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7p21

A chromosome band present on 7p
National Institutes of Health

Papers overview

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Highly Cited
2012
Highly Cited
2012
Frontotemporal lobar degeneration with TDP-43 inclusions (FTLD-TDP) is a fatal neurodegenerative disease with no available… Expand
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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… Expand
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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… Expand
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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… Expand
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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… Expand
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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… Expand
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Highly Cited
2002
Highly Cited
2002
Primary ciliary dyskinesia (PCD; MIM 242650) is an autosomal recessive disorder of ciliary dysfunction with extensive genetic… Expand
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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… Expand
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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… Expand
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Highly Cited
1988
Highly Cited
1988
The human interferon-beta 2 gene (IFNB2) product is identical to that for the B-cell stimulation factor-2 (BSF-2), the hybridoma… Expand
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