F
Fawz S. Al Harthi
Researcher at King Abdulaziz City for Science and Technology
Publications - 2
Citations - 66
Fawz S. Al Harthi is an academic researcher from King Abdulaziz City for Science and Technology. The author has contributed to research in topics: Population & Candidate gene. The author has an hindex of 2, co-authored 2 publications receiving 24 citations.
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Journal ArticleDOI
Rare loss-of-function variants in type I IFN immunity genes are not associated with severe COVID-19
Gundula Povysil,Guillaume Butler-Laporte,Ning Shang,Chen Wang,Atlas Khan,Manal Alaamery,Tomoko Nakanishi,Sirui Zhou,Vincenzo Forgetta,Robert Eveleigh,Mathieu Bourgey,Naveed Aziz,Steven J.M. Jones,Bartha Maria Knoppers,Stephen W. Scherer,Lisa J. Strug,Pierre Lepage,Jiannis Ragoussis,Guillaume Bourque,Jahad Alghamdi,Nora Aljawini,Nour Albes,Hani M. Al-Afghani,Bader Alghamdi,Mansour S Almutairi,Ebrahim Mahmoud,Leen Abu-Safieh,Hadeel El Bardisy,Fawz S. Al Harthi,Abdulraheem Alshareef,Bandar A. Suliman,Saleh A. Alqahtani,Abdulaziz Almalik,May Alrashed,Salam Massadeh,Vincent Mooser,Mark Lathrop,Mohamed Fawzy,Yaseen M. Arabi,Hamdi Mbarek,Chadi Saad,Wadha Al-Muftah,Junghyun Jung,Serghei Mangul,Radja Badji,Asma Al Thani,Said I. Ismail,Ali G. Gharavi,Malak Abedalthagafi,J. Brent Richards,David Goldstein,Krzysztof Kiryluk +51 more
TL;DR: In this article, 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.
Posted ContentDOI
Failure to replicate the association of rare loss-of-function variants in type I IFN immunity genes with severe COVID-19
Gundula Povysil,Guillaume Butler-Laporte,Ning Shang,Chen Weng,Atlas Khan,Manal Alaamery,Manal Alaamery,Tomoko Nakanishi,Sirui Zhou,Vincenzo Forgetta,Robert Eveleigh,Mathieu Bourgey,Naveed Aziz,Steven J.M. Jones,Bartha Maria Knoppers,Stephen W. Scherer,Lisa J. Strug,Pierre Lepage,Jiannis Ragoussis,Guillaume Bourque,Jahad Alghamdi,Nora Aljawini,Nora Aljawini,Nour Albes,Nour Albes,Hani M. Al-Afghani,Bader Alghamdi,Mansour Almutair,Ebrahim Mahmoud,Leen Abu Safie,Hadeel El Bardisy,Fawz S. Al Harthi,Abdulraheem Alshareef,Bandar A. Suliman,Saleh A. Alqahtani,Abdulaziz Almalik,May Alrashed,Salam Massadeh,Salam Massadeh,Vincent Mooser,Mark Lathrop,Yaseen Arabi,Yaseen Arabi,Hamdi Mbarek,Chadi Saad,Wadha Al-Muftah,Radja Badji,Asma Al Thani,Said I. Ismail,Ali G. Gharavi,Malak Abedalthagafi,J. Brent Richards,David Goldstein,Krzysztof Kiryluk +53 more
TL;DR: In this article, 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.