Rare NRXN1 promoter variants in patients with schizophrenia (Q33821726)

29 July 2017

Rare NRXN1 promoter variants in patients with schizophrenia (English)

1 reference

29 July 2017

1 reference

Abhishek K Shah

1

1 reference

29 July 2017

Nina M Tioleco

2

1 reference

29 July 2017

Karen Nolan

3

1 reference

29 July 2017

Joseph Locker

4

1 reference

29 July 2017

Katherine Groh

5

1 reference

29 July 2017

Catalina Villa

6

1 reference

29 July 2017

Pavla Stopkova

7

1 reference

29 July 2017

Erika Pedrosa

8

1 reference

29 July 2017

Herbert M Lachman

9

1 reference

29 July 2017

language of work or name

English

0 references

publication date

25 March 2010

1 reference

29 July 2017

5

1 reference

based on heuristic

inferred from page(s)

published in

Neuroscience Letters

1 reference

29 July 2017

475

1 reference

29 July 2017

2

1 reference

29 July 2017

80-84

1 reference

ChIP-chip analysis of neurexins and other candidate genes for addiction and neuropsychiatric disorders

29 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862389

Common variants in polygenic schizophrenia.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862389

Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862389

Schizophrenia genetics: advancing on two fronts

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862389

A genome-wide investigation of SNPs and CNVs in schizophrenia

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862389

Disruption of the neurexin 1 gene is associated with schizophrenia

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862389

Recurrent CNVs disrupt three candidate genes in schizophrenia patients

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862389

Expression of Runx2 transcription factor in non-skeletal tissues, sperm and brain

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862389

Neurexin 1alpha structural variants associated with autism

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862389

Significant association of the neurexin-1 gene (NRXN1) with nicotine dependence in European- and African-American smokers

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862389

Structural variation of chromosomes in autism spectrum disorder

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862389

Induction of GABAergic postsynaptic differentiation by alpha-neurexins

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862389

Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862389

Regulation of the GABA cell phenotype in hippocampus of schizophrenics and bipolars

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862389

Genomewide suggestive linkage of opioid dependence to chromosome 14q.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862389

The neuroligin and neurexin families: from structure to function at the synapse

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862389

The transcription factor regulatory factor X1 increases the expression of neuronal glutamate transporter type 3.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862389

Preliminary investigation of gene expression profiles in peripheral blood lymphocytes in schizophrenia

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862389

Alpha-neurexins couple Ca2+ channels to synaptic vesicle exocytosis

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862389

Copy number variation in schizophrenia in the Japanese population

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862389

Proto-oncogene FBI-1 (Pokemon) and SREBP-1 synergistically activate transcription of fatty-acid synthase gene (FASN).

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862389

Association of missense variants of the PRKC, apoptosis, WT1, regulator (PAWR) gene with schizophrenia

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862389

Disruption of neurexin 1 associated with autism spectrum disorder

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862389

Deletion of alpha-neurexins does not cause a major impairment of axonal pathfinding or synapse formation.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862389

Novel genes identified in a high-density genome wide association study for nicotine dependence

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862389

Addiction molecular genetics: 639,401 SNP whole genome association identifies many "cell adhesion" genes

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862389

Position-dependent repression and promotion of DQB1 intron 3 splicing by GGGG motifs

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862389

Characterization of an intron splice enhancer that regulates alternative splicing of human GH pre-mRNA.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862389

c-Myb Is Required for Neural Progenitor Cell Proliferation and Maintenance of the Neural Stem Cell Niche in Adult Brain

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862389

CDKN1C mutation in Wiedemann-Beckwith syndrome patients reduces RNA splicing efficiency and identifies a splicing enhancer

29 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20347009

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.NEULET.2010.03.047

1 reference

29 July 2017

1 reference

29 July 2017

1 reference