Anne Rensing‐Ehl

University of Freiburg — Germany

Immunology and Microbiology · Life Sciences

34h-index4.5kcitations66works16.52yr avg
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Research Topics

Immune Cell Function and Interaction(33), Immunodeficiency and Autoimmune Disorders(27), T-cell and B-cell Immunology(15), Chronic Lymphocytic Leukemia Research(13), Viral-associated cancers and disorders(9)

Publications66 total

Diagnostic evaluation of paediatric autoimmune lymphoproliferative immunodeficiencies (ALPID): a prospective cohort study
The Lancet Haematology·2024· 15 cited
Non-apoptotic FAS signaling controls mTOR activation and extrafollicular maturation in human B cells
Science Immunology·2024· 18 cited
Abnormal biomarkers predict complex FAS or FADD defects missed by exome sequencing
Journal of Allergy and Clinical Immunology·2023· 5 citedOpen Access
Autoimmune lymphoproliferative immunodeficiencies (ALPIDs): A proposed approach to redefining ALPS and other lymphoproliferative immune disorders
Journal of Allergy and Clinical Immunology·2023· 20 citedOpen Access
Combined germline and somatic human FADD mutations cause autoimmune lymphoproliferative syndrome
Journal of Allergy and Clinical Immunology·2023· 18 citedOpen Access
Single-cell transcriptomics reveal different maturation stages and sublineage commitment of human thymic invariant natural killer T cells
Journal of Leukocyte Biology·2023· 7 citedOpen Access
AKT activity orchestrates marginal zone B cell development in mice and humans
Cell Reports·2023· 10 citedOpen Access
Autoimmunity and immunodeficiency associated with monoallelic LIG4 mutations via haploinsufficiency
Journal of Allergy and Clinical Immunology·2023· 15 citedOpen Access
Revisiting autoimmune lymphoproliferative syndrome caused by Fas ligand mutations
Journal of Allergy and Clinical Immunology·2023· 14 citedOpen Access
Diagnostic Evaluation of Pediatricautoimmune-Lymphoproliferative Immunodeficiencies (ALPID): A Prospective Cohort Study
SSRN Electronic Journal·2023Open Access
Detection of Signature Double-Negative T Cells Is a Reliable Marker for ALPS Associated with FAS Mutation
Blood·2022
Monogenic early-onset lymphoproliferation and autoimmunity: Natural history of STAT3 gain-of-function syndrome
Journal of Allergy and Clinical Immunology·2022· 110 citedOpen Access
The expansion of human T-bet <sup>high</sup> CD21 <sup>low</sup> B cells is T cell dependent
Science Immunology·2021· 138 cited
Complete CD95/FAS deficiency due to complex homozygous germline TNFRSF6 mutations in an adult patient with mild autoimmune lymphoproliferative syndrome (ALPS)
Clinical Immunology·2021· 4 cited
A distinct CD38+CD45RA+ population of CD4+, CD8+, and double-negative T cells is controlled by FAS
The Journal of Experimental Medicine·2020· 45 citedOpen Access
Germline TET2 loss of function causes childhood immunodeficiency and lymphoma
Blood·2020· 83 citedOpen Access
THU0053 CONTRIBUTION OF DEFECTIVE NON-APOPTOTIC FAS SIGNALING TO IMMUNE DYSREGULATION IN AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME (ALPS)
Annals of the Rheumatic Diseases·2020Open Access
Distinct molecular response patterns of activating STAT3 mutations associate with penetrance of lymphoproliferation and autoimmunity
Clinical Immunology·2019· 56 cited
<scp>CD</scp>57 identifies T cells with functional senescence before terminal differentiation and relative telomere shortening in patients with activated <scp>PI</scp>3 kinase delta syndrome
Immunology and Cell Biology·2018· 24 citedOpen Access
Leukämien und Lymphome
2017· 1 cited
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Frequent Co-authors

Stephan Ehl(32), Carsten Speckmann(21), Klaus Schwarz(21), Myriam Ricarda Lorenz(14), Klaus Warnatz(10), Bodo Grimbacher(10), Sebastian Fuchs(10), Ilka Fuchs(10), Marta Rizzi(8), Christian Klemann(8), Frédéric Rieux‐Laucat(8), Aleš Janda(7), Sophie Hambleton(7), Aude Magérus(7), Kai Lehmberg(6), Maximilian Heeg(6), Olaf Neth(6), Jan Rohr(6), Maximilian Seidl(5), Thomas Vraetz(5)