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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
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Afacan, E., Dündar, G., Başkaya, F., Pusane, A.E., Yelten, M.B., “On Chip Reconfigurable CMOS Analog Circuit Design and Automation Against Aging Phenomena: Sense and React”, ACM Transactions on Design Automation of Electronic Systems (TODAES), 24(44), 2019. Dil Türkçe
Akyol, C., "Validated Innovative Approaches for Energy-efficient Resource Recovery and Re-use From Municipal Wastewater: From Anaerobic Treatment Systems to a Biorefinery Concept", Ciritical Reviews in Environmental Science and Technology, 2019. Dil Türkçe
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