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Hamìt Özyürek

Ondokuz Mayis University

14H指数
75论文数
1.4K被引数
收录论文 9
发表时间
Joubert syndrome: a model for untangling recessive disorders with extreme genetic heterogeneity
err2015-06-19
err227
errOAAI
errBachmann-Gagescu, R.; Dempsey, J. C.; Phelps, I. G.; O'Roak, B. J.; Knutzen, D. M.; Rue, T. C.; Ishak, G. E.; Isabella, C. R.; Gorden, N.; Adkins, J.; Boyle, E. A.; de Lacy, N.; O'Day, D.; Alswaid, A.; Ramadevi, Radha A.; Lingappa, L.; Lourenco, C.; Martorell, L.; Garcia-Cazorla, A.; Ozyurek, H.; Haliloglu, G.; Tuysuz, B.; Topcu, M.; Chance, P.; Parisi, M. A.; Glass, I. A.; Shendure, J.; Doherty, D.
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Charles Bonnet Syndrome After Herpes Simplex Encephalitis
err2012-04-01
err4
PREAI
errAydin, Omer Faruk; Ince, Hulya; Tasdemir, Haydar Ali; Ozyurek, Hamit
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The relationship between migraine and right-to-left shunt in children
err2010-09-28
err4
PREAI
errSarisoy, Sevcan; Aydin, Omer Faruk; Sungur, Metin; Bayrak, Ilkay Koray; Aker, Servet; Ozyurek, Hamit; Tasdemir, Haydar Ali; Baysal, Kemal
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Mutations in 3 genes (MKS3, CC2D2A and RPGRIP1L) cause COACH syndrome (Joubert syndrome with congenital hepatic fibrosis)
err2009-07-01
err126
errOAAI
errDoherty, D.; Parisi, M. A.; Finn, L. S.; Gunay-Aygun, M.; Al-Mateen, M.; Bates, D.; Clericuzio, C.; Demir, H.; Dorschner, M.; van Essen, A. J.; Gahl, W. A.; Gentile, M.; Gorden, N. T.; Hikida, A.; Knutzen, D.; Ozyurek, H.; Phelps, I.; Rosenthal, P.; Verloes, A.; Weigand, H.; Chance, P. F.; Dobyns, W. B.; Glass, I. A.
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Establishment of interdisciplinary child protection teams in Turkey 2002-2006: Identifying the strongest link can make a difference!
err2009-04-01
err31
PREAI
errAgirtan, Canan A.; Akar, Taner; Akbas, Seher; Akdur, Recep; Aydin, Cahide; Aytar, Gulsen; Ayyildiz, Suat; Baskan, Sevgi; Belgemen, Tugba; Bezirci, Ozdecan; Beyazova, Ufuk; Beyaztas, Fatma Yucel; Buken, Bora; Buken, Erhan; Camurdan, Aysu D.; Can, Demet; Canbaz, Sevgi; Canturk, Gurol; Ceyhan, Meltem; Coskun, Abdulhakim; Celik, Ahmet; Cetin, Fusun C.; Coskun, Ayse Gul; Dagcinar, Adnan; Dallar, Yildiz; Demirel, Birol; Demirogullari, Billur; Derman, Orhan; Dilli, Dilek; Ersahin, Yusuf; Esiyok, Burcu; Evinc, Gulin; Gencer, Ozlem; Gokler, Bahar; Hanci, Hamit; Iseri, Elvan; Isir, Aysun Baransel; Isiten, Nukhet; Kale, Gulsev; Karadag, Ferda; Kanbur, Nuray; Kilic, Birim; Kultur, Ebru; Kurtay, Derya; Kuruoglu, Asli; Miral, Suha; Odabasi, Aysun B.; Oral, Resmiye; Orhon, Filiz Simsek; Ozbesler, Cengiz; Ozdemir, Dilsad Foto; Ozkok, M. Selim; Ozmert, Elif; Oztop, Didem B.; Ozyurek, Hamit; Pasli, Figen; Peksen, Yildiz; Polat, Onur; Sabin, Figen; Sabin, Ahmet Rifat; Salacin, Serpil; Suskan, Emine; Tander, Burak; Tekin, Deniz; Teksam, Ozlern; Tiras, Ulku; Tomak, Yilmaz; Tumer, Ali Riza; Turla, Ahmet; Ulukol, Betul; Uslu, Runa; Tas, Fatma V.; Vatandas, Nilgun; Velipasaoglu, Sevtap; Yagmur, Fatih; Yagmurlu, Aydin; Yalcin, Songul; Yavuz, Sukruye; Yurdakok, Kadriye
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CC2D2A Is Mutated in Joubert Syndrome and Interacts with the Ciliopathy-Associated Basal Body Protein CEP290
err2008-11-01
err214
errOAAI
errGorden, Nicholas T.; Arts, Heleen H.; Parisi, Melissa A.; Coene, Karlien L. M.; Letteboer, Stef J. F.; van Beersum, Sylvia E. C.; Mans, Dorus A.; Hikida, Abigail; Eckert, Melissa; Knutzen, Dana; Alswaid, Abdulrahman F.; Ozyurek, Hamit; Dibooglu, Sel; Otto, Edgar A.; Liu, Yangfan; Davis, Erica E.; Hutter, Carolyn M.; Bammler, Theo K.; Farin, Frederico M.; Dorschner, Michael; Topcu, Meral; Zackai, Elaine H.; Rosenthal, Phillip; Owens, Kelly N.; Katsanis, Nicholas; Vincent, John B.; Hildebrandt, Friedhelm; Rubel, Edwin W.; Raible, David W.; Knoers, Nine V. A. M.; Chance, Phillip F.; Roepman, Ronald; Moens, Cecilia B.; Glass, Ian A.; Doherty, Dan
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Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome
err2007-06-10
err286
PREAI
errArts, Heleen H.; Doherty, Dan; van Beersum, Sylvia E. C.; Parisi, Melissa A.; Letteboer, Stef J. F.; Gorden, Nicholas T.; Peters, Theo A.; Maerker, Tina; Voesenek, Krysta; Kartono, Aileen; Ozyurek, Hamit; Farin, Federico M.; Kroes, Hester Y.; Wolfrum, Uwe; Brunner, Han G.; Cremers, Frans P. M.; Glass, Ian A.; Knoers, Nine V. A. M.; Roepman, Ronald
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Rare association of Hirschsprung's disease and Joubert syndrome
err2007-05-22
err10
PREAI
errOzyurek, Hamit; Kayacik, Ozlem Eroglu; Gungor, Olcay; Karagoz, Filiz
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