMed publication ID

7 August 2017

James Sutcliffe

12

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Europe PubMed Central

PubMed publication ID

7 August 2017

Michael Gill

13

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Europe PubMed Central

PubMed publication ID

7 August 2017

Louise Gallagher

14

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Europe PubMed Central

PubMed publication ID

7 August 2017

publication date

27 April 2011

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Europe PubMed Central

PubMed publication ID

7 August 2017

European Journal of Human Genetics

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Europe PubMed Central

PubMed publication ID

7 August 2017

19

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Europe PubMed Central

PubMed publication ID

7 August 2017

10

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Europe PubMed Central

PubMed publication ID

7 August 2017

1082-1089

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Europe PubMed Central

PubMed publication ID

7 August 2017

describes a project that uses

1 reference

Europe PubMed Central

9 June 2022

https://europepmc.org/search?query=(METHODS:'Cytoscape')

based on heuristic

inferred from PubMed Central ID database lookup

Enrichment map: a network-based method for gene-set enrichment visualization and interpretation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3190264

27 July 2018

Analysing biological pathways in genome-wide association studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3190264

27 July 2018

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=3190264

27 July 2018

Functional impact of global rare copy number variation 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=3190264

27 July 2018

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=3190264

27 July 2018

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3190264

27 July 2018

Gene ontology analysis of GWA study data sets provides insights into the biology of bipolar disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3190264

27 July 2018

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=3190264

27 July 2018

The utility F-box for protein destruction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3190264

27 July 2018

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=3190264

27 July 2018

Genome-wide expression profiling of lymphoblastoid cell lines distinguishes different forms of autism and reveals shared pathways

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3190264

27 July 2018

MAP kinase signalling pathways in cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3190264

27 July 2018

p38 MAPK in development and cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3190264

27 July 2018

p38 MAP kinase's emerging role as a tumor suppressor

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3190264

27 July 2018

Cytoscape: a software environment for integrated models of biomolecular interaction networks

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3190264

27 July 2018

Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3190264

27 July 2018

Gene ontology: tool for the unification of biology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3190264

27 July 2018

Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3190264

27 July 2018

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

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3190264

27 July 2018

https://api.crossref.org/works/10.1038%2FEJHG.2011.75

21 January 2018

Autism diagnostic observation schedule: a standardized observation of communicative and social behavior

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3190264

27 July 2018

Autism and mitochondrial disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3190264

26 September 2018

Autism spectrum disorder diagnoses in Stockholm preschoolers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3190264

26 September 2018

Discovering genetic ancestry using spectral graph theory

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3190264

26 September 2018

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=3190264

26 September 2018

Epidemiology of Pervasive Developmental Disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3190264

26 September 2018

Pathway-based approaches for analysis of genomewide association studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3190264

26 September 2018

Combining information from multiple sources in the diagnosis of autism spectrum disorders.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3190264

26 September 2018

Polymorphisms in xenobiotic metabolism genes and autism.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3190264

26 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3190264

26 September 2018

A simple and fast two-locus quality control test to detect false positives due to batch effects in genome-wide association studies

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2011.75

21 January 2018

The SNP ratio test: pathway analysis of genome-wide association datasets

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2011.75

21 January 2018

Identifiers

10.1038/EJHG.2011.75

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Dimensions Publication ID

0 references

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

ResearchGate publication ID

0 references

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