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1p36.12
A chromosome band present on 1p
National Institutes of Health
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Related topics
Related topics
4 relations
C1QA wt Allele
Chromosome 1 Short Arm
Chromosomes
KDM1A 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
C. Gregson
,
F. Newell
,
+17 authors
E. Duncan
Bone
2018
Corpus ID: 47001043
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.
Xiao-Feng Chen
,
Dong-Li Zhu
,
+12 authors
Tie-Lin Yang
American journal of human genetics
2018
Corpus ID: 14005168
Highly Cited
2017
Highly Cited
2017
Genetic architecture of epigenetic and neuronal ageing rates in human brain regions
A. Lu
,
E. Hannon
,
+5 authors
S. Horvath
Nature communications
2017
Corpus ID: 205310481
Identifying genes regulating the pace of epigenetic ageing represents a new frontier in genome-wide association studies (GWASs…
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Highly Cited
2016
Highly Cited
2016
Endometriosis risk alleles at 1p36.12 act through inverse regulation of CDC42 and LINC00339.
J. Powell
,
J. Fung
,
+17 authors
G. Montgomery
Human molecular genetics
2016
Corpus ID: 3535096
Genome-wide association studies (GWAS) have identified markers within the WNT4 region on chromosome 1p36.12 showing consistent…
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Highly Cited
2014
Highly Cited
2014
Multistage genome-wide association meta-analyses identified two new loci for bone mineral density.
Lei Zhang
,
H. Choi
,
+53 authors
H. Deng
Human molecular genetics
2014
Corpus ID: 25932457
Aiming to identify novel genetic variants and to confirm previously identified genetic variants associated with bone mineral…
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Highly Cited
2013
Highly Cited
2013
Genome-Wide Association Study Link Novel Loci to Endometriosis
H. Albertsen
,
R. Chettier
,
P. Farrington
,
K. Ward
PloS one
2013
Corpus ID: 27804409
Endometriosis is a common gynecological condition with complex etiology defined by the presence of endometrial glands and stroma…
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Highly Cited
2012
Highly Cited
2012
Genome-wide association meta-analysis identifies new endometriosis risk loci
D. Nyholt
,
Siew-Kee Low
,
+20 authors
G. Montgomery
Nature Genetics
2012
Corpus ID: 193844
We conducted a genome-wide association meta-analysis of 4,604 endometriosis cases and 9,393 controls of Japanese and European…
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2004
2004
Characterization and expression of the human WNT4; lack of associated germline mutations in high--to moderate--risk breast and ovarian cancer.
H. Peltoketo
,
M. Allinen
,
+5 authors
S. Vainio
Cancer letters
2004
Corpus ID: 1953045
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
M. Sun
,
J. Eshleman
,
+5 authors
O. Sudilovsky
Hepatology
2001
Corpus ID: 20480097
Loss of heterozygosity (LOH) of chromosome 1 has been suggested, by karyotyping, to be an initial episode in human…
Expand
Highly Cited
2000
Highly Cited
2000
Genome-wide linkage disequilibrium mapping of late onset Alzheimer's disease in Finland
M. Hiltunen
,
A. Mannermaa
,
+5 authors
H. Soininen
Neurobiology of Aging
2000
Corpus ID: 27712072
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