PLoS Genetics Audain, E, Wilsdon, A, Breckpot, J, Izarzugaza, J M G, Fitzgerald, T W, Kahlert, A K, Sifrim, A, Wünnemann, F, Perez-Riverol, Y, Abdul-Khaliq, H, Bak, M, Bassett, A S, Benson, W D, Berger, F, Daehnert, I, Devriendt, K, Dittrich, S, Daubeney, P E F, Garg, V, Hackmann, K, Hoff, K, Hofmann, P, Dombrowsky, G, Pickardt, T, Bauer, U, Keavney, B D, Klaassen, S, Kramer, H H, Marshall, C R, Milewicz, D M, Lemaire, S, Coselli, J S, Mitchell, M E, Tomita-Mitchell, A, Prakash, S K, Stamm, K, Stewart, A F R, Silversides, C K, Siebert, R, Stiller, B, Rosenfeld, J A, Vater, I, Postma, A V, Caliebe, A, Brook, J D, Andelfinger, G, Hurles, M E, Thienpont, B, Larsen, L A & Hitz, M P 2021, ' Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease ', PLOS Genetics, vol. 17, no. 7, e1009679 . https://doi.org/10.1371/journal.pgen.1009679 PLoS genetics, 17(7):e1009679. Public Library of Science PLoS Genetics, Vol 17, Iss 7, p e1009679 (2021) PLoS Genetics, Vol 17, Iss 9, p e1009809 (2021)