FAQ

ASTN2 gene

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

Topic mentions per year

Topic mentions per year

2005-2016
02420052016

Related topics

Related topics

3 relations
Astrotactin-2NeurogenesisSchizophrenia

Related mentions per year

Related mentions per year

1936-2018
19401960198020002020
ASTN2 gene
Schizophrenia
Neurogenesis
Astrotactin-2

Papers overview

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2014
2014
Polymorphisms within ASTN2 gene are associated with age at onset of Alzheimer’s disease
Alzheimer’s disease (AD) is a multifactorial neurological condition associated with genetic profiles that are still not… (More)
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2014
2014
Accurate gene expression-based biodosimetry using a minimal set of human gene transcripts.
PURPOSE Rapid and reliable methods for conducting biological dosimetry are a necessity in the event of a large-scale nuclear… (More)
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2014
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… (More)
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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… (More)
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Highly Cited
2012
Highly Cited
2012
Identification of new susceptibility loci for osteoarthritis (arcOGEN): a genome-wide association study
BACKGROUND Osteoarthritis is the most common form of arthritis worldwide and is a major cause of pain and disability in elderly… (More)
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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… (More)
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2010
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… (More)
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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… (More)
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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… (More)
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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… (More)
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