Mehmet Burak Mutlu

9PUBLICATIONS
51CO-AUTHORS
NeonatologyNeurology and neuromuscular diseasesNeurogeneticsCancer geneticsMedical molecular engineering of nucleic acids and proteins
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Publications (9)

|Aug 14, 2026
Biallelic SLC20A2 loss-of-function in severe early-onset neurodevelopmental disorder with brain calcification.

|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

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Frequent Collaborators

3 joint publications

Ayşe Gül Bayrak Tokaç

3 joint publications

Özlem Öz

2 joint publications

Aynur Aday

2 joint publications

Fahrettin Duymuş