METAP1 mutation is a novel candidate for autosomal recessive intellectual disability by Caglayan, Ahmet Okay, Aktar, Fesih, Bilguvar, Kaya, Baranoski, Jacob F, Akgumus, Gozde Tugce, Harmanci, Akdes Serin, Erson-Omay, Emine Zeynep, Yasuno, Katsuhito, Caksen, Huseyin, Gunel, Murat

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NGLY1 mutation causes neuromotor impairment, intellectual disability, and neuropathy by Caglayan, Ahmet Okay, Comu, Sinan, Baranoski, Jacob F, Parman, Yesim, Kaymakçalan, Hande, Akgumus, Gozde Tugce, Caglar, Caner, Dolen, Duygu, Erson-Omay, Emine Zeynep, Harmanci, Akdes Serin, Mishra-Gorur, Ketu, Freeze, Hudson H, Yasuno, Katsuhito, Bilguvar, Kaya, Gunel, Murat

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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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Mutations inKATNB1Cause Complex Cerebral Malformations by Disrupting Asymmetrically Dividing Neural Progenitors by Mishra-Gorur, Ketu, Çaglayan, Ahmet Okay, Schaffer, Ashleigh E, Chabu, Chiswili, Henegariu, Octavian, Vonhoff, Fernando, Akgümüs, Gözde Tugce, Nishimura, Sayoko, Han, Wenqi, Tu, Shu, Baran, Burçin, Gümüs, Hakan, Dilber, Cengiz, Zaki, Maha S, Hossni, Heba AA, Rivière, Jean-Baptiste, Kayserili, Hülya, Spencer, Emily G, Rosti, Rasim Ö, Schroth, Jana, Per, Hüseyin, Çaglar, Caner, Çaglar, Çagri, Dölen, Duygu, Baranoski, Jacob F, Kumandas, Sefer, Minja, Frank J, Erson-Omay, E Zeynep, Mane, Shrikant M, Lifton, Richard P, Xu, Tian, Keshishian, Haig, Dobyns, William B, Chi, Neil C, Sestan, Nenad, Louvi, Angeliki, Bilgüvar, Kaya, Yasuno, Katsuhito, Gleeson, Joseph G, Günel, Murat

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Mutations in KATNB1 Cause Complex Cerebral Malformations by Disrupting Asymmetrically Dividing Neural Progenitors by Mishra-Gorur, Ketu, Çağlayan, Ahmet Okay, Schaffer, Ashleigh E, Chabu, Chiswili, Henegariu, Octavian, Vonhoff, Fernando, Akgümüş, Gözde Tuğce, Nishimura, Sayoko, Han, Wenqi, Tu, Shu, Baran, Burçin, Gümüş, Hakan, Dilber, Cengiz, Zaki, Maha S, Hossni, Heba A A, Rivière, Jean-Baptiste, Kayserili, Hülya, Spencer, Emily G, Rosti, Rasim Ö, Schroth, Jana, Per, Hüseyin, Çağlar, Caner, Çağlar, Çağri, Dölen, Duygu, Baranoski, Jacob F, Kumandaş, Sefer, Minja, Frank J, Erson-Omay, E Zeynep, Mane, Shrikant M, Lifton, Richard P, Xu, Tian, Keshishian, Haig, Dobyns, William B, Chi, Neil C, Šestan, Nenad, Louvi, Angeliki, Bilgüvar, Kaya, Yasuno, Katsuhito, Gleeson, Joseph G, Günel, Murat

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Mutations in KATNB1 Cause Complex Cerebral Malformations by Disrupting Asymmetrically Dividing Neural Progenitors by Mishra-Gorur, Ketu, Çağlayan, Ahmet Okay, Schaffer, Ashleigh E., Chabu, Chiswili, Henegariu, Octavian, Vonhoff, Fernando, Akgümüş, Gözde Tuğce, Nishimura, Sayoko, Han, Wenqi, Tu, Shu, Baran, Burçin, Gümüş, Hakan, Dilber, Cengiz, Zaki, Maha S., Hossni, Heba A.A., Rivière, Jean-Baptiste, Kayserili, Hülya, Spencer, Emily G., Rosti, Rasim Ö., Schroth, Jana, Per, Hüseyin, Çağlar, Caner, Çağlar, Çağri, Dölen, Duygu, Baranoski, Jacob F., Kumandaş, Sefer, Minja, Frank J., Erson-Omay, E. Zeynep, Mane, Shrikant M., Lifton, Richard P., Xu, Tian, Keshishian, Haig, Dobyns, William B., Chi, Neil C., Šestan, Nenad, Louvi, Angeliki, Bilgüvar, Kaya, Yasuno, Katsuhito, Gleeson, Joseph G., Günel, Murat

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Loss of Protocadherin‐12 Leads to Diencephalic‐Mesencephalic Junction Dysplasia Syndrome by Guemez‐Gamboa, Alicia, Çağlayan, Ahmet Okay, Stanley, Valentina, Gregor, Anne, Zaki, Maha S., Saleem, Sahar N., Musaev, Damir, McEvoy‐Venneri, Jennifer, Belandres, Denice, Akizu, Naiara, Silhavy, Jennifer L., Schroth, Jana, Rosti, Rasim Ozgur, Copeland, Brett, Lewis, Steven M., Fang, Rebecca, Issa, Mahmoud Y., Per, Huseyin, Gumus, Hakan, Bayram, Ayse Kacar, Kumandas, Sefer, Akgumus, Gozde Tugce, Erson‐Omay, Emine Z., Yasuno, Katsuhito, Bilguvar, Kaya, Heimer, Gali, Pillar, Nir, Shomron, Noam, Weissglas‐Volkov, Daphna, Porat, Yuval, Einhorn, Yaron, Gabriel, Stacey, Ben‐Zeev, Bruria, Gunel, Murat, Gleeson, Joseph G.

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Loss of Protocadherin‐12 L eads to D iencephalic‐ M esencephalic J unction D ysplasia S yndrome by Guemez‐Gamboa, Alicia, Çağlayan, Ahmet Okay, Stanley, Valentina, Gregor, Anne, Zaki, Maha S., Saleem, Sahar N., Musaev, Damir, McEvoy‐Venneri, Jennifer, Belandres, Denice, Akizu, Naiara, Silhavy, Jennifer L., Schroth, Jana, Rosti, Rasim Ozgur, Copeland, Brett, Lewis, Steven M., Fang, Rebecca, Issa, Mahmoud Y., Per, Huseyin, Gumus, Hakan, Bayram, Ayse Kacar, Kumandas, Sefer, Akgumus, Gozde Tugce, Erson‐Omay, Emine Z., Yasuno, Katsuhito, Bilguvar, Kaya, Heimer, Gali, Pillar, Nir, Shomron, Noam, Weissglas‐Volkov, Daphna, Porat, Yuval, Einhorn, Yaron, Gabriel, Stacey, Ben‐Zeev, Bruria, Gunel, Murat, Gleeson, Joseph G.

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