1q41

A chromosome band present on 1q
National Institutes of Health

Papers overview

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2012
2012
As one of the leading causes of visual impairment and blindness, myopia poses a significant public health burden in Asia. The… (More)
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Highly Cited
2010
Highly Cited
2010
Genome-wide association studies (GWAS) have identified ten loci harboring common variants that influence risk of developing… (More)
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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… (More)
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2008
2008
BACKGROUND Recent large-scale genome-wide association studies have identified several loci associated with the risk of coronary… (More)
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Highly Cited
2005
Highly Cited
2005
Systemic lupus erythematosus (SLE) is an autoimmune disease with a complex genetic basis that includes susceptibility gene(s… (More)
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Highly Cited
2001
Highly Cited
2001
Abnormalities in cellular differentiation are frequent occurrences in human cancers. Treatment of human melanoma cells with… (More)
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1999
1999
OBJECTIVE Genetic susceptibility to systemic lupus erythematosus (SLE) is undoubtedly complex and, presumably, involves multiple… (More)
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Highly Cited
1998
Highly Cited
1998
Systemic lupus erythematosus (SLE) is an autoimmune disorder characterized by production of autoantibodies against intracellular… (More)
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Highly Cited
1998
Highly Cited
1998
p53 is a tumor suppressor protein that controls cell proliferation by regulating the expression of growth control genes. In a… (More)
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Highly Cited
1998
Highly Cited
1998
Usher syndrome type IIa (OMIM 276901), an autosomal recessive disorder characterized by moderate to severe sensorineural hearing… (More)
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