1p31

A chromosome band present on 1p
National Institutes of Health

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Chromosome 1 Short ArmChromosomesDIRAS3 wt AlleleDNAJB4 wt Allele
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Papers overview

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2014
2014
Severe osteoarthritis of the hand associates with common variants within the ALDH1A2 gene and with rare variants at 1p31
Osteoarthritis is the most common form of arthritis and is a major cause of pain and disability in the elderly. To search for… (More)
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Highly Cited
2012
Highly Cited
2012
Immunochip analyses identify a novel risk locus for primary biliary cirrhosis at 13q14, multiple independent associations at four established risk loci and epistasis between 1p31 and 7q32 risk…
To further characterize the genetic basis of primary biliary cirrhosis (PBC), we genotyped 2426 PBC patients and 5731 unaffected… (More)
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2011
2011
Aberrations of NEGR1 on 1p31 and MYEOV on 11q13 in neuroblastoma.
MYEOV and NEGR1 are novel candidate gene targets in neuroblastoma that were identified by chromosomal gain in 11q13 and loss in… (More)
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2010
2010
A genome-wide association analysis reveals 1p31 and 2p13.3 as susceptibility loci for Kawasaki disease
Kawasaki disease (KD) is an acute self-limited vasculitis of infants and children that manifests as fever and signs of… (More)
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Highly Cited
2006
Highly Cited
2006
A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.
The inflammatory bowel diseases Crohn's disease and ulcerative colitis are common, chronic disorders that cause abdominal pain… (More)
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2004
2004
CLCA2 tumour suppressor gene in 1p31 is epigenetically regulated in breast cancer
The calcium-activated chloride channel gene family is clustered in the 1p31 region, which is frequently deleted in sporadic… (More)
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2002
2002
Locus for elevated apolipoprotein B levels on chromosome 1p31 in families with familial combined hyperlipidemia.
Familial combined hyperlipidemia (FCH), a common cause of premature coronary artery disease, is genetically complex and poorly… (More)
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Highly Cited
2000
Highly Cited
2000
Genome screen for asthma and related phenotypes in the French EGEA study.
A genome-wide search was conducted in 107 nuclear families with at least two siblings with asthma, as part of the French EGEA… (More)
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Highly Cited
1998
Highly Cited
1998
Autosomal genomic scan for loci linked to obesity and energy metabolism in Pima Indians.
An autosomal genomic scan to search for linkage to obesity and energy metabolism was completed in Pima Indians, a population… (More)
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Highly Cited
1996
Highly Cited
1996
Genesis, a winged helix transcriptional repressor with expression restricted to embryonic stem cells.
A novel member of the winged helix (formerly HNF-3/Forkhead) transcriptional regulatory family, termed Genesis, was isolated and… (More)
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