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

Circulation: Cardiovascular Genetics

Volumn 2, Issue 2, 2009, Pages 159-164

  Smith, J Gustav ^a,b   Melander, Olle ^b   Lövkvist, Håkan ^b   Hedblad, Bo ^b   Engström, Gunnar ^b   Nilsson, Peter ^b   Carlson, Joyce ^b   Berglund, Göran ^b   Norrving, Bo ^b   Lindgren, Arne ^b  

^a MASSACHUSETTS INSTITUTE OF TECHNOLOGY   (United States)

^b LUND UNIVERSITY   (Sweden)

Author keywords

Atherosclerosis; Cardiovascular diseases; Cerebral infarction; Genetics; Stroke

Indexed keywords

ADULT; AGED; ARTICLE; CARDIOVASCULAR RISK; CEREBROVASCULAR ACCIDENT; CHROMOSOME 9P; CHROMOSOME 9P21; CONTROLLED STUDY; CORONARY ARTERY DISEASE; DIABETES MELLITUS; FEMALE; GENE FREQUENCY; GENETIC ASSOCIATION; GENETIC SELECTION; GENETIC VARIABILITY; GENOTYPE; HEART INFARCTION; HUMAN; HYPERTENSION; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; SMOKING HABIT; CASE CONTROL STUDY; CHROMOSOME 9; GENETIC PREDISPOSITION; GENETICS; ISCHEMIA; MIDDLE AGED; PROSPECTIVE STUDY; RISK FACTOR; STROKE; SWEDEN;

AGED; AGED, 80 AND OVER; CASE-CONTROL STUDIES; CHROMOSOMES, HUMAN, PAIR 9; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENETIC VARIATION; GENOME-WIDE ASSOCIATION STUDY; HUMANS; ISCHEMIA; MALE; MIDDLE AGED; POLYMORPHISM, SINGLE NUCLEOTIDE; PROSPECTIVE STUDIES; RISK FACTORS; STROKE; SWEDEN;

EID: 70449110469     PISSN: 1942325X     EISSN: 19423268     Source Type: Journal    
DOI: 10.1161/CIRCGENETICS.108.835173     Document Type: Article

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