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1q41

A chromosome band present on 1q
National Institutes of Health

Papers overview

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Highly Cited
2012
Highly Cited
2012
As one of the leading causes of visual impairment and blindness, myopia poses a significant public health burden in Asia. The… Expand
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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… Expand
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Highly Cited
2008
Highly Cited
2008
BACKGROUND Recent large-scale genome-wide association studies have identified several loci associated with the risk of coronary… Expand
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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… Expand
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Review
2002
Review
2002
With λs estimates of 10 to 20 and other evidence of familial aggregation, as well as a monozygotic twin concordance rate >20… Expand
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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… Expand
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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… Expand
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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… Expand
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Highly Cited
1998
Highly Cited
1998
Remarkable structural and functional similarities exist between the Drosophila Toll/Cactus/Dorsal signaling pathway and the… Expand
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Highly Cited
1995
Highly Cited
1995
Usher syndrome type II is associated with hearing loss and retinitis pigmentosa but not with any vestibular problems. It is known… Expand
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