- Witte, John;
- Hoffmann, Thomas;
- Risch, Neil;
- Hoffmann, TJ;
- Sakoda, LC;
- Shen, L;
- Jorgenson, E;
- Habel, LA;
- Liu, J;
- Kvale, MN;
- Asgari, MM;
- Banda, Y;
- Corley, D
© 2015 Hoffmann et al.An efficient approach to characterizing the disease burden of rare genetic variants is to impute them into large well-phenotyped cohorts with existing genome-wide genotype data using large sequenced referenced panels. The success of t