Failure to replicate the association of rare loss-of-function variants in type I IFN immunity genes with severe COVID-19

A recent report found that rare predicted loss-of-function (pLOF) variants across 13 candidate genes in TLR3- and IRF7-dependent type I IFN pathways explain up to 3.5% of severe COVID-19 cases. We performed whole-exome or whole-genome sequencing of 1,934 COVID-19 cases (713 with severe and 1,221 wit...

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Detalhes bibliográficos
Publicado no:medRxiv
Main Authors: Povysil, Gundula, Butler-Laporte, Guillaume, Shang, Ning, Weng, Chen, Khan, Atlas, Alaamery, Manal, Nakanishi, Tomoko, Zhou, Sirui, Forgetta, Vincenzo, Eveleigh, Robert, Bourgey, Mathieu, Aziz, Naveed, Jones, Steven, Knoppers, Bartha, Scherer, Stephen, Strug, Lisa, Lepage, Pierre, Ragoussis, Jiannis, Bourque, Guillaume, Alghamdi, Jahad, Aljawini, Nora, Albes, Nour, Al-Afghani, Hani M., Alghamdi, Bader, Almutair, Mansour, Mahmoud, Ebrahim Sabri, Safie, Leen Abu, Bardisy, Hadeel El, Al Harthi, Fawz S., Alshareef, Abdulraheem, Suliman, Bandar Ali, Alqahtani, Saleh, AlMalik, Abdulaziz, Alrashed, May M., Massadeh, Salam, Mooser, Vincent, Lathrop, Mark, Arabi, Yaseen, Mbarek, Hamdi, Saad, Chadi, Al-Muftah, Wadha, Badji, Radja, Al Thani, Asma, Ismail, Said I., Gharavi, Ali G., Abedalthagafi, Malak S., Richards, J Brent, Goldstein, David B., Kiryluk, Krzysztof
Formato: Artigo
Idioma:Inglês
Publicado em: Cold Spring Harbor Laboratory 2020
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7781338/
https://ncbi.nlm.nih.gov/pubmed/33398295
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/2020.12.18.20248226
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