Erika Van Nieuwenhove

Utrecht University — Netherlands

Immunology and Microbiology · Life Sciences

14h-index849citations29works2.22yr avg
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Research Topics

Immunodeficiency and Autoimmune Disorders(8), Inflammasome and immune disorders(6), Neutrophil, Myeloperoxidase and Oxidative Mechanisms(4), Autoimmune and Inflammatory Disorders Research(4), Blood disorders and treatments(4)

Publications28 total

Safety, immunogenicity and efficacy of the Shingrix vaccine in immunocompromised varicella zoster virus naïve pediatric patients
Vaccine·2025· 1 citedOpen Access
Safety, Immunogenicity and Efficacy of the Shingrix Vaccine in Immunocompromised Varicella Zoster Virus Naïve Pediatric Patients
SSRN Electronic Journal·2025Open Access
Highlight of 2023: Advances in pediatric immunology
Immunology and Cell Biology·2024· 1 citedOpen Access
OTULIN haploinsufficiency predisposes to environmentally directed inflammation
Frontiers in Immunology·2024· 5 citedOpen Access
Humoral and cellular immunogenicity, effectiveness and safety of COVID-19 mRNA vaccination in patients with pediatric rheumatic diseases: A prospective cohort study
Vaccine·2024· 4 citedOpen Access
Homozygous DBF4 mutation as a cause of severe congenital neutropenia
Journal of Allergy and Clinical Immunology·2023· 8 citedOpen Access
Author Correction: Disrupted Ca2+ homeostasis and immunodeficiency in patients with functional IP3 receptor subtype 3 defects
Cellular and Molecular Immunology·2022Open Access
Disrupted Ca2+ homeostasis and immunodeficiency in patients with functional IP3 receptor subtype 3 defects
Cellular and Molecular Immunology·2022· 22 citedOpen Access
A disease‐associated missense mutation in CYP4F3 affects the metabolism of leukotriene B4 via disruption of electron transfer
Journal of Cachexia Sarcopenia and Muscle·2022· 18 citedOpen Access
Human OTULIN haploinsufficiency impairs cell-intrinsic immunity to staphylococcal α-toxin
Science·2022· 59 citedOpen Access
Primary Sjögren's syndrome and high type I interferon signalling in a kindred with C2 deficiency
Rheumatology Advances in Practice·2022· 1 citedOpen Access
Enhanced cGAS-STING–dependent interferon signaling associated with mutations in ATAD3A
The Journal of Experimental Medicine·2021· 83 citedOpen Access
Disrupted Ca <sup>2+</sup> homeostasis and immunodeficiency in patients with functional Inositol 1,4,5-trisphosphate receptor subtype 3 defects
2021· 1 citedOpen Access
Enhanced cGAS-STING-dependent interferon signaling associated with mutations in ATAD3A
2021· 11 citedOpen Access
Phenotypical and Functional Characterization of Neutrophils in Two Pyrin-Associated Auto-inflammatory Diseases
Journal of Clinical Immunology·2021· 10 citedOpen Access
Phenotypic analysis of pyrin-associated autoinflammation with neutrophilic dermatosis patients during treatment
Lara D. Veeken·2021· 14 citedOpen Access
Defective Sec61α1 underlies a novel cause of autosomal dominant severe congenital neutropenia
Journal of Allergy and Clinical Immunology·2020· 44 citedOpen Access
Machine learning identifies an immunological pattern associated with multiple juvenile idiopathic arthritis subtypes
Annals of the Rheumatic Diseases·2019· 49 cited
NFIL3 mutations alter immune homeostasis and sensitise for arthritis pathology
Annals of the Rheumatic Diseases·2018· 35 citedOpen Access
ADA2 Deficiency Mimicking Idiopathic Multicentric Castleman Disease
PEDIATRICS·2018· 36 citedOpen Access
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Frequent Co-authors

Carine Wouters(16), Adrian Liston(16), Stéphanie Humblet‐Baron(16), Isabelle Meyts(9), James Dooley(8), Susan Schlenner(8), Mathijs Willemsen(8), Vasiliki Lagou(7), Lien De Somer(7), Frederik Staels(7), Rik Schrijvers(7), Julika Neumann(6), Lien Van Eyck(5), John S. Barber(5), Margaux Gerbaux(5), Josselyn E. Garcia‐Perez(4), Emanuela Pasciuto(4), An Goris(4), Brigitte Bader‐Meunier(4), Patrick Matthys(4)