List of works - Sebastian Fuchs

A human inferred germline antibody binds to an immunodominant epitope and neutralizes Zika virus

scientific article

A prospective study on the natural history of patients with profound combined immunodeficiency: An interim analysis.

scientific article

Antiviral and regulatory T cell immunity in a patient with stromal interaction molecule 1 deficiency

scientific article published on 21 December 2011

Clinical and immunological overlap between autoimmune lymphoproliferative syndrome and common variable immunodeficiency.

scientific article published on 15 September 2010

Common variable immunodeficiency, impaired neurological development and reduced numbers of T regulatory cells in a 10-year-old boy with a STAT1 gain-of-function mutation.

scientific article published on 5 April 2016

Deficiency of innate and acquired immunity caused by an IKBKB mutation.

scientific article published on December 2013

Dengue Virus Evades AAV-Mediated Neutralizing Antibody Prophylaxis in Rhesus Monkeys

scientific article published on 24 July 2017

Early-onset Evans syndrome, immunodeficiency, and premature immunosenescence associated with tripeptidyl-peptidase II deficiency

scientific article

Hemophagocytic lymphohistiocytosis as presenting manifestation of profound combined immunodeficiency due to an ORAI1 mutation

scientific article published on 17 June 2017

High-dimensional single-cell proteomics analysis identifies immune checkpoint signatures and therapeutic targets in ulcerative colitis

scientific article published on 09 January 2019

Insulin modulates the inflammatory granulocyte response to streptococci via phosphatidylinositol 3-kinase.

scientific article

Missense mutation in immunodeficient patients shows the multifunctional roles of coiled-coil domain 3 (CC3) in STIM1 activation

scientific article published on 27 April 2015

Omenn syndrome associated with a functional reversion due to a somatic second-site mutation in CARD11 deficiency

scientific article

Oncogenic JAK2V617F causes PD-L1 expression, mediating immune escape in myeloproliferative neoplasms.

scientific article published in February 2018

Potent Plasmablast-Derived Antibodies Elicited by the National Institutes of Health Dengue Vaccine

scientific article published on 6 September 2017

SYK expression endows human ZAP70-deficient CD8 T cells with residual TCR signaling

scientific article published on 14 July 2015

The Extended Clinical Phenotype of 26 Patients with Chronic Mucocutaneous Candidiasis due to Gain-of-Function Mutations in STAT1

scientific article

List of works by Sebastian Fuchs

A human inferred germline antibody binds to an immunodominant epitope and neutralizes Zika virus

A prospective study on the natural history of patients with profound combined immunodeficiency: An interim analysis.

Antiviral and regulatory T cell immunity in a patient with stromal interaction molecule 1 deficiency

Clinical and immunological overlap between autoimmune lymphoproliferative syndrome and common variable immunodeficiency.

Common variable immunodeficiency, impaired neurological development and reduced numbers of T regulatory cells in a 10-year-old boy with a STAT1 gain-of-function mutation.

Deficiency of innate and acquired immunity caused by an IKBKB mutation.

Dengue Virus Evades AAV-Mediated Neutralizing Antibody Prophylaxis in Rhesus Monkeys

Early-onset Evans syndrome, immunodeficiency, and premature immunosenescence associated with tripeptidyl-peptidase II deficiency

Hemophagocytic lymphohistiocytosis as presenting manifestation of profound combined immunodeficiency due to an ORAI1 mutation

High-dimensional single-cell proteomics analysis identifies immune checkpoint signatures and therapeutic targets in ulcerative colitis

Insulin modulates the inflammatory granulocyte response to streptococci via phosphatidylinositol 3-kinase.

Missense mutation in immunodeficient patients shows the multifunctional roles of coiled-coil domain 3 (CC3) in STIM1 activation

Omenn syndrome associated with a functional reversion due to a somatic second-site mutation in CARD11 deficiency

Oncogenic JAK2V617F causes PD-L1 expression, mediating immune escape in myeloproliferative neoplasms.

Potent Plasmablast-Derived Antibodies Elicited by the National Institutes of Health Dengue Vaccine

SYK expression endows human ZAP70-deficient CD8 T cells with residual TCR signaling

The Extended Clinical Phenotype of 26 Patients with Chronic Mucocutaneous Candidiasis due to Gain-of-Function Mutations in STAT1