Author:
Denny Joshua C.,Tenenbaum Jessica D.,Might Matt
Publisher
Springer International Publishing
Reference84 articles.
1. 1000 Genomes Project Consortium, Auton, A., Brooks, L. D., Durbin, R. M., Garrison, E. P., Kang, H. M., et al. (2015). A global reference for human genetic variation. Nature, 526(7571), 68–74. https://doi.org/10.1038/nature15393.
2. 23andWe: The First Annual Update – 23andMe Blog. (n.d.). Retrieved from https://blog.23andme.com/23andme-and-you/23andwe-the-first-annual-update/
3. Ahmad, T., Pencina, M. J., Schulte, P. J., O’Brien, E., Whellan, D. J., Piña, I. L., et al. (2014). Clinical implications of chronic heart failure phenotypes defined by cluster analysis. Journal of the American College of Cardiology, 64(17), 1765–1774. https://doi.org/10.1016/j.jacc.2014.07.979.
4. Bastarache, L., Hughey, J. J., Hebbring, S., Marlo, J., Zhao, W., Ho, W. T., et al. (2018). Phenotype risk scores identify patients with unrecognized Mendelian disease patterns. Science, 359(6381), 1233–1239. https://doi.org/10.1126/science.aal4043.
5. Bentley, A. R., Callier, S., & Rotimi, C. N. (2017). Diversity and inclusion in genomic research: Why the uneven progress? Journal of Community Genetics, 8(4), 255–266. https://doi.org/10.1007/s12687-017-0316-6.