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15q15.2

A chromosome band present on 15q
National Institutes of Health

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4 relations
15qCDAN1 wt AlleleChromosomesUSP8 wt Allele

Papers overview

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2016
2016
Abstract 5229: Candidate gene analysis of exome sequencing data in smokers susceptible and resistant to chronic obstructive pulmonary disease
Background: Chronic obstructive pulmonary disease (COPD) is a major comorbidity for Lung cancer (LC), the presence of COPD… Expand
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2015
2015
Implication of a Chromosome 15q15.2 Locus in Regulating UBR1 and Predisposing Smokers to MGMT Methylation in Lung.
O(6)-Methylguanine-DNA methyltransferase (MGMT) is a DNA repair enzyme that protects cells from carcinogenic effects of… Expand
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2011
2011
Genome-wide significant association between a sequence variant at 15q15.2 and lung cancer risk.
Genome-wide association studies (GWAS) have identified 3 genomic regions, at 15q24-25.1, 5p15.33, and 6p21.33, which associate… Expand
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Highly Cited
2009
Highly Cited
2009
Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study.
To explore the impact of common variation on the risk of developing lung cancer, we conducted a two-phase genome-wide association… Expand
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2008
2008
Craniosynostosis in a patient with a de novo 15q15-q22 deletion.
Interstitial deletions involving the chromosomal band 15q15 are very rare. A total of five cases were previously reported. Here… Expand
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Highly Cited
2005
Highly Cited
2005
A homozygous missense mutation in TGM5 abolishes epidermal transglutaminase 5 activity and causes acral peeling skin syndrome.
Peeling skin syndrome is an autosomal recessive genodermatosis characterized by the shedding of the outer epidermis. In the acral… Expand
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Highly Cited
2001
Highly Cited
2001
Evolution of Transglutaminase Genes: Identification of a Transglutaminase Gene Cluster on Human Chromosome 15q15
We isolated and characterized the gene encoding human transglutaminase (TG)X(TGM5) and mapped it to the 15q15.2 region of… Expand
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2001
2001
The C/At is out of the bag: a gene for mental illness
  • M-L Wong
  • The Pharmacogenomics Journal
  • 2001
    • Corpus ID: 5750492
Has the first ‘schizophrenia’ gene been identified? The knowledge that genes play a considerable role in the etiology of… Expand
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1995
1995
An STS map of the limb girdle muscular dystrophy type 2A region
A gene for the recessive limb girdle muscular dystrophy LGMD2A (MIM 253600) was mapped within a 7-cM interval along Chromosome… Expand
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