Ibrahim Baris
Istanbul, 34450, Turkey
Last Updated: 09/26/2026
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Found 28 publications
Phenotype-Driven Next-Generation Sequencing and Structure-Based In Silico Analysis Reveal Disease-Specific Diagnostic Yield and Genotype-Phenotype Correlations in Inherited Kidney Diseases.
Journal: Life (Basel, Switzerland)
Published: February 13, 2026
Expanding the Phenotypic Spectrum of NDUFS6-Related Disease: From Neonatal Mitochondrial Encephalopathy to Childhood-Onset Axonal Neuropathy.
Journal: International journal of molecular sciences
Published: January 09, 2026
Biallelic Truncating DNAH14 Variant in Siblings with Neurodevelopmental Disorder and Predominant Ataxia: Clinical Report and Literature Review.
Journal: International journal of molecular sciences
Published: December 09, 2025
Whole Exome Sequencing in Patients With Developmental Delay/Intellectual Disability (DD/ID), Epilepsy and the First Turkish Patient Diagnosed With BCL11A-Related Intellectual Disability.
Journal: Molecular genetics & genomic medicine
Published: October 14, 2025
M54 selectively stabilizes the circadian clock component of CRY1 and enhances the period of circadian rhythm at cellular level.
Journal: The Journal of biological chemistry
Published: August 07, 2024
Functional characterization of the CRY2 circadian clock component variant p.Ser420Phe revealed a new degradation pathway for CRY2.
Journal: The Journal of biological chemistry
Published: September 14, 2023
Single nucleotide polymorphisms (SNPs) in circadian genes: Impact on gene function and phenotype.
Journal: Advances in protein chemistry and structural biology
Published: September 14, 2023
TW68, cryptochromes stabilizer, regulates fasting blood glucose levels in diabetic ob/ob and high fat-diet-induced obese mice.
Journal: Biochemical pharmacology
Published: July 10, 2023
Protein interaction networks of the mammalian core clock proteins.
Journal: Advances in protein chemistry and structural biology
Published: July 25, 2022
The secondary pocket of cryptochrome 2 is important for the regulation of its stability and localization.
Journal: The Journal of biological chemistry
Published: March 22, 2022
Clinical and Molecular Findings in a Turkish Family Who Had a (c.869- 1G>A) Splicing Variant in PSEN1 Gene with A Rare Condition: The Variant Alzheimer's Disease with Spastic Paraparesis.
Journal: Current Alzheimer research
Published: September 30, 2021
Last Updated: 09/26/2026