6q26

A chromosome band present on 6q
National Institutes of Health

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ChromosomesIGF2R wt AlleleQKI wt Allele

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Highly Cited
2010
Highly Cited
2010
Genetic loci influencing kidney function and chronic kidney disease
Using genome-wide association, we identify common variants at 2p12–p13, 6q26, 17q23 and 19q13 associated with serum creatinine, a… (More)
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Highly Cited
2009
Highly Cited
2009
Genetic variants associated with Lp(a) lipoprotein level and coronary disease.
BACKGROUND An increased level of Lp(a) lipoprotein has been identified as a risk factor for coronary artery disease that is… (More)
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Highly Cited
2006
Highly Cited
2006
The epigenetic imprinting defect of patients with Beckwith-Wiedemann syndrome born after assisted reproductive technology is not restricted to the 11p15 region.
BACKGROUND Genomic imprinting refers to an epigenetic marking resulting in monoallelic gene expression and has a critical role in… (More)
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2006
2006
Small regions of overlapping deletions on 6q26 in human astrocytic tumours identified using chromosome 6 tile path array-CGH
Deletions of chromosome 6 are a common abnormality in diverse human malignancies including astrocytic tumours, suggesting the… (More)
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Highly Cited
2003
Highly Cited
2003
Alterations in the common fragile site gene Parkin in ovarian and other cancers
The cloning and characterization of the common fragile site (CFS) FRA6E (6q26) identified Parkin, the gene involved in the… (More)
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Highly Cited
1999
Highly Cited
1999
Cloning and characterization of a novel human phosphodiesterase that hydrolyzes both cAMP and cGMP (PDE10A).
cDNA encoding a novel phosphodiesterase (PDE) was isolated from a human fetal lung cDNA library and designated PDE10A. The… (More)
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Highly Cited
1998
Highly Cited
1998
Genome scan of human systemic lupus erythematosus: evidence for linkage on chromosome 1q in African-American pedigrees.
Systemic lupus erythematosus (SLE) is an autoimmune disorder characterized by production of autoantibodies against intracellular… (More)
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1997
1997
The two human organic cation transporter genes SLC22A1 and SLC22A2 are located on chromosome 6q26.
Polyspecific transporters for organic cations (OCT) belong to a new protein family which also include organic anion transporters… (More)
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1987
1987
Linkage disequilibrium of plasminogen polymorphisms and assignment of the gene to human chromosome 6q26-6q27.
Linkage disequilibrium was observed between newly identified DNA polymorphisms and a previously described protein polymorphism… (More)
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Highly Cited
1984
Highly Cited
1984
DNA polymerase α inhibition by aphidicolin induces gaps and breaks at common fragile sites in human chromosomes
Aphidicolin, a specific inhibitor of DNA polymerase α, is known to induce chromosomal aberrations. At concentrations that did not… (More)
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