(Q33637520)

28 July 2017

Polymorphisms associated with both noncardioembolic stroke and coronary heart disease: vienna stroke registry (English)

1 reference

28 July 2017

coronary artery disease

1 reference

Christine Mannhalter

10

0 references

author name string

May M Luke

1

1 reference

28 July 2017

Wolfgang Lalouschek

2

1 reference

28 July 2017

Charles M Rowland

3

1 reference

28 July 2017

Joseph J Catanese

4

1 reference

28 July 2017

Joel I Bolonick

5

1 reference

28 July 2017

Nam D Bui

6

1 reference

28 July 2017

Stefan Greisenegger

7

1 reference

28 July 2017

Georg Endler

8

1 reference

28 July 2017

James J Devlin

9

1 reference

28 July 2017

12 September 2009

1 reference

28 July 2017

Cerebrovascular Diseases

1 reference

28 July 2017

28

1 reference

28 July 2017

5

1 reference

28 July 2017

499-504

1 reference

Sequence variants on chromosome 9p21.3 confer risk for atherosclerotic stroke

28 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2818395

Classification of stroke subtypes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2818395

A genetic variant on chromosome 9p21 and incident heart failure in the ARIC study

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2818395

Variant on 9p21 strongly associates with coronary heart disease, but lacks association with common stroke

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2818395

Genetic association studies in ischaemic stroke: replication failure and prospects

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2818395

Gene variants associated with ischemic stroke: the cardiovascular health study

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2818395

Single nucleotide polymorphisms associated with coronary heart disease predict incident ischemic stroke in the atherosclerosis risk in communities study

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2818395

Single-nucleotide polymorphisms of MMP-2 gene in stroke subtypes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2818395

Heart Disease and Stroke Statistics--2008 Update: A Report From the American Heart Association Statistics Committee and Stroke Statistics Subcommittee

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2818395

Five common gene variants identify elevated genetic risk for coronary heart disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2818395

PHOSIDA (phosphorylation site database): management, structural and evolutionary investigation, and prediction of phosphosites

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2818395

A common allele on chromosome 9 associated with coronary heart disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2818395

Global, in vivo, and site-specific phosphorylation dynamics in signaling networks

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2818395

Identification of four gene variants associated with myocardial infarction

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2818395

Current strategies of secondary prevention after a cerebrovascular event: the Vienna stroke registry

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2818395

The Vienna Stroke Registry--objectives and methodology. The Vienna Stroke Study Group.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2818395

Inference of population structure using multilocus genotype data

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2818395

New approach to stroke subtyping: the A-S-C-O (phenotypic) classification of stroke.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2818395

Ischaemic stroke subtypes and their genetic basis: a comprehensive meta-analysis of small and large vessel stroke

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2818395

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

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2818395

Two common gene variants on chromosome 9 and risk of atherothrombosis

30 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19752551

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Common genetic variants on chromosome 9p21 confers risk of ischemic stroke: a large-scale genetic association study

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19752551

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1159/000236914

1 reference

28 July 2017

1 reference

28 July 2017

1 reference