Mehmet Burak Mutlu

8PUBLICATIONS
42CO-AUTHORS
Neurology and neuromuscular diseasesNeurogeneticsCancer geneticsMedical molecular engineering of nucleic acids and proteinsGene expression (incl. microarray and other genome-wide approaches)
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Publications (8)

|Jul 21, 2026
Clinical and Electrodiagnostic Characterization of Pediatric Triple A Syndrome: A Cohort of 17 Patients.

|Jun 15, 2026
Structural Variant and Repeat Expansion Findings Identified by Optical Genome Mapping in Complex Autism Spectrum Disorder With Concomitant Neurodevelopmental Disorders.

|May 11, 2026
Mutation analysis of the FOXL2 and BMP15 genes in patients with premature ovarian insufficiency.

|Dec 10, 2025
Revealing Monogenic Diabetes: Clinical and Genetic Features of Pediatric MODY Cases in Türkiye: Single Center Experience.

Aslihan Sanri, Tugba Kontbay Cetin, Emel Gul Acikgoz

|Nov 03, 2025
Pilot evaluation of optical genome mapping in chronic lymphocytic leukemia: complementing FISH analysis.

Simge Erdem, Ayşe Gül Bayrak Tokaç, Aynur Aday

|Apr 15, 2025
Optical Genome Mapping as a New Approach to Detecting Cytogenetic Abnormalities: Why Is It Difficult in Multiple Myeloma?

Ayşe Gül Bayrak Tokaç, Mehmet Burak Mutlu, Simge Erdem

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Frequent Collaborators

3 joint publications

Ayşe Gül Bayrak Tokaç

2 joint publications

Aynur Aday

2 joint publications

Fahrettin Duymuş

2 joint publications

Serhat Seyhan