| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1012078260 |
| P356 | DOI | 10.1186/1471-2350-3-1 |
| P932 | PMC publication ID | 79001 |
| P698 | PubMed publication ID | 11882254 |
| P5875 | ResearchGate publication ID | 11481284 |
| P50 | author | John Anthony Hardy | Q6237755 |
| James F Meschia | Q78887459 | ||
| Thomas G Brott | Q87844681 | ||
| P2093 | author name string | Stephen S Rich | |
| Robert D Brown | |||
| P2860 | cites work | Classification of subtype of acute ischemic stroke. Definitions for use in a multicenter clinical trial. TOAST. Trial of Org 10172 in Acute Stroke Treatment | Q22306370 |
| Effect of oral nimodipine on cerebral infarction and outcome after subarachnoid haemorrhage: British aneurysm nimodipine trial | Q24675435 | ||
| A genome-wide search for human type 1 diabetes susceptibility genes | Q28247197 | ||
| Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients | Q28255796 | ||
| A genome screen in multiple sclerosis reveals susceptibility loci on chromosome 6p21 and 17q22 | Q28283861 | ||
| Complete multipoint sib-pair analysis of qualitative and quantitative traits | Q28763550 | ||
| A genome-wide search for susceptibility genes in human systemic lupus erythematosus sib-pair families | Q28776415 | ||
| Ethical and methodological issues in pedigree stroke research | Q30440503 | ||
| A randomized controlled trial of high-dose intravenous nicardipine in aneurysmal subarachnoid hemorrhage. A report of the Cooperative Aneurysm Study | Q30467610 | ||
| Verifying the stroke-free phenotype by structured telephone interview | Q33910376 | ||
| Validating the Questionnaire for Verifying Stroke-Free Status (QVSFS) by neurological history and examination | Q34392784 | ||
| Use of human tissues in research: clarifying clinician and researcher roles and information flows | Q34434744 | ||
| Linkage strategies for genetically complex traits. II. The power of affected relative pairs | Q35201348 | ||
| Chromosomal mapping of quantitative trait loci contributing to stroke in a rat model of complex human disease | Q38563272 | ||
| Mendelian etiologies of stroke | Q39672446 | ||
| Drugs and surgery in the prevention of ischemic stroke | Q40561483 | ||
| Linkage strategies for genetically complex traits. I. Multilocus models | Q40623210 | ||
| Carotid stenosis: factors affecting symptomatology | Q40672711 | ||
| The genetics of multiple sclerosis: principles, background and updated results of the United Kingdom systematic genome screen | Q40837236 | ||
| Predictive Genetic Tests: Problems and Pitfalls | Q40856273 | ||
| Accuracy of initial stroke subtype diagnosis in the TOAST study. Trial of ORG 10172 in Acute Stroke Treatment | Q40968365 | ||
| The generalized sib pair IBD distribution: its use in the detection of linkage | Q41042260 | ||
| Using discordant sib pairs to map loci for qualitative traits with high sibling recurrence risk. | Q42589526 | ||
| Efficiency of typing unaffected relatives in an affected-sib-pair linkage study with single-locus and multiple tightly linked markers. | Q42672500 | ||
| Linkage and mode of inheritance in complex traits. | Q43770036 | ||
| Prospective study of serum total homocysteine concentration and risk of stroke in middle-aged British men. | Q44040534 | ||
| Familial history of stroke and stroke risk. The Family Heart Study | Q44681410 | ||
| Apolipoprotein E4 Phenotype Is Not an Important Risk Factor for Coronary Heart Disease or Stroke in Elderly Subjects | Q45128303 | ||
| Trends in acute ischemic stroke trials through the 20th century | Q46087072 | ||
| FV-ARG-506-GLN-Mutation-associated resistance to activated protein C in ischemic stroke | Q47686776 | ||
| Naming Names in Human Genetic Variation Research | Q47750911 | ||
| Rules for research on human genetic variation--lessons from Iceland | Q47852953 | ||
| ACE, MTHFR, factor V Leiden, and APOE polymorphisms in patients with vascular and Alzheimer's dementia | Q47860994 | ||
| The prothrombin G20210A mutation and factor V Leiden mutation in patients with cerebrovascular disease | Q47869534 | ||
| Private company wins rights to Icelandic gene database | Q47998026 | ||
| Endothelial Nitric Oxide Synthase Exon 7 Polymorphism, Ischemic Cerebrovascular Disease, and Carotid Atheroma | Q48398492 | ||
| The Apolipoprotein E ε4 Allele and Outcome in Cerebrovascular Disease | Q48398522 | ||
| Patterns of MRI lesions in CADASIL | Q48408751 | ||
| Lipoprotein and apolipoprotein profile in men with ischemic stroke. Role of lipoprotein(a), triglyceride-rich lipoproteins, and apolipoprotein E polymorphism | Q48412906 | ||
| SPECT study of a German CADASIL family: a phenotype with migraine and progressive dementia only | Q48444580 | ||
| Prevalence of apolipoprotein E alleles in healthy subjects and survivors of ischemic stroke: an Italian Case-Control Study. | Q48530017 | ||
| A Common Polymorphism in the Methylenetetrahydrofolate Reductase Gene, Homocysteine, and Ischemic Cerebrovascular Disease | Q48626130 | ||
| Parental history of cardiovascular disease and risk of stroke. A prospective follow-up of 14371 middle-aged men and women in Finland | Q48670263 | ||
| Feasibility of an affected sibling pair study in ischemic stroke: results of a 2-center family history registry | Q48691811 | ||
| Epidemiology of ischemic stroke subtypes according to TOAST criteria: incidence, recurrence, and long-term survival in ischemic stroke subtypes: a population-based study | Q48691914 | ||
| Deletion polymorphism in the angiotensin-converting enzyme gene in patients with a history of ischemic stroke. | Q49152412 | ||
| Apolipoprotein E ε2 Allele and Risk of Stroke in the Older Population | Q50627123 | ||
| Ischemic stroke subtypes: a population-based study of incidence and risk factors | Q50654471 | ||
| Paraoxonase PON1 polymorphism leu-Met54 is associated with carotid atherosclerosis: results of the Austrian Stroke Prevention Study | Q50864296 | ||
| Prevalence of apolipoprotein E phenotypes in ischemic cerebrovascular disease. A case-control study | Q51055127 | ||
| Genetic studies on chromosome 12 in late-onset Alzheimer disease | Q51991719 | ||
| Complete genomic screen in late-onset familial Alzheimer disease. Evidence for a new locus on chromosome 12. | Q53219806 | ||
| A full genome scan for late onset Alzheimer's disease | Q53333524 | ||
| A genome-wide search for human non-insulin-dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2. | Q53780537 | ||
| Age-related effects on atherogenesis and scavenger enzymes of intracranial and extracranial arteries in men without classic risk factors for atherosclerosis | Q53989239 | ||
| If I am only for myself, what am I? A communitarian look at the privacy stalemate | Q56909642 | ||
| A full genome search in multiple sclerosis | Q57264092 | ||
| Loci on chromosomes 2 (NIDDM1) and 15 interact to increase susceptibility to diabetes in Mexican Americans | Q57308002 | ||
| Familial aggregation of stroke. The Framingham Study | Q57629057 | ||
| Task force 3: clinical research in a molecular era and the need to expand its ethical imperatives | Q58674999 | ||
| A study of twins and stroke | Q68093509 | ||
| The World Health Organization MONICA Project (monitoring trends and determinants in cardiovascular disease): a major international collaboration. WHO MONICA Project Principal Investigators | Q68250496 | ||
| Ischemic stroke in the elderly. Role of the common factor V mutation causing resistance to activated protein C | Q70878586 | ||
| A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex. The Multiple Sclerosis Genetics Group | Q71230101 | ||
| Apolipoprotein E polymorphism and stroke in a population sample aged 75 years or more | Q71269697 | ||
| Affected-sib-pair interval mapping and exclusion for complex genetic traits: sampling considerations | Q71300195 | ||
| Apolipoprotein E variants in ischemic stroke | Q71568570 | ||
| Arg506Gln factor V mutation (factor V Leiden) in patients with ischaemic cerebrovascular disease and survivors of myocardial infarction | Q71575892 | ||
| Angiotensin-converting enzyme gene deletion polymorphism. A new risk factor for lacunar stroke but not carotid atheroma | Q71948032 | ||
| Factor V Leiden gene mutation and thrombin generation in relation to the development of acute stroke | Q72294581 | ||
| Brief clinical report on a deletion 5q35.3. | Q72306583 | ||
| Genetic testing and insurance. The Ad Hoc Committee on Genetic Testing/Insurance Issues | Q72419255 | ||
| Mutation in the gene coding for coagulation factor V and the risk of myocardial infarction, stroke, and venous thrombosis in apparently healthy men | Q72596362 | ||
| Molecular approach to assessing the genetic risk of cerebral infarction: deletion polymorphism in the gene encoding angiotensin 1-converting enzyme | Q72880524 | ||
| A genome-wide search for asthma susceptibility loci in ethnically diverse populations. The Collaborative Study on the Genetics of Asthma (CSGA) | Q73196409 | ||
| Factor V Leiden (resistance to activated protein C) increases the risk of myocardial infarction in young women | Q73235510 | ||
| 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 | Q73520139 | ||
| A common prothrombin variant (20210 G to A) increases the risk of myocardial infarction in young women | Q73686426 | ||
| Divergent association of apolipoprotein E polymorphism with vascular disease in patients with NIDDM and control subjects | Q73704570 | ||
| Risk of Stroke in Young Women and Two Prothrombotic Mutations: Factor V Leiden and Prothrombin Gene Variant (G20210A) | Q74324113 | ||
| Platelet glycoprotein receptor IIIa polymorphism P1A2 and ischemic stroke risk: the Stroke Prevention in Young Women Study | Q74324120 | ||
| Endothelial changes in muscle and skin biopsies in patients with CADASIL | Q74458985 | ||
| Subtyping in ischemic stroke genetic research | Q81370684 | ||
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | sibling | Q31184 |
| P304 | page(s) | 1 | |
| P577 | publication date | 2002-01-01 | |
| P1433 | published in | BMC Medical Genetics | Q15759918 |
| P1476 | title | The Siblings With Ischemic Stroke Study (SWISS) protocol | |
| P478 | volume | 3 |
| Q30436684 | A survey of the SWISS researchers on the impact of sibling privacy protections on pedigree recruitment |
| Q33834878 | Bio-Repository of DNA in stroke (BRAINS): a study protocol |
| Q24649888 | Candidate gene polymorphisms for ischemic stroke |
| Q30428008 | Common mitochondrial sequence variants in ischemic stroke |
| Q30414654 | Common variants within oxidative phosphorylation genes influence risk of ischemic stroke and intracerebral hemorrhage |
| Q30410263 | Early-onset stroke and vasculopathy associated with mutations in ADA2 |
| Q30430617 | Effect modification by population dietary folate on the association between MTHFR genotype, homocysteine, and stroke risk: a meta-analysis of genetic studies and randomised trials |
| Q37344485 | Genetic considerations relevant to intracranial hemorrhage and brain arteriovenous malformations |
| Q24793784 | Genetic risk factors for cerebrovascular disease in children with sickle cell disease: design of a case-control association study and genomewide screen |
| Q37012822 | Genetic variants associated with myocardial infarction in the PSMA6 gene and Chr9p21 are also associated with ischaemic stroke |
| Q36018306 | Genetics of cerebrovascular disorders |
| Q36713912 | Genetics of ischaemic stroke |
| Q30430623 | Genomic risk profiling of ischemic stroke: results of an international genome-wide association meta-analysis |
| Q39436645 | Genomics, Biology, and Human Illness: Advances in the Monogenic Autoinflammatory Diseases |
| Q30440385 | IL1RN VNTR polymorphism in ischemic stroke: analysis in 3 populations |
| Q48203208 | In search of genes for stroke |
| Q92086026 | Interaction between an ATP-Binding Cassette A1 (ABCA1) Variant and Egg Consumption for the Risk of Ischemic Stroke and Carotid Atherosclerosis: a Family-Based Study in the Chinese Population |
| Q30444346 | Interobserver agreement in the trial of org 10172 in acute stroke treatment classification of stroke based on retrospective medical record review |
| Q36870175 | Ischemic stroke risk, smoking, and the genetics of inflammation in a biracial population: the stroke prevention in young women study |
| Q30438484 | Joint Commission primary stroke center certification does not affect proband enrollment: the siblings with ischemic stroke study |
| Q49476953 | Joint Effects of PON1 Polymorphisms and Vegetable Intake on Ischemic Stroke: A Family-Based Case Control Study. |
| Q30279161 | Meta-Analysis of Genome-Wide Association Studies Identifies Genetic Risk Factors for Stroke in African Americans |
| Q36418529 | Multilingual Validation of the Questionnaire for Verifying Stroke-Free Status in West Africa |
| Q33303923 | Neuroserpin polymorphisms and stroke risk in a biracial population: the stroke prevention in young women study |
| Q35148409 | New advances in identifying genetic anomalies in stroke-prone probands |
| Q80482540 | New advances in identifying genetic anomalies in stroke-prone probands |
| Q30445412 | Phosphodiesterase 4D and 5-lipoxygenase activating protein in ischemic stroke |
| Q35126776 | Phosphodiesterase 4D polymorphisms and the risk of cerebral infarction in a biracial population: the Stroke Prevention in Young Women Study |
| Q34544496 | Principal-component analysis for assessment of population stratification in mitochondrial medical genetics |
| Q30439096 | Proband race/ethnicity affects pedigree completion rate in a genetic study of ischemic stroke |
| Q34247395 | Rare variants in ischemic stroke: an exome pilot study |
| Q33592108 | Sibling history of myocardial infarction or stroke and risk of cardiovascular disease in the elderly: the Cardiovascular Health Study |
| Q30424818 | Siblings with ischemic stroke study: results of a genome-wide scan for stroke loci |
| Q30310914 | Spouses and unrelated friends of probands as controls for stroke genetics studies |
| Q30440501 | Stroke genetic research and adults with impaired decision-making capacity: a survey of IRB and investigator practices |
| Q33297927 | The Fangshan/Family-based Ischemic Stroke Study In China (FISSIC) protocol |
| Q24794936 | The Ischemic Stroke Genetics Study (ISGS) Protocol |
| Q30446682 | The Siblings With Ischemic Stroke Study (SWISS): a progress report |
| Q30436022 | The impact of privacy protections on recruitment in a multicenter stroke genetics study |
| Q36854881 | Validation of the 8-item questionnaire for verifying stroke free status with and without pictograms in three West African languages |
Search more.