The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism (Q33764400)

29 July 2017

The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism (English)

1 reference

29 July 2017

0 references

1

Dexter Hadley

1 reference

29 July 2017

15

Hakon Hakonarson

1 reference

29 July 2017

Renata Pellegrino

10

0 references

Joseph Glessner

object named as

Joseph Glessner

14

1 reference

ORCID Public Data File 2021

Kelly A Thomas

6

object named as

Kelly Thomas

1 reference

29 July 2017

9

Frank Mentch

1 reference

29 July 2017

3

Charlly Kao

1 reference

29 July 2017

8

Haijun Qiu

1 reference

29 July 2017

Zhi-Liang Wu

2

1 reference

29 July 2017

Akshata Kini

4

1 reference

29 July 2017

Alisha Mohamed-Hadley

5

1 reference

29 July 2017

Lyam Vazquez

7

1 reference

29 July 2017

Cecilia Kim

11

1 reference

29 July 2017

John Connolly

12

1 reference

29 July 2017

AGP Consortium

13

1 reference

29 July 2017

language of work or name

English

0 references

publication date

13 June 2014

1 reference

29 July 2017

Nature Communications

1 reference

29 July 2017

5

1 reference

29 July 2017

4074

1 reference

Creative Commons Attribution 3.0 Unported

29 July 2017

start time

13 June 2014

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

exact match

https://scigraph.springernature.com/pub.10.1038/ncomms5074

0 references

cites work

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1 reference

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Network topologies and convergent aetiologies arising from deletions and duplications observed in individuals with autism

22 June 2018

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Identification of rare recurrent copy number variants in high-risk autism families and their prevalence in a large ASD population

22 June 2018

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22 June 2018

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

22 June 2018

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Pharmacogenomics and personalized medicine in neuropsychiatry

22 June 2018

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De Novo Gene Disruptions in Children on the Autistic Spectrum

22 June 2018

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

22 June 2018

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

22 June 2018

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

22 June 2018

1 reference

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Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder

22 June 2018

1 reference

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Mutations causing syndromic autism define an axis of synaptic pathophysiology

22 June 2018

1 reference

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Recurrence risk for autism spectrum disorders: a Baby Siblings Research Consortium study

22 June 2018

1 reference

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

22 June 2018

1 reference

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Protein interactome reveals converging molecular pathways among autism disorders

22 June 2018

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Prevalence of autism spectrum disorders in a total population sample

22 June 2018

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Etiological heterogeneity in autism spectrum disorders: more than 100 genetic and genomic disorders and still counting

22 June 2018

1 reference

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Sibling recurrence and the genetic epidemiology of autism

22 June 2018

1 reference

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Integrating common and rare genetic variation in diverse human populations

22 June 2018

1 reference

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

22 June 2018

1 reference

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Functional impact of global rare copy number variation in autism spectrum disorders

22 June 2018

1 reference

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Strong synaptic transmission impact by copy number variations in schizophrenia

22 June 2018

1 reference

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The correlation between rates of cancer and autism: an exploratory ecological investigation

22 June 2018

1 reference

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Prevalence of autism spectrum disorders - Autism and Developmental Disabilities Monitoring Network, United States, 2006

22 June 2018

1 reference

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Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4059929

Gene-network analysis identifies susceptibility genes related to glycobiology in autism

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4059929

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

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4059929

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

22 June 2018

1 reference

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Autism-specific copy number variants further implicate the phosphatidylinositol signaling pathway and the glutamatergic synapse in the etiology of the disorder.

22 June 2018

1 reference

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An empirical framework for binary interactome mapping

22 June 2018

1 reference

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The association analysis of RELN and GRM8 genes with autistic spectrum disorder in Chinese Han population

22 June 2018

1 reference

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BAG-1 associates with Hsc70.Tau complex and regulates the proteasomal degradation of Tau protein.

22 June 2018

1 reference

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PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data

22 June 2018

1 reference

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22 June 2018

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Mapping autism risk loci using genetic linkage and chromosomal rearrangements

22 June 2018

1 reference

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Prevalence of autism spectrum disorders--autism and developmental disabilities monitoring network, 14 sites, United States, 2002.

22 June 2018

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Patterns of sequence conservation in presynaptic neural genes

22 June 2018

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Investigation of autism and GABA receptor subunit genes in multiple ethnic groups

22 June 2018

1 reference

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Towards a proteome-scale map of the human protein–protein interaction network

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4059929

Identification of significant association and gene-gene interaction of GABA receptor subunit genes in autism

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4059929

Familial symptom domains in monozygotic siblings with autism

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4059929

22 June 2018

The genetics of autism

1 reference

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HUGE: a database for human KIAA proteins, a 2004 update integrating HUGEppi and ROUGE.

22 June 2018

1 reference

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Postnatal Neurodevelopmental Disorders: Meeting at the Synapse?

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4059929

Positive associations of polymorphisms in the metabotropic glutamate receptor type 3 gene (GRM3) with schizophrenia

22 June 2018

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4059929

22 June 2018

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4059929

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4059929

X-ray structures of Myc-Max and Mad-Max recognizing DNA. Molecular bases of regulation by proto-oncogenic transcription factors

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4059929

22 June 2018

The prevalence of autism

1 reference

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N-CoR controls differentiation of neural stem cells into astrocytes

22 June 2018

1 reference

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22 June 2018

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A human genome diversity cell line panel

22 June 2018

1 reference

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Association between a GABRB3 polymorphism and autism.

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4059929

Genetics of austim: complex aetiology for a heterogeneous disorder

22 June 2018

1 reference

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Polymorphisms in the genes for mGluR types 7 and 8: association studies with schizophrenia

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4059929

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

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4059929

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

22 June 2018

1 reference

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Infantile autism: a genetic study of 21 twin pairs

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4059929

Association study of polymorphisms in the group III metabotropic glutamate receptor genes, GRM4 and GRM7, with schizophrenia

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4059929

BAG-1M is up-regulated in hippocampus of Alzheimer's disease patients and associates with tau and APP proteins

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4059929

The association between glutamate receptor gene SNP and schizophrenia

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4059929

Positive associations of polymorphisms in the metabotropic glutamate receptor type 8 gene (GRM8) with schizophrenia

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4059929

The metabotropic glutamate receptor 8 gene at 7q31: partial duplication and possible association with autism

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4059929

A polymorphism of the metabotropic glutamate receptor mGluR7 (GRM7) gene is associated with schizophrenia

30 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24927284

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Changes in prevalence of parent-reported autism spectrum disorder in school-aged U.S. children: 2007 to 2011-2012.

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24927284

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NCOMMS5074

1 reference

Dimensions Publication ID

29 July 2017

0 references

0 references

1 reference

29 July 2017

1 reference