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Duygu Duman
212  results:
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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/..
 
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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/..
 
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3

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/..
 
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4

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/..
 
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5

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/..
 
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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/..
 
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7

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/..
 
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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/..
 
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9

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/..
 
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10

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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11

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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12

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/..
 
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13

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/..
 
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14

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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15

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/..
 
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