@misc{indiciaefbf45189412b,
  title = {Identification of rare-disease genes in diverse undiagnosed cases using whole blood transcriptome sequencing and large control cohorts},
  author = {Fresard, L. and Smail, C. and Smith, K. S. and Ferraro, N. M. and Teran, N. A. and Kernohan, K. D. and Bonner, D. and Li, X. and Marwaha, S. and Zappala, Z. and Balliu, B. and Davis, J. R. and Liu, B. and Prybol, C. J. and Kholer, J. N. and Zastrow, D. B. and Fisk, D. G. and Grove, M. E. and Davidson, J. M. and Hartley, T. and Joshi, R. and Strober, B. J. and Utiramerur, S. and Care4Rare Canada Consortium, and Undiagnosed Diseases Network, and Lind, L. and Ingelsson, E. and Battle, A. and Bejerano, G. and Bernstein, J. A. and Ashley, E. A. and Boycott, K. M. and Merker, J. D. and Wheeler, M. T. and Montgomery, S. B.},
  year = {2018},
  doi = {10.1101/408492},
  url = {https://www.biorxiv.org/content/10.1101/408492v1},
  note = {Source identifier: 10.1101/408492}
}