A genome-wide association study identifies genetic variants in the CDKN2BAS locus associated with endometriosis in Japanese (Q28286993)

7

Daisuke Aoki

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Michiaki Kubo

5

Michiaki Kubo

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Atsushi Takahashi

4

Atsushi Takahashi

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Yūsuke Nakamura

10

Yusuke Nakamura

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Hitoshi Zembutsu

2

Hitoshi Zembutsu

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Satoko Uno

1

Satoko Uno

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Akira Hirasawa

3

Akira Hirasawa

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author name string

Tomoko Akahane

6

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Koichi Hirata

describes a project that uses

9

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language of work or name

English

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publication date

August 2010

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published in

Nature Genetics

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volume

42

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page(s)

707-10

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issue

8

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genome-wide association study

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INK4/ARF transcript expression is associated with chromosome 9p21 variants linked to atherosclerosis

inferred from title

cites work

1 reference

Molecular cloning, expression pattern, and chromosomal localization of human CDKN2D/INK4d, an inhibitor of cyclin D-dependent kinases

21 April 2017

1 reference

Genomewide association analysis of coronary artery disease

21 April 2017

1 reference

Genome-wide association study of intracranial aneurysm identifies three new risk loci

21 April 2017

1 reference

New common variants affecting susceptibility to basal cell carcinoma

21 April 2017

1 reference

Chromosome 9p21 SNPs Associated with Multiple Disease Phenotypes Correlate with ANRIL Expression

21 April 2017

1 reference

Female development in mammals is regulated by Wnt-4 signalling

21 April 2017

1 reference

Sexually dimorphic development of the mammalian reproductive tract requires Wnt-7a

21 April 2017

1 reference

Epithelial transformation of metanephric mesenchyme in the developing kidney regulated by Wnt-4

21 April 2017

1 reference

Efficiency and power in genetic association studies

21 April 2017

1 reference

Haploview: analysis and visualization of LD and haplotype maps

21 April 2017

1 reference

PLINK: a tool set for whole-genome association and population-based linkage analyses

21 April 2017

1 reference

A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants

21 April 2017

1 reference

Genome-wide association study identifies five susceptibility loci for glioma

21 April 2017

1 reference

21 April 2017

1 reference

Familial aggregation of endometriosis in the Yale Series.

21 January 2018

1 reference

Post-operative use of oral contraceptive pills for prevention of anatomical relapse or symptom-recurrence after conservative surgery for endometriosis

21 January 2018

1 reference

Haplotype analysis of the matrix metalloproteinase-9 gene associated with advanced-stage endometriosis

21 January 2018

1 reference

Functional analysis of the chromosome 9p21.3 coronary artery disease risk locus.

21 January 2018

1 reference

Characterization of a germ-line deletion, including the entire INK4/ARF locus, in a melanoma-neural system tumor family: identification of ANRIL, an antisense noncoding RNA whose expression coclusters with ARF.

21 January 2018

1 reference

Insertional mutagenesis in mice deficient for p15Ink4b, p16Ink4a, p21Cip1, and p27Kip1 reveals cancer gene interactions and correlations with tumor phenotypes

21 January 2018

1 reference

Alteration of p16 and p15 genes in human uterine tumours

21 January 2018

1 reference

Association between four SNPs on chromosome 9p21 and myocardial infarction is replicated in an Italian population.

21 January 2018

1 reference

Worldwide patterns of haplotype diversity at 9p21.3, a locus associated with type 2 diabetes and coronary heart disease

21 January 2018

1 reference

Replication of genome-wide association studies of type 2 diabetes susceptibility in Japan.

21 January 2018

1 reference

The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm

21 January 2018

1 reference

Genome-wide association study identifies three loci associated with melanoma risk

21 January 2018

1 reference

Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi

21 January 2018

1 reference

Four SNPs on chromosome 9p21 in a South Korean population implicate a genetic locus that confers high cross-race risk for development of coronary artery disease.

21 January 2018

1 reference

Association of CDKAL1, IGF2BP2, CDKN2A/B, HHEX, SLC30A8, and KCNJ11 with susceptibility to type 2 diabetes in a Japanese population.

21 January 2018

1 reference

Endometriosis may be generated by mimicking the ontogenetic development of the female genital tract.

21 January 2018

1 reference

Theories of endometriosis

21 January 2018

1 reference

A high-throughput SNP typing system for genome-wide association studies

21 January 2018

1 reference

N-acetyl transferase 2 polymorphism and advanced stages of endometriosis in South Indian women

21 January 2018

1 reference

Aberrant DNA hypermethylation of hMLH-1 and CDKN2A/p16 genes in benign, premalignant and malignant endometrial lesions

21 January 2018

1 reference

12 December 2020

The BioBank Japan Project.

1 reference

12 December 2020

Rates of endometriosis recurrence and pregnancy 1 year after treatment with intranasal buserelin acetate (Suprecur) (a prospective study)

1 reference

12 December 2020

Malignancy in endometriosis: frequency and comparison of ovarian and extraovarian types

1 reference

12 December 2020

P16 alterations increase the metastatic potential of endometrial carcinoma

1 reference

12 December 2020

Hypermethylation in the p16 promoter region in the carcinogenesis of endometrial cancer in Japanese patients.

1 reference

12 December 2020

The function of the SNP in the MMP1 and MMP3 promoter in susceptibility to endometriosis in China

1 reference

12 December 2020

Intron 1 and exon 1 alpha estrogen receptor gene polymorphisms in women with endometriosis

1 reference

12 December 2020

Possible involvement of hMLH1, p16(INK4a) and PTEN in the malignant transformation of endometriosis

1 reference

12 December 2020

1 reference

12 December 2020

Loss of heterozygosity in adenomyosis on hMSH2, hMLH1, p16Ink4 and GALT loci

1 reference

12 December 2020

CYP17, CYP1A1 and COMT polymorphisms and the risk of adenomyosis and endometriosis in Taiwanese women

1 reference

12 December 2020

Metastatic or Embolic Endometriosis, due to the Menstrual Dissemination of Endometrial Tissue into the Venous Circulation

1 reference

12 December 2020

CYP17 and CYP19 gene polymorphisms in women affected with endometriosis

1 reference

12 December 2020