Ghent University Academic Bibliography

Your filters: cql: author="Arias, Andrés A." or (type any "bookEditor issueEditor" and editor="Arias, Andrés A.")

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Deleterious variants in the autophagy-related gene RB1CC1/FIP200 impair immunity to SARS-CoV-2

Lili Hu, Renee M. van der Sluis, Kennith Brian Castelino, Bao-Cun Zhang, Andreas Ronit, Thomas Zillinger, Marvin Werner, Sofie Eg Jørgensen, Anne Louise Hansen, Alice Pedersen, et al.

(2025) NATURE COMMUNICATIONS. 16(1).
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Higher COVID-19 pneumonia risk associated with anti-IFN-α than with anti-IFN-ω auto-Abs in children

Paul Bastard, Adrian Gervais, Maki Taniguchi, Liisa Saare, Karita Särekannu, Tom Le Voyer, Quentin Philippot, Jérémie Rosain, Lucy Bizien, Takaki Asano, et al.

(2024) JOURNAL OF EXPERIMENTAL MEDICINE. 221(2).
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Impact of SARS-CoV-2 infection and COVID-19 on patients with inborn errors of immunity

Stuart G. Tangye, Laurent Abel, Salah Al-Muhsen, Alessandro Aiuti, Saleh Al-Muhsen, Fahd Al-Mulla, Mark S. Anderson, Evangelos Andreakos, Antonio Novelli, Andrés A. Arias, et al.

(2023) JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY. 151(4). p.818-831
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Inherited and acquired errors of type I interferon immunity govern susceptibility to COVID-19 and multisystem inflammatory syndrome in children

Giorgia Bucciol, Isabelle Meyts, Laurent Abel, Salah Al-Muhsen, Alessandro Aiuti, Fahd Al-Mulla, Evangelos Andreakos, Novelli Antonio, Andrés A. Arias, Sophie Trouillet-Assant, et al.

(2023) JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY. 151(4). p.832-840
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Inborn errors of OAS–RNase L in SARS-CoV-2–related multisystem inflammatory syndrome in children

Danyel Lee, Jérémie Le Pen, Ahmad Yatim, Beihua Dong, Yann Aquino, Masato Ogishi, Rémi Pescarmona, Estelle Talouarn, Darawan Rinchai, Peng Zhang, et al.

(2023) SCIENCE. 379(6632).
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Humans with inherited MyD88 and IRAK-4 deficiencies are predisposed to hypoxemic COVID-19 pneumonia

Ana García-García, Rebeca Pérez de Diego, Carlos Flores, Darawan Rinchai, Jordi Solé-Violán, Àngela Deyà-Martínez, Blanca García-Solis, José M. Lorenzo-Salazar, Elisa Hernández-Brito, Anna-Lisa Lanz, et al.

(2023) JOURNAL OF EXPERIMENTAL MEDICINE. 220(5).
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Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency

Tom Le Voyer, Audrey V. Parent, Xian Liu, Axel Cederholm, Adrian Gervais, Jérémie Rosain, Tina Nguyen, Malena Perez Lorenzo, Elze Rackaityte, Darawan Rinchai, et al.

(2023) NATURE. 623(7988). p.803-813
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Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19

Daniela Matuozzo, Estelle Talouarn, Astrid Marchal, Peng Zhang, Jeremy Manry, Yoann Seeleuthner, Yu Zhang, Alexandre Bolze, Matthieu Chaldebas, Baptiste Milisavljevic, et al.

(2023) GENOME MEDICINE. 15(1).
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- Miscellaneous
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Decoding the human genetic and immunological basis of COVID-19 mRNA vaccine-induced myocarditis

Alexandre Bolze, Trine H. Mogensen, Shen-Ying Zhang, Laurent Abel, Evangelos Andreakos, Lisa M. Arkin, Alessandro Borghesi, Petter Brodin, David Hagin, Giuseppe Novelli, et al.

(2022) JOURNAL OF CLINICAL IMMUNOLOGY. 42(7). p.1354-1359
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Studying severe long COVID to understand post-infectious disorders beyond COVID-19

Petter Brodin, Giorgio Casari, Liam Townsend, Cliona O’Farrelly, Ivan Tancevski, Judith Löffler-Ragg, Trine H. Mogensen, Jean Laurent Casanova, Laurent Abel, Alessandro Aiuti, et al.

(2022) NATURE MEDICINE. 28(5). p.879-882

Academic Bibliography

Deleterious variants in the autophagy-related gene RB1CC1/FIP200 impair immunity to SARS-CoV-2

Higher COVID-19 pneumonia risk associated with anti-IFN-α than with anti-IFN-ω auto-Abs in children

Impact of SARS-CoV-2 infection and COVID-19 on patients with inborn errors of immunity

Inherited and acquired errors of type I interferon immunity govern susceptibility to COVID-19 and multisystem inflammatory syndrome in children

Inborn errors of OAS–RNase L in SARS-CoV-2–related multisystem inflammatory syndrome in children

Humans with inherited MyD88 and IRAK-4 deficiencies are predisposed to hypoxemic COVID-19 pneumonia

Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency

Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19

Decoding the human genetic and immunological basis of COVID-19 mRNA vaccine-induced myocarditis

Studying severe long COVID to understand post-infectious disorders beyond COVID-19

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