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15q15

A chromosome band present on 15q
National Institutes of Health

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7 relations
15qBUB1B wt AlleleChromosomesPDIA3 wt Allele
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Papers overview

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Highly Cited
2012
Highly Cited
2012
Influence of common genetic variation on lung cancer risk: meta-analysis of 14 900 cases and 29 485 controls
Recent genome-wide association studies (GWASs) have identified common genetic variants at 5p15.33, 6p21-6p22 and 15q25.1… Expand
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Highly Cited
2012
Highly Cited
2012
Common variants near TARDBP and EGR2 are associated with susceptibility to Ewing sarcoma
Ewing sarcoma, a pediatric tumor characterized by EWSR1-ETS fusions, is predominantly observed in populations of European… Expand
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2004
2004
A locus on 15q15-15qter influences dyslexia: further support from a transmission/disequilibrium study in an Italian speaking population.
Developmental dyslexia (dyslexia) is a heritable condition typically diagnosed in the first school years, characterised by an… Expand
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Highly Cited
2003
Highly Cited
2003
CATSPER2, a human autosomal nonsyndromic male infertility gene
In the course of positional cloning of the Congenital Dyserythropoietic Anemia type I (CDAI) [MIM 224120] gene on 15q15.1–15.3… Expand
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Highly Cited
2002
Highly Cited
2002
Congenital dyserythropoietic anemia type I is caused by mutations in codanin-1.
Congenital dyserythropoietic anemias (CDAs) constitute a rare group of inherited red-blood-cell disorders associated with… Expand
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Highly Cited
2001
Highly Cited
2001
Evolution of Transglutaminase Genes: Identification of a Transglutaminase Gene Cluster on Human Chromosome 15q15
We isolated and characterized the gene encoding human transglutaminase (TG)X(TGM5) and mapped it to the 15q15.2 region of… Expand
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Highly Cited
2001
Highly Cited
2001
Mutations in a new gene encoding a protein of the hair bundle cause non-syndromic deafness at the DFNB16 locus
Hearing impairment affects about 1 in 1,000 children at birth. Approximately 70 loci implicated in non-syndromic forms of… Expand
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Highly Cited
2000
Highly Cited
2000
Splitting schizophrenia: periodic catatonia-susceptibility locus on chromosome 15q15.
The nature of subtypes in schizophrenia and the meaning of heterogeneity in schizophrenia have been considered a principal… Expand
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Highly Cited
1999
Highly Cited
1999
Purification of a Novel Flavoprotein Involved in the Thyroid NADPH Oxidase
Hydrogen peroxide is the final electron acceptor for the biosynthesis of thyroid hormone catalyzed by thyroperoxidase at the… Expand
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Highly Cited
1998
Highly Cited
1998
Stimulation of p53-mediated Transcriptional Activation by the p53-binding Proteins, 53BP1 and 53BP2*
p53 is a tumor suppressor protein that controls cell proliferation by regulating the expression of growth control genes. In a… Expand
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