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15q15.2

A chromosome band present on 15q
National Institutes of Health

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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… 
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… 
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… 
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… 
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… 
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… 
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… 
2001
2001
The C/At is out of the bag: a gene for mental illness
Has the first ‘schizophrenia’ gene been identified? The knowledge that genes play a considerable role in the etiology of… 
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… 
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