Canberk Ipsir

Ankara, Turkey

Last Updated: 09/26/2026

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Found 9 publications

Clinical Heterogeneity of TNFRSF13B Variants: A Monogenic Cause or a Genetic Modifier?

Clinical Heterogeneity of TNFRSF13B Variants: A Monogenic Cause or a Genetic Modifier?

Journal: Immunology

Published: March 17, 2026

From Interferon Signature to the Clinical Landscape: Type I Interferonopathies.

From Interferon Signature to the Clinical Landscape: Type I Interferonopathies.

Journal: Arthritis & rheumatology (Hoboken, N.J.)

Published: November 20, 2025

From Interferon Signature to the Clinical Landscape: Type I Interferonopathies.

From Interferon Signature to the Clinical Landscape: Type I Interferonopathies.

Journal: Arthritis & rheumatology (Hoboken, N.J.)

Published: November 20, 2025

Comprehensive αβ T-Cell Receptor Repertoire Analysis Reveals a Unique CD8+ TCR Landscape in DOCK8-Deficient Patients.

Comprehensive αβ T-Cell Receptor Repertoire Analysis Reveals a Unique CD8+ TCR Landscape in DOCK8-Deficient Patients.

Journal: Allergy

Published: January 21, 2025

Correction to: Genetic Evaluation of the Patients with Clinically Diagnosed Inborn Errors of Immunity by Whole Exome Sequencing: Results from a Specialized Research Center for Immunodeficiency in Türkiye.

Correction to: Genetic Evaluation of the Patients with Clinically Diagnosed Inborn Errors of Immunity by Whole Exome Sequencing: Results from a Specialized Research Center for Immunodeficiency in Türkiye.

Journal: Journal of clinical immunology

Published: November 14, 2024

Beyond the Classical Triad: Atypical Presentations and Regulatory T Cell Phenotyping in a Cohort of IPEX Patients.

Beyond the Classical Triad: Atypical Presentations and Regulatory T Cell Phenotyping in a Cohort of IPEX Patients.

Journal: Journal of clinical immunology

Published: October 31, 2024

Defective kinase activity of IKKα leads to combined immunodeficiency and disruption of immune tolerance in humans.

Defective kinase activity of IKKα leads to combined immunodeficiency and disruption of immune tolerance in humans.

Journal: Nature communications

Published: April 23, 2024

Genetic Evaluation of the Patients with Clinically Diagnosed Inborn Errors of Immunity by Whole Exome Sequencing: Results from a Specialized Research Center for Immunodeficiency in Türkiye.

Genetic Evaluation of the Patients with Clinically Diagnosed Inborn Errors of Immunity by Whole Exome Sequencing: Results from a Specialized Research Center for Immunodeficiency in Türkiye.

Journal: Journal of clinical immunology

Published: March 09, 2024

A Novel Homozygous Germline Mutation in Transferrin Receptor 1 (TfR1) Leads to Combined Immunodeficiency and Provides New Insights into Iron-Immunity Axis.

A Novel Homozygous Germline Mutation in Transferrin Receptor 1 (TfR1) Leads to Combined Immunodeficiency and Provides New Insights into Iron-Immunity Axis.

Journal: Journal of clinical immunology

Published: November 08, 2023

Showing 1-9 of 9

Last Updated: 09/26/2026