(Q28277540)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27479844%20AND%20SRC:MED&resulttype=core&format=json

20 March 2020

title

Genome-wide prediction and functional characterization of the genetic basis of autism spectrum disorder (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27479844%20AND%20SRC:MED&resulttype=core&format=json

20 March 2020

main subject

autism spectrum disorder

0 references

0 references

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27479844%20AND%20SRC:MED&resulttype=core&format=json

20 March 2020

Alex Lash

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27479844%20AND%20SRC:MED&resulttype=core&format=json

20 March 2020

Arjun Krishnan

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27479844%20AND%20SRC:MED&resulttype=core&format=json

20 March 2020

Ran Zhang

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27479844%20AND%20SRC:MED&resulttype=core&format=json

20 March 2020

Victoria Yao

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27479844%20AND%20SRC:MED&resulttype=core&format=json

20 March 2020

10

Olga G Troyanskaya

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27479844%20AND%20SRC:MED&resulttype=core&format=json

20 March 2020

4

Chandra L Theesfeld

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27479844%20AND%20SRC:MED&resulttype=core&format=json

20 March 2020

author name string

Alicja Tadych

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27479844%20AND%20SRC:MED&resulttype=core&format=json

20 March 2020

Natalia Volfovsky

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27479844%20AND%20SRC:MED&resulttype=core&format=json

20 March 2020

Alan Packer

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27479844%20AND%20SRC:MED&resulttype=core&format=json

20 March 2020

language of work or name

English

0 references

publication date

1 August 2016

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27479844%20AND%20SRC:MED&resulttype=core&format=json

20 March 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27479844%20AND%20SRC:MED&resulttype=core&format=json

20 March 2020

volume

19

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27479844%20AND%20SRC:MED&resulttype=core&format=json

20 March 2020

issue

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27479844%20AND%20SRC:MED&resulttype=core&format=json

20 March 2020

page(s)

1454-1462

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27479844%20AND%20SRC:MED&resulttype=core&format=json

The human disease network

20 March 2020

cites work

1 reference

Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations

21 April 2017

1 reference

Patterns and rates of exonic de novo mutations in autism spectrum disorders

21 April 2017

1 reference

De Novo Gene Disruptions in Children on the Autistic Spectrum

21 April 2017

1 reference

The contribution of de novo coding mutations to autism spectrum disorder

21 April 2017

1 reference

Synaptic, transcriptional and chromatin genes disrupted in autism

21 April 2017

1 reference

FMRP stalls ribosomal translocation on mRNAs linked to synaptic function and autism

21 April 2017

1 reference

Low load for disruptive mutations in autism genes and their biased transmission

21 April 2017

1 reference

Shank3 mutant mice display autistic-like behaviours and striatal dysfunction

21 April 2017

1 reference

Rosbin: a novel homeobox-like protein gene expressed exclusively in round spermatids

21 April 2017

1 reference

Association between microdeletion and microduplication at 16p11.2 and autism

21 April 2017

1 reference

Associating genes and protein complexes with disease via network propagation

21 April 2017

1 reference

SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs)

21 April 2017

1 reference

Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders

21 April 2017

1 reference

A framework for the interpretation of de novo mutation in human disease

21 April 2017

1 reference

NCBI GEO: archive for functional genomics data sets--update

21 April 2017

1 reference

A comparison of normalization methods for high density oligonucleotide array data based on variance and bias

21 April 2017

1 reference

Evolving gene/transcript definitions significantly alter the interpretation of GeneChip data

21 April 2017

1 reference

Fast unfolding of communities in large networks

21 April 2017

1 reference

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

21 April 2017

1 reference

HOCOMOCO: a comprehensive collection of human transcription factor binding sites models

21 April 2017

1 reference

De novo mutations revealed by whole-exome sequencing are strongly associated with autism

21 April 2017

1 reference

Spatio-temporal transcriptome of the human brain

21 April 2017

1 reference

Transcriptomic analysis of autistic brain reveals convergent molecular pathology

21 April 2017

1 reference

The genetic association database

21 April 2017

1 reference

NETWORK ASSISTED ANALYSIS TO REVEAL THE GENETIC BASIS OF AUTISM.

21 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5803797

Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5803797

Neural variability: friend or foe?

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5803797

Understanding multicellular function and disease with human tissue-specific networks

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5803797

Association of maternal report of infant and toddler gastrointestinal symptoms with autism: evidence from a prospective birth cohort

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5803797

The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5803797

Spatiotemporal 16p11.2 protein network implicates cortical late mid-fetal brain development and KCTD13-Cul3-RhoA pathway in psychiatric diseases

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5803797

Integrated systems analysis reveals a molecular network underlying autism spectrum disorders

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5803797

Genotype to phenotype relationships in autism spectrum disorders

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5803797

The relationship between sleep and behavior in autism spectrum disorder (ASD): a review

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5803797

The discovery of integrated gene networks for autism and related disorders

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5803797

Anatomical Abnormalities in Autism?

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5803797

The cerebellum, sensitive periods, and autism.

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5803797

Cytokine aberrations in autism spectrum disorder: a systematic review and meta-analysis

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5803797

Convergence of genes and cellular pathways dysregulated in autism spectrum disorders

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5803797

Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism.

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5803797

Patches of disorganization in the neocortex of children with autism

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5803797

Sensory symptoms in autism spectrum disorders

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5803797

The role of de novo mutations in the genetics of autism spectrum disorders

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5803797

Integrative functional genomic analyses implicate specific molecular pathways and circuits in autism

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5803797

Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5803797

Topoisomerases facilitate transcription of long genes linked to autism

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5803797

Genic intolerance to functional variation and the interpretation of personal genomes

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5803797

Integrated model of de novo and inherited genetic variants yields greater power to identify risk genes

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5803797

The autism brain imaging data exchange: towards a large-scale evaluation of the intrinsic brain architecture in autism

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5803797

The Disease and Gene Annotations (DGA): an annotation resource for human disease.

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5803797

Standardizing ADOS domain scores: separating severity of social affect and restricted and repetitive behaviors

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5803797

Using large clinical data sets to infer pathogenicity for rare copy number variants in autism cohorts

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5803797

Network- and attribute-based classifiers can prioritize genes and pathways for autism spectrum disorders and intellectual disability

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5803797

Integrative gene network analysis provides novel regulatory relationships, genetic contributions and susceptible targets in autism spectrum disorders

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5803797

The Gene Ontology: enhancements for 2011

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5803797

D³: Data-Driven Documents

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5803797

Rare de novo variants associated with autism implicate a large functional network of genes involved in formation and function of synapses

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5803797

FIMO: scanning for occurrences of a given motif

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5803797

Characterization of the proteome, diseases and evolution of the human postsynaptic density.

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5803797

The Simons Simplex Collection: A Resource for Identification of Autism Genetic Risk Factors

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5803797

Depletion of protein phosphatase 4 in human cells reveals essential roles in centrosome maturation, cell migration and the regulation of Rho GTPases

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5803797

Elevated rates of protein secretion, evolution, and disease among tissue-specific genes

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5803797

Assessing experimentally derived interactions in a small world

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5803797

The human genome browser at UCSC

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5803797

Combined analysis of exome sequencing points toward a major role for transcription regulation during brain development in autism

2 June 2018

1 reference

Brain-expressed exons under purifying selection are enriched for de novo mutations in autism spectrum disorder

21 January 2018

1 reference

A navigator for human genome epidemiology.

21 January 2018

1 reference

Predicting good probabilities with supervised learning

21 January 2018

1 reference

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/NN.4353

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27479844%20AND%20SRC:MED&resulttype=core&format=json

20 March 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27479844%20AND%20SRC:MED&resulttype=core&format=json

20 March 2020

PubMed publication ID

27479844

1 reference