Safa Barış

A sex-biased imbalance between Tfr, Tph, and atypical B cells determines antibody responses in COVID-19 patients

Regulatory T cells in autoimmune kidney diseases and transplantation

Human Inborn Errors of Immunity: 2019 Update on the Classification from the International Union of Immunological Societies Expert Committee

Transcriptional and epigenetic basis of Treg cell development and function: its genetic anomalies or variations in autoimmune diseases

Tregopathies: Monogenic diseases resulting in regulatory T-cell deficiency

Control of Germinal Center Responses by T-Follicular Regulatory Cells

Interaction between microbiota and immunity in health and disease

Asthma

Mechanism-Based Precision Therapy for the Treatment of Primary Immunodeficiency and Primary Immunodysregulatory Diseases

Clinical, Immunological, and Molecular Heterogeneity of 173 Patients With the Phenotype of Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked (IPEX) Syndrome

Lessons learned from the study of human inborn errors of innate immunity

Transcription factor Ikzf1 associates with Foxp3 to repress gene expression in Treg cells and limit autoimmunity and anti-tumor immunity

Unexpected Help: Follicular Regulatory T Cells in the Germinal Center

Regulatory T Cells and Human Disease

From IPEX syndrome to FOXP3 mutation: a lesson on immune dysregulation

Sublingual immunotherapy for asthma

Control of foreign Ag‐specific Ab responses by Treg and Tfr

Cataracts

Resetting microbiota by Lactobacillus reuteri inhibits T reg deficiency–induced autoimmunity via adenosine A2A receptors

XRCC1 and XPD genetic polymorphisms and susceptibility to age-related cataract: a meta-analysis.

Severe Early-Onset Combined Immunodeficiency due to Heterozygous Gain-of-Function Mutations in STAT1

Clinical Heterogeneity of Immunodysregulation, Polyendocrinopathy, Enteropathy, X-linked: Pulmonary Involvement as a Non-Classical Disease Manifestation

JAGN1 Deficient Severe Congenital Neutropenia: Two Cases from the Same Family

DNA repair gene XPD and XRCC1 polymorphisms and the risk of childhood acute lymphoblastic leukemia

Exaggerated follicular helper T-cell responses in patients with LRBA deficiency caused by failure of CTLA4-mediated regulation

Long-Term Effect of Sublingual and Subcutaneous Immunotherapy in Dust Mite-Allergic Children With Asthma/Rhinitis: A 3-Year Prospective Randomized Controlled Trial.