Genomic Analysis of Non-NF2 Meningiomas Reveals Mutations in TRAF7, KLF4, AKT1, and SMO by Clark, Victoria E., Erson-Omay, E. Zeynep, Serin, Akdes, Yin, Jun, Cotney, Justin, Özduman, Koray, Avşar, Timuçin, Li, Jie, Murray, Phillip B., Henegariu, Octavian, Yilmaz, Saliha, Günel, Jennifer Moliterno, Carrión-Grant, Geneive, Yılmaz, Baran, Grady, Conor, Tanrıkulu, Bahattin, Bakırcıoǧlu, Mehmet, Kaymakçalan, Hande, Caglayan, Ahmet Okay, Sencar, Leman, Ceyhun, Emre, Atik, A. Fatih, Bayri, Yaşar, Bai, Hanwen, Kolb, Luis E., Hebert, Ryan M., Omay, S. Bulent, Mishra-Gorur, Ketu, Choi, Murim, Overton, John D., Holland, Eric C., Mane, Shrikant, State, Matthew W., Bilgüvar, Kaya, Baehring, Joachim M., Gutin, Philip H., Piepmeier, Joseph M., Vortmeyer, Alexander, Brennan, Cameron W., Pamir, M. Necmettin, Kılıç, Türker, Lifton, Richard P., Noonan, James P., Yasuno, Katsuhito, Günel, Murat

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Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations by Lifton, Richard P, State, Matthew W, Günel, Murat, Bilgüvar, Kaya, Öztürk, Ali Kemal, Louvi, Angeliki, Kwan, Kenneth Y, Choi, Murim, Tatl, Burak, Yaln zo lu, Dilek, Tüysüz, Beyhan, Ça layan, Ahmet Okay, Gökben, Sarenur, Kaymakçalan, Hande, Barak, Tanyeri, Bak rc o lu, Mehmet, Yasuno, Katsuhito, Ho, Winson, Sanders, Stephan, Zhu, Ying, Y lmaz, Sanem, Dinçer, Alp, Johnson, Michele H, Bronen, Richard A, Koçer, Naci, Per, Hüseyin, Mane, Shrikant, Pamir, Mehmet Necmettin, Yalç nkaya, Cengiz, Kumanda, Sefer, Topçu, Meral, Özmen, Meral, Šestan, Nenad

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Common variant near the endothelin receptor type A (EDNRA) gene is associated with intracranial aneurysm risk by Yasuno, Katsuhito, Bakırcıoğlu, Mehmet, Low, Siew-Kee, Bilgüvar, Kaya, Gaál, Emília, Ruigrok, Ynte M, Niemelä, Mika, Hata, Akira, Bijlenga, Philippe, Kasuya, Hidetoshi, Jääskeläinen, Juha E, Krex, Dietmar, Auburger, Georg, Simon, Matthias, Krischek, Boris, Ozturk, Ali K, Mane, Shrikant, Rinkel, Gabriel J. E, Steinmetz, Helmuth, Hernesniemi, Juha, Schaller, Karl, Zembutsu, Hitoshi, Inoue, Ituro, Palotie, Aarno, Cambien, François, Nakamura, Yusuke, Lifton, Richard P, Günel, Murat

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Recessive loss of function of the neuronal ubiquitin hydrolase UCHL1 leads to early-onset progressive neurodegeneration by Bilguvar, Kaya, Tyagi, Navneet K., Ozkara, Cigdem, Tuysuz, Beyhan, Bakircioglu, Mehmet, Choi, Murim, Delil, Sakir, Caglayan, Ahmet O., Baranoski, Jacob F., Erturk, Ozdem, Yalcinkaya, Cengiz, Karacorlu, Murat, Dincer, Alp, Johnson, Michele H., Mane, Shrikant, Chandra, Sreeganga S., Louvi, Angeliki, Boggon, Titus J., Lifton, Richard P., Horwich, Arthur L., Gunel, Murat

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Somatic POLE mutations cause an ultramutated giant cell high-grade glioma subtype with better prognosis by Erson-Omay, E Zeynep, Çağlayan, Ahmet Okay, Schultz, Nikolaus, Weinhold, Nils, Omay, S Bülent, Özduman, Koray, Köksal, Yavuz, Li, Jie, Serin Harmancı, Akdes, Clark, Victoria, Carrión-Grant, Geneive, Baranoski, Jacob, Çağlar, Caner, Barak, Tanyeri, Coşkun, Süleyman, Baran, Burçin, Köse, Doğan, Sun, Jia, Bakırcıoğlu, Mehmet, Moliterno Günel, Jennifer, Pamir, M Necmettin, Mishra-Gorur, Ketu, Bilguvar, Kaya, Yasuno, Katsuhito, Vortmeyer, Alexander, Huttner, Anita J, Sander, Chris, Günel, Murat

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The Essential Role of Centrosomal NDE1 in Human Cerebral Cortex Neurogenesis by Bakircioglu, Mehmet, Carvalho, Ofélia P., Khurshid, Maryam, Cox, James J., Tuysuz, Beyhan, Barak, Tanyeri, Yilmaz, Saliha, Caglayan, Okay, Dincer, Alp, Nicholas, Adeline K., Quarrell, Oliver, Springell, Kelly, Karbani, Gulshan, Malik, Saghira, Gannon, Caroline, Sheridan, Eamonn, Crosier, Moira, Lisgo, Steve N., Lindsay, Susan, Bilguvar, Kaya, Gergely, Fanni, Gunel, Murat, Woods, C. Geoffrey

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Brain Malformations Associated With Knobloch Syndrome—Review of Literature, Expanding Clinical Spectrum, and Identification of Novel Mutations by Caglayan, Ahmet Okay, MD, Baranoski, Jacob F, Aktar, Fesih, MD, Han, Wengi, PhD, Tuysuz, Beyhan, MD, Guzel, Aslan, MD, Guclu, Bulent, MD, Kaymakcalan, Hande, MD, Aktekin, Berrin, MD, Akgumus, Gozde Tugce, MS, Murray, Phillip B., MS, Erson-Omay, Emine Z., PhD, Caglar, Caner, MS, Bakircioglu, Mehmet, MS, Sakalar, Yildirim Bayezit, MD, Guzel, Ebru, MD, Demir, Nihat, MD, Tuncer, Oguz, MD, Senturk, Senem, MD, Ekici, Baris, MD, Minja, Frank J., MD, Šestan, Nenad, Yasuno, Katsuhito, PhD, Bilguvar, Kaya, MD, Caksen, Huseyin, MD, Gunel, Murat, MD

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Longitudinal analysis of treatment-induced genomic alterations in gliomas by Erson-Omay, E Zeynep, Henegariu, Octavian, Omay, S Bülent, Harmancı, Akdes Serin, Youngblood, Mark W, Mishra-Gorur, Ketu, Li, Jie, Özduman, Koray, Carrión-Grant, Geneive, Clark, Victoria E, Çağlar, Caner, Bakırcıoğlu, Mehmet, Pamir, M Necmettin, Tabar, Viviane, Vortmeyer, Alexander O, Bilguvar, Kaya, Yasuno, Katsuhito, DeAngelis, Lisa M, Baehring, Joachim M, Moliterno, Jennifer, Günel, Murat

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Proximal Humerus Tumors: Higher-than-Expected Risk of Revision With Constrained Reverse Shoulder Arthroplasty by Ayvaz, Mehmet, Cetik, Riza Mert, Bakircioglu, Sancar, Tokgozoglu, A. Mazhar

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Management preferences of orthopedic surgeons in developmental dysplasia of the hip under 1 year of age in Türkiye: Results of a nationwide cross-sectional survey by Volkan Çetin, Baki, Bakırcıoğlu, Sancar, Çiftci, Sadettin, Salih Söylemez, Mehmet, Erkuş, Serkan, Turhan, Yalçın, Yalkın Çamurcu, İsmet, Duman, Serda, Yıldırım, Timur, Memişoğlu, Kaya, Şenaran, Hakan, Ömeroğlu, Hakan

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Closed versus medial open reduction in the treatment of developmental dysplasia of the hip under age 1: A retrospective comparative study by Bakircioglu, Sancar, Mert Cetik, Riza, Danisman, Murat, Askin, Mehmet, Abdulkadir Bulut, Muhammed, Yilmaz, Guney

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Osteochondral autograft transplantation of the femoral head in sequelae of developmental dysplasia of hip: A case report and review of the literature by Kaymaz, Burak, Bakırcıoğlu, Sancar, Yılmaz, Güney, Atay, Özgür Ahmet, Aksoy, Mehmet Cemalettin

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