Common NOTCH3 Variants and Cerebral Small-Vessel Disease

Stroke

Volumn 46, Issue 6, 2015, Pages 1482-1487

  Rutten Jacobs, Loes C A ^a   Traylor, Matthew ^a   Adib Samii, Poneh ^b   Thijs, Vincent ^c,d   Sudlow, Cathie ^e   Rothwell, Peter M ^f   Boncoraglio, Giorgio ^g   Dichgans, Martin ^h   Bevan, Steve ^a   Meschia, James ⁱ   Levi, Christopher ^j   Rost, Natalia S ^k   Rosand, Jonathan ^k   Hassan, Ahamad ^l   Markus, Hugh S ^a  

^a UNIVERSITY OF CAMBRIDGE   (United Kingdom)

^b ST GEORGE'S UNIVERSITY OF LONDON   (United Kingdom)

^c UNIVERSITY OF LEUVEN   (Belgium)

^d DEPARTMENT OF PLANT SYSTEMS BIOLOGY   (Belgium)

^e UNIVERSITY OF EDINBURGH   (United Kingdom)

^f UNIVERSITY OF OXFORD   (United Kingdom)

^g DEPARTMENT OF NEUROSURGERY   (Italy)

^h LUDWIG MAXIMILIANS UNIVERSITY   (Germany)

ⁱ MAYO CLINIC   (United States)

^j UNIVERSITY OF NEWCASTLE   (Australia)

^k MASSACHUSETTS GENERAL HOSPITAL   (United States)

^l LEEDS GENERAL INFIRMARY   (United Kingdom)

more..

Author keywords

CADASIL; cerebral small vessel diseases; genetic association studies; stroke, lacunar

Indexed keywords

NOTCH3 RECEPTOR; PROTEIN VARIANT; NOTCH RECEPTOR; NOTCH3 PROTEIN, HUMAN;

ADULT; ARTICLE; BRAIN ISCHEMIA; BRAIN SIZE; CARDIOVASCULAR RISK; CEREBROVASCULAR DISEASE; CONTROLLED STUDY; FEMALE; GENE FREQUENCY; GENETIC ASSOCIATION; GENETIC CODE; GENETIC RISK; GENOME; HUMAN; HYPERTENSION; LACUNAR STROKE; MAJOR CLINICAL STUDY; MALE; NUCLEAR MAGNETIC RESONANCE IMAGING; POPULATION GENETICS; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; STROKE PATIENT; WHITE MATTER; ALLELE; CLINICAL TRIAL; COMPLICATION; GENETICS; GENOME-WIDE ASSOCIATION STUDY; MIDDLE AGED; MULTICENTER STUDY; STROKE, LACUNAR;

ALLELES; FEMALE; GENE FREQUENCY; GENOME-WIDE ASSOCIATION STUDY; HUMANS; HYPERTENSION; MALE; MIDDLE AGED; POLYMORPHISM, SINGLE NUCLEOTIDE; RECEPTORS, NOTCH; STROKE, LACUNAR;

EID: 84942940873     PISSN: 00392499     EISSN: 15244628     Source Type: Journal    
DOI: 10.1161/STROKEAHA.114.008540     Document Type: Article

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