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14q13.3

Part of the chromosome bands present on the long (q) arm of chromosome 14.
National Institutes of Health

Papers overview

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2016
2016
Few high penetrance variants that explain risk in late‐onset Alzheimer's disease (LOAD) families have been found. 
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Highly Cited
2012
Highly Cited
2012
Aim  Chromosome microarray (CMA) can determine copy number variants such as microdeletions or microduplications. Microdeletions… Expand
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Highly Cited
2012
Highly Cited
2012
A genome-wide association study of papillary thyroid carcinoma (PTC) pinpointed two independent SNPs (rs944289 and rs965513… Expand
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Highly Cited
2012
Highly Cited
2012
To search for sequence variants conferring risk of nonmedullary thyroid cancer, we focused our analysis on 22 SNPs with a P < 5… Expand
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2010
2010
Purpose: Because loss of Nkx2-8 increases lung cancer in the mouse, we studied suppressive mechanisms in human lung cancer… Expand
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Highly Cited
2009
Highly Cited
2009
In order to search for sequence variants conferring risk of thyroid cancer we conducted a genome-wide association study in 192… Expand
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Highly Cited
2009
Highly Cited
2009
Acquired chromosomal aberrations play an important role in tumour development and progression. Such genetic alterations occur in… Expand
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Highly Cited
2008
Highly Cited
2008
Lung cancer is a leading cause of cancer death, where the amplification of oncogenes contributes to tumorigenesis. Genomic… Expand
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Highly Cited
2007
Highly Cited
2007
Somatic alterations in cellular DNA underlie almost all human cancers. The prospect of targeted therapies and the development of… Expand
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Highly Cited
2007
Highly Cited
2007
  • J. Kendall, Q. Liu, +6 authors D. Mu
  • Proceedings of the National Academy of Sciences
  • 2007
  • Corpus ID: 15785642
We used high-resolution array analysis to discover a recurrent lung cancer amplicon located at 14q13.3. Low-level gain of this… Expand
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