A stroke gene panel for whole-exome sequencing

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A stroke gene panel for whole-exome sequencing is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1038/S41431-018-0274-4
P932PMC publication ID6336868
P698PubMed publication ID30356112

P50authorAndreea IlincaQ87020181
Ulf KristofferssonQ114337615
P2093author name stringMaria Soller
Paul Piccinelli
Arne G Lindgren
Sofie Samuelsson
P2860cites workClassification of subtype of acute ischemic stroke. Definitions for use in a multicenter clinical trial. TOAST. Trial of Org 10172 in Acute Stroke TreatmentQ22306370
Genetic Risk Factors for Ischemic and Hemorrhagic StrokeQ28079249
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's diseaseQ28244731
Genetic overlap between diagnostic subtypes of ischemic strokeQ30360595
New insights into mechanisms of small vessel disease stroke from genetics.Q30400024
Hereditary cerebral small vessel disease and strokeQ31169895
Stroke genetics: a review and updateQ34357593
Lombardia GENS: a collaborative registry for monogenic diseases associated with stroke.Q34480067
Application of next-generation sequencing technologies in NeurologyQ34658348
Systematic review of methods and results of studies of the genetic epidemiology of ischemic strokeQ35611174
Family aggregation of cardiovascular disease mortality: a register-based prospective study of pooled Nordic twin cohorts.Q38879596
Familial aggregation of stroke amongst young patients in Lund Stroke RegisterQ38950143
Family history in ischemic stroke before 70 years of age: the Sahlgrenska Academy Study on Ischemic StrokeQ40417012
Next generation sequencing for systematic assessment of genetics of small-vessel disease and lacunar stroke.Q41331897
Global, regional, and national disability-adjusted life-years (DALYs) for 333 diseases and injuries and healthy life expectancy (HALE) for 195 countries and territories, 1990-2016: a systematic analysis for the Global Burden of Disease Study 2016.Q41686289
Cathepsin A-related arteriopathy with strokes and leukoencephalopathy (CARASAL).Q48461635
Feasibility of an affected sibling pair study in ischemic stroke: results of a 2-center family history registryQ48691811
Clinical Pregenetic Screening for Stroke Monogenic Diseases: Results From Lombardia GENS RegistryQ48704656
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypesQ50531000
A computerized algorithm for etiologic classification of ischemic stroke: the Causative Classification of Stroke SystemQ51905089
Multiplicity of risk factors in ischemic stroke patients: relations to age, sex, and subtype--a study of 2,505 patients from the lund stroke register.Q64915420
Prevalence of stroke and vascular risk factors among first-degree relatives of stroke patients and control subjects. A prospective consecutive studyQ81310275
P433issue2
P407language of work or nameEnglishQ1860
P304page(s)317-324
P577publication date2018-10-24
P1433published inEuropean Journal of Human GeneticsQ2155433
P1476titleA stroke gene panel for whole-exome sequencing
P478volume27

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cites work (P2860)
Q90332812Whole-Exome Sequencing in 22 Young Ischemic Stroke Patients With Familial Clustering of Stroke
Q103836788Whole-exome sequencing of Finnish patients with vascular cognitive impairment

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