Follow-up of a major linkage peak on chromosome 1 reveals suggestive QTLs associated with essential hypertension: GenNet study (Q24650582)

22 June 2017

Follow-up of a major linkage peak on chromosome 1 reveals suggestive QTLs associated with essential hypertension: GenNet study (English)

1 reference

22 June 2017

arterial hypertension

1 reference

based on heuristic

inferred from title

essential hypertension

1 reference

4

Richard S Cooper

1 reference

22 June 2017

Georg B Ehret

1

1 reference

22 June 2017

Ashley A O'Connor

series ordinal

2

1 reference

22 June 2017

Alan Weder

series ordinal

3

1 reference

22 June 2017

Aravinda Chakravarti

series ordinal

5

1 reference

22 June 2017

language of work or name

English

0 references

publication date

17 June 2009

1 reference

European Journal of Human Genetics

22 June 2017

1 reference

22 June 2017

17

1 reference

22 June 2017

12

1 reference

22 June 2017

1650-1657

1 reference

A second generation human haplotype map of over 3.1 million SNPs

22 June 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2783544

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2783544

Highly multiplexed molecular inversion probe genotyping: over 10,000 targeted SNPs genotyped in a single tube assay

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2783544

The human A33 antigen is a transmembrane glycoprotein and a novel member of the immunoglobulin superfamily

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2783544

Haploview: analysis and visualization of LD and haplotype maps

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2783544

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2783544

Aliskiren: the first renin inhibitor for clinical treatment

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2783544

Global and regional burden of disease and risk factors, 2001: systematic analysis of population health data

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2783544

Multiplexed genotyping with sequence-tagged molecular inversion probes

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2783544

Replication of the Wellcome Trust genome-wide association study of essential hypertension: the Family Blood Pressure Program

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2783544

Multiple genes for essential-hypertension susceptibility on chromosome 1q.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2783544

Optimal genotype determination in highly multiplexed SNP data

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2783544

Molecular cloning of the zeta chain of the T cell antigen receptor.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2783544

Randomised double-blind comparison of placebo and active treatment for older patients with isolated systolic hypertension. The Systolic Hypertension in Europe (Syst-Eur) Trial Investigators.

30 May 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.94

A multivariate family-based association test using generalized estimating equations: FBAT-GEE.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.94

Adjusting for treatment effects in studies of quantitative traits: antihypertensive therapy and systolic blood pressure.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.94

Does the relation of blood pressure to coronary heart disease risk change with aging? The Framingham Heart Study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.94

Renin Gene Polymorphisms and Haplotypes, Blood Pressure, and Responses to Renin-Angiotensin System Inhibition

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.94

The risk of venous thromboembolism in family members with mutations in the genes of factor V or prothrombin or both

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.94

Multi-center genetic study of hypertension: The Family Blood Pressure Program (FBPP).

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2783544

Established risk factors and coronary artery disease: the Framingham Study.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2783544

Resistance to activated protein C and FV leiden mutation in patients with a history of acute myocardial infarction or primary hypertension

28 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19536175

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A genome-wide linkage analysis investigating the determinants of blood pressure in whites and African Americans

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19536175

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/EJHG.2009.94

1 reference

Dimensions Publication ID

22 June 2017

1033791358

0 references

OpenCitations bibliographic resource ID

3269948

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference