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15q22.33
Part of the chromosome bands present on the long (q) arm of chromosome 15.
National Institutes of Health
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2 relations
15q
Chromosomes
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Atopic asthma after rhinovirus‐induced wheezing is associated with DNA methylation change in the SMAD3 gene promoter
R. Lund
,
Maria Osmala
,
+13 authors
T. Jartti
Allergy. European Journal of Allergy and Clinical…
2018
Corpus ID: 19083407
Children with rhinovirus‐induced severe early wheezing have an increased risk of developing asthma later in life. The exact…
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Highly Cited
2017
Highly Cited
2017
A genome-wide association study yields five novel thyroid cancer risk loci
J. Gudmundsson
,
G. Thorleifsson
,
+37 authors
K. Stefánsson
Nature Communications
2017
Corpus ID: 196776
The great majority of thyroid cancers are of the non-medullary type. Here we report findings from a genome-wide association study…
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2014
2014
The impact of coronary artery disease risk loci on ischemic heart failure severity and prognosis: association analysis in the COntrolled ROsuvastatin multiNAtional trial in heart failure (CORONA)
Vincent G. Haver
,
N. Verweij
,
+7 authors
P. van der Harst
BMC Medical Genetics
2014
Corpus ID: 1432799
BackgroundRecent genome-wide association studies have identified multiple loci that are associated with an increased risk of…
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2011
2011
Replication of Putative Susceptibility Loci from Genome-Wide Association Studies Associated with Coronary Atherosclerosis in Chinese Han Population
Fang Xie
,
X. Chu
,
+7 authors
Wei Huang
PLoS ONE
2011
Corpus ID: 404331
Background Coronary atherosclerosis, the main cause of cardiovascular disease, is a progressive disease. Recent Genome Wide…
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2009
2009
Exclusion of known corneal dystrophy genes in an autosomal dominant pedigree of a unique anterior membrane corneal dystrophy
A. Vincent
,
D. Markie
,
+4 authors
C. McGhee
Molecular Vision
2009
Corpus ID: 15608004
Purpose With advances in phenotyping tools and availability of molecular characterization, an increasing number of phenotypically…
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2008
2008
Genome-wide association analysis with selective genotyping identifies candidate loci for adult height at 8q21.13 and 15q22.33-q23 in Mongolians
Tetsuaki Kimura
,
Terukazu Kobayashi
,
+10 authors
H. Inoko
Human Genetics
2008
Corpus ID: 15477481
We performed a genome-wide association study with 23,465 microsatellite markers to identify genes related to adult height…
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Highly Cited
2007
Highly Cited
2007
Genomewide association analysis of coronary artery disease.
N. Samani
,
J. Erdmann
,
+31 authors
H. Schunkert
New England Journal of Medicine
2007
Corpus ID: 9786737
BACKGROUND Modern genotyping platforms permit a systematic search for inherited components of complex diseases. We performed a…
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2004
2004
Correlation of Major Cytogenetic Response with a Pharmacogenetic Marker in Chronic Myeloid Leukemia Patients Treated with Imatinib (STI571)
M. Dressman
,
R. Malinowski
,
+4 authors
M. Polymeropoulos
Clinical Cancer Research
2004
Corpus ID: 2283320
Purpose: Imatinib, an inhibitor of the Bcr-Abl tyrosine kinase, is indicated for the treatment of patients with Philadelphia…
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2000
2000
Assignment1 of the NR2E3 gene to mouse chromosome 9 and to human chromosome 15q22.33→q23
N. D. Rendtorff
,
H. Vissing
,
Z. Tümer
,
A. Silahtaroglu
,
N. Tommerup
Cytogenetic and Genome Research
2000
Corpus ID: 34825159
Supported by grants from the Danish Biotechnological Research and Development Program 1996–1998, the Danish Cancer Society, the…
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1997
1997
Assignment of the gene for ERC-55 (RCN2) to human chromosome band 15q22.33-->q24.1 by in situ hybridization.
J. Y. Wang
,
D. Zhen
,
D. Bianchi
,
E. Androphy
,
J. J. Chen
Cytogenetics and Cell Genetics
1997
Corpus ID: 46847024
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