Genetics update: Impact of the human genome projects and identification of a stroke gene

Stroke

Volumn 32, Issue 6, 2001, Pages 1239-1241

  Alberts, Mark J ^a  

^a NORTHWESTERN UNIVERSITY   (United States)

Author keywords

Genetics; Stroke

Indexed keywords

EDITORIAL; GENE MAPPING; GENE MUTATION; GENETIC ANALYSIS; GENETIC PREDISPOSITION; HUMAN; PRIORITY JOURNAL; SEQUENCE ANALYSIS; STROKE;

EID: 0034986193     PISSN: 00392499     EISSN: None     Source Type: Journal    
DOI: 10.1161/01.STR.32.6.1239     Document Type: Editorial

References (15)

1. Initial sequencing and analysis of the human genome
2. The sequence of the human genome
3. A physical map of the human genome
4. A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms
5. Dissecting human disease in the postgenomic era
6. Identification of a gene for common stroke
7. Genetics and ischemic stroke
8. Apolipoprotein E genotype and cerebral amyloid angiopathy-related hemorrhage
9. Apolipoprotein E genotype and the risk of recurrent lobar intracerebral hemorrhage
10. Intracerebral hemorrhage outcome: Apolipoprotein E genotype, hematoma, and edema volumes
11. De novo mutation in the Notch3 gene causing CADASIL
12. Truncating mutations in CCM1, encoding KRIT1, cause hereditary cavernous angiomas
13. Linkage of familial moyamoya disease (spontaneous occlusion of the circle of Willis) to chromosome 17q25
14. Linkage analysis of moyamoya disease on chromosome 6