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2q36.3

A chromosome band present on 2q
National Institutes of Health

Papers overview

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2016
2016
AIM Cardiovascular disease (CVD) is a major cause of morbidity and mortality in developed countries. This study aimed to confirm… Expand
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2014
2014
Large population-based registry studies have shown that breast cancer prognosis is inherited. Here we analyse single-nucleotide… Expand
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2013
2013
White matter hyperintensities (WMHs) of the brain are important markers of aging and small-vessel disease. WMHs are rare in… Expand
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Highly Cited
2011
Highly Cited
2011
Background— Genome-wide association studies identified several single nucleotide polymorphisms (SNP) associated with prevalent… Expand
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Highly Cited
2009
Highly Cited
2009
Background—Combined analysis of 2 genome-wide association studies in cases enriched for family history recently identified 7 loci… Expand
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2009
2009
OBJECTIVES The chromosomal loci 9p21.3, 6q25.1, and 2q36.3, represented by their respective leading variants rs1333049, rs6922269… Expand
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Highly Cited
2009
Highly Cited
2009
Recently, genome wide association studies (GWAS) have identified a number of single nucleotide polymorphisms (SNPs) as being… Expand
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Highly Cited
2007
Highly Cited
2007
BACKGROUND Modern genotyping platforms permit a systematic search for inherited components of complex diseases. We performed a… Expand
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Highly Cited
2005
Highly Cited
2005
Biotin-responsive basal ganglia disease (BBGD) is a recessive disorder with childhood onset that presents as a subacute… Expand
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Highly Cited
2002
Highly Cited
2002
We have delineated regions of interest at chromosome 2q21.2, 2q36.3, and 2q37.1 by deletion mapping of 114 urothelial cancers (UC… Expand
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