Funda E. Cipe

Istanbul, Turkey

Last Updated: 09/26/2026

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Found 42 publications

A Novel GATA2 Splice-Site Mutation Associated with Familial Myelodysplastic Syndrome.

A Novel GATA2 Splice-Site Mutation Associated with Familial Myelodysplastic Syndrome.

Journal: Pediatric allergy, immunology, and pulmonology
Published: July 01, 2026

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

A Rare Genetic Intersection: Down Syndrome With Coexisting Spinal Muscular Atrophy.

A Rare Genetic Intersection: Down Syndrome With Coexisting Spinal Muscular Atrophy.

Journal: Cureus
Published: August 17, 2024

A Novel Variant of the PIK3R1 Gene Mutation Associated With SHORT Syndrome and Agammaglobulinemia.

A Novel Variant of the PIK3R1 Gene Mutation Associated With SHORT Syndrome and Agammaglobulinemia.

Journal: Cureus
Published: June 23, 2024

Adenosine Deaminase (ADA)-Deficient Severe Combined Immunodeficiency Unmasked by Persistent Lymphopenia and Prolonged Severe SARS-CoV-2 Infection in a Three-Week-Old Neonate.

Adenosine Deaminase (ADA)-Deficient Severe Combined Immunodeficiency Unmasked by Persistent Lymphopenia and Prolonged Severe SARS-CoV-2 Infection in a Three-Week-Old Neonate.

Journal: Cureus
Published: April 05, 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

Primary immune regulatory disorders (PIRD): expanding the mutation spectrum in Turkey and identification of sixteen novel variants.

Primary immune regulatory disorders (PIRD): expanding the mutation spectrum in Turkey and identification of sixteen novel variants.

Journal: Immunologic research
Published: October 13, 2023

Malignancies and Lymphoproliferations in Children With Primary Immune Deficiency-A Single-center Experience.

Malignancies and Lymphoproliferations in Children With Primary Immune Deficiency-A Single-center Experience.

Journal: Journal of pediatric hematology/oncology
Published: August 15, 2023

Neurologic Status of Patients with Purine Nucleoside Phosphorylase Deficiency Before and After Hematopoetic Stem Cell Transplantation.

Neurologic Status of Patients with Purine Nucleoside Phosphorylase Deficiency Before and After Hematopoetic Stem Cell Transplantation.

Journal: Journal of clinical immunology
Published: July 10, 2023

The impact of Treosulfan-based conditioning for inborn errors of immunity: Is dose monitoring crucial?

The impact of Treosulfan-based conditioning for inborn errors of immunity: Is dose monitoring crucial?

Journal: Clinical transplantation
Published: June 13, 2023

Subcutaneous Fat Necrosis of the Newborn After Whole-Body Cooling for Birth Asphyxia.

Subcutaneous Fat Necrosis of the Newborn After Whole-Body Cooling for Birth Asphyxia.

Journal: Cureus
Published: February 01, 2023

Hepatocellular Carcinoma in ADA-SCID Patient After Hematopoietic Stem Cell Transplantation.

Hepatocellular Carcinoma in ADA-SCID Patient After Hematopoietic Stem Cell Transplantation.

Journal: Journal of pediatric hematology/oncology
Published: November 27, 2022
Showing 1-12 of 42

Last Updated: 09/26/2026