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1q23

A chromosome band present on 1q
National Institutes of Health

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Highly Cited
2006
Highly Cited
2006
Age-related macular degeneration (AMD; OMIM #603075) is the most frequent cause of visual impairment in the elderly population… Expand
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Highly Cited
2003
Highly Cited
2003
Headache attacks and autonomic dysfunctions characterize migraine, a very common, disabling disorder with a prevalence of 12% in… Expand
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Highly Cited
2003
Highly Cited
2003
Alzheimer's disease (AD) is a devastating neurodegenerative disorder of late life with complex inheritance. Mutations in three… Expand
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Highly Cited
2003
Highly Cited
2003
Familial hemiplegic migraine (FHM) is a rare, severe, autosomal dominant subtype of migraine with aura. Up to 75% of FHM families… Expand
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Highly Cited
2002
Highly Cited
2002
OBJECTIVE Although low-affinity alleles of human Fcgamma receptor types IIA and IIIA (FcgammaRIIA and FcgammaRIIIA, respectively… Expand
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Highly Cited
1999
Highly Cited
1999
Considerable evidence supports a major inherited component of type 2 diabetes. We initially conducted a genome-wide scan with 440… 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
1997
Highly Cited
1997
Comparative genomic hybridization was used to screen 25 adenocarcinomas and 25 squamous cell carcinomas of the lung for… Expand
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Highly Cited
1994
Highly Cited
1994
Fas ligand (FasL) is a 40 kDa type II membrane protein belonging to the tumor necrosis factor family, which induces apoptosis by… Expand
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Highly Cited
1989
Highly Cited
1989
A cDNA encoding a new human lymphocyte cell surface molecule has been isolated and shown to identify a fourth member of a… Expand
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