Works by Cengiz, F.


Results: 19
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    SLITRK6 mutations cause myopia and deafness in humans and mice.

    Published in:
    Journal of Clinical Investigation, 2013, v. 123, n. 5, p. 2094, doi. 10.1172/JCI65853
    By:
    • Tekin, Mustafa;
    • Chioza, Barry A.;
    • Yoshifumi Matsumoto;
    • Diaz-Horta, Oscar;
    • Cross, Harold E.;
    • Duygu Duman;
    • Kokotas, Haris;
    • Moore-Barton, Heather L.;
    • Kazuto Sakoori;
    • Maya Ota;
    • Yuri S. Odaka;
    • Foster II, Joseph;
    • Cengiz, F. Basak;
    • Suna Tokgoz-Yilmaz;
    • Oya Tekeli;
    • Grigoriadou, Maria;
    • Petersen, Michael B.;
    • Sreekantan-Nair, Ajith;
    • Gurtz, Kay;
    • Xia-Juan Xia
    Publication type:
    Article
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    Spectrum of DNA variants for non-syndromic deafness in a large cohort from multiple continents.

    Published in:
    Human Genetics, 2016, v. 135, n. 8, p. 953, doi. 10.1007/s00439-016-1697-z
    By:
    • Yan, Denise;
    • Tekin, Demet;
    • Bademci, Guney;
    • Foster, Joseph;
    • Cengiz, F.;
    • Kannan-Sundhari, Abhiraami;
    • Guo, Shengru;
    • Mittal, Rahul;
    • Zou, Bing;
    • Grati, Mhamed;
    • Kabahuma, Rosemary;
    • Kameswaran, Mohan;
    • Lasisi, Taye;
    • Adedeji, Waheed;
    • Lasisi, Akeem;
    • Menendez, Ibis;
    • Herrera, Marianna;
    • Carranza, Claudia;
    • Maroofian, Reza;
    • Crosby, Andrew
    Publication type:
    Article
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    Variations in Multiple Syndromic Deafness Genes Mimic Non-syndromic Hearing Loss.

    Published in:
    Scientific Reports, 2016, p. 31622, doi. 10.1038/srep31622
    By:
    • Bademci, G.;
    • Cengiz, F. B.;
    • Foster II, J.;
    • Duman, D.;
    • Sennaroglu, L.;
    • Diaz-Horta, O.;
    • Atik, T.;
    • Kirazli, T.;
    • Olgun, L.;
    • Alper, H.;
    • Menendez, I.;
    • Loclar, I.;
    • Sennaroglu, G.;
    • Tokgoz-Yilmaz, S.;
    • Guo, S.;
    • Olgun, Y.;
    • Mahdieh, N.;
    • Bonyadi, M.;
    • Bozan, N.;
    • Ayral, A.
    Publication type:
    Article