Murat H. Yarar

Istanbul, Turkey

Last Updated: 09/26/2026

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Found 18 publications

Heterozygous TSHR Variants in Pediatric Idiopathic Subclinical Hypothyroidism: Association with a Variable and Compensated Thyroid Phenotype

Heterozygous TSHR Variants in Pediatric Idiopathic Subclinical Hypothyroidism: Association with a Variable and Compensated Thyroid Phenotype

Journal: Journal of clinical research in pediatric endocrinology

Published: June 05, 2026

Unmasking JIA mimics: skeletal dysplasias in pediatric rheumatology.

Unmasking JIA mimics: skeletal dysplasias in pediatric rheumatology.

Journal: European journal of pediatrics

Published: May 06, 2026

A pediatric CAPS patient with an unusual presentation and resistance to standard treatment.

A pediatric CAPS patient with an unusual presentation and resistance to standard treatment.

Journal: ARP rheumatology

Published: April 12, 2026

Next-Generation Sequencing-Based Detection of KRAS G12D Variants in Colorectal Cancer: A Retrospective Cohort Study.

Next-Generation Sequencing-Based Detection of KRAS G12D Variants in Colorectal Cancer: A Retrospective Cohort Study.

Journal: Genes

Published: January 09, 2026

Paediatric macrophage activation syndrome: clinical features and outcomes across diverse aetiologies.

Paediatric macrophage activation syndrome: clinical features and outcomes across diverse aetiologies.

Journal: Rheumatology (Oxford, England)

Published: December 30, 2025

Response to the letter by Schmitt et al.

Response to the letter by Schmitt et al.

Journal: European journal of endocrinology

Published: August 07, 2025

Clinical and molecular results in 15 Turkish patients with Wiedemann-Steiner syndrome: identification of eight novel KMT2A variants and a case of dual molecular diagnosis in the CSNK2A1.

Clinical and molecular results in 15 Turkish patients with Wiedemann-Steiner syndrome: identification of eight novel KMT2A variants and a case of dual molecular diagnosis in the CSNK2A1.

Journal: European journal of pediatrics

Published: June 17, 2025

Novel IGF1R Variants in Short Stature: Lessons from Two Patients and Outcome of Growth Hormone Therapy

Novel IGF1R Variants in Short Stature: Lessons from Two Patients and Outcome of Growth Hormone Therapy

Journal: Journal of clinical research in pediatric endocrinology

Published: April 24, 2025

Novel IGF1R Variants in Short Stature: Lessons from Two Patients and Outcome of Growth Hormone Therapy.

Novel IGF1R Variants in Short Stature: Lessons from Two Patients and Outcome of Growth Hormone Therapy.

Journal: Journal of clinical research in pediatric endocrinology

Published: April 24, 2025

A rare autoinflammatory syndrome associated with a C2orf69 frameshift mutation: a case report.

A rare autoinflammatory syndrome associated with a C2orf69 frameshift mutation: a case report.

Journal: Immunologic research

Published: March 23, 2025

Genetic Profiling of Huntington's Disease: Insights from CAG Repeat Analysis for Precision Diagnosis and Management.

Genetic Profiling of Huntington's Disease: Insights from CAG Repeat Analysis for Precision Diagnosis and Management.

Journal: Noro psikiyatri arsivi

Published: February 07, 2025

Expanding the Genetic Landscape of RASopathies: Significance of Including NF1 in Targeted Panels.

Expanding the Genetic Landscape of RASopathies: Significance of Including NF1 in Targeted Panels.

Journal: Molecular syndromology

Published: November 10, 2024

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Last Updated: 09/26/2026