Julia C. Korholz
Dresden, SN, Germany
Last Updated: 09/26/2026
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Found 26 publications
Timing is everything: outcomes of allogeneic HSCT in adults with inborn errors of immunity.
Journal: Bone marrow transplantation
Published: April 26, 2026
Human germline biallelic loss-of-function OSMR variants cause severe allergic disease.
Journal: Journal of human immunity
Published: April 15, 2026
Guidance on JAK inhibitor treatment for inborn errors of JAK-STAT signaling, 2026: International consensus statement on behalf of the European Society for Immunodeficiencies/European Society for Blood and Marrow Transplantation-Inborn Errors Working Party and ERN-RITA.
Journal: The Journal of allergy and clinical immunology
Published: March 09, 2026
Guidance on JAK inhibitor treatment for inborn errors of JAK-STAT signaling (2026). An international consensus statement on behalf of the ESID/EBMT-IEWP and ERN-RITA.
Journal: The Journal of allergy and clinical immunology
Published: March 09, 2026
Primary atopic disorders: Monogenic insights into immunity.
Journal: Journal of human immunity
Published: January 16, 2026
Phenotypic spectrum of RNU4ATAC-related spliceosomopathies: four novel cases and integrated reevaluation of previously reported patients.
Journal: Orphanet journal of rare diseases
Published: September 10, 2025
Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings.
Journal: Nature genetics
Published: June 24, 2025
IKBKB gain of function: An inborn error with clinical heterogeneity progressing toward combined immunodeficiency.
Journal: The Journal of allergy and clinical immunology
Published: October 22, 2024
A randomised, placebo-controlled, phase III trial of leniolisib in activated phosphoinositide 3-kinase delta (PI3Kδ) syndrome (APDS): Adolescent and adult subgroup analysis.
Journal: Clinical immunology (Orlando, Fla.)
Published: August 23, 2024
Clinical manifestations, disease penetrance, and treatment in individuals with SOCS1 insufficiency: a registry-based and population-based study.
Journal: The Lancet. Rheumatology
Published: August 06, 2024
One gene to rule them all - clinical perspectives of a potent suppressor of cytokine signaling - SOCS1.
Journal: Frontiers in immunology
Published: February 12, 2024
IKAROS-how many feathers have you lost: mild and severe phenotypes in IKZF1 deficiency.
Journal: Frontiers in pediatrics
Published: November 28, 2023
Last Updated: 09/26/2026