18q21.1

A chromosome band present on 18q
National Institutes of Health

Papers overview

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Highly Cited
2010
Highly Cited
2010
To identify new risk variants for chronic lymphocytic leukemia (CLL), we conducted a genome-wide association study of 299,983… (More)
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Highly Cited
2009
Highly Cited
2009
While conventional LDL-C, HDL-C, and triglyceride measurements reflect aggregate properties of plasma lipoprotein fractions, NMR… (More)
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Highly Cited
2007
Highly Cited
2007
Pitt-Hopkins syndrome (PHS) is a rare syndromic encephalopathy characterized by daily bouts of hyperventilation and a facial… (More)
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Highly Cited
2001
Highly Cited
2001
Juvenile polyposis (JP; OMIM 174900) is an autosomal dominant gastrointestinal hamartomatous polyposis syndrome in which patients… (More)
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Highly Cited
1998
Highly Cited
1998
Familial juvenile polyposis is an autosomal dominant disease characterized by a predisposition to hamartomatous polyps and… (More)
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1998
1998
Familial juvenile polyposis (FJP) is a hamartomatouspolyposis syndrome in which affected family members develop upper and lower… (More)
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1997
1997
There are currently 13 diseases known to be caused by unstable triplet repeat mutations; however, there are some instances (as… (More)
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Highly Cited
1996
Highly Cited
1996
About 90 percent of human pancreatic carcinomas show allelic loss at chromosome 18q. To identify candidate tumor suppressor genes… (More)
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Highly Cited
1996
Highly Cited
1996
Absolute genetic differences between neoplastic and nonneoplastic cells can be discerned at sites of homozygous deletions. These… (More)
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Highly Cited
1996
Highly Cited
1996
We recently identified a novel tumor-suppressor gene, DPC4, at chromosome 18q21.1 and found that both alleles of DPC4 were… (More)
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