Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 210,223,306 papers from all fields of science
Search
Sign In
Create Free Account
NRXN2 gene
Known as:
Neurexin 2 Gene
, NRXN2
, neurexin 2
Expand
This gene may play a role in cell adhesion.
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
6 relations
Cell Adhesion
Ligand Binding
Neurexin-2, human
Signal Transduction
Expand
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2017
Review
2017
Neurexins and neuropsychiatric disorders
Enas A. Kasem
,
Taiga Kurihara
,
K. Tabuchi
Neurosciences research
2017
Corpus ID: 207154295
Highly Cited
2015
Highly Cited
2015
Genetic targeting of NRXN2 in mice unveils role in excitatory cortical synapse function and social behaviors
Gesche Born
,
H. Grayton
,
+6 authors
M. Missler
Frontiers in Synaptic Neuroscience
2015
Corpus ID: 15153117
Human genetics has identified rare copy number variations and deleterious mutations for all neurexin genes (NRXN1-3) in patients…
Expand
Highly Cited
2015
Highly Cited
2015
Heterozygous Deletion of α-Neurexin I or α-Neurexin II Results in Behaviors Relevant to Autism and Schizophrenia
J. Dachtler
,
J. L. Ivorra
,
T. Rowland
,
C. Lever
,
R. Rodgers
,
S. Clapcote
Behavioral Neuroscience
2015
Corpus ID: 15127733
The neurexins are a family of presynaptic cell adhesion molecules. Human genetic studies have found heterozygous deletions…
Expand
Highly Cited
2014
Highly Cited
2014
SMN deficiency alters Nrxn2 expression and splicing in zebrafish and mouse models of spinal muscular atrophy.
K. See
,
Preeti Yadav
,
+8 authors
C. Winkler
Human Molecular Genetics
2014
Corpus ID: 189865
Spinal muscular atrophy (SMA) is a progressive neurodegenerative disease affecting lower motor neurons. SMA is caused by…
Expand
Highly Cited
2012
Highly Cited
2012
Rare deletions at the neurexin 3 locus in autism spectrum disorder.
A. Vaags
,
A. C. Lionel
,
+24 authors
S. Scherer
American Journal of Human Genetics
2012
Corpus ID: 2979632
Highly Cited
2011
Highly Cited
2011
Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia
J. Gauthier
,
Tabrez J. Siddiqui
,
+18 authors
G. Rouleau
Human Genetics
2011
Corpus ID: 31196781
Growing genetic evidence is converging in favor of common pathogenic mechanisms for autism spectrum disorders (ASD), intellectual…
Expand
Highly Cited
2009
Highly Cited
2009
Disruption of the neurexin 1 gene is associated with schizophrenia.
D. Rujescu
,
A. Ingason
,
+49 authors
D. Collier
Human Molecular Genetics
2009
Corpus ID: 13928932
Deletions within the neurexin 1 gene (NRXN1; 2p16.3) are associated with autism and have also been reported in two families with…
Expand
Highly Cited
2009
Highly Cited
2009
Prenatal exposure to valproic acid leads to reduced expression of synaptic adhesion molecule neuroligin 3 in mice
E. Kolozsi
,
R. N. MacKenzie
,
F. Roullet
,
D. deCatanzaro
,
J. Foster
Neuroscience
2009
Corpus ID: 10759425
Highly Cited
2009
Highly Cited
2009
LAD-1/variant syndrome is caused by mutations in FERMT3.
T. Kuijpers
,
Edith van de Vijver
,
+12 authors
F. Baas
Blood
2009
Corpus ID: 16062006
Leukocyte adhesion deficiency-1/variant (LAD1v) syndrome presents early in life and manifests by infections without pus formation…
Expand
2007
2007
Ca2+ -dependent splicing of neurexin IIalpha.
G. Rozic-Kotliroff
,
N. Zisapel
Biochemical and Biophysical Research…
2007
Corpus ID: 9951749
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE