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Genomics
Citations 1-10 of 27 total displayed.
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Most recent content
(1 Dec 2009):
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- Original Contributions
Analysis of Genetic Variability and Whole Genome Linkage of Whole-Brain, Subcortical, and Ependymal Hyperintense White Matter Volume
- Peter Kochunov, David Glahn, Anderson Winkler, Ravindranath Duggirala, Rene L. Olvera, Shelley Cole, Thomas D. Dyer, Laura Almasy, Peter T. Fox, and John Blangero
Stroke 2009;40:3685-3690; published online before print as doi:10.1161/STROKEAHA.109.565390
[Abstract]
[Full text]
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Past content
(since Apr 2000):
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- Topical Review
Pharmacogenetics and Stroke
- James F. Meschia
Stroke 2009;40:3641-3645; published online before print as doi:10.1161/STROKEAHA.109.562231
[Abstract]
[Full text]
- Articles
Analysis of Genetic Variability and Whole Genome Linkage of Whole-Brain, Subcortical, and Ependymal Hyperintense White Matter Volume
- Peter Kochunov, David Glahn, Anderson Winkler, Ravindranath Duggirala, Rene L. Olvera, Shelley Cole, Thomas D. Dyer, Laura Almasy, Peter T. Fox, and John Blangero
Stroke published October 15, 2009, doi:10.1161/STROKEAHA.109.565390
[Abstract]
- Original Contributions
Multi-Ethnic Genetic Association Study of Carotid Intima-Media Thickness Using a Targeted Cardiovascular SNP Microarray
- Matthew B. Lanktree, Robert A. Hegele, Salim Yusuf, and Sonia S. Anand
Stroke 2009;40:3173-3179; published online before print as doi:10.1161/STROKEAHA.109.556563
[Abstract]
[Full text]
- Articles
Pharmacogenetics and Stroke
- James F. Meschia
Stroke published September 17, 2009, doi:10.1161/STROKEAHA.109.562231
[Abstract]
- Articles
Multi-Ethnic Genetic Association Study of Carotid Intima-Media Thickness Using a Targeted Cardiovascular SNP Microarray
- Matthew B. Lanktree, Robert A. Hegele, Salim Yusuf, and Sonia S. Anand
Stroke published August 13, 2009, doi:10.1161/STROKEAHA.109.556563
[Abstract]
- Case Reports
Novel LMNA Mutation in Atypical Werner Syndrome Presenting With Ischemic Disease
- Dimitri Renard, Genevieve Fourcade, Didier Milhaud, Didier Bessis, Vera Esteves-Vieira, Amandine Boyer, Patrice Roll, Patrice Bourgeois, Nicolas Levy, and Annachiara De Sandre-Giovannoli
Stroke 2009;40:e11-14e; published online before print as doi:10.1161/STROKEAHA.108.531780
[Abstract]
[Full text]
- Articles
Novel LMNA Mutation in Atypical Werner Syndrome Presenting With Ischemic Disease
- Dimitri Renard, Genevieve Fourcade, Didier Milhaud, Didier Bessis, Vera Esteves-Vieira, Amandine Boyer, Patrice Roll, Patrice Bourgeois, Nicolas Levy, and Annachiara De Sandre-Giovannoli
Stroke published December 18, 2008, doi:10.1161/STROKEAHA.108.531780
[Abstract]
- Original Contributions
Evaluation of the Paraoxonases as Candidate Genes for Stroke: Gln192Arg Polymorphism in the Paraoxonase 1 Gene Is Associated With Increased Risk of Stroke
- Koustubh Ranade, Todd G. Kirchgessner, Olga A. Iakoubova, James J. Devlin, Terrye DelMonte, Priya Vishnupad, Lester Hui, Zenta Tsuchihashi, Frank M. Sacks, Marc S. Sabatine, Eugene Braunwald, Thomas J. White, Peter M. Shaw, and Nicholas C. Dracopoli
Stroke 2005;36:2346-2350; published online before print as doi:10.1161/01.STR.0000185703.88944.7d
[Abstract]
[Full text]
- Articles
Evaluation of the Paraoxonases as Candidate Genes for Stroke. Gln192Arg Polymorphism in the Paraoxonase 1 Gene Is Associated With Increased Risk of Stroke
- Koustubh Ranade, Todd G. Kirchgessner, Olga A. Iakoubova, James J. Devlin, Terrye DelMonte, Priya Vishnupad, Lester Hui, Zenta Tsuchihashi, Frank M. Sacks, Marc S. Sabatine, Eugene Braunwald, Thomas J. White, Peter M. Shaw, and Nicholas C. Dracopoli
Stroke published October 20, 2005, doi:10.1161/01.STR.0000185703.88944.7d
[Abstract]
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