Ghent University Academic Bibliography

Your filters: cql: author="Seeleuthner, Yoann" or (type any "bookEditor issueEditor" and editor="Seeleuthner, Yoann")

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Somatic deficiency of the human E3 ubiquitin ligase CBL in leukocytes impairs B cell but not T cell development and function

Taja Vatovec, Anna-Lena Neehus, Katherine J. L. Jackson, Danielle T. Avery, Ivan Bagarić, Lucia Erazo, Carlos A. Arango-Franco, Masato Ogishi, Syed F. Ahmed, Axel Cederholm, et al.

(2026) NATURE IMMUNOLOGY. 27(2). p.308-322
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SARS-CoV-2 brainstem encephalitis in human inherited DBR1 deficiency

Yi-Hao Chan, Vanja Lundberg, Jérémie Le Pen, Jiayi Yuan, Danyel Lee, Francesca Pinci, Stefano Volpi, Koji Nakajima, Vincent Bondet, Sanna Åkesson, et al.

(2024) JOURNAL OF EXPERIMENTAL MEDICINE. 221(9).
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Heterozygous BTNL8 variants in individuals with multisystem inflammatory syndrome in children (MIS-C)

Evangelos Bellos, Dilys Santillo, Pierre Vantourout, Heather R. Jackson, Amedine Duret, Henry Hearn, Yoann Seeleuthner, Estelle Talouarn, Stephanie Hodeib, Harsita Patel, et al.

(2024) JOURNAL OF EXPERIMENTAL MEDICINE. 221(12).
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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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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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X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19

Takaki Asano, Bertrand Boisson, Fanny Onodi, Daniela Matuozzo, Marcela Moncada-Velez, Majistor Raj Luxman Maglorius Renkilaraj, Peng Zhang, Laurent Meertens, Alexandre Bolze, Marie Materna, et al.

(2021) SCIENCE IMMUNOLOGY. 6(62).
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SARS-CoV-2–related MIS-C : a key to the viral and genetic causes of Kawasaki disease?

Vanessa Sancho-Shimizu, Petter Brodin, Aurélie Cobat, Catherine M. Biggs, Julie Toubiana, Carrie L. Lucas, Sarah E. Henrickson, Alexandre Belot, Elie Haddad, Kathie Beland, et al.

(2021) JOURNAL OF EXPERIMENTAL MEDICINE. 218(6).
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Dominant-negative mutations in human IL6ST underlie hyper-IgE syndrome

Vivien Béziat, Simon Tavernier (UGent) , Yin-Huai Chen, Cindy S. Ma, Marie Materna, Arian Laurence, Jens Staal (UGent) , Dominik Aschenbrenner, Lisa Roels (UGent) , Lisa Worley, et al.

(2020) JOURNAL OF EXPERIMENTAL MEDICINE. 217(6).
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Autoantibodies against type I IFNs in patients with life-threatening COVID-19

Paul Bastard, Lindsey B. Rosen, Qian Zhang, Eleftherios Michailidis, Hans-Heinrich Hoffmann, Yu Zhang, Karim Dorgham, Quentin Philippot, Jeremie Rosain, Vivien Beziat, et al.

(2020) SCIENCE. 370(6515).
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Inborn errors of type I IFN immunity in patients with life-threatening COVID-19

Qian Zhang, Paul Bastard, Zhiyong Liu, Jérémie Le Pen, Marcela Moncada-Velez, Jie Chen, Masato Ogishi, Ira K. D. Sabli, Stephanie Hodeib, Cecilia Korol, et al.

(2020) SCIENCE. 370(6515). p.422-+

Academic Bibliography

Somatic deficiency of the human E3 ubiquitin ligase CBL in leukocytes impairs B cell but not T cell development and function

SARS-CoV-2 brainstem encephalitis in human inherited DBR1 deficiency

Heterozygous BTNL8 variants in individuals with multisystem inflammatory syndrome in children (MIS-C)

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

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

X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19

SARS-CoV-2–related MIS-C : a key to the viral and genetic causes of Kawasaki disease?

Dominant-negative mutations in human IL6ST underlie hyper-IgE syndrome

Autoantibodies against type I IFNs in patients with life-threatening COVID-19

Inborn errors of type I IFN immunity in patients with life-threatening COVID-19

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