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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

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Genome-wide association study of extreme high bone mass: Contribution of common genetic variation to extreme BMD phenotypes and potential novel BMD-associated genes
Highly Cited
2018
Highly Cited
2018
An Osteoporosis Risk SNP at 1p36.12 Acts as an Allele-Specific Enhancer to Modulate LINC00339 Expression via Long-Range Loop Formation.
Highly Cited
2017
Highly Cited
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… 
Highly Cited
2016
Highly Cited
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… 
Highly Cited
2014
Highly Cited
2014
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… 
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… 
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… 
2004
2004
Characterization and expression of the human WNT4; lack of associated germline mutations in high--to moderate--risk breast and ovarian cancer.
Highly Cited
2001
Highly Cited
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… 
Highly Cited
2000
Highly Cited
2000
Genome-wide linkage disequilibrium mapping of late onset Alzheimer's disease in Finland
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