Area of research
Immunology · Infectious Diseases
Research interest
Research interests include Immunodeficiency and Autoimmune Disorders, SARS-CoV-2 and COVID-19 Research, DNA Repair Mechanisms, and T-cell and B-cell Immunology.
Conversion of monoclonal IgG to dimeric and secretory IgA restores neutralizing ability and prevents infection of Omicron lineages
SARS-CoV-2 brainstem encephalitis in human inherited DBR1 deficiency
Orientation Regulation of Class-switch Recombination in Human B Cells
Causal relationship between hypothyroidism and coronary atherosclerotic cardiovascular disease: a bidirectional two-sample Mendelian randomization
Heterologous immunization with inactivated vaccine followed by mRNA-booster elicits strong immunity against SARS-CoV-2 Omicron variant
Human serum from SARS-CoV-2-vaccinated and COVID-19 patients shows reduced binding to the RBD of SARS-CoV-2 Omicron variant
Human T-bet governs the generation of a distinct subset of CD11c <sup>high</sup> CD21 <sup>low</sup> B cells
Immunity to SARS-CoV-2 up to 15 months after infection
Inherited IFNAR1 Deficiency in a Child with Both Critical COVID-19 Pneumonia and Multisystem Inflammatory Syndrome
Genetic and immunologic evaluation of children with inborn errors of immunity and severe or critical COVID-19
Genomic characterization of lymphomas in patients with inborn errors of immunity
Persistence of SARS-CoV-2-specific B and T cell responses in convalescent COVID-19 patients 6–8 months after the infection
SARS-CoV-2–specific B- and T-cell immunity in a population-based study of young Swedish adults
X-Linked TLR7 Deficiency Underlies Critical COVID-19 Pneumonia in a Male Patient with Ataxia-Telangiectasia
Genome-wide CRISPR screens reveal synthetic lethal interaction between CREBBP and EP300 in diffuse large B-cell lymphoma
APRIL-dependent lifelong plasmacyte maintenance and immunoglobulin production in humans
The H2B deubiquitinase Usp22 promotes antibody class switch recombination by facilitating non-homologous end joining
<i>EXTL3</i> mutations cause skeletal dysplasia, immune deficiency, and developmental delay
Combined immunodeficiency and Epstein-Barr virus–induced B cell malignancy in humans with inherited CD70 deficiency
Modeling altered T-cell development with induced pluripotent stem cells from patients with RAG1-dependent immune deficiencies
Human HOIP and LUBAC deficiency underlies autoinflammation, immunodeficiency, amylopectinosis, and lymphangiectasia
Differential role of nonhomologous end joining factors in the generation, DNA damage response, and myeloid differentiation of human induced pluripotent stem cells
IgA subclass switch recombination in human mucosal and systemic immune compartments
Deleterious Mutations in LRBA Are Associated with a Syndrome of Immune Deficiency and Autoimmunity