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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
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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2009
2009
A recent genome-wide association study suggested seven new loci as associated with prostate cancer susceptibility. The strongest… Expand
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Highly Cited
2004
Highly Cited
2004
  • Ching C. Lau, Charles P. Harris, +11 authors Pulivarthi H. Rao
  • Genes, chromosomes & cancer
  • 2004
  • Corpus ID: 35648718
Osteosarcoma (OS) is a highly malignant bone neoplasm of children and young adults. It is characterized by chaotic karyotypes… Expand
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
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
1999
Highly Cited
1999
Little is known about sequence organization close to human centromeres, despite empirical and theoretical data which suggest that… 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