Atypical phenotype of an old disease or typical phenotype of a new disease: deficiency of adenosine deaminase 2 by Mustafa Çakan, Nuray Aktay-Ayaz, Şerife Gül Karadağ, Eda Tahir-Turanlı, Kelsey Stafstrom, Wayne Bainter, Raif S Geha, Janet Chou

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Profiling of five urinary exosomal miRNAs for the differential diagnosis of patients with diabetic kidney disease and focal segmental glomerulosclerosis. by Sinan Trabulus, Mehmet Seyit Zor, Selma Alagoz, Mevlut Tamer Dincer, Meral Meşe, Erkan Yilmaz, Eda Tahir Turanli, Nurhan Seyahi

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Exome sequencing reveals low-frequency and rare variant contributions to multiple sclerosis susceptibility in Turkish families by Furkan Büyükgöl, Berk Gürdamar, Mehmet Ufuk Aluçlu, Yeşim Beckmann, Kaya Bilguvar, Cavit Boz, Alper Bülbül, Sena Destan Bünül, Özge Çetin, Caner Feyzi Demir, Serkan Demir, Taşkın Duman, Hüsnü Efendi, Özgül Ekmekçi, Utku Ertetik, Özlem Ethemoğlu, Elif Everest, Haluk Gümüş, Tuncay Gündüz, Rana Karabudak, Bedriye Karaman, Murat Kürtüncü, Muzaffer Mutluer, Meziyet Dilara Reda, Sabahattin Saip, Meral Seferoğlu, Elif Sever, Osman Ugur Sezerman, Sedat Şen, Beril Taşdelen, Mehmet Tecellioğlu, Murat Terzi, Aslı Tuncer, Ömer Faruk Turan, Melih Tütüncü, Gülgün Uncu, Uğur Uygunoğlu, Cihat Uzunköprü, Umut Voyvoda, Mehmet Fatih Yetkin, Nur Yüceyar, Aksel Siva, Eda Tahir Turanlı

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