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15q24
A chromosome band present on 15q
National Institutes of Health
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Related topics
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9 relations
15q
ARNT2 wt Allele
CHRNA5 wt Allele
CHRNB4 wt Allele
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2011
Highly Cited
2011
Genome-Wide Meta-Analysis Identifies Regions on 7p21 (AHR) and 15q24 (CYP1A2) As Determinants of Habitual Caffeine Consumption
PLoS Genetics
2011
Corpus ID: 13759165
We report the first genome-wide association study of habitual caffeine intake. We included 47,341 individuals of European descent…
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Highly Cited
2011
Highly Cited
2011
Sequence variants at CYP1A1-CYP1A2 and AHR associate with coffee consumption.
P. Sulem
,
D. Gudbjartsson
,
+31 authors
K. Stefánsson
Human Molecular Genetics
2011
Corpus ID: 6880211
Coffee is the most commonly used stimulant and caffeine is its main psychoactive ingredient. The heritability of coffee…
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Highly Cited
2010
Highly Cited
2010
Identifying loci for the overlap between attention-deficit/hyperactivity disorder and autism spectrum disorder using a genome-wide QTL linkage approach.
J. Nijmeijer
,
A. Arias-Vásquez
,
+23 authors
P. Hoekstra
Journal of the American Academy of Child and…
2010
Corpus ID: 28542160
Highly Cited
2008
Highly Cited
2008
Familial aggregation of common sequence variants on 15q24-25.1 in lung cancer.
Pengyuan Liu
,
H. Vikis
,
+26 authors
M. You
Journal of the National Cancer Institute
2008
Corpus ID: 7386832
Three recent genome-wide association studies identified associations between markers in the chromosomal region 15q24-25.1 and the…
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2003
2003
DNA copy number changes detected by comparative genomic hybridization and their association with clinicopathologic parameters in breast tumors.
Sultan Cingoz
,
O. Altungoz
,
T. Canda
,
S. Saydam
,
G. Aksakoğlu
,
M. Sakızlı
Cancer Genetics and Cytogenetics
2003
Corpus ID: 26057272
Highly Cited
2001
Highly Cited
2001
A Polymorphic Genomic Duplication on Human Chromosome 15 Is a Susceptibility Factor for Panic and Phobic Disorders
M. Gratacós
,
M. Nadal
,
+8 authors
X. Estivill
Cell
2001
Corpus ID: 14401895
Highly Cited
2001
Highly Cited
2001
Deletion 15q24‐26 in prenatally detected diaphragmatic hernia: increasing evidence of a candidate region for diaphragmatic development
D. Schlembach
,
M. Zenker
,
U. Trautmann
,
R. Ulmer
,
E. Beinder
Prenatal Diagnosis
2001
Corpus ID: 37090518
Survival of children with congenital diaphragmatic hernia (CDH) is mainly dependent on the extent of lung hypoplasia and the…
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Highly Cited
2000
Highly Cited
2000
Genetic imbalances with impact on survival in head and neck cancer patients.
U. Bockmühl
,
K. Schlüns
,
I. Küchler
,
S. Petersen
,
I. Petersen
American Journal of Pathology
2000
Corpus ID: 40389548
Highly Cited
1998
Highly Cited
1998
Autosomal dominant nocturnal frontal-lobe epilepsy: genetic heterogeneity and evidence for a second locus at 15q24.
H. Phillips
,
I. Scheffer
,
+15 authors
J. Mulley
American Journal of Human Genetics
1998
Corpus ID: 31521910
Autosomal dominant nocturnal frontal-lobe epilepsy (ADNFLE) is a recently identified partial epilepsy in which two different…
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1987
1987
Monosomy and trisomy of 15q24→qter in a family with a translocation t(6;15)(P25;q24)
U. Kristoffersson
,
S. Heim
,
N. Mandahl
,
Lennart Sundkvist
,
Jan Szelest
,
I. Hägerstrand
Clinical Genetics
1987
Corpus ID: 35723497
A child with multiple anomalies, including growth retardation, a left‐sided diaphragmatic hernia with lung hypoplasia, and…
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