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15q23

A chromosome band present on 15q
National Institutes of Health

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6 relations
15qANP32A wt AlleleCSPG4 wt AlleleChromosomes

Papers overview

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Highly Cited
2020
Highly Cited
2020
A Transcriptome-Wide Association Study (TWAS) Identifies Novel Candidate Susceptibility Genes for Pancreatic Cancer.
BACKGROUND Although 20 pancreatic cancer susceptibility loci have been identified through genome-wide association studies (GWAS… 
Highly Cited
2014
Highly Cited
2014
Genome-wide association study of lung function phenotypes in a founder population.
2014
2014
A genome scan for loci shared by autism spectrum disorder and language impairment.
OBJECTIVE The authors conducted a genetic linkage study of families that have both autism spectrum disorder (ASD) and language… 
2010
2010
Verification that common variation at 2q37.1, 6p25.3, 11q24.1, 15q23, and 19q13.32 influences chronic lymphocytic leukaemia risk
A recent genome wide association study of chronic lymphocytic leukaemia (CLL) provided evidence that common variation at 2q13… 
Highly Cited
2010
Highly Cited
2010
Inherited genetic susceptibility to monoclonal B-cell lymphocytosis.
Monoclonal B-cell lymphocytosis (MBL) is detectable in > 3% of the general population. Recent data are compatible, at least in a… 
Highly Cited
2007
Highly Cited
2007
Array CGH identifies distinct DNA copy number profiles of oncogenes and tumor suppressor genes in chromosomal- and microsatellite-unstable sporadic colorectal carcinomas
DNA copy number changes represent molecular fingerprints of solid tumors and are as such relevant for better understanding of… 
Highly Cited
2004
Highly Cited
2004
Evidence for linkage between regulatory enzymes in glycolysis and schizophrenia in a multiplex sample
Observations of impaired glucose regulation in schizophrenia are long‐standing, although their pathological and etiological… 
2003
2003
Genetic imbalances with impact on survival in colorectal cancer patients
Aims:  To investigate the prognostic significance of chromosomal alterations in colorectal cancer patients. Histopathological… 
Review
2001
Review
2001
Update on the molecular genetics of retinitis pigmentosa
Retinitis pigmentosa (RP) is a heterogeneous group of retinal dystrophies characterized by photoreceptor cell degeneration. RP… 
Highly Cited
1999
Highly Cited
1999
cDNA cloning and chromosomal localization of human alpha(11) integrin. A collagen-binding, I domain-containing, beta(1)-associated integrin alpha-chain present in muscle tissues.
We previously identified a novel integrin alpha-chain in human fetal muscle cells (Gullberg, D., Velling, T., Sjöberg, G., and… 
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