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1p36.12

A chromosome band present on 1p
National Institutes of Health

Related topics

Related topics

4 relations
C1QA wt AlleleChromosome 1 Short ArmChromosomesKDM1A wt Allele

Papers overview

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2018
2018
An Osteoporosis Risk SNP at 1p36.12 Acts as an Allele-Specific Enhancer to Modulate LINC00339 Expression via Long-Range Loop Formation.
Genome-wide association studies (GWASs) have reproducibly associated variants within intergenic regions of 1p36.12 locus with… Expand
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2017
2017
Genetic architecture of epigenetic and neuronal ageing rates in human brain regions
Identifying genes regulating the pace of epigenetic ageing represents a new frontier in genome-wide association studies (GWASs… Expand
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2016
2016
Endometriosis risk alleles at 1p36.12 act through inverse regulation of CDC42 and LINC00339.
Genome-wide association studies (GWAS) have identified markers within the WNT4 region on chromosome 1p36.12 showing consistent… Expand
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Highly Cited
2013
Highly Cited
2013
Genome-Wide Association Study Link Novel Loci to Endometriosis
Endometriosis is a common gynecological condition with complex etiology defined by the presence of endometrial glands and stroma… Expand
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Highly Cited
2013
Highly Cited
2013
Multistage genome-wide association meta-analyses identified two new loci for bone mineral density.
Aiming to identify novel genetic variants and to confirm previously identified genetic variants associated with bone mineral… Expand
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Highly Cited
2012
Highly Cited
2012
Genome-wide association meta-analysis identifies new endometriosis risk loci
We conducted a genome-wide association meta-analysis of 4,604 endometriosis cases and 9,393 controls of Japanese and European… Expand
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2005
2005
Involvement of multiple developmental genes on chromosome 1p in lung tumorigenesis.
Lung cancer is the leading cause of cancer death in North America. Despite advances in lung cancer treatment, the overall 5 year… Expand
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2001
2001
An early lesion in hepatic carcinogenesis: loss of heterozygosity in human cirrhotic livers and dysplastic nodules at the 1p36-p34 region.
Loss of heterozygosity (LOH) of chromosome 1 has been suggested, by karyotyping, to be an initial episode in human… Expand
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2000
2000
Genome-wide linkage disequilibrium mapping of late onset Alzheimer's disease in Finland
BACKGROUND AD is a complex neurodegenerative disorder comprising several disease-associated chromosome loci. To find novel… Expand
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1999
1999
Cloning and characterization of novel mouse and human secretory phospholipase A(2)s.
Mammalian secretory phospholipase A(2)s (sPLA(2)s) are classified into several groups according to molecular structure and the… Expand
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