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ASTN2 gene
Known as:
ASTN2
, Astrotactin 2 Gene
, ASTROTACTIN 2
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This gene may play a role in neural development.
National Institutes of Health
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Related topics
Related topics
3 relations
Astrotactin-2
Neurogenesis
Schizophrenia
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2017
Highly Cited
2017
Corrigendum: 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function
M. Gorski
,
P. J. Most
,
+123 authors
C. Fuchsberger
Scientific reports
2017
Corpus ID: 52856661
This corrects the article DOI: 10.1038/srep45040.
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
,
R. Anney
,
+160 authors
M. 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…
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Highly Cited
2015
Highly Cited
2015
Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation
M. S. Artigas
,
L. Wain
,
+96 authors
M. Tobin
Nature communications
2015
Corpus ID: 15488955
Lung function measures are used in the diagnosis of chronic obstructive pulmonary disease. In 38,199 European ancestry…
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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.
A. C. Lionel
,
K. Tammimies
,
+81 authors
S. Scherer
Human molecular genetics
2014
Corpus ID: 12528045
Rare copy number variants (CNVs) disrupting ASTN2 or both ASTN2 and TRIM32 have been reported at 9q33.1 by genome-wide studies in…
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Highly Cited
2012
Highly Cited
2012
Identification of new susceptibility loci for osteoarthritis (arcOGEN): a genome-wide association study
E. Zeggini
,
K. Panoutsopoulou
,
+73 authors
J. Loughlin
The Lancet
2012
Corpus ID: 12875446
Highly Cited
2011
Highly Cited
2011
Rare Copy Number Variation Discovery and Cross-Disorder Comparisons Identify Risk Genes for ADHD
A. C. Lionel
,
J. Crosbie
,
+22 authors
S. Scherer
Science Translational Medicine
2011
Corpus ID: 21521749
A high-resolution analysis of copy number variation in patients with ADHD reveals new gene associations, few de novo mutations…
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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
P. Wilson
,
R. Fryer
,
Yin Fang
,
M. Hatten
The Journal of Neuroscience
2010
Corpus ID: 14877823
Glial-guided neuronal migration is a key step in the development of laminar architecture of cortical regions of the mammalian…
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Highly Cited
2009
Highly Cited
2009
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes
J. Glessner
,
Kai Wang
,
+56 authors
H. Hakonarson
Nature
2009
Corpus ID: 2748240
Autism spectrum disorders (ASDs) are childhood neurodevelopmental disorders with complex genetic origins. Previous studies…
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Highly Cited
2008
Highly Cited
2008
Recurrent CNVs disrupt three candidate genes in schizophrenia patients.
T. Vrijenhoek
,
J. Buizer-Voskamp
,
+6 authors
J. Veltman
American journal of human genetics
2008
Corpus ID: 27883497
Highly Cited
2008
Highly Cited
2008
Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies
K. Lesch
,
N. Timmesfeld
,
+15 authors
C. Jacob
Journal of Neural Transmission
2008
Corpus ID: 7036114
A genome-wide association (GWA) study with pooled DNA in adult attention-deficit/hyperactivity disorder (ADHD) employing ~500K…
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