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11q13.5
A chromosome band present on 11q
National Institutes of Health
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Related topics
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4 relations
ACER3 wt Allele
Chromosomes
UVRAG wt Allele
chromosome 11q
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Targeted Resequencing and Functional Testing Identifies Low-Frequency Missense Variants in the Gene Encoding GARP as Significant Contributors to Atopic Dermatitis Risk.
Judith Manz
,
E. Rodriguez
,
+11 authors
S. Weidinger
Journal of Investigative Dermatology
2016
Corpus ID: 25426243
Highly Cited
2011
Highly Cited
2011
META-ANALYSIS OF GENOME-WIDE ASSOCIATION STUDIES IDENTIFIES THREE NEW RISK LOCI FOR ATOPIC DERMATITIS
L. Paternoster
,
M. Standl
,
+106 authors
S. Weidinger
Nature Genetics
2011
Corpus ID: 1362495
Atopic dermatitis (AD) is a commonly occurring chronic skin disease with high heritability. Apart from filaggrin (FLG), the genes…
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Highly Cited
2009
Highly Cited
2009
A common variant on chromosome 11q13 is associated with atopic dermatitis
J. Esparza-Gordillo
,
S. Weidinger
,
+24 authors
A. Ruether
Nature Genetics
2009
Corpus ID: 205350994
We conducted a genome-wide association study in 939 individuals with atopic dermatitis and 975 controls as well as 270 complete…
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Highly Cited
2009
Highly Cited
2009
Functional analysis of 11q13.5 amplicon identifies Rsf-1 (HBXAP) as a gene involved in paclitaxel resistance in ovarian cancer.
Jung-Hye Choi
,
J. Sheu
,
+4 authors
I. Shih
Cancer Research
2009
Corpus ID: 1739272
The chromosome 11q13.5 locus is frequently amplified in several types of human cancer. We have previously shown that 11q13.5…
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Highly Cited
2006
Highly Cited
2006
Amplification of EMSY, a novel oncogene on 11q13, in high grade ovarian surface epithelial carcinomas.
Lindsay A. Brown
,
J. Irving
,
+9 authors
D. Huntsman
Gynecologic Oncology
2006
Corpus ID: 28473362
Highly Cited
2006
Highly Cited
2006
MYO7A mutation screening in Usher syndrome type I patients from diverse origins
T. Jaijo
,
E. Aller
,
+10 authors
J. M. Millán
Journal of Medical Genetics
2006
Corpus ID: 3026905
Usher syndrome (USH) (OMIM 276901) is an autosomal recessive disorder characterised by hearing impairment associated with…
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Highly Cited
2005
Highly Cited
2005
Amplification of a chromatin remodeling gene, Rsf-1/HBXAP, in ovarian carcinoma.
I. Shih
,
J. Sheu
,
+9 authors
Tian-Li Wang
Proceedings of the National Academy of Sciences…
2005
Corpus ID: 33025685
A genomewide technology, digital karyotyping, was used to identify subchromosomal alterations in ovarian cancer. Amplification at…
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Highly Cited
2004
Highly Cited
2004
Prevention of venous thromboembolism with low molecular-weight heparin in patients with multiple myeloma treated with thalidomide and chemotherapy
Monique C. Minnema
,
Iris Breitkreutz
,
+7 authors
H. Lokhorst
Leukemia
2004
Corpus ID: 6851900
Prevention of venous thromboembolism with low molecular-weight heparin in patients with multiple myeloma treated with thalidomide…
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2003
2003
11q13 Alterations in two cases of hibernoma: Large heterozygous deletions and rearrangement breakpoints near GARP in 11q13.5
G. Maire
,
A. Forus
,
+5 authors
F. Pedeutour
Genes, Chromosomes and Cancer
2003
Corpus ID: 13606852
Hibernomas are rare, benign tumors with a histological appearance resembling that of brown adipose tissue. The diagnosis of…
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Highly Cited
1997
Highly Cited
1997
Detailed map of a region commonly amplified at 11q13-->q14 in human breast carcinoma.
S. Bekri
,
J. Adélaı̈de
,
+9 authors
P. Gaudray
Cytogenetics and Cell Genetics
1997
Corpus ID: 46855966
Amplification of loci present on band q13 of human chromosome 11 is a feature of a subset of estrogen receptor positive breast…
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