Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics InitiativeGuillaume Butler‐Laporte, Konrad J. Karczewski, Gundula Povysil et al.|PLoS Genetics|2022Cited by 68
Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findingsAxel Schmidt, Fabian Brand, Alexej Knaus et al.|Nature Genetics|2024Cited by 49
Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics InitiativeGuillaume Butler‐Laporte, Konrad J. Karczewski, Gundula Povysil et al.|medRxiv|2022Cited by 7
Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findingsAxel Schmidt, Fabian Brand, Magdalena Danyel et al.|Nature Genetics|2025Cited by 0