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8q24.3

A chromosome band present on 8q
National Institutes of Health

Papers overview

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Highly Cited
2013
Highly Cited
2013
Copy-number variants (CNVs) represent a significant interpretative challenge, given that each CNV typically affects the dosage of… Expand
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Highly Cited
2010
Highly Cited
2010
Recurrent chromosomal aberrations are often observed in hepatocellular carcinoma (HCC), but little is known about the functional… Expand
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Highly Cited
2010
Highly Cited
2010
We conducted a multi-stage, genome-wide association study of bladder cancer with a primary scan of 591,637 SNPs in 3,532 affected… Expand
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Highly Cited
2003
Highly Cited
2003
Representational difference analysis (RDA) of human breast cancer was used to discover a novel amplicon located at chromosomal… Expand
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Highly Cited
2001
Highly Cited
2001
To gain insights into the molecular basis for metastasis, we compared the global gene expression profile of metastatic colorectal… Expand
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Highly Cited
2001
Highly Cited
2001
Acrodermatitis enteropathica (AE) is a rare autosomal recessive pediatric disease characterized by dermatitis, diarrhea, alopecia… Expand
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Highly Cited
1999
Highly Cited
1999
Rothmund-Thomson syndrome (RTS; also known as poikiloderma congenitale) is a rare, autosomal recessive genetic disorder… Expand
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Highly Cited
1998
Highly Cited
1998
Wnt family members are critical to many developmental processes, and components of the Wnt signaling pathway have been linked to… Expand
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Highly Cited
1998
Highly Cited
1998
Through a differential screening technique, we have identified a cDNA clone with differential expression in normal versus tumor… Expand
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Highly Cited
1998
Highly Cited
1998
Aldosterone synthase (AS) is encoded by the CYP11B2 gene, a candidate for familial hypertension. CYP11B2 was previously mapped to… Expand
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