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Duygu Duman
213
results:
Search for persons
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Format
Online (213)
Mediatypes
Articles (Online) (87)
Bookchapter (Online) (1)
OpenAccess-fulltext (125)
Languages
english (177)
Sorted by: Relevance
Sorted by: Year
?
1
Genetic heterogeneity in hereditary hearing loss: Potential..:
Ramzan, Memoona
;
Zafeer, Mohammad Faraz
;
Abad, Clemer
...
European Journal of Human Genetics. 32 (2024) 6 - p. 639-646 , 2024
Link:
https://doi.org/10.1038/..
?
2
Identification of novel MYH14 variants in families with aut..:
Duman, Duygu
;
Ramzan, Memoona
;
Subasioglu, Asli
...
American Journal of Medical Genetics Part A. 194 (2024) 6 - p. , 2024
Link:
https://doi.org/10.1002/..
?
3
Genome sequencing identifies coding and non-coding variants..:
Ramzan, Memoona
;
Duman, Duygu
;
Hendricks, LeShon Chere Peart
...
Journal of Human Genetics. 68 (2023) 10 - p. 657-669 , 2023
Link:
https://doi.org/10.1038/..
?
4
Novel GPR156 variants confirm its role in moderate sensorin..:
Ramzan, Memoona
;
Bozan, Nazim
;
Seyhan, Serhat
...
Scientific Reports. 13 (2023) 1 - p. , 2023
Link:
https://doi.org/10.1038/..
?
5
Dispersed DNA variants underlie hearing loss in South Flori..:
Peart, LéShon
;
Gonzalez, Joanna
;
Morel Swols, Dayna
...
Human Genomics. 17 (2023) 1 - p. , 2023
Link:
https://doi.org/10.1186/..
?
6
Mutations inMINAR2encoding membrane integral NOTCH2-associa..:
Bademci, Guney
;
Lachgar-Ruiz, María
;
Deokar, Mangesh
...
Proceedings of the National Academy of Sciences. 119 (2022) 26 - p. , 2022
Link:
https://doi.org/10.1073/..
?
7
Novel variant p.E269K confirms causative role of PLS1 mutat..:
Diaz‐Horta, Oscar
;
Bademci, Guney
;
Tokgoz‐Yilmaz, Suna
...
Clinical Genetics. 96 (2019) 6 - p. 575-578 , 2019
Link:
https://doi.org/10.1111/..
?
8
A truncating CLDN9 variant is associated with autosomal rec..:
Sineni, Claire J.
;
Yildirim-Baylan, Muzeyyen
;
Guo, Shengru
...
Human Genetics. 138 (2019) 10 - p. 1071-1075 , 2019
Link:
https://doi.org/10.1007/..
?
9
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..
?
10
Adams–Oliver syndrome caused by mutations ofthe EOGT gene:
Schröder, Kim C.
;
Duman, Duygu
;
Tekin, Mustafa
...
American Journal of Medical Genetics Part A. 179 (2019) 11 - p. 2246-2251 , 2019
Link:
https://doi.org/10.1002/..
?
11
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/..
?
12
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/..
?
13
Elucidating the genetic architecture of Adams-Oliver syndro..:
Meester, Josephina A.N.
;
Sukalo, Maja
;
Schröder, Kim C.
...
Human Mutation. 39 (2018) 9 - p. 1246-1261 , 2018
Link:
https://doi.org/10.1002/..
?
14
MPZL2 is a novel gene associated with autosomal recessive n..:
Bademci, Guney
;
Abad, Clemer
;
Incesulu, Armagan
...
Human Genetics. 137 (2018) 6-7 - p. 479-486 , 2018
Link:
https://doi.org/10.1007/..
?
15
FOXF2is required for cochlear development in humans and mic:
Bademci, Guney
;
Abad, Clemer
;
Incesulu, Armagan
...
Human Molecular Genetics. 28 (2018) 8 - p. 1286-1297 , 2018
Link:
https://doi.org/10.1093/..
1-15