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BMC Public Health|May 30, 2023
Superspreading, overdispersion and their implications in the SARS-CoV-2 (COVID-19) pandemic: a systematic review and meta-analysis of the literatureOliver Wegehaupt, Akira Endo, Anna VassallFrontiers in Immunology|May 28, 2020
Cell Versus Cytokine - Directed Therapies for Hemophagocytic Lymphohistiocytosis (HLH) in Inborn Errors of ImmunityOliver Wegehaupt, Katharina Wustrau, Kai Lehmberg, et al.Journal of Clinical Immunology|May 21, 2024
Variable Syndromic Immunodeficiency in Patients with Biallelic PRIM1 MutationsVasil Toskov, Petra Kaiser-Labusch, Min Ae Lee-Kirsch, et al.Blood Advances|March 31, 2026
Digenic and Multigenic Heterozygous FHL Genotypes Are Common but Clinically Silent in the General PopulationOleg Borisov, Jasmin Mann, Kevin Kim Walz, et al.Pediatric Blood & Cancer|April 15, 2020
TIM-3 deficiency presenting with two clonally unrelated episodes of mesenteric and subcutaneous panniculitis-like T-cell lymphoma and hemophagocytic lymphohistiocytosisOliver Wegehaupt, Miriam Groß, Claudia Wehr, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|November 12, 2024
The role of the co-chaperone DNAJB11 in polycystic kidney disease: Molecular mechanisms and cellular origin of cyst formationTilman Busch, Björn Neubauer, Lars Schmitt, et al.European Journal of Cancer (Oxford, England : 1990)|November 4, 2021
SARS-CoV-2 in children with cancer or after haematopoietic stem cell transplant: An analysis of 131 patientsGabrielle M Haeusler, Roland A Ammann, Fabianne Carlesse, et al.Blood|March 16, 2025
Beyond genotype: challenges in predicting disease risk for carriers of biallelic perforin variantsOliver Wegehaupt, Oleg Borisov, Elena Sieni, et al.The Journal of Allergy and Clinical Immunology|November 18, 2023
Abnormal biomarkers predict complex FAS or FADD defects missed by exome sequencingAnne Rensing-Ehl, Myriam Ricarda Lorenz, Marita Führer, et al.Journal of Human Immunity|June 1, 2026
Human germline biallelic loss-of-function <i>OSMR</i> variants cause severe allergic diseaseSimran Samra, Mehul Sharma, Julia Körholz, et al.Pageof 2