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Revista Mexicana de Neurociencia

Academia Mexicana de Neurología, A.C.
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2013, Number 2

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Rev Mex Neuroci 2013; 14 (2)

Genetic heritability of ischemic stroke and the contribution of previously reported candidate gene and genomewide associations

Millán CMR, Espinosa SL
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Language: Spanish
References: 10
Page: 61-62
PDF size: 516.29 Kb.


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REFERENCES

  1. Hindorff LA, Sethupathy P, Junkins HA, Ramos EM, Mehta JP, et al. Potential etiologic and functional implications of genome-wide association loci for human diseases and traits. Proc Natl Acad Sci USA 2009;106: 9362-7.

  2. Manolio TA, Collins FS, Cox NJ, Goldstein DB, Hindorff LA, et al. Finding the missing heritability of complex diseases. Nature 2009; 461: 747-53.

  3. van Asselt KM, Kok HS, van der Schouw YT, Peeters PH, Pearson PL, et al. Role of genetic analyses in cardiology: part II: heritability estimation for gene searching in multifactorial diseases. Circulation 2006; 113: 1136-9.

  4. Atwood LD, Wolf PA, Heard-Costa NL, Massaro JM, Beiser A et al. Genetic variation in white matter hyperintensity volumen in the Framingham Study. Stroke 2004; 35: 1609-13.

  5. Moskau S, Golla A, Grothe C, Boes M, Pohl C, et al. Heritability of carotid artery atherosclerotic lesions: an ultrasound study in 154 families. Stroke 2005; 36: 5-8.

  6. International Stroke Genetics Consortium Consortium (ISGS); Wellcome Trust Case Control Consortium 2 (WTCCC2); Bellenguez C, Bevan S, Gschwendtner A, Spencer CC, Burgess AI, et al. Genomewide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke. Nat Genet 2012; 44: 328-33.

  7. Traylor M, Farrall M, Holliday EG, Sudlow C, Hopewell JC et al; Australian Stroke Genetics Collaborative, Wellcome Trust Case Control Consortium 2 (WTCCC2); International Stroke Genetics Consortium. Genetic risk factors for ischaemic stroke and its subtype (the METASTROKE Collaboration): a metaanalysis of genome-wide association studies. Lancet Neurol 2012; 11: 951-62.

  8. Bevan S, Traylor M, Adib-Samii P, Malik R, Paul NL et al. Genetic heritability of ischemic stroke and the contribution of previously reported candidate gene and genomewide associations. Stroke 2012; 43: 3161-7.

  9. Sinner MF, Ellinor PT, Hettinger T, Benjamin EJ, Kääb S. Genome-wide association studies of atrial fibrillation: past, present, and future. Cardiovasc Res 2011; 89: 701-9.

  10. Mohanty S, Santangeli P, Bai R, DI Biase L, Mohanty P et al. Variant rs2200733 on chromosome 4q25 confers increased risk of atrial fibrillation: evidence from a meta-analysis. J Cardiovasc Electrophysiol 2013; 24: 155-61.




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Rev Mex Neuroci. 2013;14