Ghent University Academic Bibliography

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Machine learning–assisted diagnosis classification of primary immune dysregulation using IDDA2.1 phenotype profiling

Malte Schwitzkowski, Sai Pavan Kumar Veeranki, Benedikt N. Seidel, Gerhard Kindle, Stephan Rusch, Dalia Abd Elaziz, Sohilla Lofty M. Abdelkader, Avigaelle Abitbol, Hassan Abolhassani, Lalash Abrahim, et al.

(2026) JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY. 157(2). p.470-485
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Changing life expectancy in European countries 1990–2021 : a subanalysis of causes and risk factors from the Global Burden of Disease Study 2021

Nicholas Steel, Clarissa Maria Mercedes Bauer-Staeb, John A Ford, Cristiana Abbafati, Mohammed Altigani Abdalla, Atef Abdelkader, Parsa Abdi, Roberto Ariel Abeldaño Zuñiga, Olugbenga Olusola Abiodun, Hassan Abolhassani, et al.

(2025) LANCET PUBLIC HEALTH. 10(3). p.e172-e188
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The state of health in the European Union (EU-27) in 2019 : a systematic analysis for the Global Burden of Disease study 2019

João Vasco Santos, Alicia Padron-Monedero, Boris Bikbov, Diana Alecsandra Grad, Dietrich Plass, Enkeleint A. Mechili, Federica Gazzelloni, Florian Fischer, Gerhard Sulo, Che Henry Ngwa, et al.

(2024) BMC PUBLIC HEALTH. 24(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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Activated phosphoinositide 3-kinase δ syndrome : update from the ESID Registry and comparison with other autoimmune-lymphoproliferative inborn errors of immunity

Maria Elena Maccari, Martin Wolkewitz, Charlotte Schwab, Tiziana Lorenzini, Jennifer W. Leiding, Nathalie Aladjdi, Hassan Abolhassani, Wadih Abou-Chahla, Alessandro Aiuti, Saba Azarnoush, et al.

(2023) JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY. 152(4). p.984-996.e10
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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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Recessive inborn errors of type I IFN immunity in children with COVID-19 pneumonia

Qian Zhang, Daniela Matuozzo, Jérémie Le Pen, Danyel Lee, Leen Moens, Takaki Asano, Jonathan Bohlen, Zhiyong Liu, Marcela Moncada-Velez, Yasemin Kendir-Demirkol, et al.

(2022) JOURNAL OF EXPERIMENTAL MEDICINE. 219(8).
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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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Initial presenting manifestations in 16,486 patients with inborn errors of immunity include infections and noninfectious manifestations

Julian Thalhammer, Gerhard Kindle, Alexandra Nieters, Stephan Rusch, Mikko R.J. Seppänen, Alain Fische, Bodo Grimbacher, David Edgar, Matthew Buckland, Nizar Mahlaoui, et al.

(2021) JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY. 148(5). p.1332-1341.e5

Academic Bibliography

Machine learning–assisted diagnosis classification of primary immune dysregulation using IDDA2.1 phenotype profiling

Changing life expectancy in European countries 1990–2021 : a subanalysis of causes and risk factors from the Global Burden of Disease Study 2021

The state of health in the European Union (EU-27) in 2019 : a systematic analysis for the Global Burden of Disease study 2019

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

Activated phosphoinositide 3-kinase δ syndrome : update from the ESID Registry and comparison with other autoimmune-lymphoproliferative inborn errors of immunity

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

Recessive inborn errors of type I IFN immunity in children with COVID-19 pneumonia

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?

Initial presenting manifestations in 16,486 patients with inborn errors of immunity include infections and noninfectious manifestations

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