Caner Aytekin - Gynecology

Author Information

Caner Aytekin is an accomplished researcher affiliated with the Pediatric Immunology Clinic at Dr. Sami Ulus Obstetrics and Gynecology and Pediatric Health and Diseases, Training and Research Hospital in Ankara, Turkey. His work primarily focuses on pediatric immunology, where he has made significant contributions to understanding genetic and immunological disorders.

Research Contributions

Caner Aytekin has authored numerous papers exploring various dimensions of pediatric immunology. Notable publications include studies on genetic mutations affecting immune response, such as the Magt1 gene and HAX1-related conditions, as well as investigations into severe combined immunodeficiency and novel genetic diseases resembling mucopolysaccharidosis-plus syndrome. His research has also delved into the genetic basis of diseases like Renpenning Syndrome and the implications of inherited PD-1 deficiency.

Aliases

Caner Aytekin is also known in academic circles by several aliases including C Aytekin, C. Aytekin, and Can Aytekin.

Publication and Citation Metrics

Metric	Value
Total Citation Count	2223
h-index	22
Total Paper Count	69

Publications:

Scales of Magt1 Gene: Novel Mutations, Different Presentations

DOI: 10.18502/ijaai.v21i1.8622

Year: 2022

Severe congenital neutropenia with mastoidectomy: A case report of HAX1.

DOI: 10.1055/a-1479-2692

Year: 2021

Pseudomonas Aeruginosa Sepsis in a Previously Healthy Infant with Subcutaneous Nodules and Mastoid Bone Destruction.

DOI: 10.1055/s-0040-1710001

Year: 2021

SARS-CoV-2–related MIS-C: A key to the viral and genetic causes of Kawasaki disease?

DOI: 10.1084/jem.20210446

Year: 2021

Single-Center Study of 72 Patients with Severe Combined Immunodeficiency: Clinical and Laboratory Features and Outcomes.

DOI: 10.1007/s10875-021-01062-y

Year: 2021

Homozygous missense VPS16 variant is associated with a novel disease, resembling mucopolysaccharidosis‐plus syndrome in two siblings

DOI: 10.1111/cge.14002

Year: 2021

Inherited PD-1 deficiency underlies tuberculosis and autoimmunity in a child.

DOI: 10.1038/s41591-021-01388-5

Year: 2021

Investigation of causative genetic defects in patients with primary immunodeficiency by next generation sequencing

DOI: 10.5455/ANNALSMEDRES.2021.03.201

Year: 2021

Renpenning Syndrome in a Turkish Patient: de novo Variant c.607C>T in PACS1 and Hypogammaglobulinemia Phenotype

DOI: 10.1159/000507562

Year: 2020

Does the Hyper IgM Phenotype Affect Prognosis in Ataxia Telangiectasia?

DOI: 10.21911/AAI.523

Year: 2020

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