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NARA Subscribed5
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Springer Nature5
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Human Genetics3
Journal of Molecular Medicine1
Molecular Genetics and Genomics1
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20191
20182
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20151
Guney Bademci results 5 · Newest (Page 1/1, per page 25)
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A truncating CLDN9 variant is associated with autosomal recessive nonsyndromic hearing lossNARA Subscribed
Human Genetics · 2019 · Vol. 138 · Issue 10 · Springer
Claire J. Sineni; Muzeyyen Yildirim-Baylan; Shengru Guo; Vladimir Camarena; Gaofeng Wang; Suna Tokgoz-Yilmaz; Duygu Duman; Guney Bademci; Mustafa Tekin
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Ripor2 is involved in auditory hair cell stereociliary bundle structure and orientationNARA Subscribed
Journal of Molecular Medicine · 2018 · Vol. 96 · Issue 11 · Springer
Oscar Diaz-Horta; Clemer Abad; Filiz Basak Cengiz; Guney Bademci; Pat Blackwelder; Katherina Walz; Mustafa Tekin
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MPZL2 is a novel gene associated with autosomal recessive nonsyndromic moderate hearing lossNARA Subscribed
Human Genetics · 2018 · Vol. 137 · Issue 6-7 · Springer
Guney Bademci; Clemer Abad; Armagan Incesulu; Abolfazl Rad; Ozgul Alper; Susanne M. Kolb; Filiz B. Cengiz; Oscar Diaz-Horta; Fatma Silan; Ercan Mihci; Emre Ocak; Maryam Najafi; Reza Maroofian; Elanur Yilmaz; Banu G. Nur; Duygu Duman; Shengru Guo; David W. Sant; Gaofeng Wang; Paula V. Monje; Thomas Haaf; Susan H. Blanton; Barbara Vona; Katherina Walz; Mustafa Tekin
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Spectrum of DNA variants for non-syndromic deafness in a large cohort from multiple continentsNARA Subscribed
Human Genetics · 2016 · Vol. 135 · Issue 8 · Springer
Denise Yan; Demet Tekin; Guney Bademci; Joseph Foster; F. Basak Cengiz; Abhiraami Kannan-Sundhari; Shengru Guo; Rahul Mittal; Bing Zou; Mhamed Grati; Rosemary I. Kabahuma; Mohan Kameswaran; Taye J. Lasisi; Waheed A. Adedeji; Akeem O. Lasisi; Ibis Menendez; Marianna Herrera; Claudia Carranza; Reza Maroofian; Andrew H. Crosby; Mariem Bensaid; Saber Masmoudi; Mahdiyeh Behnam; Majid Mojarrad; Yong Feng; Duygu Duman; Alex M. Mawla; Alex S. Nord; Susan H. Blanton; Xue Z. Liu; Mustafa Tekin
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Novel mutations confirm that COL11A2 is responsible for autosomal recessive non-syndromic hearing loss DFNB53NARA Subscribed
Molecular Genetics and Genomics · 2015 · Vol. 290 · Issue 4 · Springer
Imen Chakchouk; M’hamed Grati; Guney Bademci; Mariem Bensaid; Qi Ma; Amine Chakroun; Joseph Foster; Denise Yan; Duygu Duman; Oscar Diaz-Horta; Abdelmonem Ghorbel; Rahul Mittal; Amjad Farooq; Mustafa Tekin; Saber Masmoudi; Xue Zhong Liu
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