22q13.1

A chromosome band present on 22q

Topic mentions per year

Topic mentions per year

1980-2017
0246819802017

Papers overview

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2013
2013
To identify variants for multiple myeloma risk, we conducted a genome-wide association study with validation in additional series… (More)
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2010
Highly Cited
2010
We conducted a multi-stage, genome-wide association study of bladder cancer with a primary scan of 591,637 SNPs in 3,532 affected… (More)
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2010
Highly Cited
2010
Male development in mammals is normally initiated by the Y-linked gene Sry, which activates expression of Sox9, leading to a… (More)
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2009
Highly Cited
2009
A high melanocytic nevi count is the strongest known risk factor for cutaneous melanoma. We conducted a genome-wide association… (More)
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2006
2006
Infantile neuroaxonal dystrophy (INAD) is an autosomal recessive progressive neurodegenerative disease that presents within the… (More)
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2000
2000
This paper reports the characterization of the human tubulin tyrosine ligase-like 1 gene (TTLL1), which maps to the chromosome… (More)
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1999
1999
An 85-kDa Group VI phospholipase A2 enzyme (iPLA2) that does not require Ca2+ for catalysis has recently been cloned from three… (More)
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1998
1998
Allelic losses on chromosome arm 22q are frequently observed in human meningiomas and in carcinomas of the colon, ovary, and… (More)
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1993
1993
The Na+/glucose cotransporter gene SGLT1 encodes the primary carrier protein responsible for the uptake of the dietary sugars… (More)
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1993
1993
Using a combination of somatic cell hybrids, in situ hybridization, and linkage mapping, we have been able to localize the… (More)
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