Genome-wide association study of hematological and biochemical traits in a Japanese population (Q34097468)

31 July 2017

title

Genome-wide association study of hematological and biochemical traits in a Japanese population (English)

1 reference

genome-wide association study

31 July 2017

main subject

0 references

Koichi Matsuda

2

0 references

Michiaki Kubo

series ordinal

4

object named as

Michiaki Kubo

1 reference

31 July 2017

6

Yataro Daigo

1 reference

31 July 2017

7

Yusuke Nakamura

1 reference

31 July 2017

1

Yoichiro Kamatani

1 reference

31 July 2017

5

Naoya Hosono

1 reference

31 July 2017

8

Naoyuki Kamatani

1 reference

31 July 2017

Yukinori Okada

3

1 reference

31 July 2017

language of work or name

English

0 references

publication date

7 February 2010

1 reference

31 July 2017

1 reference

31 July 2017

volume

42

1 reference

31 July 2017

issue

3

1 reference

31 July 2017

page(s)

210-215

1 reference

describes a project that uses

31 July 2017

genome-wide association study

1 reference

Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans

inferred from title

cites work

1 reference

12 December 2020

Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels

1 reference

12 December 2020

Nonsense mutation in the glycoprotein Ib alpha coding sequence associated with Bernard-Soulier syndrome

1 reference

12 December 2020

Common variants in TMPRSS6 are associated with iron status and erythrocyte volume

1 reference

12 December 2020

Mouse development and cell proliferation in the absence of D-cyclins.

1 reference

12 December 2020

Increased high-density lipoprotein levels caused by a common cholesteryl-ester transfer protein gene mutation

1 reference

12 December 2020

Principal components analysis corrects for stratification in genome-wide association studies

1 reference

12 December 2020

A genome-wide association study identifies protein quantitative trait loci (pQTLs)

1 reference

12 December 2020

The BioBank Japan Project.

1 reference

12 December 2020

Cloning and characterization of the human urea transporter UT-A1 and mapping of the human Slc14a2 gene

1 reference

12 December 2020

Age and origin of the G774A mutation in SLC22A12 causing renal hypouricemia in Japanese

1 reference

12 December 2020

A second generation human haplotype map of over 3.1 million SNPs

1 reference

12 December 2020

The HBS1L-MYB intergenic region on chromosome 6q23.3 influences erythrocyte, platelet, and monocyte counts in humans.

1 reference

12 December 2020

Mutation in the gene encoding the alpha chain of platelet glycoprotein Ib in platelet-type von Willebrand disease

1 reference

12 December 2020

Inhibition of eukaryotic DNA replication by geminin binding to Cdt1

1 reference

12 December 2020

Measuring inconsistency in meta-analyses

1 reference

12 December 2020

RNPC1, an RNA-binding protein and a target of the p53 family, is required for maintaining the stability of the basal and stress-induced p21 transcript

1 reference

12 December 2020

Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations

1 reference

12 December 2020

Mutations in TERT, the gene for telomerase reverse transcriptase, in aplastic anemia

1 reference

12 December 2020

A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium

1 reference

12 December 2020

Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes

1 reference

12 December 2020

Association of three genetic loci with uric acid concentration and risk of gout: a genome-wide association study

1 reference

12 December 2020

An activating splice donor mutation in the thrombopoietin gene causes hereditary thrombocythaemia.

1 reference

12 December 2020

Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium

1 reference

12 December 2020

Japanese population structure, based on SNP genotypes from 7003 individuals compared to other ethnic groups: effects on population-based association studies

1 reference

12 December 2020

Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts

1 reference

12 December 2020

Statistical analysis of the associations between polymorphisms within aldehyde dehydrogenase 2 (ALDH2), and quantitative and qualitative traits extracted from a large-scale database of Japanese single-nucleotide polymorphisms (SNPs).

1 reference

12 December 2020

Sequence variation at the human ABO locus.

1 reference

12 December 2020

Two candidate genes for low platelet count identified in an Asian Indian kindred by genome-wide linkage analysis: glycoprotein IX and thrombopoietin

1 reference

12 December 2020

Polymorphisms in Platelet Glycoprotein 1bα and Factor VII and Risk of Ischemic Stroke

1 reference

12 December 2020

Intergenic variants of HBS1L-MYB are responsible for a major quantitative trait locus on chromosome 6q23 influencing fetal hemoglobin levels in adults

1 reference

12 December 2020

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

1 reference

12 December 2020

Protein tyrosine phosphatases: a diverse family of intracellular and transmembrane enzymes

1 reference

12 December 2020

Common variants at 30 loci contribute to polygenic dyslipidemia

1 reference

12 December 2020

Mutations in TNFRSF13B encoding TACI are associated with common variable immunodeficiency in humans.

1 reference

12 December 2020

TACI is mutant in common variable immunodeficiency and IgA deficiency

1 reference

12 December 2020

Genome-wide association study identifies variants in TMPRSS6 associated with hemoglobin levels

1 reference

12 December 2020

Genome-wide association analysis of metabolic traits in a birth cohort from a founder population

1 reference

12 December 2020

The glycocalicin portion of platelet glycoprotein Ib expresses both high and moderate affinity receptor sites for thrombin. A soluble radioreceptor assay for the interaction of thrombin with platelets

1 reference

12 December 2020

Identifiers

DOI

10.1038/NG.531

1 reference

31 July 2017

1 reference