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
Çorapçı, F., Duman, E.A., "Differential Patterns of Diurnal Cortisol by Home and Daycare Chaos in Young Children", Psychoneuroendocrınology, 2019. Dil Türkçe
Ecevitogğlu, A., Ateşyakar, N., Duman, E.A., "Study Protocol of a Pregnancy Cohort from Turkey: Bogazici Mother-Baby Relationship Project", Psychoneuroendocrınology, 2019. Dil Türkçe
Duman, E.A., "Impact of Different Characteristics of Early Adversity on Stress-related Endophenotypes and Mental Health Problems", Psychoneuroendocrınology, 2019. Dil Türkçe
Tolun, A., Köprülü, M., Nalbant, G., "Linked Homozygous CRADD and USP44 Variants in Intellectual Disability", European Journal of Human Genetics, 2019. Dil Türkçe
Savun-Hekimoğlu, B., Ince, N.H., "Optimization of Methylparaben Degradation by Sonocatalysis", Ultrasonics Sonochemistry, 2019. Dil Türkçe