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Schulz, H., Ruppert A.K., Zara, F, Çağlayan, H., et al, “No Evidence for a BRD2 Promoter Hypermethylation Inblood Leukocytes of Europeans With Juvenile Myoclonic Epilepsy”, Epilepsia, 60 (5), E31-E36, 2019. Dil Türkçe
Sahbaz, I., Gündoğdu-Eken, A., Koçoğlu, C., Başak, A.N., "Phenotypic and Genotypic Analysis of Hereditary Ataxia Patients in Sakarya City, Turkey", Noropsikiyatri Arşivi-archives of Neuropsychiatry, 2019. Dil Türkçe
Pareyson, D., Stojkovic, T., Reilly, M.M., Leonard-Louis, S., Laurà, M., Blake, J., Parman, Y., Battaloğlu, E., et al., "A Multicenter Retrospective Study of Charcot-Marie-Tooth Disease Type 4B (CMT4B) Associated with Mutations in Myotubularin-Ielated Proteins (MTMRs)", Annals of Neurology, 86 (1), 55-67, 2019. Dil Türkçe
Tolun, A., Nalbant, G., "A Small Homozygous CHST11 Deletion in Chondrodysplasia, Brachydactyly, Overriding Digits, Clino-symphalangism and Synpolydactyly", European Journal of Human Genetics, 2019. Dil Türkçe
Tolun, A., "Candidate Gene Search For Autosomal Dominant Behcet's Disease Through Whole Exome Sequencing", European Journal of Human Genetics, 2019. Dil Türkçe
Tolun, A., Bölükbaşı, E.Y., "Search for a Genetic Factor for Pleuroparenchymal Fibroelastosis (PPFE)", European Journal of Human Genetics, 2019. Dil Türkçe
Akçimen, F., Başak, A.N., "Genomic Variants in the FTO Gene Are Associated With Sporadic Amyotrophic Lateral Sclerosis in Greek Patients", European Journal of Human Genetics, 2019. Dil Türkçe
Sahbaz, I., Başak, N., Gündoğdu, A., Kocoğlu, C., "Genetic and Clinical Analysis of Spinocerebellar Ataxia Type 36 in a Turkish Family with Review of Literature", European Journal of Human Genetics, 2019. Dil Türkçe
Bilir, B., Battaloğlu, E., "Genotype-phenotype Correlation in Pelizaeus Merzbacher Disease and Pelizaeus Merzbacher-like Disease", Bezmialem Science, 2019. Dil Türkçe
