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10q11

A chromosome band present on 10q
National Institutes of Health

Papers overview

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Review
2011
Review
2011
AIMS Two single-nucleotide polymorphisms (SNPs), rs1746048 and rs501120, from genome wide association studies of coronary artery… Expand
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Highly Cited
2010
Highly Cited
2010
Genome-wide association studies (GWAS) have established a variant, rs10993994, on chromosome 10q11 as being associated with… Expand
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Highly Cited
2010
Highly Cited
2010
Sequence variants in the human genome are associated with serum levels of prostate-specific antigen. SNPping Away at Prostate… Expand
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2010
2010
OBJECTIVE To investigate whether chromosome 10q11.21 influences common carotid intima-media thickness (IMT) and atherosclerosis… Expand
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Highly Cited
2009
Highly Cited
2009
We conducted a genome-wide association study testing single nucleotide polymorphisms (SNPs) and copy number variants (CNVs) for… Expand
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Highly Cited
2009
Highly Cited
2009
A single nucleotide polymorphism (SNP) at 10q11 (rs10993994) in the 5' region of the MSMB gene was recently implicated in… Expand
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Highly Cited
2004
Highly Cited
2004
Osteosarcoma (OS) is a highly malignant bone neoplasm of children and young adults. It is characterized by chaotic karyotypes… Expand
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Highly Cited
2002
Highly Cited
2002
Genetic studies of Hirschsprung disease, a common congenital malformation, have identified eight genes with mutations that can be… Expand
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Highly Cited
2002
Highly Cited
2002
Hirschsprung disease (HSCR), the most common hereditary cause of intestinal obstruction, shows considerable variation and complex… Expand
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Highly Cited
1996
Highly Cited
1996
Hereditary hyperparathyroidism-jaw tumor syndrome (HPT-JT) is an autosomal dominant disease (OMIM 145001) that has recently been… Expand
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