7p21

A chromosome band present on 7p
National Institutes of Health

Topic mentions per year

Topic mentions per year

1976-2017
051019762017

Papers overview

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Highly Cited
2011
Highly Cited
2011
We report the first genome-wide association study of habitual caffeine intake. We included 47,341 individuals of European descent… (More)
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Highly Cited
2010
Highly Cited
2010
Frontotemporal lobar degeneration (FTLD) is the second most common cause of presenile dementia. The predominant neuropathology is… (More)
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Highly Cited
2008
Highly Cited
2008
Primary ciliary dyskinesia (PCD) is an inherited disorder characterized by perturbed or absent beating of motile cilia, which is… (More)
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Highly Cited
2007
Highly Cited
2007
Recently, we identified recurrent gene fusions involving the 5' untranslated region of the androgen-regulated gene TMPRSS2 and… (More)
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Highly Cited
2005
Highly Cited
2005
Mantle cell lymphoma (MCL) is characterized by 11q13 chromosomal translocation and CCND1 overexpression, but additional genomic… (More)
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Highly Cited
2003
Highly Cited
2003
hAG-2 and hAG-3 are recently discovered human homologues of the secreted Xenopus laevis proteins XAG-1/2 (AGR-1/2) that are… (More)
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Highly Cited
1997
Highly Cited
1997
Saethre-Chotzen syndrome (acrocephalo-syndactyly type III, ACS III) is an autosomal dominant craniosynostosis with brachydactyly… (More)
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1997
1997
The TWIST gene maps to 7p21 and mutations in the gene have been reported in the Saethre-Chotzen form of craniosynostosis. The… (More)
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1994
1994
We isolated the human arylhydrocarbon receptor (AhR) cDNA from a human lung cDNA library, by using mouse AhR cDNA as a labeled… (More)
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1988
1988
The human interferon-beta 2 gene (IFNB2) product is identical to that for the B-cell stimulation factor-2 (BSF-2), the hybridoma… (More)
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