@misc{indiciae226b4bf64bc3,
  title = {Impact of rare and common genetic variants on diabetes diagnosis by hemoglobin A1c in multi-ancestry cohorts: The Trans-Omics for Precision Medicine Program.},
  author = {Sarnowski, C. and Leong, A. and Raffield, L. M. and Wu, P. and de Vries, P. S. and DiCorpo, D. and Guo, X. and Xu, H. and Liu, Y. and Zheng, X. and Hu, Y. and Brody, J. A. and Goodarzi, M. O. and Hidalgo, B. A. and Highland, H. M. and Jain, D. and Liu, C.-T. and Naik, R. P. and Perry, J. A. and Porneala, B. C. and Selvin, E. and Wessel, J. and Psaty, B. M. and Curran, J. E. and Peralta, J. M. and Blangero, J. and Kooperberg, C. and Mathias, R. and Johnson, A. D. and Reiner, A. P. and Mitchell, B. D. and Cupples, L. A. and Vasan, R. S. and Correa, A. and Morrison, A. C. and Boerwinkle, E. and Rotter, J. I. and Rich, S. S. and Manning, A. K. and Dupuis, J. and Meigs, J. B. and the TOPMed Diabetes working group, and t},
  year = {2019},
  doi = {10.1101/643932},
  url = {https://www.biorxiv.org/content/10.1101/643932v1},
  note = {Source identifier: 10.1101/643932}
}