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Research Square|September 18, 2023
Mechanisms of mRNA processing defects in inherited THOC6 intellectual disability syndromeElizabeth Werren, Geneva LaForce, Anshika Srivastava, et al.Journal of Clinical Immunology|January 14, 2022
Low Density Granulocytes and Dysregulated Neutrophils Driving Autoinflammatory Manifestations in NEMO DeficiencyNaz Surucu Yilmaz, Sevgi Bilgic Eltan, Basak Kayaoglu, et al.Iscience|May 26, 2023
Dominant-negative heterozygous mutations in AIRE confer diverse autoimmune phenotypesBergithe E Oftedal, Kristian Assing, Safa Baris, et al.Journal of Clinical Immunology|January 26, 2022
Expanding the Clinical and Immunological Phenotypes and Natural History of MALT1 DeficiencyAsena Pinar Sefer, Hassan Abolhassani, Franziska Ober, et al.Clinical Immunology (Orlando, Fla.)|July 11, 2023
Defective Treg generation and increased type 3 immune response in leukocyte adhesion deficiency 1Serife Erdem, Sule Haskologlu, Yesim Haliloglu, et al.Frontiers in Pediatrics|June 18, 2026
Genomic diagnosis and multisystem phenotyping in pediatric congenital analbuminemia: clinical, coagulation, and immune signaturesAsena Pinar Sefer, Melek Yorgun Altunbas, Baran Erman, et al.Allergy|October 10, 2019
ILC3 deficiency and generalized ILC abnormalities in DOCK8-deficient patientsAhmet Eken, Murat Cansever, Fatma Zehra Okus, et al.Journal of Clinical Immunology|August 9, 2024
DIAPH1-Deficiency is Associated with Major T, NK and ILC Defects in HumansZehra Busra Azizoglu, Royala Babayeva, Zehra Sule Haskologlu, et al.Nature Immunology|May 15, 2012
DOCK8 functions as an adaptor that links TLR-MyD88 signaling to B cell activationHaifa H Jabara, Douglas R McDonald, Erin Janssen, et al.Molecular Genetics and Metabolism|February 20, 2026
From genotype to outcome: Zygosity-specific insights in 63 cases of CLPB-related mitochondrial diseaseOliver Heath, Francisco Del Caño-Ochoa, Safa Baris, et al.Pageof 14