Common genetic variants do not predict recurrent events in coronary heart disease patients

BACKGROUND: It is unclear whether genetic variants identified from single nucleotide polymorphisms (SNPs) strongly associated with coronary heart disease (CHD) in genome-wide association studies (GWAS), or a genetic risk score (GRS) derived from them, can help stratify risk of recurrent events in pa...

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Detalles Bibliográficos
Autores principales: Thompson, P. L., Hui, J., Beilby, J., Palmer, L. J., Watts, G. F., West, M. J., Kirby, A., Marschner, S., Simes, R. J., Sullivan, D. R., White, H. D., Stewart, R., Tonkin, A. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8908687/
https://www.ncbi.nlm.nih.gov/pubmed/35264114
http://dx.doi.org/10.1186/s12872-022-02520-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8908687/
https://www.ncbi.nlm.nih.gov/pubmed/35264114
http://dx.doi.org/10.1186/s12872-022-02520-0

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