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15q15.2
A chromosome band present on 15q
National Institutes of Health
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4 relations
15q
CDAN1 wt Allele
Chromosomes
USP8 wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Abstract 5229: Candidate gene analysis of exome sequencing data in smokers susceptible and resistant to chronic obstructive pulmonary disease
Yanhong Liu
,
M. Cho
,
+8 authors
M. Spitz
2016
Corpus ID: 78629249
Background: Chronic obstructive pulmonary disease (COPD) is a major comorbidity for Lung cancer (LC), the presence of COPD…
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2015
2015
Implication of a Chromosome 15q15.2 Locus in Regulating UBR1 and Predisposing Smokers to MGMT Methylation in Lung.
S. Leng
,
Guodong Wu
,
+16 authors
S. Belinsky
Cancer Research
2015
Corpus ID: 5787080
O(6)-Methylguanine-DNA methyltransferase (MGMT) is a DNA repair enzyme that protects cells from carcinogenic effects of…
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2011
2011
Genome-wide significant association between a sequence variant at 15q15.2 and lung cancer risk.
T. Rafnar
,
P. Sulem
,
+29 authors
K. Stefánsson
Cancer Research
2011
Corpus ID: 6874387
Genome-wide association studies (GWAS) have identified 3 genomic regions, at 15q24-25.1, 5p15.33, and 6p21.33, which associate…
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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.
P. Broderick
,
Yufei Wang
,
+5 authors
R. Houlston
Cancer Research
2009
Corpus ID: 6204967
To explore the impact of common variation on the risk of developing lung cancer, we conducted a two-phase genome-wide association…
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2008
2008
Craniosynostosis in a patient with a de novo 15q15‐q22 deletion
Y. Hiraki
,
Miyuki Moriuchi
,
+8 authors
N. Matsumoto
American Journal of Medical Genetics. Part A
2008
Corpus ID: 35356291
Interstitial deletions involving the chromosomal band 15q15 are very rare. A total of five cases were previously reported. Here…
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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.
A. Cassidy
,
M. V. van Steensel
,
+7 authors
W. McLean
American Journal of Human Genetics
2005
Corpus ID: 45217057
Peeling skin syndrome is an autosomal recessive genodermatosis characterized by the shedding of the outer epidermis. In the acral…
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Highly Cited
2001
Highly Cited
2001
Evolution of Transglutaminase Genes: Identification of a Transglutaminase Gene Cluster on Human Chromosome 15q15
P. Grenard
,
Margaret Bates
,
D. Aeschlimann
Journal of Biological Chemistry
2001
Corpus ID: 24276644
We isolated and characterized the gene encoding human transglutaminase (TG)X(TGM5) and mapped it to the 15q15.2 region of…
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2001
2001
The C/At is out of the bag: a gene for mental illness
Melissa 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…
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1995
1995
An STS map of the limb girdle muscular dystrophy type 2A region
I. Richard
,
C. Roudaut
,
F. Fougerousse
,
N. Chiannilkulchai
,
J. Beckmann
Mammalian Genome
1995
Corpus ID: 38576980
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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