The Siblings With Ischemic Stroke Study (SWISS) protocol (Q24803218)

3

object named as

Thomas G Brott

0 references

James F Meschia

1

object named as

James F Meschia

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author name string

Robert D Brown

2

0 references

Stephen S Rich

https://scigraph.springernature.com/pub.10.1186/1471-2350-3-1

6

0 references

language of work or name

English

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publication date

2002

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published in

BMC Medical Genetics

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volume

3

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issue

1

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page(s)

1

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exact match

0 references

cites work

Effect of oral nimodipine on cerebral infarction and outcome after subarachnoid haemorrhage: British aneurysm nimodipine trial

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=79001

Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=79001

A genome screen in multiple sclerosis reveals susceptibility loci on chromosome 6p21 and 17q22

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=79001

A genome-wide search for human type 1 diabetes susceptibility genes

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=79001

Classification of subtype of acute ischemic stroke. Definitions for use in a multicenter clinical trial. TOAST. Trial of Org 10172 in Acute Stroke 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=79001

A genome-wide search for susceptibility genes in human systemic lupus erythematosus sib-pair families

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=79001

Complete multipoint sib-pair analysis of qualitative and quantitative traits

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=79001

Carotid stenosis: factors affecting symptomatology

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=79001

Validating the Questionnaire for Verifying Stroke-Free Status (QVSFS) by neurological history and examination

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=79001

Ethical and methodological issues in pedigree stroke research

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=79001

Verifying the stroke-free phenotype by structured telephone interview

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=79001

The genetics of multiple sclerosis: principles, background and updated results of the United Kingdom systematic genome screen

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=79001

Predictive genetic tests: problems and pitfalls

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=79001

Use of human tissues in research: clarifying clinician and researcher roles and information flows

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=79001

Chromosomal mapping of quantitative trait loci contributing to stroke in a rat model of complex human disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=79001

A randomized controlled trial of high-dose intravenous nicardipine in aneurysmal subarachnoid hemorrhage. A report of the Cooperative Aneurysm Study

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=79001

Drugs and surgery in the prevention of ischemic stroke

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=79001

Accuracy of initial stroke subtype diagnosis in the TOAST study. Trial of ORG 10172 in Acute Stroke Treatment

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=79001

Mendelian etiologies of stroke

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=79001

Linkage strategies for genetically complex traits. II. The power of affected relative pairs

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=79001

Linkage strategies for genetically complex traits. I. Multilocus models

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=79001

The generalized sib pair IBD distribution: its use in the detection of linkage

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=79001

Trends in acute ischemic stroke trials through the 20th century

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=79001

Private company wins rights to Icelandic gene database.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=79001

Endothelial nitric oxide synthase exon 7 polymorphism, ischemic cerebrovascular disease, and carotid atheroma.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=79001

The apolipoprotein E epsilon4 allele and outcome in cerebrovascular disease.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=79001

Naming names in human genetic variation research.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=79001

Patterns of MRI lesions in CADASIL.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=79001

ACE, MTHFR, factor V Leiden, and APOE polymorphisms in patients with vascular and Alzheimer's dementia.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=79001

The prothrombin G20210A mutation and factor V Leiden mutation in patients with cerebrovascular disease.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=79001

Parental history of cardiovascular disease and risk of stroke. A prospective follow-up of 14371 middle-aged men and women in Finland.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=79001

Using discordant sib pairs to map loci for qualitative traits with high sibling recurrence risk.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=79001

Efficiency of typing unaffected relatives in an affected-sib-pair linkage study with single-locus and multiple tightly linked markers.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=79001

Lipoprotein and apolipoprotein profile in men with ischemic stroke. Role of lipoprotein(a), triglyceride-rich lipoproteins, and apolipoprotein E polymorphism.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=79001

Familial history of stroke and stroke risk. The Family Heart Study

30 May 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-1

SPECT study of a German CADASIL family: a phenotype with migraine and progressive dementia only.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-1

FV-ARG-506-GLN-Mutation-associated resistance to activated protein C in ischemic stroke

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-1

Prospective study of serum total homocysteine concentration and risk of stroke in middle-aged British men.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-1

A common polymorphism in the methylenetetrahydrofolate reductase gene, homocysteine, and ischemic cerebrovascular disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-1

Deletion polymorphism in the angiotensin-converting enzyme gene in patients with a history of ischemic stroke.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-1

Apolipoprotein E4 phenotype is not an important risk factor for coronary heart disease or stroke in elderly subjects

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-1

Apolipoprotein E epsilon 2 allele and risk of stroke in the older population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-1

Prevalence of apolipoprotein E phenotypes in ischemic cerebrovascular disease. A case-control study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-1

Prevalence of apolipoprotein E alleles in healthy subjects and survivors of ischemic stroke: an Italian Case-Control Study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-1

Paraoxonase PON1 polymorphism leu-Met54 is associated with carotid atherosclerosis: results of the Austrian Stroke Prevention Study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-1

A full genome scan for late onset Alzheimer's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-1

Complete genomic screen in late-onset familial Alzheimer disease. Evidence for a new locus on chromosome 12.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-1

Genetic studies on chromosome 12 in late-onset Alzheimer disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-1

A genome-wide search for human non-insulin-dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-1

Feasibility of an affected sibling pair study in ischemic stroke: results of a 2-center family history registry.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-1

Epidemiology of ischemic stroke subtypes according to TOAST criteria: incidence, recurrence, and long-term survival in ischemic stroke subtypes: a population-based study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-1

Ischemic stroke subtypes: a population-based study of incidence and risk factors.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-1

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-1

Rules for research on human genetic variation--lessons from Iceland.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-1

A full genome search in multiple sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-1

Loci on chromosomes 2 (NIDDM1) and 15 interact to increase susceptibility to diabetes in Mexican Americans

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-1

Familial aggregation of stroke. The Framingham Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-1

If I am only for myself, what am I? A communitarian look at the privacy stalemate

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=79001

Task force 3: clinical research in a molecular era and the need to expand its ethical imperatives

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=79001

Linkage and mode of inheritance in complex traits.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=79001

A study of twins and stroke

28 November 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-1

Endothelial changes in muscle and skin biopsies in patients with CADASIL

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-1

Risk of stroke in young women and two prothrombotic mutations: factor V Leiden and prothrombin gene variant (G20210A)

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-1

Ischemic stroke in the elderly. Role of the common factor V mutation causing resistance to activated protein C

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-1

Factor V Leiden gene mutation and thrombin generation in relation to the development of acute stroke

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-1

Mutation in the gene coding for coagulation factor V and the risk of myocardial infarction, stroke, and venous thrombosis in apparently healthy men

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-1

Polymorphisms of the human platelet antigens HPA-1, HPA-2, HPA-3, and HPA-5 on the platelet receptors for fibrinogen (GPIIb/IIIa), von Willebrand factor (GPIb/IX), and collagen (GPIa/IIa) are not correlated with an increased risk for stroke

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-1

Platelet glycoprotein receptor IIIa polymorphism P1A2 and ischemic stroke risk: the Stroke Prevention in Young Women Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-1

Angiotensin-converting enzyme gene deletion polymorphism. A new risk factor for lacunar stroke but not carotid atheroma

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-1

Apolipoprotein E polymorphism and stroke in a population sample aged 75 years or more

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-1

Divergent association of apolipoprotein E polymorphism with vascular disease in patients with NIDDM and control subjects

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-1

A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex. The Multiple Sclerosis Genetics Group

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-1

A genome-wide search for asthma susceptibility loci in ethnically diverse populations. The Collaborative Study on the Genetics of Asthma (CSGA)

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-1

The World Health Organization MONICA Project (monitoring trends and determinants in cardiovascular disease): a major international collaboration. WHO MONICA Project Principal Investigators

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-1

Affected-sib-pair interval mapping and exclusion for complex genetic traits: sampling considerations

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-1

Brief clinical report on a deletion 5q35.3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-1

Apolipoprotein E variants in ischemic stroke

21 January 2018

1 reference

12 December 2020

Genetic testing and insurance. The Ad Hoc Committee on Genetic Testing/Insurance Issues

1 reference

12 December 2020

A common prothrombin variant (20210 G to A) increases the risk of myocardial infarction in young women

1 reference

12 December 2020

Subtyping in ischemic stroke genetic research

1 reference

12 December 2020

Molecular approach to assessing the genetic risk of cerebral infarction: deletion polymorphism in the gene encoding angiotensin 1-converting enzyme

1 reference

12 December 2020

Arg506Gln factor V mutation (factor V Leiden) in patients with ischaemic cerebrovascular disease and survivors of myocardial infarction

1 reference

12 December 2020

Factor V Leiden (resistance to activated protein C) increases the risk of myocardial infarction in young women

1 reference

12 December 2020