Skip to search formSkip to main content
You are currently offline. Some features of the site may not work correctly.

ASTN2 gene

Known as: ASTN2, Astrotactin 2 Gene, ASTROTACTIN 2 
This gene may play a role in neural development.
National Institutes of Health

Related topics

Related topics

3 relations
Astrotactin-2NeurogenesisSchizophrenia

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2017
Highly Cited
2017
Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia
  • Richard J. L. Stephan Verneri Jakob Peter Hailiang Lambert Anney Ripke Anttila Grove Holmans Huang Klei Lee M, Richard Anney, +160 authors Mark J. Daly
  • Molecular Autism
  • 2017
    • Corpus ID: 4243803
Over the past decade genome-wide association studies (GWAS) have been applied to aid in the understanding of the biology of… Expand
  • table 1
  • figure 1
  • figure 2
  • table 2
  • table 3
Is this relevant?
Highly Cited
2017
Highly Cited
2017
Novel genetic loci associated with hippocampal volume
The hippocampal formation is a brain structure integrally involved in episodic memory, spatial navigation, cognition and stress… Expand
  • figure 1
  • figure 2
  • figure 3
  • table 1
Is this relevant?
Highly Cited
2014
Highly Cited
2014
Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes.
Rare copy number variants (CNVs) disrupting ASTN2 or both ASTN2 and TRIM32 have been reported at 9q33.1 by genome-wide studies in… Expand
  • table 1
  • figure 1
  • figure 2
  • table 2
  • figure 3
Is this relevant?
Highly Cited
2012
Highly Cited
2012
Identification of new susceptibility loci for osteoarthritis (arcOGEN): a genome-wide association study
Summary Background Osteoarthritis is the most common form of arthritis worldwide and is a major cause of pain and disability in… Expand
  • table 1
  • table 2
Is this relevant?
Highly Cited
2012
Highly Cited
2012
Common variants at 12q14 and 12q24 are associated with hippocampal volume
Aging is associated with reductions in hippocampal volume that are accelerated by Alzheimer's disease and vascular risk factors… Expand
  • figure 1
  • figure 2
  • figure 3
Is this relevant?
Highly Cited
2011
Highly Cited
2011
Rare copy number variation discovery and cross-disorder comparisons identify risk genes for ADHD.
Attention deficit hyperactivity disorder (ADHD) is a common and persistent condition characterized by developmentally atypical… Expand
Is this relevant?
Highly Cited
2010
Highly Cited
2010
Astn2, a novel member of the astrotactin gene family, regulates the trafficking of ASTN1 during glial-guided neuronal migration.
Glial-guided neuronal migration is a key step in the development of laminar architecture of cortical regions of the mammalian… Expand
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 5
Is this relevant?
Highly Cited
2009
Highly Cited
2009
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes
Autism spectrum disorders (ASDs) are childhood neurodevelopmental disorders with complex genetic origins. Previous studies… Expand
  • table 1
  • table 2
  • figure 1
  • figure 2
Is this relevant?
Highly Cited
2008
Highly Cited
2008
Recurrent CNVs disrupt three candidate genes in schizophrenia patients.
Schizophrenia is a severe psychiatric disease with complex etiology, affecting approximately 1% of the general population. Most… Expand
Is this relevant?
Highly Cited
2008
Highly Cited
2008
Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies
A genome-wide association (GWA) study with pooled DNA in adult attention-deficit/hyperactivity disorder (ADHD) employing ~500K… Expand
  • table 1
  • figure 1
  • table 2
  • figure 2
Is this relevant?
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy, Terms of Service, and Dataset License
ACCEPT & CONTINUE