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Cengiz, Başak
179  results:
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1

Congenital defects of glycosylation: Novel presentations wi..:

İnci, Aslı ; Cengiz, Başak ; Biberoğlu, Gürsel...
American Journal of Medical Genetics Part A.  185 (2021)  9 - p. 2739-2747 , 2021
Link: https://doi.org/10.1002/..
 
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2

Dysfunction of GRAP, encoding the GRB2-related adaptor prot..:

Li, Chong ; Bademci, Guney ; Subasioglu, Asli...
Proceedings of the National Academy of Sciences of the United States of America.  116 (2019)  4 - p. 1347-1352 , 2019
Link: https://www.jstor.org/st..
 
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3

Dysfunction ofGRAP, encoding the GRB2-related adaptor prote..:

Li, Chong ; Bademci, Guney ; Subasioglu, Asli...
Proceedings of the National Academy of Sciences.  116 (2019)  4 - p. 1347-1352 , 2019
Link: https://doi.org/10.1073/..
 
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4

Identification of candidate gene FAM183A and novel pathogen..:

McSherry, Megan ; Masih, Katherine E. ; Elcioglu, Nursel H....
PLOS ONE.  13 (2018)  11 - p. e0208324 , 2018
Link: https://doi.org/10.1371/..
 
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5

Monosomy chromosome 21 compensated by 21q22.11q22.3 duplica..:

Su, Meng ; Benke, Paul J. ; Bademci, Guney...
Molecular Cytogenetics.  11 (2018)  1 - p. , 2018
Link: https://doi.org/10.1186/..
 
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6

Ripor2 is involved in auditory hair cell stereociliary bund..:

Diaz-Horta, Oscar ; Abad, Clemer ; Cengiz, Filiz Basak...
Journal of Molecular Medicine.  96 (2018)  11 - p. 1227-1238 , 2018
Link: https://doi.org/10.1007/..
 
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7

Dominant deafness–onychodystrophy syndrome caused by an ATP..:

Menendez, Ibis ; Carranza, Claudia ; Herrera, Mariana...
Clinical Case Reports.  5 (2017)  4 - p. 376-379 , 2017
Link: https://doi.org/10.1002/..
 
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8

Novel pathogenic variants underlie SLC26A4 -related hearing..:

Cengiz, Filiz Basak ; Yilmazer, Rasim ; Olgun, Levent...
International Journal of Pediatric Otorhinolaryngology.  101 (2017)  - p. 167-171 , 2017
Link: https://doi.org/10.1016/..
 
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9

Novel EYA1 variants causing Branchio-oto-renal syndrome:

Klingbeil, Kyle D. ; Greenland, Christopher M. ; Arslan, Selcuk...
International Journal of Pediatric Otorhinolaryngology.  98 (2017)  - p. 59-63 , 2017
Link: https://doi.org/10.1016/..
 
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10

Audiological findings in Noonan syndrome:

Tokgoz-Yilmaz, Suna ; Turkyilmaz, Meral Didem ; Cengiz, Filiz Basak...
International Journal of Pediatric Otorhinolaryngology.  89 (2016)  - p. 50-54 , 2016
Link: https://doi.org/10.1016/..
 
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11

Targeted Resequencing of Deafness Genes Reveals a FounderMY..:

Manzoli, Gabrielle N. ; Bademci, Guney ; Acosta, Angelina X....
Annals of Human Genetics.  80 (2016)  6 - p. 327-331 , 2016
Link: https://doi.org/10.1111/..
 
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12

ROR1 is essential for proper innervation of auditory hair c..:

Diaz-Horta, Oscar ; Abad, Clemer ; Sennaroglu, Levent...
Proceedings of the National Academy of Sciences of the United States of America.  113 (2016)  21 - p. 5993-5998 , 2016
Link: https://www.jstor.org/st..
 
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13

ROR1 is essential for proper innervation of auditory hair c..:

Diaz-Horta, Oscar ; Abad, Clemer ; Sennaroglu, Levent...
Proceedings of the National Academy of Sciences.  113 (2016)  21 - p. 5993-5998 , 2016
Link: https://doi.org/10.1073/..
 
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14

Comprehensive analysis via exome sequencing uncovers geneti..:

Bademci, Guney ; Foster II, Joseph ; Mahdieh, Nejat...
Genetics in Medicine.  18 (2016)  4 - p. 364-371 , 2016
Link: https://doi.org/10.1038/..
 
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15

Spectrum of DNA variants for non-syndromic deafness in a la..:

Yan, Denise ; Tekin, Demet ; Bademci, Guney...
Human Genetics.  135 (2016)  8 - p. 953-961 , 2016
Link: https://doi.org/10.1007/..
 
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