Ozan Baytas

Loss of mitochondrial enzyme GPT2 causes early neurodegeneration in locus coeruleus

J. Kauer, E. Morrow, Ozan Baytas, 2022, Neurobiology of Disease.

GPT2 mutations in autosomal recessive developmental disability: extending the clinical phenotype and population prevalence estimates

J. Vincent, Judy S. H. Liu, E. Morrow, 2019, Human Genetics.

Mutations in mitochondrial enzyme GPT2 cause metabolic dysfunction and neurological disease with developmental and progressive features

R. Deberardinis, D. Housman, A. Barkovich, 2016, Proceedings of the National Academy of Sciences.

Longitudinal MRI findings in patient with SLC25A12 pathogenic variants inform disease progression and classification

C. Phornphutkul, D. Merck, E. Morrow, 2019, American journal of medical genetics. Part A.

Cellular resilience: 5-HT neurons in Tph2−/− mice retain normal firing behavior despite the lack of brain 5-HT

K. Lesch, R. Corradetti, B. Mlinar, 2015, European Neuropsychopharmacology.