Open AccessCorrection: Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease
Author(s) -
Enrique Audain,
Anna Wilsdon,
Jeroen Breckpot,
Jose M. G. Izarzugaza,
Tomas Fitzgerald,
AnneKarin Kahlert,
Alejandro Sifrim,
Florian Wünnemann,
Yasset PerezRiverol,
Hashim AbdulKhaliq,
Mads Bak,
Anne S. Bassett,
D. Woodrow Benson,
Felix Berger,
Ingo Daehnert,
Koenraad Devriendt,
Sven Dittrich,
Piers E.F. Daubeney,
Vidu Garg,
Karl Hackmann,
Kirstin Hoff,
Philipp Hofmann,
Gregor Dombrowsky,
Thomas Pickardt,
Ulrike Bauer,
Bernard Keavney,
Sabine Klaassen,
HansHeiner Kramer,
Christian R. Marshall,
Dianna M. Milewicz,
Scott A. LeMaire,
Joseph S. Coselli,
Michael E. Mitchell,
Aoy TomitaMitchell,
Siddharth K. Prakash,
Karl Stamm,
Alexandre F.R. Stewart,
Candice K. Silversides,
Reiner Siebert,
Brigitte Stiller,
Jill A. Rosenfeld,
Inga Vater,
Alex V. Postma,
Almuth Caliebe,
J. David Brook,
Grégor Andelfinger,
Matthew E. Hurles,
Bernard Thienpont,
Lars Allan Larsen,
MarcPhillip Hitz
Publication year - 2021
Publication title -
plos genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.587
H-Index - 233
eISSN - 1553-7404
pISSN - 1553-7390
DOI - 10.1371/journal.pgen.1009809
Subject(s) - haploinsufficiency , biology , genetics , candidate gene , computational biology , gene , bioinformatics , phenotype