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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
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
2000
Highly Cited
2000
DNA copy number changes were characterized by comparative genomic hybridization (CGH) in 18 breast cancer cell lines. In 5 of… Expand
Highly Cited
1998
Highly Cited
1998
Usher syndrome type IIa (OMIM 276901), an autosomal recessive disorder characterized by moderate to severe sensorineural hearing… Expand
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
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