@misc{indiciaea19094d1f1da,
  title = {Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease},
  author = {Audain, E. and Wilsdon, A. and Breckpot, J. and Izarzugaza, J. M. and Fitzgerald, T. W. and Anne-Karin, K. and Sifrim, A. and Wuennemann, F. and Perez-Riverol, Y. and Abdul-Khaliq, H. and Bak, M. and Bassett, A. S. and Belmont, J. and Benson, W. D. and Berger, F. and Daehnert, I. and Devriendt, K. and Dittrich, S. and Daubeney, P. and Garg, V. and Hackmann, K. and Hoff, K. and Hofmann, P. and Dombrowsky, G. and Pickardt, T. and Bauer, U. and Keavney, B. and Klaassen, S. and Kramer, H.-H. and Marshall, C. R. and Milewicz, D. M. and Lemaire, S. and Coselli, J. and Mitchell, M. E. and Tomita-Mitchell, A. and Prakash, S. K. and Stamm, K. and Stewart, A. F. and Silversides, C. K. and Siebert, R. and Stiller, B. and Ros},
  year = {2020},
  doi = {10.1101/2020.06.25.169573},
  url = {https://www.biorxiv.org/content/10.1101/2020.06.25.169573v1},
  note = {Source identifier: 10.1101/2020.06.25.169573}
}